FN Thomson Reuters Web of Science™
VR 1.0
PT J
AU Pope, C
North-Lee, B
Davis, B
AF Pope, Charlene
North-Lee, Bertha
Davis, Boyd
TI Dropped Cues in Patient-Physician Interactions: How Discourse Analysis
Finds Areas for Coaching
SO INTERNATIONAL JOURNAL OF QUALITATIVE METHODS
LA English
DT Meeting Abstract
C1 [Pope, Charlene; North-Lee, Bertha] Ralph H Johnson VA Med Ctr, Charleston, SC USA.
[Davis, Boyd] Univ North Carolina Charlotte, Charlotte, NC USA.
NR 0
TC 0
Z9 0
U1 4
U2 4
PU SAGE PUBLICATIONS INC
PI THOUSAND OAKS
PA 2455 TELLER RD, THOUSAND OAKS, CA 91320 USA
SN 1609-4069
J9 INT J QUAL METH
JI Int. J. Qual. Meth.
PD DEC
PY 2017
VL 16
IS 1
PG 1
WC Social Sciences, Interdisciplinary
SC Social Sciences - Other Topics
GA EL7CA
UT WOS:000394777500099
ER
PT J
AU Salazar, R
Dwivedi, AK
Royall, DR
AF Salazar, Ricardo
Dwivedi, Alok Kumar
Royall, Donald R.
TI Cross-Ethnic Differences in the Severity of Neuropsychiatric Symptoms in
Persons With Mild Cognitive Impairment and Alzheimer's Disease
SO JOURNAL OF NEUROPSYCHIATRY AND CLINICAL NEUROSCIENCES
LA English
DT Article
ID BRIEF CLINICAL FORM; MEXICAN-AMERICANS; NPI-Q; DEMENTIA; HISPANICS;
PREVALENCE; DEPRESSION; POPULATION; VALIDATION; INVENTORY
AB In this cross-sectional study, we examined the neuropsychiatric profile of mild cognitive impairment (MCI) and Alzheimer's disease (AD) using the Neuropsychiatric Inventory Questionnaire (NPI-Q). Data were available on 875 controls, 339 MCI cases, and 975 AD participants. Surprisingly, differences in neuropsychiatric symptom (NPS) severity by ethnicity in subjects with AD, but not with MCI, were found. More so, in Hispanics with AD, a higher frequency in most of the individual NPI-Q symptom items of the scale was observed, except for apathy. After adjustment for clinical features, some individual NPI-Q symptoms also showed an association with Hispanic ethnicity in the control group that nearly reached statistical significance. There may be cross-ethnic differences in the neuropsychiatric presentation of AD in Hispanics versus non-Hispanic whites. Future studies are needed to clarify the etiology of these differences, and to assess the need for ethnicity-specific treatment and care-giving interventions.
C1 [Salazar, Ricardo] Texas Tech Univ Hlth Sci Ctr El Paso, Div Geriatr Psychiat & Behav Neurosci, Dept Psychiat, El Paso, TX 79905 USA.
Texas Tech Univ Hlth Sci Ctr El Paso, Paul L Foster Sch Med, El Paso, TX 79905 USA.
Texas Tech Univ Hlth Sci Ctr El Paso, Paul L Foster Sch Med, Dept Biomed Sci, Div Biostat & Epidemiol, El Paso, TX 79905 USA.
Texas Tech Univ Hlth Sci Ctr El Paso, Biostat & Epidemiol Consulting Lab, El Paso, TX 79905 USA.
Univ Texas Hlth Sci Ctr San Antonio, Dept Psychiat & Behav Med, San Antonio, TX 78229 USA.
Univ Texas Hlth Sci Ctr San Antonio, Depts Med Family & Community Med, San Antonio, TX 78229 USA.
South Texas Vet Hlth Care Syst, GRECC, San Antonio, TX USA.
RP Salazar, R (reprint author), Texas Tech Univ Hlth Sci Ctr El Paso, Div Geriatr Psychiat & Behav Neurosci, Dept Psychiat, El Paso, TX 79905 USA.
FU Texas Alzheimer's Research and Care Consortium (TARCC) - state of Texas
through the Texas Council on Alzheimer's Disease and Related Disorders
FX This study was made possible by the Texas Alzheimer's Research and Care
Consortium (TARCC) funded by the state of Texas through the Texas
Council on Alzheimer's Disease and Related Disorders.
NR 41
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U1 42
U2 42
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 0895-0172
EI 1545-7222
J9 J NEUROPSYCH CLIN N
JI J. Neuropsychiatr. Clin. Neurosci.
PD WIN
PY 2017
VL 29
IS 1
BP 13
EP 21
DI 10.1176/appi.neuropsych.15120423
PG 9
WC Clinical Neurology; Neurosciences; Psychiatry
SC Neurosciences & Neurology; Psychiatry
GA EP0WO
UT WOS:000397107600003
PM 27417070
ER
PT J
AU Turgeman, L
May, JH
Sciulli, R
AF Turgeman, Lior
May, Jerrold H.
Sciulli, Roberta
TI Insights from a machine learning model for predicting the hospital
Length of Stay (LOS) at the time of admission
SO EXPERT SYSTEMS WITH APPLICATIONS
LA English
DT Article
DE Cubist decision tree; Continuous association rule mining algorithm
(CARMA); Support vector machine (SVM); Decision function; Error
distribution; Length of Stay (LOS)
ID CONGESTIVE-HEART-FAILURE; PHASE-TYPE DISTRIBUTIONS; ELDERLY PATIENTS;
READMISSION; MORTALITY; SURVIVAL; ANEMIA; ADULTS; COSTS; COPD
AB A model that accurately predicts, at the time of admission, the Length of Stay (LOS) for hospitalized patients could be an effective tool for healthcare providers. It could enable early interventions to prevent complications, enabling more efficient utilization of manpower and facilities in hospitals. In this study, we apply a regression tree (Cubist) model for predicting the LOS, based on static inputs, that is, values that are known at the time of admission and that do not change during patient's hospital stay. The model was trained and validated on de-identified administrative data from the Veterans Health Administration (VHA) hospitals in Pittsburgh, PA. We chose to use a Cubist model because it produced more accurate predictions than did alternative techniques. In addition, tree models enable us to examine the classification rules learned from the data, in order to better understand the factors that are most correlated with hospital LOS. Cubist recursively partitions the data set as it estimates linear regressions for each partition, and the error level differs for different partitions, so that it is possible to deduce what are the characteristics of patients whose LOS can be accurately predicted at admission, and what are the characteristics of patients for whom the LOS estimate at that point in time is more highly uncertain. For example, our model indicates that the prediction error is greater for patients who had more admissions in the recent past, and for those who had longer previous hospital stays. Our approach suggests that mapping the cases into a higher dimensional space, using a Radial Basis Function (RBF) kernel, helps to separate them by their level of Cubist error, using a Support Vector Machine (SVM). (C) 2017 Elsevier Ltd. All rights reserved.
C1 [Turgeman, Lior; May, Jerrold H.] Univ Pittsburgh, Joseph M Katz Grad Sch Business, Mervis Hall, Pittsburgh, PA 15260 USA.
[Sciulli, Roberta] Vet Affairs Pittsburgh Healthcare Syst, Vet Engn Resource Ctr, Pittsburgh, PA 15215 USA.
RP Turgeman, L (reprint author), IBM Res, Univ Haifa Campus, Haifa, Israel.
EM tur.lior@gmail.com; jerrymay@katz.pitt.edu; RLS150@PITT.EDU
FU U.S. Department of Veterans Affairs [VA244-13-C-0581, VA240-14-D-0038];
University of Pittsburgh
FX This work was supported by the U.S. Department of Veterans Affairs,
through master contract numbers VA244-13-C-0581 and VA240-14-D-0038 with
the University of Pittsburgh. This work is an outcome of a continuing
partnership between the Katz Graduate School of Business and the
Pittsburgh Veterans Engineering Resource Center (VERC). Inpatient
admissions data were pulled from the VA corporate data warehouse by Dr.
Youxu C. Tjader. We thank the RRTICT project group of the Pittsburgh
Veterans Engineering Resource Center (VERC) for helpful discussions.
NR 52
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U2 11
PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0957-4174
EI 1873-6793
J9 EXPERT SYST APPL
JI Expert Syst. Appl.
PD JUL 15
PY 2017
VL 78
BP 376
EP 385
DI 10.1016/j.eswa.2017.02.023
PG 10
WC Computer Science, Artificial Intelligence; Engineering, Electrical &
Electronic; Operations Research & Management Science
SC Computer Science; Engineering; Operations Research & Management Science
GA ER5XK
UT WOS:000398877400027
ER
PT J
AU Lynn, DD
Zukin, LM
Dellavalle, R
AF Lynn, Darren D.
Zukin, Leonid M.
Dellavalle, Robert
TI The safety and efficacy of Diphoterine for ocular and cutaneous burns in
humans
SO CUTANEOUS AND OCULAR TOXICOLOGY
LA English
DT Review
DE Prevor; amphoteric; chemical burn; alkaloid burn; acid burn
ID DECONTAMINATION SOLUTION; SPLASH DECONTAMINATION; ACTIVE
DECONTAMINATION; EMERGENCY TREATMENT; CHEMICAL SPLASHES; EYE BURNS; SKIN
AB Context: Diphoterine, developed by the French company Prevor, is a polyvalent, chelating, amphoteric and slightly hypertonic solution used in the management of chemical cutaneous and ocular burns. While used extensively in Europe and Canada, it is has not been approved by the United States Occupational Safety and Health Administration (OSHA) as an alternative to the water-rinse method due to a lack of evidence of its safety and efficacy on human subjects. An unbiased and extensive systematic review was undertaken in order to better understand Diphoterine's safety and efficaciousness on humans.Objective: Review the safety and efficacy of Diphoterine for treating chemical burns of the skin and eyes in humans.Methods: Data sources: Information sources included Pubmed, the National Library of Medicine's Medline Database and the Publications sections of the Prevor website. Search terms included Diphoterine, chemical burn, ocular burn and cutaneous burn. Study selection: Any study type published through a peer-reviewed journal up to May 2016 was considered eligible. Published data must have included Diphoterine in the treatment of chemical burns on the skin or eyes as well as meet other specified criteria. Acceptable studies had to use either a quantitative (e.g. number of work days lost) or qualitative (e.g. level of erythema) approach when measuring cutaneous or ocular lesion outcomes. Data extraction: Independent assessment of article inclusion by two authors using predefined criteria.Results and Conclusion: Diphoterine is safe and highly effective in improving healing time, healing sequelae and pain management of chemical burns on the skin and eyes of humans. Outcomes are significantly improved when compared to water or a physiologic solution equivalent. We recommend that this product be readily available to emergency responders and companies that expose their employees to hazardous chemical substances in order to improve healing sequelae, pain management and lost work days from these types of burns.
C1 [Lynn, Darren D.] Univ Colorado, Denver Sch Med, Dept Dermatol, Anschutz Med Campus, Aurora, CO 80045 USA.
[Zukin, Leonid M.] Univ Colorado, Denver Sch Med, Dept Opthamol, Aurora, CO USA.
[Dellavalle, Robert] US Dept Vet Affairs, Eastern Colorado Hlth Care Syst, Dermatol Serv, Denver, CO USA.
RP Lynn, DD (reprint author), Univ Colorado, Denver Sch Med, Dept Dermatol, Anschutz Med Campus, Aurora, CO 80045 USA.
EM darren.lynn@ucdenver.edu
NR 17
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U1 0
U2 0
PU TAYLOR & FRANCIS LTD
PI ABINGDON
PA 2-4 PARK SQUARE, MILTON PARK, ABINGDON OR14 4RN, OXON, ENGLAND
SN 1556-9527
EI 1556-9535
J9 CUTAN OCUL TOXICOL
JI Cutan. Ocul. Toxicol.
PD JUN
PY 2017
VL 36
IS 2
BP 185
EP 192
DI 10.1080/15569527.2016.1217423
PG 8
WC Ophthalmology; Toxicology
SC Ophthalmology; Toxicology
GA ES4JV
UT WOS:000399501400015
PM 27486965
ER
PT J
AU Krivinko, JM
Erickson, SL
Abrahamson, EE
Wills, ZP
Ikonomovic, MD
Penzes, P
Sweet, RA
AF Krivinko, Josh M.
Erickson, Susan L.
Abrahamson, Eric E.
Wills, Zachary P.
Ikonomovic, Milos D.
Penzes, Peter
Sweet, Robert A.
TI Kalirin reduction rescues psychosis-associated behavioral deficits in
APPswe/PSEN1dE9 transgenic mice
SO NEUROBIOLOGY OF AGING
LA English
DT Article
DE Psychosis; Alzheimer disease; Kalirin
ID AMYLOID PRECURSOR PROTEIN; PLACEBO-CONTROLLED TRIALS; INCREASED FAMILIAL
RISK; ALZHEIMERS-DISEASE; MOUSE MODEL; COGNITIVE IMPAIRMENT;
PSYCHOLOGICAL SYMPTOMS; P21-ACTIVATED KINASES; PREPULSE INHIBITION;
MENTAL-RETARDATION
AB Psychosis in Alzheimer's disease (AD+P) represents a distinct clinical and neurobiological AD phenotype and is associated with more rapid cognitive decline, higher rates of abnormal behaviors, and increased caregiver burden compared with AD without psychosis. On a molecular level, AD+P is associated with greater reductions in the protein kalirin, a guanine exchange factor which has also been linked to the psychotic disease, schizophrenia. In this study, we sought to determine the molecular and behavioral consequences of kalirin reduction in APPswe/PSEN1dE9 mice. We evaluated mice with and without kalirin reduction during tasks measuring psychosis-associated behaviors and spatial memory. We found that kalirin reduction in APPswe/PSEN1dE9 mice significantly attenuated psychosis-associated behavior at 12 months of age without changing spatial memory performance. The 12-month-old APPswe/PSEN1dE9 mice with reduced kalirin levels also had increased levels of the active, phosphorylated forms of p21 protein (Cdc42/Rac) eactivated kinases (PAKs), which function in signaling pathways for maintenance of dendritic spine density, morphology, and function. Published by Elsevier Inc.
C1 [Krivinko, Josh M.; Erickson, Susan L.; Ikonomovic, Milos D.; Sweet, Robert A.] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA USA.
[Abrahamson, Eric E.; Ikonomovic, Milos D.; Sweet, Robert A.] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15261 USA.
[Wills, Zachary P.] Univ Pittsburgh, Sch Med, Dept Neurobiol, Pittsburgh, PA USA.
[Ikonomovic, Milos D.] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA USA.
[Penzes, Peter] Northwestern Univ, Dept Physiol, Feinberg Sch Med, Chicago, IL 60611 USA.
[Penzes, Peter] Northwestern Univ, Dept Psychiat & Behav Sci, Feinberg Sch Med, Chicago, IL 60611 USA.
[Sweet, Robert A.] VA Pittsburgh Healthcare Syst, Mental Illness Res Educ & Clin Ctr, Pittsburgh, PA USA.
RP Sweet, RA (reprint author), Biomed Sci Tower,Rm W-1645,3811 OHara St, Pittsburgh, PA 15213 USA.
EM sweetra@upmc.edu
FU [BX000452]; [MH071533]; [AG014449]; [MH071316]; [MH097216];
[MH107966]
FX The authors would like to thank Dr. Patrick Murray for his input on the
design of the experiments and Dr. Floh Thiels for her input on the
behavioral test battery. All behavioral testing was conducted in the
Rodent Behavioral Assessment Core in the Department of Neurobiology at
the University of Pittsburgh. This work was supported by grants BX000452
(R.A.S.), MH071533 (R.A.S.), AG014449 (M.D.I.), MH071316 (P.P.),
MH097216 (P.P.), and MH107966 (Z.W.). The content is solely the
responsibility of the authors and does not necessarily represent the
official views of the National Institute of Mental Health, the National
Institutes of Health, the Department of Veterans Affairs, or the United
States Government.
NR 63
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U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0197-4580
EI 1558-1497
J9 NEUROBIOL AGING
JI Neurobiol. Aging
PD JUN
PY 2017
VL 54
BP 59
EP 70
DI 10.1016/j.neurobiolaging.2017.02.006
PG 12
WC Geriatrics & Gerontology; Neurosciences
SC Geriatrics & Gerontology; Neurosciences & Neurology
GA ES4JZ
UT WOS:000399501800007
PM 28319837
ER
PT J
AU Geerling, JC
Yokota, S
Rukhadze, I
Roe, D
Chamberlin, NL
AF Geerling, Joel C.
Yokota, Shigefumi
Rukhadze, Irma
Roe, Dan
Chamberlin, Nancy L.
TI Kolliker-Fuse GABAergic and glutamatergic neurons project to distinct
targets
SO JOURNAL OF COMPARATIVE NEUROLOGY
LA English
DT Article
DE respiratory; whisking; FoxP2; trigeminal; parabrachial; PBel; RRID:
AB_10015246; RRID: AB_2107107; RRID: AB_2107133
ID VENTRAL RESPIRATORY GROUP; PARABRACHIAL NUCLEUS; BRAIN-STEM; LATERAL
LEMNISCUS; TOPOGRAPHIC ORGANIZATION; EFFERENT CONNECTIONS; FOXP2
EXPRESSION; PHRENIC NUCLEUS; RAT; MATH1
AB The Kolliker-Fuse nucleus (KF) is known primarily for its respiratory function as the "pneumotaxic center" or 'pontine respiratory group." Considered part of the parabrachial (PB) complex, KF contains glutamatergic neurons that project to respiratory-related targets in the medulla and spinal cord (Yokota, Oka, Tsumori, Nakamura, & Yasui, 2007). Here we describe an unexpected population of neurons in the caudal KF and adjacent lateral crescent subnucleus (PBlc), which are -aminobutyric acid (GABA)ergic and have an entirely different pattern of projections than glutamatergic KF neurons. First, immunofluorescence, in situ hybridization, and Cre-reporter labeling revealed that many of these GABAergic neurons express FoxP2 in both rats and mice. Next, using Cre-dependent axonal tracing in Vgat-IRES-Cre and Vglut2-IRES-Cre mice, we identified different projection patterns from GABAergic and glutamatergic neurons in this region. GABAergic neurons in KF and PBlc project heavily and almost exclusively to trigeminal sensory nuclei, with minimal projections to cardiorespiratory nuclei in the brainstem, and none to the spinal cord. In contrast, glutamatergic KF neurons project heavily to the autonomic, respiratory, and motor regions of the medulla and spinal cord previously identified as efferent targets mediating KF cardiorespiratory effects. These findings identify a novel, GABAergic subpopulation of KF/PB neurons with a distinct efferent projection pattern targeting the brainstem trigeminal sensory system. Rather than regulating breathing, we propose that these neurons influence vibrissal sensorimotor function.
C1 [Geerling, Joel C.; Yokota, Shigefumi; Rukhadze, Irma; Roe, Dan; Chamberlin, Nancy L.] Beth Israel Deaconess Med Ctr, Dept Neurol, 330 Brookline Ave, Boston, MA 02215 USA.
[Geerling, Joel C.; Yokota, Shigefumi; Rukhadze, Irma; Roe, Dan; Chamberlin, Nancy L.] Harvard Med Sch, Boston, MA USA.
[Geerling, Joel C.; Rukhadze, Irma; Chamberlin, Nancy L.] Beth Israel Deaconess Med Ctr, Div Sleep Med, Boston, MA 02215 USA.
[Geerling, Joel C.] Univ Iowa Hosp & Clin, Dept Neurol, Iowa City, IA 52242 USA.
[Yokota, Shigefumi] Shimane Univ, Sch Med, Dept Anat & Morphol Neurosci, Izumo, Shimane, Japan.
[Rukhadze, Irma] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Rukhadze, Irma] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
RP Geerling, JC; Chamberlin, NL (reprint author), Beth Israel Deaconess Med Ctr, Dept Neurol, 330 Brookline Ave, Boston, MA 02215 USA.
EM jgeerlin@bidmc.harvard.edu; nchamber@bidmc.harvard.edu
OI Geerling, Joel/0000-0001-9956-4006
FU National Institutes of Health [P01 HL095491, NS070682]
FX National Institutes of Health, Grant/Award Numbers: P01 HL095491 (to
N.L.C.) and R25 #NS070682 (to J.C.G.).
NR 59
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Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0021-9967
EI 1096-9861
J9 J COMP NEUROL
JI J. Comp. Neurol.
PD JUN 1
PY 2017
VL 525
IS 8
BP 1844
EP 1860
DI 10.1002/cne.24164
PG 17
WC Neurosciences; Zoology
SC Neurosciences & Neurology; Zoology
GA ER2JL
UT WOS:000398620100006
PM 28032634
ER
PT J
AU Xu, DH
Zhu, ZW
Xiao, HP
Wakefield, MR
Bai, Q
Nicholl, MB
Ding, VA
Fang, YJ
AF Xu, Dixon H.
Zhu, Ziwen
Xiao, Huaping
Wakefield, Mark R.
Bai, Qian
Nicholl, Michael B.
Ding, Vivi A.
Fang, Yujiang
TI Unveil the mysterious mask of cytokine-based immunotherapy for melanoma
SO CANCER LETTERS
LA English
DT Review
DE Cytokine; Melanoma; Immunotherapy
ID CD8(+) T-CELLS; DIFFERENTIATION-ASSOCIATED GENE-7; DOSE RECOMBINANT
INTERLEUKIN-2; ACTIVATED KILLER-CELLS; INHIBITS TUMOR-GROWTH; LONG-TERM
SURVIVAL; METASTATIC MELANOMA; MALIGNANT-MELANOMA; NK CELLS;
ANTITUMOR-ACTIVITY
AB Melanoma is the leading cause of death among all skin cancers and its incidence continues to rise rapidly worldwide in the past decades. The available treatment options for melanoma remain limited despite extensive clinical research. Melanoma is an immunogenic tumor and great advances in immunology in recent decades allow for the development of immunotherapeutic agents against melanoma. In recent years, immunotherapy utilizing cytokines has been particularly successful in certain cancers and holds promise for patients with advanced melanoma. In this review, an overview of the current status and emerging perspectives on cytokine immunotherapy for melanoma are discussed in details. Such a study will be helpful to unveil the mysterious mask of cytokine-based immunotherapy for melanoma. (C) 2017 Elsevier B.V. All rights reserved.
C1 [Xu, Dixon H.; Xiao, Huaping; Ding, Vivi A.; Fang, Yujiang] Des Moines Univ, Dept Microbiol Immunol & Pathol, Des Moines, IA 50312 USA.
[Zhu, Ziwen; Wakefield, Mark R.; Bai, Qian; Fang, Yujiang] Univ Missouri, Sch Med, Dept Surg, Columbia, MO 65212 USA.
[Xiao, Huaping] Xiangnan Univ, Affiliated Hosp, Chenzhou, Hunan, Peoples R China.
[Nicholl, Michael B.] South Texas Vet Hlth Care Syst, San Antonio, TX 78229 USA.
RP Fang, YJ (reprint author), Des Moines Univ, Coll Osteopath Med, Dept Microbiol Immunol & Pathol, Des Moines, IA 50312 USA.
EM yujiang.fang@dmu.edu
FU Iowa Science Foundation [ISF 16-8, IOER 05-14-01, IOER 112-3749, IOER
112-3114]
FX This study was supported by grants for Yujiang Fang (Iowa Science
Foundation Grant ISF 16-8, IOER 05-14-01, IOER 112-3749 and IOER
112-3114).
NR 153
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U1 6
U2 6
PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0304-3835
EI 1872-7980
J9 CANCER LETT
JI Cancer Lett.
PD MAY 28
PY 2017
VL 394
BP 43
EP 51
DI 10.1016/j.canlet.2017.02.022
PG 9
WC Oncology
SC Oncology
GA ES5ZZ
UT WOS:000399626900005
PM 28254411
ER
PT J
AU Raghuram, V
Weber, S
Raber, J
Chen, DH
Bird, TD
Maylie, J
Adelman, JP
AF Raghuram, Vijeta
Weber, Sydney
Raber, Jacob
Chen, Dong-Hui
Bird, Thomas D.
Maylie, James
Adelman, John P.
TI Assessment of mutations in KCNN2 and ZNF135 to patient neurological
symptoms
SO NEUROREPORT
LA English
DT Article
DE apamin; ataxia; CRISPR-Cas system; human exome sequencing; neuroscience;
SK potassium channel; transgenic mice; ZNF135
ID CA2+-ACTIVATED K+ CHANNELS; CONDUCTANCE
AB Exome sequencing from a patient with neurological and developmental symptoms revealed two mutations in separate genes. One was a homozygous transition mutation that results in an in-frame, premature translational stop codon in the ZNF135 gene predicted to encode a transcriptional repressor. Another mutation was heterozygous, a single nucleotide duplication in the KCNN2 gene that encodes a Ca2+ -activated K+ channel, SK2, and leads to a translational frame shift and a premature stop codon. Heterologous expression studies, brain slice recordings, and coordination tests from a transgenic mouse line carrying the SK2 mutation suggest that it does not contribute to the patient's symptoms. ZNF135 is expressed in human brain and it is likely that the homozygous mutation underlies the human phenotype. Copyright (C) 2017 The Author(s). Published by Wolters Kluwer Health, Inc.
C1 [Raghuram, Vijeta; Adelman, John P.] Oregon Hlth & Sci Univ, Vollum Inst, L474,3181 SW Sam Jackson Pk Rd, Portland, OR 97201 USA.
[Weber, Sydney; Raber, Jacob] Oregon Hlth & Sci Univ, Dept Behav Neurosci, Portland, OR 97201 USA.
[Maylie, James] Oregon Hlth & Sci Univ, Dept Obstet & Gynecol, Portland, OR 97201 USA.
[Chen, Dong-Hui; Bird, Thomas D.] Univ Washington, Geriatr Res GRECC, Dept Neurol, VA Puget Sound Healthcare Syst, Seattle, WA 98195 USA.
RP Adelman, JP (reprint author), Oregon Hlth & Sci Univ, Vollum Inst, L474,3181 SW Sam Jackson Pk Rd, Portland, OR 97201 USA.
EM adelman@ohsu.edu
FU NIH
FX This work was supported by NIH grants to J.M. and J.P.A.
NR 7
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U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0959-4965
EI 1473-558X
J9 NEUROREPORT
JI Neuroreport
PD MAY 3
PY 2017
VL 28
IS 7
BP 375
EP 379
DI 10.1097/WNR.0000000000000754
PG 5
WC Neurosciences
SC Neurosciences & Neurology
GA ES2CI
UT WOS:000399333000002
PM 28240725
ER
PT J
AU Nedjat-Haiem, FR
Carrion, IV
Gonzalez, K
Ell, K
Thompson, B
Mishra, SI
AF Nedjat-Haiem, Frances R.
Carrion, Iraida V.
Gonzalez, Krystana
Ell, Kathleen
Thompson, Beti
Mishra, Shiraz I.
TI Exploring Health Care Providers' Views About Initiating End-of-Life Care
Communication
SO AMERICAN JOURNAL OF HOSPICE & PALLIATIVE MEDICINE
LA English
DT Article
DE health care providers; end-of-life care; communication; qualitative
research; social work
ID DISCUSSIONS; PERCEPTIONS; PHYSICIANS; DECISION; NEEDS
AB Numerous factors impede effective and timely end-of-life (EOL) care communication. These factors include delays in communication until patients are seriously ill and/or close to death. Gaps in patient-provider communication negatively affect advance care planning and limit referrals to palliative and hospice care. Confusion about the roles of various health care providers also limits communication, especially when providers do not coordinate care with other health care providers in various disciplines. Although providers receive education regarding EOL communication and care coordination, little is known about the roles of all health care providers, including nonphysician support staff working with physicians to discuss the possibility of dying and help patients prepare for death. This study explores the perspectives of physicians, nurses, social workers, and chaplains on engaging seriously ill patients and families in EOL care communication. Qualitative data were from 79 (medical and nonmedical) providers practicing at 2 medical centers in Central Los Angeles. Three themes that describe providers' perceptions of their roles and responsibility in talking with seriously ill patients emerged: (1) providers' roles for engaging in EOL discussions, (2) responsibility of physicians for initiating and leading discussions, and (3) need for team co-management patient care. Providers highlighted the importance of beginning discussions early by having physicians lead them, specifically due to their medical training and need to clarify medical information regarding patients' prognosis. Although physicians are a vital part of leading EOL communication, and are at the center of communication of medical information, an interdisciplinary approach that involves nurses, social workers, and chaplains could significantly improve patient care.
C1 [Nedjat-Haiem, Frances R.; Gonzalez, Krystana] New Mexico State Univ, Sch Social Work, POB 30001,MSC 3SW, Las Cruces, NM 88003 USA.
[Nedjat-Haiem, Frances R.] Vet Affairs Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Carrion, Iraida V.] Univ S Florida, Sch Social Work, Tampa, FL USA.
[Ell, Kathleen] Univ Southern Calif, Sch Social Work, Los Angeles, CA USA.
[Thompson, Beti] Univ Washington, Sch Publ Hlth, Seattle, WA 98195 USA.
[Mishra, Shiraz I.] Univ New Mexico, Sch Med, Albuquerque, NM 87131 USA.
RP Nedjat-Haiem, FR (reprint author), New Mexico State Univ, Sch Social Work, POB 30001,MSC 3SW, Las Cruces, NM 88003 USA.
EM nedjatha@gmail.com
FU American Cancer Society Doctoral Training Grants in Oncology Social Work
[DSW-06-220-01-SW]; US Department of Veterans Affairs, Hartford/VA
Social Work Scholars Program
FX The author(s) disclosed receipt of the following financial support for
the research, authorship, and/or publication of this article: This
research was supported by the American Cancer Society Doctoral Training
Grants in Oncology Social Work DSW-06-220-01-SW (F. R. Nedjat-Haiem, PI)
and US Department of Veterans Affairs, Hartford/VA Social Work Scholars
Program.
NR 28
TC 0
Z9 0
U1 1
U2 1
PU SAGE PUBLICATIONS INC
PI THOUSAND OAKS
PA 2455 TELLER RD, THOUSAND OAKS, CA 91320 USA
SN 1049-9091
EI 1938-2715
J9 AM J HOSP PALLIAT ME
JI Am. J. Hosp. Palliat. Med.
PD MAY
PY 2017
VL 34
IS 4
BP 308
EP 317
DI 10.1177/1049909115627773
PG 10
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA ER5JM
UT WOS:000398837800003
PM 26878869
ER
PT J
AU Wong, SPY
O'Hare, AM
AF Wong, Susan P. Y.
O'Hare, Ann M.
TI Families' Perception of End-of-Life Care for Patients With Serious
Illness
SO AMERICAN JOURNAL OF KIDNEY DISEASES
LA English
DT Article
ID AGGRESSIVE CANCER CARE; HEALTH-CARE; DIALYSIS; QUALITY; PERSPECTIVES;
DISEASE; ADULTS; HEMODIALYSIS; HOSPICE; DEATH
AB If 'progress' refers to the long-held Enlightenment idea and ideal that rationality and its tools can unequivocally improve life and reduce suffering, then 'postprogress' characterizes today's medicine.. Postprogress suggests that technical ability and more and more interventions, while they extend wanted life for many, also bring with them existential quandaries about one's own relationship to medicine, to suffering, to more life, and of the apparent control that can be exercised over the timing of death.
-Sharon R. Kaufman, Ordinary Medicine(1)
C1 [O'Hare, Ann M.] Univ Washington, 1660 S Columbian Way, Seattle, WA 98108 USA.
VA Puget Sound Hlth Care Syst, Seattle, WA USA.
RP O'Hare, AM (reprint author), Univ Washington, 1660 S Columbian Way, Seattle, WA 98108 USA.
EM ann.ohare@va.gov
FU Clinical Scientist in Nephrology Fellowship from the American Kidney
Fund; National Institutes of Health; Centers for Disease Control and
Prevention; VA Health Services Research and Development Service
FX Dr Wong is supported by the Clinical Scientist in Nephrology Fellowship
from the American Kidney Fund. Dr O'Hare receives research funding from
the National Institutes of Health, Centers for Disease Control and
Prevention, and VA Health Services Research and Development Service.
NR 32
TC 0
Z9 0
U1 1
U2 1
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0272-6386
EI 1523-6838
J9 AM J KIDNEY DIS
JI Am. J. Kidney Dis.
PD MAY
PY 2017
VL 69
IS 5
BP 564
EP 567
DI 10.1053/j.ajkd.2016.10.014
PG 4
WC Urology & Nephrology
SC Urology & Nephrology
GA ES4EZ
UT WOS:000399484200004
PM 27932044
ER
PT J
AU Garimella, PS
Li, KF
Naviaux, JC
Shlipak, MG
Abdelmalek, JA
Castro, E
Capparelli, EV
Naviaux, RK
Ix, JH
AF Garimella, Pranav S.
Li, Kefeng
Naviaux, Jane C.
Shlipak, Michael G.
Abdelmalek, Joseph A.
Castro, Erick
Capparelli, Edmund V.
Naviaux, Robert K.
Ix, Joachim H.
TI Utility of Spot Urine Specimens to Assess Tubular Secretion
SO AMERICAN JOURNAL OF KIDNEY DISEASES
LA English
DT Letter
ID KIDNEY-FUNCTION DECLINE; PROGRESSION; HEALTH
C1 [Garimella, Pranav S.; Li, Kefeng; Naviaux, Jane C.; Abdelmalek, Joseph A.; Capparelli, Edmund V.; Naviaux, Robert K.; Ix, Joachim H.] Univ Calif San Diego, San Diego, CA 92103 USA.
[Shlipak, Michael G.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Castro, Erick] Vet Med Res Fdn, San Diego, CA USA.
RP Ix, JH (reprint author), Univ Calif San Diego, San Diego, CA 92103 USA.
EM joeix@ucsd.edu
FU American Heart Association Established Investigator Award
[14EIA18560026]; National Institute of Diabetes and Digestive and Kidney
Diseases [R01 DK098234]
FX This work was supported by research awards from the American Heart
Association Established Investigator Award to J.H.I. (14EIA18560026) and
the National Institute of Diabetes and Digestive and Kidney Diseases to
J.H.I. and M.G.S. (R01 DK098234). The funders had no role in study
design; collection, analysis, and interpretation of data; writing the
report; or the decision to submit the report for publication.
NR 8
TC 0
Z9 0
U1 0
U2 0
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0272-6386
EI 1523-6838
J9 AM J KIDNEY DIS
JI Am. J. Kidney Dis.
PD MAY
PY 2017
VL 69
IS 5
BP 709
EP 711
DI 10.1053/j.ajkd.2016.12.016
PG 3
WC Urology & Nephrology
SC Urology & Nephrology
GA ES4EZ
UT WOS:000399484200028
PM 28284759
ER
PT J
AU Lin, TY
Shekar, AO
Li, N
Yeh, MW
Saab, S
Wilson, M
Leung, AM
AF Lin, Tiffany Y.
Shekar, Anshula O.
Li, Ning
Yeh, Michael W.
Saab, Sammy
Wilson, Mark
Leung, Angela M.
TI Incidence of abnormal liver biochemical tests in hyperthyroidism
SO CLINICAL ENDOCRINOLOGY
LA English
DT Article
ID GRAVES-DISEASE; THYROTROPIN RECEPTOR; SERIAL CHANGES; THYROTOXICOSIS;
PROPYLTHIOURACIL; ASSOCIATIONS; METHIMAZOLE; THERAPY; COHORT
AB ObjectiveAbnormal serum liver function tests are common in patients with untreated thyrotoxicosis, even prior to the initiation of antithyroidal medications that may worsen the severity of the abnormal serum liver biochemistries. There is a wide range of the incidence of these abnormalities in the published literature. The aim of this study was to assess the risks factors and threshold of thyrotoxicosis severity for developing an abnormal liver biochemical test upon the diagnosis of new thyrotoxicosis.
DesignSingle-institution retrospective cohort study.
PatientsPatients of 18 years old receiving medical care at a large, academic, urban US medical centre between 2002-2016.
MeasurementsInclusion criteria were a serum thyroid stimulating hormone (TSH) concentration of <03 mIU/l or ICD-9 code for thyrotoxicosis, with thyrotoxicosis confirmed by either a concurrent elevated serum triiodothyronine (T3) or thyroxine (T4) concentration ([total or free] within 3 months), and an available liver biochemical test(s) within 6 months of thyrotoxicosis. The biochemical liver tests assessed were serum aspartate transaminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (AP), gamma-glutamyltransferase (GGT), total bilirubin, and conjugated bilirubin concentrations.
ResultsIn this cohort of 1514 subjects, the overall incidence of any biochemical liver test abnormality within 6 months of thyrotoxicosis was 39%. An initial serum TSH concentration <002 mIU/l, male gender, and African-American race were significant predictors of an abnormal serum liver biochemical test within 6 months of the diagnosis of new-onset untreated thyrotoxicosis.
ConclusionsThis study identifies risk factors for patients who develop an abnormal serum liver biochemical test result within 6 months of a diagnosis of untreated thyrotoxicosis.
C1 [Lin, Tiffany Y.] Univ Calif Los Angeles, David Geffen Sch Med, 11301 Wilshire Blvd 111D, Los Angeles, CA 90073 USA.
[Shekar, Anshula O.] Univ Calif Los Angeles, Dept Med, David Geffen Sch Med, 11301 Wilshire Blvd 111D, Los Angeles, CA 90073 USA.
[Li, Ning] Univ Calif Los Angeles, Dept Biomath, David Geffen Sch Med, Los Angeles, CA 90073 USA.
[Yeh, Michael W.] Univ Calif Los Angeles, Sect Endocrine Surg, Dept Surg, David Geffen Sch Med, Los Angeles, CA 90073 USA.
[Saab, Sammy] Univ Calif Los Angeles, Div Gastroenterol, Dept Med, David Geffen Sch Med, Los Angeles, CA 90073 USA.
[Wilson, Mark] Sansum Clin, Santa Barbara, CA USA.
[Leung, Angela M.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Endocrinol Diabet & Hypertens, Los Angeles, CA 90073 USA.
[Leung, Angela M.] VA Greater Los Angeles Healthcare Syst, Div Endocrinol, Los Angeles, CA USA.
RP Leung, AM (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Div Endocrinol Diabet & Hypertens, 11301 Wilshire Blvd 111D, Los Angeles, CA 90073 USA.
EM amleung@mednet.ucla.edu
FU NIH [K23HD068552]
FX Supported by NIH K23HD068552 (AML).
NR 31
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0300-0664
EI 1365-2265
J9 CLIN ENDOCRINOL
JI Clin. Endocrinol.
PD MAY
PY 2017
VL 86
IS 5
BP 755
EP 759
DI 10.1111/cen.13312
PG 5
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA ER5QF
UT WOS:000398856100016
PM 28199740
ER
PT J
AU Sheets, KM
Atta, MG
Fine, DM
Zook, K
Mcfall, AM
Estrella, MM
Schwartz, GJ
Lucas, GM
AF Sheets, Kerry M.
Atta, Mohamed G.
Fine, Derek M.
Zook, Katie
Mcfall, Allison M.
Estrella, Michelle M.
Schwartz, George J.
Lucas, Gregory M.
TI Longitudinal Assessment of Proximal Tubular Dysfunction in HIV
Seropositive and Seronegative Persons: Correlates and Implications
SO JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES
LA English
DT Article
DE HIV; proximal tubular dysfunction; tenofovir disoproxil fumarate;
antiretroviral therapy; glomerular filtration rate
ID TENOFOVIR DISOPROXIL FUMARATE; INFECTED PATIENTS; ANTIRETROVIRAL
THERAPY; URINARY ALBUMIN; TOTAL PROTEIN; DOUBLE-BLIND; NEPHROTOXICITY;
ABNORMALITIES; EMTRICITABINE; ALAFENAMIDE
AB Background: Proximal tubular dysfunction (PTD) is common in HIV-positive persons and has been associated with tenofovir disoproxil fumarate (TDF). However, few studies have assessed the natural history PTD in HIV-positive and -negative individuals, or the association of PTD with the subsequent trajectory of directly measured glomerular filtration rate (mGFR).
Methods: We followed 192 HIV-positive and 100 HIV-negative, nondiabetic participants for 3 years. We measured 3 PTD markers (normoglycemic glycosuria, fractional excretion of phosphorus, and tubular proteinuria) and mGFR (by iohexol disappearance from serum) annually. We used univariate and multivariate generalized estimating equation logistic regression to identify factors associated with PTD across all visits and linear mixed effects models to assess the association between baseline PTD and mGFR slope.
Results: Compared with HIV-negative participants, HIV-positive persons that were not taking antiretroviral therapy were at increased risk of PTD (adjusted odds ratio 3.33; 95% confidence interval: 1.65 to 6.71), whereas those taking a TDF-based or a TDF-sparing regimen were not at significantly increased risk of PTD. Among HIV-positive participants, uncontrolled viremia was a strong correlate of PTD. Forty-nine of 55 (89%) participants with PTD at baseline had at least 1 subsequent visit without PTD. There was no association between baseline PTD and rate of decline in mGFR over time.
Conclusions: Poorly controlled HIV may be a stronger risk factor for PTD than TDF use. The individual-level variability of the PTD markers over time was high, potentially limiting their usefulness for routine screening in unselected patients. Baseline PTD was not associated with subsequent mGFR slope.
C1 [Sheets, Kerry M.] Johns Hopkins Bayview Med Ctr, Internal Med Residency Training Program, Baltimore, MD USA.
[Atta, Mohamed G.; Fine, Derek M.] Johns Hopkins Univ, Sch Med, Div Nephrol, Baltimore, MD USA.
[Zook, Katie; Lucas, Gregory M.] Johns Hopkins Univ, Sch Med, Div Infect Dis, Dept Med, Baltimore, MD USA.
[Mcfall, Allison M.] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA.
[Estrella, Michelle M.] San Francisco VA Med Ctr, Kidney Hlth Res Collaborat, San Francisco, CA USA.
[Estrella, Michelle M.] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Schwartz, George J.] Univ Rochester, Med Ctr, Dept Pediat, Rochester, NY 14642 USA.
RP Lucas, GM (reprint author), Johns Hopkins Univ, Sch Med, Div Infect Dis, Dept Med, Baltimore, MD USA.
EM glucas@jhmi.edu
FU National Institute on Drug Abuse [R01DA026770, K24DA035684]; National
Institute of Allergy and Infectious Diseases [T32AI102623]; National
Institute of Diabetes and Digestive and Kidney Disease [U01DK082194,
P01DK056492]; Johns Hopkins Institute for Clinical and Translational
Research (ICTR); National Center for Advancing Translational Sciences
(NCATS), a component of the NIH [UL1-TR000424]; Johns Hopkins Center for
AIDS Research [P30AI094189]
FX Supported by the National Institute on Drug Abuse (R01DA026770,
K24DA035684). Other support was provided by the National Institute of
Allergy and Infectious Diseases (T32AI102623), the National Institute of
Diabetes and Digestive and Kidney Disease (U01DK082194, P01DK056492),
the Johns Hopkins Institute for Clinical and Translational Research
(ICTR), which is funded in part by grant number UL1-TR000424 from the
National Center for Advancing Translational Sciences (NCATS), a
component of the NIH, and by the Johns Hopkins Center for AIDS Research
(P30AI094189). GE Healthcare provided the iohexol used for glomerular
filtration rate measurements.
NR 30
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1525-4135
EI 1077-9450
J9 JAIDS-J ACQ IMM DEF
JI JAIDS
PD MAY 1
PY 2017
VL 75
IS 1
BP 45
EP 51
PG 7
WC Immunology; Infectious Diseases
SC Immunology; Infectious Diseases
GA ES2RV
UT WOS:000399376500013
PM 28151777
ER
PT J
AU Kelley, D
Jones, LT
Wu, J
Bohm, N
AF Kelley, Denise
Jones, Lauren Thornton
Wu, Jun
Bohm, Nicole
TI Evaluating the safety and effectiveness of venous thromboembolism
prophylaxis in patients with sickle cell disease
SO JOURNAL OF THROMBOSIS AND THROMBOLYSIS
LA English
DT Article
DE Venous thromboembolism; Prophylaxis; Sickle cell disease; Enoxaparin;
Heparin
AB Nearly every component of hemostasis is altered in sickle cell disease (SCD), yet little evidence exists to guide utilization of venous thromboembolism prophylaxis (VTEP) in this population. This retrospective cohort study included 135 adult patients admitted with a diagnosis of SCD vaso-occlusive crisis to the general medicine service at a tertiary care academic medical center from August 1, 2011 to August 1, 2013. If VTEP was discontinued, the medical record was reviewed for suspicion of VTE, hemorrhage, heparin-induced thrombocytopenia (HIT), or other adverse events. The primary objective was to characterize the safety and effectiveness of VTEP in SCD. The secondary objective was to assess the correlation of VTE with risk factors documented in the general medical population. Most patients (116/135, 85.9%) were prescribed VTEP upon admission, with early discontinuation in 23 patients (19.8%). Reasons for discontinuation included suspicion of VTE (10/116, 8.6%), hemorrhage (5/116, 4.3%), and/or HIT (4/116, 3.4%). Since patients with SCD receiving standard VTEP regimens appear to have similar outcomes compared to medically ill patients in prospective studies, using these regimens appears to be safe when indicated in the opinion of the provider. Once daily injections may be preferred in order to optimize adherence.
C1 [Kelley, Denise] UF Hlth Jacksonville Med Ctr, Dept Pharm, Jacksonville, FL 32209 USA.
[Jones, Lauren Thornton] Ralph H Johnson VA Med Ctr, Dept Pharm, Charleston, SC 29425 USA.
[Wu, Jun] Presbyterian Coll Pharm, Clinton, SC 29325 USA.
[Bohm, Nicole] Med Univ South Carolina, Coll Pharm, 280 Calhoun St QE 205, Charleston, SC 29425 USA.
RP Bohm, N (reprint author), Med Univ South Carolina, Coll Pharm, 280 Calhoun St QE 205, Charleston, SC 29425 USA.
EM bohm@musc.edu
FU South Carolina Clinical and Translational Research (SCTR) Institute
through NIH [UL1 TR000062]
FX This project was supported by the South Carolina Clinical and
Translational Research (SCTR) Institute, with an academic home at the
Medical University of South Carolina, through NIH Grant Number UL1
TR000062. I would like to acknowledge Petra A. Aldridge, MS for her
contributions to statistical analysis.
NR 12
TC 0
Z9 0
U1 1
U2 1
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0929-5305
EI 1573-742X
J9 J THROMB THROMBOLYS
JI J. Thromb. Thrombolysis
PD MAY
PY 2017
VL 43
IS 4
BP 463
EP 468
DI 10.1007/s11239-016-1463-z
PG 6
WC Hematology; Peripheral Vascular Disease
SC Hematology; Cardiovascular System & Cardiology
GA ER7VB
UT WOS:000399021200005
PM 27943026
ER
PT J
AU Gatto, EM
Allegri, RF
Da Prat, G
Mendez, PC
Hanna, DS
Dorschner, MO
Surace, EI
Zabetian, CP
Mata, IF
AF Gatto, Emilia M.
Allegri, Ricardo F.
Da Prat, Gustavo
Chrem Mendez, Patricio
Hanna, David S.
Dorschner, Michael O.
Surace, Ezequiel I.
Zabetian, Cyrus P.
Mata, Ignacio F.
TI Intrafamilial variable phenotype including corticobasal syndrome in a
family with p.P301L mutation in the MAPT gene: first report in South
America
SO NEUROBIOLOGY OF AGING
LA English
DT Article
DE FTD; MAPT; P301L; Cognition; CBS
ID FRONTOTEMPORAL LOBAR DEGENERATION; PROGRESSIVE SUPRANUCLEAR PALSY;
PROTEIN-TAU GENE; PARKINSONS-DISEASE; DEMENTIA; NEUROPATHOLOGY;
AGGREGATION; TAUOPATHIES; ASSOCIATION; DIAGNOSIS
AB Frontotemporal lobar degeneration is a neuropathological disorder that causes a variety of clinical syndromes including frontotemporal dementia (FTD), progressive supranuclear palsy, and corticobasal syndrome (CBS). FTD associated with parkinsonism occurs frequently as a result of mutations in the C9orf72 gene and also in the genes coding for the protein associated with microtubule tau (MAPT) and progranulin (GRN) on chromosome 17 (FTDP-17). Herein, we report an Argentinean family, of Basque ancestry, with an extensive family history of behavioral variant of FTD. Twenty-one members over 6 generations composed the pedigree. An extensive neurologic and neurocognitive examination was performed on 2 symptomatic individuals and 3 non-symptomatic individuals. Two different phenotypes were identified among affected members, CBS in the proband and FTD in his brother. DNA was extracted from blood for these 5 individuals and whole-exome sequencing was performed on 3 of them followed by Sanger sequencing of candidate genes on the other 2. In both affected individuals, a missense mutation (p.P301L; rs63751273) in exon 10 of the MAPT gene (chr17q21.3) was identified. Among MAPT mutations, p.P301L is the most frequently associated to different phenotypes: (1) aggressive, symmetrical, andearly-onset Parkinsonism; (2) late parkinsonism associated with FTD; and (3) progressive supranuclear palsy but only exceptionally it is reported associated to CBS. This is the first report of the occurrence of the p.P301L-MAPT mutation in South America and supports the marked phenotypic heterogeneity among members of the same family as previously reported. Published by Elsevier Inc.
C1 [Gatto, Emilia M.] Fdn INEBA, Dept Movement Disorders, Buenos Aires, DF, Argentina.
[Gatto, Emilia M.; Da Prat, Gustavo] Dept Neurol, Sanatorio Trinidad Mitre, Buenos Aires, DF, Argentina.
[Allegri, Ricardo F.; Chrem Mendez, Patricio] Inst Invest Neurol Dr Raul Carrea FLENI, Memory & Aging Ctr, Dept Cognit Neurol, Buenos Aires, DF, Argentina.
[Allegri, Ricardo F.] Consejo Nacl Invest Cient & Tecn, Argentine Res Council, Buenos Aires, DF, Argentina.
[Hanna, David S.; Surace, Ezequiel I.] Univ Costa CUC, Barranquilla, Colombia.
[Chrem Mendez, Patricio; Dorschner, Michael O.; Zabetian, Cyrus P.] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Da Prat, Gustavo; Hanna, David S.; Zabetian, Cyrus P.] Univ Washington, Dept Pathol, Seattle, WA 98195 USA.
[Hanna, David S.] FLEN, Dept Neuropathol, Lab Biol Mol, Buenos Aires, DF, Argentina.
[Chrem Mendez, Patricio; Hanna, David S.; Surace, Ezequiel I.; Mata, Ignacio F.] Vet Affairs Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA USA.
[Chrem Mendez, Patricio; Dorschner, Michael O.] Univ Washington, Dept Neurol, Seattle, WA 98195 USA.
RP Mata, IF (reprint author), VA Puget Sound Hlth Care Syst, GRECC S 182, 1660 S Columbian Way, Seattle, WA 98108 USA.
EM nachofm@uw.edu
FU Parkinson's Disease Foundation; Department of Veterans Affairs
[1I01BX000531]; National Institutes of Health [R01 NS065070, P50
NS062684]
FX The authors would like to acknowledge all the individuals in this family
for their collaboration and doctors Marcelo Kauffman and Sergio
Rodriguez, Laboratorio de Neurogenetica, Hospital Ramos Mejia, Buenos
Aires Argentina for their scientific collaboration. This work was
supported by grants from the Parkinson's Disease Foundation, the
Department of Veterans Affairs (1I01BX000531) and the National
Institutes of Health (R01 NS065070, P50 NS062684). The contents do not
represent the views of the U.S. Department of Veterans Affairs or the
United States Government.
NR 34
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0197-4580
EI 1558-1497
J9 NEUROBIOL AGING
JI Neurobiol. Aging
PD MAY
PY 2017
VL 53
AR 195.e11
DI 10.1016/j.neurobiolaging.2017.02.002
PG 7
WC Geriatrics & Gerontology; Neurosciences
SC Geriatrics & Gerontology; Neurosciences & Neurology
GA ES4JU
UT WOS:000399501300032
ER
PT J
AU Lee, AD
Spiegel, BM
Hays, RD
Melmed, GY
Bolus, R
Khanna, D
Khanna, PP
Chang, L
AF Lee, A. D.
Spiegel, B. M.
Hays, R. D.
Melmed, G. Y.
Bolus, R.
Khanna, D.
Khanna, P. P.
Chang, L.
TI Gastrointestinal symptom severity in irritable bowel syndrome,
inflammatory bowel disease and the general population
SO NEUROGASTROENTEROLOGY AND MOTILITY
LA English
DT Article
DE gender; inflammatory bowel disease; irritable bowel syndrome; symptom
severity
ID PATIENT-REPORTED OUTCOMES; GASTROESOPHAGEAL-REFLUX DISEASE; COMPUTERIZED
ADAPTIVE TESTS; QUALITY-OF-LIFE; ULCERATIVE-COLITIS; FECAL INCONTINENCE;
BRAIN RESPONSES; RATING-SCALE; PREVALENCE; METAANALYSIS
AB Background: Irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD) patients report similar gastrointestinal (GI) symptoms, yet comparisons of symptom severity between groups and with the general population (GP) are lacking.
Methods: We compared Patient-Reported Outcomes Measurement Information System (PROMIS (R)) GI symptom scales measuring gastro-esophageal reflux (GER), disrupted swallowing, diarrhea, bowel incontinence, nausea/vomiting, constipation, belly pain, and gas/bloating in: (i) USA GP sample, (ii) IBS patients, and (iii) IBD patients from tertiary care and community populations. Symptom severity scores were based on T-score metric with mean 5010 (standard deviation) relative to the GP.
Key Results: Of 1643 patients enrolled, there were 253 IBS patients (68% F, mean age 45 +/- 15years), 213 IBD patients (46% F, mean age 41 +/- 14years), and 1177 GP subjects (57% F, mean age 46 +/- 16years). IBS patients reported greater severity of GER, disrupted swallowing, nausea/vomiting, belly pain, gas/bloating, and constipation symptoms than their IBD counterparts (all P<.05). Compared to the GP, IBD patients had worse belly pain, gas/bloating, diarrhea, and bowel incontinence, but less severe GER and disrupted swallowing (all P<.05), and IBS patients had more severe nausea/vomiting, belly pain, gas/bloating, and constipation (all P<.05). Women had more severe belly pain and gas/bloating than men, whereas men had more severe bowel incontinence (all P<.05).
Conclusion & Inferences: IBS and IBD are associated with more severe GI symptoms compared to the GP excluding esophageal symptoms. Unlike IBD, IBS is not characterized by observable GI inflammation but patients report more severe upper and lower GI symptoms.
C1 [Lee, A. D.; Spiegel, B. M.; Melmed, G. Y.] Cedars Sinai Med Ctr, Ctr Outcomes Res & Educ, Los Angeles, CA 90048 USA.
[Lee, A. D.; Spiegel, B. M.] VA Greater Los Angeles Healthcare Syst, Dept Med, Div Gastroenterol, Los Angeles, CA USA.
[Lee, A. D.; Hays, R. D.] RAND Hlth Program, Santa Monica, CA USA.
[Lee, A. D.; Spiegel, B. M.; Bolus, R.] UCLA VA Ctr Outcomes Res & Educ CORE, Los Angeles, CA USA.
[Lee, A. D.] Kaiser Permanente Los Angeles Med Ctr, Div Gastroenterol, Los Angeles, CA USA.
[Spiegel, B. M.; Bolus, R.; Chang, L.] Univ Calif Los Angeles, David Geffen Sch Med, Div Digest Dis, Dept Med, Los Angeles, CA 90095 USA.
[Spiegel, B. M.; Hays, R. D.] Univ Calif Los Angeles, Dept Med, Div Gen Internal Med, Los Angeles, CA 90024 USA.
[Hays, R. D.] Univ Calif Los Angeles, Dept Hlth Serv, Fielding Sch Publ Hlth, Los Angeles, CA USA.
[Khanna, D.; Khanna, P. P.] Univ Michigan, Div Rheumatol, Ann Arbor, MI 48109 USA.
[Chang, L.] Univ Calif Los Angeles, David Geffen Sch Med, G Oppenheimer Ctr Neurobiol Stress & Resilience, Los Angeles, CA 90095 USA.
RP Chang, L (reprint author), G Oppenheimer Ctr Neurobiol Stress & Resilience, Los Angeles, CA 90095 USA.
EM linchang@ucla.edu
FU NIH/NIAMS [U01 AR057936A]; National Institutes of Health through the NIH
Roadmap for Medical Research Grant [AR052177]; NIAMS [K24 AR063120];
National Research Service Award (NRSA) Institutional Research Training
Grant [NIAMS 1 T32 AR053463]; ACR Research and Education Foundation
Clinical Investigator Fellowship [2009_11]; NIH/NIA [P30-AG028748,
P30-AG021684]; NCMHD [2P20MD000182]; NIDDK [P50 DK64539]
FX This research was supported by NIH/NIAMS U01 AR057936A, the National
Institutes of Health through the NIH Roadmap for Medical Research Grant
(AR052177). Dinesh Khanna was also supported by. NIAMS K24 AR063120 Puja
Khanna was supported by Ruth L. Kirschstein National Research Service
Award (NRSA) Institutional Research Training Grant NIAMS 1 T32 AR053463
and ACR Research and Education Foundation Clinical Investigator
Fellowship Award 2009_11. Ron D. Hays was also supported by NIH/NIA
Grants P30-AG028748 and P30-AG021684, and NCMHD Grant 2P20MD000182. Lin
Chang was also supported by NIDDK P50 DK64539.
NR 52
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1350-1925
EI 1365-2982
J9 NEUROGASTROENT MOTIL
JI Neurogastroenterol. Motil.
PD MAY
PY 2017
VL 29
IS 5
AR UNSP e13003
DI 10.1111/nmo.13003
PG 9
WC Gastroenterology & Hepatology; Clinical Neurology; Neurosciences
SC Gastroenterology & Hepatology; Neurosciences & Neurology
GA ES6UK
UT WOS:000399685100011
ER
PT J
AU Mori, T
Crandall, CJ
Ganz, DA
AF Mori, T.
Crandall, C. J.
Ganz, D. A.
TI Cost-effectiveness of denosumab versus oral alendronate for elderly
osteoporotic women in Japan
SO OSTEOPOROSIS INTERNATIONAL
LA English
DT Article
DE Alendronate; Cost-effectiveness analysis; Denosumab; Osteoporosis
ID HIP FRACTURE; POSTMENOPAUSAL OSTEOPOROSIS; FRAGILITY FRACTURES;
METAANALYSIS; BISPHOSPHONATES; PERSISTENCE; TRENDS; RISK; MORTALITY;
THERAPY
AB We constructed a Markov microsimulation model among hypothetical cohorts of community-dwelling elderly osteoporotic Japanese women without prior hip or vertebral fractures over a lifetime horizon. Compared with weekly oral alendronate for 5 years, denosumab every 6 months for 5 years is cost-saving or cost-effective at a conventionally accepted threshold.
The objective of the study was to examine the cost-effectiveness of subcutaneous denosumab every 6 months for 5 years compared with weekly oral alendronate for 5 years in Japan.
We calculated incremental cost-effectiveness ratios [ICERs] (2016 US dollars [$] per quality-adjusted life year [QALY]), using a Markov microsimulation model among hypothetical cohorts of community-dwelling osteoporotic Japanese women without prior hip or vertebral fractures at various ages of therapy initiation (65, 70, 75, and 80 years) over a lifetime horizon from three perspectives: societal, healthcare sector, and government.
Denosumab was cost-saving compared with alendronate at ages 75 and 80 years from any of the three perspectives. The ICERs of denosumab compared with alendronate were $25,700 and $5000 per QALY at ages 65 and 70 years from a societal perspective and did not exceed a willingness-to-pay of $50,000 per QALY from the other two perspectives. In deterministic sensitivity analyses, results were sensitive to changes in the effectiveness of denosumab for reducing hip fracture and clinical vertebral fracture and the rate ratio of non-persistence with denosumab compared to alendronate. In probabilistic sensitivity analyses, the probabilities of denosumab being cost-effective compared with alendronate were 89-100% at a willingness-to-pay of $50,000 per QALY.
Among community-dwelling elderly osteoporotic women in Japan, denosumab every 6 months for 5 years is cost-saving or cost-effective at a conventionally accepted threshold of willingness-to-pay at all ages examined, compared with weekly alendronate for 5 years. This study provides insight to clinicians and policymakers regarding the relative economic value of osteoporosis treatments in elderly women.
C1 [Mori, T.] Kameda Med Ctr, Dept Gen Internal Med, 929 Higashi Cho, Kamogawa City, Chiba 2968602, Japan.
[Mori, T.] Univ Tsukuba, Grad Sch Comprehens Human Sci, Dept Primary Care & Med Educ, Tsukuba, Ibaraki, Japan.
[Mori, T.] Univ Tsukuba, Dept Hlth Serv Res, Fac Med, Tsukuba, Ibaraki, Japan.
[Crandall, C. J.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Gen Internal Med & Hlth Serv Res, Los Angeles, CA 90095 USA.
[Ganz, D. A.] Vet Affairs Greater Los Angeles Healthcare Syst, Geriatr Res Educ & Clin Ctr, Los Angeles, CA USA.
[Ganz, D. A.] Vet Affairs Greater Los Angeles Healthcare Syst, HSR&D Ctr Healthcare Innovat Implementat & Policy, Los Angeles, CA USA.
[Ganz, D. A.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Geriatr, Los Angeles, CA 90095 USA.
[Ganz, D. A.] RAND Corp, Hlth Unit, Santa Monica, CA USA.
RP Mori, T (reprint author), Kameda Med Ctr, Dept Gen Internal Med, 929 Higashi Cho, Kamogawa City, Chiba 2968602, Japan.; Mori, T (reprint author), Univ Tsukuba, Grad Sch Comprehens Human Sci, Dept Primary Care & Med Educ, Tsukuba, Ibaraki, Japan.; Mori, T (reprint author), Univ Tsukuba, Dept Hlth Serv Res, Fac Med, Tsukuba, Ibaraki, Japan.
EM takahiromori@outlook.com
NR 43
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER LONDON LTD
PI LONDON
PA 236 GRAYS INN RD, 6TH FLOOR, LONDON WC1X 8HL, ENGLAND
SN 0937-941X
EI 1433-2965
J9 OSTEOPOROSIS INT
JI Osteoporosis Int.
PD MAY
PY 2017
VL 28
IS 5
BP 1733
EP 1744
DI 10.1007/s00198-017-3940-4
PG 12
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA ES3QH
UT WOS:000399443600024
PM 28210776
ER
PT J
AU Woolley, JD
Chuang, B
Fussell, C
Scherer, S
Biagianti, B
Fulford, D
Mathalon, DH
Vinogradov, S
AF Woolley, J. D.
Chuang, B.
Fussell, C.
Scherer, S.
Biagianti, B.
Fulford, D.
Mathalon, D. H.
Vinogradov, S.
TI Intranasal oxytocin increases facial expressivity, but not ratings of
trustworthiness, in patients with schizophrenia and healthy controls
SO PSYCHOLOGICAL MEDICINE
LA English
DT Article
DE Blunted affect; facial expressivity; oxytocin; schizophrenia; social
cognition; trustworthiness
ID RANDOMIZED CONTROLLED-TRIAL; SOCIAL COGNITION; NEGATIVE SYMPTOMS; FLAT
AFFECT; EMOTION; JUDGMENTS; RESPONSES; AMYGDALA; FACES; VALIDATION
AB Background. Blunted facial affect is a common negative symptom of schizophrenia. Additionally, assessing the trustworthiness of faces is a social cognitive ability that is impaired in schizophrenia. Currently available pharmacological agents are ineffective at improving either of these symptoms, despite their clinical significance. The hypothalamic neuropeptide oxytocin has multiple prosocial effects when administered intranasally to healthy individuals and shows promise in decreasing negative symptoms and enhancing social cognition in schizophrenia. Although two small studies have investigated oxytocin's effects on ratings of facial trustworthiness in schizophrenia, its effects on facial expressivity have not been investigated in any population.
Method. We investigated the effects of oxytocin on facial emotional expressivity while participants performed a facial trustworthiness rating task in 33 individuals with schizophrenia and 35 age-matched healthy controls using a double-blind, placebo-controlled, cross-over design. Participants rated the trustworthiness of presented faces interspersed with emotionally evocative photographs while being video-recorded. Participants' facial expressivity in these videos was quantified by blind raters using a well-validated manualized approach (i.e. the Facial Expression Coding System; FACES).
Results. While oxytocin administration did not affect ratings of facial trustworthiness, it significantly increased facial expressivity in individuals with schizophrenia (Z=-2.33, p=0.02) and at trend level in healthy controls (Z=-1.87, p=0.06).
Conclusions. These results demonstrate that oxytocin administration can increase facial expressivity in response to emotional stimuli and suggest that oxytocin may have the potential to serve as a treatment for blunted facial affect in schizophrenia.
C1 [Woolley, J. D.; Chuang, B.; Fussell, C.; Mathalon, D. H.; Vinogradov, S.] San Francisco VA Med Ctr, Dept Psychiat, San Francisco, CA USA.
[Woolley, J. D.; Chuang, B.; Fussell, C.; Biagianti, B.; Mathalon, D. H.; Vinogradov, S.] Univ Calif San Francisco, Dept Psychiat, 4150 Clement St,116C-1, San Francisco, CA 94121 USA.
[Scherer, S.] Univ Southern Calif, Inst Creat Technol, Los Angeles, CA USA.
[Fulford, D.] Boston Univ, Dept Occupat Therapy, Boston, MA 02215 USA.
[Fulford, D.] Boston Univ, Dept Psychol & Brain Sci, Boston, MA 02215 USA.
RP Woolley, JD (reprint author), Univ Calif San Francisco, Dept Psychiat, 4150 Clement St,116C-1, San Francisco, CA 94121 USA.
EM Josh.Woolley@ucsf.edu
FU Veterans Health Administration Office of Research and Development Career
Development Award (CDA) [1IK2CX000758-01A1]; National Institute of
Mental Health Diversity Supplement [3R01MH068725-09S1]
FX Grant support was provided by the Veterans Health Administration Office
of Research and Development Career Development Award (CDA)
1IK2CX000758-01A1 and National Institute of Mental Health Diversity
Supplement 3R01MH068725-09S1.
NR 61
TC 0
Z9 0
U1 0
U2 0
PU CAMBRIDGE UNIV PRESS
PI NEW YORK
PA 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA
SN 0033-2917
EI 1469-8978
J9 PSYCHOL MED
JI Psychol. Med.
PD MAY
PY 2017
VL 47
IS 7
BP 1311
EP 1322
DI 10.1017/S0033291716003433
PG 12
WC Psychology, Clinical; Psychiatry; Psychology
SC Psychology; Psychiatry
GA ER4UO
UT WOS:000398797100013
PM 28091349
ER
PT J
AU Deming, Y
Li, ZR
Kapoor, M
Harari, O
Del-Aguila, JL
Black, K
Carrell, D
Cai, YF
Fernandez, MV
Budde, J
Ma, SM
Saef, B
Howells, B
Huang, KL
Bertelsen, S
Fagan, AM
Holtzman, DM
Morris, JC
Kim, S
Saykin, AJ
De Jager, PL
Albert, M
Moghekar, A
O'Brien, R
Riemenschneider, M
Petersen, RC
Blennow, K
Zetterberg, H
Minthon, L
Van Deerlin, VM
Lee, VMY
Shaw, LM
Trojanowski, JQ
Schellenberg, G
Haines, JL
Mayeux, R
Pericak-Vance, MA
Farrer, LA
Peskind, ER
Li, G
Di Narzo, AF
Kauwe, JSK
Goate, AM
Cruchaga, C
AF Deming, Yuetiva
Li, Zeran
Kapoor, Manav
Harari, Oscar
Del-Aguila, Jorge L.
Black, Kathleen
Carrell, David
Cai, Yefei
Fernandez, Maria Victoria
Budde, John
Ma, Shengmei
Saef, Benjamin
Howells, Bill
Huang, Kuan-lin
Bertelsen, Sarah
Fagan, Anne M.
Holtzman, David M.
Morris, John C.
Kim, Sungeun
Saykin, Andrew J.
De Jager, Philip L.
Albert, Marilyn
Moghekar, Abhay
O'Brien, Richard
Riemenschneider, Matthias
Petersen, Ronald C.
Blennow, Kaj
Zetterberg, Henrik
Minthon, Lennart
Van Deerlin, Vivianna M.
Lee, Virginia Man-Yee
Shaw, Leslie M.
Trojanowski, John Q.
Schellenberg, Gerard
Haines, Jonathan L.
Mayeux, Richard
Pericak-Vance, Margaret A.
Farrer, Lindsay A.
Peskind, Elaine R.
Li, Ge
Di Narzo, Antonio F.
Kauwe, John S. K.
Goate, Alison M.
Cruchaga, Carlos
CA Alzheimer's Dis Neuroimaging
Alzheimer Dis Genetic Consor
TI Genome-wide association study identifies four novel loci associated with
Alzheimer's endophenotypes and disease modifiers
SO ACTA NEUROPATHOLOGICA
LA English
DT Article
DE Alzheimer's disease; Endophenotype; Cerebrospinal fluid biomarkers;
Genome-wide association study
ID CEREBROSPINAL-FLUID A-BETA(42); MILD COGNITIVE IMPAIRMENT; RATING-SCALE
SUM; TAU LEVELS; BIOMARKER SIGNATURE; COMMON VARIANTS; RISK VARIANTS;
SCORE; CSF; METAANALYSIS
AB More than 20 genetic loci have been associated with risk for Alzheimer's disease (AD), but reported genome-wide significant loci do not account for all the estimated heritability and provide little information about underlying biological mechanisms. Genetic studies using intermediate quantitative traits such as biomarkers, or endophenotypes, benefit from increased statistical power to identify variants that may not pass the stringent multiple test correction in case-control studies. Endophenotypes also contain additional information helpful for identifying variants and genes associated with other aspects of disease, such as rate of progression or onset, and provide context to interpret the results from genome-wide association studies (GWAS). We conducted GWAS of amyloid beta (A beta(42)), tau, and phosphorylated tau (ptau181) levels in cerebrospinal fluid (CSF) from 3146 participants across nine studies to identify novel variants associated with AD. Five genome-wide significant loci (two novel) were associated with ptau181, including loci that have also been associated with AD risk or brain-related phenotypes. Two novel loci associated with A beta(42) near GLIS1 on 1p32.3 (beta = -0.059, P = 2.08 x 10(-8)) and within SERPINB1 on 6p25 (beta = -0.025, P = 1.72 x 10(-8)) were also associated with AD risk (GLIS1: OR = 1.105, P = 3.43 x 10(-2)), disease progression (GLIS1: beta = 0.277, P = 1.92 x 10(-2)), and age at onset (SER-PINB1: beta = 0.043, P = 4.62 x 10(-3)). Bioinformatics indicate that the intronic SERPINB1 variant (rs316341) affects expression of SERPINB1 in various tissues, including the hippocampus, suggesting that SERPINB1 influences AD through an A beta-associated mechanism. Analyses of known AD risk loci suggest CLU and FERMT2 may influence CSF A beta(42) (P = 0.001 and P = 0.009, respectively) and the INPP5D locus may affect ptau181 levels (P = 0.009); larger studies are necessary to verify these results. Together the findings from this study can be used to inform future AD studies.
C1 [Deming, Yuetiva; Li, Zeran; Harari, Oscar; Del-Aguila, Jorge L.; Black, Kathleen; Carrell, David; Cai, Yefei; Fernandez, Maria Victoria; Budde, John; Ma, Shengmei; Saef, Benjamin; Howells, Bill; Cruchaga, Carlos] Washington Univ, Sch Med, Dept Psychiat, 660 S Euclid Ave B8134, St Louis, MO 63110 USA.
[Kapoor, Manav; Bertelsen, Sarah; Goate, Alison M.] Icahn Sch Med Mt Sinai, Dept Neurosci, Ronald M Loeb Ctr Alzheimers Dis, New York, NY 10029 USA.
[Huang, Kuan-lin] Washington Univ, Sch Med, Dept Med, 660 S Euclid Ave B8134, St Louis, MO 63110 USA.
[Huang, Kuan-lin] Washington Univ, Sch Med, McDonnell Genome Inst, 660 S Euclid Ave B8134, St Louis, MO 63110 USA.
[Fagan, Anne M.; Holtzman, David M.; Morris, John C.] Washington Univ, Sch Med, Dept Neurol, 660 S Euclid Ave, St Louis, MO 63110 USA.
[Fagan, Anne M.; Holtzman, David M.; Morris, John C.] Washington Univ, Sch Med, Knight Alzheimers Dis Res Ctr, 660 S Euclid Ave, St Louis, MO 63110 USA.
[Fagan, Anne M.; Holtzman, David M.; Morris, John C.] Washington Univ, Sch Med, Hope Ctr Neurol Disorders, 660 S Euclid Ave B8111, St Louis, MO 63110 USA.
[Holtzman, David M.; Morris, John C.; Cruchaga, Carlos] Washington Univ, Sch Med, Dept Dev Biol, 660 S Euclid Ave, St Louis, MO 63110 USA.
[Kim, Sungeun; Saykin, Andrew J.] Indiana Univ, Sch Med, Indiana Alzheimer Dis Ctr, Indianapolis, IN USA.
[Kim, Sungeun; Saykin, Andrew J.] Indiana Univ, Sch Med, Ctr Neuroimaging, Indianapolis, IN USA.
[Kim, Sungeun] SUNY Coll Oswego, Dept Elect & Comp Engn, Oswego, NY 13126 USA.
[De Jager, Philip L.] Brigham & Womens Hosp, Program Translat NeuroPsychiat Gen, Dept Neurol, Inst Neurosci, 75 Francis St, Boston, MA 02115 USA.
[De Jager, Philip L.] Harvard Med Sch, Boston, MA 02115 USA.
[De Jager, Philip L.] Harvard Univ, Broad Inst, Program Med & Populat Genet, Cambridge, MA 02142 USA.
[De Jager, Philip L.] MIT, Cambridge, MA 02142 USA.
[Albert, Marilyn; Moghekar, Abhay] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA.
[O'Brien, Richard] Duke Med Ctr, Dept Neurol, Box 2900, Durham, NC 27710 USA.
[Riemenschneider, Matthias] Saarland Univ, Clin Psychiat & Psychotherapy, Homburg, Germany.
[Petersen, Ronald C.] Mayo Clin, Dept Neurol, Rochester, MN USA.
[Blennow, Kaj; Zetterberg, Henrik] Univ Gothenburg, Dept Psychiat & Neurochem, Inst Neurosci & Physiol, Sahlgrenska Acad, Molndal, Sweden.
[Blennow, Kaj; Zetterberg, Henrik] Univ Gothenburg, Clin Neurochem Lab, Dept Neurosci & Physiol, Sahlgrenska Univ Hosp, Molndal, Sweden.
[Zetterberg, Henrik] UCL Inst Neurol, Dept Mol Neurosci, London, England.
[Minthon, Lennart] Lund Univ, Clin Memory Res Unit, Dept Clin Sci, Lund, Sweden.
[Van Deerlin, Vivianna M.; Lee, Virginia Man-Yee; Shaw, Leslie M.; Trojanowski, John Q.; Schellenberg, Gerard] Univ Penn, Dept Pathol & Lab Med, Perelman Sch Med, Philadelphia, PA USA.
[Haines, Jonathan L.] Vanderbilt Univ, Dept Mol Physiol & Biophys, Vanderbilt Ctr Human Genet Res, Nashville, TN 37232 USA.
[Mayeux, Richard] Columbia Univ, Dept Neurol, Taub Inst Alzheimers Dis & Aging Brain, New York, NY USA.
[Mayeux, Richard] Columbia Univ, Gertrude H Sergievsky Ctr, New York, NY 10027 USA.
[Pericak-Vance, Margaret A.] Univ Miami, John P Hussman Inst Human Gen, Miami, FL USA.
[Pericak-Vance, Margaret A.] Univ Miami, Dr John T Macdonald Fdn, Dept Human Genet, Miami, FL USA.
[Farrer, Lindsay A.] Boston Univ, Dept Biostat, Boston, MA 02215 USA.
[Farrer, Lindsay A.] Boston Univ, Dept Med, Genet Program, Boston, MA 02215 USA.
[Farrer, Lindsay A.] Boston Univ, Dept Ophthalmol, Boston, MA 02215 USA.
[Farrer, Lindsay A.] Boston Univ, Dept Epidemiol, Boston, MA 02215 USA.
[Farrer, Lindsay A.] Boston Univ, Dept Neurol, Boston, MA 02215 USA.
[Peskind, Elaine R.; Li, Ge] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Peskind, Elaine R.] VA Puget Sound Hlth Care Syst, VISN Mental Illness Res Educ & Clin Ctr 20, Seattle, WA USA.
[Li, Ge] VA Puget Sound Hlth Care Syst, VISN Geriatr Res Educ & Clin Ctr 20, Seattle, WA USA.
[Di Narzo, Antonio F.] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA.
[Kauwe, John S. K.] Brigham Young Univ, Dept Biol, Provo, UT 84602 USA.
RP Cruchaga, C (reprint author), Washington Univ, Sch Med, Dept Psychiat, 660 S Euclid Ave B8134, St Louis, MO 63110 USA.; Cruchaga, C (reprint author), Washington Univ, Sch Med, Dept Dev Biol, 660 S Euclid Ave, St Louis, MO 63110 USA.
EM ccruchaga@wustl.edu
FU National Institutes of Health [R01AG044546, P01AG003991, RF1AG053303,
R01AG035083, R01NS085419]; Alzheimer's Association [NIRG-11-200110];
American Federation for Aging Research; BrightFocus Foundation
Alzheimer's Disease Research Grant [A2013359S]; NIH [P50 AG05681, P01
AG03991, P01 AG026276, U01AG032984]; GERAD from the Wellcome Trust
[GR082604MA]; Medical Research Council [G0300429]; NCRAD [U24 AG21886];
NACC [U01 AG016976]; NIAGADS [U24-AG041689]; UPENN [P30 AG010124]; NIA
[R03AG050856]; Alzheimer's Association; Michael J. Fox Foundation; ARUK
Biomarkers Across Neurodegenerative Diseases (BAND); German Federal
Ministry of Education and Research (BMBF) National Genome Research
Network (NGFN) [01GS08125]; Helmholtz Alliance for Mental Health in an
Aging Society (HELMA) [Ha-15]; [U01 AG024904]; [R01 AG19771]; [P30
AG10133]; [R01 AG048015]; [AG05136]
FX This work was supported by grants from the National Institutes of Health
(R01AG044546, P01AG003991, RF1AG053303, R01AG035083, and R01NS085419),
and the Alzheimer's Association (NIRG-11-200110). This research was
conducted while C.C. was a recipient of a New Investigator Award in
Alzheimer's disease from the American Federation for Aging Research.
C.C. is a recipient of a BrightFocus Foundation Alzheimer's Disease
Research Grant (A2013359S). The recruitment and clinical
characterization of research participants at Washington University were
supported by NIH P50 AG05681, P01 AG03991, and P01 AG026276. ADGC is
supported by grants from the NIH (#U01AG032984) and GERAD from the
Wellcome Trust (GR082604MA) and the Medical Research Council (G0300429);
additional support was provided by NCRAD (U24 AG21886), NACC (U01
AG016976), NIAGADS (U24-AG041689) and UPENN (P30 AG010124). Support for
A.S. was provided by U01 AG024904, R01 AG19771, and P30 AG10133. P.D.J.
received support from R01 AG048015. UW ADRC received funding from
AG05136. S.K. received support from NIA R03AG050856, Alzheimer's
Association, Michael J. Fox Foundation, and ARUK Biomarkers Across
Neurodegenerative Diseases (BAND). M.R. received support from the German
Federal Ministry of Education and Research (BMBF) National Genome
Research Network (NGFN) Grant No. 01GS08125 and through the Helmholtz
Alliance for Mental Health in an Aging Society (HELMA) Grant No. Ha-15.
This work was supported by access to equipment made possible by the Hope
Center for Neurological Disorders and the Departments of Neurology and
Psychiatry at Washington University School of Medicine.
NR 85
TC 0
Z9 0
U1 11
U2 11
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0001-6322
EI 1432-0533
J9 ACTA NEUROPATHOL
JI Acta Neuropathol.
PD MAY
PY 2017
VL 133
IS 5
BP 839
EP 856
DI 10.1007/s00401-017-1685-y
PG 18
WC Clinical Neurology; Neurosciences; Pathology
SC Neurosciences & Neurology; Pathology
GA ES2ZS
UT WOS:000399397300010
PM 28247064
ER
PT J
AU Wood, AE
Prins, A
Bush, NE
Hsia, JF
Bourn, LE
Earley, MD
Walser, RD
Ruzek, J
AF Wood, Amanda Ernst
Prins, Annabel
Bush, Nigel E.
Hsia, Jennifer F.
Bourn, Laura E.
Earley, Michael D.
Walser, Robyn D.
Ruzek, Josef
TI Reduction of Burnout in Mental Health Care Providers Using the Provider
Resilience Mobile Application
SO COMMUNITY MENTAL HEALTH JOURNAL
LA English
DT Article
DE Burnout; Employee health; Mobile applications
ID COMPASSION FATIGUE; VETERANS; SUPPORT; TRAUMA; SAMPLE
AB This pilot study examined the usability, acceptability, and effectiveness of a free Provider Resilience (PR) mobile application (app) designed by the National Center for Telehealth and Technology to reduce provider burnout. Outpatient mental health providers (N = 30) used the PR app for 1 month. Participants rated the PR app on the System Usability Scale with an overall score of 79.7, which is in the top quartile for usability. Results of paired sample t tests on the Professional Quality of Life Scale indicated significant decreases on the Burnout (t = 3.65, p < .001) and Compassion Fatigue (t = 4.54, p < .001) subscales. The Provider Resilience app shows promise in reducing burnout and compassion fatigue in mental health care providers.
C1 [Wood, Amanda Ernst; Hsia, Jennifer F.; Bourn, Laura E.; Earley, Michael D.] VA Puget Sound Hlth Care Syst, Amer Lake Div A116R, Tacoma, WA 98493 USA.
[Wood, Amanda Ernst] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Prins, Annabel; Walser, Robyn D.; Ruzek, Josef] VA Palo Alto Hlth Care Syst, Natl Ctr PTSD, Menlo Pk, CA USA.
[Prins, Annabel] San Jose State Univ, Dept Psychol, San Jose, CA 95192 USA.
[Bush, Nigel E.] Natl Ctr Telehlth & Technol, Tacoma, WA USA.
[Walser, Robyn D.] Univ Calif Berkeley, Dept Psychol, 3210 Tolman Hall, Berkeley, CA 94720 USA.
RP Wood, AE (reprint author), VA Puget Sound Hlth Care Syst, Amer Lake Div A116R, Tacoma, WA 98493 USA.; Wood, AE (reprint author), Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
EM Amanda.wood@va.gov
FU National Center for PTSD
FX Support for this study was provided by the National Center for PTSD.
NR 22
TC 0
Z9 0
U1 3
U2 3
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0010-3853
EI 1573-2789
J9 COMMUNITY MENT HLT J
JI Community Ment. Health J.
PD MAY
PY 2017
VL 53
IS 4
BP 452
EP 459
DI 10.1007/s10597-016-0076-5
PG 8
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ES0TM
UT WOS:000399239600010
PM 28070775
ER
PT J
AU Mridha, AR
Wree, A
Robertson, AAB
Yeh, MM
Johnson, CD
Van Rooyen, DM
Haczeyni, F
Teoh, NCH
Savard, C
Ioannou, GN
Masters, SL
Schroder, K
Cooper, MA
Feldstein, AE
Farrell, GC
AF Mridha, Auvro R.
Wree, Alexander
Robertson, Avril A. B.
Yeh, Matthew M.
Johnson, Casey D.
Van Rooyen, Derrick M.
Haczeyni, Fahrettin
Teoh, Narci C. -H.
Savard, Christopher
Ioannou, George N.
Masters, Seth L.
Schroder, Kate
Cooper, Matthew A.
Feldstein, Ariel E.
Farrell, Geoffrey C.
TI NLRP3 inflammasome blockade reduces liver inflammation and fibrosis in
experimental NASH in mice
SO JOURNAL OF HEPATOLOGY
LA English
DT Article
DE NAFLD; NLRP3; Inflammasomes; Cholesterol crystals; Kupffer cells;
Hepatocytes; Interleukin-1 beta; Fibrosis; Diet, atherogenic;
Methionine; NLR proteins
ID CROWN-LIKE STRUCTURES; NONALCOHOLIC STEATOHEPATITIS; CHOLESTEROL
CRYSTALS; DIABETIC MICE; FATTY-ACID; DISEASE; ACTIVATION; LIPOTOXICITY;
PATHOGENESIS; INJURY
AB Background & Aims: NOD-like receptor protein 3 (NLRP3) inflammasome activation occurs in Non-alcoholic fatty liver disease (NAFLD). We used the first small molecule NLRP3 inhibitor, MCC950, to test whether inflammasome blockade alters inflammatory recruitment and liver fibrosis in two murine models of steatohepatitis.
Methods: We fed foz/foz and wild-type mice an atherogenic diet for 16 weeks, gavaged MCC950 or vehicle until 24 weeks, then determined NAFLD phenotype. In mice fed an methionine/choline deficient (MCD) diet, we gavaged MCC950 or vehicle for 6 weeks and determined the effects on liver fibrosis.
Results: In vehicle-treated foz/foz mice, hepatic expression of NLRP3, pro-IL-1 beta, active caspase-1 and IL-1 beta increased at 24 weeks, in association with cholesterol crystal formation and NASH pathology; plasma IL-1 beta, IL-6, MCP-1, ALT/AST all increased. MCC950 treatment normalized hepatic caspase 1 and IL-1b expression, plasma IL-1 beta, MCP-1 and IL-6, lowered ALT/AST, and reduced the severity of liver inflammation including designation as NASH pathology, and liver fibrosis. In vitro, cholesterol crystals activated Kupffer cells and macrophages to release IL-1 beta; MCC950 abolished this, and the associated neutrophil migration. MCD diet-fed mice developed fibrotic steatohepatitis; MCC950 suppressed the increase in hepatic caspase 1 and IL-1 beta, lowered numbers of macrophages and neutrophils in the liver, and improved liver fibrosis.
Conclusion: MCC950, an NLRP3 selective inhibitor, improved NAFLD pathology and fibrosis in obese diabetic mice. This is potentially attributable to the blockade of cholesterol crystal-mediated NLRP3 activation in myeloid cells. MCC950 reduced liver fibrosis in MCD-fed mice. Targeting NLRP3 is a logical direction in pharmacotherapy of NASH.
Lay summary: Fatty liver disease caused by being overweight with diabetes and a high risk of heart attack, termed nonalcoholic steatohepatitis (NASH), is the most common serious liver disease with no current treatment. There could be several causes of inflammation in NASH, but activation of a protein scaffold within cells termed the inflammasome (NLRP3) has been suggested to play a role. Here we show that cholesterol crystals could be one pathway to activate the inflammasome in NASH. We used a drug called MCC950, which has already been shown to block NLRP3 activation, in an attempt to reduce liver injury in NASH. This drug partly reversed liver inflammation, particularly in obese diabetic mice that most closely resembles the human context of NASH. In addition, such dampening of liver inflammation in NASH achieved with MCC950 partly reversed liver scarring, the process that links NASH to the development of cirrhosis. (C) 2017 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
C1 [Mridha, Auvro R.; Van Rooyen, Derrick M.; Haczeyni, Fahrettin; Teoh, Narci C. -H.; Farrell, Geoffrey C.] Australian Natl Univ, Canberra Hosp, ANU Med Sch, Liver Res Grp, Garran, ACT, Australia.
[Wree, Alexander] RWTH Aachen Univ Hosp, Dept Internal Med 3, Aachen, Germany.
[Wree, Alexander; Johnson, Casey D.; Feldstein, Ariel E.] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA.
[Robertson, Avril A. B.; Schroder, Kate; Cooper, Matthew A.] Univ Queensland, Inst Mol Biosci, St Lucia, Qld, Australia.
[Yeh, Matthew M.] Univ Washington, Dept Pathol, Seattle, WA 98195 USA.
[Savard, Christopher; Ioannou, George N.] Vet Affairs Puget Sound Hlth Care Syst, Dept Gastroenterol & Hepatol, Seattle, WA USA.
[Savard, Christopher; Ioannou, George N.] Univ Washington, Seattle, WA 98195 USA.
[Masters, Seth L.] Walter & Eliza Hall Inst Med Res, Parkville, Vic, Australia.
RP Farrell, GC (reprint author), Canberra Hosp, Gastroenterol & Hepatol Unit, POB 111, Woden, ACT 2605, Australia.
EM geoff.farrell@anu.edu.au
FU NIH [R2 AA023574, U01 AA022489]; Australian NHMRC [1084136, 1044288,
1086786]; Deutsche Forschungsgemeinschaft [WR 173/3-1]
FX Supported by NIH Project grants R2 AA023574 and U01 AA022489 (to AEF),
Australian NHMRC project grants 1084136 and 1044288 (to GCF), and
1086786 (to MAC and AABR), and Deutsche Forschungsgemeinschaft WR
173/3-1 (to AW). Matthew Cooper is an NHMRC Principle Research Fellow
(1059354).
NR 50
TC 0
Z9 0
U1 3
U2 3
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 0168-8278
EI 1600-0641
J9 J HEPATOL
JI J. Hepatol.
PD MAY
PY 2017
VL 66
IS 5
BP 1037
EP 1046
DI 10.1016/j.jhep.2017.01.022
PG 10
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA ES0DM
UT WOS:000399196300021
PM 28167322
ER
PT J
AU Aghazadehsanai, N
Chang, TI
Garrett, NR
Friedlander, AH
AF Aghazadehsanai, Nona
Chang, Tina I.
Garrett, Neal R.
Friedlander, Arthur H.
TI Prevalence of calcified carotid artery atheromas on digital panoramic
images among perimenopausal and postmenopausal African American women
SO ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY
LA English
DT Article
ID HEART; ASSOCIATION; RADIOGRAPHS; DISEASE; HEALTH; PLAQUE; RISK;
ATHEROSCLEROSIS; CALCIFICATIONS; POPULATION
AB Objective. Health care disparities, often of an obscure nature, result in African American women (AAw) having enhanced risk of adverse cardiovascular events. Therefore, we sought to determine the prevalence of calcified carotid artery atheromas (CCAA), a validated risk indicator of these events, on their digital panoramic images.
Study Design. Comprehensive electronic medical records and digital panoramic images of self-identified AAw aged >= 45 years treated between 2007 and 2014 were retrieved from a Veterans Affairs Dental Service. Images were reviewed for CCAA in the cervical bifurcation region, and medical records were reviewed for atherogenic risk factors: hypertension, diabetes, and dyslipidemia.
Results. The study sample of 171 AAw (mean age 58.2 +/- 8.0 years) evidenced a 24% CCAA positive prevalence rate. In comparison with the CCAA negative group, those with atheromas were significantly older (61.4 +/- 10.1 vs. 57.2 +/- 7.0), diabetic, and dyslipidemic. Also observed among the full study sample was significant concordant increase of CCAA prevalence with age. Among those who were CCAA positive, there was a significant increased prevalence of dyslipidemia with age.
Conclusions. Panoramic images of older AAw frequently revealed carotid atheromas, a risk indicator of generalized atherosclerosis and future adverse cardiovascular events.
C1 [Aghazadehsanai, Nona] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Chang, Tina I.] VA Greater Los Angeles Healthcare Syst, Res Fellowship & Inpatient Oral & Maxillofacial S, Los Angeles, CA USA.
[Chang, Tina I.; Friedlander, Arthur H.] Univ Calif Los Angeles, Sch Dent, Oral & Maxillofacial Surg, Los Angeles, CA 90024 USA.
[Garrett, Neal R.] Univ Calif Los Angeles, Sch Dent, Los Angeles, CA 90024 USA.
[Friedlander, Arthur H.] VA Greater Los Angeles Healthcare Syst, Grad Med Educ, Los Angeles, CA USA.
[Friedlander, Arthur H.] Ronald Reagan UCLA Med Ctr, Hosp Dent Serv, Qual Assurance, Los Angeles, CA USA.
RP Friedlander, AH (reprint author), Hosp Dent Serv, 11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM arthur.friedlander@va.gov
FU VA Greater Los Angeles Healthcare System
FX This material is the result of work supported with resources and use of
facilities at the VA Greater Los Angeles Healthcare System. Its contents
do not represent the views of the U. S. Department of Veterans Affairs
or the United States Government. The authors have no conflicts of
interest to disclose.
NR 22
TC 0
Z9 0
U1 3
U2 3
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 2212-4403
EI 1528-395X
J9 OR SURG OR MED OR PA
JI Oral Surg. Oral Med. Oral Pathol. Oral Radiol.
PD MAY
PY 2017
VL 123
IS 5
BP 621
EP 625
DI 10.1016/j.oooo.2017.01.011
PG 5
WC Dentistry, Oral Surgery & Medicine
SC Dentistry, Oral Surgery & Medicine
GA ER6XT
UT WOS:000398954000021
PM 28407989
ER
PT J
AU Moon, AM
Green, PK
Berry, K
Ioannou, GN
AF Moon, A. M.
Green, P. K.
Berry, K.
Ioannou, G. N.
TI Transformation of hepatitis C antiviral treatment in a national
healthcare system following the introduction of direct antiviral agents
SO ALIMENTARY PHARMACOLOGY & THERAPEUTICS
LA English
DT Article
ID SUSTAINED VIROLOGICAL RESPONSE; GENOTYPE 1 INFECTION;
OF-VETERANS-AFFAIRS; VIRUS-INFECTION; HEPATOCELLULAR-CARCINOMA;
UNITED-STATES; COST-EFFECTIVENESS; HCV; SOFOSBUVIR; DASABUVIR
AB BackgroundHighly effective direct antiviral agents (DAAs) for hepatitis C virus (HCV) were introduced recently. Their utilisation has been limited by high cost and low access to care.
AimTo describe the effect of DAAs on HCV treatment and cure rates in the United States Veterans Affairs (VA) national healthcare system.
MethodsWe identified all HCV antiviral treatment regimens initiated from 1 January 1999 to 31 December 2015 (n = 105 369) in the VA national healthcare system, and determined if they resulted in sustained virological response (SVR).
ResultsHCV antiviral treatment rates were low (1981-6679 treatments/year) in the interferon era (1999-2010). The introduction of simeprevir and sofosbuvir in 2013 and ledipasvir/sofosbuvir and paritaprevir/ombitasvir/ritonavir/dasabuvir in 2014 were followed by increases in annual treatment rates to 9180 in 2014 and 31 028 in 2015. The number of patients achieving SVR was 1313 in 2010, the last year of the interferon era, and increased 5.6-fold to 7377 in 2014 and 21-fold to 28 084 in 2015. The proportion of treated patients who achieved SVR increased from 19.2% in 1999 and 36.0% in 2010 to 90.5% in 2015. Within 2015, monthly treatment rates ranged from 727 in July to 6868 in September correlating with the availability of funds for DAAs.
ConclusionsDAAs resulted in a 21-fold increase in the number of patients achieving HCV cure. Treatment rates in 2015 were limited primarily by the availability of funds. Further increases in funding and cost reductions of DAAs in 2016 suggest that the VA could cure the majority of HCV-infected Veterans in VA care within the next few years.
C1 [Moon, A. M.; Ioannou, G. N.] Univ Washington, Div Gen Internal Med, Seattle, WA 98195 USA.
[Green, P. K.; Berry, K.; Ioannou, G. N.] Vet Affairs Puget Sound Healthcare Syst, Hlth Serv Res, Seattle, WA USA.
[Green, P. K.; Berry, K.; Ioannou, G. N.] Vet Affairs Puget Sound Healthcare Syst, Hlth Serv Dev, Seattle, WA USA.
[Ioannou, G. N.] Vet Affairs Puget Sound Healthcare Syst, Gastroenterol, S-111 Gastro,1660 S Columbian Way, Seattle, WA 98108 USA.
[Ioannou, G. N.] Univ Washington, Seattle, WA 98195 USA.
RP Ioannou, GN (reprint author), Vet Affairs Puget Sound Healthcare Syst, Gastroenterol, S-111 Gastro,1660 S Columbian Way, Seattle, WA 98108 USA.
EM georgei@medicine.washington.edu
FU Merit Review grant, Clinical Science Research and Development, Office of
Research and Development, Veterans Affairs [I01CX001156]
FX The study was funded by a Merit Review grant (I01CX001156), Clinical
Science Research and Development, Office of Research and Development,
Veterans Affairs (GNI).
NR 48
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0269-2813
EI 1365-2036
J9 ALIMENT PHARM THER
JI Aliment. Pharmacol. Ther.
PD MAY
PY 2017
VL 45
IS 9
BP 1201
EP 1212
DI 10.1111/apt.14021
PG 12
WC Gastroenterology & Hepatology; Pharmacology & Pharmacy
SC Gastroenterology & Hepatology; Pharmacology & Pharmacy
GA ER3EM
UT WOS:000398678600003
PM 28271521
ER
PT J
AU Cook, DB
Light, AR
Light, KC
Broderick, G
Shields, MR
Dougherty, RJ
Meyer, JD
VanRiper, S
Stegner, AJ
Ellingson, LD
Vernon, SD
AF Cook, Dane B.
Light, Alan R.
Light, Kathleen C.
Broderick, Gordon
Shields, Morgan R.
Dougherty, Ryan J.
Meyer, Jacob D.
VanRiper, Stephanie
Stegner, Aaron J.
Ellingson, Laura D.
Vernon, Suzanne D.
TI Neural consequences of post-exertion malaise in Myalgic
Encephalomyelitis/Chronic Fatigue Syndrome
SO BRAIN BEHAVIOR AND IMMUNITY
LA English
DT Article
DE Exercise; Symptoms; Brain; Cognitive performance
ID ANTERIOR CINGULATE CORTEX; STATE FUNCTIONAL CONNECTIVITY; BRAIN MRI
ABNORMALITIES; GULF-WAR ILLNESS; MULTIPLE-SCLEROSIS; COGNITIVE FATIGUE;
WORKING-MEMORY; POSTEXERTIONAL MALAISE; PROCESSING SPEED; MENTAL FATIGUE
AB Post exertion malaise is one of the most debilitating aspects of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, yet the neurobiological consequences are largely unexplored. The objective of the study was to determine the neural consequences of acute exercise using functional brain imaging. Fifteen female Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients and 15 healthy female controls completed 30 min of submaximal exercise (70% of peak heart rate) on a cycle ergometer. Symptom assessments (e.g. fatigue, pain, mood) and brain imaging data were collected one week prior to and 24 h following exercise. Functional brain images were obtained during performance of: 1) a fatiguing cognitive task - the Paced Auditory Serial Addition Task, 2) a non-fatiguing cognitive task - simple number recognition, and 3) a non fatiguing motor task - finger tapping. Symptom and exercise data were analyzed using independent samples t-tests. Cognitive performance data were analyzed using mixed-model analysis of variance with repeated measures. Brain responses to fatiguing and non-fatiguing tasks were analyzed using linear mixed effects with cluster-wise (101-voxels) alpha of 0.05. Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients reported large symptom changes compared to controls (effect size >= 0.8, p < 0.05). Patients and controls had similar physiological responses to exercise (p > 0.05). However, patients exercised at significantly lower Watts and reported greater exertion and leg muscle pain (p < 0.05). For cognitive performance, a significant Group by Time interaction (p < 0.05), demonstrated pre- to post-exercise improvements for controls and worsening for patients. Brain responses to finger tapping did not differ between groups at either time point. During number recognition, controls exhibited greater brain activity (p < 0.05) in the posterior cingulate cortex, but only for the pre-exercise scan. For the Paced Serial Auditory Addition Task, there was a significant Group by Time interaction (p < 0.05) with patients exhibiting increased brain activity from pre- to postexercise compared to controls bilaterally for inferior and superior parietal and cingulate cortices. Changes in brain activity were significantly related to symptoms for patients (p < 0.05). Acute exercise exacerbated symptoms, impaired cognitive performance and affected brain function in Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome patients. These converging results, linking symptom exacerbation with brain function, provide objective evidence of the detrimental neurophysiological effects of post-exertion malaise. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license.
C1 [Cook, Dane B.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
[Cook, Dane B.; Shields, Morgan R.; Dougherty, Ryan J.; Meyer, Jacob D.; VanRiper, Stephanie; Stegner, Aaron J.] Univ Wisconsin, Madison, WI USA.
[Light, Alan R.; Light, Kathleen C.] Univ Utah, Salt Lake City, UT USA.
[Broderick, Gordon] Nova Southeastern Univ, Ft Lauderdale, FL USA.
[Ellingson, Laura D.] Iowa State Univ, Ames, IA USA.
[Vernon, Suzanne D.] Bateman Horne Ctr, Salt Lake City, UT USA.
RP Cook, DB (reprint author), Univ Wisconsin, Dept Kinesiol, 2000 Observ Dr, Madison, WI 53706 USA.
EM dane.cook@wisc.edu
FU Solve ME/CFS Initiative (SMCI) United States
FX Supported by a grant from the Solve ME/CFS Initiative (SMCI) United
States - Dane B Cook PI
NR 88
TC 0
Z9 0
U1 2
U2 2
PU ACADEMIC PRESS INC ELSEVIER SCIENCE
PI SAN DIEGO
PA 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA
SN 0889-1591
EI 1090-2139
J9 BRAIN BEHAV IMMUN
JI Brain Behav. Immun.
PD MAY
PY 2017
VL 62
BP 87
EP 99
DI 10.1016/j.bbi.2017.02.009
PG 13
WC Immunology; Neurosciences
SC Immunology; Neurosciences & Neurology
GA ER2TS
UT WOS:000398647300012
PM 28216087
ER
PT J
AU Wile, DJ
Agarwal, PA
Schulzer, M
Mak, E
Dinelle, K
Shahinfard, E
Vafai, N
Hasegawa, K
Zhang, J
McKenzie, J
Neilson, N
Strongosky, A
Uitti, RJ
Guttman, M
Zabetian, CP
Ding, YS
Adam, M
Aasly, J
Wszolek, ZK
Farrer, M
Sossi, V
Stoessl, AJ
AF Wile, Daryl J.
Agarwal, Pankaj A.
Schulzer, Michael
Mak, Edwin
Dinelle, Katherine
Shahinfard, Elham
Vafai, Nasim
Hasegawa, Kazuko
Zhang, Jing
McKenzie, Jessamyn
Neilson, Nicole
Strongosky, Audrey
Uitti, Ryan J.
Guttman, Mark
Zabetian, Cyrus P.
Ding, Yu-Shin
Adam, Mike
Aasly, Jan
Wszolek, Zbigniew K.
Farrer, Matthew
Sossi, Vesna
Stoessl, A. Jon
TI Serotonin and dopamine transporter PET changes in the premotor phase of
LRRK2 parkinsonism: cross-sectional studies
SO LANCET NEUROLOGY
LA English
DT Article
ID G2019S MUTATION CARRIERS; DISEASE; DYSFUNCTION; BINDING; PROGRESSION
AB Background People with Parkinson's disease can show premotor neurochemical changes in the dopaminergic and non-dopaminergic systems. Using PET, we assessed whether dopaminergic and serotonin transporter changes are similar in LRRK2 mutation carriers with Parkinson's disease and individuals with sporadic Parkinson's disease, and whether LRRK2 mutation carriers without motor symptoms show PET changes.
Methods We did two cross-sectional PET studies at the Pacific Parkinson's Research Centre in Vancouver, BC, Canada. We included LRRK2 mutation carriers with or without manifest Parkinson's disease, people with sporadic Parkinson's disease, and age-matched healthy controls, all aged 18 years or older. People with Parkinson's disease were diagnosed by a neurologist with movement disorder training, in accordance with the UK Parkinson's Disease Society Brain Bank criteria. LRRK2 carrier status was confirmed by bidirectional Sanger sequencing. In the first study, LRRK2 mutation carriers with or without manifest Parkinson's disease who were referred for investigation between July, 1999, and January, 2012, were scanned with PET tracers for the membrane dopamine transporter, and dopamine synthesis and storage (F-18-6-fluoro-L-dopa; F-18-FDOPA). We compared findings with those in people with sporadic Parkinson's disease and age-matched healthy controls. In the second study, distinct groups of LRRK2 mutation carriers, individuals with sporadic Parkinson's disease, and age-matched healthy controls seen from November, 2012, to May, 2016, were studied with tracers for the serotonin transporter and vesicular monoamine transporter 2 (VMAT2). Striatal dopamine transporter binding, VMAT2 binding, F-18-FDOPA uptake, and serotonin transporter binding in multiple brain regions were compared by ANCOVA, adjusted for age.
Findings Between January, 1997, and January, 2012, we obtained data for our first study from 40 LRRK2 mutation carriers, 63 individuals with sporadic Parkinson's disease, and 35 healthy controls. We identified significant group differences in striatal dopamine transporter binding (all age ranges in caudate and putamen, p<0.0001) and F-18-FDOPA uptake (in caudate: age <= 50 years, p=0.0002; all other age ranges, p<0.0001; in putamen: all age ranges, p<0.0001). LRRK2 mutation carriers with manifest Parkinson's disease (n=15) had reduced striatal dopamine transporter binding and F-18-FDOPA uptake, comparable with amounts seen in individuals with sporadic Parkinson's disease of similar duration. LRRK2 mutation carriers without manifest Parkinson's disease (n=25) had greater F-18-FDOPA uptake and dopamine transporter binding than did individuals with sporadic Parkinson's disease, with F-18-FDOPA uptake comparable with controls and dopamine transporter binding lower than in controls. Between November, 2012, and May, 2016, we obtained data for our second study from 16 LRRK2 mutation carriers, 13 individuals with sporadic Parkinson's disease, and nine healthy controls. Nine LRRK2 mutation carriers without manifest Parkinson's disease had significantly elevated serotonin transporter binding in the hypothalamus (compared with controls, individuals with LRRK2 Parkinson's disease, and people with sporadic Parkinson's disease, p<0.0001), striatum (compared with people with sporadic Parkinson's disease, p=0.02), and brainstem (compared with LRRK2 mutation carriers with manifest Parkinson's disease, p=0.01), after adjustment for age. Serotonin transporter binding in the cortex did not differ significantly between groups after age adjustment. Striatal VMAT2 binding was reduced in all individuals with manifest Parkinson's disease and reduced asymmetrically in one LRRK2 mutation carrier without manifest disease.
Interpretation Dopaminergic and serotonergic changes progress in a similar fashion in LRRK2 mutation carriers with manifest Parkinson's disease and individuals with sporadic Parkinson's disease, but LRRK2 mutation carriers without manifest Parkinson's disease show increased serotonin transporter binding in the striatum, brainstem, and hypothalamus, possibly reflecting compensatory changes in serotonergic innervation preceding the motor onset of Parkinson's disease. Increased serotonergic innervation might contribute to clinical differences in LRRK2 Parkinson's disease, including the emergence of non-motor symptoms and, potentially, differences in the long-term response to levodopa.
C1 [Wile, Daryl J.; Stoessl, A. Jon] Univ British Columbia, Dept Med, Vancouver, BC, Canada.
[Schulzer, Michael] Univ British Columbia, Dept Stat, Vancouver, BC, Canada.
[Dinelle, Katherine; Shahinfard, Elham; Vafai, Nasim; Sossi, Vesna] Univ British Columbia, Dept Phys & Astron, Vancouver, BC, Canada.
[Farrer, Matthew] Univ British Columbia, Dept Med Genet, Vancouver, BC, Canada.
[Agarwal, Pankaj A.] Global Hosp, Bombay, Maharashtra, India.
[Aasly, Jan] Norwegian Univ Sci & Technol, Trondheim, Norway.
[Strongosky, Audrey; Uitti, Ryan J.; Wszolek, Zbigniew K.] Mayo Clin, Jacksonville, FL 32224 USA.
[Mak, Edwin; McKenzie, Jessamyn; Neilson, Nicole; Stoessl, A. Jon] Pacific Parkinsons Res Ctr, Vancouver, BC, Canada.
[Hasegawa, Kazuko] Sagamihara Natl Hosp, Sagamihara, Kanagawa, Japan.
[Zhang, Jing; Zabetian, Cyrus P.] Univ Washington, Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA 98195 USA.
[Guttman, Mark] Ctr Movement Disorders, Toronto, ON, Canada.
[Ding, Yu-Shin] NYU, Sch Med, New York, NY USA.
[Adam, Mike] TRIUMF, Vancouver, BC, Canada.
RP Wile, DJ (reprint author), Univ British Columbia, Southern Med Program, Kelowna, BC V1W 4V5, Canada.
EM dwile@mail.ubc.ca
FU Canada Research Chairs; Michael J Fox Foundation; National Institutes of
Health; Pacific Alzheimer Research Foundation; Pacific Parkinson's
Research Institute; National Research Council of Canada
FX Canada Research Chairs, Michael J Fox Foundation, National Institutes of
Health, Pacific Alzheimer Research Foundation, Pacific Parkinson's
Research Institute, National Research Council of Canada.
NR 28
TC 1
Z9 1
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1474-4422
EI 1474-4465
J9 LANCET NEUROL
JI Lancet Neurol.
PD MAY
PY 2017
VL 16
IS 5
BP 351
EP 359
DI 10.1016/S1474-4422(17)30056-X
PG 9
WC Clinical Neurology
SC Neurosciences & Neurology
GA ER4PH
UT WOS:000398782100012
PM 28336296
ER
PT J
AU Parang, B
Kaz, AM
Barrett, CW
Short, SP
Ning, W
Keating, CE
Mittal, MK
Naik, RD
Washington, MK
Revetta, FL
Smith, J
Chen, X
Wilson, KT
Brand, T
Bader, DM
Tansey, WP
Chen, R
Brentnall, TA
Grady, WM
Williams, CS
AF Parang, Bobak
Kaz, Andrew M.
Barrett, Caitlyn W.
Short, Sarah P.
Ning, Wei
Keating, Cody E.
Mittal, Mukul K.
Naik, Rishi D.
Washington, Mary K.
Revetta, Frank L.
Smith, Joshua
Chen, Xi
Wilson, Keith T.
Brand, Thomas
Bader, David M.
Tansey, William P.
Chen, Ru
Brentnall, Teresa A.
Grady, William M.
Williams, Christopher S.
TI BVES regulates c-Myc stability via PP2A and suppresses colitis-induced
tumourigenesis
SO GUT
LA English
DT Article
ID INFLAMMATORY-BOWEL-DISEASE; JUNCTIONAL ADHESION MOLECULE; DEXTRAN
SODIUM-SULFATE; ULCERATIVE-COLITIS; TIGHT JUNCTION; COLORECTAL-CANCER;
COLON-CARCINOMA; GASTRIC-CANCER; E-CADHERIN; EXPRESSION
AB Objective Blood vessel epicardial substance (BVES) is a tight junction-associated protein that regulates epithelial-mesenchymal states and is underexpressed in epithelial malignancy. However, the functional impact of BVES loss on tumourigenesis is unknown. Here we define the in vivo role of BVES in colitis-associated cancer (CAC), its cellular function and its relevance to patients with IBD.
Design We determined BVES promoter methylation status using an Infinium HumanMethylation450 array screen of patients with UC with and without CAC. We also measured BVES mRNA levels in a tissue microarray consisting of normal colons and CAC samples. Bves(-/-) and wild-type mice (controls) were administered azoxymethane (AOM) and dextran sodium sulfate (DSS) to induce tumour formation. Last, we used a yeast two-hybrid screen to identify BVES interactors and performed mechanistic studies in multiple cell lines to define how BVES reduces c-Myc levels.
Results BVES mRNA was reduced in tumours from patients with CAC via promoter hypermethylation. Importantly, BVES promoter hypermethylation was concurrently present in distant non-malignant-appearing mucosa. As seen in human patients, Bves was underexpressed in experimental inflammatory carcinogenesis, and Bves(-/-) mice had increased tumour multiplicity and degree of dysplasia after AOM/DSS administration. Molecular analysis of Bves(-/-) tumours revealed Wnt activation and increased c-Myc levels. Mechanistically, we identified a new signalling pathway whereby BVES interacts with PR61 alpha, a protein phosphatase 2A regulatory subunit, to mediate c-Myc destruction.
Conclusion Loss of BVES promotes inflammatory tumourigenesis through dysregulation of Wnt signalling and the oncogene c-Myc. BVES promoter methylation status may serve as a CAC biomarker.
C1 [Parang, Bobak; Barrett, Caitlyn W.; Short, Sarah P.; Ning, Wei; Keating, Cody E.; Mittal, Mukul K.; Naik, Rishi D.; Wilson, Keith T.; Williams, Christopher S.] Vanderbilt Univ, Dept Med, Div Gastroenterol, Nashville, TN USA.
[Parang, Bobak; Barrett, Caitlyn W.; Short, Sarah P.; Ning, Wei; Keating, Cody E.; Mittal, Mukul K.; Wilson, Keith T.; Williams, Christopher S.] Vanderbilt Univ, Dept Canc Biol, 221 Kirkland Hall, Nashville, TN 37235 USA.
[Kaz, Andrew M.] VA Puget Sound Hlth Care Syst, Gastroenterol Sect, Seattle, WA USA.
[Kaz, Andrew M.; Chen, Ru; Brentnall, Teresa A.; Grady, William M.] Univ Washington, Dept Med, Div Gastroenterol, Seattle, WA USA.
[Washington, Mary K.; Revetta, Frank L.] Vanderbilt Univ, Dept Pathol Microbiol & Immunol, 221 Kirkland Hall, Nashville, TN 37235 USA.
[Smith, Joshua] Mem Sloan Kettering Canc Ctr, Dept Surg, Colorectal Serv, 1275 York Ave, New York, NY 10021 USA.
[Chen, Xi] Univ Miami, Miller Sch Med, Sylvester Comprehens Canc Ctr, Dept Publ Hlth Sci,Div Biostat, Miami, FL 33136 USA.
[Wilson, Keith T.; Williams, Christopher S.] Vanderbilt Ingram Canc Ctr, Nashville, TN USA.
[Wilson, Keith T.; Williams, Christopher S.] Vet Affairs Tennessee Valley Hlth Care Syst, Nashville, TN USA.
[Brand, Thomas] Imperial Coll London, Heart Sci Ctr, Natl Heart & Lung Inst, London, England.
[Bader, David M.; Tansey, William P.] Vanderbilt Univ, Dept Cell & Dev Biol, 221 Kirkland Hall, Nashville, TN 37235 USA.
RP Williams, CS (reprint author), Vanderbilt Univ, Sch Med, Med & Canc Biol, 1065D MRB-4,B2215 Garland Ave, Nashville, TN 37232 USA.; Williams, CS (reprint author), Vanderbilt Univ, Sch Med, Phys Scientist Training Programme, 1065D MRB-4,B2215 Garland Ave, Nashville, TN 37232 USA.; Williams, CS (reprint author), Vanderbilt Univ, Sch Med, VA Hlth Syst, 1065D MRB-4,B2215 Garland Ave, Nashville, TN 37232 USA.
EM christopher.williams@vanderbilt.edu
FU VA Merit [1I01BX001426]; Medical Research Council [MR/J010383/J1];
Vanderbilt Institute for Clinical and Translational Research
[UL1TR000445]; NIH [1F30DK096718-01A1, R01AT004821, T32 GM07347,
DK080221, P50CA095103]; ACS [ACS-RSG 116552]
FX VA Merit (1I01BX001426), Medical Research Council (MR/J010383/J1),
Vanderbilt Institute for Clinical and Translational Research
(UL1TR000445), NIH (1F30DK096718-01A1, R01AT004821, T32 GM07347), NIH
(DK080221, P50CA095103) and ACS (ACS-RSG 116552).
NR 46
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U1 3
U2 3
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 0017-5749
EI 1468-3288
J9 GUT
JI Gut
PD MAY
PY 2017
VL 66
IS 5
BP 852
EP 862
DI 10.1136/gutjnl-2015-310255
PG 11
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA ER1QH
UT WOS:000398566800012
PM 28389570
ER
PT J
AU Singh, JA
AF Singh, Jasvinder A.
TI Lesinurad combination therapy with allopurinol in gout: do CLEAR studies
make the treatment of gout clearer?
SO ANNALS OF THE RHEUMATIC DISEASES
LA English
DT Editorial Material
ID PREVALENCE; HYPERURICEMIA
C1 [Singh, Jasvinder A.] Birmingham VA Med Ctr, Birmingham, AL USA.
[Singh, Jasvinder A.] Univ Alabama Birmingham, Sch Med, Dept Med, Birmingham, AL 35294 USA.
[Singh, Jasvinder A.] Univ Alabama Birmingham, Sch Publ Hlth, Div Epidemiol, Birmingham, AL 35294 USA.
RP Singh, JA (reprint author), Univ Alabama Birmingham, Fac Off Tower B805, 510 20th St S, Birmingham, AL 35294 USA.
EM Jasvinder.md@gmail.com
FU Takeda; Savient; Regeneron; Merz; Iroko; Bioiberica; Crealta; Allergan
pharmaceuticals; WebMD; UBM LLC; American College of Rheumatology;
Horizon pharmaceuticals; ACR's Annual Meeting Planning Committee; Chair
of the ACR Meet-the-Professor, Workshop and Study Group Subcommittee;
Veterans Affairs Rheumatology Field Advisory Committee
FX JAS has received research grants from Takeda and Savient and consultant
fees from Savient, Takeda, Regeneron, Merz, Iroko, Bioiberica, Crealta
and Allergan pharmaceuticals, WebMD, UBM LLC and the American College of
Rheumatology. JAS serves as the principal investigator for an
investigator-initiated study funded by Horizon pharmaceuticals through a
grant to DINORA, a 501 (c) (3) entity. JAS is a member of the executive
of OMERACT, an organisation that develops outcome measures in
rheumatology and receives arms-length funding from 36 companies; a
member of the ACR's Annual Meeting Planning Committee; Chair of the ACR
Meet-the-Professor, Workshop and Study Group Subcommittee; and a member
of the Veterans Affairs Rheumatology Field Advisory Committee. JAS is
supported by the resources and the use of facilities at the VA Medical
Center at Birmingham, Alabama, USA.
NR 13
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U1 4
U2 4
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 0003-4967
EI 1468-2060
J9 ANN RHEUM DIS
JI Ann. Rheum. Dis.
PD MAY
PY 2017
VL 76
IS 5
DI 10.1136/annrheumdis-2016-210519
PG 3
WC Rheumatology
SC Rheumatology
GA EQ9EM
UT WOS:000398387200004
PM 28039184
ER
PT J
AU Kishan, AU
Shaikh, T
Wang, PC
Reiter, RE
Said, J
Raghavan, G
Nickols, NG
Aronson, WJ
Sadeghi, A
Kamrava, M
Demanes, DJ
Steinberg, ML
Horwitz, EM
Kupelian, PA
King, CR
AF Kishan, Amar U.
Shaikh, Talha
Wang, Pin-Chieh
Reiter, Robert E.
Said, Jonathan
Raghavan, Govind
Nickols, Nicholas G.
Aronson, William J.
Sadeghi, Ahmad
Kamrava, Mitchell
Demanes, David Jeffrey
Steinberg, Michael L.
Horwitz, Eric M.
Kupelian, Patrick A.
King, Christopher R.
TI Clinical Outcomes for Patients with Gleason Score 9-10 Prostate
Adenocarcinoma Treated With Radiotherapy or Radical Prostatectomy: A
Multi-institutional Comparative Analysis
SO EUROPEAN UROLOGY
LA English
DT Article
DE Gleason 9; Gleason 10; Radiotherapy; Radical prostatectomy
ID ANDROGEN-DEPRIVATION THERAPY; ISUP CONSENSUS CONFERENCE;
INTERNATIONAL-SOCIETY; RANDOMIZED-TRIALS; RADIATION-THERAPY; BEAM
RADIOTHERAPY; HORMONAL-THERAPY; SHORT-TERM; CANCER; CARCINOMA
AB Background: The long natural history of prostate cancer (CaP) limits comparisons of efficacy between radical prostatectomy (RP) and external beam radiotherapy (EBRT), since patients treated years ago received treatments considered suboptimal by modern standards (particularly with regards to androgen deprivation therapy [ADT] and radiotherapy dose-escalation]. Gleason score (GS) 9-10 CaP is particularly aggressive, and clinically-relevant endpoints occur early, facilitating meaningful comparisons.
Objective: To compare outcomes of patientswithGS 9-10 CaP following EBRT, extremely-dose escalatedradiotherapy(as exemplifiedbyEBRT + brachytherapy[EBRT + BT]), andRP.
Design, setting, participants: Retrospective analysis of 487 patients with biopsy GS 9-10 CaP treated between 2000 and 2013 (230 with EBRT, 87 with EBRT + BT, and 170 with RP). Most radiotherapy patients received ADT and dose-escalated radiotherapy.
Outcome measurements and statistical analysis: Kaplan-Meier analysis and multivariate Cox regression estimated and compared 5-yr and 10-yr rates of distant metastasisfree survival, cancer-specific survival (CSS), and overall survival (OS).
Results and limitations: The median follow-up was 4.6 yr. Local salvage and systemic salvage were performed more frequently in RP patients (49.0% and 30.1%) when compared with either EBRT patients (0.9% and 19.7%) or EBRT + BT patients (1.2% and 16.1%, p < 0.0001). Five-yr and 10-yr distant metastasis-free survival rates were significantly higher with EBRT + BT (94.6% and 89.8%) than with EBRT (78.7% and 66.7%, p = 0.0005) or RP (79.1% and 61.5%, p < 0.0001). The 5-yr and 10-yr CSS and OS rates were similar across all three cohorts.
Conclusions: Radiotherapy and RP provide equivalent CSS and OS. Extremely dose-escalated radiotherapy with ADT in particular offers improved systemic control when compared with either EBRT or RP. These data suggest that extremely dose-escalated radiotherapy with ADT might be the optimal upfront treatment for patients with biopsy GS 9-10 CaP.
Patient summary: While some prostate cancers are slow-growing requiring many years, sometimes decades, of follow-up in order to compare between radiation and surgery, high-risk and very aggressive cancers follow a much shorter time course allowing such comparisons to bemade and updated as treatments, especially radiation, rapidly evolve. We showed that radiation-based treatments and surgery, with contemporary standards, offer equivalent survival for patientswith very aggressive cancers (defined asGleason score 9-10). Extremely-dose escalated radiotherapy with short-course androgen deprivation therapy offered the least risk of developing metastases, and equivalent long term survival. (C) 2016 European Association of Urology. Published by Elsevier B. V. All rights reserved.
C1 [Kishan, Amar U.; Wang, Pin-Chieh; Raghavan, Govind; Nickols, Nicholas G.; Kamrava, Mitchell; Demanes, David Jeffrey; Steinberg, Michael L.; Kupelian, Patrick A.; King, Christopher R.] Univ Calif Los Angeles, Dept Radiat Oncol, Los Angeles, CA 90024 USA.
[Shaikh, Talha; Horwitz, Eric M.] Fox Chase Canc Ctr, Dept Radiat Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA.
[Reiter, Robert E.; Aronson, William J.] Univ Calif Los Angeles, Dept Urol, Los Angeles, CA USA.
[Said, Jonathan] Univ Calif Los Angeles, Dept Pathol, Los Angeles, CA 90024 USA.
[Nickols, Nicholas G.; Sadeghi, Ahmad] Vet Affairs Greater Los Angeles Healthcare Syst, Dept Radiat Oncol, Los Angeles, CA USA.
[Aronson, William J.] Vet Affairs Greater Los Angeles Healthcare Syst, Dept Urol, Los Angeles, CA USA.
RP Kishan, AU (reprint author), Dept Radiat Oncol, Suite B265,200 Med Plaza, Los Angeles, CA 90095 USA.
EM aukishan@mednet.ucla.edu
NR 34
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U1 4
U2 4
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 0302-2838
EI 1873-7560
J9 EUR UROL
JI Eur. Urol.
PD MAY
PY 2017
VL 71
IS 5
BP 766
EP 773
DI 10.1016/j.eururo.2016.06.046
PG 8
WC Urology & Nephrology
SC Urology & Nephrology
GA EQ0PO
UT WOS:000397773300031
PM 27452951
ER
PT J
AU Abdallah, CG
AF Abdallah, Chadi G.
TI What's the Buzz About Hydroxynorketamine? Is It the History, the Story,
the Debate, or the Promise?
SO BIOLOGICAL PSYCHIATRY
LA English
DT Editorial Material
ID ANTIDEPRESSANT; KETAMINE; METABOLITES; DEPRESSION; RECEPTORS
C1 [Abdallah, Chadi G.] US Dept Vet Affairs, Natl Ctr PTSD, Clin Neurosci Div, West Haven, CT USA.
[Abdallah, Chadi G.] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA.
RP Abdallah, CG (reprint author), Yale Univ, Sch Med, VA Natl Ctr PTSD, Dept Psychiat,Clin Neurosci Div, 950 Campbell Ave,151E, West Haven, CT 06516 USA.
EM chadi.abdallah@yale.edu
FU U.S. Department of Veterans Affairs; National Center for PTSD; Patterson
Trust Award; National Institute of Mental Health [K23MH101498]
FX This work was supported by the U. S. Department of Veterans Affairs,
National Center for PTSD, the Patterson Trust Award, and the National
Institute of Mental Health (Grant No. K23MH101498). The views expressed
in this article are those of the author and do not necessarily reflect
the position or policy of the Department of Veterans Affairs or other
sponsoring institutions.
NR 10
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U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0006-3223
EI 1873-2402
J9 BIOL PSYCHIAT
JI Biol. Psychiatry
PD APR 15
PY 2017
VL 81
IS 8
BP E61
EP E63
DI 10.1016/j.biopsych.2017.01.002
PG 3
WC Neurosciences; Psychiatry
SC Neurosciences & Neurology; Psychiatry
GA EP3SA
UT WOS:000397300800002
PM 28317551
ER
PT J
AU Peralta, CA
Frigaard, M
Rubinsky, AD
Rolon, L
Lo, L
Voora, S
Seal, K
Tuot, D
Chao, S
Lui, K
Chiao, P
Powe, N
Shlipak, M
AF Peralta, Carmen A.
Frigaard, Martin
Rubinsky, Anna D.
Rolon, Leticia
Lo, Lowell
Voora, Santhi
Seal, Karen
Tuot, Delphine
Chao, Shirley
Lui, Kimberly
Chiao, Phillip
Powe, Neil
Shlipak, Michael
TI Implementation of a pragmatic randomized trial of screening for chronic
kidney disease to improve care among non-diabetic hypertensive veterans
SO BMC NEPHROLOGY
LA English
DT Article
DE Chronic kidney disease; Blood pressure; Hypertension; Screening
ID CLINICAL-PRACTICE GUIDELINE; RE-AIM FRAMEWORK; QUALITY-OF-CARE;
COST-EFFECTIVENESS; CYSTATIN C; UNITED-STATES; HEALTH; RISK;
INTERVENTIONS; CREATININE
AB Background: Whether screening for chronic kidney disease (CKD) can improve the care of persons at high risk for complications remains uncertain. We describe the design and early implementation experience of a pilot, cluster-randomized pragmatic trial to evaluate the feasibility, implementation, and effectiveness of a "triple marker" CKD screening program (creatinine, cystatin C and albumin to creatinine ratio) for improving care among hypertensive veterans seen in primary care at one Veterans Administration Hospital.
Methods/design: Non-diabetic hypertensive veterans age 18-80 without known CKD were randomized in clusters determined by primary care provider (unit of randomization) into three arms. Usual care will be compared with two incrementally intensified treatment strategies: (1) screen for CKD followed by patient and provider education or (2) screen-educate plus a clinical pharmacist-led CKD and BP management program. The primary clinical outcome is systolic blood pressure (BP) change from baseline. Secondary clinical outcome is BP control. The primary process outcomes is triple marker screening (across three arms), and secondary process outcomes include use of inhibitors of the renin-angiotensin system (ACE/ARB) overall and in persons with albuminuria, CKD recognition by PCP, use of non-steroidal anti-inflammatory drugs (NSAIDs) and NSAID education by PCP. The design uses the Veterans Health Administration electronic health record (EHR) to identify participants, deliver the interventions and ascertain study outcomes. Assessment of the program implementation will use the Reach, Effectiveness, Adoption, Implementation, and Maintenance (RE-AIM) framework. Study duration is 12 months.
Results: A total of 1,819 patients have been randomized within 41 provider clusters. The median age (interquartile range) is 68 years (61-72), and 99% of participants are male. Approximately 16% are Black, and 5% Hispanic. In the first 6 months of the trial, 434 triple marker screening tests have been ordered, and 217(50%) have been tested. A total of 48 new CKD cases have been identified among those tested, for a preliminary yield of 22%.
Conclusion: We have successfully implemented a pragmatic protocol that uses the EHR to identify and characterize eligible participants, deliver the intervention, and ascertain study outcomes with high rates of participation by providers and patients. Results from this study can guide design of pragmatic trials in the field of CKD.
C1 [Peralta, Carmen A.; Frigaard, Martin; Rubinsky, Anna D.; Seal, Karen; Chao, Shirley; Lui, Kimberly; Chiao, Phillip; Shlipak, Michael] San Francisco VA Med Ctr, 4150 Clement St,111A1, San Francisco, CA 94121 USA.
[Rolon, Leticia; Lo, Lowell] Univ Calif San Francisco, 533 Parnassus Ave, San Francisco, CA 94117 USA.
[Voora, Santhi] Univ Calif San Francisco, 533 Parnassus Ave,UC Hall, San Francisco, CA 94143 USA.
[Tuot, Delphine; Powe, Neil] San Francisco Gen Hosp, 1001 Potrero Ave,SFGH 100, San Francisco, CA 94110 USA.
RP Peralta, CA (reprint author), San Francisco VA Med Ctr, 4150 Clement St,111A1, San Francisco, CA 94121 USA.
EM carmenalicia.peralta@ucsf.edu
FU National Kidney Foundation; [1R34DK102152]
FX This work is supported by 1R34DK102152 (PI: Peralta) and the National
Kidney Foundation.
NR 26
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U1 0
U2 0
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1471-2369
J9 BMC NEPHROL
JI BMC Nephrol.
PD APR 12
PY 2017
VL 18
AR 132
DI 10.1186/s12882-017-0541-6
PG 10
WC Urology & Nephrology
SC Urology & Nephrology
GA ES0AD
UT WOS:000399187400001
PM 28399844
ER
PT J
AU Williams, JS
Bishu, K
Dismuke, CE
Egede, LE
AF Williams, Joni S.
Bishu, Kinfe
Dismuke, Clara E.
Egede, Leonard E.
TI Sex differences in healthcare expenditures among adults with diabetes:
evidence from the medical expenditure panel survey, 2002-2011
SO BMC HEALTH SERVICES RESEARCH
LA English
DT Article
DE Sex differences; Healthcare expenditures; Adults; Diabetes
ID UNITED-STATES; US ADULTS; COSTS; MODELS
AB Background: The evidence assessing differences in medical costs between men and women with diabetes living in the United States is sparse; however, evidence suggests women generally have higher healthcare expenditures compared to men. Since little is known about these differences, the aim of this study was to assess differences in out-of-pocket (OOP) and total healthcare expenditures among adults with diabetes.
Methods: Data were used from 20,442 adults (>= 18 years of age) with diabetes from the 2002-2011 Medical Expenditure Panel Survey. Dependent variables were OOP and total direct expenditures for multiple health services (prescription, office-based, inpatient, outpatient, emergency, dental, home healthcare, and other services). The independent variable was sex. Covariates included sociodemographic characteristics, comorbid conditions, and time. Sample demographics were summarized. Mean OOP and total direct expenditures for health services by sex status were analyzed. Regression models were performed to assess incremental costs of healthcare expenditures by sex among adults with diabetes.
Results: Fifty-six percent of the sample was composed of women. Unadjusted mean OOP costs were higher for women for prescriptions ($1177; 95% CI $1117-$1237 vs. $959; 95% CI $918-$1000; p < 0.001) compared to men. Unadjusted mean total direct expenditures were also higher for women for prescriptions ($3797; 95% CI $3660-$3934 vs. $3334; 95% CI $3208-$3460; p < 0.001) and home healthcare ($752; 95% CI $646-$858 vs. $397; 95% CI $332-$462; p < 0.001). When adjusting for covariates, higher OOP and total direct costs persisted for women for prescription services (OOP: $156; 95% CI $87-$ 225; p < 0.001 and total: $184; 95% CI $50-$318; p = 0.007). Women also paid > $50 OOP for office-based visits (p < 0.001) and > $55 total expenditures for home healthcare (p = 0.041) compared to men after adjustments.
Conclusions: Our findings show women with diabetes have higher OOP and total direct expenditures compared to men. Additional research is needed to investigate this disparity between men and women and to understand the associated drivers and clinical implications. Policy recommendations are warranted to minimize the higher burden of costs for women with diabetes.
C1 [Williams, Joni S.; Egede, Leonard E.] Med Coll Wisconsin, Ctr Patient Care & Outcomes Res, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA.
[Williams, Joni S.; Egede, Leonard E.] Med Coll Wisconsin, Dept Med, Div Gen Internal Med, 9200 Wisconsin Ave, Milwaukee, WI 53226 USA.
[Bishu, Kinfe; Dismuke, Clara E.] Med Univ South Carolina, Dept Med, Ctr Hlth Dispar Res, 135 Rutledge Ave,Room 280,MSC 250593, Charleston, SC 29425 USA.
[Bishu, Kinfe; Dismuke, Clara E.] Med Univ South Carolina, Dept Med, Div Gen Internal Med & Geriat, 171 Ashley Ave, Charleston, SC 29425 USA.
[Dismuke, Clara E.] Vet Affairs Med Ctr, Ctr Innovat COIN, Hlth Equity & Rural Outreach Innovat Ctr HEROIC, Ralph H Johnson Dept, 109 Bee St,Mail Code 151, Charleston, SC 29401 USA.
RP Egede, LE (reprint author), Med Coll Wisconsin, Ctr Patient Care & Outcomes Res, 8701 Watertown Plank Rd, Milwaukee, WI 53226 USA.; Egede, LE (reprint author), Med Coll Wisconsin, Dept Med, Div Gen Internal Med, 9200 Wisconsin Ave, Milwaukee, WI 53226 USA.
EM legede@mcw.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases
[K24DK093699]
FX This study was supported by the National Institute of Diabetes and
Digestive and Kidney Diseases (grant K24DK093699, Principal
Investigator: Leonard Egede, MD).
NR 34
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U2 1
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1472-6963
J9 BMC HEALTH SERV RES
JI BMC Health Serv. Res.
PD APR 11
PY 2017
AR 259
DI 10.1186/s12913-017-2178-3
PG 8
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA ER8MH
UT WOS:000399073100001
PM 28399859
ER
PT J
AU Young, MRI
AF Young, M. Rita I.
TI Redirecting the focus of cancer immunotherapy to premalignant conditions
SO CANCER LETTERS
LA English
DT Review
DE Cancer; Immune infiltrate; Immunotherapy; Premalignant
ID SQUAMOUS-CELL CARCINOMA; ORAL LESIONS; T-CELLS; ESOPHAGEAL
ADENOCARCINOMA; BARRETTS-ESOPHAGUS; INFLAMMATORY MICROENVIRONMENT;
PRECANCEROUS LESIONS; COLORECTAL-CANCER; ACTINIC KERATOSES; IMMUNE
REACTIVITY
AB Much progress has been made in introducing immunological treatment approaches for cancer, with lessons learned from both the successes and failures of immunotherapy. Among the challenges of immunotherapeutic approaches for cancer are the multitudes of mechanisms by which cancers are known to subvert the immune defenses. This has led to the incorporation into the immunotherapeutic arsenal strategies by which to overcome the cancer's immunological blockades. What has been only superficially explored is the immunological milieu of premalignant lesions and the possibility of immunological approaches for the treatment of premalignant lesions so as to prevent secondary pre malignant lesions and their progression to cancer. This review discusses the immunological environment associated with premalignant lesions, and the possible missed opportunity of utilizing immunological treatment strategies in the less hostile environment of premalignant lesions as compared to the immune subversive cancer environment. Published by Elsevier Ireland Ltd.
C1 [Young, M. Rita I.] Ralph H Johnson VA Med Ctr, Res Serv, Charleston, SC 29401 USA.
[Young, M. Rita I.] Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, Charleston, SC 29425 USA.
RP Young, MRI (reprint author), Ralph H Johnson VA Med Ctr, Res Serv, Charleston, SC 29401 USA.; Young, MRI (reprint author), Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, Charleston, SC 29425 USA.
EM youngmr@musc.edu
FU Clinical Sciences Research and Development Program of the Department of
Veterans Affairs [1 I01CX000851]
FX MRI Young is funded by Clinical Sciences Research and Development
Program of the Department of Veterans Affairs (1 I01CX000851).
NR 76
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U1 4
U2 4
PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0304-3835
EI 1872-7980
J9 CANCER LETT
JI Cancer Lett.
PD APR 10
PY 2017
VL 391
BP 83
EP 88
DI 10.1016/j.canlet.2017.01.022
PG 6
WC Oncology
SC Oncology
GA EP4RG
UT WOS:000397367000009
PM 28130162
ER
PT J
AU Lee, HJ
Lee, DY
Mariappan, MM
Feliers, D
Ghosh-Choudhury, G
Abboud, HE
Gorin, Y
Kasinath, BS
AF Lee, Hak Joo
Lee, Doug Yoon
Mariappan, Meenalakshmi M.
Feliers, Denis
Ghosh-Choudhury, Goutam
Abboud, Hanna E.
Gorin, Yves
Kasinath, Balakuntalam S.
TI Hydrogen sulfide inhibits high glucose-induced NADPH oxidase 4
expression and matrix increase by recruiting inducible nitric oxide
synthase in kidney proximal tubular epithelial cells
SO JOURNAL OF BIOLOGICAL CHEMISTRY
LA English
DT Article
DE AMP-activated kinase (AMPK); diabetic nephropathy; laminin; oxidative
stress; reactive oxygen species (ROS)
ID ACTIVATED PROTEIN-KINASE; DIABETIC-NEPHROPATHY; OXIDATIVE STRESS;
FIBRONECTIN EXPRESSION; SODIUM HYDROSULFIDE; S-NITROSYLATION;
ANGIOTENSIN-II; MOUSE MODEL; TGF-BETA; MICE
AB High-glucose increases NADPH oxidase 4 (NOX4) expression, reactive oxygen species generation, and matrix protein synthesis by inhibiting AMP-activated protein kinase (AMPK) in renal cells. Because hydrogen sulfide (H2S) inhibits high glucose-induced matrix protein increase by activating AMPK in renal cells, we examined whether H2S inhibits high glucose-induced expression of NOX4 and matrix protein and whether H2S and NO pathways are integrated. High glucose increased NOX4 expression and activity at 24 h in renal proximal tubular epithelial cells, which was inhibited by sodium hydrosulfide (NaHS), a source of H2S. High glucose decreased AMPK phosphorylation and activity, which was restored by NaHS. Compound C, an AMPK inhibitor, prevented NaHS inhibition of high glucose-induced NOX4 expression. NaHS inhibition of high glucose-induced NOX4 expression was abrogated by N()-nitro-l-arginine methyl ester, an inhibitor of NOS. NaHS unexpectedly augmented the expression of inducible NOS (iNOS) but not endothelial NOS. iNOS siRNA and 1400W, a selective iNOS inhibitor, abolished the ameliorative effects of NaHS on high glucose-induced NOX4 expression, reactive oxygen species generation, and, matrix laminin expression. Thus, H2S recruits iNOS to generate NO to inhibit high glucose-induced NOX4 expression, oxidative stress, and matrix protein accumulation in renal epithelial cells; the two gasotransmitters H2S and NO and their interaction may serve as therapeutic targets in diabetic kidney disease.
C1 [Lee, Hak Joo; Lee, Doug Yoon; Mariappan, Meenalakshmi M.; Feliers, Denis; Ghosh-Choudhury, Goutam; Abboud, Hanna E.; Gorin, Yves; Kasinath, Balakuntalam S.] Univ Texas Hlth Sci Ctr San Antonio, MC7882,7703 Floyd Curl Dr, San Antonio, TX 78229 USA.
[Lee, Hak Joo; Mariappan, Meenalakshmi M.; Feliers, Denis; Ghosh-Choudhury, Goutam; Abboud, Hanna E.; Kasinath, Balakuntalam S.] South Texas Vet Hlth Care Syst, San Antonio, TX 78229 USA.
RP Kasinath, BS (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Med, MC7882,7703 Floyd Curl Dr, San Antonio, TX 78229 USA.
EM Kasinath@uthscsa.edu
FU University of Texas Health Science Center at San Antonio (UTHSCSA); NCI,
National Institutes of Health [P30 CA54174]
FX Images were generated in the Core Optical Imaging Facility, which is
supported by University of Texas Health Science Center at San Antonio
(UTHSCSA) and NCI, National Institutes of Health Grant P30 CA54174
(Cancer Therapy & Research Center (CTRC) at UTHSCSA).
NR 55
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U1 2
U2 2
PU AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3996 USA
SN 0021-9258
EI 1083-351X
J9 J BIOL CHEM
JI J. Biol. Chem.
PD APR 7
PY 2017
VL 292
IS 14
BP 5665
EP 5675
DI 10.1074/jbc.M116.766758
PG 11
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA ER5AI
UT WOS:000398813200005
PM 28188286
ER
PT J
AU Carcamo-Orive, I
Hoffman, GE
Cundiff, P
Beckmann, ND
D'Souza, SL
Knowles, JW
Patel, A
Papatsenko, D
Abbasi, F
Reaven, GM
Whalen, S
Lee, P
Shahbazi, M
Henrion, MYR
Zhu, KX
Wang, S
Roussos, P
Schadt, EE
Pandey, G
Chang, R
Quertermous, T
Lemischka, I
AF Carcamo-Orive, Ivan
Hoffman, Gabriel E.
Cundiff, Paige
Beckmann, Noam D.
D'Souza, Sunita L.
Knowles, Joshua W.
Patel, Achchhe
Papatsenko, Dimitri
Abbasi, Fahim
Reaven, Gerald M.
Whalen, Sean
Lee, Philip
Shahbazi, Mohammad
Henrion, Marc Y. R.
Zhu, Kuixi
Wang, Sven
Roussos, Panos
Schadt, Eric E.
Pandey, Gaurav
Chang, Rui
Quertermous, Thomas
Lemischka, Ihor
TI Analysis of Transcriptional Variability in a Large Human iPSC Library
Reveals Genetic and Non-genetic Determinants of Heterogeneity
SO CELL STEM CELL
LA English
DT Article
ID PLURIPOTENT STEM-CELLS; DIFFERENTIAL EXPRESSION ANALYSIS; POLYCOMB
COMPLEXES; CHROMOSOMAL-ABERRATIONS; R/BIOCONDUCTOR PACKAGE; EPIGENETIC
MEMORY; NETWORK ANALYSIS; DNA METHYLATION; IDENTIFICATION; VARIANTS
AB Variability in induced pluripotent stem cell (iPSC) lines remains a concern for disease modeling and regenerative medicine. We have used RNA-sequencing analysis and linear mixed models to examine the sources of gene expression variability in 317 human iPSC lines from 101 individuals. We found that similar to 50% of genome-wide expression variability is explained by variation across individuals and identified a set of expression quantitative trait loci that contribute to this variation. These analyses coupled with allele-specific expression show that iPSCs retain a donor-specific gene expression pattern. Network, pathway, and key driver analyses showed that Polycomb targets contribute significantly to the non-genetic variability seen within and across individuals, highlighting this chromatin regulator as a likely source of reprogramming-based variability. Our findings therefore shed light on variation between iPSC lines and illustrate the potential for our dataset and other similar large-scale analyses to identify underlying drivers relevant to iPSC applications.
C1 [Carcamo-Orive, Ivan; Knowles, Joshua W.; Abbasi, Fahim; Reaven, Gerald M.; Lee, Philip; Shahbazi, Mohammad; Quertermous, Thomas] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA.
[Carcamo-Orive, Ivan; Knowles, Joshua W.; Abbasi, Fahim; Reaven, Gerald M.; Lee, Philip; Shahbazi, Mohammad; Quertermous, Thomas] Stanford Univ, Sch Med, Cardiovasc Inst, Stanford, CA 94305 USA.
[Hoffman, Gabriel E.; Beckmann, Noam D.; Henrion, Marc Y. R.; Zhu, Kuixi; Wang, Sven; Roussos, Panos; Schadt, Eric E.; Pandey, Gaurav; Chang, Rui] Icahn Sch Med Mt Sinai, Inst Genom & Multiscale Biol, Dept Genet & Genom Sci, New York, NY 10029 USA.
[Cundiff, Paige; Patel, Achchhe; Papatsenko, Dimitri; Lemischka, Ihor] Icahn Sch Med Mt Sinai, Black Family Stem Cell Inst, Dept Dev & Regenerat Biol, New York, NY 10029 USA.
[D'Souza, Sunita L.] Icahn Sch Med Mt Sinai, Expt Therapeut Inst, Black Family Stem Cell Inst, Dept Dev & Regenerat Biol, New York, NY 10029 USA.
[Papatsenko, Dimitri] Skolkovo Inst Sci & Technol, Nobel St,Bldg 3, Moscow 143026, Russia.
[Whalen, Sean] Univ Calif San Francisco, Gladstone Inst, San Francisco, CA 94148 USA.
[Roussos, Panos] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.
[Roussos, Panos] James J Peters VA Med Ctr, Mental Illness Res Educ & Clin Ctr VISN 3, Bronx, NY 10468 USA.
[Lemischka, Ihor] Icahn Sch Med Mt Sinai, Dept Pharmacol & Syst Therapeut, New York, NY 10029 USA.
RP Quertermous, T (reprint author), Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA.; Quertermous, T (reprint author), Stanford Univ, Sch Med, Cardiovasc Inst, Stanford, CA 94305 USA.; Chang, R (reprint author), Icahn Sch Med Mt Sinai, Inst Genom & Multiscale Biol, Dept Genet & Genom Sci, New York, NY 10029 USA.
EM rui.r.chang@mssm.edu; tomq1@stanford.edu
OI Carcamo-Orive, Ivan/0000-0001-8823-4925
FU NIH [U01HL107388, R01GM114434, 1RF1AG051504-01, R01AG043076,
R01DK107437, R01MH097276]; IBM faculty award; AHA [10FTF3360005]
FX This work was supported by NIH grants U01HL107388 (T.Q., E.E.S., and
I.L.) and R01GM114434; an IBM faculty award (G.P.); the AHA (grant
10FTF3360005, J.W.K.); and NIH grants 1RF1AG051504-01, R01AG043076,
R01DK107437 (T.Q.), and R01MH097276 (R.C.).
NR 72
TC 0
Z9 0
U1 5
U2 5
PU CELL PRESS
PI CAMBRIDGE
PA 50 HAMPSHIRE ST, FLOOR 5, CAMBRIDGE, MA 02139 USA
SN 1934-5909
EI 1875-9777
J9 CELL STEM CELL
JI Cell Stem Cell
PD APR 6
PY 2017
VL 20
IS 4
BP 518
EP +
DI 10.1016/j.stem.2016.11.005
PG 24
WC Cell & Tissue Engineering; Cell Biology
SC Cell Biology
GA EQ8QO
UT WOS:000398350800015
PM 28017796
ER
PT J
AU Lavery, K
Gilden, DJ
Saint, S
Judson, MA
Dhaliwal, G
AF Lavery, Karen
Gilden, Daniel J.
Saint, Sanjay
Judson, Marc A.
Dhaliwal, Gurpreet
TI A Bare-Bones Approach
SO NEW ENGLAND JOURNAL OF MEDICINE
LA English
DT Editorial Material
ID VITAMIN-D; SARCOIDOSIS; ADALIMUMAB; THERAPY; PET/CT
C1 [Lavery, Karen; Gilden, Daniel J.] Legacy Emanuel Hosp, Dept Med, Portland, OR USA.
[Lavery, Karen; Gilden, Daniel J.] Legacy Good Samaritan Hosp, 1015 NW 22nd Ave, Portland, OR 97210 USA.
[Saint, Sanjay] Univ Michigan Hlth Syst, Ann Arbor Vet Affairs VA Hlth Serv Res & Dev Ctr, Patient Safety Enhancement Program, Ann Arbor, MI USA.
[Saint, Sanjay] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI USA.
[Judson, Marc A.] Albany Med Coll, Dept Med, Albany, NY 12208 USA.
[Judson, Marc A.] Albany Med Coll, Div Pulm & Crit Care Med, Albany, NY 12208 USA.
[Dhaliwal, Gurpreet] San Francisco VA Med Ctr, Med Serv, San Francisco, CA USA.
[Dhaliwal, Gurpreet] Univ Calif San Francisco, Sch Med, Dept Med, San Francisco, CA USA.
RP Gilden, DJ (reprint author), Legacy Good Samaritan Hosp, 1015 NW 22nd Ave, Portland, OR 97210 USA.; Gilden, DJ (reprint author), Legacy Emanuel Hosp, 1015 NW 22nd Ave, Portland, OR 97210 USA.
EM dgilden@lhs.org
NR 14
TC 0
Z9 0
U1 2
U2 2
PU MASSACHUSETTS MEDICAL SOC
PI WALTHAM
PA WALTHAM WOODS CENTER, 860 WINTER ST,, WALTHAM, MA 02451-1413 USA
SN 0028-4793
EI 1533-4406
J9 NEW ENGL J MED
JI N. Engl. J. Med.
PD APR 6
PY 2017
VL 376
IS 14
BP 1371
EP 1376
DI 10.1056/NEJMcps1516629
PG 6
WC Medicine, General & Internal
SC General & Internal Medicine
GA EQ9SJ
UT WOS:000398424800014
PM 28379797
ER
PT J
AU Ellerbe, LS
Manfredi, L
Gupta, S
Phelps, TE
Bowe, TR
Rubinsky, AD
Burden, JL
Harris, AHS
AF Ellerbe, Laura S.
Manfredi, Luisa
Gupta, Shalini
Phelps, Tyler E.
Bowe, Thomas R.
Rubinsky, Anna D.
Burden, Jennifer L.
Harris, Alex H. S.
TI VA residential substance use disorder treatment program providers'
perceptions of facilitators and barriers to performance on pre-admission
processes
SO ADDICTION SCIENCE & CLINICAL PRACTICE
LA English
DT Article
DE Substance use disorders; Residential treatment; Standards of care;
Quality measurement; Quality improvement
ID QUALITY MEASURES
AB Background: In the U.S. Department of Veterans Affairs (VA), residential treatment programs are an important part of the continuum of care for patients with a substance use disorder (SUD). However, a limited number of program-specific measures to identify quality gaps in SUD residential programs exist. This study aimed to: (1) Develop metrics for two pre-admission processes: Wait Time and Engagement While Waiting, and (2) Interview program management and staff about program structures and processes that may contribute to performance on these metrics. The first aim sought to supplement the VA's existing facility-level performance metrics with SUD program-level metrics in order to identify high-value targets for quality improvement. The second aim recognized that not all key processes are reflected in the administrative data, and even when they are, new insight may be gained from viewing these data in the context of day-to-day clinical practice.
Methods: VA administrative data from fiscal year 2012 were used to calculate pre-admission metrics for 97 programs (63 SUD Residential Rehabilitation Treatment Programs (SUD RRTPs); 34 Mental Health Residential Rehabilitation Treatment Programs (MH RRTPs) with a SUD track). Interviews were then conducted with management and front-line staff to learn what factors may have contributed to high or low performance, relative to the national average for their program type. We hypothesized that speaking directly to residential program staff may reveal innovative practices, areas for improvement, and factors that may explain system-wide variability in performance.
Results: Average wait time for admission was 16 days (SUD RRTPs: 17 days; MH RRTPs with a SUD track: 11 days), with 60% of Veterans waiting longer than 7 days. For these Veterans, engagement while waiting occurred in an average of 54% of the waiting weeks (range 3-100% across programs). Fifty-nine interviews representing 44 programs revealed factors perceived to potentially impact performance in these domains. Efficient screening processes, effective patient flow, and available beds were perceived to facilitate shorter wait times, while lack of beds, poor staffing levels, and lengths of stay of existing patients were thought to lengthen wait times. Accessible outpatient services, strong patient outreach, and strong encouragement of pre-admission outpatient treatment emerged as facilitators of engagement while waiting; poor staffing levels, socioeconomic barriers, and low patient motivation were viewed as barriers.
Conclusions: Metrics for pre-admission processes can be helpful for monitoring residential SUD treatment programs. Interviewing program management and staff about drivers of performance metrics can play a complementary role by identifying innovative and other strong practices, as well as high-value targets for quality improvement. Key facilitators of high-performing facilities may offer programs with lower performance useful strategies to improve specific pre-admission processes.
C1 [Ellerbe, Laura S.; Manfredi, Luisa; Gupta, Shalini; Phelps, Tyler E.; Bowe, Thomas R.; Harris, Alex H. S.] Dept Vet Affairs VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat, 795 Willow Rd MPD 152, Menlo Pk, CA 94025 USA.
[Rubinsky, Anna D.] Univ Calif San Francisco, Dept Med, San Francisco, CA USA.
[Rubinsky, Anna D.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Burden, Jennifer L.] Salem VA Med Ctr, Salem, VA USA.
RP Manfredi, L (reprint author), Dept Vet Affairs VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat, 795 Willow Rd MPD 152, Menlo Pk, CA 94025 USA.
EM Luisa.Manfredi@va.gov
FU Department of Veterans Affairs (VA) Quality Enhancement Research
Initiative [RRP-12-468]; VA Research Career Scientist Award [RCS-14-232]
FX This work was funded in part by the Department of Veterans Affairs (VA)
Quality Enhancement Research Initiative (RRP-12-468) and a VA Research
Career Scientist Award to Dr. Harris (RCS-14-232). The views expressed
are those of the authors and do not represent the position or policy of
the Department of Veterans Affairs or the United States Government.
NR 11
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PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1940-0640
J9 ADDICT SCI CLIN PRAC
JI Addict. Sci. Clin. Pract.
PD APR 4
PY 2017
VL 12
BP 1
EP 11
AR 10
DI 10.1186/s13722-017-0075-z
PG 11
WC Substance Abuse
SC Substance Abuse
GA EQ9QL
UT WOS:000398419100001
PM 28372579
ER
PT J
AU Simmons, MM
Gabrielian, S
Byrne, T
McCullough, MB
Smith, JL
Taylor, TJ
O'Toole, TP
Kane, V
Yakovchenko, V
McInnes, DK
Smelson, DA
AF Simmons, Molly M.
Gabrielian, Sonya
Byrne, Thomas
McCullough, Megan B.
Smith, Jeffery L.
Taylor, Thom J.
O'Toole, Tom P.
Kane, Vincent
Yakovchenko, Vera
McInnes, D. Keith
Smelson, David A.
TI A Hybrid III stepped wedge cluster randomized trial testing an
implementation strategy to facilitate the use of an evidence-based
practice in VA Homeless Primary Care Treatment Programs
SO IMPLEMENTATION SCIENCE
LA English
DT Article
DE Facilitation; Step wedge design; Co-occurring disorders; Vulnerable
populations
ID MENTAL-ILLNESS; NATIONAL DISSEMINATION; EXTERNAL FACILITATION;
SUBSTANCE-ABUSE; QUERI SERIES; HEALTH; INTERVENTION; INDIVIDUALS;
VETERANS; DESIGNS
AB Background: Homeless veterans often have multiple health care and psychosocial needs, including assistance with access to housing and health care, as well as support for ongoing treatment engagement. The Department of Veterans Affairs (VA) developed specialized Homeless Patient Alignment Care Teams (HPACT) with the goal of offering an integrated, " one-stop program" to address housing and health care needs of homeless veterans. However, while 70% of HPACT's veteran enrollees have co-occurring mental health and substance use disorders, HPACT does not have a uniform, embedded treatment protocol for this subpopulation. One wraparound intervention designed to address the needs of homeless veterans with co-occurring mental health and substance use disorders which is suitable to be integrated into HPACT clinic sites is the evidence-based practice called Maintaining Independence and Sobriety through Systems Integration, Outreach, and Networking-Veterans Edition, or MISSION-Vet. Despite the promise of MISSION-Vet within HPACT clinics, implementation of an evidence-based intervention within a busy program like HPACT can be difficult. The current study is being undertaken to identify an appropriate implementation strategy for MISSION-Vet within HPACT. The study will test the implementation platform called Facilitation and compared to implementation as usual (IU). The aims of this study are as follows: (1) Compare the extent to which IU or Facilitation strategies achieve fidelity to the MISSION-Vet intervention as delivered by HPACT homeless provider staff. (2) Compare the effects of Facilitation and IU strategies on the National HPACT Performance Measures. (3) Compare the effects of IU and Facilitation on the permanent housing status. (4) Identify and describe key stakeholders' (patients, providers, staff) experiences with, and perspectives on, the barriers to, and facilitators of implementing MISSION.
Design: Type III Hybrid modified stepped wedge implementation comparing IU to Facilitation across seven HPACT teams in three sites in the greater Los Angeles VA system. This is a cluster randomized trial.
Discussion: Integrating MISSION-Vet within HPACT has the potential to improve the health of thousands of veterans, but it is crucial to implement the intervention appropriately in order for it to succeed. The lessons learned in this protocol could assist with a larger roll-out of MISSION within HPACT. This protocol is registered with clinicaltrials. gov and was assigned the number NCT 02942979.
C1 [Simmons, Molly M.; Byrne, Thomas; O'Toole, Tom P.; Smelson, David A.] VA Natl Ctr Homelessness Vet, Washington, DC 20420 USA.
[Simmons, Molly M.; McCullough, Megan B.; Yakovchenko, Vera; McInnes, D. Keith; Smelson, David A.] VA Ctr Hlth Org & Implementat Res, Bedford, MA 01730 USA.
[Simmons, Molly M.; McCullough, Megan B.; Yakovchenko, Vera; McInnes, D. Keith] Boston Univ, Sch Publ Hlth, Boston, MA USA.
[Gabrielian, Sonya; Smith, Jeffery L.] VA Greater Los Angeles Hlth Care Syst, Los Angeles, CA USA.
[Gabrielian, Sonya] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
[Byrne, Thomas] Boston Univ, Sch Social Work, Boston, MA 02215 USA.
[Smith, Jeffery L.] Univ Arkansas Med Sci, Coll Med, Little Rock, AR 72205 USA.
[Taylor, Thom J.] VA Palo Alto Hlth Care Syst, Palo Alto, CA USA.
[Smith, Jeffery L.; Taylor, Thom J.] VA Qual Enhancement Res Initiat Team Based Behav, Palo Alto, CA USA.
[O'Toole, Tom P.] Brown Univ, Alpert Med Sch, Providence, RI 02912 USA.
[Kane, Vincent] VA Med Ctr Wilmington, Wilmington, DE USA.
[McInnes, D. Keith; Smelson, David A.] VA Bridging Care Continuum Qual Enhancement Res I, Bedford, MA USA.
[Smelson, David A.] Univ Massachusetts, Med Sch, Worcester, MA 01605 USA.
RP Simmons, MM (reprint author), VA Natl Ctr Homelessness Vet, Washington, DC 20420 USA.; Simmons, MM (reprint author), VA Ctr Hlth Org & Implementat Res, Bedford, MA 01730 USA.
EM msimmons@post.harvard.edu
FU VA Health Services Research and Development Quality Enhancement Research
Initiative [QUE 15-284]
FX This project was funded by a grant from the VA Health Services Research
and Development Quality Enhancement Research Initiative, "Bridging the
Care Continuum" (QUE 15-284).
NR 57
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U1 1
U2 1
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1748-5908
J9 IMPLEMENT SCI
JI Implement. Sci.
PD APR 4
PY 2017
VL 12
AR 46
DI 10.1186/s13012-017-0563-2
PG 10
WC Health Care Sciences & Services; Health Policy & Services
SC Health Care Sciences & Services
GA ER0YU
UT WOS:000398516200003
PM 28376839
ER
PT J
AU Nguyen, KL
Han, F
Zhou, ZW
Brunengraber, DZ
Ayad, I
Levi, DS
Satou, GM
Reemtsen, BL
Hu, P
Finn, JP
AF Kim-Lien Nguyen
Han, Fei
Zhou, Ziwu
Brunengraber, Daniel Z.
Ayad, Ihab
Levi, Daniel S.
Satou, Gary M.
Reemtsen, Brian L.
Hu, Peng
Finn, J. Paul
TI 4D MUSIC CMR: value-based imaging of neonates and infants with
congenital heart disease
SO JOURNAL OF CARDIOVASCULAR MAGNETIC RESONANCE
LA English
DT Article
DE Congenital heart disease; Magnetic resonance angiography; Cardiovascular
magnetic resonance; Ferumoxytol; 4-D imaging
ID CARDIOVASCULAR MAGNETIC-RESONANCE; ENHANCED MR-ANGIOGRAPHY; CONTRAST
AGENT; HIGH-RESOLUTION; THORACIC AORTA; STEADY-STATE; YOUNG-ADULTS;
FERUMOXYTOL; CHILDREN; SAFETY
AB Background: 4D Multiphase Steady State Imaging with Contrast (MUSIC) acquires high-resolution volumetric images of the beating heart during uninterrupted ventilation. We aim to evaluate the diagnostic performance and clinical impact of 4D MUSIC in a cohort of neonates and infants with congenital heart disease (CHD).
Methods: Forty consecutive neonates and infants with CHD (age range 2 days to 2 years, weight 1 to 13 kg) underwent 3.0 T CMR with ferumoxytol enhancement (FE) at a single institution. Independently, two readers graded the diagnostic image quality of intra-cardiac structures and related vascular segments on FE-MUSIC and breath held FE-CMRA images using a four-point scale. Correlation of the CMR findings with surgery and other imaging modalities was performed in all patients. Clinical impact was evaluated in consensus with referring surgeons and cardiologists. One point was given for each of five key outcome measures: 1) change in overall management, 2) change in surgical approach, 3) reduction in the need for diagnostic catheterization, 4) improved assessment of risk-to-benefit for planned intervention and discussion with parents, 5) accurate pre-procedural roadmap.
Results: All FE-CMR studies were completed successfully, safely and without adverse events. On a four-point scale, the average FE-MUSIC image quality scores were >3.5 for intra-cardiac structures and >3.0 for coronary arteries. Intra-cardiac morphology and vascular anatomy were well visualized with good interobserver agreement (r = 0.46). Correspondence between the findings on MUSIC, surgery, correlative imaging and autopsy was excellent. The average clinical impact score was 4.2 +/- 0.9. In five patients with discordant findings on echo/MUSIC (n = 5) and catheter angiography/MUSIC (n = 1), findings on FE-MUSIC were shown to be accurate at autopsy (n = 1) and surgery (n = 4). The decision to undertake biventricular vs univentricular repair was amended in 2 patients based on FE-MUSIC findings. Plans for surgical approaches which would have involved circulatory arrest were amended in two of 28 surgical cases. In all 28 cases requiring procedural intervention, FE-MUSIC provided accurate dynamic 3D roadmaps and more confident risk-to-benefit assessments for proposed interventions.
Conclusions: FE-MUSIC CMR has high clinical impact by providing accurate, high quality, simple and safe dynamic 3D imaging of cardiac and vascular anatomy in neonates and infants with CHD. The findings influenced patient management in a positive manner.
C1 [Kim-Lien Nguyen; Han, Fei; Zhou, Ziwu; Brunengraber, Daniel Z.; Hu, Peng; Finn, J. Paul] UCLA, Dept Radiol Sci, David Geffen Sch Med, Diag Cardiovasc Imaging Lab, Los Angeles, CA 90095 USA.
[Kim-Lien Nguyen] UCLA, David Geffen Sch Med, Div Cardiol, Los Angeles, CA USA.
[Kim-Lien Nguyen] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Han, Fei; Zhou, Ziwu; Hu, Peng; Finn, J. Paul] Univ Calif Los Angeles, Dept Biomed Phys, Los Angeles, CA 90095 USA.
[Ayad, Ihab] UCLA, David Geffen Sch Med, Dept Anesthesiol, Los Angeles, CA USA.
[Levi, Daniel S.; Satou, Gary M.] UCLA, David Geffen Sch Med, Div Pediat Cardiol, Los Angeles, CA USA.
[Reemtsen, Brian L.] UCLA, David Geffen Sch Med, Div Cardiothorac Surg, Los Angeles, CA USA.
[Han, Fei; Zhou, Ziwu; Brunengraber, Daniel Z.; Hu, Peng; Finn, J. Paul] Univ Calif Los Angeles, Dept Radiol Sci, Peter V Ueberroth Bldg Suite 3371, Los Angeles, CA 90095 USA.
RP Finn, JP (reprint author), UCLA, Dept Radiol Sci, David Geffen Sch Med, Diag Cardiovasc Imaging Lab, Los Angeles, CA 90095 USA.; Finn, JP (reprint author), Univ Calif Los Angeles, Dept Biomed Phys, Los Angeles, CA 90095 USA.; Finn, JP (reprint author), Univ Calif Los Angeles, Dept Radiol Sci, Peter V Ueberroth Bldg Suite 3371, Los Angeles, CA 90095 USA.
EM pfinn@mednet.ucla.edu
FU National Heart, Lung, and Blood Institute [R01HL127153]
FX This work is supported by grant R01HL127153 from the National Heart,
Lung, and Blood Institute.
NR 35
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U1 0
U2 0
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1097-6647
EI 1532-429X
J9 J CARDIOVASC MAGN R
JI J. Cardiov. Magn. Reson.
PD APR 3
PY 2017
VL 19
AR 40
DI 10.1186/s12968-017-0352-8
PG 15
WC Cardiac & Cardiovascular Systems; Radiology, Nuclear Medicine & Medical
Imaging
SC Cardiovascular System & Cardiology; Radiology, Nuclear Medicine &
Medical Imaging
GA EQ2SA
UT WOS:000397919600001
PM 28366171
ER
PT J
AU Reid, AT
Hoffstaedter, F
Gong, GL
Laird, AR
Fox, P
Evans, AC
Amunts, K
Eickhoff, SB
AF Reid, Andrew T.
Hoffstaedter, Felix
Gong, Gaolang
Laird, Angela R.
Fox, Peter
Evans, Alan C.
Amunts, Katrin
Eickhoff, Simon B.
TI A seed-based cross-modal comparison of brain connectivity measures
SO BRAIN STRUCTURE & FUNCTION
LA English
DT Article
DE Multimodal comparison; Cortical thickness; VBM; Resting-state fMRI; MACM
ID STATE FUNCTIONAL CONNECTIVITY; AUTOMATED 3-D EXTRACTION; GLOBAL SIGNAL
REGRESSION; VOXEL-BASED MORPHOMETRY; HUMAN CEREBRAL-CORTEX; SMALL VESSEL
DISEASE; CORTICAL THICKNESS; ALZHEIMERS-DISEASE; CORPUS-CALLOSUM;
DEFAULT MODE
AB Human neuroimaging methods have provided a number of means by which the connectivity structure of the human brain can be inferred. For instance, correlations in blood-oxygen-level-dependent (BOLD) signal time series are commonly used to make inferences about "functional connectivity." Correlations across samples in structural morphometric measures, such as voxel-based morphometry (VBM) or cortical thickness (CT), have also been used to estimate connectivity, putatively through mutually trophic effects on connected brain areas. In this study, we have compared seed-based connectivity estimates obtained from four common correlational approaches: resting-state functional connectivity (RS-fMRI), meta-analytic connectivity modeling (MACM), VBM correlations, and CT correlations. We found that the two functional approaches (RS-fMRI and MACM) had the best agreement. While the two structural approaches (CT and VBM) had better-than-random convergence, they were no more similar to each other than to the functional approaches. The degree of correspondence between modalities varied considerably across seed regions, and also depended on the threshold applied to the connectivity distribution. These results demonstrate some degrees of similarity between connectivity inferred from structural and functional covariances, particularly for the most robust functionally connected regions (e.g., the default mode network). However, they also caution that these measures likely capture very different aspects of brain structure and function.
C1 [Reid, Andrew T.; Hoffstaedter, Felix; Amunts, Katrin; Eickhoff, Simon B.] Julich Res Ctr, Inst Neurosci & Med INM 1, Wilhelm Johnen Str, D-52428 Julich, Germany.
[Hoffstaedter, Felix; Eickhoff, Simon B.] Heinrich Heine Univ, Dept Clin Neurosci & Med, Dusseldorf, Germany.
[Gong, Gaolang] Sch Brain & Cognit Sci, Natl Key Lab Cognit Neurosci & Learning, Beijing, Peoples R China.
[Laird, Angela R.] Florida Int Univ, Dept Phys, Miami, FL 33199 USA.
[Fox, Peter] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Fox, Peter] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Evans, Alan C.] McGill Univ, Montreal Neurol Inst, McConnell Brain Imaging Ctr, Montreal, PQ, Canada.
[Amunts, Katrin] Heinrich Heine Univ, C&O Vogt Inst Brain Res, Dusseldorf, Germany.
[Reid, Andrew T.] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands.
RP Reid, AT (reprint author), Julich Res Ctr, Inst Neurosci & Med INM 1, Wilhelm Johnen Str, D-52428 Julich, Germany.; Reid, AT (reprint author), Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands.
EM a.reid@donders.ru.nl
FU Deutsche Forschungsgemeinschaft (DFG) [EI 816/4-1, EI 816/6-1, LA
3071/3-1]; National Institute of Mental Health [R01-MH074457]; European
EFT program (Human Brain Project)
FX This study was supported by the Deutsche Forschungsgemeinschaft (DFG, EI
816/4-1; EI 816/6-1 and LA 3071/3-1.), the National Institute of Mental
Health (R01-MH074457) and the European EFT program (Human Brain
Project).
NR 105
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PU SPRINGER HEIDELBERG
PI HEIDELBERG
PA TIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY
SN 1863-2653
EI 1863-2661
J9 BRAIN STRUCT FUNCT
JI Brain Struct. Funct.
PD APR
PY 2017
VL 222
IS 3
BP 1131
EP 1151
DI 10.1007/s00429-016-1264-3
PG 21
WC Anatomy & Morphology; Neurosciences
SC Anatomy & Morphology; Neurosciences & Neurology
GA ER6QH
UT WOS:000398930700002
ER
PT J
AU Niquet, J
Baldwin, R
Suchomelova, L
Lumley, L
Eavey, R
Wasterlain, CG
AF Niquet, Jerome
Baldwin, Roger
Suchomelova, Lucie
Lumley, Lucille
Eavey, Roland
Wasterlain, Claude G.
TI Treatment of experimental status epilepticus with synergistic drug
combinations
SO EPILEPSIA
LA English
DT Article
DE Refractory status epilepticus; Cholinergic seizures; Polytherapy;
Diazepam; Ketamine; Valproate
ID GABA(A) RECEPTORS; PILOCARPINE MODEL; KETAMINE; ACCUMULATION; INCREASES;
DIAZEPAM; EPILEPSY; ADULTS
AB During status epilepticus (SE), synaptic -aminobutyric acid A receptors (GABA(A)Rs) become internalized and inactive, whereas spare N-methyl-d-aspartate receptors (NMDARs) assemble, move to the membrane, and become synaptically active. When treatment of SE is delayed, the number of synaptic GABA(A)Rs is drastically reduced, and a GABA(A) agonist cannot fully restore inhibition. We used a combination of low-dose diazepam (to stimulate the remaining GABA(A)Rs), ketamine (to mitigate the effect of the NMDAR increase), and valproate (to enhance inhibition at a nonbenzodiazepine site) to treat seizures in a model of severe cholinergic SE. High doses of diazepam failed to stop electrographic SE, showing that benzodiazepine pharmacoresistance had developed. The diazepam-ketamine-valproate combination was far more effective in stopping SE than triple-dose monotherapy using the same individual drugs. Isobolograms showed that this drug combination's therapeutic actions were synergistic, with positive cooperativity between drugs, whereas drug toxicity was simply additive, without positive or negative cooperativity. As a result, the therapeutic index was improved by this drug combination compared to monotherapy. These results suggest that synergistic drug combinations that target receptor changes can control benzodiazepine-refractory SE.
C1 [Niquet, Jerome; Suchomelova, Lucie; Eavey, Roland; Wasterlain, Claude G.] Univ Calif Los Angeles, Dept Neurol, David Geffen Sch Med, Los Angeles, CA 90024 USA.
[Niquet, Jerome; Baldwin, Roger; Suchomelova, Lucie; Eavey, Roland; Wasterlain, Claude G.] Vet Affairs Greater Los Angeles Healthcare Syst, Epilepsy Res Lab 151, Los Angeles, CA USA.
[Lumley, Lucille] US Army Med Res Inst Chem Def USAMRICD, Aberdeen Proving Ground, MD USA.
[Wasterlain, Claude G.] Univ Calif Los Angeles, David Geffen Sch Med, Brain Res Inst, Los Angeles, CA 90095 USA.
RP Niquet, J (reprint author), VA Greater Los Angeles Healthcare Syst, Epilepsy Res Lab, 11301 Wilshire Blvd,Bldg 114,Room 139, West Los Angeles, CA 90073 USA.
EM jniquet@ucla.edu
FU Department of Veterans Health Affairs [I01 BX000273-07]; NINDS (NIH
Counteract Program) [UO1 NS074926]; James and Debbie Cho Foundation
FX This work was supported by Merit Review Award # I01 BX000273-07 from the
Department of Veterans Health Affairs, by NINDS (NIH Counteract Program;
grant UO1 NS074926), and by the James and Debbie Cho Foundation
NR 19
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0013-9580
EI 1528-1167
J9 EPILEPSIA
JI Epilepsia
PD APR
PY 2017
VL 58
IS 4
BP E49
EP E53
DI 10.1111/epi.13695
PG 5
WC Clinical Neurology
SC Neurosciences & Neurology
GA ER5RU
UT WOS:000398861000001
PM 28225161
ER
PT J
AU Best, SL
AF Best, Sara L.
TI Editorial Comment for Jones et al.
SO JOURNAL OF ENDOUROLOGY
LA English
DT Editorial Material
ID OUTCOMES
C1 [Best, Sara L.] Univ Wisconsin, Dept Urol, Sch Med & Publ Hlth, 1685 Highland Ave,MFCB 3229, Madison, WI 53705 USA.
[Best, Sara L.] William S Middleton Mem Vet Adm Med Ctr, Dept Urol, Madison, WI USA.
RP Best, SL (reprint author), Univ Wisconsin, Dept Urol, Sch Med & Publ Hlth, 1685 Highland Ave,MFCB 3229, Madison, WI 53705 USA.
EM best@urology.wisc.edu
NR 2
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PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 0892-7790
EI 1557-900X
J9 J ENDOUROL
JI J. Endourol.
PD APR
PY 2017
VL 31
IS 4
BP 341
EP 341
DI 10.1089/end.2017.0183
PG 1
WC Urology & Nephrology
SC Urology & Nephrology
GA ES2BJ
UT WOS:000399330400003
PM 28322584
ER
PT J
AU Doupnik, SK
Feudtner, C
Marcus, SC
AF Doupnik, Stephanie K.
Feudtner, Chris
Marcus, Steven C.
TI Family Report Compared to Clinician-Documented Diagnoses for Psychiatric
Conditions Among Hospitalized Children
SO JOURNAL OF HOSPITAL MEDICINE
LA English
DT Article
ID MENTAL-HEALTH DISORDERS; COLLABORATIVE CARE; UNITED-STATES; SERVICES
ASSESSMENT; ANXIETY DISORDERS; PERCEIVED STIGMA; DEPRESSION; TRIAL;
ILLNESS; YOUTH
AB BACKGROUND: Psychiatric comorbidity is common in pediatric medical and surgical hospitalizations and is associated with worse hospital outcomes. Integrating medical or surgical and psychiatric hospital care depends on accurate estimates of which hospitalized children have psychiatric comorbidity.
OBJECTIVE: We conducted a study to determine agreement of family report (FR) and clinician documentation (CD) identification of psychiatric diagnoses in hospitalized children.
DESIGN AND SETTING: This was a cross-sectional study at a tertiary-care children's hospital.
PATIENTS: The patients were children and adolescents (age, 4-21 years) who were hospitalized for medical or surgical indications.
MEASUREMENTS: Psychiatric diagnoses were identified from structured interviews (FR) and from inpatient notes and International Classification of Diseases codes in medical records (CD). We compared estimates of point prevalence of any comorbid psychiatric diagnosis using each method, and estimated FR-CD agreement in identifying psychiatric comorbidity in hospitalized children.
RESULTS: Of 119 study patients, 26 (22%; 95% confidence interval [CI], 14%-29%) had a psychiatric comorbidity identified by FR, 30 (25%; 95% CI, 17%-34%) had it identified by CD, and 37 (23%-40%) had it identified by FR or CD. Agreement between FR and CD was low overall (kappa = .46; 95% CI, .27-.66), highest for attention-deficit/hyperactivity disorder (kappa=.78; 95% CI, .59-.97), and lowest for anxiety disorders (kappa = .11; 95% CI, -.16 to.56).
CONCLUSIONS: Current methods may underestimate the prevalence of psychiatric conditions in hospitalized children. Information from multiple sources may be needed to develop accurate estimates of the scope of the population in need of services so that mental health resources can be appropriately allocated. (C) 2017 Society of Hospital Medicine
C1 [Doupnik, Stephanie K.; Feudtner, Chris] Childrens Hosp Philadelphia, Ctr Pediat Clin Effectiveness, Div Gen Pediat, Philadelphia, PA 19104 USA.
[Doupnik, Stephanie K.; Feudtner, Chris] Childrens Hosp Philadelphia, PolicyLab, Philadelphia, PA 19104 USA.
[Doupnik, Stephanie K.; Feudtner, Chris; Marcus, Steven C.] Univ Penn, Leonard Davis Inst Hlth Econ, Philadelphia, PA 19104 USA.
[Feudtner, Chris] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA.
[Feudtner, Chris] Univ Penn, Perelman Sch Med, Dept Med Eth & Hlth Policy, Philadelphia, PA 19104 USA.
[Marcus, Steven C.] Philadelphia VA Med Ctr, Ctr Hlth Equ Res & Promot, Philadelphia, PA USA.
[Marcus, Steven C.] Univ Penn, Sch Social Policy & Practice, Philadelphia, PA 19104 USA.
[Marcus, Steven C.] Univ Penn, Ctr Mental Hlth Policy & Serv Res, Philadelphia, PA 19104 USA.
RP Doupnik, SK (reprint author), Childrens Hosp Philadelphia, Div Gen Pediat, Room 1451,CHOP North,3401 Civ Ctr Blvd, Philadelphia, PA 19104 USA.
EM doupniks@chop.edu
FU Center for Pediatric Health Disparities at Children's Hospital of
Philadelphia; Ruth L. Kirschstein National Research Service Award
[T32-HP010026-11]; National Institutes of Health
FX The direct costs of this project were funded by an internal pilot grant
from the Center for Pediatric Health Disparities at Children's Hospital
of Philadelphia. Dr. Doupnik was supported by Ruth L. Kirschstein
National Research Service Award T32-HP010026-11, funded by the National
Institutes of Health. The sponsors had no role in study design;
collection, analysis, or interpretation of data; manuscript writing; or
deciding to submit this article for publication.
NR 38
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PU FRONTLINE MEDICAL COMMUNICATIONS
PI THE WOODLANDS
PA WRIGHTS MEDIA, 2407 TIMBERLOCH PLACE, SUITE B, THE WOODLANDS, TX 77386
USA
SN 1553-5592
EI 1553-5606
J9 J HOSP MED
JI J. Hosp. Med.
PD APR
PY 2017
VL 12
IS 4
BP 245
EP 250
DI 10.12788/jhm.2698
PG 6
WC Medicine, General & Internal
SC General & Internal Medicine
GA ES5KQ
UT WOS:000399578000006
ER
PT J
AU Han, S
Pistole, MC
Caldwell, JM
AF Han, Suejung
Pistole, M. Carole
Caldwell, Jarred M.
TI Acculturative Stress, Parental and Professor Attachment, and College
Adjustment in Asian International Students
SO JOURNAL OF MULTICULTURAL COUNSELING AND DEVELOPMENT
LA English
DT Article
DE attachment; acculturative stress; Asian international students; college
adjustment; apego; estres aculturativo; estudiantes internacionales
asiaticos; adaptacion al entorno academico
ID ADULT ATTACHMENT; PERFECTIONISM; SYMPTOMS; SCALE
AB This study examined parental and professor attachment as buffers against acculturative stress and as predictors of college adjustment of 210 Asian international students (AISs). Moderated hierarchical regression analyses revealed that acculturative stress negatively and secure parental and professor attachment positively predicted academic integration. Secure professor attachment positively predicted grade point average. Mother attachment may buffer against acculturative stress on academic integration; father attachment may exacerbate it. Counselors may use these findings to enhance AISs' attachment functioning for their college adjustment. Este estudio examino el apego parental y el apego al profesor como protectores contra el estres aculturativo y como indicadores de adaptacion al entorno academico en 210 estudiantes internacionales asiaticos (AIS, por sus siglas en ingles). Los analisis de regresion jerarquica moderada revelaron que el estres aculturativo fue un indicador negativo de integracion academica, mientras que el apego parental y el apego al profesor fueron indicadores positivos. El apego seguro al profesor fue un indicador positivo de la media de las calificaciones academicas. El apego materno puede proteger contra el estres aculturativo en la integracion academica; el apego paterno puede agravarlo. Los consejeros pueden usar estos descubrimientos para enfatizar el funcionamiento del apego en los AIS para su adaptacion al entorno academico.
C1 [Han, Suejung] Illinois State Univ, Dept Psychol, Normal, IL 61761 USA.
[Pistole, M. Carole] Purdue Univ, Dept Educ Studies, W Lafayette, IN 47907 USA.
[Caldwell, Jarred M.] Ralph H Johnson VA Med Ctr, Charleston, SC USA.
RP Han, S (reprint author), Illinois State Univ, Dept Psychol, Normal, IL 61761 USA.
EM shan3@ilstu.edu
FU Purdue Research Foundation
FX Suejung Han, Department of Psychology, Illinois State University; M.
Carole Pistole, Department of Educational Studies, Purdue University;
Jarred M. Caldwell, Ralph H. Johnson VA Medical Center, Charleston,
South Carolina. This study was supported by a grant from the Purdue
Research Foundation awarded to M. Carole Pistole. Correspondence
concerning this article should be addressed to Suejung Han, Department
of Psychology, Illinois State University, Normal, IL 61761 (e-mail:
shan3@ilstu.edu).
NR 35
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0883-8534
EI 2161-1912
J9 J MULTICULT COUNS D
JI J. Multicult. Couns. Dev.
PD APR
PY 2017
VL 45
IS 2
BP 111
EP 126
DI 10.1002/jmcd.12068
PG 16
WC Psychology, Applied
SC Psychology
GA ER5NC
UT WOS:000398847600003
ER
PT J
AU Zullo, AR
Lee, Y
Daiello, LA
Mor, V
Boscardin, WJ
Dore, DD
Miao, YH
Fung, KZ
Komaiko, KDR
Steinman, MA
AF Zullo, Andrew R.
Lee, Yoojin
Daiello, Lori A.
Mor, Vincent
Boscardin, W. John
Dore, David D.
Miao, Yinghui
Fung, Kathy Z.
Komaiko, Kiya D. R.
Steinman, Michael A.
TI Beta-Blocker Use in US Nursing Home Residents After Myocardial
Infarction: A National Study
SO JOURNAL OF THE AMERICAN GERIATRICS SOCIETY
LA English
DT Article
DE nursing homes; myocardial infarction; beta-blockers; elderly; drug
utilization
ID CONVERTING ENZYME-INHIBITORS; CALCIUM-CHANNEL BLOCKERS;
CORONARY-ARTERY-DISEASE; MINIMUM DATA SET; OLDER PATIENTS;
HEART-FAILURE; PRACTICE GUIDELINES; ELDERLY SURVIVORS; PRIMARY-CARE;
THERAPY
AB ObjectivesTo evaluate how often beta-blockers were started after acute myocardial infarction (AMI) in nursing home (NH) residents who previously did not use these drugs and to evaluate which factors were associated with post-AMI use of beta-blockers.
DesignRetrospective cohort using linked national Minimum Data Set assessments; Online Survey, Certification and Reporting records; and Medicare claims.
SettingU.S. NHs.
ParticipantsNational cohort of 15,720 residents aged 65 and older who were hospitalized for AMI between May 2007 and March 2010, had not taken beta-blockers for at least 4 months before their AMI, and survived 14 days or longer after NH readmission.
MeasurementsThe outcome was beta-blocker initiation within 30 days of NH readmission.
ResultsFifty-seven percent (n = 8,953) of residents initiated a beta-blocker after AMI. After covariate adjustment, use of beta-blockers was less in older residents (ranging from odds ratio (OR) = 0.89, 95% confidence interval (CI) = 0.79-1.00 for aged 75-84 to OR = 0.65, 95% CI = 0.54-0.79 for 95 vs 65-74) and less in residents with higher levels of functional impairment (dependent or totally dependent vs independent to limited assistance: OR = 0.84, 95% CI = 0.75-0.94) and medication use (15 vs 10 medications: OR = 0.89, 95% CI = 0.80-0.99). A wide variety of resident and NH characteristics were not associated with beta-blocker use, including sex, cognitive function, comorbidity burden, and NH ownership.
ConclusionAlmost half of older NH residents in the United States do not initiate a beta-blocker after AMI. The absence of observed factors that strongly predict beta-blocker use may indicate a lack of consensus on how to manage older NH residents, suggesting the need to develop and disseminate thoughtful practice standards.
C1 [Zullo, Andrew R.; Lee, Yoojin; Daiello, Lori A.; Mor, Vincent; Dore, David D.] Brown Univ, Sch Publ Hlth, Dept Hlth Serv Policy & Practice, 121 South Main St,Box G-S121-8, Providence, RI 02912 USA.
[Mor, Vincent] Providence Vet Affairs Med Ctr, Ctr Innovat, Providence, RI USA.
[Boscardin, W. John; Miao, Yinghui; Fung, Kathy Z.; Komaiko, Kiya D. R.; Steinman, Michael A.] Univ Calif San Francisco, Div Geriatr, San Francisco, CA 94143 USA.
[Boscardin, W. John; Miao, Yinghui; Fung, Kathy Z.; Komaiko, Kiya D. R.; Steinman, Michael A.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Boscardin, W. John] Univ Calif San Francisco, Div Biostat, San Francisco, CA 94143 USA.
[Dore, David D.] Optum Epidemiol, Boston, MA USA.
RP Zullo, AR (reprint author), Brown Univ, Sch Publ Hlth, Dept Hlth Serv Policy & Practice, 121 South Main St,Box G-S121-8, Providence, RI 02912 USA.
EM andrew_zullo@brown.edu
FU National Heart, Lung, and Blood Institute [5R01HL111032]; National
Institute on Aging [K24AG049057]; Agency for Healthcare Research and
Quality Award [5K12HS022998]; HCR Manor Care, Inc., a NH chain;
NaviHealth, a postacute care service organization; iodine.com
FX Financial support for this study was provided by the National Heart,
Lung, and Blood Institute (5R01HL111032) and National Institute on Aging
(K24AG049057). Dr. Zullo is supported by Agency for Healthcare Research
and Quality Award 5K12HS022998.; V.M.'s research is in a related area to
that of several different paid activities. V.M. also periodically serves
as a paid speaker at national conferences, where he discusses trends and
research findings in long-term and postacute care. V.M. holds stock of
unknown value in PointRight, Inc., an information services company
providing advice and consultation to various components of the LTC and
postacute care industry, including suppliers and insurers. PointRight
sells information on the measurement of NH quality to NHs and liability
insurers. V.M. was a founder of the company but has subsequently
divested much of his equity in the company and relinquished his seat on
board. In addition, V.M. chairs the Independent Quality Committee for
HCR Manor Care, Inc., a NH chain, for which he receives compensation in
the range of $ 20,000 to $ 40,000. V.M. also serves as chair of a
Scientific Advisory Committee for NaviHealth, a postacute care service
organization, for which he also receives compensation in the range of $
20,000 to $ 40,000 per year. V.M. serves as a technical expert panel
member on several Centers for Medicare and Medicaid Services quality
measurement panels. V.M. is a member of the board of directors of Tufts
Health Plan Foundation; Hospice Care of Rhode Island; and Jewish
Alliance of Rhode Island. D.D.D. is an employee of Optum and stockholder
in UnitedHealth Group, Optum's parent company. M.A.S. is a paid
consultant for iodine.com.
NR 48
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0002-8614
EI 1532-5415
J9 J AM GERIATR SOC
JI J. Am. Geriatr. Soc.
PD APR
PY 2017
VL 65
IS 4
BP 754
EP 762
DI 10.1111/jgs.14671
PG 9
WC Geriatrics & Gerontology; Gerontology
SC Geriatrics & Gerontology
GA ES7CL
UT WOS:000399707100016
PM 27861719
ER
PT J
AU Nitzburg, GC
Cuesta-Diaz, A
Ospina, LH
Russo, M
Shanahan, M
Perez-Rodriguez, M
Larsen, E
Mulaimovic, S
Burdick, KE
AF Nitzburg, George C.
Cuesta-Diaz, Armando
Ospina, Luz H.
Russo, Manuela
Shanahan, Megan
Perez-Rodriguez, Mercedes
Larsen, Emmett
Mulaimovic, Sandra
Burdick, Katherine E.
TI Organizational Learning Strategies and Verbal Memory Deficits in Bipolar
Disorder
SO JOURNAL OF THE INTERNATIONAL NEUROPSYCHOLOGICAL SOCIETY
LA English
DT Article
DE Cognitive deficits; Cognitive remediation; Functional remediation; Mood
disorder; Semantic clustering; Serial clustering
ID COGNITIVE IMPAIRMENT; I DISORDER; NEUROCOGNITIVE IMPAIRMENT; 1ST-DEGREE
RELATIVES; EXECUTIVE CONTROL; EUTHYMIC PATIENTS; RATING-SCALE;
FOLLOW-UP; METAANALYSIS; SCHIZOPHRENIA
AB Background: Verbal memory (VM) impairment is prominent in bipolar disorder (BD) and is linked to functional outcomes. However, the intricacies of VM impairment have not yet been studied in a large sample of BD patients. Moreover, some have proposed VM deficits that may be mediated by organizational strategies, such as semantic or serial clustering. Thus, the exact nature of VM break-down in BD patients is not well understood, limiting remediation efforts. We investigated the intricacies of VM deficits in BD patients versus healthy controls (HCs) and examined whether verbal learning differences were mediated by use of clustering strategies. Methods: The California Verbal Learning Test (CVLT) was administered to 113 affectively stable BD patients and 106 HCs. We compared diagnostic groups on all CVLT indices and investigated whether group differences in verbal learning were mediated by clustering strategies. Results: Although BD patients showed significantly poorer attention, learning, and memory, these indices were only mildly impaired. However, BD patients evidenced poorer use of effective learning strategies and lower recall consistency, with these indices falling in the moderately impaired range. Moreover, relative reliance on semantic clustering fully mediated the relationship between diagnostic category and verbal learning, while reliance on serial clustering partially mediated this relationship. Conclusions: VM deficits in affectively stable bipolar patients were widespread but were generally mildly impaired. However, patients displayed inadequate use of organizational strategies with clear separation from HCs on semantic and serial clustering. Remediation efforts may benefit from education about mnemonic devices or chunking" techniques to attenuate VM deficits in BD.
C1 [Nitzburg, George C.; Cuesta-Diaz, Armando; Ospina, Luz H.; Russo, Manuela; Shanahan, Megan; Perez-Rodriguez, Mercedes; Larsen, Emmett; Mulaimovic, Sandra; Burdick, Katherine E.] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.
[Nitzburg, George C.; Cuesta-Diaz, Armando; Ospina, Luz H.; Russo, Manuela; Shanahan, Megan; Perez-Rodriguez, Mercedes; Larsen, Emmett; Mulaimovic, Sandra; Burdick, Katherine E.] Icahn Sch Med Mt Sinai, Dept Neurosci, New York, NY 10029 USA.
[Burdick, Katherine E.] James J Peters VA Hosp, Bronx, NY USA.
RP Nitzburg, GC (reprint author), Icahn Sch Med Mt Sinai, One Gustave L Levy Pl,Box 1230, New York, NY 10029 USA.
EM george.nitzburg@gmail.com
FU National Institute of Mental Health (NIMH) [K23MH077807, R01MH100125]
FX Dr. Burdick has served as an advisory board member for Dainippon
Sumitomo Pharmaceutical and for Takeda Lundbeck, which had no impact
upon the work presented in this manuscript. Dr. Nitzburg has received
research funding from Talkspace Incorporated, which had no impact upon
the work presented in this manuscript. All other authors report no
competing interests regarding the present study. This study was funded
by grants from the National Institute of Mental Health (NIMH) to Dr.
Burdick (K23MH077807; R01MH100125).
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PU CAMBRIDGE UNIV PRESS
PI NEW YORK
PA 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA
SN 1355-6177
EI 1469-7661
J9 J INT NEUROPSYCH SOC
JI J. Int. Neuropsychol. Soc.
PD APR
PY 2017
VL 23
IS 4
BP 358
EP 366
DI 10.1017/S1355617717000133
PG 9
WC Clinical Neurology; Neurosciences; Psychiatry; Psychology
SC Neurosciences & Neurology; Psychiatry; Psychology
GA ES2YO
UT WOS:000399394000008
PM 28382899
ER
PT J
AU Nelson, HN
Borrero, S
Lehman, E
Velott, DL
Chuang, CH
AF Nelson, Hallie N.
Borrero, Sonya
Lehman, Erik
Velott, Diana L.
Chuang, Cynthia H.
TI MEASURING ORAL CONTRACEPTIVE ADHERENCE USING SELF-REPORT VERSUS PHARMACY
CLAIMS DATA
SO JOURNAL OF WOMENS HEALTH
LA English
DT Meeting Abstract
C1 [Nelson, Hallie N.] Penn State Coll Med, Hershey, PA USA.
[Borrero, Sonya] Univ Pittsburgh, Div Gen Internal Med, Ctr Hlth Equ Res & Promot, VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Lehman, Erik; Velott, Diana L.; Chuang, Cynthia H.] Penn State Coll Med, Dept Publ Hlth Sci, Hershey, PA USA.
[Chuang, Cynthia H.] Penn State Coll Med, Div Gen Internal Med, Hershey, PA USA.
NR 0
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U2 0
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1540-9996
EI 1931-843X
J9 J WOMENS HEALTH
JI J. Womens Health
PD APR
PY 2017
VL 26
IS 4
MA 105
BP A42
EP A42
PG 1
WC Public, Environmental & Occupational Health; Medicine, General &
Internal; Obstetrics & Gynecology; Women's Studies
SC Public, Environmental & Occupational Health; General & Internal
Medicine; Obstetrics & Gynecology; Women's Studies
GA ES4HB
UT WOS:000399492100106
ER
PT J
AU Bush, NE
Smolenski, DJ
Denneson, LM
Williams, HB
Thomas, EK
Dobscha, SK
AF Bush, Nigel E.
Smolenski, Derek J.
Denneson, Lauren M.
Williams, Holly B.
Thomas, Elissa K.
Dobscha, Steven K.
TI A Virtual Hope Box: Randomized Controlled Trial of a Smartphone App for
Emotional Regulation and Coping With Distress
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID COGNITIVE THERAPY; SUICIDE ATTEMPTS; LIVING INVENTORY; KILLING YOURSELF;
STAYING ALIVE; SCALE; INTERVENTION; MILITARY; VALIDITY; BEHAVIOR
AB Objective: The purpose of this study was to assess the impact of the Virtual Hope Box (VHB), a smartphone app to improve stress coping skills, suicidal ideation, and perceived reasons for living among patients at elevated risk of suicide and self-harm.
Methods: The authors conducted a parallel-group randomized controlled trial with two groups of U.S. service veterans in active mental health treatment who had recently expressed suicidal ideation. Between March 2014 and April 2015, 118 patients were enrolled in the study. Participants were assigned to use the VHB (N=58) or to a control group that received printed materials about coping with suicidality (N=60) to supplement treatment as usual over a 12-week period. Three measures-the Coping Self-Efficacy Scale, Beck Scale for Suicidal Ideation, and Brief Reasons for Living Inventory-were collected at baseline (before randomization) and three, six, and 12 weeks. Secondary measures-the Interpersonal Needs Questionnaire, Perceived Stress Scale, and Columbia-Suicide Severity Rating Scale-were collected at baseline and 12 weeks.
Results: VHB users reported significantly greater ability to cope with unpleasant emotions and thoughts (Coping Self-Efficacy Scale) at three (b=2.41, 95% confidence interval [CI]=.29-4.55) and 12 weeks (b=2.99, 95% CI=.08-5.90) compared with the control group. No significant advantage was found on other outcome measures for treatment augmented by the VHB.
Conclusions: The VHB is a demonstrably useful accessory to treatment-an easily accessible tool that can increase stress coping skills. Because the app is easily disseminated across a large population, it is likely to have broad, positive utility in behavioral health care.
C1 [Bush, Nigel E.; Smolenski, Derek J.; Thomas, Elissa K.] US Dept Def, Natl Ctr Telehlth & Technol, Joint Base Lewis McChord, Tacoma, WA 98409 USA.
[Denneson, Lauren M.; Williams, Holly B.] US Dept Vet Affairs, Ctr Improve Veteran Involvement Carc, Portland Hlth Care Syst, Portland, OR USA.
[Dobscha, Steven K.] Oregon Hlth & Sci Univ, Mental Hlth Div, Portland, OR 97201 USA.
[Dobscha, Steven K.] Oregon Hlth & Sci Univ, Dept Psychiat, Portland, OR 97201 USA.
RP Bush, NE (reprint author), US Dept Def, Natl Ctr Telehlth & Technol, Joint Base Lewis McChord, Tacoma, WA 98409 USA.
EM nigele.bush.civ@mail.mil
FU Military Suicide Research Consortium [W81XWH-10-2-0178]
FX This randomized controlled trial of the Virtual Hope Box was supported
by grant W81XWH-10-2-0178 from the Military Suicide Research Consortium,
with oversight by the Military Operational Medicine Research Program.
NR 37
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PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 330
EP 336
DI 10.1176/appi.ps.201600283
PG 7
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600006
PM 27842473
ER
PT J
AU Lagomasino, IT
Dwight-Johnson, M
Green, JM
Tang, LQ
Zhang, LL
Duan, NH
Miranda, J
AF Lagomasino, Isabel T.
Dwight-Johnson, Megan
Green, Jennifer M.
Tang, Lingqi
Zhang, Lily
Duan, Naihua
Miranda, Jeanne
TI Effectiveness of Collaborative Care for Depression in Public-Sector
Primary Care Clinics Serving Latinos
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID RANDOMIZED CONTROLLED-TRIAL; LOW-INCOME LATINOS; TREATMENT PREFERENCES;
QUALITY IMPROVEMENT; MAJOR DEPRESSION; UNITED-STATES; MANAGEMENT;
DISPARITIES; VALIDATION; DISORDERS
AB Objective: Quality improvement interventions for depression care have been shown to be effective for improving quality of care and depression outcomes in settings with primarily insured patients. The aim of this study was to determine the impact of a collaborative care intervention for depression that was tailored for low-income Latino patients seen in public-sector clinics.
Methods: A total of 400 depressed patients from three public-sector primary care clinics were enrolled in a randomized controlled trial of a tailored collaborative care intervention versus enhanced usual care. Social workers without previous mental health experience served as depression care specialists for the intervention patients (N=196). Depending on patient preference, they delivered a cognitive-behavioral therapy (CBT) intervention or facilitated antidepressant medication given by primary care providers or both. In enhanced usual care, patients (N=204) received a pamphlet about depression, a letter for their primary care provider stating that they had a positive depression screen, and a list of local mental health resources. Intent-to-treat analyses examined clinical and process-of-care outcomes at 16 weeks.
Results: Compared with patients in the enhanced usual care group, patients in the intervention group had significantly improved depression, quality of life, and satisfaction outcomes (p<.001 for all). Intervention patients also had significantly improved quality-of-care indicators, including the proportion of patients receiving either psychotherapy or antidepressant medication (77% versus 21%, p<.001).
Conclusions: Collaborative care for depression can greatly improve care and outcomes in public-sector clinics. Social workers without prior mental health experience can effectively provide CBT and manage depression care.
C1 [Lagomasino, Isabel T.; Green, Jennifer M.] Univ Southern Calif, Keck Sch Med, Dept Psychiat & Behav Sci, Los Angeles, CA 90033 USA.
[Dwight-Johnson, Megan] US Dept Vet Affairs, Greater Los Angeles Healthcare Syst, Dept Psychiat, Los Angeles, CA USA.
[Tang, Lingqi; Zhang, Lily; Miranda, Jeanne] Univ Calif Los Angeles, Dept Psychiat, Ctr Hlth Serv & Soc, Los Angeles, CA 90095 USA.
[Duan, Naihua] Columbia Univ, Div Biostat, New York, NY USA.
[Duan, Naihua] New York State Psychiat Inst & Hosp, New York, NY 10032 USA.
RP Miranda, J (reprint author), Univ Calif Los Angeles, Dept Psychiat, Ctr Hlth Serv & Soc, Los Angeles, CA 90095 USA.
EM jmmiranda@mednet.ucla.edu
FU National Institute of Mental Health [5R01MH067949]
FX This work was sponsored by grant 5R01MH067949 from the National
Institute of Mental Health. The authors acknowledge Maribel Avila,
Jeannette Hilgert, Gustavo Rodriguez, Ricardo Romero, Melissa Van Dyk,
and Maribel Vega for their contributions to this project and Kenneth
Wells, M.D, M.P.H, for his invaluable consultation and mentorship.
NR 33
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U1 1
U2 1
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 353
EP 359
DI 10.1176/appi.ps.201600187
PG 7
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600009
PM 27842470
ER
PT J
AU Lucksted, A
Drapalski, AL
Brown, CH
Wilson, C
Charlotte, M
Mullane, A
Fang, LJ
AF Lucksted, Alicia
Drapalski, Amy L.
Brown, Clayton H.
Wilson, Camille
Charlotte, Melanie
Mullane, Audrina
Fang, Li Juan
TI Outcomes of a Psychoeducational Intervention to Reduce Internalized
Stigma Among Psychosocial Rehabilitation Clients
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID RANDOMIZED CONTROLLED-TRIAL; SEVERE MENTAL-ILLNESS; SCHIZOPHRENIA
SPECTRUM DISORDERS; MEASURING COGNITIVE INSIGHT; SELF-STIGMA;
NEUROPSYCHOLOGICAL STATUS; NARRATIVE ENHANCEMENT; REPEATABLE BATTERY;
PERCEIVED STIGMA; HEALTH PROBLEMS
AB Objective: This community-based randomized controlled trial was carried out to test the Ending SelfStigma (ESS) psychoeducational intervention, which is designed to help adults with serious mental illnesses reduce internalization of mental illness stigma and its effects.
Methods: A total of 268 adults from five different mental health programs in Maryland took part. After baseline interview, consenting participants were randomly assigned to the nine-week ESS intervention or a minimally enhanced treatment-as-usual control condition. Participants were assessed by using symptom, psychosocial functioning, and self-stigma measures at baseline, postintervention, and sixmonth follow-up. Demographic characteristics were assessed at baseline.
Results: Compared with participants in the control condition, ESS group participants showed significant decreases on the stereotype agreement and self-concurrence subscales of the Self Stigma of Mental Illness Scale, significant improvement on the alienation and stigma resistance subscales of the Internalized Stigma Mental Illness measure, and a significant increase in recovery orientation from baseline to postintervention. None of these differences were sustained at six-month follow-up.
Conclusions: Results indicate that ESS was useful in helping to reduce key aspects of internalized stigma among individuals with mental illnesses and that advances in the delivery, targeting, and content of the intervention in the field may be warranted to increase its potency.
C1 [Lucksted, Alicia; Charlotte, Melanie; Fang, Li Juan] Univ Maryland, Sch Med, Dept Psychiat, Div Psychiat Serv Res, Baltimore, MD 21201 USA.
[Brown, Clayton H.] Univ Maryland, Sch Med, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA.
[Drapalski, Amy L.] US Dept Vet Affairs, Maryland Hlth Care Syst, Mental Illness Res Educ & Clin Ctr, Baltimore, MD USA.
[Wilson, Camille] Univ Maryland Baltimore Cty, Dept Psychol, Baltimore, MD 21228 USA.
[Mullane, Audrina] Cleveland Clin, Dept Psychiat & Psychol, Cleveland, OH 44106 USA.
RP Lucksted, A (reprint author), Univ Maryland, Sch Med, Dept Psychiat, Div Psychiat Serv Res, Baltimore, MD 21201 USA.
EM aluckste@psych.umaryland.edu
FU National Institutes of Health [1R01MH090036-01A1]
FX This project was supported by National Institutes of Health grant
1R01MH090036-01A1.
NR 73
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U1 0
U2 0
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 360
EP 367
DI 10.1176/appi.ps.201600037
PG 8
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600010
PM 27903136
ER
PT J
AU Tsai, J
Flatley, B
Kasprow, WJ
Clark, S
Finlay, A
AF Tsai, Jack
Flatley, Bessie
Kasprow, Wesley J.
Clark, Sean
Finlay, Andrea
TI Diversion of Veterans With Criminal Justice Involvement to Treatment
Courts: Participant Characteristics and Outcomes
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID PEER-SUPPORT; ERA VETERANS; AFGHANISTAN; IRAQ; INCARCERATION
AB Objective: This study compared characteristics and outcomes between veterans who participated in veterans treatment courts (VTCs) and veterans involved in criminal justice who participated in other treatment courts (TCs) or who participated in neither VTCs or TCs.
Methods: Data from 22,708 veterans (N=8,083 VTC participants, 680 participants in other TCs [other-TC participants], and 13,945 participants in neither VTCs nor TCs [non-TC participants]) in the Veterans Justice Outreach (VJO) program were analyzed by using multilevel regression models.
Results: VTC participants were more likely than other VJO participants to have served in Iraq or Afghanistan, but there were no sociodemographic disparities in access to VTCs. VTC participants were more likely than non-TC participants to have drug or public-order offenses, and they were more likely than other-TC participants to have DUI offenses. VTC participants had better independent housing outcomes than other VJO participants, and they had better employment outcomes than non-TC participants. However, VTC and other-TC participants were also more likely to have jail sanctions and new incarcerations compared with non-TC participants.
Conclusions: VTCs are a growing service model that serves a broad group of veterans with a range of criminal offenses. Although VTCs show moderate benefits in housing and employment, specialized services are needed to reduce recidivism and maximize these benefits.
C1 [Tsai, Jack] US Dept Vet Affairs, Connecticut Healthcare Syst, New England Mental Illness Res Educ & Clin Ctr, West Haven, CT USA.
[Kasprow, Wesley J.] US Dept Vet Affairs, Connecticut Healthcare Syst, Northeast Program Evaluat Ctr, W Haven, NH USA.
[Tsai, Jack] Yale Sch Med, Dept Psychiat, New Haven, CT 06510 USA.
[Flatley, Bessie] US Dept Vet Affairs, Vet Justice Programs, Philadelphia, PA USA.
[Flatley, Bessie] US Dept Vet Affairs, Natl Ctr Homelessness Vet, Philadelphia, PA USA.
[Clark, Sean] Vet Hlth Adm, Vet Justice Program Off, Lexington, KY USA.
[Finlay, Andrea] VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat, Palo Alto, CA USA.
[Finlay, Andrea] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA.
[Finlay, Andrea] Stanford Univ, Sch Med, Div Gen Med Disciplines, Stanford, CA 94305 USA.
RP Tsai, J (reprint author), US Dept Vet Affairs, Connecticut Healthcare Syst, New England Mental Illness Res Educ & Clin Ctr, West Haven, CT USA.; Tsai, J (reprint author), Yale Sch Med, Dept Psychiat, New Haven, CT 06510 USA.
EM jack.tsai@yale.edu
NR 28
TC 0
Z9 0
U1 1
U2 1
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 375
EP 383
DI 10.1176/appi.ps.201600233
PG 9
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600012
PM 27903139
ER
PT J
AU Meshberg-Cohen, S
DeViva, JC
Rosen, MI
AF Meshberg-Cohen, Sarah
DeViva, Jason C.
Rosen, Marc I.
TI Counseling Veterans Applying for Service Connection Status for Mental
Health Conditions
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID POSTTRAUMATIC-STRESS-DISORDER; DISABILITY; STIGMA; PTSD; CARE;
COMPENSATION; ATTITUDES; CLINICIAN
AB Veterans with mental health conditions that were either caused or aggravated by their military service are eligible to receive service-connected disability benefits from the Department of Veterans Affairs. The process of applying for service connection status is complex, and it is not surprising that veterans frequently develop beliefs about service connection that may not be accurate and that could interfere with treatment. The authors describe some of these beliefs and offer suggestions to clinicians for addressing them. Veterans may believe that their clinician is directly involved in service connection determination or that therapy notes will determine the outcome of the claim. Veterans may not understand the basis for award of service connection and may interpret rejection of their claim as reflecting disrespect for their service or degree of distress. The authors argue that discussing these beliefs with veterans might enhance therapy by demonstrating familiarity with an important aspect of veterans' experience and by helping veterans address a significant and distressing issue.
C1 [Meshberg-Cohen, Sarah; DeViva, Jason C.; Rosen, Marc I.] Yale Sch Med, Dept Psychiat, New Haven, CT 06510 USA.
[Meshberg-Cohen, Sarah; DeViva, Jason C.; Rosen, Marc I.] US Dept Vet Affairs, Connecticut Healthcare Syst, Dept Psychiat, West Haven, CT USA.
RP Meshberg-Cohen, S (reprint author), Yale Sch Med, Dept Psychiat, New Haven, CT 06510 USA.; Meshberg-Cohen, S (reprint author), US Dept Vet Affairs, Connecticut Healthcare Syst, Dept Psychiat, West Haven, CT USA.
EM sarah.meshberg-cohen@yale.edu
NR 15
TC 0
Z9 0
U1 0
U2 0
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 396
EP 399
DI 10.1176/appi.ps.201500533
PG 4
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600015
PM 27629795
ER
PT J
AU Quinn, AE
Rubinsky, AD
Fernandez, AC
Hahm, HC
Samet, JH
AF Quinn, Amity E.
Rubinsky, Anna D.
Fernandez, Anne C.
Hahm, Hyeouk Chris
Samet, Jeffrey H.
TI A Research Agenda to Advance the Coordination of Care for General
Medical and Substance Use Disorders
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID ADDICTION TREATMENT; RANDOMIZED-TRIAL; UNITED-STATES; ALCOHOL; BURDEN;
MANAGEMENT; DISEASE; HEALTH
AB The separation of addiction care from the general medical care system has a negative impact on patients' receipt of high-quality medical care. Clinical and policy-level strategies to improve the coordination of addiction care and general medical care include identifying and engaging patients with unhealthy substance use in general medical settings, providing effective chronic disease management of substance use disorders in primary care, including patient and family perspectives in care coordination, and implementing pragmatic models to pay for the coordination of addiction and general medical care. This Open Forum discusses practice and research recommendations to advance the coordination of general medical and addiction care. The discussion is based on the proceedings of a national meeting of experts in 2014.
C1 [Quinn, Amity E.] Brandeis Univ, Heller Sch Social Policy & Management, Inst Behav Hlth, Waltham, MA 02453 USA.
[Rubinsky, Anna D.] Vet Affairs Puget Sound Hlth Care Syst, Hlth Serv Res & Dev Ctr Innovat, Seattle, WA USA.
[Rubinsky, Anna D.] Univ Calif San Francisco, Kidney Hlth Res Collaborat, San Francisco, CA 94143 USA.
[Rubinsky, Anna D.] VA Med Ctr, San Francisco, CA USA.
[Fernandez, Anne C.] Brown Univ, Ctr Alcohol & Addict Studies, Providence, RI 02912 USA.
[Hahm, Hyeouk Chris] Boston Univ, Sch Social Work, Boston, MA 02215 USA.
[Samet, Jeffrey H.] Boston Univ, Sch Med, Boston, MA 02215 USA.
[Samet, Jeffrey H.] Boston Univ, Sch Publ Hlth, Boston, MA 02215 USA.
[Samet, Jeffrey H.] Boston Med Ctr, Boston, MA USA.
RP Quinn, AE (reprint author), Brandeis Univ, Heller Sch Social Policy & Management, Inst Behav Hlth, Waltham, MA 02453 USA.
EM amity@brandeis.edu
FU [F31 AA023711]; [T32 AA007459]; [R25-DA13582]; [P30DA040500]
FX The contributions of Dr. Quinn and Dr. Fernandez were funded in part by
grants F31 AA023711 and T32 AA007459, respectively. The contribution of
Dr. Samet was funded in part by grants R25-DA13582 and P30DA040500. The
results presented are from a preconference session, which was part of
the Addiction Health Services Research conference, held in Boston,
October 15-17, 2014. The preconference and report were supported by the
Blending Initiative of the National Institute on Drug Abuse under the
leadership of the Center for the National Drug Abuse Treatment Clinical
Trials Network. The authors thank preconference presenters Katharine
Bradley, M.D., M.P.H., Constance Horgan, Sc.D., Richard Saitz, M.D.,
M.P.H., and Constance Weisner, Dr.P.H., M.S.W., and commentators JudyAnn
Bigby, M.D., and Mary Jane England, M.D. The views expressed arc those
of the authors and do not necessarily represent the position or policy
of the Department of Veterans Affairs, the United States Government, or
the authors' institutions.
NR 17
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U1 1
U2 1
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 400
EP 404
DI 10.1176/appi.ps.201600070
PG 5
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600017
PM 27629798
ER
PT J
AU Herbst, E
Zaman, T
Rife, T
AF Herbst, Ellen
Zaman, Tauheed
Rife, Tessa
TI Prescriptions Filled Following an Opioid-Related Hospitalization
SO PSYCHIATRIC SERVICES
LA English
DT Letter
C1 [Herbst, Ellen; Zaman, Tauheed; Rife, Tessa] San Francisco VA Med Ctr, Addict Recovery Treatment Serv, San Francisco, CA 94121 USA.
[Herbst, Ellen; Zaman, Tauheed] Univ Calif San Francisco, Sch Med, Dept Psychiat, San Francisco, CA 94143 USA.
[Rife, Tessa] Univ Calif San Francisco, Sch Pharm, San Francisco, CA 94143 USA.
RP Herbst, E (reprint author), San Francisco VA Med Ctr, Addict Recovery Treatment Serv, San Francisco, CA 94121 USA.; Herbst, E (reprint author), Univ Calif San Francisco, Sch Med, Dept Psychiat, San Francisco, CA 94143 USA.
EM ellen.herbst@va.gov
NR 3
TC 0
Z9 0
U1 0
U2 0
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD APR 1
PY 2017
VL 68
IS 4
BP 422
EP 423
DI 10.1176/appi.ps.68304
PG 2
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA ER5DV
UT WOS:000398822600028
PM 28366126
ER
PT J
AU Krejsgaard, T
Lindahl, LM
Mongan, NP
Wasik, MA
Litvinov, IV
Iversen, L
Langhoff, E
Woetmann, A
Odum, N
AF Krejsgaard, Thorbjorn
Lindahl, Lise M.
Mongan, Nigel P.
Wasik, Mariusz A.
Litvinov, Ivan V.
Iversen, Lars
Langhoff, Erik
Woetmann, Anders
Odum, Niels
TI Malignant inflammation in cutaneous TaEurocell lymphoma-a hostile
takeover
SO SEMINARS IN IMMUNOPATHOLOGY
LA English
DT Review
DE Cutaneous T-cell lymphoma; Malignant T cells; Inflammation;
Pathogenesis; Cancer; Infection; Mycosis fungoides; Sezary syndrome
ID T-CELL LYMPHOMA; ENDOTHELIAL GROWTH-FACTOR; STAPHYLOCOCCUS-AUREUS
COLONIZATION; LIGAND-MEDIATED APOPTOSIS; MESSENGER-RNA EXPRESSION; EARLY
MYCOSIS-FUNGOIDES; NF-KAPPA-B; SEZARY-SYNDROME; INTERFERON-GAMMA; TUMOR
MICROENVIRONMENT
AB Cutaneous T-cell lymphomas (CTCL) are characterized by the presence of chronically inflamed skin lesions containing malignant T cells. Early disease presents as limited skin patches or plaques and exhibits an indolent behavior. For many patients, the disease never progresses beyond this stage, but in approximately one third of patients, the disease becomes progressive, and the skin lesions start to expand and evolve. Eventually, overt tumors develop and the malignant T cells may disseminate to the blood, lymph nodes, bone marrow, and visceral organs, often with a fatal outcome. The transition from early indolent to progressive and advanced disease is accompanied by a significant shift in the nature of the tumor-associated inflammation. This shift does not appear to be an epiphenomenon but rather a critical step in disease progression. Emerging evidence supports that the malignant T cells take control of the inflammatory environment, suppressing cellular immunity and anti-tumor responses while promoting a chronic inflammatory milieu that fuels their own expansion. Here, we review the inflammatory changes associated with disease progression in CTCL and point to their wider relevance in other cancer contexts. We further define the term "malignant inflammation" as a pro-tumorigenic inflammatory environment orchestrated by the tumor cells and discuss some of the mechanisms driving the development of malignant inflammation in CTCL.
C1 [Krejsgaard, Thorbjorn; Woetmann, Anders; Odum, Niels] Univ Copenhagen, Dept Immunol & Microbiol, Blegdamsvej 3c, DK-2200 Copenhagen N, Denmark.
[Lindahl, Lise M.; Iversen, Lars] Aarhus Univ Hosp, Dept Dermatol, Aarhus, Denmark.
[Mongan, Nigel P.] Univ Nottingham, Sch Vet Med & Sci, Loughborough, Leics, England.
[Wasik, Mariusz A.] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA.
[Litvinov, Ivan V.] Univ Ottawa, Div Dermatol, Ottawa, ON, Canada.
[Langhoff, Erik] James J Peters VA Med Ctr, Vet Affairs, Bronx, NY USA.
RP Krejsgaard, T; Odum, N (reprint author), Univ Copenhagen, Dept Immunol & Microbiol, Blegdamsvej 3c, DK-2200 Copenhagen N, Denmark.
EM thorkr@sund.ku.dk; ndum@sund.ku.dk
FU Danish Research Council; Novo Nordic Foundation; Novo Nordic Foundation
Tandem program; Lundbeck Foundation; Danish Cancer Society (Kraeftens
Bekaempelse); Danish Cancer Society; TV2 "Knaek-Cancer-Program"; Sapera
Aude Talent Grant from Danish Council for Independent Research
[DFF-4092-00122]
FX This work was supported by research funding from the Danish Research
Council, the Novo Nordic Foundation, the Novo Nordic Foundation Tandem
program, the Lundbeck Foundation, the Danish Cancer Society (Kraeftens
Bekaempelse), and the Danish Cancer Society and TV2
"Knaek-Cancer-Program". TK was further supported by a Sapera Aude Talent
Grant (DFF-4092-00122) from the Danish Council for Independent Research.
NR 165
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PU SPRINGER HEIDELBERG
PI HEIDELBERG
PA TIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY
SN 1863-2297
EI 1863-2300
J9 SEMIN IMMUNOPATHOL
JI Semin. Immunopathol.
PD APR
PY 2017
VL 39
IS 3
BP 269
EP 282
DI 10.1007/s00281-016-0594-9
PG 14
WC Immunology; Pathology
SC Immunology; Pathology
GA ER6PR
UT WOS:000398928500004
PM 27717961
ER
PT J
AU Jia, H
Pan, YL
Guo, XG
Zhao, LN
Wang, XP
Zhang, LH
Dong, T
Luo, H
Ge, ZZ
Liu, J
Hao, JY
Yao, P
Zhang, Y
Ren, HY
Zhou, WZ
Guo, YJ
Zhang, W
Chen, XL
Sun, DY
Yang, XQ
Kang, XY
Liu, N
Liu, ZG
Leung, F
Wu, KC
Fan, DM
AF Jia, Hui
Pan, Yanglin
Guo, Xuegang
Zhao, Lina
Wang, Xiangping
Zhang, Linhui
Dong, Tao
Luo, Hui
Ge, Zhizheng
Liu, Jun
Hao, Jianyu
Yao, Ping
Zhang, Yao
Ren, Hongyu
Zhou, Weizhen
Guo, Yujie
Zhang, Wei
Chen, Xiaolin
Sun, Dayong
Yang, Xiaoqiang
Kang, Xiaoyu
Liu, Na
Liu, Zhiguo
Leung, Felix
Wu, Kaichun
Fan, Daiming
TI Water Exchange Method Significantly Improves Adenoma Detection Rate: A
Multicenter, Randomized Controlled Trial
SO AMERICAN JOURNAL OF GASTROENTEROLOGY
LA English
DT Article
ID LONGER WITHDRAWAL TIME; SCREENING COLONOSCOPY; QUALITY INDICATORS;
COLORECTAL-CANCER; AIDED COLONOSCOPY; AIR INSUFFLATION; CECAL
INTUBATION; INTERVAL CANCER; IMMERSION; RISK
AB OBJECTIVES: Adenoma detection rate (ADR) is a key colonoscopy quality indicator in Western clinical literature. Our low ADR prompted us to assess novel methods to improve performance. Western retrospective reports suggested that water exchange (WE) could increase ADR. However, most of these studies used pain score or intubation rate as the primary outcome. Here we test the hypothesis that WE significantly increases ADR among Chinese colonoscopists and design a prospective randomized controlled trial using ADR as our primary outcome.
METHODS: This prospective, randomized controlled trial was performed at six centers in China. Screening, surveillance, and diagnostic cases were randomized to be examined by WE or traditional air insufflation (AI) method. The primary outcome was ADR.
RESULTS: From April 2014 to July 2015, 3,303 patients were randomized to WE (n = 1,653) and AI (n = 1,650). The baseline characteristics were comparable. Overall ADR was 18.3% (WE) and 13.4% (AI) (relative risk 1.45, 95% confidential interval: 1.20-1.75, P < 0.001). ADR in screening patients using AI was 25.8% (male) and 15.7% (female). ADR in screening patients aged > 50 years old was 29.4% (WE) and 22.9% (AI) (relative risk 1.09, 95% confidential interval: 1.00-1.19, P = 0.040). The increase by WE was reproducibly observed in all indication categories, and significant in screening and diagnostic cases. The limitation imposed by the unblinded investigators was mitigated by comparable inspection times in cases without polyps, similar adenoma per positive colonoscopy, and reproducible enhancement of ADR and adenoma per colonoscopy by WE across all eight investigators.
CONCLUSIONS: This prospective study confirms Western retrospective data that WE significantly improves ADR among Chinese colonoscopists. WE may be superior to AI for screening colonoscopy in China. Colonoscopists elsewhere with low ADR might consider evaluating WE for performance improvement.
C1 [Jia, Hui; Pan, Yanglin; Guo, Xuegang; Wang, Xiangping; Zhang, Linhui; Dong, Tao; Luo, Hui; Kang, Xiaoyu; Liu, Na; Liu, Zhiguo; Wu, Kaichun; Fan, Daiming] Fourth Mil Med Univ, Xijing Hosp Digest Dis, 127 Changle West Rd, Xian 710032, Shaanxi, Peoples R China.
[Jia, Hui] Weinan Cent Hosp, Dept Gastroenterol, Weinan, Peoples R China.
[Zhao, Lina] Fourth Mil Med Univ, Xijing Hosp, Dept Radiotherapy, Xian, Peoples R China.
[Ge, Zhizheng; Zhang, Yao; Zhang, Wei] Shanghai Jiao Tong Univ, Div Gastroenterol, Shanghai Renji Hosp, Sch Med, Shanghai, Peoples R China.
[Liu, Jun; Ren, Hongyu; Chen, Xiaolin] Huazhong Sci Technol Univ, Tongji Med Union Hosp, Dept Gastroenterol, Wuhan, Peoples R China.
[Hao, Jianyu; Zhou, Weizhen] Capital Med Univ, Beijing Chao Yang Hosp, Dept Gastroenterol, Beijing, Peoples R China.
[Guo, Yujie] Xinjiang Med Univ, Dept Gastroenterol, Affiliated Hosp 1, Urumqi, Peoples R China.
[Sun, Dayong; Yang, Xiaoqiang] Guangzhou Gen Hosp Guangzhou Mil Command Peoples, Dept Gastroenterol, Guangzhou, Guangdong, Peoples R China.
[Leung, Felix] Vet Affairs Greater Los Angeles Healthcare Syst, Div Gastroenterol, Dept Med, Sepulveda Ambulatory Care Ctr, North Hills, CA USA.
[Leung, Felix] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
RP Pan, YL; Wu, KC (reprint author), Fourth Mil Med Univ, Xijing Hosp Digest Dis, 127 Changle West Rd, Xian 710032, Shaanxi, Peoples R China.; Leung, F (reprint author), Vet Affairs Greater Los Angeles Healthcare Syst, Sepulveda Ambulatory Care Ctr, 111G,16111 Plummer St, North Hills, CA 91343 USA.
EM yanglinpan@hotmail.com; felix.leung@va.gov; kaicwu@fmmu.edu.cn
FU National Natural Science Foundation of China [81172288, 81370585];
National Key Technology RD Program [2015BAI13B07]
FX National Natural Science Foundation of China (81172288 and 81370585) and
National Key Technology R&D Program (2015BAI13B07).
NR 38
TC 1
Z9 1
U1 1
U2 1
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 0002-9270
EI 1572-0241
J9 AM J GASTROENTEROL
JI Am. J. Gastroenterol.
PD APR
PY 2017
VL 112
IS 4
BP 568
EP 576
DI 10.1038/ajg.2016.501
PG 9
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA ES2MG
UT WOS:000399362000013
PM 27922025
ER
PT J
AU Cui, CW
Basen, T
Philipp, AT
Yusin, J
Krishnaswamy, G
AF Cui, Chongwei
Basen, Tyler
Philipp, Ami Thakor
Yusin, Joseph
Krishnaswamy, Guha
TI Celiac disease and nonceliac gluten sensitivity
SO ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
LA English
DT Article
C1 [Cui, Chongwei; Basen, Tyler; Philipp, Ami Thakor; Yusin, Joseph] Vet Affairs Greater Los Angeles Healthcare Syst, Dept Allergy & Immunol, Los Angeles, CA USA.
[Krishnaswamy, Guha] Wake Forest Sch Med, Med Ctr Blvd,Watlington Tower,Second Floor, Winston Salem, NC 27157 USA.
[Krishnaswamy, Guha] Wake Baptist Hosp, Med Ctr Blvd,Watlington Tower,Second Floor, Winston Salem, NC 27157 USA.
[Krishnaswamy, Guha] WG Bill Hefner Vet Affairs Med Ctr & Affiliated C, Salisbury, NC USA.
RP Krishnaswamy, G (reprint author), Wake Forest Sch Med, Med Ctr Blvd,Watlington Tower,Second Floor, Winston Salem, NC 27157 USA.; Krishnaswamy, G (reprint author), Wake Baptist Hosp, Med Ctr Blvd,Watlington Tower,Second Floor, Winston Salem, NC 27157 USA.
EM gkrishna@wakehealth.edu
NR 16
TC 0
Z9 0
U1 3
U2 3
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1081-1206
EI 1534-4436
J9 ANN ALLERG ASTHMA IM
JI Ann. Allergy Asthma Immunol.
PD APR
PY 2017
VL 118
IS 4
BP 389
EP 393
DI 10.1016/j.anai.2017.01.008
PG 5
WC Allergy; Immunology
SC Allergy; Immunology
GA ER6SE
UT WOS:000398936900002
PM 28390579
ER
PT J
AU Weinstock, MA
Lott, JP
Wang, Q
Titus, LJ
Onega, T
Nelson, HD
Pearson, L
Piepkorn, M
Barnhill, RL
Elmore, JG
Tosteson, ANA
AF Weinstock, M. A.
Lott, J. P.
Wang, Q.
Titus, L. J.
Onega, T.
Nelson, H. D.
Pearson, L.
Piepkorn, M.
Barnhill, R. L.
Elmore, J. G.
Tosteson, A. N. A.
TI Skin biopsy utilization and melanoma incidence among Medicare
beneficiaries
SO BRITISH JOURNAL OF DERMATOLOGY
LA English
DT Article
ID UNITED-STATES; CANCER; OVERDIAGNOSIS; POPULATION
AB Background Melanoma incidence has increased in recent decades in the U.S.A. Uncertainty remains regarding how much of this increase is attributable to greater melanoma screening activities, potential detection bias and overdiagnosis. Objectives To use a cross-sectional ecological analysis to evaluate the relationship between skin biopsy and melanoma incidence rates over a more recent time period than prior reports.
Methods Examination of the association of biopsy rates and melanoma incidence (invasive and in situ) in SEER-Medicare data (including 10 states) for 2002-2009.
Results The skin biopsy rate increased by approximately 50% (6% per year) throughout this 8-year period, from 7012 biopsies per 100 000 persons in 2002 to 10 528 biopsies per 100 000 persons in 2009. The overall melanoma incidence rate increased approximately 4% (< 1% per year) over the same time period. The incidence of melanoma in situ increased approximately 10% (1% per year), while the incidence of invasive melanoma increased from 2002 to 2005 then decreased from 2006 to 2009. Regression models estimated that, on average, for every 1000 skin biopsies performed, an additional 5.2 (95% confidence interval 4.1-6.3) cases of melanoma in situ were diagnosed and 8.1 (95% confidence interval 6.7-9.5) cases of invasive melanoma were diagnosed. When considering individual states, some demonstrated a positive association between biopsy rate and invasive melanoma incidence, others an inverse association, and still others a more complex pattern.
Conclusions Increased skin biopsies over time are associated with increased diagnosis of in situ melanoma, but the association with invasive melanoma is more complex.
C1 [Weinstock, M. A.] US Dept Vet Affairs, Ctr Dermatoepidemiol, Med Ctr, Providence, RI USA.
[Weinstock, M. A.] Rhode Isl Hosp, Dept Dermatol, Providence, RI USA.
[Weinstock, M. A.] Brown Univ, Dept Dermatol, Providence, RI 02912 USA.
[Weinstock, M. A.] Brown Univ, Dept Epidemiol, Providence, RI 02912 USA.
[Lott, J. P.] Cornell Scott Hill Hlth Ctr, New Haven, CT USA.
[Wang, Q.; Pearson, L.; Tosteson, A. N. A.] Geisel Sch Med Dartmouth, Dartmouth Inst Hlth Policy & Clin Practice, Lebanon, NH USA.
[Titus, L. J.; Onega, T.] Geisel Sch Med Dartmouth, Dept Epidemiol, Lebanon, NH USA.
[Onega, T.] Geisel Sch Med Dartmouth, Dept Biomed Data Sci, Lebanon, NH USA.
[Tosteson, A. N. A.] Geisel Sch Med Dartmouth, Dept Med, Lebanon, NH USA.
[Titus, L. J.; Onega, T.; Tosteson, A. N. A.] Norris Cotton Canc Ctr, Lebanon, NH USA.
[Nelson, H. D.] Oregon Hlth & Sci Univ, Dept Med Informat, Portland, OR 97201 USA.
[Nelson, H. D.] Oregon Hlth & Sci Univ, Dept Clin Epidemiol, Portland, OR 97201 USA.
[Nelson, H. D.] Oregon Hlth & Sci Univ, Dept Med, Portland, OR 97201 USA.
[Nelson, H. D.] Providence Hlth & Serv, Providence Canc Ctr, Providence, OR USA.
[Piepkorn, M.] Univ Washington, Sch Med, Dept Med, Div Dermatol, Seattle, WA 98195 USA.
[Elmore, J. G.] Univ Washington, Sch Med, Dept Internal Med, Seattle, WA 98105 USA.
[Piepkorn, M.] Dermatopathol Northwest, Bellevue, WA USA.
[Barnhill, R. L.] Univ Paris 05, Dept Pathol, Inst Curie, Paris, France.
[Barnhill, R. L.] Univ Paris 05, Fac Med, Paris, France.
RP Elmore, JG (reprint author), Univ Washington, Sch Med, Dept Internal Med, Seattle, WA 98105 USA.
EM jelmore@u.washington.edu
FU National Cancer Institute [R01 CA151306, K05 CA104699]
FX This work was supported by the National Cancer Institute (R01 CA151306
and K05 CA104699). The funder was not involved in the design and conduct
of the study; the collection, management, analysis and interpretation of
data; the preparation, review and approval of the manuscript; or the
decision to submit the manuscript for publication.
NR 13
TC 1
Z9 1
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0007-0963
EI 1365-2133
J9 BRIT J DERMATOL
JI Br. J. Dermatol.
PD APR
PY 2017
VL 176
IS 4
BP 949
EP 954
DI 10.1111/bjd.15077
PG 6
WC Dermatology
SC Dermatology
GA ES2MR
UT WOS:000399363100039
PM 27639256
ER
PT J
AU Dasgupta, SK
Le, A
Vijayan, KV
Thiagarajan, P
AF Dasgupta, Swapan K.
Le, Anhquyen
Vijayan, K. Vinod
Thiagarajan, Perumal
TI Dasatinib inhibits actin fiber reorganization and promotes endothelial
cell permeability through RhoA-ROCK pathway
SO CANCER MEDICINE
LA English
DT Article
DE Actin fibers; dasatinib; endothelial permeability; tyrosine
phosphorylation
ID FOCAL ADHESION FORMATION; CHRONIC MYELOID-LEUKEMIA; TYROSINE
PHOSPHORYLATION; VASCULAR-PERMEABILITY; KINASE; PAXILLIN;
HYPERPERMEABILITY; SRC; ACTIVATION; MECHANISM
AB Treatment with dasatinib, a tyrosine kinase inhibitor, is associated with edema, pleural effusion, and pulmonary edema. We investigated the effect of dasatinib on the barrier function of human microvascular endothelial cells-1 (HMEC-1) in vitro and in vivo. The permeability of HMEC-1 to fluorescein isothiocyante (FITC)-dextran increased in Transwell chambers within 5min following the addition of therapeutic concentrations of dasatinib. The change in permeability was associated with increased activation of RhoA GTPase and its effector Rho-associated coiled-coil kinase 1(ROCK1). RhoA inhibitor C3 transferase almost completely inhibited dasatinib-induced increase in permeability. Under similar conditions, imatinib had no effect on permeability or activation of RhoA. Since integrin-induced cell spreading suppresses RhoA activation, we examined the effect of dasatinib on cell spreading on fibronectin substrate. Dasatinib impaired endothelial cell spreading in a concentration-dependent manner and induced disorganization of actin fibers. Tyrosine kinases play an essential role in transmitting signals from integrins to RhoA and we examined tyrosine phosphorylation of several cytoskeletal proteins. Dasatinib markedly inhibited tyrosine phosphorylation of p130 Crk-associated substrate (p130cas), paxillin and vinculin. These results suggest that the inhibition of tyrosine phosphorylation of the focal adhesion plaque components by dasatinib may alter the assembly of actin fibers resulting in the activation of RhoA/ROCK pathway. Consistent with these findings, dasatinib-induced increase in the permeability was blocked by ROCK inhibitor y27632. In vivo administration of y27632, significantly inhibited the dasatinib-induced extravasation of Evans blue in mice and dasatinib-induced increase in microvascular permeability was attenuated in ROCK1-deficient mice. These findings suggest that ROCK inhibitors could serve as therapeutic modalities to ameliorate the dasatinib-induced pulmonary changes.
C1 [Dasgupta, Swapan K.; Le, Anhquyen; Thiagarajan, Perumal] Baylor Coll Med, Dept Pathol, Michael E DeBakey Vet Affairs Med Ctr, CTRID, Houston, TX 77030 USA.
[Vijayan, K. Vinod; Thiagarajan, Perumal] Baylor Coll Med, Dept Med, Michael E DeBakey Vet Affairs Med Ctr, CTRID, Houston, TX 77030 USA.
RP Dasgupta, SK; Thiagarajan, P (reprint author), Michael E DeBakey VA Med Ctr, Mail Stop 113, Houston, TX 77030 USA.
EM swapand@bcm.edu; perumalt@bcm.edu
FU Department of Veterans Affairs, Veterans Health Administration; Office
of Research and Development, Biomedical Laboratory Research and
Development; American Heart Association; Gulf Coast Blood Center;
National Institutes of Health [HL08163, GM112806]
FX This study was supported in part by grants from the Department of
Veterans Affairs, Veterans Health Administration, Office of Research and
Development, Biomedical Laboratory Research and Development, American
Heart Association, a grant from Gulf Coast Blood Center, and National
Institutes of Health HL08163 and GM112806.
NR 39
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2045-7634
J9 CANCER MED-US
JI Cancer Med.
PD APR
PY 2017
VL 6
IS 4
BP 809
EP 818
DI 10.1002/cam4.1019
PG 10
WC Oncology
SC Oncology
GA ER5ND
UT WOS:000398847700010
PM 28316141
ER
PT J
AU El-Sherief, AH
Lau, CT
Obuchowski, NA
Mehta, AC
Rice, TW
Blackstone, EH
AF El-Sherief, Ahmed H.
Lau, Charles T.
Obuchowski, Nancy A.
Mehta, Atul C.
Rice, Thomas W.
Blackstone, Eugene H.
TI Cross-Disciplinary Analysis of Lymph Node Classification in Lung Cancer
on CT Scanning
SO CHEST
LA English
DT Article
DE lung cancer; lymph nodes; staging
ID INTERNATIONAL ASSOCIATION
AB BACKGROUND: Accurate and consistent regional lymph node classification is an important element in the staging and multidisciplinary management of lung cancer. Regional lymph node definition sets-lymph node maps-have been created to standardize regional lymph node classification. In 2009, the International Association for the Study of Lung Cancer (IASLC) introduced a lymph node map to supersede all preexisting lymph node maps. Our aim was to study if and how lung cancer specialists apply the IASLC lymph node map when classifying thoracic lymph nodes encountered on CT scans during lung cancer staging.
METHODS: From April 2013 through July 2013, invitations were distributed to all members of the Fleischner Society, Society of Thoracic Radiology, General Thoracic Surgical Club, and the American Association of Bronchology and Interventional Pulmonology to participate in an anonymous online image-based and text-based 20-question survey regarding lymph node classification for lung cancer staging on CT imaging.
RESULTS: Three hundred thirty-seven people responded (approximately 25% participation). Respondents consisted of self-reported thoracic radiologists (n = 158), thoracic surgeons (n = 102), and pulmonologists who perform endobronchial ultrasonography (n = 77). Half of the respondents (50%; 95% CI, 44%-55%) reported using the IASLC lymph node map in daily practice, with no significant differences between subspecialties. A disparity was observed between the IASLC definition sets and their interpretation and application on CT scans, in particular for lymph nodes near the thoracic inlet, anterior to the trachea, anterior to the tracheal bifurcation, near the ligamentum arteriosum, between the bronchus intermedius and esophagus, in the internal mammary space, and adjacent to the heart.
CONCLUSIONS: Use of older lymph node maps and inconsistencies in interpretation and application of definitions in the IASLC lymph node map may potentially lead to misclassification of stage and suboptimal management of lung cancer in some patients.
C1 [El-Sherief, Ahmed H.; Lau, Charles T.] Cleveland Clin, Sect Thorac Imaging, Heart & Vasc Inst, Cleveland, OH 44106 USA.
[Obuchowski, Nancy A.; Blackstone, Eugene H.] Cleveland Clin, Imaging Inst, Dept Qualitat Hlth Sci, Heart & Vasc Inst, Cleveland, OH 44106 USA.
[Mehta, Atul C.] Cleveland Clin, Sect Pulm Med, Heart & Vasc Inst, Cleveland, OH 44106 USA.
[Rice, Thomas W.; Blackstone, Eugene H.] Cleveland Clin, Resp Inst, Heart & Vasc Inst, Cleveland, OH 44106 USA.
[Rice, Thomas W.; Blackstone, Eugene H.] Cleveland Clin, Sect Thorac & Cardiovasc Surg, Heart & Vasc Inst, Cleveland, OH 44106 USA.
[El-Sherief, Ahmed H.] Vet Affairs Greater Angeles Healthcare Syst, Dept Diagnost Radiol, Sect Thorac Imaging, Los Angeles, CA USA.
[El-Sherief, Ahmed H.] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
RP El-Sherief, AH (reprint author), Greater Los Angeles Vet Adm Healthcare Syst, Sect Thorac Imaging, Dept Diagnost Radiol, 11301 Wilshire Blvd,Bldg 500, Los Angeles, CA 90073 USA.
EM ahelsherief@gmail.com
NR 10
TC 1
Z9 1
U1 0
U2 0
PU AMER COLL CHEST PHYSICIANS
PI GLENVIEW
PA 2595 PATRIOT BLVD, GLENVIEW, IL 60026 USA
SN 0012-3692
J9 CHEST
JI Chest
PD APR
PY 2017
VL 151
IS 4
BP 776
EP 785
DI 10.1016/j.chest.2016.09.016
PG 10
WC Critical Care Medicine; Respiratory System
SC General & Internal Medicine; Respiratory System
GA ER3WV
UT WOS:000398731500019
PM 27713056
ER
PT J
AU Meyer, S
Teerlink, JR
Metra, M
Ponikowski, P
Cotter, G
Davison, BA
Felker, GM
Filippatos, G
Greenberg, BH
Hua, TA
Severin, T
Qian, M
Voors, AA
AF Meyer, Sven
Teerlink, John R.
Metra, Marco
Ponikowski, Piotr
Cotter, Gad
Davison, Beth A.
Felker, G. Michael
Filippatos, Gerasimos
Greenberg, Barry H.
Hua, Tsushung A.
Severin, Thomas
Qian, Min
Voors, Adriaan A.
TI Sex differences in early dyspnea relief between men and women
hospitalized for acute heart failure: insights from the RELAX-AHF study
SO CLINICAL RESEARCH IN CARDIOLOGY
LA English
DT Article
DE Serelaxin; Acute heart failure; Sex; Gender; Dyspnea
ID RENAL IMPAIRMENT; OUTCOMES; SERELAXIN; ASSOCIATION; PROTECT; GENDER;
DETERMINANTS; REGISTRY
AB Women with heart failure are typically older, and more often have hypertension and a preserved left ventricular ejection fraction as compared with men. We sought to analyze if these sex differences influence the course and outcome of acute heart failure.
We analyzed sex differences in acute heart failure in 1161 patients enrolled in the RELAX-AHF study. The pre-specified study endpoints were used. At baseline, women (436/1161 patients) were older, had a higher left ventricular ejection fraction, a higher rate of hypertension, and were treated differently from men. Early dyspnea improvement (moderate or marked dyspnea improvement measured by Likert scale during the first 24 h) was greater in women. However, dyspnea improvement over the first 5 days (change from baseline in the visual analog scale area under the curve (VAS AUC) to day 5) was similar between men and women. Women reported greater improvements in general wellbeing by Likert, but no such benefits were evident with the VAS score. Multi-variable predictors of moderate or marked dyspnea improvement were female sex (p = 0.0011), lower age (p = 0.0026) and lower diuretic dose (p = 0.0067). The additional efficacy endpoints of RELAX-AHF were similar between men and women and serelaxin was equally effective in men and women.
Women exhibit better earlier dyspnea relief and improvement in general wellbeing compared with men, even adjusted for age and left ventricular ejection fraction. However, in-hospital and post-discharge clinical outcomes were similar between men and women.
This trial is registered at ClinicalTrials.gov, NCT00520806.
C1 [Meyer, Sven; Voors, Adriaan A.] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands.
[Meyer, Sven] Carl von Ossietzky Univ Oldenburg, European Med Sch Oldenburg Groningen, Heart Ctr Oldenburg, Dept Cardiol, Oldenburg, Germany.
[Teerlink, John R.] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Teerlink, John R.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Metra, Marco] Univ Brescia, Cardiol, Dept Med & Surg Specialties, Radiol Sci & Publ Hlth, Brescia, Italy.
[Ponikowski, Piotr] Med Univ, Clin Mil Hosp, Wroclaw, Poland.
[Cotter, Gad; Davison, Beth A.] Momentum Res Inc, Durham, NC USA.
[Felker, G. Michael] Duke Univ, Sch Med, Duke Heart Ctr, Durham, NC USA.
[Filippatos, Gerasimos] Athens Univ Hosp, Athens, Greece.
[Greenberg, Barry H.] Univ Calif San Diego, La Jolla, CA 92093 USA.
[Hua, Tsushung A.] Novartis Pharmaceut, E Hanover, NJ USA.
[Severin, Thomas] Novartis Pharma AG, Basel, Switzerland.
[Qian, Min] Columbia Univ, Med Ctr, New York, NY USA.
RP Voors, AA (reprint author), Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands.
EM a.a.voors@umcg.nl
FU Servier; Novartis; Amgen; Bayer; Cardio3 Bioscience; Cytokinetics; Mast
Therapeutics; Medtronic; St. Jude; Trevena; Abbott Vascular; Corthera;
Abbott; Merck; PDL BioPharma; Otsuka; Roche Diagnostics; Bristol Myers
Squibb; NHLBI; European Union; Alere; Boehringer Ingelheim;
Cardio3Biosciences; Celladon; GSK; Merck/MSD; Stealth Peptides;
Singulex; Sphingotec; Vifor; ZS Pharma
FX SM received consulting fees, travel support and honoraria from Servier
and Novartis. JRT has received research grants or consulting fees from
Amgen, Bayer, Cardio3 Bioscience, Cytokinetics, Mast Therapeutics,
Medtronic, Novartis, St. Jude and Trevena. MM has received consulting
income from Abbott Vascular, Bayer, Corthera, and Novartis, as well as
travel support and honoraria from Servier and Novartis. PP was a
consultant for Astellas, Bayer, EKR Therapeutics, J&J, the Medicines
Company, Medtronic, Novartis, Otsuka, Palatin Technologies, PDL
BioPharma, Pericor Therapeutics, SigmaTau, Solvay Pharmaceuticals, and
Trevena; has received honoraria from Alere, Beckman-Coulter, BiogenIdec,
Corthera, Ikaria, Nile Therapeutics, Momentum Research, and Overcome;
has received research support from Abbott, Merck and PDL BioPharma; and
has received travel support from MyLife and equipment support from
Sonosite. PSP, in the last one year is or has been a Consultant for:
Intersection Medical, INSYS, Janssen, Medtronic, Novartis, Trevena,
scPharmaceuticals, Cardioxyl, Roche Diagnostics, Relypsa, Honoraria:
Palatin Technologies. GC and BAD are employees of Momentum Research,
which has provided consulting and trial management services to
NovaCardia, Merck, Corthera, Novartis, Nile Therapeutics, Bioheart,
Cardio3 Biosciences, Amgen, Celadon, Targegen, Trevena, Sorbent
Therapeutics, and NIH. GMF reports consulting income from Novartis,
Amgen, Otsuka, Trevena, Roche Diagnostics, Merck, Medtronic, Bristol
Myers Squibb and grant fundings from Novartis, Amgen, Otsuka, Roche
Diagnostics, and NHLBI. GF is an executive committee member and
consultant to Corthera (a Novartis company), Bayer, Cardiorentis, and
has received research grants from Amgen, European Union. BHG served as a
consultant for Novartis, Teva, Celladon, Janssen, Zensun, Relypsa, MAST
and ZS Pharma. MQ receives partial salary support from Novartis for
statistical analysis of the data for this trial. TS and TAH are
employees and receive salary, benefits, and stocks options from Novartis
Pharma. AAV reports consultancy fees and/or research grants from: Alere,
Amgen, Bayer, Boehringer Ingelheim, Cardio3Biosciences, Celladon, GSK,
Merck/MSD, Novartis, Servier, Stealth Peptides, Singulex, Sphingotec,
Trevena, Vifor, ZS Pharma.
NR 22
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER HEIDELBERG
PI HEIDELBERG
PA TIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY
SN 1861-0684
EI 1861-0692
J9 CLIN RES CARDIOL
JI Clin. Res. Cardiol.
PD APR
PY 2017
VL 106
IS 4
BP 280
EP 292
DI 10.1007/s00392-016-1051-4
PG 13
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA ER3VG
UT WOS:000398727100005
PM 27838739
ER
PT J
AU Flores, LE
Berenbaum, H
AF Flores, Luis E., Jr.
Berenbaum, Howard
TI The Effect of the Social Regulation of Emotion on Emotional Long-Term
Memory
SO EMOTION
LA English
DT Article
DE emotional memory; social regulation of emotion; interpersonal
ID HUMAN AMYGDALA; OXYTOCIN; PERSONALITY; INVOLVEMENT; PERFORMANCE;
MECHANISMS; REACTIVITY; CLOSENESS; EXPLICIT; SUPPORT
AB Memories for emotional events tend to be stronger than for neutral events, and weakening negative memories can be helpful to promote well-being. The present study examined whether the social regulation of emotion (in the form of handholding) altered the strength of emotional long-term memory. A sample of 219 undergraduate students viewed sets of negative, neutral, and positive images. Each participant held a stress ball while viewing half of the images and held someone's hand while viewing the other half. Participants returned 1 week later to complete a recognition task. Performance on the recognition task demonstrated that participants had lower memory accuracy for negative but not for positive pictures that were shown while they were holding someone's hand compared with when they were holding a stress ball. Although handholding altered the strength of negative emotional long-term memory, it did not down-regulate negative affective response as measured by self-report or facial expressivity. The present findings provide evidence that the social regulation of emotion can help weaken memory for negative information. Given the role of strong negative memories in different forms of psychopathology (e.g., depression, posttraumatic stress disorder), these findings may help better understand how close relationships protect against psychopathology.
C1 [Flores, Luis E., Jr.] VA Pittsburgh Healthcare Syst, VISN Mental Illness Res Educ & Clin Ctr MIRECC 4, Pittsburgh, PA USA.
[Flores, Luis E., Jr.] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15260 USA.
[Berenbaum, Howard] Univ Illinois, Dept Psychol, Champaign, IL USA.
RP Flores, LE (reprint author), VA Pittsburgh Healthcare Syst, MIRECC Res Off Bldg 151R,Univ Dr Campus, Pittsburgh, PA 15240 USA.
EM floresle@pitt.edu
NR 50
TC 0
Z9 0
U1 5
U2 5
PU AMER PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST NE, WASHINGTON, DC 20002-4242 USA
SN 1528-3542
EI 1931-1516
J9 EMOTION
JI Emotion
PD APR
PY 2017
VL 17
IS 3
BP 547
EP 556
DI 10.1037/emo0000259
PG 10
WC Psychology, Experimental
SC Psychology
GA ER6JE
UT WOS:000398910600014
PM 27936815
ER
PT J
AU Snowden, MB
Steinman, LE
Bryant, LL
Cherrier, MM
Greenlund, KJ
Leith, KH
Levy, C
Logsdon, RG
Copeland, C
Vogel, M
Anderson, LA
Atkins, DC
Bell, JF
Fitzpatrick, AL
AF Snowden, Mark B.
Steinman, Lesley E.
Bryant, Lucinda L.
Cherrier, Monique M.
Greenlund, Kurt J.
Leith, Katherine H.
Levy, Cari
Logsdon, Rebecca G.
Copeland, Catherine
Vogel, Mia
Anderson, Lynda A.
Atkins, David C.
Bell, Janice F.
Fitzpatrick, Annette L.
TI Dementia and co-occurring chronic conditions: a systematic literature
review to identify what is known and where are the gaps in the evidence?
SO INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Review
DE dementia; cognitive impairment; multiple chronic conditions; systematic
literature review; public health; aging
ID NURSING-HOME RESIDENTS; COMMUNITY-BASED COHORT; AFRICAN-AMERICAN
PATIENTS; CONGESTIVE-HEART-FAILURE; COGNITIVE IMPAIRMENT;
ALZHEIMERS-DISEASE; OLDER-ADULTS; PARKINSONS-DISEASE; VASCULAR DEMENTIA;
INCIDENT DEMENTIA
AB ObjectiveThe challenges posed by people living with multiple chronic conditions are unique for people with dementia and other significant cognitive impairment. There have been recent calls to action to review the existing literature on co-occurring chronic conditions and dementia in order to better understand the effect of cognitive impairment on disease management, mobility, and mortality.
MethodsThis systematic literature review searched PubMed databases through 2011 (updated in 2016) using key constructs of older adults, moderate-to-severe cognitive impairment (both diagnosed and undiagnosed dementia), and chronic conditions. Reviewers assessed papers for eligibility and extracted key data from each included manuscript. An independent expert panel rated the strength and quality of evidence and prioritized gaps for future study.
ResultsFour thousand thirty-three articles were identified, of which 147 met criteria for review. We found that moderate-to-severe cognitive impairment increased risks of mortality, was associated with prolonged institutional stays, and decreased function in persons with multiple chronic conditions. There was no relationship between significant cognitive impairment and use of cardiovascular or hypertensive medications for persons with these comorbidities. Prioritized areas for future research include hospitalizations, disease-specific outcomes, diabetes, chronic pain, cardiovascular disease, depression, falls, stroke, and multiple chronic conditions.
ConclusionsThis review summarizes that living with significant cognitive impairment or dementia negatively impacts mortality, institutionalization, and functional outcomes for people living with multiple chronic conditions. Our findings suggest that chronic-disease management interventions will need to address co-occurring cognitive impairment. Copyright (c) 2017 John Wiley & Sons, Ltd.
C1 [Snowden, Mark B.; Cherrier, Monique M.; Atkins, David C.] Univ Washington, Sch Med, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Steinman, Lesley E.; Copeland, Catherine; Vogel, Mia] Univ Washington, Hlth Promot Res Ctr, Seattle, WA 98195 USA.
[Bryant, Lucinda L.] Univ Colorado, Dept Community & Behav Hlth, Colorado Sch Publ Hlth, Anschutz Med Campus, Aurora, CO USA.
[Greenlund, Kurt J.; Anderson, Lynda A.] Ctr Dis Control & Prevent, Natl Ctr Chron Dis Prevent & Hlth Promot, Atlanta, GA USA.
[Leith, Katherine H.] Univ South Carolina, Coll Social Work, Hamilton Coll, Columbia, SC USA.
[Levy, Cari] Univ Colorado, Sch Med, Div Hlth Care Policy & Res, Denver, CO USA.
[Levy, Cari] Denver Vet Affairs Med Ctr, Denver, CO USA.
[Logsdon, Rebecca G.] UW Sch Nursing, Northwest Res Grp Aging, Seattle, WA USA.
[Anderson, Lynda A.] Emory Univ, Rollins Sch Publ Hlth, Atlanta, GA 30322 USA.
[Bell, Janice F.] Univ Calif Davis, Betty Irene Moore Sch Nursing, Davis, CA 95616 USA.
[Fitzpatrick, Annette L.] Univ Washington, Sch Med, Dept Family Med, Seattle, WA 98195 USA.
[Fitzpatrick, Annette L.] Univ Washington, Dept Epidemiol, Sch Med, Seattle, WA 98195 USA.
[Fitzpatrick, Annette L.] Univ Washington, Sch Med, Dept Global Hlth, Seattle, WA USA.
[Fitzpatrick, Annette L.] Univ Washington, Sch Publ Hlth, Seattle, WA 98195 USA.
RP Steinman, LE (reprint author), Univ Washington, Hlth Promot Res Ctr, Seattle, WA 98195 USA.
EM lesles@uw.edu
FU Centers for Disease Control and Prevention's (CDC) Healthy Aging Program
through the CDC Prevention Research Centers Program, Special Interest
Project [U48-DP000050]
FX This research was funded by the Centers for Disease Control and
Prevention's (CDC) Healthy Aging Program through the CDC Prevention
Research Centers Program, Special Interest Project grant (U48-DP000050)
to the University of Washington Health Promotion Research Center.
Special thanks to Lucinda L. Bryant, PhD, MSHA, and Catherine Copeland,
MPA for their contributions to the literature search and data
abstraction, to Angie Deokar for grant management, and to Oejin Shin for
her work preparing the manuscript. Please contact the corresponding
author for further information about categories not presented or for
detailed summary data tables. The findings and conclusions in this
article are those of the authors and do not necessarily represent the
official position of the CDC. Please contact the corresponding author
for copies of the underlying research materials related to our paper
(e.g., detailed summary data tables, article abstraction instruments).
NR 165
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0885-6230
EI 1099-1166
J9 INT J GERIATR PSYCH
JI Int. J. Geriatr. Psychiatr.
PD APR
PY 2017
VL 32
IS 4
BP 357
EP 371
DI 10.1002/gps.4652
PG 15
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA ES1PV
UT WOS:000399300400001
PM 28146334
ER
PT J
AU Harrington, KD
Gould, E
Lim, YY
Ames, D
Pietrzak, RH
Rembach, A
Rainey-Smith, S
Martins, RN
Salvado, O
Villemagne, VL
Rowe, CC
Masters, CL
Maruff, P
AF Harrington, Karra D.
Gould, Emma
Lim, Yen Ying
Ames, David
Pietrzak, Robert H.
Rembach, Alan
Rainey-Smith, Stephanie
Martins, Ralph N.
Salvado, Olivier
Villemagne, Victor L.
Rowe, Christopher C.
Masters, Colin L.
Maruff, Paul
CA AIBL Res Grp
TI Amyloid burden and incident depressive symptoms in cognitively normal
older adults
SO INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Article
DE amyloid; depression; Alzheimer's disease; cognitively normal
ID LATE-LIFE DEPRESSION; ALZHEIMERS ASSOCIATION WORKGROUPS; BETA PROTEIN;
DIAGNOSTIC GUIDELINES; ELDERLY DEPRESSION; NATIONAL INSTITUTE; MAJOR
DEPRESSION; A-BETA; DISEASE; IMPAIRMENT
AB ObjectiveSeveral studies have reported that non-demented older adults with clinical depression show changes in amyloid- (A) levels in blood, cerebrospinal fluid and on neuroimaging that are consistent with those observed in patients with Alzheimer's disease. These findings suggest that A may be one of the mechanisms underlying the relation between the two conditions. We sought to determine the relation between elevated cerebral A and the presence of depression across a 54-month prospective observation period.
MethodsCognitively normal older adults from the Australian Imaging Biomarkers and Lifestyle study who were not depressed and had undergone a positron emission tomography scan to classify them as either high A (n=81) or low A (n=278) participated. Depressive symptoms were assessed using the Geriatric Depression Scale Short Form at 18-month intervals over 54months.
ResultsWhilst there was no difference in probable depression between groups at baseline, incidence was 4.5 (95% confidence interval [CI] 1.3-16.4) times greater within the high A group (9%) than the low A group (2%) by the 54-month assessment.
ConclusionsResults of this study suggest that elevated A levels are associated with a 4.5-fold increased likelihood of developing clinically significant depressive symptoms on follow-up in preclinical Alzheimer's disease. This underscores the importance of assessing, monitoring and treating depressive symptoms in older adults with elevated A. Copyright (c) 2016 John Wiley & Sons, Ltd.
C1 [Harrington, Karra D.; Gould, Emma] Deakin Univ, Sch Psychol, Geelong, Vic, Australia.
[Harrington, Karra D.; Lim, Yen Ying; Rembach, Alan; Villemagne, Victor L.; Masters, Colin L.; Maruff, Paul] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia.
[Harrington, Karra D.; Ames, David] Univ Melbourne, Acad Unit Psychiat Old Age, Dept Psychiat, Parkville, Vic, Australia.
[Ames, David] Natl Ageing Res Inst, Parkville, Vic, Australia.
[Pietrzak, Robert H.] VA Connecticut Healthcare Syst, Clin Neurosci Div, Natl Ctr Posttraumat Stress Disorder, US Dept Vet Affairs, West Haven, CT USA.
[Pietrzak, Robert H.] Yale Sch Med, Dept Psychiat, New Haven, CT USA.
[Rainey-Smith, Stephanie; Martins, Ralph N.] Edith Cowan Univ, Sch Exercise Biomed & Hlth Sci, Ctr Excellence Alzheimers Dis Res & Care, Perth, WA, Australia.
[Rainey-Smith, Stephanie; Martins, Ralph N.] Hollywood Private Hosp, Sir James McCusker Alzheimers Dis Res Unit, Nedlands, WA, Australia.
[Salvado, Olivier] Australian E Hlth Res Ctr BioMedIA, CSIRO Preventat Hlth Natl Res Flagship, Herston, Qld, Australia.
[Villemagne, Victor L.; Rowe, Christopher C.] Austin Hlth, Ctr PET, Dept Nucl Med, Heidelberg, Vic, Australia.
[Villemagne, Victor L.; Rowe, Christopher C.] Univ Melbourne, Dept Med, Austin Hlth, Heidelberg, Vic, Australia.
[Maruff, Paul] CogState Ltd, Melbourne, Vic, Australia.
RP Harrington, KD (reprint author), Deakin Univ, Sch Psychol, Geelong, Vic, Australia.; Harrington, KD (reprint author), Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Parkville, Vic, Australia.; Harrington, KD (reprint author), Univ Melbourne, Acad Unit Psychiat Old Age, Dept Psychiat, Parkville, Vic, Australia.
EM karra.harrington@florey.edu.au
FU Australian Commonwealth Scientific Industrial and Research Organization
[CSIRO]; Edith Cowan University [ECU]; Mental Health Research Institute
[MHRI]; Alzheimer's Australia [AA]; National Ageing Research Institute
[NARI]; Austin Health; CogState Ltd.; Hollywood Private Hospital; Sir
Charles Gardner Hospital; National Health and Medical Research Council
(NHMRC); Dementia Collaborative Research Centres program (DCRC2);
Science and Industry Endowment Fund (SIEF); Cooperative Research Centre
(CRC) for Mental Health from the Australian Government
FX Funding for the study was provided in part by the study partners
(Australian Commonwealth Scientific Industrial and Research Organization
[CSIRO], Edith Cowan University [ECU], Mental Health Research Institute
[MHRI], Alzheimer's Australia [AA], National Ageing Research Institute
[NARI], Austin Health, CogState Ltd., Hollywood Private Hospital, Sir
Charles Gardner Hospital). The study also received support from the
National Health and Medical Research Council (NHMRC) and the Dementia
Collaborative Research Centres program (DCRC2), as well as ongoing
funding from the Science and Industry Endowment Fund (SIEF). The authors
also acknowledge the financial support of the Cooperative Research
Centre (CRC) for Mental Health, from the Australian Government.
NR 52
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PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0885-6230
EI 1099-1166
J9 INT J GERIATR PSYCH
JI Int. J. Geriatr. Psychiatr.
PD APR
PY 2017
VL 32
IS 4
BP 455
EP 463
DI 10.1002/gps.4489
PG 9
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA ES1PV
UT WOS:000399300400011
PM 27114112
ER
PT J
AU Horan, WP
Johnson, MW
Green, MF
AF Horan, William P.
Johnson, Matthew W.
Green, Michael F.
TI Altered Experiential, But Not Hypothetical, Delay Discounting in
Schizophrenia
SO JOURNAL OF ABNORMAL PSYCHOLOGY
LA English
DT Article
DE cost-benefit decision making; prospection; psychosis; reward valuation;
reliability
ID TEST-RETEST RELIABILITY; CIGARETTE-SMOKING STATUS; DECISION-MAKING;
INTERTEMPORAL CHOICE; QUALITY-ASSURANCE; REWARDS; TASK; IMPULSIVITY;
REAL; DEFICITS
AB Delay discounting (DD) is a future-oriented decision-making process that refers to whether one is willing to forego a smaller, sooner reward for the sake of a larger, later reward. It can be assessed using hypothetical tasks, which involve choices between hypothetical rewards of varying amounts over delay periods of days to years, or experiential tasks, which involve receiving actual rewards in real time over delay periods of seconds to minutes. Initial studies in schizophrenia have only used hypothetical tasks and have been mixed in finding either elevated or normal levels of DD. One hundred thirty-one outpatients with schizophrenia and 70 healthy controls completed hypothetical and experiential DD tasks involving monetary rewards, and the schizophrenia group was retested after 4 weeks. Although both groups showed qualitatively similar hyperbolic discounting functions on both tasks, they showed a quantitative DD difference. The schizophrenia showed higher DD than controls on the experiential task but normal DD on the hypothetical task. This pattern was not attributable to a range of potential confounds, including smoking status, substance use disorder status, or neurocognition. It was also not attributable to differences in the test-retest reliability, which was good for both tasks. The schizophrenia group's robust pattern of altered experiential but normal hypothetical task performance points to key factors that may contribute to impaired DD in this disorder. These may include increased valuation of small (but not large) monetary rewards, or a hypersensitivity to costs associated with waiting inactively for those rewards.
C1 [Horan, William P.; Green, Michael F.] VISN 22 Mental Illness Res Educ & Clin Ctr, Dept Vet Affairs, Los Angeles, CA USA.
[Horan, William P.; Green, Michael F.] Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA.
[Johnson, Matthew W.] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Baltimore, MD 21218 USA.
RP Horan, WP (reprint author), Vet Affairs Greater Los Angeles Healthcare Syst, MIRECC 210A,Bldg 210,11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM horan@ucla.edu
FU VA Merit Award; [R01DA035277]
FX This project was funded by a VA Merit Award (to William P. Horan).
Support of Matthew W. Johnson's time was provided by Grants R01DA035277
and R01DA035277.
NR 73
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PU AMER PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST NE, WASHINGTON, DC 20002-4242 USA
SN 0021-843X
EI 1939-1846
J9 J ABNORM PSYCHOL
JI J. Abnorm. Psychol.
PD APR
PY 2017
VL 126
IS 3
BP 301
EP 311
DI 10.1037/abn0000249
PG 11
WC Psychology, Clinical; Psychology, Multidisciplinary
SC Psychology
GA ER4AD
UT WOS:000398740500004
PM 28165261
ER
PT J
AU Walker, RJ
Neelon, B
Egede, LE
AF Walker, Rebekah J.
Neelon, Brian
Egede, Leonard E.
TI Advancing the Understanding of Social Determinants of Health Through
Geospatial Analysis
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Editorial Material
ID EMERGENCY-DEPARTMENT EXPENDITURES; MODEL
C1 [Walker, Rebekah J.; Neelon, Brian; Egede, Leonard E.] Ralph H Johnson Vet Affairs Med Ctr, HEROIC, Charleston, SC USA.
[Walker, Rebekah J.; Egede, Leonard E.] Med Univ South Carolina, Ctr Hlth Dispar Res, 135 Rutledge Ave,Room 280G, Charleston, SC 29425 USA.
[Walker, Rebekah J.; Egede, Leonard E.] Med Univ South Carolina, Div Gen Internal Med & Geriatr, Dept Med, Charleston, SC USA.
[Neelon, Brian] Med Univ South Carolina, Dept Publ Hlth Sci, Charleston, SC USA.
RP Egede, LE (reprint author), Med Univ South Carolina, Ctr Hlth Dispar Res, 135 Rutledge Ave,Room 280G, Charleston, SC 29425 USA.
EM egedel@musc.edu
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U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD APR
PY 2017
VL 32
IS 4
BP 371
EP 372
DI 10.1007/s11606-016-3942-5
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA ER5NH
UT WOS:000398848100002
PM 27957663
ER
PT J
AU Nelson, K
Schwartz, G
Hernandez, S
Simonetti, J
Curtis, I
Fihn, SD
AF Nelson, Karin
Schwartz, Greg
Hernandez, Susan
Simonetti, Joseph
Curtis, Idamay
Fihn, Stephan D.
TI The Association Between Neighborhood Environment and Mortality: Results
from a National Study of Veterans
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Article
DE risk adjustment; veteran; socioeconomic factors; public health; clinical
epidemiology
ID SOCIOECONOMIC-STATUS; UNITED-STATES; POPULATION HEALTH; OLDER-ADULTS; US
ADULTS; MULTILEVEL; DETERMINANTS; MODELS; SAMPLE; CARE
AB As the largest integrated US health system, the Veterans Health Administration (VHA) provides unique national data to expand knowledge about the association between neighborhood socioeconomic status (NSES) and health. Although living in areas of lower NSES has been associated with higher mortality, previous studies have been limited to higher-income, less diverse populations than those who receive VHA care.
To describe the association between NSES and all-cause mortality in a national sample of veterans enrolled in VHA primary care.
One-year observational cohort of veterans who were alive on December 31, 2011. Data on individual veterans (vital status, and clinical and demographic characteristics) were abstracted from the VHA Corporate Data Warehouse. Census tract information was obtained from the US Census Bureau American Community Survey. Logistic regression was used to model the association between NSES deciles and all-cause mortality during 2012, adjusting for individual-level income and demographics, and accounting for spatial autocorrelation.
Veterans who had vital status, demographic, and NSES data, and who were both assigned a primary care physician and alive on December 31, 2011 (n = 4,814,631).
Census tracts were used as proxies for neighborhoods. A summary score based on census tract data characterized NSES. Veteran addresses were geocoded and linked to census tract NSES scores. Census tracts were divided into NSES deciles.
In adjusted analysis, veterans living in the lowest-decile NSES tract were 10 % (OR 1.10, 95 % CI 1.07, 1.14) more likely to die than those living in the highest-decile NSES tract.
Lower neighborhood SES is associated with all-cause mortality among veterans after adjusting for individual-level socioeconomic characteristics. NSES should be considered in risk adjustment models for veteran mortality, and may need to be incorporated into strategies aimed at improving veteran health.
C1 [Nelson, Karin; Simonetti, Joseph] VA Puget Sound Healthcare Syst, Hlth Serv Res & Dev Seattle Denver COIN, Seattle, WA 98108 USA.
[Nelson, Karin; Fihn, Stephan D.] VA Puget Sound Healthcare Syst, Gen Internal Med Serv, Seattle, WA USA.
[Nelson, Karin; Simonetti, Joseph; Fihn, Stephan D.] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA.
[Nelson, Karin; Hernandez, Susan; Fihn, Stephan D.] Univ Washington, Sch Publ Hlth, Dept Hlth Serv, Seattle, WA 98195 USA.
[Schwartz, Greg; Curtis, Idamay; Fihn, Stephan D.] VHA Off Analyt & Business Intelligence, Seattle, WA USA.
RP Nelson, K (reprint author), VA Puget Sound Healthcare Syst, Hlth Serv Res & Dev Seattle Denver COIN, Seattle, WA 98108 USA.
EM Karin.Nelson@va.gov
FU US Department of Veterans Affairs, VHA Office of Analytics and Business
Intelligence
FX This material is based upon work supported by the US Department of
Veterans Affairs, VHA Office of Analytics and Business Intelligence.
This work was presented at the Society for General Internal Medicine
National Meeting (May, 2015) and at Academy Health (June, 2015). The
views expressed in this article are those of the authors and do not
necessarily represent the views of the Department of Veterans Affairs.
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PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD APR
PY 2017
VL 32
IS 4
BP 416
EP 422
DI 10.1007/s11606-016-3905-x
PG 7
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA ER5NH
UT WOS:000398848100013
PM 27815763
ER
PT J
AU Haas, JS
Barlow, WE
Schapira, MM
MacLean, CD
Klabunde, CN
Sprague, BL
Beaber, EF
Chen, JS
Bitton, A
Onega, T
Harris, K
Tosteson, ANA
AF Haas, Jennifer S.
Barlow, William E.
Schapira, Marilyn M.
MacLean, Charles D.
Klabunde, Carrie N.
Sprague, Brian L.
Beaber, Elisabeth F.
Chen, Jane S.
Bitton, Asaf
Onega, Tracy
Harris, Kimberly
Tosteson, Anna N. A.
CA PROSPR Population-Based Res
TI Primary Care Providers' Beliefs and Recommendations and Use of Screening
Mammography by their Patients
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Article
DE mammography; variation in care; provider beliefs
ID SERVICES TASK-FORCE; BREAST-CANCER; PREVENTIVE CARE; WOMEN; ATTITUDES;
GUIDELINES; UPDATE; TRENDS; OLDER
AB Revised breast cancer screening guidelines have fueled debate about the effectiveness and frequency of screening mammography, encouraging discussion between women and their providers.
To examine whether primary care providers' (PCPs') beliefs about the effectiveness and frequency of screening mammography are associated with utilization by their patients.
Cross-sectional survey data from PCPs (2014) from three primary care networks affiliated with the Population-based Research Optimizing Screening through Personalized Regimens (PROSPR) consortium, linked with data about their patients' mammography use (2011-2014).
PCPs (n = 209) and their female patients age 40-89 years without breast cancer (n = 30,233).
Outcomes included whether (1) women received a screening mammogram during a 2-year period; and (2) screened women had > 1 mammogram during that period, reflecting annual screening. Principal independent variables were PCP beliefs about the effectiveness of mammography and their recommendations for screening frequency.
Overall 65.2% of women received > 1 screening mammogram. For women 40-48 years, mammography use was modestly lower for those cared for by PCPs who believed that screening was ineffective compared with those who believed it was somewhat or very effective (59.1%, 62.3%, and 64.7%; p = 0.019 after controlling for patient characteristics). Of women with PCPs who reported they did not recommend screening before age 50, 48.1% were nonetheless screened. For women age 49-74 years, the vast majority were cared for by providers who believed that screening was effective. Provider recommendations were not associated with screening frequency. For women >= 75 years, those cared for by providers who were uncertain about effectiveness had higher screening use (50.7%) than those cared for by providers who believed it was somewhat effective (42.8%). Patients of providers who did not recommend screening were less likely to be screened than were those whose providers recommended annual screening, yet 37.1% of patients whose providers recommended against screening still received screening.
PCP beliefs about mammography effectiveness and screening recommendations are only modestly associated with use, suggesting other likely influences on patient participation in mammography.
C1 [Haas, Jennifer S.; Chen, Jane S.; Bitton, Asaf; Harris, Kimberly] Brigham & Womens Hosp, Div Gen Med & Primary Care, 1620 Tremont St, Boston, MA 02120 USA.
[Haas, Jennifer S.; Bitton, Asaf] Harvard Med Sch, Boston, MA USA.
[Haas, Jennifer S.] Harvard TH Chan Sch Publ Hlth, Boston, MA USA.
[Barlow, William E.; Beaber, Elisabeth F.] Fred Hutchinson Canc Res Ctr, 1124 Columbia St, Seattle, WA 98104 USA.
[Schapira, Marilyn M.] Univ Penn, Philadelphia, PA 19104 USA.
[Schapira, Marilyn M.] Philadelphia VA Med Ctr, Philadelphia, PA USA.
[Klabunde, Carrie N.] NIH, Off Dis Prevent, Off Director, Bldg 10, Bethesda, MD 20892 USA.
[MacLean, Charles D.; Sprague, Brian L.] Univ Vermont, Burlington, VT USA.
[Onega, Tracy; Tosteson, Anna N. A.] Geisel Sch Med Dartmouth, Lebanon, NH USA.
[Onega, Tracy; Tosteson, Anna N. A.] Norris Cotton Canc Ctr, Lebanon, NH USA.
RP Haas, JS (reprint author), Brigham & Womens Hosp, Div Gen Med & Primary Care, 1620 Tremont St, Boston, MA 02120 USA.
EM jhaas@partners.org
FU National Cancer Institute-funded consortium, Population-Based Research
Optimizing Screening through Personalized Regimens (PROSPR) [U54
CA163307, U54 CA163313, U54 CA163303, U01 CA163304]
FX This study was conducted as part of the National Cancer Institute-funded
consortium, Population-Based Research Optimizing Screening through
Personalized Regimens (PROSPR) (Grant numbers U54 CA163307, U54
CA163313, U54 CA163303, U01 CA163304).
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PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD APR
PY 2017
VL 32
IS 4
BP 449
EP 457
DI 10.1007/s11606-016-3973-y
PG 9
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA ER5NH
UT WOS:000398848100017
PM 28070772
ER
PT J
AU Anderson, E
Stevenson, K
Johnson, D
Ebert, J
Blair, T
AF Anderson, E.
Stevenson, K.
Johnson, D.
Ebert, J.
Blair, T.
TI Controlled Substance Advisory: A review of patient outcomes in the year
following a prohibition of opioids for chronic conditions due to safety
concerns
SO JOURNAL OF PAIN
LA English
DT Meeting Abstract
C1 [Anderson, E.; Stevenson, K.; Johnson, D.; Ebert, J.; Blair, T.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
NR 0
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U1 0
U2 0
PU CHURCHILL LIVINGSTONE
PI EDINBURGH
PA JOURNAL PRODUCTION DEPT, ROBERT STEVENSON HOUSE, 1-3 BAXTERS PLACE,
LEITH WALK, EDINBURGH EH1 3AF, MIDLOTHIAN, SCOTLAND
SN 1526-5900
J9 J PAIN
JI J. Pain
PD APR
PY 2017
VL 18
IS 4
SU 1
MA 235
BP S34
EP S34
PG 1
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA ER4FV
UT WOS:000398755400140
ER
PT J
AU Domanski, A
Bair, M
Balk, R
Brandt, C
Brody, A
Dismore, R
Gaetano, V
Garrido, M
Gittleman, D
Kerns, R
Krebs, E
Linden, E
Morrison, R
Natividad, D
Penrod, J
Rinaldi, A
Stefanis, L
Sun, D
Hwang, U
AF Domanski, A.
Bair, M.
Balk, R.
Brandt, C.
Brody, A.
Dismore, R.
Gaetano, V.
Garrido, M.
Gittleman, D.
Kerns, R.
Krebs, E.
Linden, E.
Morrison, R.
Natividad, D.
Penrod, J.
Rinaldi, A.
Stefanis, L.
Sun, D.
Hwang, U.
TI Evaluating the agreement between self-reported and documented analgesic
use in older veterans with osteoarthritis
SO JOURNAL OF PAIN
LA English
DT Meeting Abstract
C1 [Domanski, A.; Bair, M.; Balk, R.; Brandt, C.; Brody, A.; Dismore, R.; Gaetano, V.; Garrido, M.; Gittleman, D.; Kerns, R.; Krebs, E.; Linden, E.; Morrison, R.; Natividad, D.; Penrod, J.; Rinaldi, A.; Stefanis, L.; Sun, D.; Hwang, U.] James J Peters VAMC, Geriatr Res Educ & Clin Ctr, Bronx, NY USA.
FU VA HSRD; Icahn School of Medicine's Summer Student Investigator Program
Award
FX This project was supported by VA HSR&D as well as the Icahn School of
Medicine's Summer Student Investigator Program Award.
NR 0
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U2 0
PU CHURCHILL LIVINGSTONE
PI EDINBURGH
PA JOURNAL PRODUCTION DEPT, ROBERT STEVENSON HOUSE, 1-3 BAXTERS PLACE,
LEITH WALK, EDINBURGH EH1 3AF, MIDLOTHIAN, SCOTLAND
SN 1526-5900
J9 J PAIN
JI J. Pain
PD APR
PY 2017
VL 18
IS 4
SU 1
MA 233
BP S34
EP S34
PG 1
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA ER4FV
UT WOS:000398755400138
ER
PT J
AU Hausmann, L
Hanlon, J
Sileanu, F
Zhao, X
Thorpe, C
Thorpe, J
Cashy, J
Mor, M
Hale, J
Radomski, T
Fine, M
Good, C
Gellad, W
AF Hausmann, L.
Hanlon, J.
Sileanu, F.
Zhao, X.
Thorpe, C.
Thorpe, J.
Cashy, J.
Mor, M.
Hale, J.
Radomski, T.
Fine, M.
Good, C.
Gellad, W.
TI Use of potentially unsafe high opioid dosage varies by demographic
characteristics among Veterans dually-enrolled in Veterans Affairs and
Medicare
SO JOURNAL OF PAIN
LA English
DT Meeting Abstract
C1 [Hausmann, L.; Hanlon, J.; Sileanu, F.; Zhao, X.; Thorpe, C.; Thorpe, J.; Cashy, J.; Mor, M.; Hale, J.; Radomski, T.; Fine, M.; Good, C.; Gellad, W.] Vet Affairs Pittsburgh Healthcare Syst, CHERP, Pittsburgh, PA USA.
FU VA HSRD IIR [14-297]
FX Funded by VA HSR&D IIR 14-297.
NR 0
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U1 0
U2 0
PU CHURCHILL LIVINGSTONE
PI EDINBURGH
PA JOURNAL PRODUCTION DEPT, ROBERT STEVENSON HOUSE, 1-3 BAXTERS PLACE,
LEITH WALK, EDINBURGH EH1 3AF, MIDLOTHIAN, SCOTLAND
SN 1526-5900
J9 J PAIN
JI J. Pain
PD APR
PY 2017
VL 18
IS 4
SU 1
MA 229
BP S33
EP S33
PG 1
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA ER4FV
UT WOS:000398755400134
ER
PT J
AU Kaji, I
Akiba, Y
Kato, I
Maruta, K
Kuwahara, A
Kaunitz, JD
AF Kaji, Izumi
Akiba, Yasutada
Kato, Ikuo
Maruta, Koji
Kuwahara, Atsukazu
Kaunitz, Jonathan D.
TI Xenin Augments Duodenal Anion Secretion via Activation of Afferent
Neural Pathways
SO JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
LA English
DT Article
ID RAT GASTROINTESTINAL-TRACT; BICARBONATE SECRETION; NEUROTENSIN RECEPTOR;
5-HT3 RECEPTORS; NONPEPTIDE ANTAGONIST; ENTEROENDOCRINE CELLS;
DEFENSE-MECHANISMS; CL-SECRETION; DISTAL COLON; IN-VITRO
AB Xenin-25, a neurotensin (NT)-related anorexigenic gut hormone generated mostly in the duodenal mucosa, is believed to increase the rate of duodenal ion secretion, because xenin-induced diarrhea is not present after Roux-en-Y gastric bypass surgery. Because the local effects of xenin on duodenal ion secretion have remained uninvestigated, we thus examined the neural pathways underlying xenin-induced duodenal anion secretion. Intravenous infusion of xenin-8, a bioactive C-terminal fragment of xenin-25, dose dependently increased the rate of duodenal HCO (3) (-) secretion in perfused duodenal loops of anesthetized rats. Xenin was immunolocalized to a subset of enteroendocrine cells in the rat duodenum. The mRNA of the xenin/NT receptor 1 (NTS1) was predominantly expressed in the enteric plexus, nodose and dorsal root ganglia, and in the lamina propria rather than in the epithelium. The serosal application of xenin-8 or xenin-25 rapidly and transiently increased short-circuit current in Ussing-chambered mucosa-submucosa preparations in a concentration-dependent manner in the duodenum and jejunum, but less so in the ileum and colon. The selective antagonist for NTS1, substance P (SP) receptor (NK1), or 5-hydroxytryptamine (5-HT) (3), but not NTS2, inhibited the responses to xenin. Xenin-evoked Cl-secretion was reduced by tetrodotoxin (TTX) or capsaicin-pretreatment, and abolished by the inhibitor of TTX-resistant sodiumchannel Nav1.8 in combination with TTX, suggesting that peripheral xenin augments duodenal HCO3- and Cl- secretion through NTS1 activation on intrinsic and extrinsic afferent nerves, followed by release of SP and 5-HT. Afferent nerve activation by postprandial, peripherally released xeninmay account for its secretory effects in the duodenum.
C1 [Kaji, Izumi; Akiba, Yasutada; Kaunitz, Jonathan D.] Greater Los Angeles Vet Affairs Healthcare Syst, Los Angeles, CA USA.
[Kaji, Izumi; Akiba, Yasutada; Maruta, Koji; Kaunitz, Jonathan D.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
[Kaunitz, Jonathan D.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA.
[Kato, Ikuo] Kobe Pharmaceut Univ, Dept Med Biochem, Kobe, Hyogo, Japan.
[Kuwahara, Atsukazu] Univ Shizuoka, Grad Sch Integrated Pharmaceut & Nutr Sci, Shizuoka, Japan.
RP Kaunitz, JD (reprint author), Greater LA VAHS, Bldg 114,Rm 217,11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM jake@ucla.edu
FU VA Merit Review; National Institutes of Health National Institute of
Diabetes and Digestive and Kidney Diseases [R01-DK54221]; American
Gastroenterology Association-Rome Foundation Functional Gastroenterology
and Motility Disorders Pilot Research Award
FX This study was supported by VA Merit Review (J.D.K.); the National
Institutes of Health National Institute of Diabetes and Digestive and
Kidney Diseases [Grant R01-DK54221] (J.D.K.); and American
Gastroenterology Association-Rome Foundation Functional Gastroenterology
and Motility Disorders Pilot Research Award (I.K.).
NR 54
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PU AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3995 USA
SN 0022-3565
EI 1521-0103
J9 J PHARMACOL EXP THER
JI J. Pharmacol. Exp. Ther.
PD APR 1
PY 2017
VL 361
IS 1
BP 151
EP 161
DI 10.1124/jpet.116.238485
PG 11
WC Pharmacology & Pharmacy
SC Pharmacology & Pharmacy
GA ER5EF
UT WOS:000398823700016
PM 28115552
ER
PT J
AU Gannon, BM
Galindo, KI
Rice, KC
Collins, GT
AF Gannon, Brenda M.
Galindo, Kayla I.
Rice, Kenner C.
Collins, Gregory T.
TI Individual Differences in the Relative Reinforcing Effects of
3,4-Methylenedioxypyrovalerone under Fixed and Progressive Ratio
Schedules of Reinforcement in Rats
SO JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS
LA English
DT Article
ID SALT CONSTITUENT 3,4-METHYLENEDIOXYPYROVALERONE; MICE DRUG
DISCRIMINATION; BATH SALTS; LOCOMOTOR-ACTIVITY; SYNTHETIC CATHINONES;
WHEEL ACTIVITY; UNITED-STATES; LEGAL HIGHS; MDPV; COCAINE
AB The recreational use of designer drugs, including synthetic cathinones (bath salts), is associated with high levels of abuse and toxicity, and represents a growing threat to public health. 3,4-Methylenedioxypyrovalerone (MDPV) is a cocaine-like monoamine uptake inhibitor, and one of the most widely available and abused synthetic cathinones. The present study used male Sprague-Dawley rats to directly compare: (1) the acquisition of responding for MDPV and cocaine under a fixed ratio (FR) 1 schedule of reinforcement; (2) full dose-response curves for MDPV and cocaine under a FR5 schedule; and (3) progressive ratio (PR) schedules of reinforcement. Selfadministration of MDPV and cocaine was acquired at comparable rates, and by a similar percentage of rats. Compared with cocaine, MDPV was similar to 10-fold more potent and similar to 3-fold more effective at maintaining responding (PR; final ratio completed). Unlike cocaine, for which little variability was observed among rats, the FR5 dose-response curve for MDPV was shifted similar to 3-fold upward for a subset of rats (high-responders) relative to other rats with identical histories (low-responders). Compared with low-responding rats, high responders also self-administered more cocaine under the FR5 schedule, and earned significantly more MDPV, cocaine, and methamphetamine under a PR schedule of reinforcement. In addition to functioning as a significantly more effective reinforcer than either cocaine or methamphetamine, MDPV also appears to be unique in its capacity to establish an enduring phenotype in rats, characterized by unusually high levels of drug intake. Although the factors underlying this high-responder phenotype are unclear, they might be related to individual differences in human drug-taking behavior.
C1 [Gannon, Brenda M.; Galindo, Kayla I.; Collins, Gregory T.] Univ Texas Hlth Sci Ctr San Antonio, Dept Pharmacol, 7703 Floyd Curl Dr,MC 7764, San Antonio, TX 78229 USA.
[Collins, Gregory T.] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Rice, Kenner C.] NIDA, Chem Biol Res Branch, NIH, Bethesda, MD 20892 USA.
[Rice, Kenner C.] NIAAA, NIH, Bethesda, MD USA.
RP Collins, GT (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Pharmacol, 7703 Floyd Curl Dr,MC 7764, San Antonio, TX 78229 USA.
EM CollinsG@uthscsa.edu
FU National Institutes of Health National Institute on Drug Abuse
[R01DA039146, T32DA031115]; Intramural Research Programs of the National
Institutes of Health National Institute on Drug Abuse; National
Institutes of Health National Institute of Alcohol Abuse and Alcoholism
FX This research was supported by the National Institutes of Health
National Institute on Drug Abuse [Grants R01DA039146 and T32DA031115].
The work of the Drug Design and Synthesis Section was supported by the
Intramural Research Programs of the National Institutes of Health
National Institute on Drug Abuse and the National Institutes of Health
National Institute of Alcohol Abuse and Alcoholism.
NR 31
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PU AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3995 USA
SN 0022-3565
EI 1521-0103
J9 J PHARMACOL EXP THER
JI J. Pharmacol. Exp. Ther.
PD APR 1
PY 2017
VL 361
IS 1
BP 181
EP 189
DI 10.1124/jpet.116.239376
PG 9
WC Pharmacology & Pharmacy
SC Pharmacology & Pharmacy
GA ER5EF
UT WOS:000398823700019
PM 28179474
ER
PT J
AU Strand, V
Singh, JA
AF Strand, Vibeke
Singh, Jasvinder A.
TI Evaluation and Management of the Patient With Suspected Inflammatory
Spine Disease
SO MAYO CLINIC PROCEEDINGS
LA English
DT Article
ID NONRADIOGRAPHIC AXIAL SPONDYLOARTHRITIS; CHRONIC BACK-PAIN;
ANKYLOSING-SPONDYLITIS; PRIMARY-CARE; REFERRAL RECOMMENDATIONS;
DIAGNOSTIC-CRITERIA; PREVALENCE; UVEITIS; DELAY; CLASSIFICATION
AB Axial spondyloarthritis (AxSpA) is a chronic inflammatory rheumatic disease characterized by inflammatory back pain (IBP) that manifests in childhood, late adolescence, or early adulthood. Ankylosing spondylitis (AS) and nonradiographic AxSpA represent 2 ends of the AxSpA spectrum. Diagnosis can be challenging because patients develop IBP that may not be associated with radiographic changes in the sacroiliac joints. Patients early in the course of disease are estimated to have at least the same level of disease activity and pain as patients with established disease; thus, they could benefit substantially from earlier diagnosis. Although the recent use of magnetic resonance imaging and its inclusion in diagnostic criteria has enhanced the identification of early AxSpA, improvement in early diagnosis has not been consistently reported across all studies. Limited knowledge of the continuum of AxSpA disease manifestations and lack of recognition of IBP in primary practice may contribute to this. Implementing a referral strategy that identifies patients with IBP for additional testing and assessment may lead to better recognition of early signs and symptoms of AxSpA, thereby offering the potential for improved patient outcomes. This review presents an overview of the epidemiology, clinical characteristics, and burdens of AxSpA, followed by a case presentation outlining approaches to the evaluation and management of a patient with suspected inflammatory spine disease. (C) 2016 Mayo Foundation for Medical Education and Research. Published by Elsevier Inc.
C1 [Strand, Vibeke] Stanford Univ, Sch Med, Div Immunol Rheumatol, Palo Alto, CA 94304 USA.
[Singh, Jasvinder A.] Univ Alabama Birmingham, Sch Med, Div Clin Immunol & Rheumatol, Birmingham, AL USA.
[Singh, Jasvinder A.] Birmingham Vet Affairs Med Ctr, Med Serv, Birmingham, AL USA.
[Singh, Jasvinder A.] Mayo Clin, Coll Med, Dept Orthoped Surg, Rochester, MN USA.
RP Strand, V (reprint author), 306 Ramona Rd, Portola Valley, CA 94028 USA.
EM vstrand@stanford.edu
FU Novartis Pharmaceuticals Corporation
FX Technical assistance with editing, figure preparation, and styling of
the manuscript for submission was provided by Oxford PharmaGenesis Inc
and was funded by Novartis Pharmaceuticals Corporation. The authors are
fully responsible for all content and editorial decisions and received
no financial support or other form of compensation related to the
development of this manuscript.
NR 59
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PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0025-6196
EI 1942-5546
J9 MAYO CLIN PROC
JI Mayo Clin. Proc.
PD APR
PY 2017
VL 92
IS 4
BP 555
EP 564
DI 10.1016/j.mayocp.2016.12.008
PG 10
WC Medicine, General & Internal
SC General & Internal Medicine
GA ER6WF
UT WOS:000398949300012
PM 28233529
ER
PT J
AU Mayl, P
Morrison, RS
Murtagh, FEM
AF Mayl, Peter
Morrison, R. Sean
Murtagh, Fliss E. M.
TI Current state of the economics of palliative and end-of-life care: A
clinical view
SO PALLIATIVE MEDICINE
LA English
DT Editorial Material
ID CANCER
C1 [Mayl, Peter] Trinity Coll Dublin, Ctr Hlth Policy & Management, 3-4 Foster Pl, Dublin 2, Ireland.
[Murtagh, Fliss E. M.] Kings Coll London, Cicely Saunders Inst, Dept Palliat Care Policy & Rehabil, London, England.
[Morrison, R. Sean] Icahn Sch Med Mt Sinai, Brookdale Dept Geriatr & Palliat Med, New York, NY 10029 USA.
[Morrison, R. Sean] James J Peters VA Med Ctr, Dept Geriatr & Palliat Med, Bronx, NY USA.
RP Mayl, P (reprint author), Trinity Coll Dublin, Ctr Hlth Policy & Management, 3-4 Foster Pl, Dublin 2, Ireland.
EM peter.may@tcd.ie
NR 13
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U1 0
U2 0
PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 0269-2163
EI 1477-030X
J9 PALLIATIVE MED
JI Palliat. Med.
PD APR
PY 2017
VL 31
IS 4
SI SI
BP 293
EP 295
DI 10.1177/0269216317695680
PG 3
WC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Medicine, General & Internal
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; General & Internal Medicine
GA ER5UO
UT WOS:000398869300002
ER
PT J
AU May, P
Garrido, MM
Cassel, JB
Kelley, AS
Meier, DE
Normand, C
Smith, TJ
Morrison, RS
AF May, Peter
Garrido, Melissa M.
Cassel, J. Brian
Kelley, Amy S.
Meier, Diane E.
Normand, Charles
Smith, Thomas J.
Morrison, R. Sean
TI Cost analysis of a prospective multi-site cohort study of palliative
care consultation teams for adults with advanced cancer: Where do
cost-savings come from?
SO PALLIATIVE MEDICINE
LA English
DT Article
DE Palliative care; economics; cancer; hospital costs; length of stay
ID LENGTH-OF-STAY; ECONOMIC-IMPACT; GUIDANCE; LARGER
AB Background: Studies report cost-savings from hospital-based palliative care consultation teams compared to usual care only, but drivers of observed differences are unclear.
Aim: To analyse cost-differences associated with palliative care consultation teams using two research questions: (Q1) What is the association between early palliative care consultation team intervention, and intensity of services and length of stay, compared to usual care only? (Q2) What is the association between early palliative care consultation team intervention and day-to-day hospital costs, compared to a later intervention?
Design: Prospective multi-site cohort study (2007-2011). Patients who received a consultation were placed in the intervention group, those who did not in the comparison group. Intervention group was stratified by timing, and groups were matched using propensity scores.
Setting/participants: Adults admitted to three US hospitals with advanced cancer. Principle analytic sample contains 863 patients (n(UC) = 637; n(PC EARLY) = 177; n(PC LATE)=49) discharged alive.
Results: Cost-savings from early palliative care accrue due to both reduced length of stay and reduced intensity of treatment, with an estimated 63% of savings associated with shorter length of stay. A reduction in day-to-day costs is observable in the days immediately following initial consult but does not persist indefinitely. A comparison of early and late palliative care consultation team cost-effects shows negligible difference once the intervention is administered.
Conclusion: Reduced length of stay is the biggest driver of cost-saving from early consultation for patients with advanced cancer. Patient- and family-centred discussions on goals of care and transition planning initiated by palliative care consultation teams may be at least as important in driving cost-savings as the reduction of unnecessary tests and pharmaceuticals identified by previous studies.
C1 [May, Peter; Normand, Charles] Trinity Coll Dublin, Ctr Hlth Policy & Management, 3-4 Foster Pl, Dublin 2, Ireland.
[Garrido, Melissa M.; Morrison, R. Sean] James J Peters VA Med Ctr, Dept Geriatr & Palliat Med, Bronx, NY USA.
[Garrido, Melissa M.; Kelley, Amy S.; Meier, Diane E.; Morrison, R. Sean] Icahn Sch Med Mt Sinai, Brookdale Dept Geriatr & Palliat Med, New York, NY 10029 USA.
[Cassel, J. Brian] Virginia Commonwealth Univ, Massey Canc Ctr, Div Hematol Oncol & Palliat Care, Richmond, VA USA.
[Smith, Thomas J.] Johns Hopkins Med Inst, Palliat Med, Baltimore, MD 21205 USA.
RP May, P (reprint author), Trinity Coll Dublin, Ctr Hlth Policy & Management, 3-4 Foster Pl, Dublin 2, Ireland.
EM peter.may@tcd.ie
FU National Cancer Institute [R01 CA116227]; HRB/NCI Health Economics
Fellowship; Veterans Affairs HSRD [CDA 11-201/CDP 12-255]; National
Institute on Aging [1K23AG040774-01A1]; American Federation for Aging;
NCI [P 30 006973, 1-R01 CA177562-01A1, 1-R01 NR014050 01]; Harry J.
Duffey Family Endowment for Palliative Care; Midcareer Investigator
Award in Patient-Oriented Research [5K24AG022345]; NIA; Claude D. Pepper
Older Americans Independence Center at the Icahn School of Medicine at
Mount Sinai [5P30AG028741]; National Palliative Care Research Center
FX The author(s) disclosed receipt of the following financial support for
the research, authorship and/or publication of this article: This work
was supported by the National Cancer Institute (Grant/ Award Number: '#
R01 CA116227'). Dr May was supported by a HRB/NCI Health Economics
Fellowship during this work. Dr Garrido is supported by a Veterans
Affairs HSR&D career development award (CDA 11-201/CDP 12-255); the
views expressed in this article are those of the authors and do not
necessarily reflect the position or policy of the Department of VA or
the United States government. Dr Kelley's time was funded by the
National Institute on Aging (1K23AG040774-01A1) and the American
Federation for Aging. Dr Smith is funded by the NCI Core Grant P 30
006973, 1-R01 CA177562-01A1, 1-R01 NR014050 01, and the Harry J. Duffey
Family Endowment for Palliative Care. Dr Morrison was the recipient of a
Midcareer Investigator Award in Patient-Oriented Research (5K24AG022345)
during the course of this work. This work was supported by the NIA,
Claude D. Pepper Older Americans Independence Center at the Icahn School
of Medicine at Mount Sinai [5P30AG028741], and the National Palliative
Care Research Center.
NR 34
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PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 0269-2163
EI 1477-030X
J9 PALLIATIVE MED
JI Palliat. Med.
PD APR
PY 2017
VL 31
IS 4
SI SI
BP 378
EP 386
DI 10.1177/0269216317690098
PG 9
WC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Medicine, General & Internal
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; General & Internal Medicine
GA ER5UO
UT WOS:000398869300010
PM 28156192
ER
PT J
AU Hanson, ER
Finley, EP
Petershack, JA
AF Hanson, Elizabeth R.
Finley, Erin P.
Petershack, Jean A.
TI What Do Pediatric Residents Gain From an Experience in Juvenile Justice?
A Qualitative Analysis of Community-Based Learning
SO ACADEMIC PEDIATRICS
LA English
DT Article
DE advocacy training; community pediatrics; juvenile justice; qualitative
analysis; resident education
ID MEDICAL-EDUCATION; HIDDEN CURRICULUM; REFLECTIVE CAPACITY; CHILD
ADVOCACY; SERVICE; ROTATION; HEALTH; PROGRAM; PROFESSIONALISM;
COMPETENCE
AB BACKGROUND: Training in advocacy and community pediatrics often involves the use of community site visits. However, data on the specific knowledge, skills, and attitudes gained from these experiences are limited. In this study we used qualitative analysis of written narratives to explore the response of residents to a juvenile justice experience.
METHODS: Pediatric residents participated in a week-long experience in the juvenile probation department and completed a written narrative. Narratives were analyzed using grounded theory to explore the effects of this experience on residents' views of youth in the juvenile justice system.
RESULTS: Analysis of 29 narratives revealed 13 themes relating to 5 core concepts: social determinants of behavior, role of professionals and institutions, achieving future potential, resolving discrepancies, and distancing. A conceptual model was developed to explore the interactions of these concepts in the resident view of youth in the juvenile justice system. Of the themes only 3 (23%) were related to content explicitly covered in the assigned reading materials.
CONCLUSIONS: Several important concepts emerged as elements of this experience, many of which were not covered in the explicit curriculum. Variability in attitudinal response to the experience raised important questions about the influence of the ideological framework of the learner and the hidden curriculum on the learning that occurs in community settings. We propose a theoretical model that delineates the factors that influence learning in community settings to guide educators in planning these types of experiences.
C1 [Hanson, Elizabeth R.; Petershack, Jean A.] Univ Texas Hlth Sci Ctr San Antonio, Dept Pediat, 7703 Floyd Curl Dr,MSC 7808, San Antonio, TX 78229 USA.
[Finley, Erin P.] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA.
[Finley, Erin P.] Univ Texas Hlth Sci Ctr San Antonio, Dept Psychiat, San Antonio, TX 78229 USA.
[Finley, Erin P.] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
RP Hanson, ER (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Pediat, 7703 Floyd Curl Dr,MSC 7808, San Antonio, TX 78229 USA.
EM Hansone3@uthscsa.edu
NR 35
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U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1876-2859
EI 1876-2867
J9 ACAD PEDIATR
JI Acad. Pediatr.
PD APR
PY 2017
VL 17
IS 3
BP 296
EP 302
PG 7
WC Pediatrics
SC Pediatrics
GA ER2UF
UT WOS:000398648600013
PM 27988206
ER
PT J
AU Williams, NR
Bentzley, BS
Sahlem, GL
Pannu, J
Korte, JE
Revuelta, G
Short, EB
George, MS
AF Williams, N. R.
Bentzley, B. S.
Sahlem, G. L.
Pannu, J.
Korte, J. E.
Revuelta, G.
Short, E. B.
George, M. S.
TI Unilateral ultra-brief pulse electroconvulsive therapy for depression in
Parkinson's disease
SO ACTA NEUROLOGICA SCANDINAVICA
LA English
DT Article
DE depression; electroconvulsive therapy; Parkinson's disease; ultra-brief
pulse
ID RATING-SCALE; ELECTRODE PLACEMENT; RECEPTOR-BINDING; DISORDERS;
PSYCHOSIS; RECOMMENDATIONS; PERFORMANCE; CRITIQUE; NUCLEUS; ECT
AB Objectives: Electroconvulsive therapy (ECT) has demonstrated efficacy in treating core symptoms of Parkinson's disease (PD); however, widespread use of ECT in PD has been limited due to concern over cognitive burden. We investigated the use of a newer ECT technology known to have fewer cognitive side effects (right unilateral [RUL] ultra-brief pulse [UBP]) for the treatment of medically refractory psychiatric dysfunction in PD.
Materials and methods: This open-label pilot study included 6 patients who were assessed in the motoric, cognitive, and neuropsychiatric domains prior to and after RUL UBP ECT. Primary endpoints were changes in total score on the HAM-D-17 and GDS-30 rating scales.
Results: Patients were found to improve in motoric and psychiatric domains following RUL UBP ECT without cognitive side effects, both immediately following ECT and at 1-month follow- up.
Conclusions: This study demonstrates that RUL UBP ECT is safe, feasible, and potentially efficacious in treating multiple domains of PD, including motor and mood, without clear cognitive side effects.
C1 [Williams, N. R.; Bentzley, B. S.; Pannu, J.] Stanford Univ, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA.
[Revuelta, G.; George, M. S.] Med Univ South Carolina, Dept Neurol, Charleston, SC USA.
[Sahlem, G. L.; Short, E. B.; George, M. S.] Med Univ South Carolina, Dept Psychiat, Charleston, SC USA.
[Korte, J. E.] Med Univ South Carolina, Dept Publ Hlth Sci, Charleston, SC USA.
[George, M. S.] Ralph H Johnson VA Med Ctr, Charleston, SC USA.
RP Williams, NR (reprint author), Dept Psychiat & Behav Sci, Stanford, CA 94305 USA.
EM nolanw@stanford.edu
OI Williams, Nolan/0000-0003-4368-3203; Bentzley,
Brandon/0000-0001-6014-4514
FU NIH [F30 DA035065, T32 GM008716, R25 DA020537, 1K23NS091391-01A1,
UL1TR000062]
FX This work was supported by NIH grants F30 DA035065,T32 GM008716,R25
DA020537,1K23NS091391- -01A1, UL1TR000062.
NR 33
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U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0001-6314
EI 1600-0404
J9 ACTA NEUROL SCAND
JI Acta Neurol. Scand.
PD APR
PY 2017
VL 135
IS 4
BP 407
EP 411
DI 10.1111/ane.12614
PG 5
WC Clinical Neurology
SC Neurosciences & Neurology
GA EQ4HE
UT WOS:000398035900004
PM 27241213
ER
PT J
AU Wimberly, AS
Ivey, M
Rennert, L
McKay, JR
AF Wimberly, Alexandra S.
Ivey, Megan
Rennert, Lior
McKay, James R.
TI Effect of Continuing Care for Cocaine Dependence on HIV Sex-Risk
Behaviors
SO AIDS AND BEHAVIOR
LA English
DT Article
DE HIV; Sex-risk; Continuing care; Cocaine
ID SEXUALLY-TRANSMITTED-DISEASES; RANDOMIZED CONTROLLED-TRIAL; ADDICTION
SEVERITY INDEX; INJECTION-DRUG USERS; METAANALYTIC EVIDENCE; SMOKE
CRACK; REDUCTION; INTERVENTIONS; RELIABILITY; EFFICACY
AB Evaluate the effect of continuing care interventions for cocaine use with HIV risk-reduction components on HIV sex-risk. Explore whether cocaine use at treatment initiation interacts with the type of continuing care intervention to affect HIV sex-risk. Cocaine dependent participants (N = 321) were randomized to: (1) Treatment as usual (TAU): intensive outpatient treatment, (2) TAU and telephone monitoring and counseling (TMC), and (3) TAU and TMC plus incentives for participation in telephone contacts (TMC+). Participants in TMC and TMC+ received a brief HIV intervention, with booster sessions as needed. Generalized estimating equations analysis compared TAU, TMC and TMC+ at 6, 12, 18, 24 months post-baseline on the following outcomes: overall HIV sex-risk, number of sexual partners, condom usage, exchange of drugs for sex, exchange of sex for drugs, exchange of money for sex, exchange of sex for money, and crack house visits. Overall sex-risk decreased for all treatment conditions at follow-up, with no treatment main effects. For people with no cocaine use at baseline, TAU experienced greater sex-risk reductions than TMC (p < .01) and TMC+ (p < .001). The three treatment conditions are effective in reducing HIV sex-risk. TMC with HIV risk-reduction components is unnecessary for cocaine-dependent clients who stop using cocaine early in treatment.
C1 [Wimberly, Alexandra S.] Univ Penn, Sch Social Policy & Practice, Philadelphia, PA 19104 USA.
[Ivey, Megan; McKay, James R.] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Rennert, Lior] Univ Penn, Biomed Grad Studies, Philadelphia, PA 19104 USA.
[McKay, James R.] Philadelphia Vet Affairs Med Ctr, Dept Behav Hlth, Philadelphia, PA USA.
RP Wimberly, AS (reprint author), Univ Penn, Sch Social Policy & Practice, Philadelphia, PA 19104 USA.
EM schepa@sp2.upenn.edu
FU National Institute on Drug Abuse [F31 DA038429, R01 DA020623, K02
DA000361, K24 DA029062]
FX This study was funded by National Institute on Drug Abuse Grants F31
DA038429, R01 DA020623, K02 DA000361, and K24 DA029062. Additional
support was provided by the Center of Excellence in Substance Abuse
Treatment and Education of the Department of Veterans Affairs.
NR 33
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PU SPRINGER/PLENUM PUBLISHERS
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1090-7165
EI 1573-3254
J9 AIDS BEHAV
JI AIDS Behav.
PD APR
PY 2017
VL 21
IS 4
BP 1082
EP 1090
DI 10.1007/s10461-016-1434-6
PG 9
WC Public, Environmental & Occupational Health; Social Sciences, Biomedical
SC Public, Environmental & Occupational Health; Biomedical Social Sciences
GA EN6QM
UT WOS:000396128500014
PM 27224980
ER
PT J
AU Becker, WC
Gordon, K
Edelman, EJ
Kerns, RD
Crystal, S
Dziura, JD
Fiellin, LE
Gordon, AJ
Goulet, JL
Justice, AC
Fiellin, DA
AF Becker, William C.
Gordon, Kirsha
Edelman, E. Jennifer
Kerns, Robert D.
Crystal, Stephen
Dziura, James D.
Fiellin, Lynn E.
Gordon, Adam J.
Goulet, Joseph L.
Justice, Amy C.
Fiellin, David A.
TI Trends in Any and High-Dose Opioid Analgesic Receipt Among Aging
Patients With and Without HIV (vol 20, pg 679, 2016)
SO AIDS AND BEHAVIOR
LA English
DT Correction
C1 [Becker, William C.; Gordon, Kirsha; Justice, Amy C.] VA Connecticut Healthcare Syst, West Haven VA Med Ctr, Internal Med, Mail Stop 151B,950 Campbell Ave, West Haven, CT 06516 USA.
[Kerns, Robert D.; Goulet, Joseph L.] VA Connecticut Healthcare Syst, Psychol, West Haven, CT USA.
[Becker, William C.; Edelman, E. Jennifer; Dziura, James D.; Fiellin, Lynn E.; Justice, Amy C.; Fiellin, David A.] Yale Univ, Sch Med, Internal Med, New Haven, CT USA.
[Kerns, Robert D.; Goulet, Joseph L.] Yale Univ, Sch Med, Psychol, New Haven, CT USA.
[Crystal, Stephen] Rutgers State Univ, Ctr Hlth Serv Res, New Brunswick, NJ USA.
[Gordon, Adam J.] Univ Pittsburgh, Pittsburgh, PA USA.
[Gordon, Adam J.] VA Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA USA.
RP Becker, WC (reprint author), VA Connecticut Healthcare Syst, West Haven VA Med Ctr, Internal Med, Mail Stop 151B,950 Campbell Ave, West Haven, CT 06516 USA.; Becker, WC (reprint author), Yale Univ, Sch Med, Internal Med, New Haven, CT USA.
EM william.becker@yale.edu
NR 1
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER/PLENUM PUBLISHERS
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1090-7165
EI 1573-3254
J9 AIDS BEHAV
JI AIDS Behav.
PD APR
PY 2017
VL 21
IS 4
BP 1228
EP 1228
DI 10.1007/s10461-017-1725-6
PG 1
WC Public, Environmental & Occupational Health; Social Sciences, Biomedical
SC Public, Environmental & Occupational Health; Biomedical Social Sciences
GA EN6QM
UT WOS:000396128500026
PM 28188459
ER
PT J
AU Simpson, TL
Lehavot, K
Petrakis, IL
AF Simpson, Tracy L.
Lehavot, Keren
Petrakis, Ismene L.
TI No Wrong Doors: Findings from a Critical Review of Behavioral Randomized
Clinical Trials for Individuals with Co-Occurring Alcohol/Drug Problems
and Posttraumatic Stress Disorder
SO ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH
LA English
DT Review
DE Posttraumatic Stress Disorder; Substance Use Disorders; Behavioral
Intervention; Psychotherapy; Critical Review
ID SUBSTANCE USE DISORDERS; CONTINGENCY MANAGEMENT PROCEDURES; NATIONAL
EPIDEMIOLOGIC SURVEY; CHRONIC CARE MANAGEMENT; DEPENDENT PATIENTS;
EXPOSURE THERAPY; PTSD; TRAUMA; INTERVENTIONS; METAANALYSIS
AB Prior reviews of behavioral treatments for individuals with comorbid alcohol and drug use disorders (substance use disorder SUD) and posttraumatic stress disorder (PTSD) have not systematically considered whether comparison conditions are matched to target treatments on time and attention. A systematic literature search using PubMed MESH terms for alcohol and substance use disorders, PTSD, and treatment identified relevant behavioral randomized clinical trials (RCTs) that evaluated PTSD-oriented exposure-based treatments, addiction-focused treatments, and coping-based treatments that do not involve exposure to trauma memories. Information pertaining to within-subject changes over time and between-subject differences, quality of control condition, recruitment efficiency, and assessment and treatment retention was synthesized. Alcohol and drug outcomes were described separately when possible. Twenty-four behavioral RCTs were identified: 7 exposure based, 6 addiction focused, and 11 coping based. Seven studies included SUD intervention comparison conditions matched to the target intervention on time and attention. Most of the 24 studies found that participants in both the experimental and control conditions improved significantly over time on SUD and PTSD outcomes. No study found significant between-group differences in both SUD and PTSD outcomes favoring the experimental treatment. Despite greater treatment dropout, there was greater improvement in some PTSD outcomes for exposure-based interventions than the control conditions, including when the control conditions were matched for time and attention. Addiction-focused and coping-based interventions did not generally show an advantage over comparably robust controls, although some coping-based interventions yielded better drug use outcomes than control conditions. When available, interventions that integrate exposure-based PTSD treatment and behavioral SUD treatment are recommended as they are associated with better PTSD outcomes than SUD care matched for time and attention. However, the results of this critical review also suggest that people with SUD/PTSD can benefit from a variety of treatment options, including standard SUD care.
C1 [Simpson, Tracy L.] VA Puget Sound Hlth Care, CESATE, Seattle, WA USA.
[Simpson, Tracy L.; Lehavot, Keren] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Lehavot, Keren] VA Puget Sound Hlth Care, Ctr Innovat Vet Ctr & Value Driven Care, HSR&D, Seattle, WA USA.
[Lehavot, Keren] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA.
[Petrakis, Ismene L.] Mental Illness Res Educ & Clin Ctr MIRECC VA Conn, West Haven, CT USA.
[Petrakis, Ismene L.] Yale Univ, Dept Psychiat, New Haven, CT 06520 USA.
RP Petrakis, IL (reprint author), Yale Univ, West Haven VA Med Ctr, 116A,950 Campbell Ave 116-A, West Haven, CT 06516 USA.
EM Ismene.Petrakis@Yale.Edu
FU CSRD VA [IK2 CX000867]
NR 52
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0145-6008
EI 1530-0277
J9 ALCOHOL CLIN EXP RES
JI Alcoholism (NY)
PD APR
PY 2017
VL 41
IS 4
BP 681
EP 702
DI 10.1111/acer.13325
PG 22
WC Substance Abuse
SC Substance Abuse
GA ER2KF
UT WOS:000398622200002
PM 28055143
ER
PT J
AU George, JF
Lever, JM
Agarwal, A
AF George, James F.
Lever, Jeremie M.
Agarwal, Anupam
TI Mononuclear phagocyte subpopulations in the mouse kidney
SO AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY
LA English
DT Review
DE acute kidney injury; inflammation; ischemia-reperfusion; macrophages;
renal fibrosis
ID ISCHEMIA-REPERFUSION INJURY; RENAL ISCHEMIA/REPERFUSION INJURY; TUBULAR
EPITHELIAL-CELLS; REGULATORY T-CELLS; DENDRITIC CELLS; RESIDENT
MACROPHAGES; ALTERNATIVE ACTIVATION; ADRIAMYCIN NEPHROPATHY; TISSUE
MACROPHAGES; STEADY-STATE
AB Mononuclear phagocytes are the most common cells in the kidney associated with immunity and inflammation. Although the presence of these cells in the kidney has been known for decades, the study of mononuclear phagocytes in the context of kidney function and dysfunction is still at an early stage. The purpose of this review is to summarize the present knowledge regarding classification of these cells in the mouse kidney and to identify relevant questions that would further advance the field and potentially lead to new opportunities for treatment of acute kidney injury and other kidney diseases.
C1 [George, James F.] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA.
[Lever, Jeremie M.; Agarwal, Anupam] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA.
[George, James F.; Lever, Jeremie M.; Agarwal, Anupam] Univ Alabama Birmingham, Dept Nephrol, Birmingham, AL USA.
[George, James F.; Lever, Jeremie M.; Agarwal, Anupam] Univ Alabama Birmingham, Res & Training Ctr, Birmingham, AL USA.
[Agarwal, Anupam] US Dept Vet Affairs, Birmingham, AL USA.
RP Agarwal, A (reprint author), Univ Alabama Birmingham, Dept Med, Div Nephrol, Rm 647 THT,1720 2nd Ave South, Birmingham, AL 35294 USA.
EM agarwal@uab.edu
FU University of Alabama at Birmingham-University of California San Diego
O'Brien Center [P30 DK079337, R01 DK059600]; NIGMS MSTP [T32GM008361];
AHA [17PRE33370121, 16GRNT31180023]
FX The authors acknowledge grant support from the University of Alabama at
Birmingham-University of California San Diego O'Brien Center (P30
DK079337) and R01 DK059600 (to A. Agarwal and J. F. George), NIGMS MSTP
T32GM008361 to Dr. Robin Lorenz for J. M. Lever; AHA 17PRE33370121 to J.
M. Lever; and 16GRNT31180023 to J. F. George.
NR 63
TC 0
Z9 0
U1 1
U2 1
PU AMER PHYSIOLOGICAL SOC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 1931-857X
EI 1522-1466
J9 AM J PHYSIOL-RENAL
JI Am. J. Physiol.-Renal Physiol.
PD APR
PY 2017
VL 312
IS 4
BP F640
EP F646
DI 10.1152/ajprenal.00369.2016
PG 7
WC Physiology; Urology & Nephrology
SC Physiology; Urology & Nephrology
GA EQ2AS
UT WOS:000397871300010
PM 28100500
ER
PT J
AU Sunshine, JE
Dagal, A
Burns, SP
Bransford, RJ
Zhang, F
Newman, SF
Nair, BG
Sharar, SR
AF Sunshine, Jacob E.
Dagal, Armagan
Burns, Stephen P.
Bransford, Richard J.
Zhang, Fangyi
Newman, Shu-Fang
Nair, Bala G.
Sharar, Sam R.
TI Methylprednisolone Therapy in Acute Traumatic Spinal Cord Injury:
Analysis of a Regional Spinal Cord Model Systems Database
SO ANESTHESIA AND ANALGESIA
LA English
DT Article
ID CONTROLLED-TRIAL; STEROIDS; EPIDEMIOLOGY
AB BACKGROUND: The objective of this study was to assess the relationship between exposure to methylprednisolone (MO) and improvements in motor function among patients with acute traumatic spinal cord injury (TSCI). MP therapy for patients with TSCI is controversial because of the current conflicting evidence documenting its benefits and risks.
METHODS: We conducted a retrospective cohort study from September 2007 to November 2014 of 311 patients with acute TSCI who were enrolled into a model systems database of a regional, level I trauma center. We linked outcomes and covariate data from the model systems database with MP exposure data from the electronic medical record. The primary outcomes were rehabilitation discharge in American Spinal Injury Association (ASIA) motor scores (sum of 10 key muscles bilaterally as per International Standards for Neurological Classification of Spinal Cord Injury, range, 0-100) and Functional Independence Measure (FIM) motor scores (range, 13-91). Secondary outcomes measured infection risk and gastrointestinal (GI) complications among MP recipients. For the primary outcomes, multivariable linear regression was used.
RESULTS: There were 160 MP recipients and 151 nonrecipients. Adjusting for age, sex, weight, race, respective baseline motor score, surgical intervention, injury level, ASIA Impairment Scale (AIS) grade, education, and insurance status, there was no association with improvement in discharge ASIA motor function or FIM motor score among MP recipients: -0.34 (95% CI, -2.8, 2.1) and 0.75 (95% CI, -2.8, 4.3), respectively. Adjusting for age, sex, race, weight, injury level, and receipt of surgery, no association with increased risk of infection or GI complications was observed.
CONCLUSIONS: This retrospective cohort study involving patients with acute TSCI observed no short-term improvements in motor function among MP recipients compared with nonrecipients. Our findings support current recommendations that MP use in this population should be limited.
C1 [Sunshine, Jacob E.; Dagal, Armagan; Newman, Shu-Fang; Nair, Bala G.; Sharar, Sam R.] Univ Washington, Dept Anesthesiol & Pain Med, 1959 NE Pacific St,Box 356540, Seattle, WA 98195 USA.
[Dagal, Armagan; Bransford, Richard J.] Univ Washington, Harborview Med Ctr, Orthopaed & Sports Med, 1959 NE Pacific St,Box 356540, Seattle, WA 98195 USA.
[Burns, Stephen P.] Vet Affairs Puget Sound Hlth Care Syst, Spinal Cord Injury Serv, Seattle, WA USA.
[Burns, Stephen P.] Univ Washington, Harborview Med Ctr, Dept Rehabil, Seattle, WA USA.
[Zhang, Fangyi] Univ Washington, Harborview Med Ctr, Dept Neurosurg, 1959 NE Pacific St,Box 356540, Seattle, WA 98195 USA.
RP Dagal, A (reprint author), Univ Washington, Sch Med, Dept Anesthesiol & Pain Med, 1959 NE Pacific St,Box 356540, Seattle, WA 98195 USA.
EM dagal@uw.edu
FU National Institute on Disability, Independent Living and Rehabilitation
Research Grant [90SI5006-01-00]
FX This study was supported in part by a National Institute on Disability,
Independent Living and Rehabilitation Research Grant (90SI5006-01-00).
NR 25
TC 0
Z9 0
U1 2
U2 2
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0003-2999
J9 ANESTH ANALG
JI Anesth. Analg.
PD APR
PY 2017
VL 124
IS 4
BP 1200
EP 1205
DI 10.1213/ANE.0000000000001906
PG 6
WC Anesthesiology
SC Anesthesiology
GA EP4MH
UT WOS:000397354100025
PM 28319547
ER
PT J
AU Larson, J
AF Larson, James
TI An Alternate Take on Airside Economizing
SO ASHRAE JOURNAL
LA English
DT Article
AB In a dry, desert climate such as in Phoenix, we must still design for occasional freezing temperatures. For a Veterans Affairs medical center and campus in that climate, we found that using advanced direct digital control (DDC) strategies with airside economizers worked well, contributing to an approximate 45% reduction in air-conditioning electricity consumption between 2008 and 2013.
C1 [Larson, James] US Dept Vet Affairs, Washington, DC 20571 USA.
RP Larson, J (reprint author), US Dept Vet Affairs, Washington, DC 20571 USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU AMER SOC HEATING REFRIGERATING AIR-CONDITIONING ENG, INC,
PI ATLANTA
PA 1791 TULLIE CIRCLE NE, ATLANTA, GA 30329 USA
SN 0001-2491
EI 1943-6637
J9 ASHRAE J
JI ASHRAE J.
PD APR
PY 2017
VL 59
IS 4
BP 36
EP 41
PG 6
WC Thermodynamics; Construction & Building Technology; Engineering,
Mechanical
SC Thermodynamics; Construction & Building Technology; Engineering
GA EQ9UK
UT WOS:000398430500007
ER
PT J
AU Goldzweig, CL
AF Goldzweig, Caroline Lubick
TI Opening up to Open Notes and adding the patient to the team
SO BMJ QUALITY & SAFETY
LA English
DT Editorial Material
ID DECISION-MAKING; HEALTH RECORDS; CLINICAL NOTES; OUTCOMES; PORTALS;
EXPERIENCES; ACCESS
C1 [Goldzweig, Caroline Lubick] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Goldzweig, Caroline Lubick] Univ Calif Los Angeles, David Geffen Sch Med, Hlth Sci Clin Prof Med, Los Angeles, CA 90095 USA.
RP Goldzweig, CL (reprint author), 11301 Wilshire Blvd,Mail Code 11, Los Angeles, CA 90073 USA.
EM Caroline.Goldzweig@va.gov
NR 12
TC 0
Z9 0
U1 0
U2 0
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 2044-5415
EI 2044-5423
J9 BMJ QUAL SAF
JI BMJ Qual. Saf.
PD APR
PY 2017
VL 26
IS 4
BP 257
EP 258
DI 10.1136/bmjqs-2016-005641
PG 2
WC Health Care Sciences & Services; Health Policy & Services
SC Health Care Sciences & Services
GA EP7UR
UT WOS:000397583200002
PM 27343275
ER
PT J
AU Bowe, B
Xie, Y
Xian, H
Li, TT
Al-Aly, Z
AF Bowe, Benjamin
Xie, Yan
Xian, Hong
Li, Tingting
Al-Aly, Ziyad
TI Association between Monocyte Count and Risk of Incident CKD and
Progression to ESRD
SO CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
LA English
DT Article
ID DENSITY-LIPOPROTEIN CHOLESTEROL; CHRONIC KIDNEY-DISEASE; RENAL INJURY;
MORTALITY; ATHEROSCLEROSIS; PREDICTOR; FIBROSIS; OUTCOMES; MICE
AB Background and objectives Experimental evidence suggests a role for monocytes in the biology of kidney disease progression; however, whether monocyte count is associated with risk of incident CKD, CKD progression, and ESRD has not been examined in large epidemiologic studies.
Design, settings, participants, & measurements We built a longitudinal observational cohort of 1,594,700 United States veterans with at least one eGFR during fiscal year 2004 (date of last eGFR during this period designated time zero) and no prior history of ESRD, dialysis, or kidney transplant. Cohort participants were followed until September 30, 2013 or death. Monocyte count closest to and before time zero was categorized in quartiles: quartile 1, >0.00 to <= 0.40 thousand cells per cubic millimeter (k/cmm); quartile 2, >0.40 to <= 0.55 k/cmm; quartile 3, >0.55 to <= 0.70 k/cmm; and quartile 4, >0.70 k/cmm. Survival models were built to examine the association between monocyte count and risk of incident eGFR<60 ml/min per 1.73 m(2), risk of incident CKD, and risk of CKD progression defined as doubling of serum creatinine, eGFR decline or the composite outcome of ESRD, dialysis, or renal transplantation.
Results Over a median follow-up of 9.2 years (interquartile range, 8.3-9.4); in adjusted survival models, there was a graded association between monocyte counts and risk of renal outcomes. Compared with quartile 1, quartile 4 was associated with higher risk of incident eGFR<60 ml/min per 1.73 m(2) (hazard ratio, 1.13; 95% confidence interval, 1.12 to 1.14) and risk of incident CKD (hazard ratio, 1.15; 95% confidence interval, 1.13 to 1.16). Quartile 4 was associated with higher risk of doubling of serum creatinine (hazard ratio, 1.22; 95% confidence interval, 1.20 to 1.24), >= 30% eGFR decline (hazard ratio, 1.18; 95% confidence interval, 1.17 to 1.19), and the composite renal end point (hazard ratio, 1.19; 95% confidence interval, 1.16 to 1.22). Cubic spline analyses of the relationship between monocyte count levels and renal outcomes showed a linear relationship, in which risk was higher with higher monocyte count. Results were robust to changes in sensitivity analyses.
Conclusions Our results show a significant association between higher monocyte count and risks of incident CKD and CKD progression to ESRD.
C1 [Bowe, Benjamin; Xie, Yan; Xian, Hong; Li, Tingting; Al-Aly, Ziyad] US Dept Vet Affairs, Clin Epidemiol Ctr, Res & Educ Serv, St Louis Hlth Care Syst, St Louis, MO USA.
[Al-Aly, Ziyad] US Dept Vet Affairs, Div Nephrol, Dept Med, St Louis Hlth Care Syst, St Louis, MO USA.
[Xian, Hong] St Louis Univ, Coll Publ Hlth & Social Justice, Dept Biostat, St Louis, MO 63103 USA.
[Li, Tingting; Al-Aly, Ziyad] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA.
[Al-Aly, Ziyad] Washington Univ, Sch Med, Inst Publ Hlth, St Louis, MO USA.
RP Al-Aly, Z (reprint author), US Dept Vet Affairs, Clin Epidemiol Ctr, St Louis Hlth Care Syst, 915 North Grand Blvd,151-JC, St Louis, MO 63106 USA.
EM zalaly@gmail.com
FU US Department of Veterans Affairs (VA); VA, Veterans Health
Administration, Office of Research and Development, Health Services
Research and Development, VA Information Resource Center Project/Data
Use Agreement [Al-Aly-01]
FX This work was funded by a grant from the US Department of Veterans
Affairs (VA; to Z.A.-A.). Support for the VA/Centers for USRDS Data is
provided by VA, Veterans Health Administration, Office of Research and
Development, Health Services Research and Development, VA Information
Resource Center Project/Data Use Agreement Al-Aly-01.
NR 42
TC 0
Z9 0
U1 0
U2 0
PU AMER SOC NEPHROLOGY
PI WASHINGTON
PA 1725 I ST, NW STE 510, WASHINGTON, DC 20006 USA
SN 1555-9041
EI 1555-905X
J9 CLIN J AM SOC NEPHRO
JI Clin. J. Am. Soc. Nephrol.
PD APR
PY 2017
VL 12
IS 4
BP 603
EP 613
DI 10.2215/CJN.09710916
PG 11
WC Urology & Nephrology
SC Urology & Nephrology
GA ER2TN
UT WOS:000398646800010
PM 28348030
ER
PT J
AU Miller, MJ
Stevens-Lapsley, J
Fields, TT
Coons, D
Bray-Hall, S
Sullivan, W
Christiansen, CL
AF Miller, Matthew J.
Stevens-Lapsley, Jennifer
Fields, Thomas T.
Coons, David
Bray-Hall, Susan
Sullivan, William
Christiansen, Cory L.
TI Physical activity behavior change for older veterans after dysvascular
amputation
SO CONTEMPORARY CLINICAL TRIALS
LA English
DT Article
DE Dysvascular amputation; Physical activity; Behavior change; Veteran;
Telerehabilitation; Feasibility
ID LOWER-LIMB AMPUTATION; RANDOMIZED CONTROLLED-TRIAL; QUALITY-OF-LIFE;
PROSTHESIS EVALUATION QUESTIONNAIRE; UNILATERAL TRANSTIBIAL AMPUTATION;
PERIPHERAL ARTERIAL-DISEASE; IMPAIRED GLUCOSE-TOLERANCE; GERIATRIC
DEPRESSION SCALE; TOTAL KNEE ARTHROPLASTY; HEART-RATE RESPONSE
AB Objective: Determine the feasibility of using a physical-activity behavior-change (PABC) intervention for increasing physical activity and reducing disability in Veterans 1-5 years following dysvascular lower-limb amputation (LLA).
Design: Cross-over, feasibility trial
Setting: VA Geriatric Research Education and Clinical Center and Veterans Homes
Participants: 32 Veterans with dysvascular LLA (1-5 years after major LLA)
Intervention: The home-based study, using telerehabilitation technology, is intended to reduce participant burden by removing transportation and time bafflers. Participants will be randomized into two participation periods of three months (Months 1-3 and 4-6). PABC intervention will occur Months 1-3 for GROUP1 and Months 4-6 for GROUP2. During PABC Intervention, participants engage in weekly video interaction with a physical therapist, who uses a collaborative approach to develop self-monitoring, barrier identification, problem solving and action planning skills to improve physical activity. GROUP2 will participate in a no physical activity intervention, attention control in Months 1-3. GROUP1 will have a no contact, intervention "wash-out" period in Months 4-6.
Main outcome measures: Feasibility will be determined using measures of 1) participant retention, 2) dose goal attainment, 3) participant acceptability, 4) safety, and 5) initial effect size. Effect size will be based on accelerometer-based physical activity and self-report disability using the Late-Life Function and Disability Index.
Conclusions: This study focuses on a prevalent and understudied population with low physical activity and high levels of disability due to dysvascular LLA. The results of this study will guide future development of targeted rehabilitation research to improve long term physical activity and disability outcomes. Published by Elsevier Inc.
C1 [Miller, Matthew J.; Stevens-Lapsley, Jennifer; Coons, David; Bray-Hall, Susan; Sullivan, William; Christiansen, Cory L.] Univ Colorado Denver, Sch Med, Dept Phys Med & Rehabil, 13121 East 17th Ave, Aurora, CO 80045 USA.
[Stevens-Lapsley, Jennifer; Bray-Hall, Susan; Sullivan, William; Christiansen, Cory L.] VA Eastern Colorado Healthcare Syst, Geriatr Res Educ & Clin Ctr, 1055 Clermont St, Denver, CO 80220 USA.
[Miller, Matthew J.; Fields, Thomas T.; Coons, David; Bray-Hall, Susan; Sullivan, William] VA Eastern Colorado Healthcare Syst, Denver Vet Affairs Med Ctr, 1055 Clermont St, Denver, CO 80220 USA.
RP Miller, MJ (reprint author), 13121 East 17th Ave,Mail Stop C244, Aurora, CO 80045 USA.
EM matthew.j4.miller@ucdenver.edu
OI Miller, Matthew/0000-0002-1301-7149
FU Small Projects in Rehabilitation Research (SPiRE) [RX002054-01A1]; NIH
[K12 HD055931]
FX We would like to thank Veterans and staff devoting time and effort to
the success of the study. The contents do not represent the views of the
U.S. Department of Veterans Affairs or the United States Government.
Additionally, we would like to acknowledge Pam Wolfe for her assistance
in the statistical methods design. This study is funded by a grant from
Small Projects in Rehabilitation Research (SPiRE; RX002054-01A1) and Dr.
Christiansen's time supported in part by NIH grant (K12 HD055931).
NR 71
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1551-7144
EI 1559-2030
J9 CONTEMP CLIN TRIALS
JI Contemp. Clin. Trials
PD APR
PY 2017
VL 55
BP 10
EP 15
DI 10.1016/j.cct.2017.01.008
PG 6
WC Medicine, Research & Experimental; Pharmacology & Pharmacy
SC Research & Experimental Medicine; Pharmacology & Pharmacy
GA EP9KI
UT WOS:000397692100002
PM 28153768
ER
PT J
AU Middlebrooks, EH
Ver Hoef, L
Szaflarski, JP
AF Middlebrooks, Erik H.
Ver Hoef, Lawrence
Szaflarski, Jerzy P.
TI Neuroimaging in Epilepsy
SO CURRENT NEUROLOGY AND NEUROSCIENCE REPORTS
LA English
DT Review
DE Epilepsy; Seizure; Neuroimaging; fMRI; DiffusionMRI; EEG
ID TEMPORAL-LOBE EPILEPSY; IDIOPATHIC GENERALIZED EPILEPSY; VERBAL MEMORY
DECLINE; INTERICTAL EPILEPTIFORM DISCHARGES; GUIDELINE DEVELOPMENT
SUBCOMMITTEE; FOCAL CORTICAL DYSPLASIA; UNPROVOKED 1ST SEIZURE;
EEG-FMRI; FUNCTIONAL MRI; AMERICAN-ACADEMY
AB In recent years, the field of neuroimaging has undergone dramatic development. Specifically, of importance for clinicians and researchers managing patients with epilepsies, new methods of brain imaging in search of the seizure-producing abnormalities have been implemented, and older methods have undergone additional refinement. Methodology to predict seizure freedom and cognitive outcome has also rapidly progressed. In general, the image data processing methods are very different and more complicated than even a decade ago. In this review, we identify the recent developments in neuroimaging that are aimed at improved management of epilepsy patients. Advances in structural imaging, diffusion imaging, fMRI, structural and functional connectivity, hybrid imaging methods, quantitative neuroimaging, and machine-learning are discussed. We also briefly summarize the potential new developments that may shape the field of neuroimaging in the near future and may advance not only our understanding of epileptic networks as the source of treatment-resistant seizures but also better define the areas that need to be treated in order to provide the patients with better long-term outcomes.
C1 [Middlebrooks, Erik H.] UAB, Dept Radiol, Birmingham, AL USA.
[Ver Hoef, Lawrence; Szaflarski, Jerzy P.] UAB, Dept Neurol, UAB Epilepsy Ctr, 1719 6th Ave South,CIRC 312, Birmingham, AL 35294 USA.
[Ver Hoef, Lawrence] UAB, Birmingham VA Med Ctr, Birmingham, AL USA.
RP Szaflarski, JP (reprint author), UAB, Dept Neurol, UAB Epilepsy Ctr, 1719 6th Ave South,CIRC 312, Birmingham, AL 35294 USA.
EM jszaflarski@uabmc.edu
OI Middlebrooks, Erik/0000-0002-4418-9605
FU National Institutes of Health [K23EB008452, R01NS094743]
FX No funding was provided for this study. Data for Fig. 1 were obtained
via grants K23EB008452 and R01NS094743 from the National Institutes of
Health to LVH.
NR 113
TC 0
Z9 0
U1 4
U2 4
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1528-4042
EI 1534-6293
J9 CURR NEUROL NEUROSCI
JI Curr. Neurol. Neurosci. Rep.
PD APR
PY 2017
VL 17
IS 4
AR 32
DI 10.1007/s11910-017-0746-x
PG 11
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA EQ3VH
UT WOS:000398000900007
PM 28324301
ER
PT J
AU Willard, JR
Barrow, BM
Zraika, S
AF Willard, Joshua R.
Barrow, Breanne M.
Zraika, Sakeneh
TI Improved glycaemia in high-fat-fed neprilysin-deficient mice is
associated with reduced DPP-4 activity and increased active GLP-1 levels
SO DIABETOLOGIA
LA English
DT Article
DE DPP-4; GLP-1; Glucose tolerance; High fat diet; Insulin secretion; Mme;
Mouse; Nep; Neprilysin
ID ANGIOTENSIN-CONVERTING ENZYME; DIPEPTIDYL-PEPTIDASE-IV; NEUTRAL
ENDOPEPTIDASE ACTIVITY; GLUCAGON-LIKE PEPTIDE-1; INSULIN SENSITIVITY;
METABOLIC SYNDROME; HUMAN SERUM; INHIBITION; CELLS; DEGRADATION
AB Aim/hypothesis Neprilysin, a widely expressed peptidase, is upregulated in metabolically altered states such as obesity and type 2 diabetes. Like dipeptidyl peptidase-4 (DPP-4), neprilysin can degrade and inactivate the insulinotropic peptide glucagon-like peptide-1 (GLP-1). Thus, we investigated whether neprilysin deficiency enhances active GLP-1 levels and improves glycaemia in a mouse model of high fat feeding.
Methods Nep(+/+) and Nep(-/-) mice were fed a 60% fat diet for 16 weeks, after which active GLP-1 and DPP-4 activity levels were measured, as were glucose, insulin and C-peptide levels during an OGTT. Insulin sensitivity was assessed using an insulin tolerance test.
Results High-fat-fed Nep-/-mice exhibited elevated active GLP-1 levels (5.8 +/- 1.1 vs 3.5 +/- 0.8 pmol/l, p<0.05) in association with improved glucose tolerance, insulin sensitivity and beta cell function compared with high-fat-fed Nep+/+ mice. In addition, plasma DPP-4 activity was lower in high-fat-fed Nep-/-mice (7.4 +/- 1.0 vs 10.7 +/- 1.3 nmol ml(-1) min(-1), p<0.05). No difference in insulin: C-peptide ratio was observed between Nep(-/-) and Nep+/+ mice, suggesting that improved glycaemia does not result from changes in insulin clearance.
Conclusions/interpretation Under conditions of increased dietary fat, an improved glycaemic status in neprilysin-deficient mice is associated with elevated active GLP-1 levels, reduced plasma DPP-4 activity and improved beta cell function. Thus, neprilysin inhibition may be a novel treatment strategy for type 2 diabetes.
C1 [Willard, Joshua R.; Barrow, Breanne M.; Zraika, Sakeneh] Vet Affairs Puget Sound Hlth Care Syst, 1660 South Columbian Way 151, Seattle, WA 98108 USA.
[Zraika, Sakeneh] Univ Washington, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA 98195 USA.
RP Zraika, S (reprint author), Vet Affairs Puget Sound Hlth Care Syst, 1660 South Columbian Way 151, Seattle, WA 98108 USA.; Zraika, S (reprint author), Univ Washington, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA 98195 USA.
EM zraikas@uw.edu
FU National Institutes of Health [DK-098506, DK-080945, P30 DK-017047];
United States Department of Veterans Affairs
FX This work was supported by the National Institutes of Health (grants
DK-098506 and DK-080945 to SZ; P30 DK-017047 to the Cell Function
Analysis Core, University of Washington Diabetes Research Center) and
the United States Department of Veterans Affairs.
NR 27
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U1 1
U2 1
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0012-186X
EI 1432-0428
J9 DIABETOLOGIA
JI Diabetologia
PD APR
PY 2017
VL 60
IS 4
BP 701
EP 708
DI 10.1007/s00125-016-4172-4
PG 8
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EQ4KS
UT WOS:000398046400011
PM 27933334
ER
PT J
AU Sonnenberg, A
Turner, KO
Genta, RM
AF Sonnenberg, Amnon
Turner, Kevin O.
Genta, Robert M.
TI Interaction of Ethnicity and H-pylori Infection in the Occurrence of
Microscopic Colitis
SO DIGESTIVE DISEASES AND SCIENCES
LA English
DT Article
DE Collagenous colitis; Environmental risk factors; Epidemiology;
Lymphocytic colitis; Helicobacter
ID INFLAMMATORY-BOWEL-DISEASE; UNITED-STATES; METAANALYSIS; ASSOCIATION;
CLASSIFICATION; GASTRITIS; NEOPLASIA; RECORDS; CANCER
AB Previous studies found that microscopic colitis is inversely associated with Helicobacter pylori infection and that microscopic colitis is characterized by a marked ethnic variation.
The aim of the present study was to test whether an underlying ethnic variation of H. pylori infection is responsible for the ethnic variation of microscopic colitis.
The Miraca Life Sciences Database is a large national electronic repository of histopathologic records of patients distributed throughout the entire USA. A cross-sectional study evaluated the influence of age, gender, ethnicity, and histologic diagnosis of H. pylori on the occurrence of microscopic colitis among subjects who underwent esophago-gastro-duodenoscopies plus colonoscopy.
The total study population comprised 228,506 subjects, of whom 28,890 carried a diagnosis of H. pylori gastritis and 3460 microscopic colitis. Female sex, old age, and H. pylori infection exerted the strongest influence on the occurrence of microscopic colitis. In comparison with the population comprising Caucasians and African-Americans, microscopic colitis was less common among subjects of Hispanic (0.34, 0.27-0.47), East Asian (0.13, 0.06-0.22), Indian (0.31, 0.10-0.73), or Middle Eastern descent (0.28, 0.07-0.74). All these ethnic subgroups were also characterized by a higher prevalence of H. pylori than the comparison group. A low prevalence of H. pylori was significantly associated with a high prevalence of microscopic colitis (R (2) = 0.91, p < 0.001).
Ethnic variations in the gastric infection with H. pylori may be partly responsible for the observed ethnic distribution of microscopic colitis.
C1 [Sonnenberg, Amnon; Turner, Kevin O.; Genta, Robert M.] Miraca Life Sci, Irving, TX 75039 USA.
[Sonnenberg, Amnon] Oregon Hlth & Sci Univ, Portland VA Med Ctr, P3-GI, Portland, OR 97239 USA.
[Genta, Robert M.] Baylor Coll Med, Houston, TX 77030 USA.
RP Sonnenberg, A (reprint author), Miraca Life Sci, Irving, TX 75039 USA.; Sonnenberg, A (reprint author), Oregon Hlth & Sci Univ, Portland VA Med Ctr, P3-GI, Portland, OR 97239 USA.
EM sonnenbe@ohsu.edu
NR 26
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Z9 0
U1 3
U2 3
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0163-2116
EI 1573-2568
J9 DIGEST DIS SCI
JI Dig. Dis. Sci.
PD APR
PY 2017
VL 62
IS 4
BP 1009
EP 1015
DI 10.1007/s10620-016-4441-6
PG 7
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EN9UA
UT WOS:000396343900025
PM 28070826
ER
PT J
AU Gulati, S
Wells, JM
AF Gulati, Swati
Wells, J. Michael
TI Bringing Stability to the Chronic Obstructive Pulmonary Disease Patient:
Clinical and Pharmacological Considerations for Frequent Exacerbators
SO DRUGS
LA English
DT Review
ID PLACEBO-CONTROLLED TRIAL; TO-SEVERE COPD; RANDOMIZED CONTROLLED-TRIAL;
PDE4 INHIBITOR ROFLUMILAST; DAILY ACLIDINIUM BROMIDE; CHRONIC
LUNG-DISEASE; DOUBLE-BLIND; INHALED CORTICOSTEROIDS; INFLAMMATORY
MARKERS; N-ACETYLCYSTEINE
AB Acute exacerbations of chronic obstructive pulmonary disease (AECOPD) are critical events associated with an accelerated loss of lung function, increased morbidity, and excess mortality. AECOPD are heterogeneous in nature and this may directly impact clinical decision making, specifically in patients with frequent exacerbations. A 'frequent exacerbator' is a sub-phenotype of chronic obstructive pulmonary disease (COPD) and is defined as an individual who experiences two or more moderate-to-severe exacerbations per year. This distinct subgroup has higher mortality and accounts for more than half of COPD-related hospitalizations annually. Thus, it is imperative to identify individuals at risk for frequent exacerbations and choose optimal strategies to minimize risk for these events. New paradigms for using combination inhalers and the introduction of novel oral compounds provide expanded treatment options to reduce the risk and frequency of exacerbations. The goals of managing frequent exacerbators or patients at risk for AECOPD are: (1) maximizing bronchodilation; (2) reducing inflammation; and (3) targeting specific molecular pathways implicated in COPD and AECOPD pathogenesis. Novel inhaler therapies including combination long-acting muscarinic agents plus long-acting beta agonists show promising results compared with monotherapy or a long-acting beta agonist inhaled corticosteroid combination in reducing exacerbation risk among individuals at risk for exacerbations and among frequent exacerbators. Likewise, oral medications including macrolides and phosphodiesterase-4 inhibitors reduce the risk for AECOPD in select groups of individuals at high risk for exacerbation. Future direction in COPD management is based on the identification of various subtypes or ` endotypes' and targeting therapies based on their pathophysiology. This review describes the impact of AECOPD and the challenges posed by frequent exacerbators, and explores the rationale for different pharmacologic approaches to preventing AECOPD in these individuals.
C1 [Gulati, Swati; Wells, J. Michael] Univ Alabama Birmingham, Div Pulm Allergy & Crit Care, Lung Hlth Ctr, Birmingham, AL 35294 USA.
[Wells, J. Michael] Birmingham VA Med Ctr, Birmingham, AL 35233 USA.
RP Wells, JM (reprint author), Univ Alabama Birmingham, Div Pulm Allergy & Crit Care, Lung Hlth Ctr, Birmingham, AL 35294 USA.; Wells, JM (reprint author), Birmingham VA Med Ctr, Birmingham, AL 35233 USA.
EM jmwells@uabmc.edu
FU National Institutes of Health/National Heart, Lung, and Blood Institute
[K08 123940]; Cystic Fibrosis Foundation
FX S.G. has no conflict of interest to disclose. J.M.W. receives grant
funding from the National Institutes of Health/National Heart, Lung, and
Blood Institute (K08 123940) and the Cystic Fibrosis Foundation; has
contracts to conduct clinical trials from GlaxoSmithKline, AstraZeneca,
and Gilead; and is a consultant for Mylan and Quintiles.
NR 140
TC 0
Z9 0
U1 1
U2 1
PU ADIS INT LTD
PI NORTHCOTE
PA 5 THE WAREHOUSE WAY, NORTHCOTE 0627, AUCKLAND, NEW ZEALAND
SN 0012-6667
EI 1179-1950
J9 DRUGS
JI Drugs
PD APR
PY 2017
VL 77
IS 6
BP 651
EP 670
DI 10.1007/s40265-017-0713-5
PG 20
WC Pharmacology & Pharmacy; Toxicology
SC Pharmacology & Pharmacy; Toxicology
GA EQ4HG
UT WOS:000398036100005
PM 28255962
ER
PT J
AU Lee, JH
Kang, M
Wang, H
Naik, G
Mobley, JA
Sonpavde, G
Garvey, WT
Darley-Usmar, VM
Ponnazhagan, S
AF Lee, Joo Hyoung
Kang, Minsung
Wang, Hong
Naik, Gurudatta
Mobley, James A.
Sonpavde, Guru
Garvey, W. Timothy
Darley-Usmar, Victor M.
Ponnazhagan, Selvarangan
TI Endostatin inhibits androgen-independent prostate cancer growth by
suppressing nuclear receptor-mediated oxidative stress
SO FASEB JOURNAL
LA English
DT Article
DE androgen-deprivation therapy; reactive oxygen species; androgen
receptor; glucocorticoid receptor; castration resistance
ID GLUCOCORTICOID-RECEPTOR; RESISTANCE; THERAPY; CELLS; MODEL;
DIFFERENTIATION; ENZALUTAMIDE; CHEMOTHERAPY; DEPRIVATION; ABIRATERONE
AB Androgen-deprivation therapy has been identified to induce oxidative stress in prostate cancer (PCa), leading to reactivation of androgen receptor (AR) signaling in a hormone-refractory manner. Thus, antioxidant therapies have gained attention as adjuvants for castration-resistant PCa. Here, we report for the first time that human endostatin (ES) prevents androgen-independent growth phenotype in PCa cells through its molecular targeting of AR and glucocorticoid receptor (GR) and downstream pro-oxidant signaling. This reversal after ES treatment significantly decreased PCa cell proliferation through down-regulation of GR and up-regulation of manganese superoxide dismutase and reduced glutathione levels. Proteome and biochemical analyses of ES-treated PCa cells further indicated a significant up-regulation of enzymes in the major reactive oxygen species (ROS) scavenging machinery, including catalase, glutathione synthetase, glutathione reductase, NADPH-cytochrome P450 reductase, biliverdin reductase, and thioredoxin reductase, resulting in a concomitant reduction of intracellular ROS. ES further augmented the antioxidant system through up-regulation of glucose influx, the pentose phosphate pathway, and NAD salvaging pathways. This shift in cancer cell redox homeostasis by ES significantly decreased the effect of protumorigenic oxidative machinery on androgen-independent PCa growth, suggesting that ES can suppress GR-induced resistant phenotype upon AR antagonism and that the dual targeting action of ES on AR and GR can be further translated to PCa therapy.-Lee, J. H., Kang, M., Wang, H., Naik, G., Mobley, J. A., Sonpavde, G., Garvey, W. T., Darley-Usmar, V. M., Ponnazhagan, S. Endostatin inhibits androgen-independent prostate cancer growth by suppressing nuclear receptor-mediated oxidative stress.
C1 [Lee, Joo Hyoung; Wang, Hong; Darley-Usmar, Victor M.; Ponnazhagan, Selvarangan] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA.
[Kang, Minsung; Garvey, W. Timothy] Univ Alabama Birmingham, Dept Nutr Sci, Birmingham, AL 35294 USA.
[Naik, Gurudatta; Sonpavde, Guru] Univ Alabama Birmingham, Comprehens Canc Ctr, Birmingham, AL USA.
[Mobley, James A.] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA.
[Garvey, W. Timothy] Birmingham Vet Affairs Med Ctr, Birmingham, AL USA.
RP Ponnazhagan, S (reprint author), Univ Alabama Birmingham, Dept Pathol, 1825 Univ Blvd,SHEL 814, Birmingham, AL 35294 USA.
EM pons@uab.edu
FU U.S. National Institutes of Health, National Cancer Institute
[R01CA184770, P30CA013148]
FX This work was supported by U.S. National Institutes of Health, National
Cancer Institute Grants R01CA184770 (to S.P.) and P30CA013148 (to
J.A.M.). The authors thank UAB Mass Spectrometry/Proteomics Shared
Facility for proteome analysis. The authors declare no conflicts of
interest.
NR 42
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Z9 0
U1 3
U2 3
PU FEDERATION AMER SOC EXP BIOL
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3998 USA
SN 0892-6638
EI 1530-6860
J9 FASEB J
JI Faseb J.
PD APR
PY 2017
VL 31
IS 4
BP 1608
EP 1619
DI 10.1096/fj.201601178R
PG 12
WC Biochemistry & Molecular Biology; Biology; Cell Biology
SC Biochemistry & Molecular Biology; Life Sciences & Biomedicine - Other
Topics; Cell Biology
GA ER0UR
UT WOS:000398504300027
PM 28069826
ER
PT J
AU Hoffman, BL
Shensa, A
Wessel, C
Hoffman, R
Primack, BA
AF Hoffman, Beth L.
Shensa, Ariel
Wessel, Charles
Hoffman, Robert
Primack, Brian A.
TI Exposure to fictional medical television and health: a systematic review
SO HEALTH EDUCATION RESEARCH
LA English
DT Review
ID ENTERTAINMENT TELEVISION; GRAYS-ANATOMY; CARDIOPULMONARY-RESUSCITATION;
DRAMAS; STORYLINES; PERCEPTIONS; KNOWLEDGE; ATTITUDES; EDUCATION;
MESSAGES
AB Fictional medical television programs have long been a staple of television programming, and they remain popular today. We aimed to examine published literature assessing the influence of medical television programs on health outcomes. We conducted systematic literature searches in PubMed, PsychINFO and CINAHL. Selected studies had to be scholarly research, to involve exposure to fictionalized medical television programming, and to assess associations between exposures and outcomes. Of 3541 unique studies identified, nineteen met selection criteria. The most commonly studied programs were ER (73%), Grey's Anatomy (58%) and House M.D. (37%). Outcomes included knowledge, perceptions and behaviors related to topics as diverse as organ donation, cancer screening, sexually transmitted infections, and heart disease. Viewing fictional medical television programs had a negative influence on viewers' healthrelated knowledge, perceptions and/or behavior in 11% of studies, a positive influence in 32% of studies, and mixed influence in 58%. While most studies (58%) were characterized as having fair quality in terms of rigor of study design, 21% were classified as good and 21% were classified as poor. As such, medical television can affect health education and outcomes. Future work should utilize randomization, more longitudinal assessments, and more direct assessments of health education and behavioral outcomes.
C1 [Hoffman, Beth L.; Shensa, Ariel; Primack, Brian A.] Univ Pittsburgh, Sch Med, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15213 USA.
[Hoffman, Beth L.; Shensa, Ariel; Primack, Brian A.] Univ Pittsburgh, Sch Med, Ctr Res Media Technol & Hlth, Pittsburgh, PA 15213 USA.
[Wessel, Charles] Univ Pittsburgh, Hlth Sci Lib Syst, Pittsburgh, PA 15213 USA.
[Hoffman, Robert] VA Pittsburgh Healthcare Syst, Dept Med, Pittsburgh, PA 15213 USA.
RP Primack, BA (reprint author), Univ Pittsburgh, Sch Med, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15213 USA.; Primack, BA (reprint author), Univ Pittsburgh, Sch Med, Ctr Res Media Technol & Hlth, Pittsburgh, PA 15213 USA.
EM bprimack@pitt.edu
RI Wessel, Charles/B-2318-2013
OI Wessel, Charles/0000-0002-5018-0156
NR 37
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Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0268-1153
EI 1465-3648
J9 HEALTH EDUC RES
JI Health Educ. Res.
PD APR
PY 2017
VL 32
IS 2
BP 107
EP 123
DI 10.1093/her/cyx034
PG 17
WC Education & Educational Research; Public, Environmental & Occupational
Health
SC Education & Educational Research; Public, Environmental & Occupational
Health
GA EQ3AZ
UT WOS:000397944600001
PM 28334962
ER
PT J
AU Hebert, PL
Howell, EA
Wong, ES
Hernandez, SE
Rinne, ST
Sulc, CA
Neely, EL
Liu, CF
AF Hebert, Paul L.
Howell, Elizabeth A.
Wong, Edwin S.
Hernandez, Susan E.
Rinne, Seppo T.
Sulc, Christine A.
Neely, Emily L.
Liu, Chuan-Fen
TI Methods for Measuring Racial Differences in Hospitals Outcomes
Attributable to Disparities in Use of High-Quality Hospital Care
SO HEALTH SERVICES RESEARCH
LA English
DT Article
DE Race; disparities; hospital readmissions
ID ACUTE MYOCARDIAL-INFARCTION; MEDICARE BENEFICIARIES; BLACK PATIENTS;
SERVING HOSPITALS; UNITED-STATES; MORTALITY; WHITES; RACE; HEALTH;
CANCER
AB ObjectiveTo compare two approaches to measuring racial/ethnic disparities in the use of high-quality hospitals.
Data SourcesSimulated data.
Study DesignThrough simulations, we compared the minority-serving approach of assessing differences in risk-adjusted outcomes at minority-serving and non-minority-serving hospitals with a fixed-effect approach that estimated the reduction in adverse outcomes if the distribution of minority and white patients across hospitals was the same. We evaluated each method's ability to detect and measure a disparity in outcomes caused by minority patients receiving care at poor-quality hospitals, which we label a between-hospital disparity, and to reject it when the disparity in outcomes was caused by factors other than hospital quality.
Principal FindingsThe minority-serving and fixed-effect approaches correctly identified between-hospital disparities in quality when they existed and rejected them when racial differences in outcomes were caused by other disparities; however, the fixed-effect approach has many advantages. It does not require an ad hoc definition of a minority-serving hospital, and it estimated the magnitude of the disparity accurately, while the minority-serving approach underestimated the disparity by 35-46 percent.
ConclusionsResearchers should consider using the fixed-effect approach for measuring disparities in use of high-quality hospital care by vulnerable populations.
C1 [Hebert, Paul L.; Wong, Edwin S.; Hernandez, Susan E.; Sulc, Christine A.; Neely, Emily L.; Liu, Chuan-Fen] VA Puget Sound Hlth Care Syst, VA HSR&D Ctr Innovat Patient Ctr & Value Drive Hl, 1660 S Columbian Way HSR&D MS-152, Seattle, WA 98108 USA.
[Howell, Elizabeth A.] Mt Sinai Sch Med, Dept Populat Hlth Sci & Policy, New York, NY USA.
[Rinne, Seppo T.] Yale Pulm & Crit Care Med, New Haven, CT USA.
RP Hebert, PL (reprint author), VA Puget Sound Hlth Care Syst, VA HSR&D Ctr Innovat Patient Ctr & Value Drive Hl, 1660 S Columbian Way HSR&D MS-152, Seattle, WA 98108 USA.
EM paul.hebert2@va.gov
FU Health Services Research and Development (HSRD) Service; Office of
Research and Development; Department of Veterans Affairs [IIR 09-354];
National Institute on Minority Health and Health Disparities
[R01MD007651]; VA HSR&D Career Development Award [CDA 13-024]
FX We acknowledge the helpful suggestions of the external reviewers. The
study was supported by a grants from the Health Services Research and
Development (HSR&D) Service, the Office of Research and Development, the
Department of Veterans Affairs (IIR 09-354), and the National Institute
on Minority Health and Health Disparities R01MD007651 (Howell). Dr. Wong
is supported by a VA HSR&D Career Development Award (CDA 13-024). The
views expressed in this article are those of the authors and do not
necessarily reflect the position or policy of the Department of Veterans
Affairs, the United States Government, the University of Washington, the
Yale School of Medicine, or the Mount Sinai School of Medicine. Dr. Wong
reports ownership of common stock in Community Health Systems Inc. and
UnitedHealth Group Inc.
NR 30
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0017-9124
EI 1475-6773
J9 HEALTH SERV RES
JI Health Serv. Res.
PD APR
PY 2017
VL 52
IS 2
BP 826
EP 848
DI 10.1111/1475-6773.12514
PG 23
WC Health Care Sciences & Services; Health Policy & Services
SC Health Care Sciences & Services
GA EP8AT
UT WOS:000397599000015
PM 27256878
ER
PT J
AU Shirley, D
Scholtz, H
Osterby, K
Musuuza, J
Fox, B
Safdar, N
AF Shirley, Daniel
Scholtz, Harry
Osterby, Kurt
Musuuza, Jackson
Fox, Barry
Safdar, Nasia
TI Optimizing Inpatient Urine Culture Ordering Practices Using the
Electronic Medical Record: A Pilot Study
SO INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY
LA English
DT Article
ID HOSPITALIZED-PATIENTS; TRACT-INFECTION; CARE
AB A prospective quasi-experimental before-and-after study of an electronic medical record anchored intervention of embedded education on appropriate urine culture indications and indication selection reduced the number of urine cultures ordered for catheterized patients at an academic medical center. This intervention could be a component of CAUTI-reduction bundles.
C1 [Shirley, Daniel; Scholtz, Harry; Fox, Barry; Safdar, Nasia] Univ Wisconsin, Dept Med, Div Infect Dis, Sch Med & Publ Hlth, Madison, WI USA.
[Scholtz, Harry; Osterby, Kurt] UW Hlth, Madison, WI USA.
[Musuuza, Jackson] Univ Wisconsin, Inst Clin & Translat Res, Madison, WI USA.
[Musuuza, Jackson; Safdar, Nasia] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
RP Shirley, D (reprint author), Univ Wisconsin, Div Infect Dis, Sch Med & Publ Hlth, Med Fdn Centennial Bldg 5th Floor, Madison, WI 53706 USA.
EM dshirley@medicine.wisc.edu
FU Veterans' Affairs Patient Safety Center; Agency for Healthcare Research
and Quality
FX Nasia Safdar is supported by a grant from the Veterans' Affairs Patient
Safety Center and by an R18 grant from the Agency for Healthcare
Research and Quality.
NR 9
TC 0
Z9 0
U1 0
U2 0
PU CAMBRIDGE UNIV PRESS
PI NEW YORK
PA 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA
SN 0899-823X
EI 1559-6834
J9 INFECT CONT HOSP EP
JI Infect. Control Hosp. Epidemiol.
PD APR
PY 2017
VL 38
IS 4
BP 486
EP 488
DI 10.1017/ice.2016.301
PG 3
WC Public, Environmental & Occupational Health; Infectious Diseases
SC Public, Environmental & Occupational Health; Infectious Diseases
GA EP4LP
UT WOS:000397352300017
PM 28025951
ER
PT J
AU Mehrotra, P
Gupta, K
Strymish, J
Kramer, DB
Lambert-Kerzner, A
Ho, PM
-Elliman, WB
AF Mehrotra, Preeti
Gupta, Kalpana
Strymish, Judith
Kramer, Daniel B.
Lambert-Kerzner, Anne
Ho, P. Michael
-Elliman, Westyn Branch
TI Implementation of Infection Prevention and Antimicrobial Stewardship in
Cardiac Electrophysiology Laboratories: Results from the SHEA Research
Network
SO INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY
LA English
DT Editorial Material
ID RISK-FACTORS; METAANALYSIS; MORTALITY
AB Infection prevention in electrophysiology (EP) laboratories is poorly characterized; thus, we conducted a cross-sectional survey using the SHEA Research Network. We found limited uptake of basic interventions, such as surveillance and appropriate peri-procedural antimicrobial use. Further study is needed to identify ways to improve infection prevention in this setting.
C1 [Mehrotra, Preeti; Kramer, Daniel B.; -Elliman, Westyn Branch] Beth Israel Deaconess Med Ctr, Dept Med, Div Infect Dis & Cardiol, Boston, MA 02215 USA.
[Mehrotra, Preeti; Strymish, Judith; Kramer, Daniel B.; -Elliman, Westyn Branch] Harvard Med Sch, Boston, MA USA.
[Gupta, Kalpana; Strymish, Judith; -Elliman, Westyn Branch] Vet Affairs Boston Healthcare Syst, Dept Med, Div Infect Dis, W Roxbury, MA USA.
[Gupta, Kalpana] Boston Univ, Sch Med, Boston, MA 02118 USA.
[Lambert-Kerzner, Anne; Ho, P. Michael] Seattle Denver Ctr Veteran Centr & Value Driven C, Denver, CO USA.
[Lambert-Kerzner, Anne; Ho, P. Michael] Univ Colorado, Sch Med, Denver, CO USA.
[Ho, P. Michael] Denver VA Med Ctr, Dept Med, Div Cardiol, Denver, CO USA.
RP Mehrotra, P (reprint author), 110 Francis St, Boston, MA USA.
FU NIA NIH HHS [K23 AG045963]
NR 7
TC 0
Z9 0
U1 0
U2 0
PU CAMBRIDGE UNIV PRESS
PI NEW YORK
PA 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA
SN 0899-823X
EI 1559-6834
J9 INFECT CONT HOSP EP
JI Infect. Control Hosp. Epidemiol.
PD APR
PY 2017
VL 38
IS 4
BP 496
EP 498
DI 10.1017/ice.2016.309
PG 3
WC Public, Environmental & Occupational Health; Infectious Diseases
SC Public, Environmental & Occupational Health; Infectious Diseases
GA EP4LP
UT WOS:000397352300021
PM 28103958
ER
PT J
AU Patz, MD
Sa, RC
Darquenne, C
Elliott, AR
Asadi, AK
Theilmann, RJ
Dubowitz, DJ
Swenson, ER
Prisk, GK
Hopkins, SR
AF Patz, Michael D.
Sa, Rui C.
Darquenne, Chantal
Elliott, Ann R.
Asadi, Amran K.
Theilmann, Rebecca J.
Dubowitz, David J.
Swenson, Erik R.
Prisk, G. Kim
Hopkins, Susan R.
TI Susceptibility to high-altitude pulmonary edema is associated with a
more uniform distribution of regional specific ventilation
SO JOURNAL OF APPLIED PHYSIOLOGY
LA English
DT Article
DE high-altitude illness; high-altitude pulmonary edema; multiple-breath
washout; proton magnetic resonance imaging; specific ventilation imaging
ID EXHALED NITRIC-OXIDE; COLLATERAL VENTILATION; BLOOD-FLOW; SUSTAINED
MICROGRAVITY; SODIUM-TRANSPORT; ACUTE-HYPOXIA; GAS-EXCHANGE; PROTON MRI;
LUNG; HETEROGENEITY
AB High-altitude pulmonary edema (HAPE) is a potentially fatal condition affecting high-altitude sojourners. The biggest predictor of HAPE development is a history of prior HAPE. Magnetic resonance imaging (MRI) shows that HAPE-susceptible (with a history of HAPE), but not HAPE-resistant (with a history of repeated ascents without illness) individuals develop greater heterogeneity of regional pulmonary perfusion breathing hypoxic gas (O-2 = 12.5%), consistent with uneven hypoxic pulmonary vasoconstriction (HPV). Why HPV is uneven in HAPE-susceptible individuals is unknown but may arise from regionally heterogeneous ventilation resulting in an uneven stimulus to HPV. We tested the hypothesis that ventilation is more heterogeneous in HAPE-susceptible subjects (n = 6) compared with HAPE-resistant controls (n = 7). MRI specific ventilation imaging (SVI) was used to measure regional specific ventilation and the relative dispersion (SD/mean) of SVI used to quantify baseline heterogeneity. Ventilation heterogeneity from conductive and respiratory airways was measured in normoxia and hypoxia (O-2 = 12.5%) using multiple-breath washout and heterogeneity quantified from the indexes S-cond and S-acin, respectively. Contrary to our hypothesis, HAPE-susceptible subjects had significantly lower relative dispersion of specific ventilation than the HAPEresistant controls [susceptible = 1.33 +/- 0.67 (SD), resistant = 2.36 +/- 0.98, P = 0.05], and Sacin tended to be more uniform (susceptible = 0.085 +/- 0.009, resistant = 0.113 +/- 0.030, P = 0.07). Scond was not significantly different between groups (susceptible = 0.019 +/- 0.007, resistant = 0.020 +/- 0.004, P = 0.67). S-acin and S-cond did not change significantly in hypoxia (P = 0.56 and 0.19, respectively). In conclusion, ventilation heterogeneity does not change with short-term hypoxia irrespective of HAPE susceptibility, and lesser rather than greater ventilation heterogeneity is observed in HAPE-susceptible subjects. This suggests that the basis for uneven HPV in HAPE involves vascular phenomena.
NEW & NOTEWORTHY Uneven hypoxic pulmonary vasoconstriction (HPV) is thought to incite high-altitude pulmonary edema (HAPE). We evaluated whether greater heterogeneity of ventilation is also a feature of HAPE-susceptible subjects compared with HAPEresistant subjects. Contrary to our hypothesis, ventilation heterogene-ity was less in HAPE-susceptible subjects and unaffected by hypoxia, suggesting a vascular basis for uneven HPV.
C1 [Patz, Michael D.] Univ Washington, Dept Anesthesiol, Seattle, WA 98195 USA.
[Sa, Rui C.; Darquenne, Chantal; Elliott, Ann R.; Asadi, Amran K.; Prisk, G. Kim; Hopkins, Susan R.] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA.
[Theilmann, Rebecca J.; Dubowitz, David J.; Prisk, G. Kim] Univ Calif San Diego, Dept Radiol, La Jolla, CA 92093 USA.
[Swenson, Erik R.] Univ Washington, Vet Affairs Puget Sound Hlth Care Syst, Med Serv, Seattle, WA 98195 USA.
RP Hopkins, SR (reprint author), Univ Calif San Diego, Div Physiol 0623A, 9500 Gilman Dr, La Jolla, CA 92093 USA.
EM shopkins@ucsd.edu
FU National Heart, Lung, and Blood Institute [118539, 104118, 122753];
Seattle Foundation
FX This study was supported by National Heart, Lung, and Blood Institute
Grants 118539, 104118, and 122753 and the Seattle Foundation.
NR 48
TC 1
Z9 1
U1 0
U2 0
PU AMER PHYSIOLOGICAL SOC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 8750-7587
EI 1522-1601
J9 J APPL PHYSIOL
JI J. Appl. Physiol.
PD APR
PY 2017
VL 122
IS 4
BP 844
EP 852
DI 10.1152/japplphysiol.00494.2016
PG 9
WC Physiology; Sport Sciences
SC Physiology; Sport Sciences
GA EQ7PK
UT WOS:000398275900011
PM 28057815
ER
PT J
AU Andorko, JI
Pineault, KG
Jewell, CM
AF Andorko, James I.
Pineault, Kevin G.
Jewell, Christopher M.
TI Impact of molecular weight on the intrinsic immunogenic activity of
poly(beta amino esters)
SO JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A
LA English
DT Article
DE poly(beta amino ester); dendritic cell and lymphocyte; nanoparticle and
microparticle; degradable biomaterial; immunology and vaccine
ID PARTICULATE VACCINE ADJUVANTS; DENDRITIC CELL MATURATION;
POLYELECTROLYTE MULTILAYERS; IMMUNE-RESPONSE; IN-VIVO; POLYMERIC
NANOPARTICLES; GENE DELIVERY; SHAPE; ACTIVATION; DNA
AB Polymeric carriers are ubiquitously studied in vaccine and drug delivery to control the encapsulation, kinetics, and targeting of cargo. Recent research reveals many polymers can cause immunostimulatory and inflammatory responses, even in the absence of other immune signals. However, the extent to which this intrinsic immunogenicity evolves during degradation is understudied. Here we synthesized a small library of poly(beta amino esters) (PBAEs) that exhibit different starting molecular weights (MWs), but with similar and rapid degradation rates. Primary dendritic cells (DCs) treated with free PBAEs, either intact or degraded to form low MW fragments, were not activated. In contrast particles formed from PBAEs at different extents of degradation caused differential expression of classical DC activation markers (for example, CD40, CD80, CD86, MHCII), as well as antigen presentation. During degradation, activation levels changed with changing physicochemical properties (for example, MW, concentration, size, charge). Of note, irrespective of starting MW, immunogenicity peaked when the MW of degrading PBAEs decreased to a range of similar to 1500-3000 Da. These findings could help inform design of future carriers that exploit the dynamic interactions with the immune system as materials degrade, leading to carriers that deliver cargo but also help direct the immune responses to vaccine or immunotherapy cargo. (C) 2017 Wiley Periodicals, Inc.
C1 [Andorko, James I.; Pineault, Kevin G.; Jewell, Christopher M.] Univ Maryland, Fischell Dept Bioengn, College Pk, MD USA.
[Jewell, Christopher M.] Univ Maryland Med Sch, Dept Microbiol & Immunol, Baltimore, MD USA.
[Jewell, Christopher M.] Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD USA.
[Jewell, Christopher M.] US Dept Vet Affairs, Biomed Lab Res & Dev, Baltimore, MD USA.
RP Jewell, CM (reprint author), Univ Maryland, Fischell Dept Bioengn, College Pk, MD USA.; Jewell, CM (reprint author), Univ Maryland Med Sch, Dept Microbiol & Immunol, Baltimore, MD USA.; Jewell, CM (reprint author), Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD USA.; Jewell, CM (reprint author), US Dept Vet Affairs, Biomed Lab Res & Dev, Baltimore, MD USA.
EM cmjewell@umd.edu
FU American Association of Pharmaceutical Scientists; National Science
Foundation CAREER Award [CAREER 1351688]; Alliance for Cancer Gene
Therapy [15051543]; Damon Runyon Foundation [DRR3415]; Melanoma Research
Alliance [348963]; Alex's Lemonade Stand Foundation for Childhood Cancer
[27120]; National Multiple Sclerosis Society [RG-1501-02968]
FX Contract grant sponsors: American Association of Pharmaceutical
Scientists; Contract grant sponsor: National Science Foundation CAREER
Award; contract grant number: CAREER 1351688; Contract grant sponsor:
Alliance for Cancer Gene Therapy; contract grant number: 15051543;
Contract grant sponsor: Damon Runyon Foundation; contract grant number:
DRR3415; Contract grant sponsor: Melanoma Research Alliance; contract
grant number: 348963; Contract grant sponsor: Alex's Lemonade Stand
Foundation for Childhood Cancer; contract grant number: 27120; Contract
grant sponsor: National Multiple Sclerosis Society; contract grant
number: RG-1501-02968
NR 58
TC 1
Z9 1
U1 6
U2 6
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1549-3296
EI 1552-4965
J9 J BIOMED MATER RES A
JI J. Biomed. Mater. Res. Part A
PD APR
PY 2017
VL 105
IS 4
BP 1219
EP 1229
DI 10.1002/jbm.a.35970
PG 11
WC Engineering, Biomedical; Materials Science, Biomaterials
SC Engineering; Materials Science
GA EM0KX
UT WOS:000395008300027
PM 27977902
ER
PT J
AU Zhao, KW
Murray, EJB
Murray, SS
AF Zhao, Ke-Wei
Murray, Elsa J. Brochmann
Murray, Samuel S.
TI HK2 Proximal Tubule Epithelial Cells Synthesize and Secrete Plasma
Proteins Predominantly Through the Apical Surface
SO JOURNAL OF CELLULAR BIOCHEMISTRY
LA English
DT Article
DE alpha(2)-MACROGLOBULIN (A2M); CHAPERONE; COMPLEMENT C3; CYTOKINES; HK2;
HepG2; TGF beta
ID GROWTH-FACTOR-BETA; ACUTE KIDNEY INJURY; TGF-BETA; TRANSFORMING
GROWTH-FACTOR-BETA-1; COMPLEMENT C3; FETUIN-A; ALPHA; ACTIVATION;
PRECURSOR; BINDING
AB Renal proximal tubule epithelial cells (PTECs) are known to reabsorb salts and small plasma proteins filtered through Bowman's capsule. Following acute kidney injury, PTECs assume some characteristics of hepatocytes in producing various plasma proteins. We now demonstrate that even at a resting state, a PTEC cell line, HK2 expresses mRNAs for and synthesizes and secretes plasma proteins in a complex with complement C3, an alpha 2-macroglobulin family chaperone, including albumin, transferrin, alpha 1-antitrypsin, alpha 1-antichymotrypsin, alpha 2-HS-glycoprotein, ceruloplasmin, haptoglobin, C1-inhibitor, secreted phosphoprotein-24, and insulin-like growth factor-1. When grown on transwell inserts, HK2 cells predominantly secrete (similar to 90%) plasma proteins into the apical side and a smaller fraction into the basolateral side as determined by ELISA assays. When cultured in the presence of exogenous cytokines such as IL1 beta, IL6, TNF alpha, BMP2, or TGF beta 1, HK2 cell mRNA expressions for plasma proteins were variably affected whereas basolateral secretions were elevated to or in excess of those of the apical level. In addition, HK2 cells produce proTGF beta 1 with its intact N-terminal latency associated peptide and latent-TGF-beta-binding proteins. The complex cannot be dissociated under conditions of SDS, heating, and electrophoresis. Moreover, HK2 cells maintain their ability to quickly uptake exogenously added serum proteins from the culture medium, as if they are recognized differently by the endocytic receptors. These results provide new insight into the hepatization of PTECs. In addition to their unique uptake of plasma proteins and salts from the filtrate, they are a source of urinary proteins under normal conditions as wells as in chronic and acute kidney diseases. (C) 2016 Wiley Periodicals, Inc.
C1 [Zhao, Ke-Wei; Murray, Elsa J. Brochmann; Murray, Samuel S.] Vet Affairs Greater Los Angeles Healthcare Syst, Geriatr Res Educ & Clin Ctr 11E, Sepulveda, CA 91343 USA.
[Murray, Elsa J. Brochmann; Murray, Samuel S.] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA.
[Murray, Samuel S.] Univ Calif Los Angeles, Interdept tmental Program Biomed Engn, Los Angeles, CA 90095 USA.
RP Zhao, KW; Murray, EJB; Murray, SS (reprint author), Vet Affairs Greater Los Angeles Healthcare Syst, Geriatr Res Educ & Clin Ctr 11E, Sepulveda, CA 91343 USA.
EM keweizhao@gmail.com; elsa.murray@va.gov; samuel.murray@va.gov
FU Department of Veterans Affairs [1IPBX000511, 1IORX000383]
FX Grant sponsor: Department of Veterans Affairs; Grant numbers:
1IPBX000511, 1IORX000383.
NR 50
TC 0
Z9 0
U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0730-2312
EI 1097-4644
J9 J CELL BIOCHEM
JI J. Cell. Biochem.
PD APR
PY 2017
VL 118
IS 4
BP 924
EP 933
DI 10.1002/jcb.25786
PG 10
WC Biochemistry & Molecular Biology; Cell Biology
SC Biochemistry & Molecular Biology; Cell Biology
GA EP5LO
UT WOS:000397420300027
PM 27862254
ER
PT J
AU Hull, RL
Willard, JR
Struck, MD
Barrow, BM
Brar, GS
Andrikopoulos, S
Zraika, S
AF hull, Rebecca L.
Willard, Joshua R.
Struck, Matthias D.
Barrow, Breanne M.
Brar, Gurkirat S.
Andrikopoulos, Sofianos
Zraika, Sakeneh
TI High fat feeding unmasks variable insulin responses in male C57BL/6
mouse substrains
SO JOURNAL OF ENDOCRINOLOGY
LA English
DT Article
DE insulin secretion; C57BU6 substrains; islet; high-fat diet
ID NICOTINAMIDE NUCLEOTIDE TRANSHYDROGENASE; DIET-INDUCED OBESITY;
INTRAVENOUS GLUCOSE; SECRETORY FUNCTION; INBRED STRAINS; MICE;
SENSITIVITY; SUSCEPTIBILITY; INTOLERANCE; MECHANISMS
AB Mouse models are widely used for elucidating mechanisms underlying type 2 diabetes. Genetic background profoundly affects metabolic phenotype; therefore, selecting the appropriate model is critical. Although variability in metabolic responses between mouse strains is now well recognized, it also occurs within C57BL/6 mice, of which several substrains exist. This within-strain variability is poorly understood and could emanate from genetic and/or environmental differences. To better define the within strain variability, we performed the first comprehensive comparison of insulin secretion from C57BL/6 substrains 61, 6JWehi, 6NJ, 6NHsd, 6NTac and 6NCrl. in vitro, glucose stimulated insulin secretion correlated with Nnt mutation status, wherein responses were uniformly lower in islets from C57BL/61 vs C57BL/6N mice. In contrast, in vivo insulin responses after 18 weeks of low fat feeding showed no differences among any of the six substrains. When challenged with a high-fat diet for 18 weeks, C57BL/6J substrains responded with a similar increase in insulin release. However, variability was evident among C57BL/6N substrains. Strikingly, 6NJ mice showed no increase in insulin release after high fat feeding, contributing to the ensuing hyperglycemia. The variability in insulin responses among high-fat-fed C57BL/6N mice could not be explained by differences in insulin sensitivity, body weight, food intake or beta-cell area. Rather, as yet unidentified genetic and/or environmental factor(s) are likely contributors. Together, our findings emphasize that caution should be exercised in extrapolating data from in vitro studies to the in vivo situation and inform on selecting the appropriate C57BL/6 substrain for metabolic studies.
C1 [hull, Rebecca L.; Willard, Joshua R.; Barrow, Breanne M.; Brar, Gurkirat S.; Zraika, Sakeneh] Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA USA.
[hull, Rebecca L.; Struck, Matthias D.; Zraika, Sakeneh] Univ Washington, Dept Med, Dept Med Endocrinol & Nutr, Seattle, WA USA.
[Andrikopoulos, Sofianos] Univ Melbourne, Austin Hosp, Dept Med, Heidelberg, Vic, Australia.
RP Zraika, S (reprint author), Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA USA.; Zraika, S (reprint author), Univ Washington, Dept Med, Dept Med Endocrinol & Nutr, Seattle, WA USA.
EM zraikas@uw.edu
FU NIH [DK-080945, DK-098506, DK-088082]; University of Washington Diabetes
Research Center [DK-017047]; Department of Veterans Affairs, VA Puget
Sound Health Care System; Seattle Institute for Biomedical and Clinical
Research; NHMRC Senior Research Fellowship
FX This work was supported by: NIH grants DK-080945 and DK-098506 to S Z,
DK-088082 to R L H, and DK-017047 (University of Washington Diabetes
Research Center); the Department of Veterans Affairs, VA Puget Sound
Health Care System; Seattle Institute for Biomedical and Clinical
Research; and a NHMRC Senior Research Fellowship to S A.
NR 31
TC 0
Z9 0
U1 0
U2 0
PU BIOSCIENTIFICA LTD
PI BRISTOL
PA EURO HOUSE, 22 APEX COURT WOODLANDS, BRADLEY STOKE, BRISTOL BS32 4JT,
ENGLAND
SN 0022-0795
EI 1479-6805
J9 J ENDOCRINOL
JI J. Endocrinol.
PD APR
PY 2017
VL 233
IS 1
BP 53
EP 64
DI 10.1530/10E-16-0377
PG 12
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EP2VS
UT WOS:000397242300009
PM 28138002
ER
PT J
AU Ffytche, DH
Pereira, JB
Ballard, C
Chaudhuri, KR
Weintraub, D
Aarsland, D
AF Ffytche, Dominic H.
Pereira, Joana B.
Ballard, Clive
Chaudhuri, K. Ray
Weintraub, Daniel
Aarsland, Dag
TI Risk factors for early psychosis in PD: insights from the Parkinson's
Progression Markers Initiative
SO JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
LA English
DT Article
ID NURSING-HOME PLACEMENT; VISUAL HALLUCINATIONS; COGNITIVE IMPAIRMENT;
MINOR HALLUCINATIONS; DIAGNOSTIC-CRITERIA; DISEASE PATIENTS; DEMENTIA;
SYMPTOMS; PREVALENCE; BRAIN
AB Background Parkinson's Disease (PD) psychosis refers to the spectrum of illusions, formed hallucinations and delusions that occur in PD. Visual hallucinations and illusions are thought to be caused by specific cognitive and higher visual function deficits and patients who develop such symptoms early in the disease course have greater rates of cognitive decline and progression to dementia. To date, no studies have investigated whether such deficits are found prior to the onset of PD psychosis.
Method Here we compare baseline cognitive, biomarker (structural imaging and cerebrospinal fluid) and other PD psychosis risk factor data in patients who go on to develop illusions or hallucinations within 3-4 years of follow-up in the Parkinson's Progression Markers Initiative cohort of newly diagnosed PD.
Results Of n=423 patients with PD, n=115 (27%) reported predominantly illusions with the median time of onset at 19.5 months follow-up. At study entry these patients had reduced CSF amyloid A beta(1-42), lower olfaction scores, higher depression scores and increased REM sleep behaviour disorder symptoms compared to patients without early onset PD psychosis but no differences in cognitive, higher visual or structural imaging measures. A subset of patients with early onset formed hallucinations (n=21) had reduced higher visual function at baseline, cortical thinning in parietal, occipital and frontal cortex and reduced hippocampal volume.
Conclusions The findings suggest early onset illusions and formed hallucinations are linked to amyloid pathology in PD and point to a difference in the underlying pathophysiological mechanism of illusions and formed hallucinations, with implications for their respective links to future cognitive decline.
C1 [Ffytche, Dominic H.; Ballard, Clive; Chaudhuri, K. Ray; Weintraub, Daniel; Aarsland, Dag] Kings Coll London, KCL PARCOG Grp, Inst Psychiat Psychol & Neurosci, PO70,de Crespigny Pk, London SE5 8AF, England.
[Ffytche, Dominic H.; Aarsland, Dag] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Old Age Psychiat, London, England.
[Pereira, Joana B.] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Stockholm, Sweden.
[Ballard, Clive] Univ Exeter, Sch Med, Exeter, Devon, England.
[Chaudhuri, K. Ray] Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England.
[Weintraub, Daniel] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Weintraub, Daniel] Univ Penn, Dept Neurol, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Weintraub, Daniel] Philadelphia Vet Affairs Med Ctr, Parkinsons Dis Res Educ & Clin Ctr, Philadelphia, PA USA.
[Weintraub, Daniel] Philadelphia Vet Affairs Med Ctr, Mental Illness Res Educ & Clin Ctr PADRECC & MIRE, Philadelphia, PA USA.
[Aarsland, Dag] Stavanger Univ Hosp, Ctr Age Related Med, Stavanger, Norway.
RP Ffytche, DH (reprint author), Kings Coll London, KCL PARCOG Grp, Inst Psychiat Psychol & Neurosci, PO70,de Crespigny Pk, London SE5 8AF, England.
EM dominic.ffytche@kcl.ac.uk
FU NIHR Maudsley Biomedical Research Centre and Dementia Unit; NIHR
Programme Grants for Applied Research [RP-PG-0610-10100 SHAPED]; Wolfson
Foundation; Royal Society
FX Data used in the preparation of this article were obtained from the
Parkinson's Progression Markers Initiative database
(http://www.ppmi-info.org/). The authors thank Dr Fabrizia D'Antonio for
help with R programming, the NIHR Maudsley Biomedical Research Centre
and Dementia Unit and NIHR Programme Grants for Applied Research
(RP-PG-0610-10100 SHAPED) for supporting involvement in this work. Dag
Aarsland is a Royal Society Wolfson Research Merit Award Holder and
thanks the Wolfson Foundation and the Royal Society for their support.
NR 41
TC 0
Z9 0
U1 1
U2 1
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 0022-3050
EI 1468-330X
J9 J NEUROL NEUROSUR PS
JI J. Neurol. Neurosurg. Psychiatry
PD APR
PY 2017
VL 88
IS 4
BP 325
EP 331
DI 10.1136/jnnp-2016-314832
PG 7
WC Clinical Neurology; Psychiatry; Surgery
SC Neurosciences & Neurology; Psychiatry; Surgery
GA EP8JO
UT WOS:000397621900010
PM 28315846
ER
PT J
AU Rule, ME
Vargas-Irwin, CE
Donoghue, JP
Truccolo, W
AF Rule, Michael E.
Vargas-Irwin, Carlos E.
Donoghue, John P.
Truccolo, Wilson
TI Dissociation between sustained single-neuron spiking and transient
beta-LFP oscillations in primate motor cortex
SO JOURNAL OF NEUROPHYSIOLOGY
LA English
DT Article
DE beta oscillations; collective dynamics; motor cortex; neural dynamics;
spike-field coupling
ID LOCAL-FIELD POTENTIALS; RECORDED IN-VIVO; TASK-DEPENDENT MODULATION;
FAST NETWORK OSCILLATIONS; PRECISION GRIP TASK; SENSORIMOTOR CORTEX;
VISUAL-CORTEX; ELECTROPHYSIOLOGICAL CHARACTERIZATION; FUNCTIONAL
CONNECTIVITY; PARKINSONS-DISEASE
AB Determining the relationship between single-neuron spiking and transient (20 Hz) beta-local field potential (beta-LFP) oscillations is an important step for understanding the role of these oscillations in motor cortex. We show that whereas motor cortex firing rates and beta spiking rhythmicity remain sustained during steady-state movement preparation periods,beta-LFP oscillations emerge, in contrast, as short transient events. Single-neuron mean firing rates within and outside transient beta-LFP events showed no differences, and no consistent correlation was found between the beta oscillation amplitude and firing rates, as was the case for movement- and visual cue-related beta-LFP suppression. Importantly, well-isolated single units featuring beta-rhythmic spiking (43%, 125/292) showed no apparent or only weak phase coupling with the transient beta-LFP oscillations. Similar results were obtained for the population spiking. These findings were common in triple microelectrode array recordings from primary motor (M1), ventral (PMv), and dorsal premotor (PMd) cortices in nonhuman primates during movement preparation. Although beta spiking rhythmicity indicates strong membrane potential fluctuations in the beta band, it does not imply strong phase coupling with beta-LFP oscillations. The observed dissociation points to two different sources of variation in motor cortex beta-LFPs: one that impacts single- neuron spiking dynamics and another related to the generation of mesoscopic beta-LFP signals. Furthermore, our findings indicate that rhythmic spiking and diverse neuronal firing rates, which encode planned actions during movement preparation, may naturally limit the ability of different neuronal populations to strongly phase-couple to a single dominant oscillation frequency, leading to the observed spiking and beta-LFP dissociation.
NEW & NOTEWORTHY We show that whereas motor cortex spiking rates and beta (similar to 20 Hz) spiking rhythmicity remain sustained during steady-state movement preparation periods, beta-local field potential (beta-LFP) oscillations emerge, in contrast, as transient events. Furthermore, the beta-LFP phase at which neurons spike drifts: phase coupling is typically weak or absent. This dissociation points to two sources of variation in the level of motor cortex beta: one that impacts single- neuron spiking and and another related to the generation of measured mesoscopic beta-LFPs.
C1 [Rule, Michael E.; Vargas-Irwin, Carlos E.; Donoghue, John P.; Truccolo, Wilson] Brown Univ, Dept Neurosci, Providence, RI 02912 USA.
[Donoghue, John P.; Truccolo, Wilson] Brown Univ, Inst Brain Sci, Providence, RI 02912 USA.
[Donoghue, John P.; Truccolo, Wilson] US Dept Vet Affairs, Ctr Neurorestorat & Neurotechnol, Providence, RI USA.
RP Truccolo, W (reprint author), Brown Univ, Dept Neurosci, Providence, RI 02912 USA.
EM wilson_truccolo@brown.edu
FU National Institutes of Neurological Disorders and Stroke (NINDS) [R01
NS25074]; K01 Career Award [NS057389]; Defense Advanced Research
Projects Agency (DARPA) REPAIR [N66001-10-C-2010]; National Science
Foundation predoctoral fellowship; Pablo J. Salame '88 Goldman Sachs
Endowed Assistant Professorship of Computational Neuroscience
FX This research is supported by National Institutes of Neurological
Disorders and Stroke (NINDS) Grants R01 NS25074 (to J.P. Donoghue) and
K01 Career Award NS057389 (to W. Truccolo), Defense Advanced Research
Projects Agency (DARPA) REPAIR Grant N66001-10-C-2010 (to J.P. Donoghue
and W. Truccolo), a National Science Foundation predoctoral fellowship
(to M.E. Rule), and the Pablo J. Salame '88 Goldman Sachs Endowed
Assistant Professorship of Computational Neuroscience (to W. Truccolo).
NR 70
TC 0
Z9 0
U1 1
U2 1
PU AMER PHYSIOLOGICAL SOC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 0022-3077
EI 1522-1598
J9 J NEUROPHYSIOL
JI J. Neurophysiol.
PD APR
PY 2017
VL 117
IS 4
BP 1524
EP 1543
DI 10.1152/jn.00651.2016
PG 20
WC Neurosciences; Physiology
SC Neurosciences & Neurology; Physiology
GA EQ7WU
UT WOS:000398296400010
PM 28100654
ER
PT J
AU Robertson, CS
McCarthy, JJ
Miller, ER
Levin, H
McCauley, SR
Swank, PR
AF Robertson, Claudia S.
McCarthy, James J.
Miller, Emmy R.
Levin, Harvey
McCauley, Stephen R.
Swank, Paul R.
CA Mission Connect Mild TBI
TI Phase II Clinical Trial of Atorvastatin in Mild Traumatic Brain Injury
SO JOURNAL OF NEUROTRAUMA
LA English
DT Article
DE clinical trial; cognitive function; traumatic brain injury
ID INTRACEREBRAL HEMORRHAGE; NEURONAL SURVIVAL; SIMVASTATIN; RATS;
INCREASE; STATINS; NEUROGENESIS; ANGIOGENESIS; THROMBOSIS; REDUCTION
AB Statins constitute a class of medications commonly used in the treatment of elevated cholesterol. However, in experimental studies, statins also have other non-cholesterol-mediated mechanisms of action, which may have neuroprotective effects. The aim of this study was to determine whether administration of atorvastatin for 7 days post-injury would improve neurological recovery in patients with mild traumatic brain injury (mTBI). The hypothesis was that atorvastatin administration would reduce post-concussion symptoms and also that atorvastatin administration for 1 week post-injury would be safe. One hundred forty patients with mTBI were planned to be enrolled and randomly assigned to receive atorvastatin 1 mg/kg (up to 80 mg/kg) per day or placebo for 7 days starting within 24 h of injury. Assessments of post-concussion syndrome, post-traumatic stress and depressive symptoms, cognition, memory, verbal fluency, functional, and work status were performed at baseline, 1 week, and 1 and 3 months. The result on the Rivermead Post-Concussion Symptoms Questionnaire at 3 months was the primary outcome. Enrollment in the trial was stopped early because of difficulty in recruiting sufficient numbers of subjects. Fifty-two patients with mTBI were enrolled; 28 patients received atorvastatin and 24 received placebo. The median Rivermead score was 2 for the atorvastatin group, compared to 3.5 for the placebo group, at 3 months post-injury (chi(2) (1) = 0.0976; p = 0.7547). The change in the Rivermead score between baseline and 3 months was also analyzed. The median decrease in score was 4 for the atorvastatin group and 10.5 for the placebo group (chi(2) (1) = 0.8750; p = 0.3496). No serious adverse events occurred, and there was no significant difference in the incidence of adverse events in the two treatment groups. Atorvastatin administration for 7 days post-injury was safe, but there were no significant differences in neurological recovery post-mTBI with atorvastatin.
C1 [Robertson, Claudia S.; Miller, Emmy R.; Levin, Harvey; McCauley, Stephen R.] Baylor Coll Med, One Baylor Plaza, Houston, TX 77030 USA.
[McCarthy, James J.] Univ Texas Hlth Sci Ctr Houston, Houston, TX 77030 USA.
[Levin, Harvey] Michael E De Bakey Vet Affairs Med Ctr, Houston, TX USA.
[Swank, Paul R.] Univ Texas Hlth Sci Ctr Houston, Sch Publ Hlth, Houston, TX 77030 USA.
[Miller, Emmy R.] Virginia Commonwealth Univ, Richmond, VA USA.
RP Robertson, CS (reprint author), Baylor Coll Med, One Baylor Plaza, Houston, TX 77030 USA.
EM claudiar@bcm.edu
FU Department of Defense [W81XWH-08-2-0132, W81XWH-08-2-0131,
W81XWH-08-2-0133, W81XWH-08-2-0142]
FX This study was supported by the Department of Defense (grant nos.
W81XWH-08-2-0132 [Robertson], W81XWH-08-2-0131 [McCarthy],
W81XWH-08-2-0133 [Levin], and W81XWH-08-2-0142 [Swank]).
NR 32
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U1 2
U2 2
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 0897-7151
EI 1557-9042
J9 J NEUROTRAUM
JI J. Neurotrauma
PD APR
PY 2017
VL 34
IS 7
BP 1394
EP 1401
DI 10.1089/neu.2016.4717
PG 8
WC Critical Care Medicine; Clinical Neurology; Neurosciences
SC General & Internal Medicine; Neurosciences & Neurology
GA ER0FB
UT WOS:000398461600009
ER
PT J
AU Watkins, LE
Sippel, LM
Pietrzak, RH
Hoff, R
Harpaz-Rotem, I
AF Watkins, Laura E.
Sippel, Lauren M.
Pietrzak, Robert H.
Hoff, Rani
Harpaz-Rotem, Ilan
TI Co-occurring aggression and suicide attempt among veterans entering
residential treatment for PTSD: The role of PTSD symptom clusters and
alcohol misuse
SO JOURNAL OF PSYCHIATRIC RESEARCH
LA English
DT Article
DE Posttraumatic stress disorder; Aggression; Suicide; Veterans; Alcohol;
Dysphoric arousal
ID POSTTRAUMATIC-STRESS-DISORDER; DIMENSIONAL STRUCTURE; AFGHANISTAN
VETERANS; MILITARY VETERANS; VIOLENT BEHAVIOR; US VETERANS; ANGER; IRAQ;
CARE; PERPETRATION
AB Aggression and suicidality are two serious public health concerns among U.S. veterans that can co-occur and share many overlapping risk factors. The current study aims to elucidate the contribution of post traumatic stress disorder (PTSD) symptom clusters defined by a five-factor model and alcohol misuse in predicting aggression and suicide attempts among veterans entering residential treatment for PTSD. Participants were 2570 U.S. veterans across 35 Veterans Health Administration sites. Multinomial logistic regression models were used to identify correlates of aggression only (n = 1471; 57.2%), suicide attempts only (n = 41; 1.6%), co-occurring aggression and suicide attempts (n = 202; 7.9%), and neither behavior (n = 856; 33.3%) over the past four months. When compared to veterans endorsing neither behavior, greater PTSD re-experiencing symptoms were related to suicide attempts (odds ratio [OR] = 1.58, 95% confidence interval [CI] = 1.09-2.30), aggression (OR = 1.13, 95% CI = 1.02-1.26), and co-occurring aggression and suicide (OR = 1.38, 95% CI = 1.13-1.68), and higher PTSD dysphoric arousal symptoms and alcohol misuse symptoms were related to aggression (OR = 1.54, 95% CI = 1.38-1.71; OR = 130, 95% CI = 1.18-1.44, respectively) and co-occurring aggression and suicide (OR = 1.66, 95% CI = 1.35-2.04; OR = 1.50, 95% CI = 1.28-1.75, respectively). Our findings suggest that assessment of PTSD symptom clusters and alcohol misuse can potentially help to identify veterans who endorse suicide attempts, aggression, or both concurrently. These results have important implications for risk assessment and treatment planning with U.S. veterans seeking care for PTSD. Published by Elsevier Ltd.
C1 [Watkins, Laura E.; Sippel, Lauren M.; Pietrzak, Robert H.; Hoff, Rani; Harpaz-Rotem, Ilan] US Dept Vet Affairs, Natl Ctr Posttraumat Stress Disorder, VA Connecticut Healthcare Syst, West Haven, CT USA.
[Watkins, Laura E.; Sippel, Lauren M.; Pietrzak, Robert H.; Hoff, Rani; Harpaz-Rotem, Ilan] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA.
[Hoff, Rani; Harpaz-Rotem, Ilan] Northeast Program Evaluat Ctr, VA Connecticut Healthcare Syst, West Haven, CT USA.
RP Watkins, LE (reprint author), VA Connecticut Healthcare Syst, 950 Campbell Ave 151D, West Haven, CT 06516 USA.
EM laura.watkins@yale.edu
FU Department of Veterans Affairs Office of Academic Affiliations, Advanced
Fellowship Program in Mental Illness Research and Treatment; Department
of Veterans Affairs National Center for Posttraumatic Stress Disorder
Clinical Neurosciences Division; VA Connecticut Healthcare System
FX Preparation of this manuscript was supported in part by the Department
of Veterans Affairs Office of Academic Affiliations, Advanced Fellowship
Program in Mental Illness Research and Treatment, the Department of
Veterans Affairs National Center for Posttraumatic Stress Disorder
Clinical Neurosciences Division, and VA Connecticut Healthcare System.
NR 38
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PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0022-3956
EI 1879-1379
J9 J PSYCHIATR RES
JI J. Psychiatr. Res.
PD APR
PY 2017
VL 87
BP 8
EP 14
DI 10.1016/j.jpsychires.2016.12.009
PG 7
WC Psychiatry
SC Psychiatry
GA EO8WK
UT WOS:000396971000002
PM 27984702
ER
PT J
AU Kumar, G
Albright, KC
Donnelly, JP
Shapshak, AH
Harrigan, MR
AF Kumar, Gyanendra
Albright, Karen C.
Donnelly, John P.
Shapshak, Angela Hays
Harrigan, Mark R.
TI Trends in Transcranial Doppler Monitoring in Aneurysmal Subarachnoid
Hemorrhage: A 10-Year Analysis of the Nationwide Inpatient Sample
SO JOURNAL OF STROKE & CEREBROVASCULAR DISEASES
LA English
DT Article
DE Aneurysmal subarachnoid hemorrhage; transcranial Doppler; cerebral
vasospasm; Nationwide Inpatient Sample
ID DELAYED CEREBRAL-ISCHEMIA; ANGIOGRAPHIC VASOSPASM; NEUROCRITICAL CARE;
CT PERFUSION; DOUBLE-BLIND; METAANALYSIS; INFARCTION; ULTRASONOGRAPHY;
RECOMMENDATIONS; MANAGEMENT
AB Background: Transcranial Doppler (TCD) is endorsed by national guidelines for use in aneurysmal subarachnoid hemorrhage (aSAH) for surveillance of cerebral vasospasm (CV). However, nationwide data on utilization of TCD for CV detection and monitoring in aSAH are lacking. Methods: Analysis of nationwide trends in TCD prevalence was performed using Nationwide Inpatient Sample (NIS) data from 2002 to 2011. Raw counts were converted into weighted counts, which were used to generate national estimates. Teaching hospitals were examined separately for TCD utilization rates. All analyses accounted for the complex sampling design and sample discharge weights of the NIS, following Healthcare Cost and Utilization Project-NIS recommendations. The objective was to estimate the proportion of patients with aSAH receiving TCD monitoring using the NIS. Results: Between 2002 and 2011, a total of 256,089 patients were discharged with a diagnosis of aSAH, of which 3850 underwent TCD monitoring. aSAH accounted for an average of 67.1 discharges per 100,000 annually (95% confidence interval [CI] 61.3-72.8). Of these, 1.5% (95% CI 0.4-2.6) underwent TCD examination. In teaching hospitals, aSAH accounted for an average of 108.5 discharges per 100,000 biennially (95% CI, 96.2-120.8), of which 2% (95% CI 1.0-4.0) underwent TCD examination. TCD utilization increased from < 1% during the 2002-2005 period to = 1.5% during the 2006-2011 period (odds ratio 2.3, 95% CI 1.0-5.7), an increase also seen in teaching hospitals. Conclusions: TCD is underused nationally in the care of aSAH. Whereas the prevalence of TCD is low in teaching hospitals, it is nearly nonexistent in nonteaching hospitals.
C1 [Kumar, Gyanendra] Mayo Clin, Dept Neurol, Phoenix, AZ USA.
[Albright, Karen C.; Shapshak, Angela Hays] Univ Alabama Birmingham, Dept Neurol, Comprehens Stroke Ctr, UAB Stn, Birmingham, AL 35294 USA.
[Albright, Karen C.] Birmingham VA Med Ctr, GRECC, Birmingham, AL USA.
[Donnelly, John P.] Univ Alabama Birmingham, COERE, Birmingham, AL USA.
[Donnelly, John P.] Univ Alabama Birmingham, Dept Prevent Med, Birmingham, AL USA.
[Harrigan, Mark R.] Univ Alabama Birmingham, Dept Neurosurg, Birmingham, AL USA.
RP Kumar, G (reprint author), 5777 E Mayo Blvd, Phoenix, AZ 85054 USA.
EM kumar.gyanendra@mayo.edu
FU [AHA14CRP20380256]
FX This study was supported by the following grant: AHA14CRP20380256.
NR 31
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U1 0
U2 0
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 1052-3057
EI 1532-8511
J9 J STROKE CEREBROVASC
JI J. Stroke Cerebrovasc. Dis.
PD APR
PY 2017
VL 26
IS 4
BP 851
EP 857
DI 10.1016/j.jstrokecerebrovasdis.2016.10.033
PG 7
WC Neurosciences; Peripheral Vascular Disease
SC Neurosciences & Neurology; Cardiovascular System & Cardiology
GA EP3AF
UT WOS:000397254200029
PM 27866915
ER
PT J
AU Porter, AL
Margolis, AR
Schoen, RR
Staresinic, CE
Ray, CA
Fletcher, CD
AF Porter, Andrea L.
Margolis, Amanda R.
Schoen, Rebecca R.
Staresinic, Carla E.
Ray, Cheryl A.
Fletcher, Christopher D.
TI Use of an extended INR follow-up interval for Veteran patients in an
anticoagulation clinic
SO JOURNAL OF THROMBOSIS AND THROMBOLYSIS
LA English
DT Article
DE Anticoagulation; Warfarin; Interval; Monitoring; International
normalized ratio (INR); Management
ID ATRIAL-FIBRILLATION; PREDICTING STROKE; WARFARIN; VALIDATION; OUTCOMES;
RISK
AB A prospective, single-arm study of 50 participants evaluated an extended INR follow-up interval to determine the implementation feasibility and safety of an extended interval in Veterans on a stable dose of warfarin. A protocol was designed to allow for a rigorous, yet pragmatic evaluation of a 12-week INR follow-up interval. Feasibility was determined by study enrollment, retention, and participant achievement rates for the extended INR interval. Safety was determined by bleeding and thromboembolism rates. Participants were monitored for 6 months. Despite the long-term stability of participants prior to enrollment, only 56% achieved a 12-week follow-up interval and only 34% of enrolled participants maintained a 12-week interval. Sixteen percent of participants were never eligible for an extension of their INR follow-up interval despite meeting initial enrollment criteria. There were two major bleeding events and one participant who experienced a thromboembolic event. Implementation of an extended interval of INR follow-up appears feasible as participant enrollment goals were met and pharmacists were able to follow the study protocol. However, a lower than expected proportion of participants were able to achieve and maintain an extended INR follow-up interval. Future evaluations are needed to confirm the safety of an extended INR interval.
C1 [Porter, Andrea L.; Margolis, Amanda R.] Univ Wisconsin, Madison Sch Pharm, 777 Highland Ave, Madison, WI 53705 USA.
[Porter, Andrea L.; Margolis, Amanda R.; Schoen, Rebecca R.; Staresinic, Carla E.; Ray, Cheryl A.; Fletcher, Christopher D.] William S Middleton Mem Vet Adm Med Ctr, 2500 Overlook Terrace 119, Madison, WI 53705 USA.
[Schoen, Rebecca R.] Texas Tech Univ, Hlth Sci Ctr, 4500 S Lancaster Rd,Bldg 7, Dallas, TX 75216 USA.
[Fletcher, Christopher D.] Univ Wisconsin, Sch Med & Publ Hlth, Div Hematol, 750 Highland Ave, Madison, WI 53726 USA.
RP Porter, AL (reprint author), Univ Wisconsin, Madison Sch Pharm, 777 Highland Ave, Madison, WI 53705 USA.; Porter, AL (reprint author), William S Middleton Mem Vet Adm Med Ctr, 2500 Overlook Terrace 119, Madison, WI 53705 USA.
EM andrea.porter@wisc.edu
FU Clinical and Translational Science Award (CTSA) program, through the NIH
National Center for Advancing Translational Sciences (NCATS)
[UL1TR000427]
FX The project described was supported by the Clinical and Translational
Science Award (CTSA) program, through the NIH National Center for
Advancing Translational Sciences (NCATS), Grant UL1TR000427. The content
is solely the responsibility of the authors and does not necessarily
represent the official views of the NIH. This material is the result of
work supported with resources and the use of facilities at the William
S. Middleton Memorial Veterans Hospital in Madison, Wisconsin. The
contents do not represent the views of the U.S. Department of Veterans
Affairs or the United States Government. Clinicaltrials.gov:
NCT02392104.
NR 18
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U1 1
U2 1
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0929-5305
EI 1573-742X
J9 J THROMB THROMBOLYS
JI J. Thromb. Thrombolysis
PD APR
PY 2017
VL 43
IS 3
BP 318
EP 325
DI 10.1007/s11239-016-1448-y
PG 8
WC Hematology; Peripheral Vascular Disease
SC Hematology; Cardiovascular System & Cardiology
GA EN2GX
UT WOS:000395829100005
PM 27803999
ER
PT J
AU Kutney-Lee, A
Smith, D
Thorpe, J
del Rosario, C
Ibrahim, S
Ersek, M
AF Kutney-Lee, Ann
Smith, Dawn
Thorpe, Joshua
del Rosario, Cindy
Ibrahim, Said
Ersek, Mary
TI Race/Ethnicity and End-of-Life Care Among Veterans
SO MEDICAL CARE
LA English
DT Article
DE disparities; end-of-life care; veterans
ID FAMILY-MEMBERS PERCEPTIONS; HOSPICE CARE; HEALTH-CARE; AFRICAN-AMERICAN;
PALLIATIVE CARE; RACIAL DISPARITIES; ETHNIC DISPARITIES; MEDICAL-CARE;
QUALITY; OUTCOMES
AB Background: Few studies have examined comprehensively racial/ ethnic variations in quality of end-of-life care.
Objective: Examine end-of-life care quality received by Veterans and their families, comparing racial/ethnic minorities to non-minorities.
Research Design: This is a retrospective, cross-sectional analysis of chart review and survey data.
Subjects: Nearly all deaths in 145 Veterans Affairs Medical Centers nationally (n = 94,697) in addition to Bereaved Family Survey (BFS) data (n = 51,859) from October 2009 to September 2014.
Measures: Outcomes included 15 BFS items and 4 indicators of high-quality end-of-life care, including receipt of a palliative care consult, chaplain visit, bereavement contact, and death in hospice/ palliative care unit. Veteran race/ethnicity was measured via chart review and defined as non-Hispanic white, non-Hispanic black, Hispanic, or other.
Results: In adjusted models, no differences were observed by race/ ethnicity in receipt of a palliative care consult or death in a hospice unit. Although black Veterans were less likely than white Veterans to receive a chaplain visit, Hispanic Veterans were more likely than white Veterans to receive a chaplain visit and to receive a bereavement contact. Less favorable outcomes for racial/ethnic minorities were noted on several BFS items. In comparison with family members of white Veterans, families of minority Veterans were less likely to report excellent overall care, and this difference was largest for black Veterans (48% vs. 62%).
Conclusions: Bereaved family members of minority Veterans generally rate the quality of end-of-life care less favorably than those of white Veterans. Family perceptions are critical to the evaluation of equity and quality of end-of-life care.
C1 [Kutney-Lee, Ann; del Rosario, Cindy; Ersek, Mary] Univ Penn, Sch Nursing, Philadelphia, PA 19104 USA.
[Kutney-Lee, Ann; Smith, Dawn; Ibrahim, Said; Ersek, Mary] Corporal Michael J Crescenz VA Med Ctr, Philadelphia, PA USA.
[Thorpe, Joshua] Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Thorpe, Joshua] Univ Pittsburgh, Sch Pharm, Pittsburgh, PA USA.
[Ibrahim, Said] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA.
RP Kutney-Lee, A (reprint author), Univ Penn, Sch Nursing, Corporal Michael J Crescenz VA Med Ctr, 418 Curie Blvd,Claire M Fagin Hall,Room 385, Philadelphia, PA 19104 USA.
EM akutney@nursing.upenn.edu
NR 44
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U2 2
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0025-7079
EI 1537-1948
J9 MED CARE
JI Med. Care
PD APR
PY 2017
VL 55
IS 4
BP 342
EP 351
PG 10
WC Health Care Sciences & Services; Health Policy & Services; Public,
Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EP8AO
UT WOS:000397598500007
PM 27579913
ER
PT J
AU Hempel, S
Graham, GD
Fu, N
Estrada, E
Chen, AY
Miake-Lye, I
Miles, JNV
Shanman, R
Shekelle, PG
Beroes, JM
Wallin, MT
AF Hempel, Susanne
Graham, Glenn D.
Fu, Ning
Estrada, Elena
Chen, Annie Y.
Miake-Lye, Isomi
Miles, Jeremy N. V.
Shanman, Roberta
Shekelle, Paul G.
Beroes, Jessica M.
Wallin, Mitchell T.
TI A systematic review of the effects of modifiable risk factor
interventions on the progression of multiple sclerosis
SO MULTIPLE SCLEROSIS JOURNAL
LA English
DT Review
DE Multiple sclerosis; MS progression; risk factors; randomized controlled
trial; systematic review
ID POLYUNSATURATED FATTY-ACIDS; TRIAL; EXERCISE
AB Background: Several risk factors are associated with multiple sclerosis (MS) progression and may be amenable to intervention.
Objective: To systematically review the evidence for interventions targeting risk factors for MS progression.
Methods: We searched six databases and existing reviews till March 2015 and consulted with experts to identify randomized controlled trials (RCTs) of interventions targeting MS risk factors (PROSPERO 2015: CRD42015016461).
Results: In total, 37 RCTs met inclusion criteria. Expanded Disability Status Scale (EDSS) scores after exercise interventions did not differ compared with untreated controls (standardized mean differences (SMDs): 0.02; confidence interval (CI): -0.40, 0.44; I-2: 0%; seven RCTs; very low quality of evidence (QoE)). Dietary interventions did not show a statistically significant effect on the relative risk (RR) of progression (RR: 0.86; CI: 0.67, 1.05; I-2: 0%; four RCTs; moderate QoE) compared to placebo. EDSS scores after vitamin D supplementation were not significantly different from placebo (SMD: -0.15; CI: -0.33, 0.02; I-2: 0%; five RCTs; very low QoE).
Conclusion: We did not identify any risk factor interventions with significant effects on MS progression, but the overall QoE was limited. More adequately powered trials are needed on vitamin D supplementation, long-term exercise, and smoking cessation.
C1 [Hempel, Susanne; Fu, Ning; Miles, Jeremy N. V.; Shanman, Roberta; Shekelle, Paul G.] RAND Corp, Southern Calif Evidence Based Practice Ctr, 1776 Main St, Santa Monica, CA 90407 USA.
[Graham, Glenn D.] US Dept Vet Affairs, Specialty Care Serv, Washington, DC USA.
[Graham, Glenn D.] Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA USA.
[Estrada, Elena; Chen, Annie Y.; Miake-Lye, Isomi; Shekelle, Paul G.; Beroes, Jessica M.] West Los Angeles VA Med Ctr, Evidence Based Synth Program ESP Ctr, Los Angeles, CA USA.
[Wallin, Mitchell T.] US Dept Vet Affairs, Multiple Sclerosis Ctr Excellence East, Washington, DC USA.
[Wallin, Mitchell T.] Georgetown Univ, Sch Med, Dept Neurol, Washington, DC USA.
RP Hempel, S (reprint author), RAND Corp, Southern Calif Evidence Based Practice Ctr, 1776 Main St, Santa Monica, CA 90407 USA.
EM susanne_hempel@rand.org
FU Department of Veterans Affairs, Veterans Health Administration, Office
of Research and Development, Quality Enhancement Research Initiative
FX The author(s) disclosed receipt of the following financial support for
the research, authorship, and/or publication of this article: This work
was funded by the Department of Veterans Affairs, Veterans Health
Administration, Office of Research and Development, Quality Enhancement
Research Initiative. The findings and conclusions in this document are
those of the author(s), and the findings and conclusions do not
necessarily represent the views of the Department of Veterans Affairs or
the US government.
NR 15
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Z9 0
U1 2
U2 2
PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 1352-4585
EI 1477-0970
J9 MULT SCLER J
JI Mult. Scler. J.
PD APR
PY 2017
VL 23
IS 4
BP 513
EP 524
DI 10.1177/1352458517690271
PG 12
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA EQ3DD
UT WOS:000397950400007
PM 28151074
ER
PT J
AU Hempel, S
Graham, GD
Fu, N
Estrada, E
Chen, AY
Miake-Lye, I
Miles, JNV
Shanman, R
Shekelle, PG
Beroes, JM
Wallin, MT
AF Hempel, Susanne
Graham, Glenn D.
Fu, Ning
Estrada, Elena
Chen, Annie Y.
Miake-Lye, Isomi
Miles, Jeremy N. V.
Shanman, Roberta
Shekelle, Paul G.
Beroes, Jessica M.
Wallin, Mitchell T.
TI A systematic review of modifiable risk factors in the progression of
multiple sclerosis
SO MULTIPLE SCLEROSIS JOURNAL
LA English
DT Review
DE Multiple sclerosis; multiple sclerosis progression; risk factors;
prognostic study; systematic review
ID VITAMIN-D STATUS; PUBLICATION BIAS; DISABILITY; METAANALYSIS; EXERCISE;
PREDICTOR; SMOKING
AB Background: The presenting symptoms and rate of progression of multiple sclerosis (MS) are very heterogeneous. The diverse clinical manifestations and the clinical course of the disease may vary with modifiable risk factors.
Objective: To systematically review modifiable risk factors and exposures associated with MS progression.
Methods: We searched six databases till March 2015, reference-mined reviews, and consulted with experts (PROSPERO 2015: CRD42015016461). Two reviewers screened and extracted data. We used random meta-analysis models and Grading of Recommendations Assessment, Development, and Evaluation (GRADE) to assess the quality of evidence.
Results: In total, 59 studies met inclusion criteria. Lower vitamin D levels were associated with higher Expanded Disability Status Scale (EDSS) scores (r = -0.22; confidence interval (CI) = -0.32, -0.12; 11 studies; I-2 = 66%), smokers had an increased risk of MS progression (hazard ratio (HR) = 1.55; CI = 1.10, 2.19; I-2 = 72%; seven studies), and there was no association of MS progression with the use of epidural analgesics during childbirth delivery (three studies). There was insufficient evidence to draw conclusions for 11 risk factors due to conflicting results or use of different predictor and outcome measures.
Conclusion: MS progression was consistently associated with low vitamin D levels, and smoking was associated with a more rapid decline in MS disability. Studies used a variety of methods, predictors, and outcomes making it difficult to draw conclusions. Future studies should focus on prospective assessments.
C1 [Hempel, Susanne; Fu, Ning; Miles, Jeremy N. V.; Shanman, Roberta; Shekelle, Paul G.] RAND Corp, Southern Calif Evidence Based Practice Ctr, 1776 Main St, Santa Monica, CA 90407 USA.
[Graham, Glenn D.] US Dept Vet Affairs, Specialty Care Serv, Washington, DC USA.
[Graham, Glenn D.] Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA USA.
[Estrada, Elena; Chen, Annie Y.; Miake-Lye, Isomi; Shekelle, Paul G.; Beroes, Jessica M.] West Los Angeles VA Med Ctr, Evidence Based Synth Program ESP Ctr, Los Angeles, CA USA.
[Wallin, Mitchell T.] US Dept Vet Affairs, Multiple Sclerosis Ctr Excellence East, Washington, DC USA.
[Wallin, Mitchell T.] Georgetown Univ, Sch Med, Dept Neurol, Washington, DC USA.
RP Hempel, S (reprint author), RAND Corp, Southern Calif Evidence Based Practice Ctr, 1776 Main St, Santa Monica, CA 90407 USA.
EM susanne_hempel@rand.org
FU Department of Veterans Affairs, Veterans Health Administration, Office
of Research and Development, Quality Enhancement Research Initiative
FX The author(s) disclosed receipt of the following financial support for
the research, authorship, and/or publication of this article: This work
was funded by the Department of Veterans Affairs, Veterans Health
Administration, Office of Research and Development, Quality Enhancement
Research Initiative. The findings and conclusions in this document are
those of the author(s) who are responsible for its contents; the
findings and conclusions do not necessarily represent the views of the
Department of Veterans Affairs or the US Government.
NR 33
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U1 1
U2 1
PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 1352-4585
EI 1477-0970
J9 MULT SCLER J
JI Mult. Scler. J.
PD APR
PY 2017
VL 23
IS 4
BP 525
EP 533
DI 10.1177/1352458517690270
PG 9
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA EQ3DD
UT WOS:000397950400008
PM 28151053
ER
PT J
AU Hawkins, T
Berman, BD
AF Hawkins, Trevor
Berman, Brian D.
TI Pimavanserin: A novel therapeutic option for Parkinson disease psychosis
SO NEUROLOGY-CLINICAL PRACTICE
LA English
DT Review
ID VISUAL HALLUCINATIONS; CLOZAPINE; QUETIAPINE; RECEPTORS; AGONIST
AB Purpose of review:In April 2016, the Food and Drug Administration (FDA) approved a first-in-class atypical antipsychotic medication called pimavanserin for the treatment of Parkinson disease psychosis (PDP). We aim to inform readers about its indications, effectiveness, and safety profile.
Recent findings:Pimavanserin acts as an inverse agonist at serotonin 5-HT2A receptors and has negligible effects on other receptors, thereby avoiding the D2 receptor antagonism that can potentially worsen motor symptoms. Its FDA approval was based primarily on the results of a single randomized, placebo-controlled phase 3 trial.
Summary:While pimavanserin appears to be a safe, effective, and well-tolerated therapeutic option for PDP, additional clinical trials and open-label extension studies are needed to determine the long-term safety and efficacy of this promising therapy. In the meantime, prescribers need to be aware of the possible adverse effects of pimavanserin including QT interval prolongation and a potential to cause a paradoxical worsening of symptoms.
C1 [Hawkins, Trevor; Berman, Brian D.] Univ Colorado, Dept Neurol, Anschutz Med Campus, Aurora, CO 80045 USA.
[Berman, Brian D.] Denver VA Med Ctr, Neurol Sect, Denver, CO 80220 USA.
RP Berman, BD (reprint author), Univ Colorado, Dept Neurol, Anschutz Med Campus, Aurora, CO 80045 USA.; Berman, BD (reprint author), Denver VA Med Ctr, Neurol Sect, Denver, CO 80220 USA.
EM brian.berman@ucdenver.edu
NR 25
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U1 1
U2 1
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 2163-0402
EI 2163-0933
J9 NEUROL-CLIN PRACT
JI Neurol.-Clin. Pract.
PD APR
PY 2017
VL 7
IS 2
BP 157
EP 162
DI 10.1212/CPJ.0000000000000342
PG 6
WC Clinical Neurology
SC Neurosciences & Neurology
GA ER5QL
UT WOS:000398856700012
ER
PT J
AU Busch, RA
Curtis, CS
Kight, CE
Leverson, GE
Ma, Y
Maursetter, L
Kudsk, KA
AF Busch, Rebecca A.
Curtis, Caitlin S.
Kight, Cassandra E.
Leverson, Glen E.
Ma, Yue
Maursetter, Laura
Kudsk, Kenneth A.
TI An Institutional Change in Continuous Renal Replacement Therapy:
Nutrition Support Team Resolves Resultant Severe Hypophosphatemia
SO NUTRITION IN CLINICAL PRACTICE
LA English
DT Article
DE parenteral nutrition; renal replacement therapy; phosphate;
hypophosphatemia; renal replacement fluids
ID ACUTE KIDNEY INJURY; DRUG SHORTAGES; FAILURE; IMPACT
AB Background: Critically ill patients with acute kidney injury may require parenteral nutrition (PN) and continuous renal replacement therapy (CRRT). Introduction of a phosphate-free premixed renal replacement fluid without system-wide education in May 2011 resulted in increased incidence of hypophosphatemia, necessitating change in practice. Changes included (1) maximizing phosphate in PN, (2) modifying the CRRT order set, and (3) developing a CRRT competency evaluation for nutrition support team members. This study evaluates the effect of these changes on the incidence of hypophosphatemia. Methods: Phosphate levels and predicated probability of hypophosphatemia were evaluated for patients receiving PN and CRRT over 3 time periods: prior to implementing the changes (preimplementation), during change implementation (intermediate), and following implementation (postimplementation). Hypophosphatemia was defined as a serum phosphate level <2.5 mg/dL. Generalized linear mixed models were applied for statistical analysis. Results: The retrospective study includes 336 measures from 49 patients. Patients in the intermediate and postimplementation periods were not significantly different from each other and had significantly higher mean phosphate levels than patients in the preimplementation period (P <.0001). They were also less likely to develop hypophosphatemia compared with preimplementation patients (intermediate: odds ratio [OR], 0.07; 95% confidence interval [CI], 0.03-0.18, P <.0001; postimplementation: OR, 0.09; 95% CI, 0.03-0.27, P <.0001). Conclusions: Modifications in phosphate dosing together with CRRT education reduced the incidence of hypophosphatemia in PN patients receiving CRRT. Communication of significant changes in clinical care should be shared with all services prior to implementation. Communication and planning between services caring for complex patients are necessary to prevent systems-based problems.
C1 [Busch, Rebecca A.; Leverson, Glen E.; Ma, Yue; Kudsk, Kenneth A.] Univ Wisconsin, Sch Med & Publ Hlth, Dept Surg, G5-341 Clinical Sci Ctr,600 Highland Ave, Madison, WI 53792 USA.
[Curtis, Caitlin S.] Univ Wisconsin, Hosp & Clin, Dept Pharm, Madison, WI 53792 USA.
[Kight, Cassandra E.] Univ Wisconsin, Hosp & Clin, Clin Nutr Serv, Madison, WI 53792 USA.
[Maursetter, Laura] Univ Wisconsin, Sch Med & Publ Hlth, Dept Internal Med, Nephrol Sect, Madison, WI USA.
[Kudsk, Kenneth A.] William S Middleton Mem Vet Adm Med Ctr, Veteran Adm Surg Serv, Madison, WI USA.
RP Kudsk, KA (reprint author), Univ Wisconsin, Sch Med & Publ Hlth, Dept Surg, G5-341 Clinical Sci Ctr,600 Highland Ave, Madison, WI 53792 USA.
EM kudsk@surgery.wisc.edu
FU Surgical Oncology Research Training Program [T32CA090217]
FX The project described was supported in part (to R.A.B.) by the Surgical
Oncology Research Training Program (grant number T32CA090217).
NR 14
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U1 0
U2 0
PU SAGE PUBLICATIONS INC
PI THOUSAND OAKS
PA 2455 TELLER RD, THOUSAND OAKS, CA 91320 USA
SN 0884-5336
EI 1941-2452
J9 NUTR CLIN PRACT
JI Nutr. Clin. Pract.
PD APR
PY 2017
VL 32
IS 2
BP 245
EP 251
DI 10.1177/0884533616662987
PG 7
WC Nutrition & Dietetics
SC Nutrition & Dietetics
GA EQ5DO
UT WOS:000398102200015
PM 27589256
ER
PT J
AU Auerbach, BJ
Wolf, FM
Hikida, A
Vallila-Buchman, P
Littman, A
Thompson, D
Louden, D
Taber, DR
Krieger, J
AF Auerbach, Brandon J.
Wolf, Fred M.
Hikida, Abigail
Vallila-Buchman, Petra
Littman, Alyson
Thompson, Douglas
Louden, Diana
Taber, Daniel R.
Krieger, James
TI Fruit Juice and Change in BMI: A Meta-analysis
SO PEDIATRICS
LA English
DT Review
ID BODY-MASS INDEX; BEVERAGE CONSUMPTION; WEIGHT STATUS; VEGETABLE INTAKE;
UNITED-STATES; CHILDREN; ADOLESCENTS; GAIN; RISK; ASSOCIATION
AB CONTEXT: Whether 100% fruit juice consumption causes weight gain in children remains abstract controversial.
OBJECTIVE: To determine the association between 100% fruit juice consumption and change in BMI or BMI z score in children.
DATA SOURCES: PubMed, Embase, CINAHL, and Cochrane databases.
STUDY SELECTION: Longitudinal studies examining the association of 100% fruit juice and change in BMI measures were included.
DATA EXTRACTION: Two independent reviewers extracted data using a predesigned data collection form.
RESULTS: Of the 4657 articles screened, 8 prospective cohort studies (n = 34 470 individual children) met the inclusion criteria. Controlling for total energy intake, 1 daily 6-to 8-oz serving increment of 100% fruit juice was associated with a 0.003 (95% CI: 0.001 to 0.004) unit increase in BMI z score over 1 year in children of all ages (0% increase in BMI percentile). In children ages 1 to 6 years, 1 serving increment was associated with a 0.087 (95% confidence interval: 0.008 to 0.167) unit increase in BMI z score (4% increase in BMI percentile). 100% fruit juice consumption was not associated with BMI z score increase in children ages 7 to 18 years.
LIMITATIONS: All observational studies; studies differed in exposure assessment and covariate adjustment.
CONCLUSIONS: Consumption of 100% fruit juice is associated with a small amount of weight gain in children ages 1 to 6 years that is not clinically significant, and is not associated with weight gain in children ages 7 to 18 years. More studies are needed in children ages 1 to 6 years.
C1 [Auerbach, Brandon J.; Krieger, James] Univ Washington, Dept Med, Seattle, WA USA.
[Auerbach, Brandon J.; Wolf, Fred M.; Littman, Alyson] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA.
[Wolf, Fred M.] Univ Washington, Dept Biomed Informat & Med Educ, Seattle, WA 98195 USA.
[Wolf, Fred M.; Hikida, Abigail; Krieger, James] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA.
[Louden, Diana] Univ Washington, Univ Lib, Seattle, WA 98195 USA.
[Hikida, Abigail; Littman, Alyson] VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Hikida, Abigail; Littman, Alyson] Northwest VA Hlth Serv, Res & Dev Ctr Excellence, Seattle, WA USA.
[Vallila-Buchman, Petra; Taber, Daniel R.; Krieger, James] Hlth Food Amer, Seattle, WA USA.
[Thompson, Douglas] Thompson Res Consulting, Chicago, IL USA.
RP Auerbach, BJ (reprint author), Univ Washington, Harborview Med Ctr, Div Gen Internal Med, Box 359780,325 Ninth Ave, Seattle, WA 98104 USA.
EM auerbach@post.harvard.edu
OI Louden, Diana/0000-0002-6161-5557
FU Ruth L. Kirschstein National Research Service of the National Institutes
of Health through the University of Washington [T32HP10002]
FX Dr Auerbach is funded by the Ruth L. Kirschstein National Research
Service of the National Institutes of Health through the University of
Washington (grant T32HP10002). The funding sources had no role in the
design, conduct, or analysis of the study, or the decision to submit the
manuscript for publication. Funded by the National Institutes of Health
(NIH).
NR 46
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U1 0
U2 0
PU AMER ACAD PEDIATRICS
PI ELK GROVE VILLAGE
PA 141 NORTH-WEST POINT BLVD,, ELK GROVE VILLAGE, IL 60007-1098 USA
SN 0031-4005
EI 1098-4275
J9 PEDIATRICS
JI Pediatrics
PD APR
PY 2017
VL 139
IS 4
AR UNSP e20162454
DI 10.1542/peds.2016-2454
PG 12
WC Pediatrics
SC Pediatrics
GA ER2CU
UT WOS:000398602400017
ER
PT J
AU Raz, M
AF Raz, Mical
TI Unintended Consequences of Expanded Mandatory Reporting Laws
SO PEDIATRICS
LA English
DT Editorial Material
ID ABUSE
C1 [Raz, Mical] Univ Penn, Perelman Sch Med, Philadelphia Vet Affairs Med Ctr, Robert Wood Johnson Clin Scholars Program, Philadelphia, PA 19104 USA.
RP Raz, M (reprint author), Univ Penn, Perelman Sch Med, Philadelphia VA Med Ctr, Robert Wood Johnson Clin Scholars Program, 1310 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
EM micalraz@mail.med.upenn.edu
NR 10
TC 0
Z9 0
U1 0
U2 0
PU AMER ACAD PEDIATRICS
PI ELK GROVE VILLAGE
PA 141 NORTH-WEST POINT BLVD,, ELK GROVE VILLAGE, IL 60007-1098 USA
SN 0031-4005
EI 1098-4275
J9 PEDIATRICS
JI Pediatrics
PD APR
PY 2017
VL 139
IS 4
AR e0163511
DI 10.1542/peds.2016-3511
PG 3
WC Pediatrics
SC Pediatrics
GA ER2CU
UT WOS:000398602400042
ER
PT J
AU Zhang, YQ
Unnikrishnan, A
Deepa, SS
Liu, YH
Li, Y
Ikeno, Y
Sosnowska, D
Van Remmen, H
Richardson, A
AF Zhang, Yiqiang
Unnikrishnan, Archana
Deepa, Sathyaseelan S.
Liu, Yuhong
Li, Yan
Ikeno, Yuji
Sosnowska, Danuta
Van Remmen, Holly
Richardson, Arlan
TI A new role for oxidative stress in aging: The accelerated aging
phenotype in Sod1(-/-) mice is correlated to increased cellular
senescence
SO REDOX BIOLOGY
LA English
DT Article
DE Cellular senescence; Superoxide dismutase; Aging; Inflammation; DNA
damage; Dietary restriction; Oxidative stress
ID LOW-GRADE INFLAMMATION; SECRETORY PHENOTYPE; NLRP3 INFLAMMASOME;
HUMAN-CELLS; DNA-DAMAGE; LIFE-SPAN; IN-VIVO; NECROPTOSIS; BIOMARKER;
DISEASES
AB In contrast to other mouse models that are deficient in antioxidant enzymes, mice null for Cu/Zn-superoxide dismutase (Sod1(-/-) mice) show a major decrease in lifespan and several accelerated aging phenotypes. The goal of this study was to determine if cell senescence might be a contributing factor in the accelerated aging phenotype observed in the Sod1(-/-) mice. We focused on kidney because it is a tissue that has been shown to a significant increase in senescent cells with age. The Sod1(-/-) mice are characterized by high levels of DNA oxidation in the kidney, which is attenuated by DR. The kidney of the Sod1(-/-) mice also have higher levels of double strand DNA breaks than wild type (WT) mice. Expression (mRNA and protein) of p16 and p21, two of the markers of cellular senescence, which increased with age, are increased significantly in the kidney of Sod1(-/-)mice as is beta-gal staining cells. In addition, the senescence associated secretory phenotype was also increased significantly in the kidney of Sod1(-/-) mice compared to WT mice as measured by the expression of transcripts for IL-6 and IL-1 beta. Dietary restriction of the Sod1(-/-) mice attenuated the increase in DNA damage, cellular senescence, and expression of IL-6 and IL-1 beta. Interestingly, the Sod1-/- mice showed higher levels of circulating cytokines than WT mice, suggesting that the accelerated aging phenotype shown by the Sod1(-/-) mice could result from increased inflammation arising from an accelerated accumulation of senescent cells. Based on our data with Sod1(-/-) mice, we propose that various bouts of increased oxidative stress over the lifespan of an animal leads to the accumulation of senescent cells. The accumulation of senescent cells in turn leads to increased inflammation, which plays a major role in the loss of function and increased pathology that are hallmark features of aging.
C1 [Zhang, Yiqiang] Univ Texas Hlth Sci Ctr San Antonio, Greehy Childrens Canc Inst, San Antonio, TX 78229 USA.
[Liu, Yuhong; Li, Yan] Univ Texas Hlth Sci Ctr San Antonio, Dept Cellular Biol, San Antonio, TX 78229 USA.
[Liu, Yuhong; Li, Yan] Univ Texas Hlth Sci Ctr San Antonio, Dept Biol Struct, San Antonio, TX 78229 USA.
[Ikeno, Yuji] Univ Texas Hlth Sci Ctr San Antonio, Dept Pathol, San Antonio, TX 78229 USA.
[Ikeno, Yuji] South Texas Vet Hlth Care Syst, GRECC, San Antonio, TX USA.
[Unnikrishnan, Archana; Deepa, Sathyaseelan S.; Sosnowska, Danuta; Richardson, Arlan] Univ Oklahoma, Hlth Sci Ctr, Dept Geriatr Med, Oklahoma City, OK 73104 USA.
[Unnikrishnan, Archana; Deepa, Sathyaseelan S.; Sosnowska, Danuta; Richardson, Arlan] Univ Oklahoma, Hlth Sci Ctr, Reynolds Oklahoma Ctr Aging, Oklahoma City, OK 73104 USA.
[Van Remmen, Holly] Oklahoma Med Res Fdn, 825 NE 13th St, Oklahoma City, OK 73104 USA.
[Van Remmen, Holly; Richardson, Arlan] Oklahoma City VA Med Ctr, Oklahoma City, OK USA.
RP Richardson, A (reprint author), Univ Oklahoma, Hlth Sci Ctr, Dept Geriatr Med, Oklahoma City, OK 73104 USA.; Richardson, A (reprint author), Univ Oklahoma, Hlth Sci Ctr, Reynolds Oklahoma Ctr Aging, Oklahoma City, OK 73104 USA.
EM Arlan-richardson@ouhsc.edu
FU NIH [P01AG020591, P01AG051442, R01 AG045693]; Senior Research Career
Scientist awards from the Department of Veteran Affairs
FX This study was supported by NIH grants to HVR and AR (P01AG020591 and
P01AG051442) and an NIH grant to AR and AU (R01 AG045693). AR and HVR
are supported by the Senior Research Career Scientist awards from the
Department of Veteran Affairs.
NR 49
TC 0
Z9 0
U1 3
U2 3
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 2213-2317
J9 REDOX BIOL
JI Redox Biol.
PD APR
PY 2017
VL 11
BP 30
EP 37
DI 10.1016/j.redox.2016.10.014
PG 8
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA EQ6RY
UT WOS:000398212000004
PM 27846439
ER
PT J
AU Redmann, M
Wani, WY
Volpicelli-Daley, L
Darley-Usmar, V
Zhang, JH
AF Redmann, Matthew
Wani, Willayat Y.
Volpicelli-Daley, Laura
Darley-Usmar, Victor
Zhang, Jianhua
TI Trehalose does not improve neuronal survival on exposure to
alpha-synuclein pre-formed fibrils
SO REDOX BIOLOGY
LA English
DT Article
DE Parkinson's disease; Alpha-synuclein fibrils; P-alpha-synuclein
trehalose; Autophagy; LC3-II
ID PARKINSONS-DISEASE; LYSOSOMAL BIOGENESIS; LEWY BODIES; AGGREGATION;
AUTOPHAGY; NEURODEGENERATION; DEGRADATION; TOLERANCE; PATHOLOGY;
CHAPERONE
AB Parkinson's disease is a debilitating neurodegenerative disorder that is pathologically characterized by intracellular inclusions comprised primarily of alpha-synuclein (alpha Syn) that can also be transmitted from neuron to neuron. Several lines of evidence suggest that these inclusions cause neurodegeneration. Thus exploring strategies to improve neuronal survival in neurons with alpha Syn aggregates is critical. Previously, exposure to alpha Syn pre-formed fibrils (PFFs) has been shown to induce aggregation of endogenous alpha Syn resulting in cell death that is exacerbated by either starvation or inhibition of mTOR by rapamycin, both of which are able to induce autophagy, an intracellular protein degradation pathway. Since mTOR inhibition may also inhibit protein synthesis and starvation itself can be detrimental to neuronal survival, we investigated the effects of autophagy induction on neurons with alpha Syn inclusions by a starvation and mTOR-independent autophagy induction mechanism. We exposed mouse primary cortical neurons to PFFs to induce inclusion formation in the presence and absence of the disaccharide trehalose, which has been proposed to induce autophagy and stimulate lysosomal biogenesis. As expected, we observed that on exposure to PFFs, there was increased abundance of pS129-alpha Syn aggregates and cell death. Trehalose alone increased LC3-II levels, consistent with increased autophagosome levels that remained elevated with PFF exposure. Interestingly, trehalose alone increased cell viability over a 14-d time course. Trehalose was also able to restore cell viability to control levels, but PFFs still exhibited toxic effects on the cells. These data provide essential information regarding effects of trehalose on aSyn accumulation and neuronal survival on exposure to PFF.
C1 [Redmann, Matthew; Wani, Willayat Y.; Darley-Usmar, Victor; Zhang, Jianhua] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL USA.
[Redmann, Matthew; Wani, Willayat Y.; Darley-Usmar, Victor; Zhang, Jianhua] Univ Alabama Birmingham, Ctr Free Rad Biol, Birmingham, AL USA.
[Volpicelli-Daley, Laura; Zhang, Jianhua] Univ Alabama Birmingham, Ctr Neurodegenerat Expt Therapeut, Birmingham, AL USA.
[Volpicelli-Daley, Laura] Univ Alabama Birmingham, Dept Neurol, Birmingham, AL 35294 USA.
[Zhang, Jianhua] Birmingham VA Med Ctr, Dept Vet Affairs, Birmingham, AL USA.
RP Zhang, JH (reprint author), Univ Alabama Birmingham, Dept Pathol, BMRII 534, 901 19th St S, Birmingham, AL 35294 USA.
EM zhanja@uab.edu
FU [NIHR01-NS064090]
FX We would like to thank Dr. Laura Volpicelli-Daley and members of the
Zhang and Darley-Usmar laboratories for discussion and technical
assistance. This work was supported by NIHR01-NS064090 (to JZ).
NR 34
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U1 1
U2 1
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 2213-2317
J9 REDOX BIOL
JI Redox Biol.
PD APR
PY 2017
VL 11
BP 429
EP 437
DI 10.1016/j.redox.2016.12.032
PG 9
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA EQ6RY
UT WOS:000398212000043
PM 28068606
ER
PT J
AU Vogelmeier, CF
Criner, GJ
Martinez, FJ
Anzueto, A
Barnes, PJ
Bourbeau, J
Celli, BR
Chen, RC
Decramer, M
Fabbri, LM
Frith, P
Halpin, DMG
Lopez Varela, MV
Nishimura, M
Roche, N
Rodriguez-Roisin, R
Sin, DD
Singh, D
Stockley, R
Vestbo, J
Wedzicha, JA
Agusti, A
AF Vogelmeier, Claus F.
Criner, Gerard J.
Martinez, Fernando J.
Anzueto, Antonio
Barnes, Peter J.
Bourbeau, Jean
Celli, Bartolome R.
Chen, Rongchang
Decramer, Marc
Fabbri, Leonardo M.
Frith, Peter
Halpin, David M. G.
Lopez Varela, M. Victorina
Nishimura, Masaharu
Roche, Nicolas
Rodriguez-Roisin, Roberto
Sin, Don D.
Singh, Dave
Stockley, Robert
Vestbo, Jorgen
Wedzicha, Jadwiga A.
Agusti, Alvar
TI Global Strategy for the Diagnosis, Management and Prevention of Chronic
Obstructive Lung Disease 2017 Report GOLD Executive Summary
SO RESPIROLOGY
LA English
DT Article
DE chronic obstructive pulmonary disease; COPD diagnosis; COPD management;
COPD prevention
ID RANDOMIZED CONTROLLED-TRIAL; AIR-FLOW OBSTRUCTION; POSITIVE-PRESSURE
VENTILATION; PLACEBO-CONTROLLED TRIAL; QUALITY-OF-LIFE; INHALED
FLUTICASONE FUROATE; CHRONIC RESPIRATORY-DISEASE; VOLUME-REDUCTION
SURGERY; BONE-MINERAL DENSITY; REQUIRING MECHANICAL VENTILATION
AB This Executive Summary of the Global Strategy for the Diagnosis, Management and Prevention of COPD, Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2017 Report focuses primarily on the revised and novel parts of the document. The most significant changes include: (i) the assessment of chronic obstructive pulmonary disease has been refined to separate the spirometric assessment from symptom evaluation. ABCD groups are now proposed to be derived exclusively from patient symptoms and their history of exacerbations; (ii) for each of the groups A to D, escalation strategies for pharmacological treatments are proposed; (iii) the concept of deescalation of therapy is introduced in the treatment assessment scheme; (iv) non-pharmacological therapies are comprehensively presented and (v) the importance of co-morbid conditions in managing COPD is reviewed.
C1 [Vogelmeier, Claus F.] Univ Marburg, German Ctr Lung Res DZL, Marburg, Germany.
[Criner, Gerard J.] Temple Univ, Lewis Katz Sch Med, Philadelphia, PA 19122 USA.
[Martinez, Fernando J.] New York Presbyterian Hosp, Weill Cornell Med Ctr, New York, NY USA.
[Anzueto, Antonio] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Anzueto, Antonio] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Barnes, Peter J.; Wedzicha, Jadwiga A.] Imperial Coll, Natl Heart & Lung Inst, London, England.
[Bourbeau, Jean] McGill Univ, Ctr Hlth, Montreal, PQ, Canada.
[Celli, Bartolome R.] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA.
[Chen, Rongchang] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Inst Resp Dis, State Key Lab Resp Dis, Guangzhou, Guangdong, Peoples R China.
[Decramer, Marc] Univ Leuven, Leuven, Belgium.
[Fabbri, Leonardo M.] Univ Modena & Reggio Emilia, Modena, Italy.
[Frith, Peter] Flinders Univ S Australia, Fac Med, Bedford Pk, SA, Australia.
[Halpin, David M. G.] Royal Devon & Exeter Hosp, Exeter, Devon, England.
[Lopez Varela, M. Victorina] Univ Republica, Hosp Maciel, Montevideo, Uruguay.
[Nishimura, Masaharu] Hokkaido Univ, Sch Med, Sapporo, Hokkaido, Japan.
[Roche, Nicolas] Univ Paris 05, Hop Cochin, AP HP, Paris, France.
[Rodriguez-Roisin, Roberto] Hosp Clin Univ Barcelona, Thorax Inst, Barcelona, Spain.
[Sin, Don D.] Univ British Columbia, St Pauls Hosp, Vancouver, BC, Canada.
[Singh, Dave; Vestbo, Jorgen] Univ Manchester, Manchester, Lancs, England.
[Stockley, Robert] Univ Hosp, Birmingham, W Midlands, England.
[Agusti, Alvar] Univ Barcelona, Hosp Clin, Ctr Invest Biomed Red Enfermedade Resp, Barcelona, Spain.
RP Vogelmeier, CF (reprint author), Univ Marburg, Dept Med Pulm & Crit Care Med, Baldingerstr 1, D-35043 Marburg, Germany.
EM Claus.Vogelmeier@med.uni-marburg.de
NR 339
TC 1
Z9 1
U1 7
U2 7
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1323-7799
EI 1440-1843
J9 RESPIROLOGY
JI Respirology
PD APR
PY 2017
VL 22
IS 3
BP 575
EP 601
DI 10.1111/resp.13012
PG 27
WC Respiratory System
SC Respiratory System
GA EQ3BY
UT WOS:000397947200023
PM 28150362
ER
PT J
AU Restrepo, MI
Chalmers, JD
Song, YL
Mallow, C
Hewlett, J
Maldonado, F
Yarmus, L
AF Restrepo, Marcos I.
Chalmers, James D.
Song, Yuanlin
Mallow, Christopher
Hewlett, Justin
Maldonado, Fabien
Yarmus, Lonny
TI Year in review 2016: Respiratory infections, acute respiratory distress
syndrome, pleural diseases, lung cancer and interventional pulmonology
SO RESPIROLOGY
LA English
DT Review
DE acute respiratory distress syndrome; bronchoscopy and interventional
techniques; lung cancer; pleural disease; respiratory infections
(non-tuberculous)
ID COMMUNITY-ACQUIRED PNEUMONIA; RESISTANT STAPHYLOCOCCUS-AUREUS;
CARE-ASSOCIATED PNEUMONIA; TUBERCULOSIS INFECTION; FLEXIBLE
BRONCHOSCOPY; PROGNOSTIC-FACTORS; METAANALYSIS; INJURY; BRONCHIECTASIS;
MANAGEMENT
C1 [Restrepo, Marcos I.] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Restrepo, Marcos I.] Univ Texas Hlth, San Antonio, TX USA.
[Mallow, Christopher; Yarmus, Lonny] Johns Hopkins Univ, Sch Med, Baltimore, MD USA.
[Hewlett, Justin; Maldonado, Fabien] Vanderbilt Univ, Sch Med, Nashville, TN 37212 USA.
[Chalmers, James D.] Univ Dundee, Ninewells Hosp & Med Sch, Scottish Ctr Resp Res, Dundee, Scotland.
[Chalmers, James D.] Univ Dundee, Ninewells Hosp & Med Sch, Sch Med, Dundee, Scotland.
[Song, Yuanlin] Fudan Univ, Zhongshan Hosp, Dept Pulm Med, Shanghai, Peoples R China.
RP Chalmers, JD (reprint author), Ninewells Hosp & Med Sch, Scottish Ctr Resp Res, Ninewells Ave, Dundee DD1 9SY, Scotland.
EM j.chalmers@dundee.ac.uk
FU AstraZeneca; Bayer Healthcare; Pfizer Ltd; GlaxoSmithKline; Centurion,
Inc; Department of Defense, USA
FX J.D.C. reports grant support from AstraZeneca, Bayer Healthcare, Pfizer
Ltd and GlaxoSmithKline. F.M. has consulted for Boston Scientific and
Intuitive, Inc; and received grant support from Centurion, Inc and from
the Department of Defense, USA.
NR 66
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1323-7799
EI 1440-1843
J9 RESPIROLOGY
JI Respirology
PD APR
PY 2017
VL 22
IS 3
BP 602
EP 611
DI 10.1111/resp.13016
PG 10
WC Respiratory System
SC Respiratory System
GA EQ3BY
UT WOS:000397947200024
PM 28244617
ER
PT J
AU Giordano, S
Zhao, XM
Chen, YF
Litovsky, SH
Hage, FG
Townes, TM
Sun, CW
Wu, LC
Oparil, S
Xing, DQ
AF Giordano, Samantha
Zhao, Xiangmin
Chen, Yiu-Fai
Litovsky, Silvio H.
Hage, Fadi G.
Townes, Tim M.
Sun, Chiao-Wang
Wu, Li-Chen
Oparil, Suzanne
Xing, Dongqi
TI Induced Pluripotent Stem Cell-Derived Endothelial Cells Overexpressing
Interleukin-8 Receptors A/B and/or C-C Chemokine Receptors 2/5 Inhibit
Vascular Injury Response
SO STEM CELLS TRANSLATIONAL MEDICINE
LA English
DT Article
DE iPS-endothelial cells; Targeted cell therapy; Vascular injury;
Interleukin 8 receptor; C-C chemokine receptor 2/5
ID MONOCYTE CHEMOATTRACTANT PROTEIN-1; SMOOTH-MUSCLE-CELLS; ADVENTITIAL
FIBROBLAST MIGRATION; CHANGES NEOINTIMAL HYPERPLASIA;
ATHEROSCLEROSIS-PRONE MICE; RAT CAROTID ARTERIES; E-DEFICIENT MICE;
KNOCKOUT MICE; IN-VITRO; HYPERCHOLESTEROLEMIC RABBITS
AB Recruitment of neutrophils and monocytes/macrophages to the site of vascular injury is mediated by binding of chemoattractants to interleukin (IL) 8 receptors RA and RB (IL8RA/B) C-C chemokine receptors (CCR) 2 and 5 expressed on neutrophil and monocyte/macrophage membranes. Endothelial cells (ECs) derived from rat-induced pluripotent stem cells (RiPS) were transduced with adenovirus containing cDNA of IL8RA/B and/or CCR2/5. We hypothesized that RiPS-ECs overexpressing IL8RA/B (RiPS-IL8RA/B-ECs), CCR2/5 (RiPS-CCR2/5-ECs), or both receptors (RiPS-IL8RA/B+CCR2/5-ECs) will inhibit inflammatory responses and neointima formation in balloon-injured rat carotid artery. Twelve-week-old male Sprague-Dawley rats underwent balloon injury of the right carotid artery and intravenous infusion of (a) saline vehicle, (b) control RiPS-Null-ECs (ECs transduced with empty virus), (c) RiPS-IL8RA/B-ECs, (d) RiPS-CCR2/5-ECs, or (e) RiPS-IL8RA/B+CCR2/5-ECs. Inflammatory mediator expression and leukocyte infiltration were measured in injured and uninjured arteries at 24 hours postinjury by enzyme-linked immunosorbent assay (ELISA) and immunohistochemistry, respectively. Neointima formation was assessed at 14 days postinjury. RiPS-ECs expressing the IL8RA/B or CCR2/5 homing device targeted the injured arteries and decreased injury-induced inflammatory cytokine expression, neutrophil/macrophage infiltration, and neointima formation. Transfused RiPS-ECs overexpressing IL8RA/B and/or CCR2/5 prevented inflammatory responses and neointima formation after vascular injury. Targeted delivery of iPS-ECs with a homing device to inflammatory mediators in injured arteries provides a novel strategy for the treatment of cardiovascular diseases.
C1 [Giordano, Samantha; Zhao, Xiangmin; Chen, Yiu-Fai; Hage, Fadi G.; Oparil, Suzanne; Xing, Dongqi] Univ Alabama Birmingham, Dept Med, Div Cardiovasc Dis, Vascu Biol & Hypertens Program, 1010 Zeigler Res Bldg,703 19th St South, Birmingham, AL 35294 USA.
[Litovsky, Silvio H.] Univ Alabama Birmingham, Dept Pathol, Div Anat Pathol, Birmingham, AL 35294 USA.
[Hage, Fadi G.] Birmingham Vet Affairs Med Ctr, Cardiol Sect, Birmingham, AL USA.
[Townes, Tim M.; Sun, Chiao-Wang; Wu, Li-Chen] Univ Alabama Birmingham, Dept Biochem & Mol Genet, Birmingham, AL USA.
RP Xing, DQ (reprint author), Univ Alabama Birmingham, Dept Med, Div Cardiovasc Dis, Vascu Biol & Hypertens Program, 1010 Zeigler Res Bldg,703 19th St South, Birmingham, AL 35294 USA.
EM dqxing@uab.edu
FU National Institutes of Health (NIH) [RO1 HL116727, RO1 HL087980, R56
HL128285-01A1, T32 HL07457]; American Heart Association (AHA) [SDG
0930098N]; Veterans Affairs Biomedical Laboratory Research & Development
Service Merit Award [OMB 4040-0001]; CCVC William W. Featheringill
Innovative Award of the University of Alabama at Birmingham
FX This study was supported by National Institutes of Health (NIH) grants:
RO1 HL116727 (Y.-F. Chen), RO1 HL087980 (S. Oparil), R56 HL128285-01A1
(D. Xing), and T32 HL07457 (S. Oparil, S. Giordano); an American Heart
Association (AHA) grant SDG 0930098N (F. G. Hage); a Veterans Affairs
Biomedical Laboratory Research & Development Service Merit Award OMB
4040-0001 (F. G. Hage); and a CCVC William W. Featheringill Innovative
Award of the University of Alabama at Birmingham (Y.-F. Chen).
NR 67
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2157-6564
EI 2157-6580
J9 STEM CELL TRANSL MED
JI Stem Cells Transl. Med.
PD APR
PY 2017
VL 6
IS 4
BP 1168
EP 1177
DI 10.1002/sctm.16-0316
PG 10
WC Cell & Tissue Engineering
SC Cell Biology
GA EQ6QB
UT WOS:000398206500012
PM 28233474
ER
PT J
AU Jay, CL
Washburn, K
Dean, PG
Helmick, RA
Pugh, JA
Stegall, MD
AF Jay, Colleen L.
Washburn, Kenneth
Dean, Patrick G.
Helmick, Ryan A.
Pugh, Jacqueline A.
Stegall, Mark D.
TI Survival Benefit in Older Patients Associated With Earlier Transplant
With High KDPI Kidneys
SO TRANSPLANTATION
LA English
DT Article
ID EUROTRANSPLANT SENIOR PROGRAM; RENAL-TRANSPLANTATION; RECIPIENTS;
DIALYSIS; OUTCOMES; RISK; AGE; THROMBOSIS; VOLUME
AB Background. Given high dialysis mortality rates for patients older than 60 years, accepting a kidney with a high Kidney Donor Profile Index (KDPI) score could enable earlier and potentially preemptive transplantation (preKT). However, evidence regarding the risks of high KDPI allografts in older patients is limited. Our objective was to determine the relative benefit for older patients of KDPI greater than 85% transplant either preemptively or not compared with remaining on the waitlist. Methods. United Network of Organ Sharing data from 2003 to 2012 for adult deceased donor kidney transplant candidates was analyzed to evaluate patient survival in patients older than 60 years for preKT and non-preKT KDPI greater than 85% transplants compared with candidates remaining on the waitlist including patients who received KDPI 0% to 85% transplants according to multivariate Cox regression models. Results. In the first year posttransplant for KDPI greater than 85% of transplants in recipients older than 60 years, preKT had a reduced mortality hazard (hazards ratio [HR], 0.61; 95% confidence interval [95% CI], 0.41-0.90) and non-preKT an increased mortality hazard (HR, 1.15; 95% CI, 1.03-1.27) compared with the waitlist including KDPI 0% to 85% transplant recipients. At 1 to 2 years and after 2 years, both KDPI greater than 85% groups had significant reductions in mortality (1-2 years: preKT HR, 0.38; 95% CI, [0.23-0.60] and non-preKT HR, 0.52; 95% CI, 0.45-0.61; and 2+ years: preKT HR, 0.50; 95% CI, 0.38-0.66 and non-preKT HR, 0.64; 95% CI, 0.58-0.70, respectively). Conclusions. PreKT and non-preKT KDPI greater than 85% transplant was associated with lower mortality hazard after the first year compared with the waitlist including KDPI 0% to 85% transplants in patients older than 60 years. Further consideration should be given to increased utilization of high KDPI grafts in older patients with the goal of avoiding or limiting time on dialysis.
C1 [Jay, Colleen L.; Washburn, Kenneth] Univ Texas Hlth Sci Ctr San Antonio, Transplant Ctr, 7703 Floyd Curl Dr, San Antonio, TX 78229 USA.
[Dean, Patrick G.; Stegall, Mark D.] Mayo Clin, Div Transplant Surg, Rochester, MN USA.
[Helmick, Ryan A.] Univ Tennessee, Ctr Hlth Sci, Methodist Univ Hosp, Transplant Inst, Memphis, TN 38163 USA.
[Pugh, Jacqueline A.] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Pugh, Jacqueline A.] Univ Texas Hlth Sci Ctr San Antonio, Div Hosp Med, San Antonio, TX 78229 USA.
RP Jay, CL (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Transplant Ctr, 7703 Floyd Curl Dr, San Antonio, TX 78229 USA.
EM jay@uthscsa.edu
FU National Center for Advancing Translational Sciences, National
Institutes of Health [KL2 TR001118]; Department of Veterans Affairs
FX The project described was supported by the National Center for Advancing
Translational Sciences, National Institutes of Health, through Grant KL2
TR001118. J.A.P.'s salary is supported by the Department of Veterans
Affairs. The content is solely the responsibility of the authors and
does not necessarily represent the official views of the National
Institutes of Health or the Department of Veterans Affairs.
NR 24
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PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0041-1337
EI 1534-6080
J9 TRANSPLANTATION
JI Transplantation
PD APR
PY 2017
VL 101
IS 4
BP 867
EP 872
DI 10.1097/TP.0000000000001405
PG 6
WC Immunology; Surgery; Transplantation
SC Immunology; Surgery; Transplantation
GA EQ5XU
UT WOS:000398157200044
PM 27495758
ER
PT J
AU Zhu, P
Bailey, SR
Lei, BA
Paulos, CM
Atkinson, C
Tomlinson, S
AF Zhu, Peng
Bailey, Stefanie R.
Lei, Biao
Paulos, Chrystal M.
Atkinson, Carl
Tomlinson, Stephen
TI Targeted Complement Inhibition Protects Vascularized Composite
Allografts From Acute Graft Injury and Prolongs Graft Survival When
Combined With Subtherapeutic Cyclosporine A Therapy
SO TRANSPLANTATION
LA English
DT Article
ID ISCHEMIA-REPERFUSION INJURY; MEMBRANE ATTACK COMPLEX; ALTERNATIVE
PATHWAY; ACUTE REJECTION; T-CELLS; ALLOTRANSPLANTATION; TRANSPLANTATION;
SYSTEM; HAND; REGENERATION
AB Background. Recipients of vascularized composite allografts require aggressive and lifelong immunosuppression, and because the surgery is usually performed in nonlife-threatening situations, the development of strategies to minimize immunosuppression is especially pertinent for this procedure. We investigated how complement affects acute graft injury, alloimmunity, and immunosuppressive therapy. Methods. Vascularized composite allografts were transplanted from Balb/C to C57BL/6 mice that were complement deficient (C3 or double C3a Receptor (R)/C5aR), or treated with a targeted complement inhibitor (CR2-Crry). Allografts were analyzed for acute inflammation and injury, subacute T cell response, and survival in the absence and presence of cyclosporine A (CsA) therapy. Results. Allografts in C3-deficient or CR2-Crry-treated recipients were protected from skin and muscle ischemia-reperfusion injury (IRI). C3aR/C5aR-deficient recipients were more modestly protected. IgM and C3d colocalized within allografts from wild type and C3aR/C5aR-deficient recipients indicating IgM-mediated complement activation, and C3d deposition was almost absent in allografts from C3-deficient and CR2-Crry-treated recipients. Inflammatory cell infiltration and P-selectin expression was also significantly reduced in C3-deficient and CR2-Crry-treated recipients. Acute treatment with CR2-Crry or with 3 mg/kg per day CsA modestly, but significantly increased median allograft survival from 5.8 to 7.4 and 7.2 days, respectively. However, combined acute CR2-Crry treatment and CsA therapy increased mean graft survival to 17.2 days. Protection was associated with significantly reduced T cell infiltration of allografts and Tc1 cells in recipient spleens. Conclusions. Complement-mediated IRI augments graft allogenicity, and appropriate complement inhibition ameliorates IRI, decreases alloimmune priming and allows more immune-sparing CsA dosing.
C1 [Zhu, Peng] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Surg, Wuhan, Peoples R China.
[Zhu, Peng; Bailey, Stefanie R.; Lei, Biao; Paulos, Chrystal M.; Atkinson, Carl; Tomlinson, Stephen] Med Univ South Carolina, Dept Microbiol & Immunol, 173 Ashley Ave, Charleston, SC 29425 USA.
[Atkinson, Carl] Med Univ South Carolina, Lee Patterson Allen Transplant Immunobiol Lab, Div Transplantat, Dept Surg, Charleston, SC USA.
[Atkinson, Carl; Tomlinson, Stephen] Med Univ South Carolina, SCIT, Charleston, SC USA.
[Tomlinson, Stephen] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA.
RP Tomlinson, S (reprint author), Med Univ South Carolina, Dept Microbiol & Immunol, 173 Ashley Ave, Charleston, SC 29425 USA.; Atkinson, C (reprint author), Med Univ South Carolina, Dept Microbiol & Immunol & Surg, 173 Ashley Ave, Charleston, SC 29425 USA.
EM atkinsoc@musc.edu; tomlinss@musc.edu
FU NIH [R56AI119026, R01DK102912]; Department of Veterans Affairs
[1I01RX001141, 1BX001218]; Department of Defense [W81XWH-16-1-0783]
FX This work was supported by grants from the NIH (R56AI119026 and
R01DK102912), Department of Veterans Affairs (Merit Award 1I01RX001141
and 1BX001218) and the Department of Defense (W81XWH-16-1-0783).
NR 43
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U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0041-1337
EI 1534-6080
J9 TRANSPLANTATION
JI Transplantation
PD APR
PY 2017
VL 101
IS 4
BP E75
EP E85
DI 10.1097/TP.0000000000001625
PG 11
WC Immunology; Surgery; Transplantation
SC Immunology; Surgery; Transplantation
GA EQ5XU
UT WOS:000398157200001
PM 28045880
ER
PT J
AU Ho, N
Lieberman, D
AF Ho, N.
Lieberman, D.
TI Editorial: smoking status and 5-year survival in patients with
colorectal cancer
SO ALIMENTARY PHARMACOLOGY & THERAPEUTICS
LA English
DT Editorial Material
C1 [Ho, N.] Portland VA Med Ctr, & Oregon Hlth & Sci Univ, Portland, OR 97239 USA.
Oregon Hlth & Sci Univ, Portland, OR 97201 USA.
RP Ho, N (reprint author), Portland VA Med Ctr, & Oregon Hlth & Sci Univ, Portland, OR 97239 USA.
EM nho4383@gmail.com; lieberma@ohsu.edu
NR 4
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U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0269-2813
EI 1365-2036
J9 ALIMENT PHARM THER
JI Aliment. Pharmacol. Ther.
PD APR
PY 2017
VL 45
IS 8
BP 1162
EP 1163
DI 10.1111/apt.13979
PG 2
WC Gastroenterology & Hepatology; Pharmacology & Pharmacy
SC Gastroenterology & Hepatology; Pharmacology & Pharmacy
GA EQ1CW
UT WOS:000397807900014
PM 28326580
ER
PT J
AU Banerjee, G
Edelman, EJ
Barry, DT
Becker, WC
Cerda, M
Crystal, S
Gaither, JR
Gordon, AJ
Gordon, KS
Kerns, RD
Martins, SS
Fiellin, DA
Marshall, BDL
AF Banerjee, Geetanjoli
Edelman, E. Jennifer
Barry, Declan T.
Becker, William C.
Cerda, Magdalena
Crystal, Stephen
Gaither, Julie R.
Gordon, Adam J.
Gordon, Kirsha S.
Kerns, Robert D.
Martins, Silvia S.
Fiellin, David A.
Marshall, Brandon D. L.
TI Reply to Ruan et al. (2017): Non-medical use of prescription opioids is
associated with heroin initiation among US veterans
SO ADDICTION
LA English
DT Letter
DE Epidemiology; heroin; longitudinal study; NMUPO; non-medical use of
prescription opioids; veterans
ID UNITED-STATES; MORTALITY; TRENDS; ABUSE
C1 [Banerjee, Geetanjoli; Marshall, Brandon D. L.] Brown Sch Publ Hlth, Dept Epidemiol, Providence, RI 02903 USA.
[Edelman, E. Jennifer; Fiellin, David A.] Yale Univ, Dept Internal Med, Yale Sch Med, New Haven, CT USA.
[Edelman, E. Jennifer; Gaither, Julie R.; Fiellin, David A.] Yale Univ, Yale Sch Publ Hlth, Yale Ctr Interdisciplinary Res AIDS, New Haven, CT USA.
[Barry, Declan T.] Yale Univ, New Haven, CT USA.
[Barry, Declan T.] APT Fdn Pain Treatment Serv, New Haven, CT USA.
[Becker, William C.; Kerns, Robert D.] Connecticut Healthcare Syst, VA, Pain Res Informat Multimorbid & Educ PRIME Ctr, West Haven, CT USA.
[Cerda, Magdalena] Univ Calif Davis, Dept Emergency Med, Sacramento, CA 95817 USA.
[Crystal, Stephen] Rutgers State Univ, Inst Hlth Hlth Cure Policy & Aging Res, New Brunswick, NJ USA.
[Gaither, Julie R.] Yale Sch Med, Yale Ctr Med Informat, New Haven, CT USA.
[Gordon, Adam J.] VA Pittsburgh Healthcare Syst, CHERP, Pittsburgh, PA USA.
[Gordon, Adam J.] VA Pittsburgh Healthcare Syst, MIRECC, Pittsburgh, PA USA.
[Gordon, Adam J.] Univ Pittsburgh, Pittsburgh, PA USA.
[Gordon, Kirsha S.] VA Connecticut Healthcare Syst, West Haven, CT USA.
[Kerns, Robert D.] Yale Univ, Dept Psychiat, New Haven, CT 06520 USA.
[Kerns, Robert D.] Yale Univ, Dept Neurol, New Haven, CT USA.
[Kerns, Robert D.] Yale Univ, Dept Psychol, New Haven, CT USA.
[Martins, Silvia S.] Columbia Univ, Mailman Sch Publ Hlth, Dept Epidemiol, New York, NY USA.
RP Marshall, BDL (reprint author), Brown Sch Publ Hlth, Dept Epidemiol, Providence, RI 02903 USA.
EM brandon_marshall@brown.edu
NR 10
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U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0965-2140
EI 1360-0443
J9 ADDICTION
JI Addiction
PD APR
PY 2017
VL 112
IS 4
BP 728
EP 729
DI 10.1111/add.13710
PG 2
WC Substance Abuse; Psychiatry
SC Substance Abuse; Psychiatry
GA EM7DJ
UT WOS:000395471400034
PM 28120531
ER
PT J
AU Borazanci, E
Dang, CV
Robey, RW
Bates, SE
Chabot, JA
Von Hoff, DD
AF Borazanci, Erkut
Dang, Chi V.
Robey, Robert W.
Bates, Susan E.
Chabot, John A.
Von Hoff, Daniel D.
TI Pancreatic Cancer: "A Riddle Wrapped in a Mystery inside an Enigma"
SO CLINICAL CANCER RESEARCH
LA English
DT Article
ID ABO BLOOD-GROUP; CONTROL CONSORTIUM PANC4; DUCTAL ADENOCARCINOMA;
STELLATE CELLS; COMBINATION THERAPY; RANDOMIZED-TRIALS; PLUS
GEMCITABINE; POOLED ANALYSIS; PD-1 BLOCKADE; UNITED-STATES
AB Pancreatic ductal adenocarcinoma (PDAC) is one of the most difficult-to-treat cancers. With an increasing incidence and inability to make major progress, it represents the very definition of unmet medical need. Progress has been made in understanding the basic biology-systematic genomic sequencing has led to the recognition that PDAC is not typically a heavily mutated tumor, although there are exceptions. The most consistently mutated genes are KRAS, CDKN2A, TP53, and SMAD4/DPC4. Study of familial PDAChas led to the recognition that a variety of defects in DNA repair genes can be associated with the emergence of pancreatic cancer. Recent studies suggest that epigenetics may play a larger role than previously recognized. A major new understanding is the recognition that PDAC should be considered a composite of tumor cells, as well as pancreatic stellate cells, immune cells, and extracellular matrix. The individual components contribute to metabolic aberration, immune dysfunction, and chemotherapy resistance, and therapeutic innovationsmaybe needed to address them individually. It has also been recognized that metastatic seeding from PDAC occurs very early in the disease course-in an estimated 73% of cases, once the tumor reaches 2 cm. The implication of this is that therapies directed toward micrometastatic disease and increasing fractional cell kill are most needed. Neoadjuvant approaches have been taken to increase resectability and improve outcome. So much work remains, and most critical is the need to understand how this tumor originates and develops.
C1 [Borazanci, Erkut; Von Hoff, Daniel D.] Arizona & TGen, HonorHealth, Phoenix, AZ USA.
[Dang, Chi V.] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA.
[Robey, Robert W.] NIH, Bethesda, MD 20892 USA.
[Bates, Susan E.; Chabot, John A.] Columbia Univ, Med Ctr, New York, NY USA.
[Bates, Susan E.] James J Peters Bronx VA Med Ctr, Bronx, NY USA.
RP Borazanci, E (reprint author), HonorHlth Res Inst, 10510 N 92nd St,Suite 200, Scottsdale, AZ 85258 USA.
EM Erkut.Borazanci@HonorHealth.com
FU Stand Up To Cancer-Cancer Research UK-Lustgarten Foundation Pancreatic
Cancer Dream Team Research Grant [SU2C-AACR-DT-20-16]; Seena Magowitz
Foundation; Mattress Firm
FX Research supported by a Stand Up To Cancer-Cancer Research UK-Lustgarten
Foundation Pancreatic Cancer Dream Team Research Grant (E. Borazanci and
D.D. Von Hoff; Grant Number: SU2C-AACR-DT-20-16). Stand Up To Cancer is
a program of the Entertainment Industry Foundation. Research grants are
administered by the American Association for Cancer Research, the
scientific partner of SU2C. E. Borazanci and D.D. Von Hoff also received
clinical research support from Seena Magowitz Foundation and Mattress
Firm.
NR 95
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U1 3
U2 3
PU AMER ASSOC CANCER RESEARCH
PI PHILADELPHIA
PA 615 CHESTNUT ST, 17TH FLOOR, PHILADELPHIA, PA 19106-4404 USA
SN 1078-0432
EI 1557-3265
J9 CLIN CANCER RES
JI Clin. Cancer Res.
PD APR 1
PY 2017
VL 23
IS 7
BP 1629
EP 1637
DI 10.1158/1078-0432.CCR-16-2070
PG 9
WC Oncology
SC Oncology
GA EQ7KK
UT WOS:000398262700003
PM 28373361
ER
PT J
AU Montgomery, AE
Cusack, M
Szymkowiak, D
Fargo, J
O'Toole, T
AF Montgomery, Ann Elizabeth
Cusack, Meagan
Szymkowiak, Dorota
Fargo, Jamison
O'Toole, Thomas
TI Factors contributing to eviction from permanent supportive housing:
Lessons from HUD-VASH
SO EVALUATION AND PROGRAM PLANNING
LA English
DT Article
DE Eviction; Permanent supportive housing; Substance use disorder; Acute
care; Veterans
ID CHRONICALLY HOMELESS INDIVIDUALS; INDEPENDENT LIVING PROGRAMS; SEVERE
ALCOHOL-PROBLEMS; SERIOUS MENTAL-ILLNESS; 1ST; PROJECT; EXPANSION;
OUTCOMES; PEOPLE; CARE
AB Introduction: Eviction from housing is associated with several negative outcomes, further exacerbated among high-need populations requiring financial and supportive services to maintain housing stability. This study investigated risk and protective factors both characteristics and precipitating events of tenant eviction informing permanent supportive housing (PSH) programs' efforts to identify tenants at risk and intervene.
Methods: Using administrative data for a cohort of 20,146 Veterans participating in PSH, this study assessed differences in Veterans who exited the program due to eviction and Veterans Who exited because they accomplished their goals. A series of logistic regressions identified patterns of health services use that may signal imminent eviction.
Results: Veterans with a drug use disorder and those who received inpatient, emergency, or outpatient care related to mental/behavioral health and substance use conditions proximal to program exit had greater risk for eviction. Receipt of outpatient primary medical care and supportive services was generally protective against eviction. The likelihood of eviction was greatest for Veterans with acute care use within 30 days of exit.
Discussion: PSH providers may use these correlates of eviction to identify Veterans in need of an intervention to prevent eviction. Future work should focus on operationalizing these findings and identifying appropriate interventions. Published by Elsevier Ltd.
C1 [Montgomery, Ann Elizabeth; Cusack, Meagan; Szymkowiak, Dorota; Fargo, Jamison; O'Toole, Thomas] US Dept Vet Affairs, Natl Ctr Homelessness Vet, Philadelphia, PA USA.
[Montgomery, Ann Elizabeth] Birmingham VA Med Ctr, Hlth Serv Res, Birmingham, AL USA.
[Montgomery, Ann Elizabeth] Univ Alabama Birmingham, Sch Publ Hlth, Birmingham, AL 35294 USA.
[Fargo, Jamison] Utah State Univ, Coll Educ & Human Serv, Logan, UT 84322 USA.
[O'Toole, Thomas] Brown Univ, Alpert Med Sch, Providence, RI 02912 USA.
[Cusack, Meagan] 4100 Chester Ave,Suite 202, Philadelphia, PA 19104 USA.
[Szymkowiak, Dorota] 4100 Chester Ave,Suite 201, Philadelphia, PA 19104 USA.
[Fargo, Jamison] 2810 Old Main Hill, Logan, UT 84322 USA.
[O'Toole, Thomas] 830 Chalkstone Ave, Providence, RI 02908 USA.
RP Montgomery, AE (reprint author), RPHB 227M,1720 2nd Ave South, Birmingham, AL 35294 USA.
EM ann.montgomery2@va.gov; meagan.cusack@va.gov; dorota.szymkowiak@va.gov;
jamison.fargo@usu.edu; thomas.o'toole@va.gov
FU U.S. Department of Veterans Affairs (VA); National Center on
Homelessness Among Veterans; U.S. Department of Housing and Urban
Development (HUD); Office of Policy Development and Research
FX Research for this paper was supported by the U.S. Department of Veterans
Affairs (VA), National Center on Homelessness Among Veterans and the
U.S. Department of Housing and Urban Development (HUD), Office of Policy
Development and Research. The authors wish to express their gratitude to
Brent Roberts of the VA Center on Health Equity Research and Promotion
and Todd Manning of the Veterans Health Administration Support Service
Center for their assistance with data management. The contents of this
paper do not represent the views of the U.S. Department of Veterans
Affairs or the United States Government.
NR 44
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U1 5
U2 5
PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0149-7189
EI 1873-7870
J9 EVAL PROGRAM PLANN
JI Eval. Program Plan.
PD APR
PY 2017
VL 61
BP 55
EP 63
DI 10.1016/j.evalprogplan.2016.11.014
PG 9
WC Social Sciences, Interdisciplinary
SC Social Sciences - Other Topics
GA EM3MZ
UT WOS:000395220600006
PM 27940343
ER
PT J
AU Levingston, CA
Young, MRI
AF Levingston, Corinne A.
Young, M. Rita I.
TI Transient immunological and clinical effectiveness of treating mice
bearing premalignant oral lesions with PD-1 antibodies
SO INTERNATIONAL JOURNAL OF CANCER
LA English
DT Article
DE cytokines; head and neck cancer; HNSCC; immunotherapy; PD-1;
premalignant oral lesions; T cell
ID SQUAMOUS-CELL CARCINOMA; REGULATORY T-CELLS; ADVANCED MELANOMA; IMMUNE
REACTIVITY; ENDOTHELIAL-CELLS; OVARIAN-CANCER; NEGATIVE HEAD;
LUNG-CANCER; NECK-CANCER; OPEN-LABEL
AB A carcinogen-induced premalignant oral lesion model that progresses to oral cancer was used to examine the impact of blocking PD-1 on cytokine expression and on progression of lesions to cancer. The results of this study show increased production of IL-2 and the inflammatory cytokines IL-6, IL-17 and TNF-a by spleen cells of lesion-bearing mice that were treated with PD-1 antibody for 1 week compared to cytokine production by spleen cells of lesion-bearing mice treated with control antibody. Production of IFN-c increased at 3 weeks of PD-1 antibody treatment, although production of the other Th1 and inflammatory mediators declined. By 5 weeks, levels of these cytokines declined for both control and PD-1 antibody-treated mice. Flow cytometric analysis for IFN-c-expressing cells showed shifts in CD4(+) 1 cells expressing IFN-c consistent with the changes in cytokine secretion. Whether or not treatment generated reactivity to lesions or HNSCC was determined. Spleen cells from PD-1 antibody- treated mice were stimulated by lysates of premalignant lesion and HNSCC tongue tissues to produce increased levels of Th1 and select inflammatory cytokines early in the course of PD-1 antibody treatment. However, with continued treatment, reactivity to lesion and HNSCC lysates declined. Analysis of clinical response to treatment suggested an early delay in lesion progression but, with continued treatment, lesions in PD-1 antibody-treated mice progressed to the same degree as in control antibody-treated mice. Overall, these results show an early beneficial response to PD-1 antibody treatment, which then fails with continued treatment and lesion progression.
C1 [Levingston, Corinne A.; Young, M. Rita I.] Ralph H Johnson VA Med Ctr, Res Serv, Charleston, SC USA.
[Young, M. Rita I.] Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, Charleston, SC 29425 USA.
RP Young, MRI (reprint author), Med Univ South Carolina, Dept Otolaryngol, 114 Doughty St, Charleston, SC 29425 USA.
EM Youngmr@musc.edu
FU Merck Investigator Studies Program [52353]; The Clinical Sciences
Research and Development Program of the Department of Veterans Affairs
[I01-CX000851]
FX Grant sponsors: Merck Investigator Studies Program; Grant sponsors:
ID#52353; Grant sponsors: The Clinical Sciences Research and Development
Program of the Department of Veterans Affairs; Grant number: Grant
number:
NR 46
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U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0020-7136
EI 1097-0215
J9 INT J CANCER
JI Int. J. Cancer
PD APR
PY 2017
VL 140
IS 7
BP 1609
EP 1619
DI 10.1002/ijc.30543
PG 11
WC Oncology
SC Oncology
GA EM2WT
UT WOS:000395177200015
PM 27914100
ER
PT J
AU Lo, B
Grady, D
AF Lo, Bernard
Grady, Deborah
TI Addressing Ethical Lapses in Research
SO JAMA INTERNAL MEDICINE
LA English
DT Editorial Material
C1 [Lo, Bernard] Greenwal Fdn, One Penn Plaza,Suite 4726, New York, NY 10119 USA.
[Grady, Deborah] Univ Calif San Francisco, San Francisco, CA USA.
[Grady, Deborah] San Francisco VA Med Ctr, San Francisco, CA USA.
RP Lo, B (reprint author), Greenwal Fdn, One Penn Plaza,Suite 4726, New York, NY 10119 USA.
EM bernardlo@greenwall.org
NR 8
TC 1
Z9 1
U1 0
U2 0
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6106
EI 2168-6114
J9 JAMA INTERN MED
JI JAMA Intern. Med.
PD APR 1
PY 2017
VL 177
IS 4
BP 461
EP 462
DI 10.1001/jamainternmed.2016.9579
PG 2
WC Medicine, General & Internal
SC General & Internal Medicine
GA EQ9SM
UT WOS:000398425200003
PM 28241241
ER
PT J
AU Stevens, VW
Nelson, RE
Schwab-Daugherty, EM
Khader, K
Jones, MM
Brown, KA
Greene, T
Croft, LD
Neuhauser, M
Glassman, P
Goetz, MB
Samore, MH
Rubin, MA
AF Stevens, Vanessa W.
Nelson, Richard E.
Schwab-Daugherty, Elyse M.
Khader, Karim
Jones, Makoto M.
Brown, Kevin A.
Greene, Tom
Croft, Lindsay D.
Neuhauser, Melinda
Glassman, Peter
Goetz, Matthew Bidwell
Samore, Matthew H.
Rubin, Michael A.
TI Comparative Effectiveness of Vancomycin and Metronidazole for the
Prevention of Recurrence and Death in Patients With Clostridium
difficile Infection
SO JAMA INTERNAL MEDICINE
LA English
DT Article
ID PSEUDOMEMBRANOUS COLITIS; STEWARDSHIP PROGRAMS; CARE FACILITIES;
DIARRHEA; DISEASE; RISK; EPIDEMIOLOGY; GUIDELINES; SEVERITY; RATIOS
AB IMPORTANCE Metronidazole hydrochloride has historically been considered first-line therapy for patients with mild to moderate Clostridium difficile infection (CDI) but is inferior to vancomycin hydrochloride for clinical cure. The choice of therapy may likewise have substantial consequences on other downstream outcomes, such as recurrence and mortality, although these secondary outcomes have been less studied.
OBJECTIVE To evaluate the risk of recurrence and all-cause 30-day mortality among patients receiving metronidazole or vancomycin for the treatment of mild to moderate and severe CDI.
DESIGN, SETTING, AND PARTICIPANTS This retrospective, propensity-matched cohort study evaluated patients treated for CDI, defined as a positive laboratory test result for the presence of C difficile toxins or toxin genes in a stool sample, in the US Department of Veterans Affairs health care system from January 1, 2005, through December 31, 2012. Data analysis was performed from February 7, 2015, through November 22, 2016.
EXPOSURES Treatment with vancomycin or metronidazole.
MAIN OUTCOMES AND MEASURES The outcomes of interest in this study were CDI recurrence and all-cause 30-day mortality. Recurrence was defined as a second positive laboratory test result within 8 weeks of the initial CDI diagnosis. All-cause 30-day mortality was defined as death from any cause within 30 days of the initial CDI diagnosis.
RESULTS A total of 47 471 patients (mean [SD] age, 68.8 [13.3] years; 1947 women [4.1%] and 45 524 men [95.9%]) developed CDI, were treated with vancomycin or metronidazole, and met criteria for entry into the study. Of 47 147 eligible first treatment episodes, 2068 (4.4%) were with vancomycin. Those 2068 patients were matched to 8069 patients in the metronidazole group for a total of 10 137 included patients. Subcohorts were constructed that comprised 5452 patients with mild to moderate disease and 3130 patients with severe disease. There were no differences in the risk of recurrence between patients treated with vancomycin vs those treated with metronidazole in any of the disease severity cohorts. Among patients in the any severity cohort, those who were treated with vancomycin were less likely to die (adjusted relative risk, 0.86; 95% CI, 0.74 to 0.98; adjusted risk difference, -0.02; 95% CI, -0.03 to -0.01). No significant difference was found in the risk of mortality between treatment groups among patients with mild to moderate CDI, but vancomycin significantly reduced the risk of all-cause 30-day mortality among patients with severe CDI (adjusted relative risk, 0.79; 95% CI, 0.65 to 0.97; adjusted risk difference, -0.04; 95% CI, -0.07 to -0.01).
CONCLUSIONS AND RELEVANCE Recurrence rates were similar among patients treated with vancomycin and metronidazole. However, the risk of 30-day mortality was significantly reduced among patients who received vancomycin. Our findings may further justify the use of vancomycin as initial therapy for severe CDI.
C1 [Stevens, Vanessa W.; Nelson, Richard E.; Khader, Karim; Jones, Makoto M.; Brown, Kevin A.; Croft, Lindsay D.; Samore, Matthew H.; Rubin, Michael A.] Vet Affairs VA Salt Lake City Hlth Care Syst, IDEAS Ctr 2 0, Salt Lake City, UT USA.
[Stevens, Vanessa W.; Nelson, Richard E.; Khader, Karim; Jones, Makoto M.; Greene, Tom; Croft, Lindsay D.; Samore, Matthew H.; Rubin, Michael A.] Univ Utah, Sch Med, Dept Internal Med, Div Epidemiol, Salt Lake City, UT USA.
[Schwab-Daugherty, Elyse M.] Univ Utah, Coll Pharm, Dept Pharmacotherapy, Salt Lake City, UT 84112 USA.
[Brown, Kevin A.] Publ Hlth Ontario, Toronto, ON, Canada.
[Neuhauser, Melinda; Glassman, Peter] VA Pharm Benefits Management Serv, Hines, IL USA.
[Glassman, Peter; Goetz, Matthew Bidwell] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
RP Stevens, VW (reprint author), Vet Affairs Salt Lake City Hlth Care Syst, IDEAS Ctr 2 0, 500 Foothill Dr, Salt Lake City, UT 84148 USA.
EM vanessa.stevens@hsc.utah.edu
FU Center of Innovation [13-414]; US Department of Veterans Affairs,
Veterans Health Administration, Office of Research and Development,
Health Services Research and Development [11-210]
FX This material is based on work supported in part by Center of Innovation
grant 13-414 (Dr Samore, principal investigator) and Career Development
Award 11-210 (Dr Nelson, principal investigator) from the US Department
of Veterans Affairs, Veterans Health Administration, Office of Research
and Development, Health Services Research and Development.
NR 38
TC 0
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U1 3
U2 3
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6106
EI 2168-6114
J9 JAMA INTERN MED
JI JAMA Intern. Med.
PD APR 1
PY 2017
VL 177
IS 4
BP 546
EP 553
DI 10.1001/jamainternmed.2016.9045
PG 8
WC Medicine, General & Internal
SC General & Internal Medicine
GA EQ9SM
UT WOS:000398425200019
PM 28166328
ER
PT J
AU Hanlon, JT
Perera, S
Newman, AB
Thorpe, JM
Donohue, JM
Simonsick, EM
Shorr, RI
Bauer, DC
Marcum, ZA
AF Hanlon, J. T.
Perera, S.
Newman, A. B.
Thorpe, J. M.
Donohue, J. M.
Simonsick, E. M.
Shorr, R. I.
Bauer, D. C.
Marcum, Z. A.
CA Hlth ABC Study
TI Potential drug-drug and drug-disease interactions in well-functioning
community-dwelling older adults
SO JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS
LA English
DT Article
DE aged; drug interaction; drug utilization
ID INAPPROPRIATE MEDICATION USE; ELDERLY-PEOPLE; RISK; HEALTH; OUTPATIENTS
AB What is known and objective: There are few studies examining both drug-drug and drug-disease interactions in older adults. Therefore, the objective of this study was to describe the prevalence of potential drug-drug and drug-disease interactions and associated factors in community-dwelling older adults.
Methods: This cross-sectional study included 3055 adults aged 70-79 without mobility limitations at their baseline visit in the Health Aging and Body Composition Study conducted in the communities of Pittsburgh PA and Memphis TN, USA. The outcome factors were potential drug-drug and drug-disease interactions as per the application of explicit criteria drawn from a number of sources to self-reported prescription and non-prescription medication use.
Results: Over one-third of participants had at least one type of interaction. Approximately one quarter (25.1%) had evidence of had one or more drug-drug interactions. Nearly 10.7% of the participants had a drug-drug interaction that involved a non-prescription medication. % The most common drug-drug interaction was non-steroidal anti-inflammatory drugs (NSAIDs) affecting antihypertensives. Additionally, 16.0% had a potential drug-disease interaction with 3.7% participants having one involving non-prescription medications. The most common drug-disease interaction was aspirin/NSAID use in those with history of peptic ulcer disease without gastroprotection. Over one-third (34.0%) had at least one type of drug interaction. Each prescription medication increased the odds of having at least one type of drug interaction by 35-40% [drug-drug interaction adjusted odds ratio (AOR) = 1.35, 95% confidence interval (CI) = 1.27-1.42; drug-disease interaction AOR = 1.30; CI = 1.21-1.40; and both AOR = 1.45; CI = 1.34-1.57]. A prior hospitalization increased the odds of having at least one type of drug interaction by 49-84% compared with those not hospitalized (drug-drug interaction AOR = 1.49, 95% CI = 1.11-2.01; drug-disease interaction AOR = 1.69, CI = 1.15-2.49; and both AOR = 1.84, CI = 1.20-2.84).
What is new and conclusionDrug interactions are common among community-dwelling older adults and are associated with the number of medications and hospitalization in the previous year. Longitudinal studies are needed to evaluate the impact of drug interactions on health-related outcomes.
C1 [Hanlon, J. T.; Perera, S.; Newman, A. B.; Marcum, Z. A.] Univ Pittsburgh, Sch Med, Dept Med, Div Geriatr, Pittsburgh, PA 15213 USA.
[Hanlon, J. T.; Thorpe, J. M.] Univ Pittsburgh, Sch Pharm, Dept Pharm & Therapeut, Pittsburgh, PA 15261 USA.
[Hanlon, J. T.; Newman, A. B.] Univ Pittsburgh, Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA.
[Hanlon, J. T.; Thorpe, J. M.] Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equ Res, Pittsburgh, PA USA.
[Hanlon, J. T.; Thorpe, J. M.] Vet Affairs Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA USA.
[Perera, S.] Univ Pittsburgh, Dept Biostat, Sch Publ Hlth, Pittsburgh, PA 15261 USA.
[Donohue, J. M.] Univ Pittsburgh, Sch Publ Hlth, Dept Hlth Policy & Management, Pittsburgh, PA 15260 USA.
[Simonsick, E. M.] NIA, Intramural Res Program, Baltimore, MD 21224 USA.
[Shorr, R. I.] Malcolm Randall Vet Affairs Med Ctr, Geriatr Res Educ & Clin Ctr, Gainesville, FL USA.
[Bauer, D. C.] Univ Calif San Francisco, San Francisco, CA 94143 USA.
RP Hanlon, JT (reprint author), Univ Pittsburgh, Dept Geriatr Med, Kaufman Med Bldg Suite 514,3471 5th Ave, Pittsburgh, PA 15213 USA.
EM jth14@pitt.edu
FU National Institute on Aging (NIA) [P30-AG024827, T32-AG021885]; NIH, NIA
[N01-AG-6-2101, N01-AG-6-2103, N01-AG-6-2106]; NIA [R01-AG028050];
National Institute of Nursing Research grant [R01-NR012459]
FX The research reported in this manuscript was primarily supported by
National Institute on Aging (NIA) grants and contracts (P30-AG024827,
T32-AG021885). This research was also supported in part by the
Intramural Research program of the NIH, NIA (N01-AG-6-2101,
N01-AG-6-2103, and N01-AG-6-2106), NIA grant (R01-AG028050), and a
National Institute of Nursing Research grant (R01-NR012459).
NR 27
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U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0269-4727
EI 1365-2710
J9 J CLIN PHARM THER
JI J. Clin. Pharm. Ther.
PD APR
PY 2017
VL 42
IS 2
BP 228
EP 233
DI 10.1111/jcpt.12502
PG 6
WC Pharmacology & Pharmacy
SC Pharmacology & Pharmacy
GA EM5TN
UT WOS:000395376300017
PM 28111765
ER
PT J
AU Miller, TR
Weiss, JJ
Brau, N
Dieterich, DT
Stivala, A
Rivera-Mindt, M
AF Miller, Theodore R.
Weiss, Jeffrey J.
Brau, Norbert
Dieterich, Douglas T.
Stivala, Alicia
Rivera-Mindt, Monica
TI Greater decline in memory and global neurocognitive function in
HIV/hepatitis C co-infected than in hepatitis C mono-infected patients
treated with pegylated interferon and ribavirin
SO JOURNAL OF NEUROVIROLOGY
LA English
DT Article
DE Hepatitis C; HIV; Pegylated interferon; Ribavirin; Neurocognitive; Side
effects
ID ANTIRETROVIRAL THERAPY; HUMAN-PAPILLOMAVIRUS; ALPHA; HIV; VIRUS; ERA;
INDIVIDUALS; IMPAIRMENT; CHARTER; ADULTS
AB The human immunodeficiency virus (HIV), hepatitis C virus (HCV), and the treatment of HCV with pegylated interferon and ribavirin (IFN/RBV) have been associated with neurocognitive and psychiatric abnormalities. The goal of this research was to prospectively evaluate neurocognitive functioning among a group of HCV mono-infected and HIV/HCV co-infected patients during the first 24 weeks of IFN/RBV treatment while accounting for practice effects, normal variations in change over time, and variations in IFN/RBV treatment exposure. Forty-four HCV mono-infected and 30 HIV/HCV co-infected patients were enrolled in a prospective study of patients beginning on IFN/RBV for chronic HCV infection. Patients were administered a depression inventory, a measure of fatigue, a structured psychiatric interview, and a neurocognitive battery at baseline and 24 weeks after initiation of treatment. Analyses were conducted to explore possible associations between neurocognitive functioning and the following: HIV/HCV co-infection vs. HCV mono-infection, IFN and RBV treatment exposure, psychiatric status, liver disease stage, and other medical characteristics. At baseline, there were no significant differences between the two groups' neuropsychiatric or neurocognitive function other than the mono-infected group had significantly higher reports of fatigue (p = 0.033). Over the course of 24 weeks of treatment after controlling for practice effects, the HIV/HCV co-infected patients experienced significantly greater declines in memory (t(56) = 2.14, p = 0.037) and global neurocognitive functioning (t(53) = 2.28, p = 0.027). In a well-characterized sample of mono-infected and co-infected patients, it appears that persons with HIV/HCV co-infection are potentially more vulnerable to neurocognitive sequalae during HCV treatment.
C1 [Miller, Theodore R.; Weiss, Jeffrey J.; Brau, Norbert; Dieterich, Douglas T.; Stivala, Alicia] Icahn Sch Med Mt Sinai, Dept Med, One Gustave L Levy Pl,POB 1087, New York, NY 10029 USA.
[Miller, Theodore R.] Yale Sch Nursing, 400 West Campus Dr, Orange, CT 06477 USA.
[Weiss, Jeffrey J.; Rivera-Mindt, Monica] Icahn Sch Med Mt Sinai, Dept Psychiat, One Gustave L Levy Pl, New York, NY 10029 USA.
[Brau, Norbert] Bronx Vet Affairs Med Ctr, Infect Dis Sect, 130 W Kingsbridge Rd, New York, NY 10468 USA.
[Rivera-Mindt, Monica] Fordham Univ, Dept Psychol, 340,441 E Fordham Rd, Bronx, NY 10458 USA.
[Rivera-Mindt, Monica] Icahn Sch Med Mt Sinai, Dept Neurol, One Gustave L Levy Pl, New York, NY 10029 USA.
RP Weiss, JJ (reprint author), Icahn Sch Med Mt Sinai, Dept Med, One Gustave L Levy Pl,POB 1087, New York, NY 10029 USA.; Weiss, JJ (reprint author), Icahn Sch Med Mt Sinai, Dept Psychiat, One Gustave L Levy Pl, New York, NY 10029 USA.
EM Jeffrey.Weiss@mountsinai.org
OI Miller, Theodore/0000-0002-3286-8176
FU National Institute of Mental Health of the National Institutes of Health
[K23MH071177]
FX This work was supported by the National Institute of Mental Health of
the National Institutes of Health (K23MH071177). The content is solely
the responsibility of the authors and does not necessarily represent the
official views of the National Institute of Mental Health or the
National Institutes of Health.
NR 66
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U1 1
U2 1
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1355-0284
EI 1538-2443
J9 J NEUROVIROL
JI J. Neurovirol.
PD APR
PY 2017
VL 23
IS 2
BP 260
EP 272
DI 10.1007/s13365-016-0494-8
PG 13
WC Neurosciences; Virology
SC Neurosciences & Neurology; Virology
GA EN7XG
UT WOS:000396214900008
PM 27896573
ER
PT J
AU Patel, AN
Lee, S
Andrews, HF
Pelton, GH
Schultz, SK
Sultzer, DL
Mintzer, J
de la Pena, D
Gupta, S
Colon, S
Schimming, C
Levin, B
Devanand, DP
AF Patel, Anjali N.
Lee, Seonjoo
Andrews, Howard F.
Pelton, Gregory H.
Schultz, Susan K.
Sultzer, David L.
Mintzer, Jacobo
de la Pena, Danilo
Gupta, Sanjay
Colon, Sylvia
Schimming, Corbett
Levin, Bruce
Devanand, D. P.
TI Prediction of Relapse After Discontinuation of Antipsychotic Treatment
in Alzheimer's Disease: The Role of Hallucinations
SO AMERICAN JOURNAL OF PSYCHIATRY
LA English
DT Article
ID NEUROPSYCHIATRIC INVENTORY; DEMENTIA; DRUGS
AB Objective: In Alzheimer's disease, antipsychotic medications are often used for a period, with relief of symptoms, and then discontinued, after which relapse may occur. The authors sought to determine which neuropsychiatric symptoms predict relapse.
Method: In the Antipsychotic Discontinuation in Alzheimer's Disease trial, 180 patients with Alzheimer's disease and symptoms of agitation or psychosis were treated with risperidone for 16 weeks, after which patients who responded (N=110) were randomly assigned to continue risperidone for 32 weeks, to continue risperidone for 16 weeks followed by switch to placebo for 16 weeks, or to receive placebo for 32 weeks. As reported previously, discontinuation of risperidone was associated with a two-to fourfold increased risk of relapse over 16-32 weeks. In planned post hoc analyses, the authors examined associations between the 12 symptom domains in the Neuropsychiatric Inventory (NPI) and relapse in the first 16-week phase after randomization.
Results: Compared with patients with mild hallucinations or no hallucinations, patients with severe hallucinations as a presenting symptom at baseline had a higher likelihood of relapse (hazard ratio=2.96, 95% CI=1.52, 5.76). This effect was present for the subgroup with auditory hallucinations, but not the subgroup with visual hallucinations. Among patients with baseline hallucinations, 13 of 17 (76.5%) who discontinued risperidone relapsed, compared with 10 of 26 (38.5%) who continued risperidone (p<0.02). This group difference remained significant for severe (77.8%) compared with mild (36%) hallucinations. NPI domain scores after the initial open-treatment phase were not associated with relapse.
Conclusions: Patients with severe baseline hallucinations were more likely to relapse after randomization, and the presence of baseline hallucinations was associated with a higher risk of relapse after discontinuation of risperidone compared with continued risperidone treatment. For patients with hallucinations, particularly auditory hallucinations, antipsychotic discontinuation should be approached cautiously because of high relapse risk.
C1 [Devanand, D. P.] Columbia Univ, Coll Physicians & Surg, New York State Psychiat Inst, Div Geriatr Psychiat, New York, NY 10027 USA.
Columbia Univ, Coll Physicians & Surg, Gertrude H Sergievsky Ctr, New York, NY USA.
Columbia Univ, Coll Physicians & Surg, Dept Neurol, New York, NY USA.
Columbia Univ, Taub Inst Res Alzheimers Dis & Aging Brain, New York, NY USA.
Columbia Univ, Mailman Sch Publ Hlth, Dept Biostat, New York, NY USA.
Med Univ South Carolina, Dept Neurosci, Div Translat Res, Charleston, SC USA.
Ralph H Johnson VA Med Ctr, Charleston, SC USA.
Univ Iowa Carver, Coll Med, Dept Psychiat, Iowa City, IA USA.
Clin Biotechnol Res Inst, Roper St Francis Healthcare, Charleston, SC USA.
Res Ctr Clin Studies, Norwalk, CT USA.
SUNY Buffalo, Sch Med & Biomed Sci, Dept Psychiat, Buffalo, NY USA.
VA Med Ctr, Dept Psychiat, Tuscaloosa, AL USA.
Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY USA.
RP Devanand, DP (reprint author), Columbia Univ, Coll Physicians & Surg, New York State Psychiat Inst, Div Geriatr Psychiat, New York, NY 10027 USA.
EM dpd3@cumc.columbia.edu
FU NIH [R01 AG021488, R01 AG17761]; Department of Veterans Affairs; NIMH;
National Institute on Aging; Alzheimer's Association; Alzheimer's
Disease Cooperative Study; Eli Lilly; Toyama Chemical Company; Avanir;
Transition Therapeutics; Biogen; Elan; EnVivo; Genentech; Hoffmann-La
Roche; Lundbeck; Merck Sharp Dohme; Neurim; Novartis; Otsuka; Pfizer;
Reckitt-Benckiser; Takeda; TauRx Therapeutics; Toyama Chemical;
Transition Therapeutics Ireland; UCSD; Wyeth; Department of Defense
FX Supported by NIH grants R01 AG021488 and R01 AG17761 and by the
Department of Veterans Affairs. Risperidone tablets and matching placebo
were donated by Janssen, a division of Johnson & Johnson.
ClinicalTrials.gov identifier: NCT00417482.; Dr. Pelton has received
grants from NIMH, the National Institute on Aging, and the Alzheimer's
Association. Dr. Schultz has received research support from the
Alzheimer's Disease Cooperative Study in partnership with Eli Lilly and
Toyama Chemical Company. Dr. Sultzer has received support from the
Department of Veterans Affairs and research support from Avanir, Eli
Lilly, and Transition Therapeutics, and he has served as a consultant
for Astellas, AbbVie, Insys, Lundbeck, and Otsuka. Dr. Mintzer is
employed by Roper St. Francis Healthcare, Medical University of South
Carolina, Ralph H. Johnson VA Medical Center, and NeuroQuest, and he is
the founder of BioPharma Connex. Dr. de la Pena has received research
support from Avanir, Biogen, Elan, Eli Lilly, EnVivo, Genentech,
Hoffmann-La Roche, Lundbeck, Merck Sharp & Dohme, Neurim, Novartis,
Otsuka, Pfizer, Reckitt-Benckiser, Takeda, TauRx Therapeutics, Toyama
Chemical, Transition Therapeutics Ireland, UCSD, and Wyeth. Dr. Gupta
has served as a speaker for Alkermes, Allergan, Avanir, Global Medical
Education, Lundbeck, Merck, Otsuka, Sunovion, and Takeda. Dr. Devanand
has received research support from Avanir, the Department of Defense,
and the National Institute on Aging, has served on scientific advisory
boards for AbbVie and Astellas, and has served as a consultant for
Intra-Cellular Therapies. The other authors report no financial
relationships with commercial interests.
NR 16
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U1 1
U2 1
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 0002-953X
EI 1535-7228
J9 AM J PSYCHIAT
JI Am. J. Psychiat.
PD APR
PY 2017
VL 174
IS 4
BP 362
EP 369
DI 10.1176/appi.ajp.2016.16020226
PG 8
WC Psychiatry
SC Psychiatry
GA EQ2SU
UT WOS:000397921800012
PM 27855483
ER
PT J
AU Waterer, G
Restrepo, MI
AF Waterer, Grant
Restrepo, Marcos I.
TI Maladaptive Suppression of Bacterial Clearance in Early Sepsis Setting
the Scene for Failure
SO AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
LA English
DT Editorial Material
C1 [Waterer, Grant] Univ Western Australia, Perth, WA, Australia.
[Waterer, Grant] Northwestern Univ, Chicago, IL 60611 USA.
[Restrepo, Marcos I.] South Texas Vet Hlth Care Syst, Dept Med, San Antonio, TX USA.
[Restrepo, Marcos I.] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
RP Waterer, G (reprint author), Univ Western Australia, Perth, WA, Australia.; Waterer, G (reprint author), Northwestern Univ, Chicago, IL 60611 USA.
NR 7
TC 0
Z9 0
U1 0
U2 0
PU AMER THORACIC SOC
PI NEW YORK
PA 25 BROADWAY, 18 FL, NEW YORK, NY 10004 USA
SN 1073-449X
EI 1535-4970
J9 AM J RESP CRIT CARE
JI Am. J. Respir. Crit. Care Med.
PD APR 1
PY 2017
VL 195
IS 7
BP 846
EP 847
PG 2
WC Critical Care Medicine; Respiratory System
SC General & Internal Medicine; Respiratory System
GA EQ4BH
UT WOS:000398017200003
PM 28362200
ER
PT J
AU Robertson, DJ
Lee, JK
Boland, CR
Dominitz, JA
Giardiello, FM
Johnson, DA
Kaltenbach, T
Lieberman, D
Levin, TR
Rex, DK
AF Robertson, Douglas J.
Lee, Jeffrey K.
Boland, C. Richard
Dominitz, Jason A.
Giardiello, Francis M.
Johnson, David A.
Kaltenbach, Tonya
Lieberman, David
Levin, Theodore R.
Rex, Douglas K.
TI Recommendations on Fecal Immunochemical Testing to Screen for Colorectal
Neoplasia: A Consensus Statement by the US Multi-Society Task Force on
Colorectal Cancer
SO GASTROENTEROLOGY
LA English
DT Article
ID OCCULT-BLOOD-TEST; RANDOMIZED CONTROLLED-TRIAL; LOW-DOSE ASPIRIN;
AVERAGE-RISK POPULATION; SAMPLE RETURN TIME; ADENOMA DETECTION;
ASYMPTOMATIC ADULTS; COLONOSCOPY SURVEILLANCE; AMBIENT-TEMPERATURE;
SEASONAL-VARIATIONS
AB The use of the fecal occult blood test ( FOBT) for colorectal cancer ( CRC) screening is supported by randomized trials demonstrating effectiveness in cancer prevention and widely recommended by guidelines for this purpose. The fecal immunochemical test ( FIT), as a direct measure of human hemoglobin in stool has a number of advantages relative to conventional FOBT and is increasingly used relative to that test. This review summarizes current evidence for FIT in colorectal neoplasia detection and the comparative effectiveness of FIT relative to other commonly used CRC screening modalities. Based on evidence, guidance statements on FIT application were developed and quality metrics for program implementation proposed.
C1 [Robertson, Douglas J.] VA Med Ctr, White River Jct, VT USA.
[Robertson, Douglas J.] Geisel Sch Med Dartmouth, Hanover, NH USA.
[Lee, Jeffrey K.] Univ Calif San Francisco, Med Ctr, San Francisco, CA USA.
[Boland, C. Richard] Baylor Univ, Med Ctr, Dallas, TX USA.
[Dominitz, Jason A.] Univ Washington, Sch Med, VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Giardiello, Francis M.] Johns Hopkins Univ, Sch Med, Baltimore, MD USA.
[Johnson, David A.] Eastern VA Med Sch, Norfolk, VA USA.
[Kaltenbach, Tonya] Univ Calif San Francisco, San Francisco Vet Affairs Med Ctr, San Francisco, CA 94143 USA.
[Lieberman, David] Oregon Hlth & Sci Univ, Portland, OR 97201 USA.
[Levin, Theodore R.] Kaiser Permanente Med Ctr, Walnut Creek, CA USA.
[Rex, Douglas K.] Indiana Univ Sch Med, Indianapolis, IN 46202 USA.
RP Robertson, DJ (reprint author), VA Med Ctr, Gastroenterol 111E, 215 N Main St, White River Jct, VT 05009 USA.
EM douglas.robertson@va.gov
FU Olympus; Endochoice
FX This authors discloses the following: David A. Johnson is a clinical
investigator for Exact Sciences and Epigenomics. David Lieberman served
on scientific advisory Board for Exact Sciences. Douglas K. Rex received
consulting fees from Olympus and research support from Endochoice.
Douglas J. Robertson is on the scientific advisory board for Medtronic.
Tonya Kaltenback served as Consultant for Olympus America. The remaining
authors disclose no conflicts.
NR 118
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U2 2
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0016-5085
EI 1528-0012
J9 GASTROENTEROLOGY
JI Gastroenterology
PD APR
PY 2017
VL 152
IS 5
BP 1217
EP +
DI 10.1053/j.gastro.2016.08.053
PG 24
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EP3QV
UT WOS:000397297700046
PM 27769517
ER
PT J
AU Chen, HI
Wolf, JA
Smith, DH
AF Chen, H. Isaac
Wolf, John A.
Smith, Douglas H.
TI Multichannel activity propagation across an engineered axon network
SO JOURNAL OF NEURAL ENGINEERING
LA English
DT Article
DE activity propagation; connectome; neural code; neural interfaces; neural
networks; optogenetics; tissue engineering
ID CORTICAL-NEURONS; IN-VIVO; LONG-RANGE; NEURAL REPRESENTATION; SYNAPTIC
INPUT; VISUAL-CORTEX; CONNECTOME; PLASTICITY; SPIKING; BRAIN
AB Objective. Although substantial progress has been made in mapping the connections of the brain, less is known about how this organization translates into brain function. In particular, the massive interconnectivity of the brain has made it difficult to specifically examine data transmission between two nodes of the connectome, a central component of the 'neural code.' Here, we investigated the propagation of multiple streams of asynchronous neuronal activity across an isolated in vitro 'connectome unit.' Approach. We used the novel technique of axon stretch growth to create a model of a long-range cortico-cortical network, a modular system consisting of paired nodes of cortical neurons connected by axon tracts. Using optical stimulation and multi-electrode array recording techniques, we explored how input patterns are represented by cortical networks, how these representations shift as they are transmitted between cortical nodes and perturbed by external conditions, and how well the downstream node distinguishes different patterns. Main results. Stimulus representations included direct, synaptic, and multiplexed responses that grew in complexity as the distance between the stimulation source and recorded neuron increased. These representations collapsed into patterns with lower information content at higher stimulation frequencies. With internodal activity propagation, a hierarchy of network pathways, including latent circuits, was revealed using glutamatergic blockade. As stimulus channels were added, divergent, non-linear effects were observed in local versus distant network layers. Pairwise difference analysis of neuronal responses suggested that neuronal ensembles generally outperformed individual cells in discriminating input patterns. Significance. Our data illuminate the complexity of spiking activity propagation in cortical networks in vitro, which is characterized by the transformation of an input into myriad outputs over several network layers. These results provide insight into how the brain potentially processes information and generates the neural code and could guide the development of clinical therapies based on multichannel brain stimulation.
C1 [Chen, H. Isaac; Wolf, John A.; Smith, Douglas H.] Univ Penn, Perelman Sch Med, Dept Neurosurg, Philadelphia, PA 19104 USA.
[Chen, H. Isaac; Wolf, John A.] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA 19104 USA.
[Chen, H. Isaac] 3rd Floor,Silverstein Pavil,3400 Spruce St, Philadelphia, PA 19104 USA.
RP Chen, HI (reprint author), Univ Penn, Perelman Sch Med, Dept Neurosurg, Philadelphia, PA 19104 USA.; Chen, HI (reprint author), Philadelphia Vet Affairs Med Ctr, Philadelphia, PA 19104 USA.; Chen, HI (reprint author), 3rd Floor,Silverstein Pavil,3400 Spruce St, Philadelphia, PA 19104 USA.
EM Isaac.Chen@uphs.upenn.edu
OI Chen, Han-Chiao/0000-0002-7431-6046
FU Department of Defense [PT110785]; National Institutes of Health
[F32NS073267, R01NS056202]; Department of Veterans Affairs
[IK2-RX002013, IK2-RX001479]
FX We would like to thank Diego Contreras and Dave Meaney for editorial
input and Andrew Jaye, J P Dolle, Mindy Ezra, and Kevin Truskowski for
technical assistance. This work was supported by the Department of
Defense (PT110785 to DHS), the National Institutes of Health
(F32NS073267 to HIC and R01NS056202 to DHS), and the Department of
Veterans Affairs (IK2-RX002013 to HIC and IK2-RX001479 to JAW). The
authors have no conflicts of interest to report.
NR 56
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PU IOP PUBLISHING LTD
PI BRISTOL
PA TEMPLE CIRCUS, TEMPLE WAY, BRISTOL BS1 6BE, ENGLAND
SN 1741-2560
EI 1741-2552
J9 J NEURAL ENG
JI J. Neural Eng.
PD APR
PY 2017
VL 14
IS 2
AR 026016
DI 10.1088/1741-2552/aa5ccd
PG 12
WC Engineering, Biomedical; Neurosciences
SC Engineering; Neurosciences & Neurology
GA EN3LL
UT WOS:000395909900003
PM 28140365
ER
PT J
AU Nowak, KL
Bartz, TM
Dalrymple, L
de Boer, IH
Kestenbaum, B
Shlipak, MG
Garimella, PS
Ix, JH
Chonchol, M
AF Nowak, Kristen L.
Bartz, Traci M.
Dalrymple, Lorien
de Boer, Ian H.
Kestenbaum, Bryan
Shlipak, Michael G.
Garimella, Pranav S.
Ix, Joachim H.
Chonchol, Michel
TI Fibroblast Growth Factor 23 and the Risk of Infection-Related
Hospitalization in Older Adults
SO JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
LA English
DT Article
ID CHRONIC KIDNEY-DISEASE; VITAMIN-D STATUS; CARDIOVASCULAR EVENTS;
24,25-DIHYDROXYVITAMIN D-3; MINERAL METABOLISM; UNITED-STATES;
CYSTATIN-C; FIBROBLAST-GROWTH-FACTOR-23; HEALTH; DEATH
AB Within monocytes, 1,25-dihydroxyvitamin D [1,25(OH)(2)D] is important for production of cathelicidins, which in turn, are critical for antibacterial action. Fibroblast growth factor 23 (FGF23) decreases 1,25(OH)(2)D production and thus, could increase infection risk. We examined this possibility in 3141 community-dwelling adults ages >= 65 years old at baseline in the Cardiovascular Health Study using Cox proportional hazards models to examine the association between FGF23 concentrations and first infection-related hospitalizations and determine whether associations differed by the presence of CKD (eGFR<60 ml/min per 1.73 m(2) [n=832] or urine albumin-to-creatinine ratio >30 mg/g [n=577]). Mean +/- SD age of participants was 78 5 years old, 60% of participants were women, and the median plasma FGF23 concentration was 70 (interquartile range, 53-99) relative units per milliliter. In fully adjusted models, higher FGF23 concentrations associated with higher risk of first infection related hospitalization (hazard ratio [HR], 1.11; 95% confidence interval [95% CI], 1.03 to 1.20 per doubling of FGF23) during a median follow-up of 8.6 years. In participants with or without CKD (defined by eGFR), FGF23 concentration associated with first infection-related hospitalization with HRs of 1.24 (95% CI, 1.08 to 1.42) and 1.06 (95% CI, 0.97 to 1.17) per doubling of FGF23, respectively (P=0.13 for interaction). Associations did not differ between groups when stratified by urine albumin-to-creatinine ratio. In sensitivity analyses, the addition of serum calcium, phosphorus, 25-hydroxyvitamin D, intact parathyroid hormone, and 24,25-dihydroxyvitamin D did not meaningfully change the estimates. In conclusion, in community-dwelling older adults, higher plasma FGF23 concentrations independently associated with the risk of first infection-related hospitalization.
C1 [Nowak, Kristen L.; Chonchol, Michel] Univ Colorado, Div Renal Dis & Hypertens, Anschutz Med Campus, Aurora, CO USA.
[Bartz, Traci M.] Univ Washington, Dept Biostat, Seattle, WA 98195 USA.
[de Boer, Ian H.] Univ Washington, Div Nephrol, Seattle, WA 98195 USA.
[de Boer, Ian H.; Kestenbaum, Bryan] Univ Washington, Kidney Res Inst, Seattle, WA 98195 USA.
[Dalrymple, Lorien] Univ Calif Davis, Dept Med, Sacramento, CA 95817 USA.
[Shlipak, Michael G.] Univ Calif San Francisco, Dept Med, San Francisco, CA USA.
[Shlipak, Michael G.] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA.
[Shlipak, Michael G.] San Francisco VA Med Ctr, Gen Internal Med Sect, San Francisco, CA USA.
[Garimella, Pranav S.] Tufts Med Ctr, Div Nephrol, Boston, MA USA.
[Ix, Joachim H.] Univ Calif San Diego, Div Nephrol, San Diego, CA 92103 USA.
[Ix, Joachim H.] Univ Calif San Diego, Div Prevent Med, San Diego, CA 92103 USA.
[Ix, Joachim H.] Vet Affairs San Diego Healthcare Syst, Nephrol Sect, San Diego, CA USA.
RP Nowak, KL (reprint author), Univ Colorado Denver, Div Renal Dis & Hypertens, Anschutz Med Campus,12700 East 19th Ave C281, Aurora, CO 80045 USA.
EM Kristen.Nowak@ucdenver.edu
FU National Heart, Lung, and Blood Institute [HHSN268201200036C,
HSN268200800007C, N01HC55222, N01HC85079, N01HC85080, N01HC85081,
N01HC85082, N01HC85083, N01HC85086, HL080295]; National Institute on
Aging; National Institute of Diabetes and Digestive and Kidney Diseases
[K01DK103678]; American Heart Association [0575021N]
FX This research was supported by contracts HHSN268201200036C,
HSN268200800007C, N01HC55222, N01HC85079, N01HC85080, N01HC85081,
N01HC85082, N01HC85083, and N01HC85086 and grant HL080295 from the
National Heart, Lung, and Blood Institute, with additional contribution
from the National Institute of Neurological Disorders and Stroke.
Additional support was provided by grants AG023629 and R01HL094555 from
the National Institute on Aging and grant K01DK103678 from the National
Institute of Diabetes and Digestive and Kidney Diseases. J.H.I. was
supported by American Heart Association award 0575021N, which supported
fibroblast growth factor 23 and the other mineral metabolism
measurements in this study.
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PU AMER SOC NEPHROLOGY
PI WASHINGTON
PA 1725 I ST, NW STE 510, WASHINGTON, DC 20006 USA
SN 1046-6673
EI 1533-3450
J9 J AM SOC NEPHROL
JI J. Am. Soc. Nephrol.
PD APR
PY 2017
VL 28
IS 4
BP 1239
EP 1246
DI 10.1681/ASN.2016040401
PG 8
WC Urology & Nephrology
SC Urology & Nephrology
GA EQ1LZ
UT WOS:000397832900025
PM 28122946
ER
PT J
AU Robinson, TN
Berian, JR
AF Robinson, Thomas N.
Berian, Julia R.
TI Incorporating Patient-centered Outcomes Into Surgical Care
SO ANNALS OF SURGERY
LA English
DT Editorial Material
ID DELIRIUM
C1 [Robinson, Thomas N.] Denver VA Med Ctr, Dept Surg, Denver, CO USA.
[Berian, Julia R.] Amer Coll Surg, Div Res & Optimal Patient Care, Chicago, IL USA.
RP Robinson, TN (reprint author), 1055 Clermont St 112, Denver, CO 80220 USA.
EM thomas.robinson@ucdenver.edu
FU John A. Hartford Foundation; University of Chicago; American College of
Surgeons
FX Dr Berian's position as the James C. Thompson Geriatric Surgery Clinical
Scholar in Residence at the American College of Surgeons is supported by
a grant from the John A. Hartford Foundation. Additional support for Dr
Berian's position as the American College of Surgeons Clinical Scholar
in Residence was provided by the University of Chicago and the American
College of Surgeons.
NR 6
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U2 2
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0003-4932
EI 1528-1140
J9 ANN SURG
JI Ann. Surg.
PD APR
PY 2017
VL 265
IS 4
BP 654
EP 655
DI 10.1097/SLA.0000000000002038
PG 2
WC Surgery
SC Surgery
GA EN4PQ
UT WOS:000395989800004
PM 27735822
ER
PT J
AU Kim, SJ
Chen, ZL
Essani, AB
Elshabrawy, HA
Volin, MV
Fantuzzi, G
McInnes, IB
Baker, JF
Finn, P
Kondos, G
Volkov, S
Swedler, W
Arami, S
Sweiss, N
Shahrara, S
AF Kim, Seung-jae
Chen, Zhenlong
Essani, Abdul B.
Elshabrawy, Hatem A.
Volin, Michael V.
Fantuzzi, Giamila
McInnes, Iain B.
Baker, Joshua F.
Finn, Patricia
Kondos, George
Volkov, Suncica
Swedler, William
Arami, Shiva
Sweiss, Nadera
Shahrara, Shiva
TI Differential impact of obesity on the pathogenesis of RA or preclinical
models is contingent on the disease status
SO ANNALS OF THE RHEUMATIC DISEASES
LA English
DT Article
ID BODY-MASS INDEX; COLLAGEN-INDUCED ARTHRITIS; OF-RHEUMATOLOGY CRITERIA;
ADIPOSE-TISSUE; INTERLEUKIN-8 PRODUCTION; INSULIN-RESISTANCE; INNATE
IMMUNITY; IN-VITRO; CLASSIFICATION; OSTEOARTHRITIS
AB Objective Studies were performed to uncover the significance of obesity in rheumatoid arthritis (RA) and preclinical models.
Methods Preclinical arthritis models were used to examine the impact of obesity on disease onset and remission. Conditioned media from RA adipose tissues were used to investigate the mechanism contributing to joint neutrophil influx and M1 macrophage differentiation observed in early and remission phases of arthritis.
Results We report that mice fed with high fat diet (HFD) have an earlier onset of collagen-induced arthritis (CIA) compared with mice on regular diet. However, the differences in CIA joint swelling between the two diet groups are lost once disease is established. We found that early arthritis triggered by obesity is due to elevated joint MIP2/interleukin-8 levels detected in CIA as well as in the RA and mouse adipose tissues and the effect of this chemokine on neutrophil recruitment. Although active disease progression is similarly affected in both diet groups, arthritis resolution is accelerated in lean mice while joint inflammation is sustained in obese mice. We document that HFD can prolong toll-like receptor (TLR) 4-induced arthritis by increasing joint monocyte migration and further remodelling the recruited cells into M1 macrophages. Consistently, we show that adipose condition media can transform RA and wild-type naive myeloid cells into M1 macrophages; however, this function is impaired by TLR4 blockade or deficiency.
Conclusions We conclude that despite established disease being unaffected by obesity, the early and the resolution phases of RA are impacted by obesity through different mechanisms.
C1 [Volin, Michael V.] Univ Illinois, Dept Med, Div Rheumatol, 840 S Woods St,Bldg CSB,Room 1113-1114, Chicago, IL 60612 USA.
[Kim, Seung-jae; Chen, Zhenlong; Essani, Abdul B.; Elshabrawy, Hatem A.; Swedler, William; Arami, Shiva; Sweiss, Nadera; Shahrara, Shiva] Jesse Brown VA Med Ctr, Div Rheumatol, Chicago, IL USA.
[Kim, Seung-jae; Chen, Zhenlong; Essani, Abdul B.; Elshabrawy, Hatem A.; Volkov, Suncica; Swedler, William; Arami, Shiva; Shahrara, Shiva] Midwestern Univ, Dept Microbiol & Immunol, Downers Grove, IL 60515 USA.
[Fantuzzi, Giamila] Univ Illinois, Dept Kinesiol & Nutr, Chicago, IL USA.
[McInnes, Iain B.] Univ Glasgow, Inst Infect Immun & Inflammat, Glasgow, Lanark, Scotland.
[Baker, Joshua F.] Philadelphia VA Med Ctr, Philadelphia, PA USA.
[Baker, Joshua F.] Hosp Univ Penn, Dept Med, Div Rheumatol, Philadelphia, PA 19104 USA.
[Finn, Patricia] Univ Illinois, Div Med, Div Pulm, Chicago, IL USA.
[Kondos, George] Univ Illinois, Div Med, Div Cardiol, Chicago, IL USA.
RP Shahrara, S (reprint author), Univ Illinois, Dept Med, Div Rheumatol, 840 S Woods St,Bldg CSB,Room 1113-1114, Chicago, IL 60612 USA.
EM shahrara@uic.edu
FU Department of Veteran's Affairs MERIT Award [1I01BX002286]; National
Institutes of Health [AR055240, AR065778]; Within Our Reach from the
ACR; Department of Defense [PR093477]; Arthritis Foundation Innovative
award; VA clinical science research and development; VA Career
Development Award [IK2 CX000955]
FX This work was supported in part by awards from Department of Veteran's
Affairs MERIT Award 1I01BX002286, the National Institutes of Health
AR055240 and AR065778, grant from Within Our Reach from the ACR, funding
provided by Department of Defense PR093477 and Arthritis Foundation
Innovative award. JFB efforts were funded by VA clinical science
research and development as well as VA Career Development Award IK2
CX000955.
NR 54
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PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 0003-4967
EI 1468-2060
J9 ANN RHEUM DIS
JI Ann. Rheum. Dis.
PD APR
PY 2017
VL 76
IS 4
AR UNSP 731
DI 10.1136/annrheumdis-2016-209206
PG 9
WC Rheumatology
SC Rheumatology
GA EO7FH
UT WOS:000396856100019
ER
PT J
AU Singh, JA
Uhlig, T
AF Singh, Jasvinder A.
Uhlig, Till
TI Chasing crystals out of the body: will treat to serum urate target for
gout help us get there?
SO ANNALS OF THE RHEUMATIC DISEASES
LA English
DT Editorial Material
ID QUALITY-OF-LIFE; LOWERING THERAPY; ALLOPURINOL; CARE; HYPERURICEMIA;
FEBUXOSTAT; ADHERENCE; RECOMMENDATIONS; PRODUCTIVITY; MANAGEMENT
C1 [Singh, Jasvinder A.] Birmingham VA Med Ctr, Birmingham, AL USA.
[Singh, Jasvinder A.] Univ Alabama Birmingham, Sch Med, Dept Med, Birmingham, AL USA.
[Singh, Jasvinder A.] Univ Alabama Birmingham, Sch Publ Hlth, Div Epidemiol, Birmingham, AL 35294 USA.
[Uhlig, Till] Diakonhjemmet Hosp, Dept Rheumatol, Natl Advisory Unit Rehabil Rheumatol, Oslo, Norway.
[Uhlig, Till] Univ Oslo, Fac Med, Oslo, Norway.
RP Singh, JA (reprint author), Univ Alabama Birmingham, Fac Off Tower 805B,510 20th St S, Birmingham, AL 35294 USA.
EM Jasvinder.md@gmail.com
FU Takeda; Savient; Regeneron; Merz; Iroko; Bioiberica; Crealta; Allergan
pharmaceuticals; WebMD; UBM LLC; American College of Rheumatology;
Horizon pharmaceuticals; AstraZeneca; Novartis; Sobi
FX JAS has received research grants from Takeda and Savient and consultant
fees from Savient, Takeda, Regeneron, Merz, Iroko, Bioiberica, Crealta
and Allergan pharmaceuticals, WebMD, UBM LLC and the American College of
Rheumatology. JAS serves as the principal investigator for an
investigator-initiated study funded by Horizon pharmaceuticals through a
grant to DINORA, a 501 (c) (3) entity. JAS is a member of the executive
of OMERACT, an organisation that develops outcome measures in
rheumatology and receives arms-length funding from 36 companies; a
member of the American College of Rheumatology's (ACR) Annual Meeting
Planning Committee (AMPC); Chair of the ACR Meet-the-Professor, Workshop
and Study Group Subcommittee and a member of the Veterans Affairs
Rheumatology Field Advisory Committee. TU has received honorarium or
consultant fees from AstraZeneca, Novartis and Sobi.
NR 34
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PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 0003-4967
EI 1468-2060
J9 ANN RHEUM DIS
JI Ann. Rheum. Dis.
PD APR
PY 2017
VL 76
IS 4
DI 10.1136/annrheumdis-2016-210436
PG 3
WC Rheumatology
SC Rheumatology
GA EO7FH
UT WOS:000396856100003
ER
PT J
AU Chawla, LS
Bellomo, R
Bihorac, A
Goldstein, SL
Siew, ED
Bagshaw, SM
Bittleman, D
Cruz, D
Endre, Z
Fitzgerald, RL
Forni, L
Kane-Gill, SL
Hoste, E
Koyner, J
Liu, KD
Macedo, E
Mehta, R
Murray, P
Nadim, M
Ostermann, M
Palevsky, PM
Pannu, N
Rosner, M
Wald, R
Zarbock, A
Ronco, C
Kellum, JA
AF Chawla, Lakhmir S.
Bellomo, Rinaldo
Bihorac, Azra
Goldstein, Stuart L.
Siew, Edward D.
Bagshaw, Sean M.
Bittleman, David
Cruz, Dinna
Endre, Zoltan
Fitzgerald, Robert L.
Forni, Lui
Kane-Gill, Sandra L.
Hoste, Eric
Koyner, Jay
Liu, Kathleen D.
Macedo, Etienne
Mehta, Ravindra
Murray, Patrick
Nadim, Mitra
Ostermann, Marlies
Palevsky, Paul M.
Pannu, Neesh
Rosner, Mitchell
Wald, Ron
Zarbock, Alexander
Ronco, Claudio
Kellum, John A.
TI Acute kidney disease and renal recovery: consensus report of the Acute
Disease Quality Initiative (ADQI) 16 Workgroup
SO NATURE REVIEWS NEPHROLOGY
LA English
DT Article
ID CRITICALLY-ILL PATIENTS; GLOMERULAR-FILTRATION-RATE; ACUTE
TUBULAR-NECROSIS; GELATINASE-ASSOCIATED LIPOCALIN; ANGIOTENSIN RECEPTOR
BLOCKERS; REPLACEMENT THERAPY MODALITY; INJURY REQUIRING DIALYSIS; SERUM
CREATININE LEVEL; LONG-TERM SURVIVAL; CARDIAC-SURGERY
AB Consensus definitions have been reached for both acute kidney injury (AKI) and chronic kidney disease (CKD) and these definitions are now routinely used in research and clinical practice. The KDIGO guideline defines AKI as an abrupt decrease in kidney function occurring over 7 days or less, whereas CKD is defined by the persistence of kidney disease for a period of > 90 days. AKI and CKD are increasingly recognized as related entities and in some instances probably represent a continuum of the disease process. For patients in whom pathophysiologic processes are ongoing, the term acute kidney disease (AKD) has been proposed to define the course of disease after AKI; however, definitions of AKD and strategies for the management of patients with AKD are not currently available. In this consensus statement, the Acute Disease Quality Initiative (ADQI) proposes definitions, staging criteria for AKD, and strategies for the management of affected patients. We also make recommendations for areas of future research, which aim to improve understanding of the underlying processes and improve outcomes for patients with AKD.
C1 [Chawla, Lakhmir S.] Vet Affairs Med Ctr, Dept Med, 50 Irving St, Washington, DC 20310 USA.
[Bellomo, Rinaldo] Monash Univ, Australian & New Zealand Intens Care Res Ctr, Clayton, Vic 3800, Australia.
[Bihorac, Azra] Univ Florida, Dept Med, Gainesville, FL 32611 USA.
[Goldstein, Stuart L.] Cincinnati Childrens Hosp Med Ctr, Div Nephrol & Hypertens, Cincinnati, OH 45229 USA.
[Siew, Edward D.] Vanderbilt Univ, Sch Med, Div Nephrol & Hypertens, Nashville, TN USA.
[Bagshaw, Sean M.] Univ Alberta, Fac Med & Dent, Div Crit Care Med, Edmonton, AB T6G 2M7, Canada.
[Bittleman, David] Univ Calif San Diego, Dept Med, San Diego, CA USA.
[Cruz, Dinna] Univ Calif San Diego, UCSD Med Ctr, San Diego, CA USA.
[Endre, Zoltan] Univ New South Wales, Prince Wales Hosp, Dept Nephrol, Kensington, NSW, Australia.
[Endre, Zoltan] Univ New South Wales, Sch Clin, Kensington, NSW, Australia.
[Forni, Lui] Surrey Cty Hosp, Surrey, England.
[Kane-Gill, Sandra L.] Univ Pittsburgh, Sch Pharm, Pittsburgh, PA 15260 USA.
[Hoste, Eric] Univ Ghent, Ghent Univ Hosp, Intens Care Unit, Ghent, Belgium.
[Koyner, Jay] Univ Chicago, Dept Med, Chicago, IL USA.
[Liu, Kathleen D.] Univ Calif San Francisco, Dept Med & Anesthesia, Divi Nephrol & Crit Care, San Francisco, CA 94143 USA.
[Murray, Patrick] Uni Coll Dublin, UCD Hlth Sci Ctr, Dublin, Ireland.
[Nadim, Mitra] Univ Southern California, Keck Sch Med, Dept Med, Div Nephrol, Los Angeles, CA USA.
[Ostermann, Marlies] Guys & St Thomas NHS Fdn Hosp, Dept Intens Care, Westminster, England.
[Palevsky, Paul M.] VA Pittsburgh Healthcare Syst, Renal Sect, Pittsburgh, PA USA.
[Palevsky, Paul M.] Univ Pittsburgh, Renal Electrolyte Div, Pittsburgh, PA USA.
[Pannu, Neesh] Univ Alberta, Fac Med & Dent, Div Crit Care Med, Edmonton, AB T6G 2M7, Canada.
[Rosner, Mitchell] Univ Virginia, Div Nephrol, Charlottesville, VA 22903 USA.
[Wald, Ron] St Michaels Hosp, Div Nephrol, Toronto, ON, Canada.
[Wald, Ron] Univ Toronto, Toronto, ON, Canada.
[Zarbock, Alexander] Univ Hosp Munster, Munster, Germany.
[Ronco, Claudio] San Bortolo Hosp, Int Renal Res Inst Vicenza, Dept Nephrol, Dept Dialysis & Transplantat, Vicenza, Italy.
[Kellum, John A.] Univ Pittsburgh, Ctr Crit Care Nephrol, Dept Crit Care Med, Pittsburgh, PA USA.
RP Chawla, LS (reprint author), Vet Affairs Med Ctr, Dept Med, 50 Irving St, Washington, DC 20310 USA.
EM minkchawla@gmail.com
FU Baxter Medical; Astute Medical; INC; Society of Critical Care Medicine;
Gambro Renal Products; VitaFlo; Mallinckrodt; Baxter Healthcare; Bellco;
AM Pharma; La Jolla Pharmaceuticals; Relypsa; Fresenius-Kabi; iSAEC;
Fresenius Medical Care; Baxter; Fresenius
FX L.S.C. has received consulting fees from Astute Medical, Nxstage Medical
and Bard Medical. R.B has received research support from Baxter Medical.
A.B. has received research support from Astute Medical, INC and the
Society of Critical Care Medicine. S.L.G. has received grants from
Gambro Renal Products, VitaFlo, Mallinckrodt, and Alexion; grants and
personal fees from Baxter Healthcare, Astute Medical, Bellco, AM Pharma,
and La Jolla Pharmaceuticals; and personal fees from Bioporto, Akebia,
Otsuka, Kaneka, and MediBeacon, all outside the submitted work. S.M.B.
has received consulting fees from Baxter and La Jolla Pharmaceuticals.
L.F. has received receiving consulting fees from Fresenius, Astute
Medical, Eras Pharma, Baxter, and Ortho Clinical. E.H. has received
speaker's fees from Alexion and a research grant from Bellco. J.K. has
received consulting fees from Nxstage Medical, Astute Medical,
Sphingotec and Pfizer. E.M. has received research funding from Relypsa
and Fresenius-Kabi. R.M. has received consulting fees from Eli Lilly,
Spectral, Keryx, Baxter, Ardea, AM Pharma, GSK, CSL Behring, Grifols,
Astute Inc. Fresenius-Kabi, Quark, Ferring Research, Ionis
Pharmaceuticals, Johnsons and Johnson and DURECT, and has received
research support from iSAEC, Relypsa, Fresenius-Kabi and Fresenius. M.O.
has received speaker honoraria and research funding from Fresenius
Medical Care, and payment for advisory services from Baxter/Gambro.
P.M.P has received consulting fees from Durect and Baxter. R.W. has
received consulting fees from Durect and MedBeacon and unrestricted
research support from Baxter. A.Z. has received unrestricted research
grants from Fresenius and Astute Medical and lecture fees from
Fresenius, Braun, Astute Medical, and Astellas. C.R. has received
consulting fees from Astute, Asahi, GE and Baxter. J.A.K. has received
consulting fees from Astute Medical, Atoc Bio, Astellas, Bard Medical,
Baxter Medical, Bioporto, Grifols, Medibeacon and Nxstage Medical.
E.D.S., D.B., D.C., Z.E., R.L.F., S.L.K.-G., K.D.L., P.M, M.N., N.P. and
M.R. declare no competing interests.
NR 152
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U1 4
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PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 1759-5061
EI 1759-507X
J9 NAT REV NEPHROL
JI Nat. Rev. Nephrol.
PD APR
PY 2017
VL 13
IS 4
BP 241
EP 257
DI 10.1038/nrneph.2017.2
PG 17
WC Urology & Nephrology
SC Urology & Nephrology
GA EP3QN
UT WOS:000397296900007
PM 28239173
ER
PT J
AU Aarsland, D
Creese, B
Politis, M
Chaudhuri, KR
Ffytche, DH
Weintraub, D
Ballard, C
AF Aarsland, Dag
Creese, Byron
Politis, Marios
Chaudhuri, K. Ray
Ffytche, Dominic H.
Weintraub, Daniel
Ballard, Clive
TI Cognitive decline in Parkinson disease
SO NATURE REVIEWS NEUROLOGY
LA English
DT Review
ID POSITRON-EMISSION-TOMOGRAPHY; DEEP BRAIN-STIMULATION; LEWY BODY
DEMENTIA; CEREBROSPINAL-FLUID BIOMARKERS; CLINICAL DIAGNOSTIC-CRITERIA;
FACTOR G196A POLYMORPHISM; 5-YEAR FOLLOW-UP; ALPHA-SYNUCLEIN;
ALZHEIMERS-DISEASE; AMYLOID-BETA
AB Dementia is a frequent problem encountered in advanced stages of Parkinson disease (PD). In recent years, research has focused on the pre-dementia stages of cognitive impairment in PD, including mild cognitive impairment (MCI). Several longitudinal studies have shown that MCI is a harbinger of dementia in PD, although the course is variable, and stabilization of cognition-or even reversal to normal cognition - is not uncommon. In addition to limbic and cortical spread of Lewy pathology, several other mechanisms are likely to contribute to cognitive decline in PD, and a variety of biomarker studies, some using novel structural and functional imaging techniques, have documented in vivo brain changes associated with cognitive impairment. The evidence consistently suggests that low cerebrospinal fluid levels of amyloid-beta(42), a marker of comorbid Alzheimer disease (AD), predict future cognitive decline and dementia in PD. Emerging genetic evidence indicates that in addition to the APOE*epsilon 4 allele (an established risk factor for AD), GBA mutations and SCNA mutations and triplications are associated with cognitive decline in PD, whereas the findings are mixed for MAPT polymorphisms. Cognitive enhancing medications have some effect in PD dementia, but no convincing evidence that progression from MCI to dementia can be delayed or prevented is available, although cognitive training has shown promising results.
C1 [Aarsland, Dag; Creese, Byron; Politis, Marios; Chaudhuri, K. Ray; Ffytche, Dominic H.; Weintraub, Daniel; Ballard, Clive] Kings Coll London, Inst Psychiat Psychol & Neurosci, KCL PARCOG Grp, De Crespigny Pk, London SE5 8AF, England.
[Aarsland, Dag; Ffytche, Dominic H.] Kings Coll London, Inst Psychiat Psychol & Neurosci, Dept Old Age Psychiat, De Crespigny Pk, London SE5 8AF, England.
[Creese, Byron; Ballard, Clive] Univ Exeter, Sch Med, Exeter EX1 2LU, Devon, England.
[Politis, Marios] Kings Coll London, Neurodegenerat Imaging Grp, Maurice Wohl Clin Neurosci Inst, Inst Psychiat Psychol & Neurosci, 125 Coldharbour Lane, London SE5 9NU, England.
[Chaudhuri, K. Ray] Kings Coll London, Dept Basic & Clin Neurosci, Maurice Wohl Clin Neurosci Inst, Natl Parkinson Fdn Ctr Excellence,Kings Coll Hosp, 5 Cutcombe Rd, London SE5 9RT, England.
[Weintraub, Daniel] Univ Penn, Perelman Sch Med, Dept Psychiat, 3615 Chestnut St,330, Philadelphia, PA 19104 USA.
[Weintraub, Daniel] Univ Penn, Perelman Sch Med, Dept Neurol, 3615 Chestnut St,330, Philadelphia, PA 19104 USA.
[Weintraub, Daniel] Philadelphia Vet Affairs Med Ctr, Parkinsons Dis Ctr, PADRECC & MIRECC, 3900 Woodland Ave, Philadelphia, PA 19104 USA.
[Weintraub, Daniel] Philadelphia Vet Affairs Med Ctr, Mental Illness Res Educ & Clin Ctr, PADRECC & MIRECC, 3900 Woodland Ave, Philadelphia, PA 19104 USA.
RP Aarsland, D (reprint author), Kings Coll London, Inst Psychiat Psychol & Neurosci, KCL PARCOG Grp, De Crespigny Pk, London SE5 8AF, England.
EM daarsland@gmail.com
OI Aarsland, Dag/0000-0001-6314-216X
FU National Institute for Health Research (NIHR) Mental Health Biomedical
Research Centre and Dementia Unit at South London and Maudsley NHS
Foundation Trust; Institute of Psychiatry, Psychology and Neuroscience,
King's College London, UK; Wolfson Foundation; Royal Society
FX The authors thank Dr Michael Haworth for help in preparing the final
manuscript. The authors would like to thank the National Institute for
Health Research (NIHR) Mental Health Biomedical Research Centre and
Dementia Unit at South London and Maudsley NHS Foundation Trust and
Institute of Psychiatry, Psychology and Neuroscience, King's College
London, UK. D.A. is a Royal Society Wolfson Research Merit Award Holder
and would like to thank the Wolfson Foundation and the Royal Society for
their support. The views expressed are those of the authors and not
necessarily those of the NHS, the NIHR or the Department of Health.
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PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 1759-4758
EI 1759-4766
J9 NAT REV NEUROL
JI Nat. Rev. Neurol.
PD APR
PY 2017
VL 13
IS 4
BP 217
EP 231
DI 10.1038/nrneurol.2017.27
PG 15
WC Clinical Neurology
SC Neurosciences & Neurology
GA EP7KU
UT WOS:000397557500005
PM 28257128
ER
PT J
AU Egervari, G
Landry, J
Callens, J
Fullard, JF
Roussos, P
Keller, E
Hurd, YL
AF Egervari, Gabor
Landry, Joseph
Callens, James
Fullard, John F.
Roussos, Panos
Keller, Eva
Hurd, Yasmin L.
TI Striatal H3K27 Acetylation Linked to Glutamatergic Gene Dysregulation in
Human Heroin Abusers Holds Promise as Therapeutic Target
SO BIOLOGICAL PSYCHIATRY
LA English
DT Article
DE Addiction; Epigenetics; Glutamate; Heroin; Histone acetylation; JQ1
ID BROMODOMAIN INHIBITOR OTX015; GLOBAL HISTONE ACETYLATION;
COCAINE-INDUCED PLASTICITY; ACTIVATES TRANSCRIPTION; EPIGENETIC
MECHANISMS; DOSE-ESCALATION; DRUG-ADDICTION; EXPRESSION; CHROMATIN;
METHYLATION
AB BACKGROUND: Opiate abuse and overdose reached epidemic levels in the United States. However, despite significant advances in animal and in vitro models, little knowledge has been directly accrued regarding the neurobiology of the opiate-addicted human brain.
METHODS: We used postmortem human brain specimens from a homogeneous European Caucasian population of heroin users for transcriptional and epigenetic profiling, as well as direct assessment of chromatin accessibility in the striatum, a brain region central to reward and emotion. A rat heroin self-administration model was used to obtain translational molecular and behavioral insights.
RESULTS: Our transcriptome approach revealed marked impairments related to glutamatergic neurotransmission and chromatin remodeling in the human striatum. A series of biochemical experiments tracked the specific location of the epigenetic disturbances to hyperacetylation of lysine 27 of histone H3, showing dynamic correlations with heroin use history and acute opiate toxicology. Targeted investigation of GRIA1, a glutamatergic gene implicated in drug-seeking behavior, verified the increased enrichment of lysine-27 acetylated histone H3 at discrete loci, accompanied by enhanced chromatin accessibility at hyperacetylated regions in the gene body. Analogous epigenetic impairments were detected in the striatum of heroin self-administering rats. Using this translational model, we showed that bromodomain inhibitor JQ1, which blocks the functional readout of acetylated lysines, reduced heroin self-administration and cue-induced drug-seeking behavior.
CONCLUSIONS: Overall, our data suggest that heroin-related histone H3 hyperacetylation contributes to glutamatergic transcriptional changes that underlie addiction behavior and identify JQ1 as a promising candidate for targeted clinical interventions in heroin use disorder.
C1 [Egervari, Gabor; Landry, Joseph; Callens, James; Fullard, John F.; Roussos, Panos; Hurd, Yasmin L.] Icahn Sch Med Mt Sinai, Friedman Brain Inst, Dept Psychiat, 1470 Madison Ave, New York, NY 10029 USA.
[Egervari, Gabor; Landry, Joseph; Callens, James; Hurd, Yasmin L.] Icahn Sch Med Mt Sinai, Friedman Brain Inst, Dept Neurosci, New York, NY USA.
[Fullard, John F.; Roussos, Panos] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY USA.
[Fullard, John F.; Roussos, Panos] Icahn Sch Med Mt Sinai, Inst Multiscale Biol, New York, NY USA.
[Roussos, Panos] James J Peters VA Med Ctr, Mental Illness Res Educ & Clin Ctr VISN 3, Bronx, NY USA.
[Keller, Eva] Semmelweis Univ, Dept Forens Med, Budapest, Hungary.
RP Hurd, YL (reprint author), Icahn Sch Med Mt Sinai, Friedman Brain Inst, Dept Psychiat, 1470 Madison Ave, New York, NY 10029 USA.
EM Yasmin.Hurd@mssm.edu
FU National Institutes of Health [DA15446, DA008227, AG050986]; Veterans
Affairs [BX002395]
FX This work was supported by grants from the National Institutes of Health
(Grant Nos. DA15446 to YLH and EK, DA008227 to YLH, AG050986 to PR) and
the Veterans Affairs (Merit Grant No. BX002395 to PR).
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PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0006-3223
EI 1873-2402
J9 BIOL PSYCHIAT
JI Biol. Psychiatry
PD APR 1
PY 2017
VL 81
IS 7
BP 585
EP 594
DI 10.1016/j.biopsych.2016.09.015
PG 10
WC Neurosciences; Psychiatry
SC Neurosciences & Neurology; Psychiatry
GA EP3RX
UT WOS:000397300500013
PM 27863698
ER
PT J
AU Morton, GJ
Muta, K
Kaiyala, KJ
Rojas, JM
Scarlett, JM
Matsen, ME
Nelson, JT
Acharya, NK
Piccinini, F
Stefanovski, D
Bergman, RN
Taborsky, GJ
Kahn, SE
Schwartz, MW
AF Morton, Gregory J.
Muta, Kenjiro
Kaiyala, Karl J.
Rojas, Jennifer M.
Scarlett, Jarrad M.
Matsen, Miles E.
Nelson, Jarrell T.
Acharya, Nikhil K.
Piccinini, Francesca
Stefanovski, Darko
Bergman, Richard N.
Taborsky, Gerald J., Jr.
Kahn, Steven E.
Schwartz, Michael W.
TI Evidence That the Sympathetic Nervous System Elicits Rapid, Coordinated,
and Reciprocal Adjustments of Insulin Secretion and Insulin Sensitivity
During Cold Exposure
SO DIABETES
LA English
DT Article
ID GLUCOSE-TOLERANCE; INTRAVENOUS GLUCOSE; PERIPHERAL-TISSUES; DISPOSITION
INDEX; B-CELL; RESISTANCE; RATS; DIET; DOGS; QUANTIFICATION
AB Dynamic adjustment of insulin secretion to compensate for changes of insulin sensitivity that result from alteration of nutritional or metabolic status is a fundamental aspect of glucose homeostasis. To investigate the role of the brain in this coupling process, we used cold exposure as an experimental paradigm because the sympathetic nervous system (SNS) helps to coordinate the major shifts of tissue glucose utilization needed to ensure that increased thermogenic needs are met. We found that glucose-induced insulin secretion declined by 50% in rats housed at 5 degrees C for 28 h, and yet, glucose tolerance did not change, owing to a doubling of insulin sensitivity. These potent effects on insulin secretion and sensitivity were fully reversed by returning animals to room temperature (22 degrees C) for 4 h or by intravenous infusion of the alpha-adrenergic receptor antagonist phentolamine for only 30 min. By comparison, insulin clearance was not affected by cold exposure or phentolamine infusion. These findings offer direct evidence of a key role for the brain, acting via the SNS, in the rapid, highly coordinated, and reciprocal changes of insulin secretion and insulin sensitivity that preserve glucose homeostasis in the setting of cold exposure.
C1 [Morton, Gregory J.; Muta, Kenjiro; Rojas, Jennifer M.; Scarlett, Jarrad M.; Matsen, Miles E.; Nelson, Jarrell T.; Acharya, Nikhil K.; Schwartz, Michael W.] Univ Washington, Dept Med, Inst Diabet, Seattle, WA 98105 USA.
[Kaiyala, Karl J.] Univ Washington, Sch Dent, Dept Oral Hlth Sci, Seattle, WA 98195 USA.
[Scarlett, Jarrad M.] Seattle Childrens Hosp, Dept Pediat Gastroenterol & Hepatol, Seattle, WA USA.
[Piccinini, Francesca; Bergman, Richard N.] Cedars Sinai Med Ctr, Diabet & Obes Res Inst, Los Angeles, CA 90048 USA.
[Stefanovski, Darko] Univ Penn, Sch Vet Med, New Bolton Ctr, Philadelphia, PA 19104 USA.
[Taborsky, Gerald J., Jr.; Kahn, Steven E.] Vet Affairs Puget Sound Hlth Care Syst, Dept Vet Affairs Med Ctr, Seattle, WA USA.
RP Schwartz, MW (reprint author), Univ Washington, Dept Med, Inst Diabet, Seattle, WA 98105 USA.
EM mschwart@u.washington.edu
FU National Institutes of Health, National Institute of Diabetes and
Digestive and Kidney Diseases [DK-089056, DK-27619, DK-29867, DK-50154,
DK-083042, DK-090320, DK-101997]; National Institute of Diabetes and
Digestive Kidney Diseases-funded Nutrition Obesity Research Center
[DK-035816]; Diabetes Research Center [DK-017047]; Nutrition, Obesity
and Atherosclerosis Training Grant from the National Heart, Lung, and
Blood Institute [T32-HL007028]; Diabetes and Metabolism Training Grant
at the University of Washington [T32-DK-0007247]; Department of Veterans
Affairs [BX001060]
FX This work was supported by National Institutes of Health, National
Institute of Diabetes and Digestive and Kidney Diseases grants DK-089056
(G.J.M.), DK-27619 and DK-29867 (R.N.B.), DK-50154 (G.J.T.), DK-083042,
DK-090320, and DK-101997 (M.W.S.); the National Institute of Diabetes
and Digestive Kidney Diseases-funded Nutrition Obesity Research Center
(DK-035816) and Diabetes Research Center (DK-017047); the Nutrition,
Obesity and Atherosclerosis Training Grant from the National Heart,
Lung, and Blood Institute (T32-HL007028) and the Diabetes and Metabolism
Training Grant (T32-DK-0007247) at the University of Washington; and the
Department of Veterans Affairs grant BX001060 (S.E.K.).
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PU AMER DIABETES ASSOC
PI ALEXANDRIA
PA 1701 N BEAUREGARD ST, ALEXANDRIA, VA 22311-1717 USA
SN 0012-1797
EI 1939-327X
J9 DIABETES
JI Diabetes
PD APR
PY 2017
VL 66
IS 4
BP 823
EP 834
DI 10.2337/db16-1351
PG 12
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EP0ZJ
UT WOS:000397114900007
PM 28115396
ER
PT J
AU Schrag, A
Weintraub, D
Schott, JM
AF Schrag, Anette
Weintraub, Daniel
Schott, Jonathan M.
TI Cognitive decline before diagnosis of Parkinson's disease Reply
SO LANCET NEUROLOGY
LA English
DT Letter
C1 [Schrag, Anette; Schott, Jonathan M.] UCL, UCL Inst Neurol, London, England.
[Weintraub, Daniel] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Weintraub, Daniel] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA USA.
RP Schrag, A (reprint author), UCL, UCL Inst Neurol, London, England.
EM a.schrag@ucl.ac.uk
FU Economic and Social Research Council; GE Healthcare; Parkinson's UK; EU
FP7; Movement Disorders Society; Medtronic; AstraZeneca; Roche; Eli
Lilly; AVID Radiopharmaceuticals
FX AS reports grants from Economic and Social Research Council, GE
Healthcare, Parkinson's UK, EU FP7, and the Movement Disorders Society;
and personal fees from Medtronic and AstraZeneca. JMS reports personal
fees from Roche and Eli Lilly, grants and non-financial support from
AVID Radiopharmaceuticals, and serves on a data safety management board
for Axon Neuroscience. DW declares no competing interests.
NR 5
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U1 4
U2 4
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1474-4422
EI 1474-4465
J9 LANCET NEUROL
JI Lancet Neurol.
PD APR
PY 2017
VL 16
IS 4
BP 262
EP 262
PG 1
WC Clinical Neurology
SC Neurosciences & Neurology
GA EN9RF
UT WOS:000396336600012
PM 28327332
ER
PT J
AU Jimenez, AM
Lee, J
Green, MF
Wynn, JK
AF Jimenez, Amy M.
Lee, Junghee
Green, Michael F.
Wynn, Jonathan K.
TI Functional connectivity when detecting rare visual targets in
schizophrenia
SO PSYCHIATRY RESEARCH-NEUROIMAGING
LA English
DT Article
DE fMRI; Psychophysiological interaction; Attention; Salience; Oddball;
Target detection
ID EVENT-RELATED FMRI; VENTRAL ATTENTION SYSTEMS; NEGATIVE SYMPTOMS; BRAIN
NETWORKS; HEMODYNAMIC-RESPONSES; ODDBALL FMRI; SEARCH; DORSAL; P300;
TASK
AB Individuals with schizophrenia demonstrate difficulties in attending to important stimuli (e.g., targets) and ignoring distractors (e.g., non-targets). We used a visual oddball task during fMRI to examine functional connectivity within and between the ventral and dorsal attention networks to determine the relative contribution of each network to detection of rare visual targets in schizophrenia. The sample comprised 25 schizophrenia patients and 27 healthy controls. Psychophysiological interaction analysis was used to examine whole-brain functional connectivity in response to targets. We used the right temporo parietal junction (TPJ) as the seed region for the ventral network and the right medial intraparietal sulcus (IPS) as the seed region for the dorsal network. We found that connectivity between right IPS and right anterior insula (AI; a component of the ventral network) was significantly greater in controls than patients. Expected patterns of within-and between network connectivity for right TPJ were observed in controls, and not significantly different in patients. These findings indicate functional connectivity deficits between the dorsal and ventral attention networks in schizophrenia that may create problems in processing relevant versus irrelevant stimuli. Understanding the nature of network disruptions underlying cognitive deficits of schizophrenia may help shed light on the pathophysiology of this disorder.
C1 [Jimenez, Amy M.; Lee, Junghee; Green, Michael F.; Wynn, Jonathan K.] VA Greater Los Angeles Healthcare Syst, Desert Pacific MIRECC, Los Angeles, CA USA.
[Jimenez, Amy M.; Lee, Junghee; Green, Michael F.; Wynn, Jonathan K.] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90024 USA.
RP Jimenez, AM (reprint author), VA Greater Los Angeles Healthcare Syst, MIRECC, Bldg 210,11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM amjimenez@ucla.edu
FU VA Career Development Award; NIMH [MH43292, MH065707]
FX This research was supported by a VA Career Development Award to Jonathan
K. Wynn, Ph.D. and NIMH Grants MH43292 and MH065707 (PI: Michael F.
Green, Ph.D.). Writing of this manuscript was supported by the Office of
Academic Affiliations, Advanced Fellowship Program in Mental Illness
Research and Treatment, Department of Veterans Affairs. For generous
support, we also thank the Brain Mapping Medical Research Organization,
Brain Mapping Support Foundation, Pierson -Lovelace Foundation, The
Ahmanson Foundation, William M. and Linda R. Dietel Philanthropic Fund
at the Northern Piedmont Community Foundation, Tamkin Foundation,
Jennifer Jones-Simon Foundation, Capital Group Companies Charitable
Foundation, Robson Family, and Northstar Fund. The authors thank Poorang
Nori and Crystal Gibson for assistance in data collection. The funders
had no role in the study design, data collection and analysis, decision
to publish, or preparation of the manuscript. These data were presented,
in part, as a poster at the 2015 Annual Meeting of the Society for
Research in Psychopathology.
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0925-4927
EI 1872-7506
J9 PSYCHIAT RES-NEUROIM
JI Psychiatry Res. Neuroimaging
PD MAR 30
PY 2017
VL 261
BP 35
EP 43
DI 10.1016/j.pscychresns.2017.01.007
PG 9
WC Clinical Neurology; Neuroimaging; Psychiatry
SC Neurosciences & Neurology; Psychiatry
GA EN4DT
UT WOS:000395958900005
PM 28126618
ER
PT J
AU AuYoung, M
Damschroder, LJ
Kinsinger, L
Moin, T
Richardson, CR
AF AuYoung, Mona
Damschroder, Laura J.
Kinsinger, Linda
Moin, Tannaz
Richardson, Caroline R.
TI Practical partnered research to improve weight loss among
overweight/obese veterans: lessons from the trenches
SO BMC MEDICAL RESEARCH METHODOLOGY
LA English
DT Article
DE Partnered research; Weight loss; Implementation; Pragmatic clinical
trials; Veterans
ID MANAGEMENT PROGRAM; DECISION-MAKING; IMPLEMENTATION; VA; TRANSLATION;
RELEVANCE; TRIALS
AB Background: Obesity and obesity-related conditions, such as type 2 diabetes, are a major issue for Veteran health. Veterans Health Administration (VA) researchers and health systems leaders have worked separately and together to provide more effective weight management programs for Veterans. Although randomized clinical trials are often considered the gold standard for establishing efficacy of interventions in controlled circumstances, pragmatic clinical trials (PCTs) provide agility for translation.
Main text: VA researchers and health system leaders collaboratively designed a PCT to compare the Diabetes Prevention Program (VA-DPP) to usual care (MOVE (R)) in promoting weight loss and glycemic control among overweight/obese Veterans with prediabetes. Together, they navigated the tensions that exist between quality improvement and research activities, facing challenges but reaping significant rewards. Early findings led to updated national guidance for delivering obesity treatment in VA.
Short conclusion: Partnered research and the use of PCTs can be powerful strategies for accelerating evidence-based findings into practice. Collaborative partnerships between researchers and health systems leaders can help enhance and sustain translation in real-world settings.
C1 [AuYoung, Mona; Richardson, Caroline R.] Ann Arbor VA Ctr Clin Management Res, CCMR, HSR&D, Mail Stop 152,P Box 130170, Ann Arbor, MI 48113 USA.
[Damschroder, Laura J.; Richardson, Caroline R.] VA Diabet QUERI, CCMR, HSR, Mail Stop 152,P Box 130170, Ann Arbor, MI 48113 USA.
[Kinsinger, Linda] Natl Ctr Hlth Promot & Dis Prevent, 3022 Croasdaile Dr 200, Durham, NC 27705 USA.
[Moin, Tannaz] VA Greater Angeles Healthcare Syst, Los Angeles, CA USA.
[Moin, Tannaz] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA USA.
[Moin, Tannaz] Greater Angeles CA Hlth Serv Res & Dev HSR & D, Ctr Healthcare Innovat Implementat & Policy, 11301 Wilshire Blvd,Mail Code 111D, Los Angeles, CA 90073 USA.
[Richardson, Caroline R.] Univ Michigan, Dept Family Med, 1018 Fuller St, Ann Arbor, MI 48104 USA.
RP AuYoung, M (reprint author), Ann Arbor VA Ctr Clin Management Res, CCMR, HSR&D, Mail Stop 152,P Box 130170, Ann Arbor, MI 48113 USA.
EM mona.auyoung@va.gov
FU Veteran Affairs (VA) Quality Enhancement Research Initiative (QUERI)
program [RRP 12-440, SDP 12-549]; clinical quality improvement funding
[XVA 41-048]; VA Office of Academic Affiliations through the VA Health
Services Research and Development Advanced Fellowship Program, VA
Greater Los Angeles [TPM65-010]; VA Health Services Research and
Development Advanced Postdoctoral Fellowship Program, VA Ann Arbor
FX This work was funded by the Veteran Affairs (VA) Quality Enhancement
Research Initiative (QUERI) program through two research grants (RRP
12-440 and SDP 12-549) and clinical quality improvement funding (XVA
41-048). Dr. Moin received support from the VA Office of Academic
Affiliations through the VA Health Services Research and Development
Advanced Fellowship Program (TPM65-010), VA Greater Los Angeles, from
2011 to 2014. Dr. AuYoung received support through the VA Health
Services Research and Development Advanced Postdoctoral Fellowship
Program, VA Ann Arbor. This quality improvement project was partially
funded by operational partners. Our partners helped to inform
feasibility of study design alternatives. However, they had no role in
final decisions regarding study design nor were they involved in data
collection or analysis, decision to publish, or preparation of this
manuscript.
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PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1471-2288
J9 BMC MED RES METHODOL
JI BMC Med. Res. Methodol.
PD MAR 29
PY 2017
VL 17
AR 50
DI 10.1186/s12874-017-0321-9
PG 8
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA EP7AT
UT WOS:000397530700001
PM 28356073
ER
PT J
AU Srinivasainagendra, V
Sandel, MW
Singh, B
Sundaresan, A
Mooga, VP
Bajpai, P
Tiwari, HK
Singh, KK
AF Srinivasainagendra, Vinodh
Sandel, Michael W.
Singh, Bhupendra
Sundaresan, Aishwarya
Mooga, Ved P.
Bajpai, Prachi
Tiwari, Hemant K.
Singh, Keshav K.
TI Migration of mitochondrial DNA in the nuclear genome of colorectal
adenocarcinoma
SO GENOME MEDICINE
LA English
DT Article
DE Cancer; Tumor; Colorectal cancer; Mitochondria; Mitochondrial DNA;
YME1L1; NUMT; Numtogenesis; mtDNA transfer; Genetic instability
ID HUMAN MYOCARDIAL-CELLS; HUMAN GENETIC-DISEASE; SACCHAROMYCES-CEREVISIAE;
INTRANUCLEAR MITOCHONDRIA; CANCER-CELLS; COPY NUMBER; DYSFUNCTION;
MUTATIONS; TRANSFORMATION; PSEUDOGENES
AB Background: Colorectal adenocarcinomas are characterized by abnormal mitochondrial DNA (mtDNA) copy number and genomic instability, but a molecular interaction between mitochondrial and nuclear genome remains unknown. Here we report the discovery of increased copies of nuclear mtDNA (NUMT) in colorectal adenocarcinomas, which supports link between mtDNA and genomic instability in the nucleus. We name this phenomenon of nuclear occurrence of mitochondrial component as numtogenesis. We provide a description of NUMT abundance and distribution in tumor versus matched blood-derived normal genomes.
Methods: Whole-genome sequence data were obtained for colon adenocarcinoma and rectum adenocarcinoma patients participating in The Cancer Genome Atlas, via the Cancer Genomics Hub, using the GeneTorrent file acquisition tool. Data were analyzed to determine NUMT proportion and distribution on a genome-wide scale. A NUMT suppressor gene was identified by comparing numtogenesis in other organisms.
Results: Our study reveals that colorectal adenocarcinoma genomes, on average, contains up to 4.2-fold more somatic NUMTs than matched normal genomes. Women colorectal tumors contained more NUMT than men. NUMT abundance in tumor predicted parallel abundance in blood. NUMT abundance positively correlated with GC content and gene density. Increased numtogenesis was observed with higher mortality. We identified YME1L1, a human homolog of yeast YME1 (yeast mitochondrial DNA escape 1) to be frequently mutated in colorectal tumors. YME1L1 was also mutated in tumors derived from other tissues. We show that inactivation of YME1L1 results in increased transfer of mtDNA in the nuclear genome.
Conclusions: Our study demonstrates increased somatic transfer of mtDNA in colorectal tumors. Our study also reveals sex-based differences in frequency of NUMT occurrence and that NUMT in blood reflects NUMT in tumors, suggesting NUMT may be used as a biomarker for tumorigenesis. We identify YME1L1 as the first NUMT suppressor gene in human and demonstrate that inactivation of YME1L1 induces migration of mtDNA to the nuclear genome. Our study reveals that numtogenesis plays an important role in the development of cancer.
C1 [Srinivasainagendra, Vinodh; Sandel, Michael W.; Sundaresan, Aishwarya; Tiwari, Hemant K.] Univ Alabama Birmingham, Sch Publ Hlth, Dept Biostatist, Birmingham, AL 35294 USA.
[Singh, Bhupendra; Mooga, Ved P.; Bajpai, Prachi] Univ Alabama Birmingham, Dept Genet, Birmingham, AL 35294 USA.
[Singh, Keshav K.] Univ Alabama Birmingham, Ctr Aging & UAB Comprehens Canc Ctr, Ctr Free Radical Biol, Dept Genet, Birmingham, AL 35294 USA.
[Singh, Keshav K.] Univ Alabama Birmingham, Ctr Aging & UAB Comprehens Canc Ctr, Ctr Free Radical Biol, Dept Pathol, Birmingham, AL 35294 USA.
[Singh, Keshav K.] Univ Alabama Birmingham, Ctr Aging & UAB Comprehens Canc Ctr, Ctr Free Radical Biol, Dept Environm Hlth, Birmingham, AL 35294 USA.
[Singh, Keshav K.] Birmingham Vet Affairs Med Ctr, Birmingham, AL 35294 USA.
[Singh, Keshav K.] Univ Alabama Birmingham, Sch Med, Dept Genet, Kaul Genet Bldg,Suite 620,720 20th St South, Birmingham, AL 35294 USA.
[Sandel, Michael W.] Univ West Alabama, Sch Nat Sci & Math, Dept Biol & Environm Sci, Livingston, NJ USA.
RP Tiwari, HK (reprint author), Univ Alabama Birmingham, Sch Publ Hlth, Dept Biostatist, Birmingham, AL 35294 USA.; Singh, KK (reprint author), Univ Alabama Birmingham, Ctr Aging & UAB Comprehens Canc Ctr, Ctr Free Radical Biol, Dept Genet, Birmingham, AL 35294 USA.; Singh, KK (reprint author), Univ Alabama Birmingham, Ctr Aging & UAB Comprehens Canc Ctr, Ctr Free Radical Biol, Dept Pathol, Birmingham, AL 35294 USA.; Singh, KK (reprint author), Univ Alabama Birmingham, Ctr Aging & UAB Comprehens Canc Ctr, Ctr Free Radical Biol, Dept Environm Hlth, Birmingham, AL 35294 USA.; Singh, KK (reprint author), Birmingham Vet Affairs Med Ctr, Birmingham, AL 35294 USA.; Singh, KK (reprint author), Univ Alabama Birmingham, Sch Med, Dept Genet, Kaul Genet Bldg,Suite 620,720 20th St South, Birmingham, AL 35294 USA.
EM htiwari@uab.edu; kksingh@uab.edu
FU Veterans Administration [1I01BX001716]; NCTN-LAPS Program Translational
Research Award; [T32HL072757]
FX This study was supported by grants from the Veterans Administration
1I01BX001716 and a NCTN-LAPS Program Translational Research Award to KKS
and T32HL072757 (PI: HKT) to MWS.
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U2 10
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1756-994X
J9 GENOME MED
JI Genome Med.
PD MAR 29
PY 2017
VL 9
AR 31
DI 10.1186/s13073-017-0420-6
PG 15
WC Genetics & Heredity
SC Genetics & Heredity
GA EP9ZA
UT WOS:000397730300001
PM 28356157
ER
PT J
AU La Fountaine, MF
Cirnigliaro, CM
Kirshblum, SC
McKenna, C
Bauman, WA
AF La Fountaine, Michael F.
Cirnigliaro, Christopher M.
Kirshblum, Steven C.
McKenna, Cristin
Bauman, William A.
TI Effect of functional sympathetic nervous system impairment of the liver
and abdominal visceral adipose tissue on circulating triglyceride-rich
lipoproteins
SO PLOS ONE
LA English
DT Article
ID SPINAL-CORD-INJURY; HOMEOSTASIS MODEL ASSESSMENT; ISOLATED RAT
HEPATOCYTES; BODY-FAT DISTRIBUTION; INSULIN-RESISTANCE;
LIPID-METABOLISM; TRIACYLGLYCEROL SECRETION; INTERNATIONAL STANDARDS;
MOLECULAR-MECHANISMS; DIABETES-MELLITUS
AB Background
Interruption of sympathetic innervation to the liver and visceral adipose tissue (VAT) in animal models has been reported to reduce VAT lipolysis and hepatic secretion of very low density lipoprotein (VLDL) and concentrations of triglyceride-rich lipoprotein particles. Whether functional impairment of sympathetic nervous system (SNS) innervation to tissues of the abdominal cavity reduce circulating concentrations of triglyceride (TG) and VLDL particles (VLDL-P) was tested in men with spinal cord injury (SCI).
Methods
One hundred-three non-ambulatory men with SCI [55 subjects with neurologic injury at or proximal to the 4th thoracic vertebrae (T up arrow 4); 48 subjects with SCI at or distal to the 5th thoracic vertebrae (down arrow T5)] and 53 able-bodied (AB) subjects were studied. Fasting blood samples were obtained for determination of TG, VLDL-P concentration by NMR spectroscopy, serum glucose by autoanalyzer, and plasma insulin by radioimmunoassay. VAT volume was determined by dual energy x-ray absorptiometry imaging with calculation by a validated proprietary software package.
Results
Significant group main effects for TG and VLDL-P were present; post-hoc tests revealed that serum TG concentrations were significantly higher in down arrow T5 group compared to AB and up arrow T4 groups [150 +/- 9 vs. 101 +/- 8 (p<0.01) and 112 +/- 8 mg/dl (p<0.05), respectively]. VLDL-P concentration was significantly elevated in down arrow T5 group compared to AB and up arrow T4 groups [74 +/- 4 vs. 58 4 (p<0.05) and 55 +/- 4 mu mol/l(p<0.05)]. VAT volume was significantly higher in both SCI groups than in the AB group, and HOMA-IR was higher and approached significance in the SCI groups compared to the AB group. A linear relationship between triglyceride rich lipoproteins (i.e., TG or Large VLDL-P) and VAT volume or HOMA-IR was significant only in the down arrow T5 group.
Conclusions
Despite a similar VAT volume and insulin resistance in both SCI groups, the down arrow T5 group had significantly higher serum TG and VLDL-P values than that observed in the up arrow T4 and the AB control groups. Thus, level of injury is an important determinate of the concentration of circulating triglyceride rich lipoproteins, which may play a role in the genesis of cardiometabolic dysfunction.
C1 [La Fountaine, Michael F.; Cirnigliaro, Christopher M.; Bauman, William A.] James J Peters Vet Affairs Med Ctr, Dept Vet Affairs, Rehabil Res & Dev Serv, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY 10468 USA.
[La Fountaine, Michael F.; Bauman, William A.] Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA.
[La Fountaine, Michael F.] Seton Hall Univ, Sch Hlth & Med Sci, S Orange, NJ 07079 USA.
[La Fountaine, Michael F.] Seton Hall Univ, Inst Adv Study Rehabil & Sports Sci, Sch Hlth & Med Sci, S Orange, NJ 07079 USA.
[Kirshblum, Steven C.; McKenna, Cristin] Kessler Inst Rehabil, W Orange, NJ USA.
[Kirshblum, Steven C.; McKenna, Cristin] Rutgers New Jersey Med Sch, Dept Phys Med & Rehabil, Newark, NJ USA.
[Bauman, William A.] Icahn Sch Med Mt Sinai, Dept Rehabil Med, New York, NY 10029 USA.
RP La Fountaine, MF (reprint author), James J Peters Vet Affairs Med Ctr, Dept Vet Affairs, Rehabil Res & Dev Serv, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY 10468 USA.; La Fountaine, MF (reprint author), Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA.; La Fountaine, MF (reprint author), Seton Hall Univ, Sch Hlth & Med Sci, S Orange, NJ 07079 USA.; La Fountaine, MF (reprint author), Seton Hall Univ, Inst Adv Study Rehabil & Sports Sci, Sch Hlth & Med Sci, S Orange, NJ 07079 USA.
EM michael.lafountaine@va.gov
FU Department of Veterans Affairs, Veterans Health Administration,
Rehabilitation Research and Development Service National Center of
Excellence for the Medical Consequences of Spinal Cord Injury [139212-C,
B2020-C]
FX This work was supported by the Department of Veterans Affairs, Veterans
Health Administration, Rehabilitation Research and Development Service
National Center of Excellence for the Medical Consequences of Spinal
Cord Injury (#139212-C and #B2020-C). The funders had no role in study
design, data collection and analysis,
NR 65
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PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1932-6203
J9 PLOS ONE
JI PLoS One
PD MAR 27
PY 2017
VL 12
IS 3
AR e0173934
DI 10.1371/joumal.pone.0173934
PG 15
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA ER9VD
UT WOS:000399174300015
PM 28346471
ER
PT J
AU Patra, A
Chen, XD
Sadowska, GB
Zhang, JY
Lim, YP
Padbury, JF
Banks, WA
Stonestreet, BS
AF Patra, Aparna
Chen, Xiaodi
Sadowska, Grazyna B.
Zhang, Jiyong
Lim, Yow-Pin
Padbury, James F.
Banks, William A.
Stonestreet, Barbara S.
TI NEUTRALIZING ANTI-INTERLEUKIN-1 beta ANTIBODIES REDUCE ISCHEMIA-RELATED
INTERLEUKIN-1 beta TRANSPORT ACROSS THE BLOOD-BRAIN BARRIER IN FETAL
SHEEP
SO NEUROSCIENCE
LA English
DT Article
DE blood-brain barrier; cytokines; interleukin-1 beta; fetus;
hypoxia-ischemia; sheep
ID EXTREMELY PRETERM INFANTS; NECROSIS-FACTOR-ALPHA; WHITE-MATTER INJURY;
IN-OVINE FETUSES; NEONATAL ENCEPHALOPATHY; INFLAMMATORY CYTOKINES;
PROTEIN EXPRESSION; CEREBRAL-ISCHEMIA; ENDOTHELIAL-CELLS; TNF-ALPHA
AB Hypoxic ischemic insults predispose to perinatal brain injury. Pro-inflammatory cytokines are important in the evolution of this injury. Interleukin-1 beta (IL-1 beta) is a key mediator of inflammatory responses and elevated IL-1b levels in brain correlate with adverse neuro developmental outcomes after brain injury. Impaired blood-brain barrier (BBB) function represents an important component of hypoxic-ischemic brain injury in the fetus. In addition, ischemia-reperfusion increases cytokine transport across the BBB of the ovine fetus. Reducing pro-inflammatory cytokine entry into brain could represent a novel approach to attenuate ischemia-related brain injury. We hypothesized that infusions of neutralizing IL-1 beta monoclonal antibody (mAb) reduce IL-1 beta transport across the BBB after ischemia in the fetus. Fetal sheep were studied 24-h after 30-min of carotid artery occlusion. Fetuses were treated with placebo-or anti-IL-1 beta mAb intravenously 15-min and 4-h after ischemia. Ovine IL-1 beta protein expressed from IL-1 beta pGEX-2T vectors in Escherichia coli (E.coli) BL-21 cells was produced, purified, and radiolabeled with (125) I. BBB permeability was quantified using the blood-to-brain transfer constant (K-i) with I-125-radiolabeled-IL-1 beta. Increases in antiIL-1 beta mAb were observed in the brain of the mAb-treated group (P < 0.001). Blood-to-brain transport of I-125-IL-1 beta was lower (P < 0.04) across brain regions in the anti-IL-1 beta mAb-treated than placebo-treated ischemic fetuses. Plasma I-125-IL-1 beta counts were higher (P < 0.001) in the anti-IL-1 beta mAb-than placebo-treated ischemic fetuses. Systemic infusions of anti-IL-1 beta mAb reduce IL-1 beta transport across the BBB after ischemia in the ovine fetus. Our findings suggest that conditions associated with increases in systemic proinflammatory cytokines and neurodevelopmental impairment could benefit from an anti-cytokine therapeutic strategy. (C) 2017 IBRO. Published by Elsevier Ltd. All rights reserved.
C1 [Patra, Aparna; Chen, Xiaodi; Sadowska, Grazyna B.; Zhang, Jiyong; Padbury, James F.; Stonestreet, Barbara S.] Brown Univ, Women & Infants Hosp Rhode Isl, Alpert Med Sch, Pediat, Providence, RI 02905 USA.
[Lim, Yow-Pin] ProThera Biol, Providence, RI 02903 USA.
[Banks, William A.] Univ Washington, Dept Med, Div Gerontol & Geriatr Med, Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA 98104 USA.
[Patra, Aparna] Univ Kentucky, Dept Pediat, 138 Leader Ave,Room 10C, Lexington, KY 40508 USA.
RP Stonestreet, BS (reprint author), Brown Univ, Women & Infants Hosp Rhode Isl, Alpert Med Sch, Dept Pediat, 101 Dudley St, Providence, RI 02905 USA.
EM aparna.patra@uky.edu; bstonestreet@wihri.org
FU National Institute of General Medical Sciences of the National
Institutes of Health [1R01-HD-057100, P20 RR018728, P20GM103537];
American Heart Association [13POST16860015]
FX Research summarized in this publication was supported by the National
Institute of General Medical Sciences of the National Institutes of
Health under award number 1R01-HD-057100, by an Institutional
Development Award (IDeA) from the National Institute of General Medical
Sciences of the National Institutes of Health under grant number P20
RR018728 and P20GM103537, and by a postdoctoral fellowship award (J.Z.)
from the American Heart Association under grant number 13POST16860015.
The content is solely the responsibility of the authors and does not
necessarily represent the official views of the National Institutes of
Health.
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PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0306-4522
EI 1873-7544
J9 NEUROSCIENCE
JI Neuroscience
PD MAR 27
PY 2017
VL 346
BP 113
EP 125
DI 10.1016/j.neuroscience.2016.12.051
PG 13
WC Neurosciences
SC Neurosciences & Neurology
GA EN1SK
UT WOS:000395790100011
PM 28089577
ER
PT J
AU Morris, BJ
Krieger, JN
Klausner, JD
AF Morris, Brian J.
Krieger, John N.
Klausner, Jeffrey D.
TI CDC's Male Circumcision Recommendations Represent a Key Public Health
Measure
SO GLOBAL HEALTH-SCIENCE AND PRACTICE
LA English
DT Editorial Material
ID SIMPLEX-VIRUS TYPE-2; HUMAN-PAPILLOMAVIRUS INFECTION; RANDOMIZED
CONTROLLED-TRIAL; AUSTRALIAN HOMOSEXUAL-MEN; TOUCH PRESSURE THRESHOLDS;
INFANT MALE CIRCUMCISION; SUB-SAHARAN AFRICA; NEWBORN CIRCUMCISION;
SEXUAL FUNCTION; HIV-INFECTION
C1 [Morris, Brian J.] Univ Sydney, Sch Med Sci, Sydney, NSW, Australia.
[Morris, Brian J.] Univ Sydney, Bosch Inst, Sydney, NSW, Australia.
[Krieger, John N.] Univ Washington, Sch Med, Seattle, WA 98195 USA.
[Krieger, John N.] VA Puget Sound Hlth Care Syst, Urol Sect, Seattle, WA USA.
[Klausner, Jeffrey D.] Univ Calif Los Angeles, Jonathan & Karin Fielding Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA USA.
RP Morris, BJ (reprint author), Univ Sydney, Sch Med Sci, Sydney, NSW, Australia.; Morris, BJ (reprint author), Univ Sydney, Bosch Inst, Sydney, NSW, Australia.
EM brian.morris@sydney.edu.au
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PU US AGENCY INT DEVELOPMENT-USAID
PI BALTIMORE
PA US AGENCY INT DEVELOPMENT-USAID, BALTIMORE, MD 00000 USA
SN 2169-575X
J9 GLOB HEALTH-SCI PRAC
JI Glob. Health
PD MAR 24
PY 2017
VL 5
IS 1
BP 15
EP 27
DI 10.9745/GHSP-D-16-00390
PG 13
WC Public, Environmental & Occupational Health
SC Public, Environmental & Occupational Health
GA ER7DK
UT WOS:000398970200004
PM 28351877
ER
PT J
AU Jadhav, S
Russo, S
Cowart, LA
Greenberg, ML
AF Jadhav, Shyamalagauri
Russo, Sarah
Cowart, L. Ashley
Greenberg, Miriam L.
TI Inositol Depletion Induced by Acute Treatment of the Bipolar Disorder
Drug Valproate Increases Levels of Phytosphingosine
SO JOURNAL OF BIOLOGICAL CHEMISTRY
LA English
DT Article
ID SACCHAROMYCES-CEREVISIAE; SPHINGOLIPID HOMEOSTASIS; PROTEIN;
BIOSYNTHESIS; YEAST; GENES; ORM2; PHOSPHORYLATION; MODULATION; LITHIUM
AB Bipolar disorder (BD) is a severe psychiatric illness affecting similar to 1% of the world population. Valproate (VPA) and lithium, widely used for the treatment of BD, are not universally effec-tive. These drugs have been shown to cause inositol depletion, but translating this observation to a specific therapeutic mech-anism has been difficult, hampering the development of more effective therapies. We have shown previously in yeast that chronic VPA treatment induces the unfolded protein response due to increasing ceramide levels. To gain insight into the mechanisms activated during acute VPA treatment, we performed a genome-wide expression study in yeast treated with VPA for 30 min. We observed increased mRNA and protein levels of RSB1, which encodes an exporter of long chain bases dihydrosphingosine (DHS) and phytosphingosine (PHS), and further saw that VPA increased sensitivity of an rsb1 Delta mutant to PHS, suggesting that VPA increases long chain base levels. Consistent with this, PHS levels were elevated in wild type and, to a greater extent, in rsb1 Delta cells. Expression of ORM genes (negative regulators of PHS synthesis) and of fatty acid elongase genes FEN1 and SUR4 were decreased, and expression of YOR1 (exporter of PHS-1P) and DPL1 (lyase that degrades DHS-1P and PHS-1P) was increased. These effects were more pronounced in medium lacking inositol, and were mirrored by inositol starvation of an ino1 Delta mutant. These findings provide a metabolic explanation as to how VPA-mediated inositol depletion causes increased synthesis of PHS and further support the therapeutic relevance of inositol depletion as a bipolar disorder treatment.
C1 [Jadhav, Shyamalagauri; Greenberg, Miriam L.] Wayne State Univ, Dept Biol Sci, Detroit, MI 48202 USA.
[Russo, Sarah; Cowart, L. Ashley] Med Univ South Carolina, Dept Biochem & Mol Biol, Charleston, SC 29425 USA.
[Russo, Sarah; Cowart, L. Ashley] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC 29425 USA.
[Jadhav, Shyamalagauri] NIDDK, NIH, Bethesda, MD 20892 USA.
RP Greenberg, ML (reprint author), Wayne State Univ, Dept Biol Sci, Detroit, MI 48202 USA.
EM mgreenberg@wayne.edu
FU National Institutes of Health [DK081367]; Graduate School of Wayne State
University
FX This work was supported, in whole or in part, by National Institutes of
Health Grant DK081367 (to M. L. G.), and support from the Graduate
School of Wayne State University (to S. J.). The authors declare that
they have no conflicts of interest with the contents of this article.
The content is solely the responsibility of the authors and does not
necessarily represent the official views of the National Institutes of
Health.
NR 25
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PU AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3996 USA
SN 0021-9258
EI 1083-351X
J9 J BIOL CHEM
JI J. Biol. Chem.
PD MAR 24
PY 2017
VL 292
IS 12
BP 4953
EP 4959
DI 10.1074/jbc.M117.775460
PG 7
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA EP7XL
UT WOS:000397590400017
PM 28100786
ER
PT J
AU Kang, SL
Li, QJ
Chen, Q
Zhou, YG
Park, S
Lee, G
Grimes, B
Krysan, K
Yu, M
Wang, W
Alber, F
Sun, FZ
Dubinett, SM
Li, WY
Zhou, XHJ
AF Kang, Shuli
Li, Qingjiao
Chen, Quan
Zhou, Yonggang
Park, Stacy
Lee, Gina
Grimes, Brandon
Krysan, Kostyantyn
Yu, Min
Wang, Wei
Alber, Frank
Sun, Fengzhu
Dubinett, Steven M.
Li, Wenyuan
Zhou, Xianghong Jasmine
TI CancerLocator: non-invasive cancer diagnosis and tissue-of-origin
prediction using methylation profiles of cell-free DNA
SO GENOME BIOLOGY
LA English
DT Article
DE Cell-free DNA; Liquid biopsy; DNA methylation; Next-generation
sequencing; Cancer diagnosis
ID COPY NUMBER ABERRATIONS; PLASMA DNA; COLORECTAL-CANCER; HYPOMETHYLATION;
CLASSIFIERS; BIOMARKERS; CARCINOMA; PATTERNS
AB We propose a probabilistic method, CancerLocator, which exploits the diagnostic potential of cell-free DNA by determining not only the presence but also the location of tumors. CancerLocator simultaneously infers the proportions and the tissue-of-origin of tumor-derived cell-free DNA in a blood sample using genome-wide DNA methylation data. CancerLocator outperforms two established multi-class classification methods on simulations and real data, even with the low proportion of tumor-derived DNA in the cell-free DNA scenarios. CancerLocator also achieves promising results on patient plasma samples with low DNA methylation sequencing coverage.
C1 [Kang, Shuli; Li, Qingjiao; Chen, Quan; Alber, Frank; Sun, Fengzhu] Univ Southern Calif, Mol & Computat Biol, Los Angeles, CA 90089 USA.
[Zhou, Yonggang; Dubinett, Steven M.; Li, Wenyuan; Zhou, Xianghong Jasmine] Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA.
[Zhou, Yonggang; Zhou, Xianghong Jasmine] Univ Calif Los Angeles, Inst Quantitat & Computat Biosci, Los Angeles, CA 90095 USA.
[Park, Stacy; Grimes, Brandon; Krysan, Kostyantyn] Univ Calif Los Angeles, David Geffen Sch Med, Div Pulm Crit Care Med Clin Immunol & Allergy, Los Angeles, CA 90095 USA.
[Lee, Gina] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Yu, Min] Univ Southern Calif, Dept Stem Cell Biol & Regenerat Med, Los Angeles, CA 90033 USA.
[Yu, Min] Univ Southern Calif, Norris Comprehens Canc Ctr, Los Angeles, CA 90033 USA.
[Wang, Wei] Zhejiang Prov Tongde Hosp, Clin Lab, Hangzhou, Zhejiang, Peoples R China.
[Dubinett, Steven M.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA.
[Dubinett, Steven M.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
[Dubinett, Steven M.] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA.
RP Dubinett, SM; Li, WY; Zhou, XHJ (reprint author), Univ Calif Los Angeles, Dept Pathol & Lab Med, David Geffen Sch Med, Los Angeles, CA 90095 USA.; Zhou, XHJ (reprint author), Univ Calif Los Angeles, Inst Quantitat & Computat Biosci, Los Angeles, CA 90095 USA.; Dubinett, SM (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Mol & Med Pharmacol, Los Angeles, CA 90095 USA.; Dubinett, SM (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.; Dubinett, SM (reprint author), Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA.
EM sdubinett@mednet.ucla.edu; WenyuanLi@mednet.ucla.edu;
XJZhou@mednet.ucla.edu
RI Sun, Fengzhu /G-4373-2010
FU NHLBI MAPGEN [U01HL108634]; NIH/NCI [1U01CA214182-01, 1U01CA196408-01];
National Institutes of Health (NIH) [NHLBI MAPGEN] [U01HL108634]
FX This work was supported by the NHLBI MAPGEN U01HL108634 grant to X.J.Z.,
the NIH/NCI 1U01CA214182-01 and the NIH/NCI 1U01CA196408-01 to S.M.D.
Funding for open access charge: National Institutes of Health (NIH)
[NHLBI MAPGEN U01HL108634 to X.J.Z.]. The authors greatly acknowledge
Dr. Yuk Ming Dennis Lo and his circulating nucleic acids research group
in the Chinese University of Hong Kong for his cfDNA data [19, 21]. We
also thank Wing Hung Wong for his constructive input for the manuscript.
NR 29
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U1 4
U2 4
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1474-760X
J9 GENOME BIOL
JI Genome Biol.
PD MAR 24
PY 2017
VL 18
AR 53
DI 10.1186/s13059-017-1191-5
PG 12
WC Biotechnology & Applied Microbiology; Genetics & Heredity
SC Biotechnology & Applied Microbiology; Genetics & Heredity
GA EP0ZI
UT WOS:000397114800001
PM 28335812
ER
PT J
AU Poewe, W
Seppi, K
Tanner, CM
Halliday, GM
Brundin, P
Volkmann, J
Schrag, AE
Lang, AE
AF Poewe, Werner
Seppi, Klaus
Tanner, Caroline M.
Halliday, Glenda M.
Brundin, Patrik
Volkmann, Jens
Schrag, Anette-Eleonore
Lang, Anthony E.
TI Parkinson disease
SO NATURE REVIEWS DISEASE PRIMERS
LA English
DT Article
ID DEEP-BRAIN-STIMULATION; CHAPERONE-MEDIATED AUTOPHAGY; QUALITY-OF-LIFE;
RANDOMIZED CONTROLLED-TRIAL; SLEEP BEHAVIOR DISORDER; MDS RESEARCH
CRITERIA; INCIDENTAL LEWY BODY; CELL-BASED THERAPIES; ALPHA-SYNUCLEIN;
DOPAMINE NEURONS
AB Parkinson disease is the second-most common neurodegenerative disorder that affects 2-3% of the population >= 65 years of age. Neuronal loss in the substantia nigra, which causes striatal dopamine deficiency, and intracellular inclusions containing aggregates of a-synuclein are the neuropathological hallmarks of Parkinson disease. Multiple other cell types throughout the central and peripheral autonomic nervous system are also involved, probably from early disease onwards. Although clinical diagnosis relies on the presence of bradykinesia and other cardinal motor features, Parkinson disease is associated with many non-motor symptoms that add to overall disability. The underlying molecular pathogenesis involves multiple pathways and mechanisms: a-synuclein proteostasis, mitochondrial function, oxidative stress, calcium homeostasis, axonal transport and neuroinflammation. Recent research into diagnostic biomarkers has taken advantage of neuroimaging in which several modalities, including PET, single-photon emission CT (SPECT) and novel MRI techniques, have been shown to aid early and differential diagnosis. Treatment of Parkinson disease is anchored on pharmacological substitution of striatal dopamine, in addition to non-dopaminergic approaches to address both motor and non-motor symptoms and deep brain stimulation for those developing intractable l-DOPA-related motor complications. Experimental therapies have tried to restore striatal dopamine by gene-based and cell-based approaches, and most recently, aggregation and cellular transport of a-synuclein have become therapeutic targets. One of the greatest current challenges is to identify markers for prodromal disease stages, which would allow novel disease-modifying therapies to be started earlier.
C1 [Poewe, Werner; Seppi, Klaus] Med Univ Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, Austria.
[Tanner, Caroline M.] San Francisco VA Med Ctr, Parkinsons Dis Res Educ & Clin, San Francisco, CA USA.
[Tanner, Caroline M.] Univ Calif San Francisco, Dept Neurol, San Francisco, CA USA.
[Halliday, Glenda M.] Univ Sydney, Sydney Med Sch, Brain & Mind Ctr, Sydney, NSW, Australia.
[Halliday, Glenda M.] Univ New South Wales, Fac Med, Sydney, NSW, Australia.
[Halliday, Glenda M.] Neurosci Res Australia, Sydney, NSW, Australia.
[Brundin, Patrik] Van Andel Res Inst, Ctr Neurodegenerat Sci, Grand Rapids, MI USA.
[Volkmann, Jens] Univ Hosp Wurzburg, Dept Neurol, Wurzburg, Germany.
[Schrag, Anette-Eleonore] UCL Inst Neurol, Dept Clin Neurosci, London, England.
[Lang, Anthony E.] Univ Toronto, Dept Med, Div Neurol, Toronto, ON, Canada.
RP Poewe, W (reprint author), Med Univ Innsbruck, Dept Neurol, Anichstr 35, A-6020 Innsbruck, Austria.
EM werner.poewe@i-med.ac.at
FU AbbVie; Allergan; AstraZeneca; BIAL; Boehringer-Ingelheim; Boston
Scientific; GlaxoSmithKline; Ipsen; Lundbeck; Medtronic; MSD;
Merck-Serono; Merz Pharmaceuticals; Neuroderm; Novartis; Orion Pharma;
Teva; UCB; Zambon; Roche; AOP Orphan Pharmaceuticals AG; Ultragenyx
Pharmaceuticals; Neurocrine Biosciences; Cynapsus; Therapeutics; Sage
Bionetworks; Adamas; American Academy of Neurology; Bionomics; Renovo
Neural; Versant Ventures/Apollo; IOS Press Partners; Parkinson's UK; GE
Healthcare; International Parkinson and Movement Disorder Society;
Grunenthal; Oxford University Press; Acorda; Avanir Pharmaceuticals;
Bristol-Myers Squibb; Cipla; Intekrin; Sun Pharma; Medichem; Merck
FX W.P. reports personal fees from AbbVie, Allergan, AstraZeneca, BIAL,
Boehringer-Ingelheim, Boston Scientific, GlaxoSmithKline, Ipsen,
Lundbeck, Medtronic, MSD, Merck-Serono, Merz Pharmaceuticals, Neuroderm,
Novartis, Orion Pharma, Teva, UCB and Zambon (consultancy and lecture
fees in relation to clinical drug development programmes for Parkinson
disease) and publishing royalties from Thieme, Wiley-Blackwell, Oxford
University Press and Cambridge University Press. K.S. reports personal
fees from Boehringer-Ingelheim, UCB, Lundbeck, AbbVie, Roche, Teva and
AOP Orphan Pharmaceuticals AG. C.M.T. has received compensation for
serving on Data Monitoring Committees from Biotie Therapeutics, Voyager
Therapeutics and Intec Pharma and personal fees for consulting services
from Ultragenyx Pharmaceuticals, Neurocrine Biosciences, Cynapsus,
Therapeutics, Sage Bionetworks and Adamas. G.M.H. has received
compensation for serving on data monitoring committees from Biotie
Therapeutics, Voyager Therapeutics and Intec Pharma, and personal fees
from the American Academy of Neurology, Bionomics and Lundbeck. P.B. has
received commercial support as a consultant from Renovo Neural, Roche,
Teva, Lundbeck, AbbVie, Neuroderm, Versant Ventures/Apollo and IOS Press
Partners. J.V. reports personal fees from Boston Scientific, Medtronic,
Bial, Allergan, Zambon (consultancy and lecture fees in relation to
clinical therapeutic development programmes for Parkinson disease) and
grants from Boston Scientific and Medtronic. A.-E.S. reports grants
from, Parkinson's UK, GE Healthcare, International Parkinson and
Movement Disorder Society, shares from AstraZeneca, and personal fees
from Grunenthal, Medtronic and Oxford University Press. A.E.L. reports
personal fees from AbbVie, Acorda, Avanir Pharmaceuticals, Bristol-Myers
Squibb, Cipla, Intekrin, Sun Pharma, Medichem, Medtronic, Teva, UCB and
Merck, and publishing royalties from Saunders, Wiley-Blackwell, Johns
Hopkins Press and Cambridge University Press.
NR 241
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U1 19
U2 19
PU NATURE PUBLISHING GROUP
PI LONDON
PA MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
SN 2056-676X
J9 NAT REV DIS PRIMERS
JI Nat. Rev. Dis. Primers
PD MAR 23
PY 2017
VL 3
AR 17013
DI 10.1038/nrdp.2017.13
PG 21
WC Medicine, General & Internal
SC General & Internal Medicine
GA EQ2JS
UT WOS:000397895800001
PM 28332488
ER
PT J
AU Singh, JA
Cleveland, J
AF Singh, Jasvinder A.
Cleveland, John
TI Allopurinol and the risk of ventricular arrhythmias in the elderly: a
study using US Medicare data
SO BMC MEDICINE
LA English
DT Article
DE Allopurinol; Ventricular arrhythmias; Risk factor; Elderly; Medicare
ID XANTHINE-OXIDASE INHIBITION; SUDDEN CARDIAC DEATH; REPERFUSION-INDUCED
ARRHYTHMIAS; ACUTE MYOCARDIAL-INFARCTION; CORONARY-ARTERY-DISEASE;
ATRIAL-FIBRILLATION; CARDIOVASCULAR-DISEASE; HEART-DISEASE;
RACIAL-DIFFERENCES; BLOOD-PRESSURE
AB Background: There are no published human studies investigating whether the use of allopurinol, the most commonly used medication for the treatment of hyperuricemia in gout, the most common type of inflammatory arthritis in adults, has any beneficial effects on ventricular electrophysiology. The objective of our study was to assess whether allopurinol use is associated with a reduction in the risk of ventricular arrhythmias (VA).
Methods: We used the 5% random sample of Medicare beneficiaries from 2006-2012 to examine new allopurinol use and the risk of incident VA. Multivariable Cox regression analyses were adjusted for demographics (age, race, sex), comorbidity, cardiac medications, and conditions associated with VA. We calculated hazard ratios (HR) and 95% confidence intervals (CI).
Results: Of the 28,755 episodes of new allopurinol use, 2538 were associated with incident VA (8.8%). Among patients with incident VA, 54% were male, 78% were White, 75% had gout as the underlying diagnosis, and the mean Charlson-Romano comorbidity score was 4.8. The crude incidence of VA per 1,000,000 person-days declined as the duration of allopurinol use increased: 1-180 days, 151; 181 days to 2 years, 105; and > 2 years, 85. In multivariableadjusted analyses, compared to non-use, allopurinol use was associated with lower HR of VA of 0.82 (95% CI, 0.76-0.90). Compared to allopurinol non-use, longer allopurinol use durations were significantly associated with lower multivariable-adjusted HR for VA: 1-180 days, 0.96 (95% CI, 0.85-1.08); 181 days to 2 years, 0.76 (95% CI, 0.68-0.85); and > 2 years, 0.72 (95% CI, 0.60-0.87). Multiple sensitivity analyses adjusting for cardiac conditions, anti-arrhythmic drugs and alternate definitions confirmed our findings with minimal/no attenuation of estimates.
Conclusion: Allopurinol use and use duration of more than 6 months were independently associated with a lower risk of VA. Future studies need to assess the pathophysiology of this potential benefit.
C1 [Singh, Jasvinder A.] Birmingham VA Med Ctr, Med Serv, Birmingham, AL 35233 USA.
[Singh, Jasvinder A.; Cleveland, John] UAB, Sch Med, Dept Med, Birmingham, AL 35294 USA.
[Singh, Jasvinder A.; Cleveland, John] UAB, Div Epidemiol, Sch Publ Hlth, Birmingham, AL 35294 USA.
[Singh, Jasvinder A.] Mayo Clin, Coll Med, Dept Orthoped Surg, Rochester, MN USA.
[Singh, Jasvinder A.; Cleveland, John] Univ Alabama Birmingham, Fac Off Tower 805B,510 20th St S, Birmingham, AL 35294 USA.
RP Singh, JA (reprint author), Birmingham VA Med Ctr, Med Serv, Birmingham, AL 35233 USA.; Singh, JA (reprint author), UAB, Sch Med, Dept Med, Birmingham, AL 35294 USA.; Singh, JA (reprint author), UAB, Div Epidemiol, Sch Publ Hlth, Birmingham, AL 35294 USA.
EM jasvinder.md@gmail.com
FU UAB Division of Rheumatology
FX This material is the result of work supported by research funds from the
UAB Division of Rheumatology and the resources and use of facilities at
the Birmingham VA Medical Center. Role of Funding Agencies: The funding
agencies played no role in study design, collection, analysis,
interpretation of data, writing of the manuscript, or in the decision to
submit the paper for publication. They accept no responsibility for the
contents.
NR 54
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U2 0
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1741-7015
J9 BMC MED
JI BMC Med.
PD MAR 22
PY 2017
VL 15
AR 59
DI 10.1186/s12916-017-0816-6
PG 11
WC Medicine, General & Internal
SC General & Internal Medicine
GA EP9FA
UT WOS:000397678300001
PM 28327188
ER
PT J
AU Rymer, J
Kaltenbach, L
Doll, J
Messenger, J
Peterson, E
Wang, T
AF Rymer, Jennifer
Kaltenbach, Lisa
Doll, Jacob
Messenger, John
Peterson, Eric
Wang, Tracy
TI BLEEDING AND PREMATURE ANTIPLATELET THERAPY DISCONTINUATION AFTER
MYOCARDIAL INFARCTION AMONG PATIENTS WITH CHRONIC KIDNEY DISEASE
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Meeting Abstract
CT 66th Annual Scientific Session and Expo of the
American-College-of-Cardiology (ACC)
CY MAR 17-19, 2017
CL Washington, DC
SP Amer Coll Cardiol
C1 Duke Univ, Durham, NC USA.
VA Puget Sound Hlth Care Syst, Seattle, WA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
SU S
MA 1296-308
BP 262
EP 262
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP4HT
UT WOS:000397342300263
ER
PT J
AU Warner, AL
Ghaznavi, Z
Lu, LY
Jackevicius, C
AF Warner, Alberta L.
Ghaznavi, Zunera
Lu, Lingyun
Jackevicius, Cynthia
TI SAFETY OF ALPHA BLOCKERS IN PATIENTS WITH HEART FAILURE
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Meeting Abstract
CT 66th Annual Scientific Session and Expo of the
American-College-of-Cardiology (ACC)
CY MAR 17-19, 2017
CL Washington, DC
SP Amer Coll Cardiol
C1 VA Greater Los Angeles, Los Angeles, CA USA.
Univ Calif Los Angeles, Los Angeles, CA USA.
NR 0
TC 0
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U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
SU S
MA 1216M-05
BP 683
EP 683
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP4HT
UT WOS:000397342301205
ER
PT J
AU Chirinos, JA
Zamani, P
Hashmath, Z
Reddy, M
Syed, KAA
Bhattacharya, P
Chahwala, J
Oldland, HG
Miller, R
Kewan, U
Varakantam, S
Tariq, A
Phan, TS
Akers, S
AF Chirinos, Julio A.
Zamani, Payman
Hashmath, Zeba
Reddy, Maheshwara
Syed, Koppula Amer Ahmed
Bhattacharya, Priyanka
Chahwala, Jugal
Oldland, Harry G.
Miller, Rachana
Kewan, Uzma
Varakantam, Swapna
Tariq, Ali
Phan, Timothy S.
Akers, Scott
TI EFFECT OF DIABETES MELLITUS ON PULSATILE ARTERIAL LOAD AND HEMODYNAMICS
IN HFPEF
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Meeting Abstract
CT 66th Annual Scientific Session and Expo of the
American-College-of-Cardiology (ACC)
CY MAR 17-19, 2017
CL Washington, DC
SP Amer Coll Cardiol
C1 Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA.
Philadelphia VA Med Ctr, Philadelphia, PA USA.
NR 0
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U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
SU S
MA 1250-275
BP 888
EP 888
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP4HT
UT WOS:000397342301410
ER
PT J
AU Lu, LY
Warner, A
Ghaznavi, Z
Chang, D
Tubert, N
Jackevicius, C
AF Lu, Lingyun
Warner, Alberta
Ghaznavi, Zunera
Chang, Donald
Tubert, Nikolas
Jackevicius, Cynthia
TI BLEEDING RISK OF DIRECT ORAL ANTICOAGULANTS COMPARED WITH WARFARIN IN
PATIENTS WITH ATRIAL FIBRILLATION AND HEART FAILURE
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Meeting Abstract
CT 66th Annual Scientific Session and Expo of the
American-College-of-Cardiology (ACC)
CY MAR 17-19, 2017
CL Washington, DC
SP Amer Coll Cardiol
C1 Calif Northstate Univ, Coll Pharm, Elk Grove, CA USA.
VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
SU S
MA 1250-287
BP 900
EP 900
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP4HT
UT WOS:000397342301422
ER
PT J
AU Armstrong, EJ
Stanislawski, M
Plomondon, M
Banerjee, S
Waldo, S
AF Armstrong, Ehrin J.
Stanislawski, Maggie
Plomondon, Meg
Banerjee, Subhash
Waldo, Stephen
TI CORONARY ATHERECTOMY FOR TREATMENT OF CALCIFIED CORONARY ARTERY LESIONS
IS ASSOCIATED WITH INCREASED PROCEDURAL SUCCESS AND LOWER PROCEDURAL
COMPLICATION RATES: INSIGHTS FROM A NATIONAL VETERAN COHORT
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Meeting Abstract
CT 66th Annual Scientific Session and Expo of the
American-College-of-Cardiology (ACC)
CY MAR 17-19, 2017
CL Washington, DC
SP Amer Coll Cardiol
C1 [Armstrong, Ehrin J.; Stanislawski, Maggie; Plomondon, Meg; Banerjee, Subhash; Waldo, Stephen] Denver VA Med Ctr, Denver, CO USA.
NR 0
TC 0
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U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
SU S
MA 1155-153
BP 1112
EP 1112
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP4HT
UT WOS:000397342301634
ER
PT J
AU Garg, V
Rezvani, B
Bersohn, M
Benharash, P
Han, J
AF Garg, Vinisha
Rezvani, Brian
Bersohn, Malcolm
Benharash, Peyman
Han, Janet
TI MYOCARDIAL FRAGILITY IN EHLERS DANLOS SYNDROME
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Meeting Abstract
CT 66th Annual Scientific Session and Expo of the
American-College-of-Cardiology (ACC)
CY MAR 17-19, 2017
CL Washington, DC
SP Amer Coll Cardiol
C1 VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
Univ Calif Los Angeles, Los Angeles, CA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
SU S
MA 1206-420
BP 2332
EP 2332
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP4HT
UT WOS:000397342303254
ER
PT J
AU Galatzer-Levy, IR
Ma, S
Statnikov, A
Yehuda, R
Shalev, AY
AF Galatzer-Levy, I. R.
Ma, S.
Statnikov, A.
Yehuda, R.
Shalev, A. Y.
TI Utilization of machine learning for prediction of post-traumatic stress:
a re-examination of cortisol in the prediction and pathways to
non-remitting PTSD
SO TRANSLATIONAL PSYCHIATRY
LA English
DT Article
ID MARKOV BLANKET INDUCTION; CIVILIAN TRAUMA VICTIMS; FEATURE-SELECTION;
CAUSAL DISCOVERY; LOCAL CAUSAL; PART II; DISORDER; TRAJECTORIES; FKBP5;
RESILIENCE
AB To date, studies of biological risk factors have revealed inconsistent relationships with subsequent post-traumatic stress disorder (PTSD). The inconsistent signal may reflect the use of data analytic tools that are ill equipped for modeling the complex interactions between biological and environmental factors that underlay post-traumatic psychopathology. Further, using symptom-based diagnostic status as the group outcome overlooks the inherent heterogeneity of PTSD, potentially contributing to failures to replicate. To examine the potential yield of novel analytic tools, we reanalyzed data from a large longitudinal study of individuals identified following trauma in the general emergency room (ER) that failed to find a linear association between cortisol response to traumatic events and subsequent PTSD. First, latent growth mixture modeling empirically identified trajectories of post-traumatic symptoms, which then were used as the study outcome. Next, support vector machines with feature selection identified sets of features with stable predictive accuracy and built robust classifiers of trajectory membership (area under the receiver operator characteristic curve (AUC) = 0.82 (95% confidence interval (CI) = 0.80-0.85)) that combined clinical, neuroendocrine, psychophysiological and demographic information. Finally, graph induction algorithms revealed a unique path from childhood trauma via lower cortisol during ER admission, to non-remitting PTSD. Traditional general linear modeling methods then confirmed the newly revealed association, thereby delineating a specific target population for early endocrine interventions. Advanced computational approaches offer innovative ways for uncovering clinically significant, non-shared biological signals in heterogeneous samples.
C1 [Galatzer-Levy, I. R.; Shalev, A. Y.] NYU, Sch Med, Dept Psychiat, 1 Pk Ave, New York, NY 10016 USA.
[Galatzer-Levy, I. R.; Shalev, A. Y.] Steven & Alexandra Cohen Ctr Study Posttraumat St, New York, NY USA.
[Ma, S.] Univ Minnesota, Dept Med, Minneapolis, MN USA.
[Statnikov, A.] New York Univ, Sch Med, Dept Med, New York, NY USA.
[Yehuda, R.] James J Peters VA Med Ctr, Mt Sinai Sch Med, Traumat Stress Studies Div, Bronx, NY USA.
RP Galatzer-Levy, IR (reprint author), NYU, Sch Med, Dept Psychiat, 1 Pk Ave, New York, NY 10016 USA.
EM Isaac.Galatzer-Levy@nyumc.org
OI Galatzer-Levy, Isaac/0000-0003-1864-064X
FU PHS Research [MH 50379]; NIMH [K01MH102415]
FX The study was supported by PHS Research grant no. MH 50379 to Dr Shalev
and an NIMH K01MH102415 to Dr Galatzer-Levy.
NR 47
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U1 5
U2 5
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 2158-3188
J9 TRANSL PSYCHIAT
JI Transl. Psychiatr.
PD MAR 21
PY 2017
VL 7
AR e1070
DI 10.1038/tp.2017.38
PG 8
WC Psychiatry
SC Psychiatry
GA EP2RB
UT WOS:000397229800007
ER
PT J
AU Konstam, MA
Kiernan, M
Chandler, A
Dhingra, R
Mody, FV
Eisen, H
Haught, WH
Wagoner, L
Gupta, D
Patten, R
Gordon, P
Korr, K
Fileccia, R
Pressler, SJ
Gregory, D
Wedge, P
Dowling, D
Romeling, M
Konstam, JM
Massaro, JM
Udelson, JE
AF Konstam, Marvin A.
Kiernan, Michael
Chandler, Arthur
Dhingra, Ravi
Mody, Freny Vaghaiwalla
Eisen, Howard
Haught, W. Herbert
Wagoner, Lynne
Gupta, Divya
Patten, Richard
Gordon, Paul
Korr, Kenneth
Fileccia, Russell
Pressler, Susan J.
Gregory, Douglas
Wedge, Patricia
Dowling, Douglas
Romeling, Matthew
Konstam, Jeremy M.
Massaro, Joseph M.
Udelson, James E.
CA SECRET CHF Investigators
TI Short-Term Effects of Tolvaptan in Patients With Acute Heart Failure and
Volume Overload
SO JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
LA English
DT Article
DE clinical trials; diuresis; dyspnea; jugular venous pressure; vasopressin
antagonism
ID WORSENING RENAL-FUNCTION; VASOPRESSIN ANTAGONIST; CONTROLLED-TRIAL;
CLINICAL-COURSE; ORAL TOLVAPTAN; OUTCOMES; DECONGESTION; DYSFUNCTION;
CHF
AB BACKGROUND In patients with acute heart failure (AHF), dyspnea relief is the most immediate goal. Renal dysfunction, diuretic resistance, and hyponatremia represent treatment impediments.
OBJECTIVES It was hypothesized that the addition of tolvaptan to a background diuretic improved dyspnea early in patients selected for an enhanced vasopressin antagonism response.
METHODS In a double-blind trial, patients were randomized to tolvaptan 30 mg/day or placebo. Study entry required hospitalization within the previous 36 h, active dyspnea, and any of the following: 1) estimated glomerular filtration rate <60 ml/min/1.73 m(2); 2) hyponatremia; or 3) diuretic resistance (urine output <= 125 ml/h following intravenous furosemide >= 40 mg). The primary endpoint was a 7-point change in self-assessed dyspnea at 8 and 16 h, using a novel standardized approach.
RESULTS We randomized 250 patients. There was no difference in the primary endpoint of day 1 dyspnea reduction, despite significantly greater weight reduction with tolvaptan (-2.4 +/- 2.1 kg vs. -0.9 +/- 1.8 kg; p < 0.001). At day 3, dyspnea reduction was greater with tolvaptan (p = 0.01). There were 2 significant treatment-by-subgroup interactions: patients without elevated jugular venous pressure and those without ascites showed directional favorability of tolvaptan over placebo for the primary endpoint compared with patients with these findings.
CONCLUSIONS Despite rapid and persistent weight loss with tolvaptan compared with placebo, in patients with AHF who were selected for greater potential benefit from vasopressin receptor inhibition, tolvaptan was not associated with greater early improvement in dyspnea. Apparent subsequent differences in dyspnea warrant further exploration of the temporal relationship between diuresis and dyspnea relief and a possible clinical role for tolvaptan. (Randomized, Double-Blind, Placebo Controlled Study of the Short Term Clinical Effects of Tolvaptan in Patients Hospitalized for Worsening Heart Failure With Challenging Volume Management [ SECRET of CHF]; NCT01584557) (J Am Coll Cardiol 2017; 69: 1409-19) (C) 2017 by the American College of Cardiology Foundation.
C1 [Konstam, Marvin A.; Kiernan, Michael; Udelson, James E.] Tufts Med Ctr, Cardiovasc Ctr, Box 108,800 Washington St, Boston, MA 02111 USA.
[Chandler, Arthur] Univ Cardiol Associates, Augusta, GA USA.
[Dhingra, Ravi] Univ Wisconsin, Cardiovasc Div, Madison, WI USA.
[Mody, Freny Vaghaiwalla] VA Greater Los Angeles, Div Cardiol, Los Angeles, CA USA.
[Eisen, Howard] Drexel Univ, Div Cardiol, Philadelphia, PA 19104 USA.
[Haught, W. Herbert] Heart Ctr Res, Huntsville, AL USA.
[Wagoner, Lynne] Mercy Hosp, Inst Heart, Fairfield, OH USA.
[Gupta, Divya] Emory Univ, Div Cardiol, Atlanta, GA 30322 USA.
[Patten, Richard] Lahey Med Ctr, Cardiovasc Med, Burlington, MA USA.
[Gordon, Paul; Korr, Kenneth] Miriam Hosp, Cardiovasc Inst, Providence, RI 02906 USA.
[Fileccia, Russell] Adv Cardiovasc Specialists, Shreveport, LA USA.
[Pressler, Susan J.] Indiana Univ, Sch Nursing, Ctr Enhancing Qual Life Chron Dis, Indianapolis, IN 46204 USA.
[Gregory, Douglas; Wedge, Patricia; Dowling, Douglas; Romeling, Matthew; Konstam, Jeremy M.] Cardiovasc Clin Sci Fdn, Boston, MA USA.
[Massaro, Joseph M.] Boston Univ, Sch Publ Hlth, Boston, MA USA.
RP Konstam, MA (reprint author), Tufts Med Ctr, Cardiovasc Ctr, Box 108,800 Washington St, Boston, MA 02111 USA.
EM mkonstam@tuftsmedicalcenter.org
FU Otsuka Pharmaceuticals Co., Rockville, Maryland; Otsuka Pharmaceuticals;
Otsuka
FX This investigation was an investigator-initiated study funded by Otsuka
Pharmaceuticals Co., Rockville, Maryland. Each of the authors and/or
their organizations received support originating from Otsuka
Pharmaceuticals to support this research. Dr. Gupta has received
additional research support from Otsuka. Drs. M.A. Konstam and Wagoner
have received honoraria from Otsuka. Randall Starling, MD, served as
Guest Editor for this paper.
NR 22
TC 1
Z9 1
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0735-1097
EI 1558-3597
J9 J AM COLL CARDIOL
JI J. Am. Coll. Cardiol.
PD MAR 21
PY 2017
VL 69
IS 11
BP 1409
EP 1419
DI 10.1016/j.jacc.2016.12.035
PG 11
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EO0AU
UT WOS:000396361500009
PM 28302292
ER
PT J
AU Low, CM
Akthar, S
Patel, DF
Loser, S
Wong, CT
Jackson, PL
Blalock, JE
Hare, SA
Lloyd, CM
Snelgrove, RJ
AF Low, Caroline M.
Akthar, Samia
Patel, Dhiren F.
Loeser, Stephan
Wong, Chi-Tung
Jackson, Patricia L.
Blalock, J. Edwin
Hare, Stephen A.
Lloyd, Clare M.
Snelgrove, Robert J.
TI The development of novel LTA(4)H modulators to selectively target LTB4
generation
SO SCIENTIFIC REPORTS
LA English
DT Article
ID LEUKOTRIENE A(4) HYDROLASE; OBSTRUCTIVE PULMONARY-DISEASE;
PROLINE-GLYCINE-PROLINE; NEUTROPHILIC INFLAMMATION; AIRWAY INFLAMMATION;
INHIBITOR; ENZYME; AMINOPEPTIDASE; DISCOVERY; EMPHYSEMA
AB The pro-inflammatory mediator leukotriene B-4 (LTB4) is implicated in the pathologies of an array of diseases and thus represents an attractive therapeutic target. The enzyme leukotriene A(4) hydrolase (LTA(4)H) catalyses the distal step in LTB4 synthesis and hence inhibitors of this enzyme have been actively pursued. Despite potent LTA(4)H inhibitors entering clinical trials all have failed to show efficacy. We recently identified a secondary anti-inflammatory role for LTA(4)H in degrading the neutrophil chemoattractant Pro-Gly-Pro (PGP) and rationalized that the failure of conventional LTA(4)H inhibitors may be that they inadvertently prevented PGP degradation. We demonstrate that these inhibitors do indeed fail to discriminate between the dual activities of LTA(4)H, and enable PGP accumulation in mice. Accordingly, we have developed novel compounds that potently inhibit LTB4 generation whilst leaving PGP degradation unperturbed. These novel compounds could represent a safer and superior class of LTA(4)H inhibitors for translation into the clinic.
C1 [Low, Caroline M.] Computat Drug Design Consultant, London SE21 8LS, England.
[Akthar, Samia; Patel, Dhiren F.; Loeser, Stephan; Lloyd, Clare M.; Snelgrove, Robert J.] Imperial Coll London, Natl Heart & Lung Inst, Inflammat Repair & Dev, London SW7 2AZ, England.
[Wong, Chi-Tung; Hare, Stephen A.] Imperial Coll London, Dept Life Sci, London SW7 2AZ, England.
[Jackson, Patricia L.; Blalock, J. Edwin] Univ Alabama Birmingham, Dept Med, Div Pulm Allergy & Crit Care Med, Birmingham, AL 35294 USA.
[Jackson, Patricia L.] Birmingham VA Med Ctr, Birmingham, AL 35294 USA.
RP Snelgrove, RJ (reprint author), Imperial Coll London, Natl Heart & Lung Inst, Inflammat Repair & Dev, London SW7 2AZ, England.
EM robert.snelgrove@imperial.ac.uk
FU Wellcome Trust Career Development Fellow [095707/Z/11/Z]; Asthma UK
Innovations award [AUK-IG-2014-286]; Imperial College Biomedical
Research Centre (BRC) Therapeutic Primer fund and MRC/Imperial College
Confidence in Concept schemes; Wellcome Trust Senior Fellow in Basic
Biomedical Sciences [086718/Z/08/Z]; MRC Career Development Fellow
[G1100332]; National Heart, Lung and Blood Institute funds [HL077783,
HL110950, HL114439, HL126596]; UAB Lung Health Center Pulmonary
Proteomics Laboratory is funded through the UAB Health Service
Foundation General Endowment Fund
FX R.J.S. is a Wellcome Trust Career Development Fellow (095707/Z/11/Z) and
is also funded through an Asthma UK Innovations award (AUK-IG-2014-286).
Aspects of this work have been funded (through R.J.S.) by the Imperial
College Biomedical Research Centre (BRC) Therapeutic Primer fund and
MRC/Imperial College Confidence in Concept schemes. C.M.L. is a Wellcome
Trust Senior Fellow in Basic Biomedical Sciences (086718/Z/08/Z). S.H.
is an MRC Career Development Fellow (G1100332). The National Heart, Lung
and Blood Institute funds J.E.B. (HL077783, HL110950, HL114439 and
HL126596). The UAB Lung Health Center Pulmonary Proteomics Laboratory is
funded through the UAB Health Service Foundation General Endowment Fund.
We would like to thank Dr. Anna Caldwell and the Centre of Excellence
for Mass Spectrometry at King's College London for the use of equipment
and technical assistance, and the staff of beamline I02 at Diamond Light
Source for facilitating X-ray crystallography studies. We would like to
thank Jen Morton, Matt Tozer, David Leese, Stuart Cameron, Seb Hallworth
and David Fengas (all Peakdale Molecular) for compound synthesis and
ADMET studies.
NR 47
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PU NATURE PUBLISHING GROUP
PI LONDON
PA MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
SN 2045-2322
J9 SCI REP-UK
JI Sci Rep
PD MAR 17
PY 2017
VL 7
AR 44449
DI 10.1038/srep44449
PG 13
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EO2PB
UT WOS:000396537300001
PM 28303931
ER
PT J
AU Bramlet, M
Olivieri, L
Farooqi, K
Ripley, B
Coakley, M
AF Bramlet, Matthew
Olivieri, Laura
Farooqi, Kanwal
Ripley, Beth
Coakley, Meghan
TI Impact of Three-Dimensional Printing on the Study and Treatment of
Congenital Heart Disease
SO CIRCULATION RESEARCH
LA English
DT Article
DE 3D printing; cardiac models; congenital heart disease; database; peer
review; segmentation
ID SIMULATION; MODELS
AB Three-dimensional (3D) printing technology allows for the translation of a 2-dimensional medical imaging study into a physical replica of a patient's individual anatomy. 3D printed models can facilitate a deeper understanding of complex patient anatomy and can aid in presurgical decision-making.(1) Although there are 3D printing case reports in almost every subspecialty of medicine to date, the rate of adoption in the field of congenital heart disease (CHD) is particularly advanced.(2,3) This is due, in no small part, to the fact that the heart is a hollow organ, which makes it a perfect substrate for 3D printing. More importantly, medical decision-making in CHD is informed by assessment of the anatomic morphology of the heart because cardiac pathology is a direct manifestation of the underlying 3D structure.
C1 [Bramlet, Matthew] Univ Illinois, Coll Med, Pediat Cardiol, 1306 N Berkeley Ave, Peoria, IL 61603 USA.
[Bramlet, Matthew] Jump Trading Simulat & Educ Ctr, Adv Imaging & Modeling Initiat, 1306 N Berkeley Ave, Peoria, IL 61603 USA.
[Olivieri, Laura] Childrens Natl Med Ctr, Div Cardiol, Washington, DC USA.
[Farooqi, Kanwal] Univ Med & Dent New Jersey, Dept Pediat, Rutgers Div Pediat Cardiol, Newark, NJ USA.
[Farooqi, Kanwal] Icahn Sch Med Mt Sinai, Dept Pediat, Div Pediat Cardiol, New York, NY USA.
[Ripley, Beth] VA Puget Sound Hlth Care Syst, Radiol, Seattle, WA USA.
[Ripley, Beth] Univ Washington, Sch Med, Seattle, WA USA.
[Coakley, Meghan] NIAID, Bioinformat & Computat Biosci Branch, Off Cyber Infrastruct & Computat Biol, NIH, Bethesda, MD USA.
RP Bramlet, M (reprint author), Univ Illinois, Coll Med, Pediat Cardiol, 1306 N Berkeley Ave, Peoria, IL 61603 USA.; Bramlet, M (reprint author), Jump Trading Simulat & Educ Ctr, Adv Imaging & Modeling Initiat, 1306 N Berkeley Ave, Peoria, IL 61603 USA.
EM Matthew.T.Bramlet@osfhealthcare.org
FU National Institutes of Allergy and Infectious Diseases [GS35F0373X]; US
Department of Health and Human Services through HHS Ignite program; US
Department of Health and Human Services through HHS Ventures program
FX The National Institutes of Health (NIH) 3D Print Exchange is operated by
the Office of Cyber Infrastructure and Computational Biology, National
Institute of Allergy and Infectious Diseases, National Institutes of
Health. Resources are provided in part through BCBB Support Services
Contract [GS35F0373X], funded by the National Institutes of Allergy and
Infectious Diseases. Initial funding for the 3D Print Exchange was
supplemented by the US Department of Health and Human Services through
the HHS Ignite and HHS Ventures programs.
NR 16
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U1 2
U2 2
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0009-7330
EI 1524-4571
J9 CIRC RES
JI Circ.Res.
PD MAR 17
PY 2017
VL 120
IS 6
BP 904
EP 907
DI 10.1161/CIRCRESAHA.116.310546
PG 4
WC Cardiac & Cardiovascular Systems; Hematology; Peripheral Vascular
Disease
SC Cardiovascular System & Cardiology; Hematology
GA EP4DL
UT WOS:000397330700004
PM 28302738
ER
PT J
AU Wu, MD
Atkinson, TM
Lindner, JR
AF Wu, Melinda D.
Atkinson, Tamara M.
Lindner, Jonathan R.
TI Platelets and von Willebrand factor in atherogenesis
SO BLOOD
LA English
DT Article
ID PROTEIN DISULFIDE-ISOMERASE; HIGH-DENSITY-LIPOPROTEIN;
ENDOTHELIAL-CELLS; GLYCOPROTEIN IB; P-SELECTIN; CORONARY
ATHEROSCLEROSIS; VASCULAR INFLAMMATION; THROMBUS FORMATION;
YOUNG-PATIENTS; IX COMPLEX
AB The role of platelet adhesion, activation, and aggregation in acute atherothrombotic events such as myocardial infarction and strokeis wellestablished. Thereis increasing evidence that platelet-endothelial interactions also contribute to early atherosclerotic plaque initiation and growth. Through these interactions, platelet-derived factors can contribute to the proinflammatory and mitogenic status of resident mural cells. Among the many putative mechanisms for platelet-endothelial interactions, increased endothelial-associated von Willebrand factor, particularly in a multimerized form, which interacts with platelet glycoproteins and integrins, is a major factor and represents a therapeutic target in early atherogenesis.
C1 [Wu, Melinda D.; Atkinson, Tamara M.; Lindner, Jonathan R.] Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
[Wu, Melinda D.; Atkinson, Tamara M.; Lindner, Jonathan R.] Oregon Hlth & Sci Univ, Dept Pediat, 3181 Sw Sam Jackson Pk Rd, Portland, OR 97201 USA.
[Atkinson, Tamara M.] Portland VA Med Ctr, Portland, OR USA.
[Lindner, Jonathan R.] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Portland, OR 97201 USA.
RP Lindner, JR (reprint author), Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
EM lindnerj@ohsu.edu
FU National Heart, Lung, and Blood Institute of the National Institutes of
Health [R01-HL078610, R01-HL111969, R01-HL120046, T32-HL094294,
K08-HL133493]; National Space Biomedical Research Institute
[14-14NSBRI10025]
FX This work was supported by grants R01-HL078610, R01-HL111969, and
R01-HL120046 (J.R.L.), T32-HL094294 (M.D.W. and T.M.A.), and
K08-HL133493 (M.D.W.) from the National Heart, Lung, and Blood Institute
of the National Institutes of Health, and 14-14NSBRI10025 from the
National Space Biomedical Research Institute (J.R.L.).
NR 84
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U1 1
U2 1
PU AMER SOC HEMATOLOGY
PI WASHINGTON
PA 2021 L ST NW, SUITE 900, WASHINGTON, DC 20036 USA
SN 0006-4971
EI 1528-0020
J9 BLOOD
JI Blood
PD MAR 16
PY 2017
VL 129
IS 11
BP 1415
EP 1419
DI 10.1182/blood-2016-07-692673
PG 5
WC Hematology
SC Hematology
GA EP3PR
UT WOS:000397294700009
PM 28174163
ER
PT J
AU Tan, Y
Richards, D
Coyle, RC
Yao, JN
Xu, RY
Gou, WY
Wang, HJ
Menick, DR
Tian, BZ
Mei, Y
AF Tan, Yu
Richards, Dylan
Coyle, Robert C.
Yao, Jenny
Xu, Ruoyu
Gou, Wenyu
Wang, Hongjun
Menick, Donald R.
Tian, Bozhi
Mei, Ying
TI Cell number per spheroid and electrical conductivity of nanowires
influence the function of silicon nanowired human cardiac spheroids
SO ACTA BIOMATERIALIA
LA English
DT Article
DE Human induced pluripotent stem cell-; derived cardiomyocytes; Spheroids;
Silicon nanowires; Oxygen transport
ID PLURIPOTENT STEM-CELLS; MYOCARDIAL-INFARCTION; OXYGEN-CONSUMPTION; RAT
HEARTS; CARDIOMYOCYTES; TISSUE; TRANSPLANTATION; VIABILITY;
BIOCOMPATIBILITY; VASCULARIZATION
AB Human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) provide an unlimited cell source to treat cardiovascular diseases, the leading cause of death worldwide. However, current hiPSCCMs retain an immature phenotype that leads to difficulties for integration with adult myocardium after transplantation. To address this, we recently utilized electrically conductive silicon nanowires (e-SiNWs) to facilitate self-assembly of hiPSC-CMs to form nanowired hiPSC cardiac spheroids. Our previous results showed addition of e-SiNWs effectively enhanced the functions of the cardiac spheroids and improved the cellular maturation of hiPSC-CMs. Here, we examined two important factors that can affect functions of the nanowired hiPSC cardiac spheroids: (1) cell number per spheroid (i.e., size of the spheroids), and (2) the electrical conductivity of the e-SiNWs. To examine the first factor, we prepared hiPSC cardiac spheroids with four different sizes by varying cell number per spheroid (similar to-0.5k, similar to 1k, similar to 3k, similar to 7k cells/ spheroid). Spheroids with similar to 3k cells/spheroid was found to maximize the beneficial effects of the 3D spheroid microenvironment. This result was explained with a semi-quantitative theory that considers two competing factors: 1) the improved 3D cell-cell adhesion, and 2) the reduced oxygen supply to the center of spheroids with the increase of cell number. Also, the critical role of electrical conductivity of silicon nanowires has been confirmed in improving tissue function of hiPSC cardiac spheroids. These results lay down a solid foundation to develop suitable nanowired hiPSC cardiac spheroids as an innovative cell delivery system to treat cardiovascular diseases.
Statement of Significance
Cardiovascular disease is the leading cause of death and disability worldwide. Due to the limited regenerative capacity of adult human hearts, human induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) have received significant attention because they provide a patient specific cell source to regenerate damaged hearts. Despite the progress, current human hiPSC-CMs retain an immature phenotype that leads to difficulties for integration with adult myocardium after transplantation. To address this, we recently utilized electrically conductive silicon nanowires (e-SiNWs) to facilitate self-assembly of hiPSC-CMs to form nanowired hiPSC cardiac spheroids. Our previous results showed addition of eSiNWs effectively enhanced the functions of the cardiac spheroids and improved the cellular maturation of hiPSC-CMs. In this manuscript, we examined the effects of two important factors on the functions of nanowired hiPSC cardiac spheroids: (1) cell number per spheroid (i.e., size of the spheroids), and (2) the electrical conductivity of the e-SiNWs. The results from these studies will allow for the development of suitable nanowired hiPSC cardiac spheroids to effectively deliver hiPSC-CMs for heart repair. (c) 2017 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
C1 [Tan, Yu; Richards, Dylan; Coyle, Robert C.; Mei, Ying] Clemson Univ, Bioengn Dept, Clemson, SC 29634 USA.
[Yao, Jenny] Acad Magnet High Sch, N Charleston, SC 29405 USA.
[Xu, Ruoyu; Tian, Bozhi] Univ Chicago, James Franck Inst, Dept Chem, Chicago, IL 60637 USA.
[Xu, Ruoyu; Tian, Bozhi] Univ Chicago, Inst Biophys Dynam, Chicago, IL 60637 USA.
[Gou, Wenyu; Wang, Hongjun] Med Univ South Carolina, Dept Surg, Charleston, SC 29425 USA.
[Menick, Donald R.] Med Univ South Carolina, Ralph H Johnson Vet Affairs Med Ctr, Gazes Cardiac Res Inst, Dept Med,Div Cardiol, Charleston, SC 29425 USA.
[Mei, Ying] Med Univ South Carolina, Dept Regenerat Med & Cell Biol, Charleston, SC 29425 USA.
RP Mei, Y (reprint author), Clemson Univ, Bioengn Dept, Clemson, SC 29634 USA.
EM mei@clemson.edu
FU National Institutes of Health [8P20 GM103444, U54 GM104941]; Clemson
University; National Science Foundation [NSF - EPS-0903795]; NIH [T32
HL007260]; US Department of Veterans Affairs Merit Review [I01
BX002327]; NIH-NIGMS [P30 GM103342]
FX The work is supported by the National Institutes of Health (8P20
GM103444, U54 GM104941), the startup funds from Clemson University, the
National Science Foundation (NSF - EPS-0903795), the NIH Cardiovascular
Training Grant (T32 HL007260), and US Department of Veterans Affairs
Merit Review (I01 BX002327). This study used the services of the
Morphology, Imaging, and Instrumentation Core, which is supported by
NIH-NIGMS P30 GM103342 to the South Carolina COBRE for Developmentally
Based Cardiovascular Diseases.
NR 49
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PU ELSEVIER SCI LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
SN 1742-7061
EI 1878-7568
J9 ACTA BIOMATER
JI Acta Biomater.
PD MAR 15
PY 2017
VL 51
BP 495
EP 504
DI 10.1016/j.actbio.2017.01.029
PG 10
WC Engineering, Biomedical; Materials Science, Biomaterials
SC Engineering; Materials Science
GA EQ4AB
UT WOS:000398014000039
PM 28087483
ER
PT J
AU Kallianos, K
Henry, TS
Yeghiazarians, Y
Zimmet, J
Shunk, KA
Tseng, EE
Mahadevan, V
Hope, MD
AF Kallianos, Kimberly
Henry, Travis S.
Yeghiazarians, Yerem
Zimmet, Jeffrey
Shunk, Kendrick A.
Tseng, Elaine E.
Mahadevan, Vaikom
Hope, Michael D.
TI Ferumoxytol MRA for transcatheter aortic valve replacement planning with
renal insufficiency
SO INTERNATIONAL JOURNAL OF CARDIOLOGY
LA English
DT Article
ID CARDIOVASCULAR MAGNETIC-RESONANCE; ANGIOGRAPHY; ECHOCARDIOGRAPHY;
REGURGITATION; IMPLANTATION; ACCURACY; CT
AB Background: Computed tomography angiography (CTA) is the test of choice for pre-procedure imaging of trans-catheter aortic valve replacement (TAVR) candidates. The iodinated contrast required, however, increases the risk of renal dysfunction in patients with pre-existing renal failure. Ferumoxytol is a magnetic resonance imaging (MRI) contrast agent that can be used with renal failure. Its long vascular resonance time allows gated MRA sequences that approach CTA in image quality. We present respiratory and cardiac gated MRA enabled by ferumoxytol that can be post-processed in an analogous fashion to CTA.
Methods: Seven patients with renal failure presenting for TAVR were imaged with respiratory and cardiac gated MRA at 3T using ferumoxtyol for contrast. Aortic annulus, root and peripheral access dimensions were calculated in a fashion identical to that used for CTA. Of these, 6 patients underwent a TAVR procedure and 5 had intraoperative valve assessment with transesophageal echocardiograph (TEE) using standard clinical protocols that employed both two-and three-dimensional techniques.
Results: Good correlation between MRA aortic annulus measurements and those from TEE were shown in 5 patients with mean annulus area of 392.4 mm(2) (290-470 range) versus 374.1 mm(2) (285-440 range), with a pairwise correlation coefficient of 0.92, p = 0.029. All patients received Sapien valve implants (one 20 mm, three 23 mm, and two 26 mm valves). Access decisions were guided by MRA with no complications. Annulus sizing resulted in no greater than trace/mild aortic regurgitation in all patients.
Conclusions: Ferumoxytol MRA is a safe alternative to CTA in patients with renal failure for pre-TAVR analysis of the aortic root and peripheral access. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
C1 [Kallianos, Kimberly; Henry, Travis S.; Hope, Michael D.] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, 505 Parnassus Ave,Box 0628, San Francisco, CA 94143 USA.
[Yeghiazarians, Yerem; Mahadevan, Vaikom] Univ Calif San Francisco, Dept Cardiol, San Francisco, CA 94143 USA.
[Zimmet, Jeffrey; Shunk, Kendrick A.] San Francisco VA Med Ctr, Dept Cardiol, San Francisco, CA USA.
[Tseng, Elaine E.] San Francisco VA Med Ctr, Dept Surg, San Francisco, CA USA.
RP Hope, MD (reprint author), Univ Calif San Francisco, Dept Radiol & Biomed Imaging, 505 Parnassus Ave,Box 0628, San Francisco, CA 94143 USA.
EM michael.hope@ucsf.edu
FU NIH/NHLBI [R01 HL123759]
FX This work was supported by NIH/NHLBI R01 HL123759.
NR 11
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U2 1
PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0167-5273
EI 1874-1754
J9 INT J CARDIOL
JI Int. J. Cardiol.
PD MAR 15
PY 2017
VL 231
BP 255
EP 257
DI 10.1016/j.ijcard.2016.12.147
PG 3
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EQ2NE
UT WOS:000397905600046
PM 28100426
ER
PT J
AU Singh, JA
Dowsey, M
Choong, PF
AF Singh, Jasvinder A.
Dowsey, Michelle
Choong, Peter F.
TI Patient Endorsement of the Outcome Measures in Rheumatology (OMERACT)
Total Joint Replacement (TJR) clinical trial draft core domain set
SO BMC MUSCULOSKELETAL DISORDERS
LA English
DT Article
ID TOTAL KNEE ARTHROPLASTY; TOTAL SHOULDER ARTHROPLASTY; TOTAL ELBOW
ARTHROPLASTY; QUALITY-OF-LIFE; PAIN OUTCOMES; INPATIENT SAMPLE; FILTER
2.0; TOTAL HIP; ARTHRITIS; TRENDS
AB Background: A patient- and surgeon-Delphi-derived Outcome Measures in Rheumatology (OMERACT) draft core domain set for total joint arthroplasty (TJR) trials was recently developed. Our objective was to obtain further patient stakeholder endorsement of draft core domain set for TJR clinical trials.
Methods: We surveyed two patient groups: (1) OMERACT patient partners; and (2) patients who had undergone hip or knee TJR. Patients received an introductory email with explanations about the core domain set and instructions to rate the core domains, i.e., important aspects, of OMERACT TJR clinical trial draft core domain set. Rating was on a nominal scale, where 1-3 indicated a domain of limited importance, 4-6 an important, but not critical domain, and 7-9 a critical domain. We used Mann-Whitney test (a non-parametric test) to compare the distribution of ratings between the two groups.
Results: Thirty one survey participants from the OMERACT patient partner group and 118 knee/hip TJR patients responded with response rates of 66 and 80%, respectively. Majority of the survey respondents were female, 87 vs. 53%, and were 55 years or older, 57 vs. 94%. Median (interquartile range [IQR]) scores for six core domains by OMERACT and knee/hip TJR patient groups were, respectively: pain, 8 [8, 9] and 9 [8, 9]; function, 9 [8, 9] and 9 [8, 9]; patient satisfaction, 8 [8, 9] and 8 [7, 9]; revision surgery, 7 [7, 8] and 7 [5, 9]; adverse events, 8 [7, 9] and 8 [6, 9]; and death, 9 [6, 9] and 9 [4, 9]. No statistically significant differences in rating were noted for any of the six core domains between the two groups (p >= 0.31). Among the additional domains, ratings for patient participation did not differ by group (p = 0.98), but ratings for cost were significantly different (p = 0.005). Patients provided qualitative feedback regarding core domains, and did not propose any modifications to the draft core domain set.
Conclusions: Two separate patient stakeholder groups endorsed the OMERACT TJR draft core domain set for TJR trials.
C1 [Singh, Jasvinder A.] Univ Alabama Birmingham, 510 20th St S,Fac Off Tower 805B, Birmingham, AL 35294 USA.
[Singh, Jasvinder A.] Birmingham Vet Affairs Med Ctr, 700 19th St S, Birmingham, AL 35233 USA.
[Dowsey, Michelle; Choong, Peter F.] Univ Melbourne, St Vincents Hosp, Dept Surg, Melbourne, Vic, Australia.
RP Singh, JA (reprint author), Univ Alabama Birmingham, 510 20th St S,Fac Off Tower 805B, Birmingham, AL 35294 USA.; Singh, JA (reprint author), Birmingham Vet Affairs Med Ctr, 700 19th St S, Birmingham, AL 35233 USA.
EM Jasvinder.md@gmail.com
FU National Health & Medical Research Council Career Development Fellowship
[APP1122526]
FX A/Prof Dowsey holds a National Health & Medical Research Council Career
Development Fellowship (APP1122526). We thank the patients for
participating in this study.
NR 31
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U2 1
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1471-2474
J9 BMC MUSCULOSKEL DIS
JI BMC Musculoskelet. Disord.
PD MAR 15
PY 2017
VL 18
AR 111
DI 10.1186/s12891-017-1464-x
PG 6
WC Orthopedics; Rheumatology
SC Orthopedics; Rheumatology
GA EQ0LE
UT WOS:000397761900001
PM 28298194
ER
PT J
AU Kyle, JE
Casey, CP
Stratton, KG
Zink, EM
Kim, YM
Zheng, XY
Monroe, ME
Weitz, KK
Bloodsworth, KJ
Orton, DJ
Ibrahim, YM
Moore, RJ
Lee, CG
Pedersen, C
Orwoll, E
Smith, RD
Burnum-Johnson, KE
Baker, ES
AF Kyle, Jennifer E.
Casey, Cameron P.
Stratton, Kelly G.
Zink, Erika M.
Kim, Young-Mo
Zheng, Xueyun
Monroe, Matthew E.
Weitz, Karl K.
Bloodsworth, Kent J.
Orton, Daniel J.
Ibrahim, Yehia M.
Moore, Ronald J.
Lee, Christine G.
Pedersen, Catherine
Orwoll, Eric
Smith, Richard D.
Burnum-Johnson, Kristin E.
Baker, Erin S.
TI Comparing identified and statistically significant lipids and polar
metabolites in 15-year old serum and dried blood spot samples for
longitudinal studies
SO RAPID COMMUNICATIONS IN MASS SPECTROMETRY
LA English
DT Article
ID MASS-SPECTROMETRY; FATTY-ACIDS; PROTEOMICS DATA; FILTER-PAPER; TERM
STABILITY; ION MOBILITY; DEGREES-C; FRAGMENTATION; LIPOPROTEINS;
METABOLOMICS
AB RATIONALE: The use of dried blood spots (DBS) has many advantages over traditional plasma and serum samples such as the smaller blood volume required, storage at room temperature, and ability to sample in remote locations. However, understanding the robustness of different analytes in DBS samples is essential, especially in older samples collected for longitudinal studies.
METHODS: Here we analyzed the stability of polar metabolites and lipids in DBS samples collected in 2000-2001 and stored at room temperature. The identified and statistically significant molecules were then compared to matched serum samples stored at-80 degrees C to determine if the DBS samples could be effectively used in a longitudinal study following metabolic disease.
RESULTS: A total of 400 polar metabolites and lipids were identified in the serum and DBS samples using gas chromatograph/mass spectrometry (GC/MS), liquid chromatography (LC)/MS, and LC/ion mobility spectrometry-MS (LC/IMS-MS). The identified polar metabolites overlapped well between the sample types, though only one statistically significant metabolite was conserved in a case-control study of older diabetic males with low amounts of high-density lipoproteins and high body mass indices, triacylglycerides and glucose levels when compared to non-diabetic patients with normal levels, indicating that degradation in the DBS samples affects polar metabolite quantitation. Differences in the lipid identifications indicated that some oxidation occurs in the DBS samples. However, 36 statistically significant lipids correlated in both sample types.
CONCLUSIONS: The difference in the number of statistically significant polar metabolites and lipids indicated that the lipids did not degrade to as great of a degree as the polar metabolites in the DBS samples and lipid quantitation was still possible. Copyright (c) 2016 John Wiley & Sons, Ltd.
C1 [Kyle, Jennifer E.; Casey, Cameron P.; Zink, Erika M.; Kim, Young-Mo; Zheng, Xueyun; Monroe, Matthew E.; Weitz, Karl K.; Bloodsworth, Kent J.; Orton, Daniel J.; Ibrahim, Yehia M.; Moore, Ronald J.; Smith, Richard D.; Burnum-Johnson, Kristin E.; Baker, Erin S.] Pacific Northwest Natl Lab, Earth & Biol Sci Directorate, Richland, WA 99352 USA.
[Stratton, Kelly G.] Pacific Northwest Natl Lab, Nat Secur Directorate, Richland, WA 99352 USA.
[Lee, Christine G.; Pedersen, Catherine; Orwoll, Eric] Oregon Hlth & Sci Univ, Dept Med, Bone & Mineral Unit, Portland, OR 97201 USA.
[Lee, Christine G.] Portland VA Med Ctr, Res Serv, Portland, OR USA.
RP Burnum-Johnson, KE; Baker, ES (reprint author), 902 Battelle Blvd,POB 999,MSIN K8-98, Richland, WA 99352 USA.
EM kristin.burnum-johnson@pnnl.gov; erin.baker@pnnl.gov
RI Kim, Young-Mo/D-3282-2009; Smith, Richard/J-3664-2012
OI Kim, Young-Mo/0000-0002-8972-7593; Smith, Richard/0000-0002-2381-2349;
Zheng, Xueyun/0000-0001-9782-4521; Casey, Cameron/0000-0001-6790-2170
FU National Institute of Environmental Health Sciences of the NIH [R01
ES022190]; NIH Eunice Kennedy Shriver National Institute of Child Health
and Human Development [R21 HD084788]; National Institute of General
Medical Sciences [P41 GM103493]; Laboratory Directed Research and
Development Program at Pacific Northwest National Laboratory; U.S.
Department of Energy Office of Biological and Environmental Research
Genome Sciences Program; National Institute of Allergy and Infectious
Diseases [U19 AI106772]; National Institute on Aging (NIA); National
Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS);
National Center for Advancing Translational Sciences (NCATS); NIH
Roadmap for Medical Research [U01 AG027810, U01 AG042124, U01 AG042139,
U01 AG042140, U01 AG042143, U01 AG042145, U01 AG042168, U01 AR066160,
UL1 TR000128]; DOE [DE-AC05-76RL0 1830]
FX The authors would like to thank Nathan Johnson for assistance in
preparing the figures. Portions of this research were supported by
grants from the National Institute of Environmental Health Sciences of
the NIH (R01 ES022190), NIH Eunice Kennedy Shriver National Institute of
Child Health and Human Development (R21 HD084788), National Institute of
General Medical Sciences (P41 GM103493), and the Laboratory Directed
Research and Development Program at Pacific Northwest National
Laboratory. This research utilized capabilities developed by the
Pan-omics program (funded by the U.S. Department of Energy Office of
Biological and Environmental Research Genome Sciences Program) and by
the National Institute of Allergy and Infectious Diseases under grant
U19 AI106772. The Osteoporotic Fractures in Men (MrOS) Study in the US
was supported by the National Institute on Aging (NIA), the National
Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS),
the National Center for Advancing Translational Sciences (NCATS), and
NIH Roadmap for Medical Research under the following grant numbers: U01
AG027810, U01 AG042124, U01 AG042139, U01 AG042140, U01 AG042143, U01
AG042145, U01 AG042168, U01 AR066160, and UL1 TR000128. This work was
performed in the W. R. Wiley Environmental Molecular Sciences Laboratory
(EMSL), a DOE national scientific user facility at the Pacific Northwest
National Laboratory (PNNL). PNNL is operated by Battelle for the DOE
under contract DE-AC05-76RL0 1830.
NR 56
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U1 8
U2 8
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0951-4198
EI 1097-0231
J9 RAPID COMMUN MASS SP
JI Rapid Commun. Mass Spectrom.
PD MAR 15
PY 2017
VL 31
IS 5
BP 447
EP 456
DI 10.1002/rcm.7808
PG 10
WC Biochemical Research Methods; Chemistry, Analytical; Spectroscopy
SC Biochemistry & Molecular Biology; Chemistry; Spectroscopy
GA EL3IK
UT WOS:000394512600006
PM 27958645
ER
PT J
AU Kort, NS
Ford, JM
Roach, BJ
Gunduz-Bruce, H
Krystal, JH
Jaeger, J
Reinhart, RMG
Mathalon, DH
AF Kort, Naomi S.
Ford, Judith M.
Roach, Brian J.
Gunduz-Bruce, Handan
Krystal, John H.
Jaeger, Judith
Reinhart, Robert M. G.
Mathalon, Daniel H.
TI Role of N-Methyl-D-Aspartate Receptors in Action-Based Predictive Coding
Deficits in Schizophrenia
SO BIOLOGICAL PSYCHIATRY
LA English
DT Article
DE Electroencephalography; Ketamine; N-methyl-D-aspartate glutamate
receptor; Predictive coding; Schizophrenia; Speech motor control
ID COROLLARY DISCHARGE DYSFUNCTION; AUDITORY SENSORY MEMORY; MISMATCH
NEGATIVITY GENERATION; SUBUNIT GENE GRIN2B; HEALTHY-VOLUNTEERS; SPEECH
PRODUCTION; SYNAPTIC PLASTICITY; NEUROPHYSIOLOGICAL EVIDENCE; COGNITIVE
DEFICITS; PSYCHOTIC SYMPTOMS
AB BACKGROUND: Recent theoretical models of schizophrenia posit that dysfunction of the neural mechanisms subserving predictive coding contributes to symptoms and cognitive deficits, and this dysfunction is further posited to result from N-methyl-D-aspartate glutamate receptor (NMDAR) hypofunction. Previously, by examining auditory cortical responses to self-generated speech sounds, we demonstrated that predictive coding during vocalization is disrupted in schizophrenia. To test the hypothesized contribution of NMDAR hypofunction to this disruption, we examined the effects of the NMDAR antagonist, ketamine, on predictive coding during vocalization in healthy volunteers and compared them with the effects of schizophrenia.
METHODS: In two separate studies, the N1 component of the event-related potential elicited by speech sounds during vocalization (talk) and passive playback(listen) were compared to assess the degree of N1 suppression during vocalization, a putative measure of auditory predictive coding. In the crossover study, 31 healthy volunteers completed two randomly ordered test days, a saline day and a ketamine day. Event- related potentials during the talk/ listen task were obtained before infusion and during infusion on both days, and N1 amplitudes were compared across days. In the case- control study, N1 amplitudes from 34 schizophrenia patients and 33 healthy control volunteers were compared.
RESULTS: N1 suppression to self produced vocalizations was significantly and similarly diminished by ketamine (Cohen's d= 1.14) and schizophrenia(Cohen's d=.85).
CONCLUSIONS: Disruption of NMDARs causes dysfunction in predictive coding during vocalization in a manner similar to the dysfunction observed in schizophrenia patients, consistent with the theorized contribution of NMDAR hypofunction to predictive coding deficits in schizophrenia.
C1 [Kort, Naomi S.; Ford, Judith M.; Mathalon, Daniel H.] Univ Calif San Francisco, San Francisco, CA USA.
[Ford, Judith M.; Mathalon, Daniel H.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Roach, Brian J.] Northern California Inst Res & Educ, San Francisco, CA USA.
[Gunduz-Bruce, Handan; Krystal, John H.; Reinhart, Robert M. G.] Yale Univ, Sch Med, New Haven, CT USA.
[Gunduz-Bruce, Handan; Krystal, John H.] Vet Affairs Connecticut Healthcare Syst, West Haven, CT USA.
[Jaeger, Judith] Clin Dev AstraZeneca Pharmaceut, Wilmington, DE USA.
[Jaeger, Judith] Albert Einstein Coll York, Yorktown Hts, NY USA.
[Jaeger, Judith] LLC, CognitionMetr, Wilmington, DC USA.
[Reinhart, Robert M. G.] Boston Univ, Boston, MA USA.
[Mathalon, Daniel H.] Mental Hlth Serv 116D, SFVAMC, 4150 Clement St, San Francisco, CA 94121 USA.
RP Mathalon, DH (reprint author), Mental Hlth Serv 116D, SFVAMC, 4150 Clement St, San Francisco, CA 94121 USA.
EM daniel.mathalon@ucsf.edu
FU AstraZeneca for an investigator-initiated study (DHM); National
Institute of Mental Health [R01 MH-58262, T32 MH089920]; Yale Center for
Clinical Investigation [UL1RR024139]; US National Institute on Alcohol
Abuse and Alcoholism [P50AA012879]
FX This work was supported by AstraZeneca for an investigator-initiated
study (DHM) and the National Institute of Mental Health Grant Nos. R01
MH-58262 (to JMF) and T32 MH089920 (to NSK). JHK was supported by the
Yale Center for Clinical Investigation Grant No. UL1RR024139 and the US
National Institute on Alcohol Abuse and Alcoholism Grant No.
P50AA012879.
NR 109
TC 1
Z9 1
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0006-3223
EI 1873-2402
J9 BIOL PSYCHIAT
JI Biol. Psychiatry
PD MAR 15
PY 2017
VL 81
IS 6
BP 514
EP 524
DI 10.1016/j.biopsych.2016.06.019
PG 11
WC Neurosciences; Psychiatry
SC Neurosciences & Neurology; Psychiatry
GA EP3RS
UT WOS:000397300000010
PM 27647218
ER
PT J
AU Reusch, JEB
Manson, JE
AF Reusch, Jane E. B.
Manson, JoAnn E.
TI Management of Type 2 Diabetes in 2017 Getting to Goal
SO JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
LA English
DT Editorial Material
ID ASSOCIATION; STATEMENT
C1 [Reusch, Jane E. B.] Univ Colorado, Anschutz Med Ctr, Ctr Womens Hlth Res, Denver, CO 80202 USA.
[Reusch, Jane E. B.] Denver VA Med Ctr, Denver, CO USA.
[Manson, JoAnn E.] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA.
[Manson, JoAnn E.] Harvard Med Sch, Boston, MA USA.
[Manson, JoAnn E.] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA.
RP Manson, JE (reprint author), Harvard Med Sch, Brigham & Womens Hosp, 900 Commonwealth Ave,Third Floor, Boston, MA 02215 USA.
EM jmanson@rics.bwh.harvard.edu
FU AstraZeneca; Merck
FX The authors have completed and submitted the ICMJE Form for Disclosure
of Potential Conflicts of Interest. Dr Reusch reported receiving grant
funding from AstraZeneca and Merck; and serving on the board of
directors for the American Diabetes Association. No other disclosures
were reported.
NR 7
TC 0
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U1 5
U2 5
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 0098-7484
EI 1538-3598
J9 JAMA-J AM MED ASSOC
JI JAMA-J. Am. Med. Assoc.
PD MAR 14
PY 2017
VL 317
IS 10
BP 1015
EP 1016
DI 10.1001/jama.2017.0241
PG 2
WC Medicine, General & Internal
SC General & Internal Medicine
GA EO5DO
UT WOS:000396713400009
PM 28249081
ER
PT J
AU Hoy, AR
Ly, M
Carlsson, CM
Okonkwo, OC
Zetterberg, H
Blennow, K
Sager, MA
Asthana, S
Johnson, SC
Alexander, AL
Bendlin, BB
AF Hoy, Andrew R.
Ly, Martina
Carlsson, Cynthia M.
Okonkwo, Ozioma C.
Zetterberg, Henrik
Blennow, Kaj
Sager, Mark A.
Asthana, Sanjay
Johnson, Sterling C.
Alexander, Andrew L.
Bendlin, Barbara B.
TI Microstructural white matter alterations in preclinical Alzheimer's
disease detected using free water elimination diffusion tensor imaging
SO PLOS ONE
LA English
DT Article
ID MILD COGNITIVE IMPAIRMENT; FIBER TRACTOGRAPHY; CORPUS-CALLOSUM;
HEALTHY-ADULTS; CSF; BRAIN; DEMENTIA; MRI; SCHIZOPHRENIA; DEGENERATION
AB Brain changes associated with Alzheimer's disease (AD) begin decades before disease diagnosis. While beta-amyloid plaques and neurofibrillary tangles are defining features of AD, neuronal loss and synaptic pathology are closely related to the cognitive dysfunction. Brain imaging methods that are tuned to assess degeneration of myelinated nerve fibers in the brain (collectively called white matter) include diffusion tensor imaging (DTI) and related techniques, and are expected to shed light on disease-related loss of structural connectivity. Participants (N = 70, ages 47-76 years) from the Wisconsin Registry for Alzheimer's Prevention study underwent DTI and hybrid diffusion imaging to determine a free-water elimination (FWE-DTI) model. The study assessed the extent to which preclinical AD pathology affects brain white matter. Preclinical AD pathology was determined using cerebrospinal fluid (CSF) biomarkers. The sample was enriched for AD risk (APOE epsilon 4 and parental history of AD). AD pathology assessed by CSF analyses was significantly associated with altered microstructure on both DTI and FWE-DTI. Affected regions included frontal, parietal, and especially temporal white matter. The f-value derived from the FWE-DTI model appeared to be the most sensitive to the relationship between the CSF AD biomarkers and microstructural alterations in white matter. These findings suggest that white matter degeneration is an early pathological feature of AD that may have utility both for early disease detection and as outcome measures for clinical trials. More complex models of microstructural diffusion properties including FWE-DTI may provide increased sensitivity to early brain changes associated with AD over standard DTI.
C1 [Hoy, Andrew R.] US Navy, Med Serv Corp, Falls Church, VA 22042 USA.
[Hoy, Andrew R.; Alexander, Andrew L.] Univ Wisconsin, Dept Med Phys, Sch Med & Publ Hlth, 1530 Med Sci Ctr, Madison, WI 53706 USA.
[Hoy, Andrew R.; Alexander, Andrew L.] Univ Wisconsin, Waisman Lab Brain Imaging & Behav, Madison, WI 53706 USA.
[Hoy, Andrew R.] Uniformed Serv Univ Hlth Sci, Dept Radiol & Radiol Sci, Bethesda, MD 20814 USA.
[Ly, Martina; Carlsson, Cynthia M.; Okonkwo, Ozioma C.; Asthana, Sanjay; Johnson, Sterling C.; Bendlin, Barbara B.] William S Middleton Mem Vet Adm Med Ctr, Geriatr Res Educ & Clin Ctr, Madison, WI USA.
[Ly, Martina; Carlsson, Cynthia M.; Okonkwo, Ozioma C.; Sager, Mark A.; Asthana, Sanjay; Johnson, Sterling C.; Bendlin, Barbara B.] Univ Wisconsin, Wisconsin Alzheimers Dis Res Ctr, Madison, WI USA.
[Ly, Martina] Univ Wisconsin, Neurosci Training Program, Madison, WI USA.
[Carlsson, Cynthia M.; Okonkwo, Ozioma C.; Sager, Mark A.; Asthana, Sanjay; Johnson, Sterling C.; Bendlin, Barbara B.] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Alzheimers Inst, Madison, WI USA.
[Zetterberg, Henrik; Blennow, Kaj] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Clin Neurochem Lab,Dept Psychiat & Neurochem, Gothenburg, Sweden.
[Zetterberg, Henrik] UCL Inst Neurol, Queen Sq, London WC1N 3BG, England.
[Alexander, Andrew L.] Univ Wisconsin, Dept Psychiat, Madison, WI 53706 USA.
RP Hoy, AR (reprint author), US Navy, Med Serv Corp, Falls Church, VA 22042 USA.; Hoy, AR (reprint author), Univ Wisconsin, Dept Med Phys, Sch Med & Publ Hlth, 1530 Med Sci Ctr, Madison, WI 53706 USA.; Hoy, AR (reprint author), Univ Wisconsin, Waisman Lab Brain Imaging & Behav, Madison, WI 53706 USA.; Hoy, AR (reprint author), Uniformed Serv Univ Hlth Sci, Dept Radiol & Radiol Sci, Bethesda, MD 20814 USA.
EM Andrew.Hoy@usuhs.edu
FU National Institutes of Health [P50AG033514, R01AG027161, P30HD003352,
P50MH100031, R01AG037639]; Torsten Soderberg Foundation at the Royal
Swedish Academy of Sciences
FX Research reported in this publication was supported in part by the
National Institutes of Health under Grant Award Numbers P50AG033514,
R01AG027161, P30HD003352, P50MH100031, and R01AG037639. The content is
solely the responsibility of the authors and does not necessarily
represent the official views of the National Institutes of Health.
Biomarker analyses in this project was supported by the Torsten
Soderberg Foundation at the Royal Swedish Academy of Sciences.
NR 88
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U2 2
PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1932-6203
J9 PLOS ONE
JI PLoS One
PD MAR 14
PY 2017
VL 12
IS 3
AR e0173982
DI 10.1371/journal.pone.0173982
PG 21
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EN6DM
UT WOS:000396094700053
PM 28291839
ER
PT J
AU Debnath, S
Velagapudi, C
Redus, L
Thameem, F
Kasinath, B
Hura, CE
Lorenzo, C
Abboud, HE
O'Connor, JC
AF Debnath, Subrata
Velagapudi, Chakradhar
Redus, Laney
Thameem, Farook
Kasinath, Balakuntalam
Hura, Claudia E.
Lorenzo, Carlos
Abboud, Hanna E.
O'Connor, Jason C.
TI Tryptophan Metabolism in Patients With Chronic Kidney Disease Secondary
to Type 2 Diabetes: Relationship to Inflammatory Markers
SO INTERNATIONAL JOURNAL OF TRYPTOPHAN RESEARCH
LA English
DT Article
DE Chronic kidney disease; indoleamine 2,3-dioxygenase 1; inflammatory
cytokines; kynurenine; tryptophan; type 2 diabetes
ID KYNURENINE PATHWAY ENZYMES; STAGE RENAL-DISEASE; INDOLEAMINE
2,3-DIOXYGENASE; AMINO-ACID; QUINOLINIC ACID; NEPHROPATHY; PROGRESSION;
PREDICTION; PLASMA; IDO2
AB OBJECTIVE : Type 2 diabetes (T2D) is the primary case of chronic kidney disease (CKD). Inflammation is associated with metabolic dysregulation in patients with T2D and CKD. Tryptophan (TRP) metabolism may have relevance to the CKD outcomes and associated symptoms. We investigated the relationships of TRP metabolism with inflammatory markers in patients with T2D and CKD.
METHODS: Data were collected from a well-characterized cohort of type 2 diabetic individuals with all stages of CKD, including patients on hemodialysis. Key TRP metabolites (kynurenine [KYN], kynurenic acid [KYNA], and quinolinic acid [QA]), proinflammatory cytokines (tumor necrosis factor-alpha [TNF-alpha] and interleukin-6 [IL-6]), and C-reactive protein were measured in plasma. The KYN/TRP ratio was utilized as a surrogate marker for indoleamine 2,3-dioxygenase 1 (IDO1) enzyme activity.
RESULTS : There was a significant inverse association between circulating TRP level and stages of CKD (P < 0.0001). Downstream bioactive TRP metabolites KYN, KYNA, and QA were positively and robustly correlated with the severity of kidney disease (P < 0.0001). In multiple linear regression, neither TNF-alpha nor IL-6 was independently related to KYN/TRP ratio after adjusting for estimated glomerular filtration rate (eGFR). Only TNF-alpha was independently related to KYN after taking into account the effect of eGFR.
CONCLUSIONS: Chronic kidney disease secondary to T2D may be associated with accumulation of toxic TRP metabolites due to both inflammation and impaired kidney function. Future longitudinal studies to determine whether the accumulation of KYN directly contributes to CKD progression and associated symptoms in patients with T2D are warranted.
C1 [Debnath, Subrata; Velagapudi, Chakradhar; Thameem, Farook; Kasinath, Balakuntalam; Hura, Claudia E.; Abboud, Hanna E.] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Nephrol, San Antonio, TX 78229 USA.
[Redus, Laney; O'Connor, Jason C.] Univ Texas Hlth Sci Ctr San Antonio, Dept Pharmacol, San Antonio, TX 78229 USA.
[Lorenzo, Carlos] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Rheumatol & Clin Immunol, San Antonio, TX 78229 USA.
[O'Connor, Jason C.] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
RP Debnath, S (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Nephrol, San Antonio, TX 78229 USA.
EM nath@uthscsa.edu; oconnorj@uthscsa.edu
FU San Antonio Area Foundation; National Institute of Diabetes and
Digestive and Kidney Diseases; National Institutes of Health (NIH)
[U01DK57292-05]; NIH [1S10OD016417-01]
FX The author(s) disclosed receipt of the following financial support for
the research, authorship, and/or publication of this article: This work
was partially supported by the San Antonio Area Foundation. The Family
Investigation of Nephropathy in Diabetes study was supported by the
National Institute of Diabetes and Digestive and Kidney Diseases, and
the National Institutes of Health (NIH) (U01DK57292-05). Mass
spectrometry analyses were conducted at the Mass Spectrometry Core
Facilities, University of Texas Health Science Center at San Antonio, on
instrumentation obtained with funding from the NIH (1S10OD016417-01).
Funding sources had no role in data analyses and interpretations.
NR 51
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U1 1
U2 1
PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 1178-6469
J9 INT J TRYPTOPHAN RES
JI Int. J. Trypotophan Res.
PD MAR 10
PY 2017
VL 10
BP 1
EP 9
DI 10.1177/1178646917694600
PG 9
WC Neurosciences
SC Neurosciences & Neurology
GA EP8TZ
UT WOS:000397649000001
ER
PT J
AU Chinman, M
McCarthy, S
Hannah, G
Byrne, TH
Smelson, DA
AF Chinman, Matthew
McCarthy, Sharon
Hannah, Gordon
Byrne, Thomas Hugh
Smelson, David A.
TI Using Getting To Outcomes to facilitate the use of an evidence-based
practice in VA homeless programs: a cluster-randomized trial of an
implementation support strategy
SO IMPLEMENTATION SCIENCE
LA English
DT Article
DE Implementation support; Co-occurring disorders; Fidelity; Training;
Technical assistance
ID TREATMENT ENGAGEMENT INTERVENTION; SUBSTANCE USE DISORDERS;
HEALTH-PROMOTION; CONSOLIDATED FRAMEWORK; MENTAL ILLNESSES; HOUSING 1ST;
INDIVIDUALS; SERVICES; ELEMENTS; IMPROVE
AB Background: Incorporating evidence-based integrated treatment for dual disorders into typical care settings has been challenging, especially among those serving Veterans who are homeless. This paper presents an evaluation of an effort to incorporate an evidence-based, dual disorder treatment called Maintaining Independence and Sobriety Through Systems Integration, Outreach, and Networking-Veterans Edition (MISSION-Vet) into case management teams serving Veterans who are homeless, using an implementation strategy called Getting To Outcomes (GTO).
Methods: This Hybrid Type III, cluster-randomized controlled trial assessed the impact of GTO over and above MISSION-Vet Implementation as Usual (IU). Both conditions received standard MISSION-Vet training and manuals. The GTO group received an implementation manual, training, technical assistance, and data feedback. The study occurred in teams at three large VA Medical Centers over 2 years. Within each team, existing sub-teams (case managers and Veterans they serve) were the clusters randomly assigned. The trial assessed MISSION-Vet services delivered and collected via administrative data and implementation barriers and facilitators, via semi-structured interview.
Results: No case managers in the IU group initiated MISSION-Vet while 68% in the GTO group did. Seven percent of Veterans with case managers in the GTO group received at least one MISSION-Vet session. Most case managers appreciated the MISSION-Vet materials and felt the GTO planning meetings supported using MISSION-Vet. Case manager interviews also showed that MISSION-Vet could be confusing; there was little involvement from leadership after their initial agreement to participate; the data feedback system had a number of difficulties; and case managers did not have the resources to implement all aspects of MISSION-Vet.
Conclusions: This project shows that GTO-like support can help launch new practices but that multiple implementation facilitators are needed for successful execution of a complex evidence-based program like MISSION-Vet.
C1 [Chinman, Matthew; McCarthy, Sharon; Hannah, Gordon] VA Pittsburgh Healthcare Syst, VISN Mental Illness Res & Clin Ctr 4, Pittsburgh, PA 15240 USA.
[Chinman, Matthew; McCarthy, Sharon; Hannah, Gordon] VA Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA 15240 USA.
[Chinman, Matthew] RAND Corp, Pittsburgh, PA 15213 USA.
[Chinman, Matthew; Byrne, Thomas Hugh; Smelson, David A.] VA Natl Ctr Homelessness Vet, Philadelphia, PA 19120 USA.
[Byrne, Thomas Hugh] Boston Univ, Sch Social Work, Boston, MA 02215 USA.
[Byrne, Thomas Hugh; Smelson, David A.] VA Ctr Healthcare Org & Implementat Res, Boston, MA USA.
[Smelson, David A.] Univ Massachusetts, Sch Med, Dept Psychiat, Worcester, MA 01605 USA.
RP Chinman, M (reprint author), VA Pittsburgh Healthcare Syst, VISN Mental Illness Res & Clin Ctr 4, Pittsburgh, PA 15240 USA.; Chinman, M (reprint author), VA Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA 15240 USA.; Chinman, M (reprint author), RAND Corp, Pittsburgh, PA 15213 USA.; Chinman, M (reprint author), VA Natl Ctr Homelessness Vet, Philadelphia, PA 19120 USA.
EM Chinman@rand.org
FU Health Services Research and Development Quality Enhancement Research
Initiative, "MISSION-Vet HUD-VASH Implementation Study" [SDP 11-240]
FX All the authors are funded by a grant from the Health Services Research
and Development Quality Enhancement Research Initiative, "MISSION-Vet
HUD-VASH Implementation Study" (SDP 11-240).
NR 43
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U1 2
U2 2
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1748-5908
J9 IMPLEMENT SCI
JI Implement. Sci.
PD MAR 9
PY 2017
VL 12
AR 34
DI 10.1186/s13012-017-0565-0
PG 12
WC Health Care Sciences & Services; Health Policy & Services
SC Health Care Sciences & Services
GA EO3RB
UT WOS:000396610800001
PM 28279207
ER
PT J
AU Bowers, JS
Nelson, MH
Majchrzak, K
Bailey, SR
Rohrer, B
Kaiser, ADM
Atkinson, C
Gattinoni, L
Paulos, CM
AF Bowers, Jacob S.
Nelson, Michelle H.
Majchrzak, Kinga
Bailey, Stefanie R.
Rohrer, Baerbel
Kaiser, Andrew D. M.
Atkinson, Carl
Gattinoni, Luca
Paulos, Chrystal M.
TI Th17 cells are refractory to senescence and retain robust antitumor
activity after long-term ex vivo expansion
SO JCI INSIGHT
LA English
DT Article
ID CD8(+) T-CELLS; TUMOR-INFILTRATING LYMPHOCYTES; ADOPTIVE IMMUNOTHERAPY;
METASTATIC MELANOMA; ESTABLISHED MELANOMA; CANCER-IMMUNOTHERAPY;
TRANSFER THERAPY; TELOMERE LENGTH; HUMAN EFFECTOR; MEMORY CELLS
AB Adoptive immunotherapy for solid tumors relies on infusing large numbers of T cells to mediate successful antitumor responses in patients. While long-term rapid-expansion protocols (REPs) produce sufficient numbers of CD8(+) T cells for treatment, they also cause decline in the cell's therapeutic fitness. In contrast, we discovered that IL-17-producing CD4(+) T cells (Th17 cells) do not require REPs to expand 5,000-fold over 3 weeks. Also, unlike Th1 cells, Th17 cells do not exhibit hallmarks of senescence or apoptosis, retaining robust antitumor efficacy in vivo. Three-week-expanded Th17 cells eliminated melanoma as effectively as Th17 cells expanded for 1 week when infused in equal numbers into mice. However, treating mice with large recalcitrant tumors required the infusion of all cells generated after 2 or 3 weeks of expansion, while the cell yield obtained after 1-week expansion was insufficient. Long-term-expanded Th17 cells also protected mice from tumor rechallenge including lung metastasis. Importantly, 2-week-expanded human chimeric antigen receptor-positive (CAR(+)) Th17 cells also retained their ability to regress human mesothelioma, while CAR(+) Th1 cells did not. Our results indicate that tumor-reactive Th17 cells are an effective cell therapy for cancer, remaining uncompromised when expanded for a long duration owing to their resistance to senescence.
C1 [Bowers, Jacob S.; Nelson, Michelle H.; Majchrzak, Kinga; Bailey, Stefanie R.; Atkinson, Carl; Paulos, Chrystal M.] Med Univ South Carolina, Dept Microbiol & Immunol, Charleston, SC 29425 USA.
[Bowers, Jacob S.; Nelson, Michelle H.; Majchrzak, Kinga; Bailey, Stefanie R.; Paulos, Chrystal M.] Med Univ South Carolina, Dept Dermatol, Charleston, SC 29425 USA.
[Bowers, Jacob S.; Nelson, Michelle H.; Majchrzak, Kinga; Bailey, Stefanie R.; Paulos, Chrystal M.] Med Univ South Carolina, Dept Surg, Charleston, SC 29425 USA.
[Majchrzak, Kinga] Warsaw Univ Life Sci, Dept Physiol Sci, Fac Vet Med, Warsaw, Poland.
[Rohrer, Baerbel] Med Univ South Carolina, Dept Ophthalmol, Charleston, SC 29425 USA.
[Rohrer, Baerbel] Ralph H Johnson VA Med Ctr, Charleston, SC USA.
[Kaiser, Andrew D. M.] NCI, Ctr Canc Res, NIH, Bethesda, MD 20892 USA.
[Gattinoni, Luca] NCI, Expt Transplantat & Immunol Branch, NIH, Bethesda, MD 20892 USA.
[Kaiser, Andrew D. M.] Miltenyi Biotec, Bergisch Gladbach, Germany.
RP Bowers, JS; Paulos, CM (reprint author), Med Univ South Carolina, Hollings Canc Ctr, 86 Jonathan Lucas St,Room 606B MSC509, Charleston, SC 29425 USA.
EM bowersjs@musc.edu; paulos@musc.edu
FU Hollings Cell Evaluation Therapy; Hollings Cell Evaluation & Therapy,
and Hollings Biostatistics Shared Resources, Hollings Cancer Center,
MUSC [P30 CA138313]; NIH [F30 CA200272, T32 GM008716, F31 CA192787];
Jeane B. Kempner Foundation; ACS [122704-PF-13-084-01-LIB]; NCI [R01
CA175061, R01 CA208514]; KL2 South Carolina Clinical & Translational
Research grant [UL1 TR000062]; ACS-IRG grant [016623-004]; MUSC start-up
funds
FX We thank Logan Huff and Hannah Knochelmann for experimental support and
Kent Armeson for help in statistical analysis of this work. This
research was supported in part by the Hollings Cell Evaluation &
Therapy, and Hollings Biostatistics Shared Resources, Hollings Cancer
Center, MUSC (P30 CA138313).; This work was supported by NIH fellowship
grant F30 CA200272 and NIH training grant T32 GM008716 to J.S. Bowers, a
Jeane B. Kempner Foundation grant and ACS Postdoctoral fellowship
(122704-PF-13-084-01-LIB) grant to M.H. Nelson, an NIH fellowship grant
F31 CA192787 to S.R. Bailey, and NCI grants R01 CA175061 and R01
CA208514, KL2 South Carolina Clinical & Translational Research grant UL1
TR000062, ACS-IRG grant 016623-004, and MUSC start-up funds to C.M.
Paulos.
NR 57
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U2 1
PU AMER SOC CLINICAL INVESTIGATION INC
PI ANN ARBOR
PA 2015 MANCHESTER RD, ANN ARBOR, MI 48104 USA
SN 2379-3708
J9 JCI INSIGHT
JI JCI Insight
PD MAR 9
PY 2017
VL 2
IS 5
AR e90772
DI 10.1172/jci.insight.90772
PG 16
WC Medicine, Research & Experimental
SC Research & Experimental Medicine
GA EN5FA
UT WOS:000396029800010
PM 28289713
ER
PT J
AU Riad, FS
Razak, E
Saba, S
Shalaby, A
Nemec, J
AF Riad, Fady S.
Razak, Eathar
Saba, Samir
Shalaby, Alaa
Nemec, Jan
TI Recent heart rate history affects QT interval duration in atrial
fibrillation
SO PLOS ONE
LA English
DT Article
ID ACTION-POTENTIAL DURATION; TORSADE-DE-POINTES; RATE DEPENDENCE;
MORTALITY; PROLONGATION; DYNAMICS; FORMULAS
AB QT interval prolongation is associated with a risk of polymorphic ventricular tachycardia. QT interval shortens with increasing heart rate and correction for this effect is necessary for meaningful QT interval assessment. We aim to improve current methods of correcting the QT interval during atrial fibrillation (AF). Digitized Holter recordings were analyzed from patients with AF. Models of QT interval dependence on RR intervals were tested by sorting the beats into 20 bins based on corrected RR interval and assessing ST-T variability within the bins. Signal-averaging within bins was performed to determine QT/RR dependence. Data from 30 patients (29 men, 69.3 7.3 years) were evaluated. QT behavior in AF is well described by a linear function (slope-0.19) of steady-state corrected RR interval. Corrected RR is calculated as a combination of an exponential weight function with time-constant of 2 minutes and a smaller "immediate response" component (weight- 0.18). This model performs significantly (p<0.0001) better than models based on instantaneous RR interval only including Bazett and Fridericia. It also outperforms models based on shorter time-constants and other previously proposed models. This model may improve detection of repolarization delay in AF. QT response to heart rate changes in AF is similar to previously published QT dynamics during atrial pacing and in sinus rhythm.
C1 [Riad, Fady S.] Univ Pittsburgh, Med Ctr, Dept Internal Med, Pittsburgh, PA USA.
[Razak, Eathar; Shalaby, Alaa] VA Pittsburgh Healthcare Syst, Dept Cardiol, Pittsburgh, PA USA.
[Saba, Samir; Nemec, Jan] Univ Pittsburgh, Med Ctr, Inst Heart & Vasc, Pittsburgh, PA 15260 USA.
[Razak, Eathar] CHI Franciscan Hlth, Franciscan Heart & Vasc Associates St Joseph, Tacoma, WA USA.
RP Nemec, J (reprint author), Univ Pittsburgh, Med Ctr, Inst Heart & Vasc, Pittsburgh, PA 15260 USA.
EM limidus@hotmail.com
NR 29
TC 0
Z9 0
U1 1
U2 1
PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1932-6203
J9 PLOS ONE
JI PLoS One
PD MAR 8
PY 2017
VL 12
IS 3
AR e0172962
DI 10.1371/journal.pone.0172962
PG 14
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EN5VL
UT WOS:000396073700033
PM 28273109
ER
PT J
AU Bibbins-Domingo, K
Grossman, DC
Curry, SJ
Barry, MJ
Davidson, KW
Doubeni, CA
Epling, J
Garcia, FAR
Kemper, AR
Krist, AH
Kurth, AE
Landefeld, CS
Mangione, CM
Phillips, WR
Phipps, MG
Silverstein, M
Simon, M
Siu, AL
Tseng, CW
AF Bibbins-Domingo, Kirsten
Grossman, David C.
Curry, Susan J.
Barry, Michael J.
Davidson, Karina W.
Doubeni, Chyke A.
Epling, Johnw., Jr.
Garcia, Francisco A. R.
Kemper, Alex R.
Krist, Alex H.
Kurth, Ann E.
Landefeld, C. Seth
Mangione, Carol M.
Phillips, William R.
Phipps, Maureen G.
Silverstein, Michael
Simon, Melissa
Siu, Albert L.
Tseng, Chien-Wen
CA US Preventive Serv Task Force
TI Screening for Gynecologic Conditions With Pelvic Examination US
Preventive Services Task Force Recommendation Statement
SO JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
LA English
DT Article
ID OVARIAN-CANCER; CLINICAL MANIFESTATIONS; BACTERIAL VAGINOSIS;
ASYMPTOMATIC WOMEN
AB IMPORTANCE Many conditions that can affect women's health are often evaluated through pelvic examination. Although the pelvic examination is a common part of the physical examination, it is unclear whether performing screening pelvic examinations in asymptomatic women has a significant effect on disease morbidity and mortality.
OBJECTIVE To issue a new US Preventive Services Task Force(USPSTF) recommendation on screening for gynecologic conditions with pelvic examination for conditions other than cervical cancer, gonorrhea, and chlamydia, for which the USPSTF has already made specific recommendations.
EVIDENCE REVIEW The USPSTF reviewed the evidence on the accuracy, benefits, and potential harms of performing screening pelvic examinations in asymptomatic, nonpregnant adult women 18 years and older who are not at increased risk for any specific gynecologic condition.
FINDINGS Overall, the USPSTF found inadequate evidence on screening pelvic examinations for the early detection and treatment of a range of gynecologic conditions in asymptomatic, nonpregnant adult women.
CONCLUSIONS AND RECOMMENDATION The USPSTF concludes that the current evidence is insufficient to assess the balance of benefits and harms of performing screening pelvic examinations in asymptomatic, nonpregnant adult women. (I statement) This statement does not apply to specific disorders for which the USPSTF already recommends screening (ie, screening for cervical cancer with a Papanicolaou smear, screening for gonorrhea and chlamydia).
C1 [Bibbins-Domingo, Kirsten] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Grossman, David C.] Grp Hlth Res Inst, Seattle, WA USA.
[Curry, Susan J.] Univ Iowa, Iowa City, IA USA.
[Barry, Michael J.] Harvard Med Sch, Boston, MA USA.
[Davidson, Karina W.] Columbia Univ, New York, NY USA.
[Doubeni, Chyke A.] Univ Penn, Philadelphia, PA 19104 USA.
[Epling, Johnw., Jr.] SUNY Upstate Med Univ, Syracuse, NY 13210 USA.
[Garcia, Francisco A. R.] Pima Cty Dept Hlth, Tucson, AZ USA.
[Kemper, Alex R.] Duke Univ, Durham, NC USA.
[Krist, Alex H.] Fairfax Family Practice Residency, Fairfax, VA USA.
[Krist, Alex H.] Virginia Commonwealth Univ, Richmond, VA 23284 USA.
[Kurth, Ann E.] Yale Univ, New Haven, CT USA.
[Landefeld, C. Seth] Univ Alabama Birmingham, Birmingham, AL USA.
[Mangione, Carol M.] Univ Calif Los Angeles, Los Angeles, CA USA.
[Phillips, William R.] Univ Washington, Seattle, WA 98195 USA.
[Phipps, Maureen G.] Brown Univ, Providence, RI 02912 USA.
[Silverstein, Michael] Boston Univ, Boston, MA 02215 USA.
[Simon, Melissa] Northwestern Univ, Evanston, IL USA.
[Siu, Albert L.] Mt Sinai Hosp, New York, NY 10029 USA.
[Siu, Albert L.] James J Peters Vet Affairs Med Ctr, Bronx, NY USA.
[Tseng, Chien-Wen] Univ Hawaii Manoa, Honolulu, HI 96822 USA.
RP Bibbins-Domingo, K (reprint author), Univ Calif San Francisco, San Francisco, CA 94143 USA.
EM chair@uspstf.net
FU USPSTF
FX The USPSTF is an independent, voluntary body. The US Congress mandates
that the Agency for Healthcare Research and Quality (AHRQ) support the
operations of the USPSTF.
NR 23
TC 0
Z9 0
U1 0
U2 0
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 0098-7484
EI 1538-3598
J9 JAMA-J AM MED ASSOC
JI JAMA-J. Am. Med. Assoc.
PD MAR 7
PY 2017
VL 317
IS 9
BP 947
EP 953
DI 10.1001/jama.2017.0807
PG 7
WC Medicine, General & Internal
SC General & Internal Medicine
GA EM8DM
UT WOS:000395541500014
ER
PT J
AU Balasubramanian, P
Kumar, R
Williams, C
Itri, V
Wang, SX
Lu, S
Hessell, AJ
Haigwood, NL
Sinangil, F
Higgins, KW
Liu, L
Li, LZ
Nyambi, P
Gorny, MK
Totrov, M
Nadas, A
Kong, XP
Zolla-Pazner, S
Hioe, CE
AF Balasubramanian, Preetha
Kumar, Rajnish
Williams, Constance
Itri, Vincenza
Wang, Shixia
Lu, Shan
Hessell, Ann J.
Haigwood, Nancy L.
Sinangil, Faruk
Higgins, Keith W.
Liu, Lily
Li, Liuzhe
Nyambi, Phillipe
Gorny, Miroslaw K.
Totrov, Maxim
Nadas, Arthur
Kong, Xiang-Peng
Zolla-Pazner, Susan
Hioe, Catarina E.
TI Differential induction of anti-V3 crown antibodies with cradle- and
ladle-binding modes in response to HIV-1 envelope vaccination
SO VACCINE
LA English
DT Article
DE HIV; HIV envelope; V3; Mimotopes; Antibodies
ID V3 LOOP; TYPE-1 GP120; NEUTRALIZING ANTIBODIES; V3-SPECIFIC ANTIBODIES;
HIV-1-INFECTED HUMANS; MONOCLONAL-ANTIBODIES; BROAD NEUTRALIZATION;
IMMUNE-RESPONSE; INFECTION; EPITOPES
AB The V3 loop in the HIV envelope gp120 is one of the immunogenic sites targeted by Abs. The V3 crown in particular has conserved structural elements recognized by cross-reactive neutralizing Abs, indicating its potential contribution in protection against HIV. Crystallographic analyses of anti-V3 crown mAbs in complex with the V3 peptides have revealed that these mAbs recognize the conserved sites on the V3 crown via two distinct strategies: a cradle-binding mode (V3C) and a ladle-binding (V3L) mode. However, almost all of the anti-V3 crown mAbs studied in the past were isolated from chronically HIV-infected individuals. The extents to which the two types of anti-V3 crown Abs are generated by vaccination are unknown. This study analyzed the prevalence of V3C-type and V3L-type Ab responses in HIV-infected individuals and in HIV envelope-immunized humans and animals using peptide mimotopes that distinguish the two Ab types. The results show that both V3L-type and V3C-type Abs were generated by the vast majority of chronically HIV-infected humans, although the V3L-type were more prevalent. In contrast, only one of the two V3 Ab types was elicited in vaccinated humans or animal models, irrespective of HIV-1 envelope clades, envelope constructs (oligomeric or monomeric), and protocols (DNA plus protein or protein alone) used for vaccinations. The V3C-type Abs were produced by vaccinated humans. macaques, and rabbits, whereas the V3L-type Abs were made by mice. The V3C-type and V3L-type Abs generated by the vaccinations were able to mediate virus neutralization. These data indicate the restricted repertoires and the species-specific differences in the functional V3-specific Ab responses induced by the HIV envelope vaccines. The study implies the need for improving immunogen designs and vaccination strategies to broaden the diversity of Abs in order to target the different conserved epitopes in the V3 loop and, by extension, in the entire HIV envelope. Published by Elsevier Ltd.
C1 [Balasubramanian, Preetha] NYU, Sch Med, Sackler Inst Grad Biomed Sci, New York, NY 10016 USA.
[Balasubramanian, Preetha; Kumar, Rajnish; Itri, Vincenza; Zolla-Pazner, Susan; Hioe, Catarina E.] Icahn Sch Med Mt Sinai, Dept Med, Div Infect Dis, New York, NY 10029 USA.
[Kumar, Rajnish; Hioe, Catarina E.] James J Peters VA Med Ctr, Bronx, NY 10468 USA.
[Williams, Constance; Liu, Lily; Li, Liuzhe; Nyambi, Phillipe; Gorny, Miroslaw K.] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA.
[Wang, Shixia; Lu, Shan] Univ Massachusetts, Sch Med, Worcester, MA 01605 USA.
[Hessell, Ann J.; Haigwood, Nancy L.] Oregon Hlth & Sci Univ, Oregon Natl Primate Res Ctr, Beaverton, OR 97006 USA.
[Haigwood, Nancy L.] Oregon Hlth & Sci Univ, Dept Mol Microbiol & Immunol, Portland, OR 97239 USA.
[Sinangil, Faruk; Higgins, Keith W.] Global Solut Infect Dis, San Francisco, CA USA.
[Totrov, Maxim] Molsoft LLC, 3366 N Torrey Pines Ct, La Jolla, CA 92037 USA.
[Nadas, Arthur] NYU, Sch Med, Dept Environm Med, New York, NY 10016 USA.
[Kong, Xiang-Peng] NYU, Sch Med, Dept Biochem & Mol Pharmacol, New York, NY 10016 USA.
RP Hioe, CE (reprint author), Dept Med, Div Infect Dis, One Gustave L Levy Pl,Box 1090, New York, NY 10029 USA.
EM catarina.hioe@mssm.edu
OI Kong, Xiang-Peng/0000-0001-5773-2681; Gorny,
Miroslaw/0000-0002-2714-8780
FU Henry M. Jackson Foundation for the Advancement of Military Medicine -
USA; NIH [R21 AI114520, HIVRAD P01 AI100151]; Department of Veterans
Affairs, Veterans Health Administration, Office of Research and
Development
FX This work was supported in part by the Henry M. Jackson Foundation for
the Advancement of Military Medicine - USA (SZP, CEH), NIH grants R21
AI114520 (CEH) and HIVRAD P01 AI100151 (XPK, SZP) and by research funds
from the Department of Veterans Affairs, Veterans Health Administration,
Office of Research and Development (VA Merit Review and Research Career
Scientist - CEH).
NR 49
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Z9 0
U1 3
U2 3
PU ELSEVIER SCI LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
SN 0264-410X
EI 1873-2518
J9 VACCINE
JI Vaccine
PD MAR 7
PY 2017
VL 35
IS 10
BP 1464
EP 1473
DI 10.1016/j.vaccine.2016.11.107
PG 10
WC Immunology; Medicine, Research & Experimental
SC Immunology; Research & Experimental Medicine
GA EM9DK
UT WOS:000395611300015
PM 28185743
ER
PT J
AU Bauer, EM
Ben-Artzi, A
Duffy, EL
Elashoff, DA
Vangala, SS
Fitzgerald, J
Ranganath, VK
AF Bauer, Erin M.
Ben-Artzi, Ami
Duffy, Erin L.
Elashoff, David A.
Vangala, Sitaram S.
Fitzgerald, John
Ranganath, Veena K.
TI Joint-specific assessment of swelling and power Doppler in obese
rheumatoid arthritis patients
SO BMC MUSCULOSKELETAL DISORDERS
LA English
DT Article
DE Ultrasound; Obesity; Outcome measures; Rheumatoid arthritis
ID BODY-MASS INDEX; ANTITUMOR NECROSIS FACTOR; DISEASE-ACTIVITY; TREATMENT
RESPONSE; AMERICAN-COLLEGE; CONTROLLED-TRIAL; ASSOCIATION; ULTRASOUND;
THERAPY; PROGRESSION
AB Background: Clinical swollen joint examination of the obese rheumatoid arthritis (RA) patient can be difficult. Musculoskeletal Ultrasound (MSUS) has higher sensitivity than physical examination for swollen joints (SJ). The purpose of this study was to determine the joint-specific association between power Doppler (PDUS) and clinical SJ in RA across body mass index (BMI) categories.
Methods: Cross-sectional clinical and laboratory data were collected on 43 RA patients. PDUS was performed on 9 joints (wrist, metacarpalphalangeal 2-5, proximal interphalgeal 2/3 and metatarsalphalangeal 2/5). DAS28 and clinical disease activity index (CDAI) were calculated. Patients were categorized by BMI: <25, 25-30, and >30. Demographic and clinical characteristics were compared across BMI groups with Kruskal-Wallis test and chi-square tests. Joint-level associations between PDUS and clinically SJ were evaluated with mixed effects logistic regression models.
Results: While demographics and clinically-determined disease activity were similar among BMI groups, PDUS scores significantly differed (p = 0.02). Using PDUS activity as the reference standard for synovitis and clinically SJ as the test, the positive predictive value of SJ was significantly lower in higher BMI groups (0.71 in BMI < 25, 0.58 in BMI 25-30 and 0.44 in BMI < 30) (p = 0.02). The logistic model demonstrated that increased BMI category resulted in decreased likelihood of PDUS positivity (OR 0.52, p = 0.03).
Conclusions: This study suggests that in an obese RA patient, a clinically assessed SJ is less likely to represent true synovitis (as measured by PDUS). Disease activity in obese RA patients may be overestimated by CDAI/DAS28 calculations and clinicians when considering change in therapy.
C1 [Bauer, Erin M.; Duffy, Erin L.; Elashoff, David A.; Vangala, Sitaram S.; Fitzgerald, John; Ranganath, Veena K.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
[Bauer, Erin M.] US Dept Vet Affairs, Los Angeles, CA USA.
[Ben-Artzi, Ami] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA.
RP Ranganath, VK (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
EM vranganath@mednet.ucla.edu
FU National Institutes of Health [NIAMS K23 AR057818-02]; National Center
for Advancing Translational Sciences through UCLA CTSI [UL1TR000124]
FX This work was supported by Grant and National Institutes of Health Award
(NIAMS K23 AR057818-02) to Veena K. Ranganath and supported by the
National Center for Advancing Translational Sciences through UCLA CTSI
Grant UL1TR000124.
NR 39
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Z9 0
U1 4
U2 4
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1471-2474
J9 BMC MUSCULOSKEL DIS
JI BMC Musculoskelet. Disord.
PD MAR 4
PY 2017
VL 18
AR 99
DI 10.1186/s12891-017-1406-7
PG 8
WC Orthopedics; Rheumatology
SC Orthopedics; Rheumatology
GA EM7AZ
UT WOS:000395465100002
PM 28259162
ER
PT J
AU Nielson, JL
Cooper, SR
Yue, JK
Sorani, MD
Inoue, T
Yuh, EL
Mukherjee, P
Petrossian, TC
Paquette, J
Lum, PY
Carlsson, GE
Vassar, MJ
Lingsma, HF
Gordon, WA
Valadka, AB
Okonkwo, DO
Manley, GT
Ferguson, AR
AF Nielson, Jessica L.
Cooper, Shelly R.
Yue, John K.
Sorani, Marco D.
Inoue, Tomoo
Yuh, Esther L.
Mukherjee, Pratik
Petrossian, Tanya C.
Paquette, Jesse
Lum, Pek Y.
Carlsson, Gunnar E.
Vassar, Mary J.
Lingsma, Hester F.
Gordon, Wayne A.
Valadka, Alex B.
Okonkwo, David O.
Manley, Geoffrey T.
Ferguson, Adam R.
CA TRACK-TBI Investigators
TI Uncovering precision phenotype-biomarker associations in traumatic brain
injury using topological data analysis
SO PLOS ONE
LA English
DT Article
ID COMMON DATA ELEMENTS; TRANSFORMING RESEARCH; CLINICAL KNOWLEDGE;
POLYMORPHISM; COMT; CLASSIFICATION; PREDICTION; PROTEIN
AB Background
Traumatic brain injury (TBI) is a complex disorder that is traditionally stratified based on clinical signs and symptoms. Recent imaging and molecular biomarker innovations provide unprecedented opportunities for improved TBI precision medicine, incorporating patho-ana-tomical and molecular mechanisms. Complete integration of these diverse data for TBI diag-nosis and patient stratification remains an unmet challenge.
Methods and findings
The Transforming Research and Clinical Knowledge in Traumatic Brain Injury (TRACK-TBI) Pilot multicenter study enrolled 586 acute TBI patients and collected diverse common data elements (TBI-CDEs) across the study population, including imaging, genetics, and clinical outcomes. We then applied topology-based data-driven discovery to identify natural sub-groups of patients, based on the TBI-CDEs collected. Our hypothesis was two-fold: 1) A machine learning tool known as topological data analysis (TDA) would reveal data-driven patterns in patient outcomes to identify candidate biomarkers of recovery, and 2) TDA-iden-tified biomarkers would significantly predict patient outcome recovery after TBI using more traditional methods of univariate statistical tests. TDA algorithms organized and mapped the data of TBI patients in multidimensional space, identifying a subset of mild TBI patients with a specific multivariate phenotype associated with unfavorable outcome at 3 and 6 months after injury. Further analyses revealed that this patient subset had high rates of post-trau-matic stress disorder (PTSD), and enrichment in several distinct genetic polymorphisms associated with cellular responses to stress and DNA damage (PARP1), and in striatal dopamine processing (ANKK1, COMT, DRD2).
Conclusions
TDA identified a unique diagnostic subgroup of patients with unfavorable outcome after mild TBI that were significantly predicted by the presence of specific genetic polymorphisms. Machine learning methods such as TDA may provide a robust method for patient stratifica-tion and treatment planning targeting identified biomarkers in future clinical trials in TBI patients.
C1 [Nielson, Jessica L.; Cooper, Shelly R.; Yue, John K.; Inoue, Tomoo; Vassar, Mary J.; Manley, Geoffrey T.; Ferguson, Adam R.] Zuckerberg San Francisco Gen Hosp, Brain & Spinal Injury Ctr BASIC, San Francisco, CA 94110 USA.
[Nielson, Jessica L.; Cooper, Shelly R.; Yue, John K.; Sorani, Marco D.; Inoue, Tomoo; Vassar, Mary J.; Manley, Geoffrey T.; Ferguson, Adam R.] Univ Calif San Francisco, Dept Neurol Surg, Weill Inst Neurosci, San Francisco, CA 94143 USA.
[Cooper, Shelly R.; Yuh, Esther L.; Mukherjee, Pratik] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA.
[Petrossian, Tanya C.; Paquette, Jesse; Lum, Pek Y.; Carlsson, Gunnar E.] Ayasdi Inc, Palo Alto, CA USA.
[Lingsma, Hester F.] Erasmus MC, Publ Hlth, Rotterdam, Netherlands.
[Gordon, Wayne A.] Icahn Sch Med Mt Sinai, Dept Rehabil Med, New York, NY 10029 USA.
[Valadka, Alex B.] Virginia Commonwealth Univ, Dept Neurosurg, Richmond, VA USA.
[Okonkwo, David O.] Univ Pittsburgh, Dept Neurosurg, Pittsburgh, PA USA.
[Ferguson, Adam R.] San Francisco VA Med Ctr, Dept Vet Affairs, San Francisco, CA 94121 USA.
RP Manley, GT; Ferguson, AR (reprint author), Zuckerberg San Francisco Gen Hosp, Brain & Spinal Injury Ctr BASIC, San Francisco, CA 94110 USA.; Manley, GT; Ferguson, AR (reprint author), Univ Calif San Francisco, Dept Neurol Surg, Weill Inst Neurosci, San Francisco, CA 94143 USA.; Ferguson, AR (reprint author), San Francisco VA Med Ctr, Dept Vet Affairs, San Francisco, CA 94121 USA.
EM manleyg@neurosurg.ucsf.edu; adam.ferguson@ucsf.edu
OI Yue, John/0000-0001-9694-7722
FU Department of Defense (DoD) [W81XWH-131-0441]; National Institutes of
Health/National Institute of Neurological Disorders and Stroke
(NIH/NINDS) [NS067092, NS069409, NS069409-0251]; Craig H. Neilsen
Foundation (ARF); Wings for Life Foundation (ARF)
FX This work was funded by the following: Department of Defense (DoD) grant
W81XWH-131-0441 (GTM): http://cdmrp.army.mil/funding/phtbi.shtml;
National Institutes of Health/National Institute of Neurological
Disorders and Stroke (NIH/NINDS) grants NS067092 (ARF), NS069409 (GTM)
and NS069409-0251 (GTM): http://www.runds.nih.govt/; Craig H. Neilsen
Foundation (ARF): http://chnfoundation.org/; and Wings for Life
Foundation (ARF): http://www.wingsforlrie.com/en/.
NR 41
TC 0
Z9 0
U1 5
U2 5
PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1932-6203
J9 PLOS ONE
JI PLoS One
PD MAR 3
PY 2017
VL 12
IS 3
AR e0169490
DI 10.1371/journal.pone.0169490
PG 19
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EN5BR
UT WOS:000396021100002
PM 28257413
ER
PT J
AU He, K
Palen, BN
Mattox, EA
Parsons, EC
AF He, Ken
Palen, Brian N.
Mattox, Elizabeth A.
Parsons, Elizabeth C.
TI Veteran Preferences Regarding Wireless Management of Positive Airway
Pressure for Obstructive Sleep Apnea at a Tertiary Health-Care System
SO RESPIRATORY CARE
LA English
DT Article
DE sleep apnea syndrome; CPAP; patient preference; telehealth;
telemedicine; e-health; home health monitoring; technology
ID RANDOMIZED CONTROLLED-TRIAL; CARDIOVASCULAR-DISEASE; HIGH-RISK;
ADHERENCE; PROGRAM; POPULATION; ADULTS; DIAGNOSIS; MEDICINE; ACCESS
AB BACKGROUND: Timely monitoring of obstructive sleep apnea (OSA) therapy can be a challenge amid conflicting pressures of rising patient volume and shortage of sleep medicine providers. Positive airway pressure (PAP) devices with wireless modem technology have the potential to improve patient access to care and streamline work load, yet little is known about patient attitudes toward telehealth integration among veterans with sleep apnea. As part of a larger quality improvement initiative at the Veterans Affairs (VA) Puget Sound Health Care System, we elicited veterans' preferences toward modem versus traditional PAP data download, including patient attitudes and factors affecting those preferences. METHODS: We conducted an anonymous survey of veterans without previous CPAP experience presenting for initial device setup and training at VA Puget Sound PAP clinics. Surveys assessed subject demographics, PAP download preferences (modem vs mail), and Likert- type scale ratings of importance placed on factors including convenience and information privacy. Using multinomial logistic regression, we examined the association between convenience rating and download preference, adjusting for information privacy rating, age, and commute time. RESULTS: Of 444 surveys analyzed, respondents were primarily male with a mean age of 52 y. Most respondents reported taking >= 30 min to commute to the PAP clinic. Convenience was rated as the most important factor affecting download preferences. Veteran preferences regarding PAP download method were mixed, with 47% preferring modem, 38% preferring memory card mail- in, and 15% undecided. A higher rating of convenience was significantly associated with modem preference, both before and after adjustment for information privacy rating, commute time, and veteran age (adjusted relative risk ratio 1.67, P <.001, 95% CI 1.40-1.99). CONCLUSIONS: PAP data download preferences were mixed among new veteran users. Veterans placed a high value on the potentially competing concerns of convenience and information privacy. Veterans preferring modem factored convenience as important in their decision making, independent of privacy concerns.
C1 [Palen, Brian N.; Parsons, Elizabeth C.] Univ Washington, Div Pulm & Crit Care Med, Seattle, WA 98195 USA.
[He, Ken; Palen, Brian N.; Mattox, Elizabeth A.; Parsons, Elizabeth C.] Vet Affairs Puget Sound Hlth Care Syst, 1600 S Columbian Way,S-111 Pulm, Seattle, WA 98108 USA.
RP Parsons, EC (reprint author), Vet Affairs Puget Sound Hlth Care Syst, 1600 S Columbian Way,S-111 Pulm, Seattle, WA 98108 USA.
EM Elizabeth.parsons@va.gov
NR 43
TC 0
Z9 0
U1 1
U2 1
PU DAEDALUS ENTERPRISES INC
PI IRVING
PA 9425 N MAC ARTHUR BLVD, STE 100, IRVING, TX 75063-4706 USA
SN 0020-1324
EI 1943-3654
J9 RESP CARE
JI Respir. Care
PD MAR 2
PY 2017
VL 62
IS 3
BP 357
EP 362
DI 10.4187/respcare.05002
PG 6
WC Critical Care Medicine; Respiratory System
SC General & Internal Medicine; Respiratory System
GA EL9WT
UT WOS:000394971500013
PM 27879382
ER
PT J
AU Geha, R
Peters, M
Gill, RM
Dhaliwal, G
AF Geha, Rabih
Peters, Marion
Gill, Ryan M.
Dhaliwal, Gurpreet
TI Histology Rings True
SO NEW ENGLAND JOURNAL OF MEDICINE
LA English
DT Editorial Material
ID Q-FEVER; HEPATIC GRANULOMAS; DIAGNOSIS; DISEASE
C1 [Peters, Marion] Univ Calif San Francisco, Div Gastroenterol, San Francisco, CA 94143 USA.
[Geha, Rabih; Peters, Marion; Dhaliwal, Gurpreet] Univ Calif San Francisco, Dept Med, San Francisco, CA USA.
[Gill, Ryan M.] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94140 USA.
[Dhaliwal, Gurpreet] San Francisco VA Med Ctr, Med Serv, San Francisco, CA USA.
RP Geha, R (reprint author), 505 Parnassus Ave,Rm 987, San Francisco, CA 94143 USA.
EM rabih.geha@ucsf.edu
FU Philips Healthcare
FX Dr. Peters reports receiving honoraria from Merck, Roche, Johnson &
Johnson, Gilead Sciences, Abbott, and Genentech; Dr. Gill, receiving
consulting fees from Philips Healthcare; and Dr. Dhaliwal, receiving
honoraria from the ISMIE Mutual Insurance and Physicians' Reciprocal
Insurers. No other potential conflict of interest relevant to this
article was reported.
NR 13
TC 0
Z9 0
U1 1
U2 1
PU MASSACHUSETTS MEDICAL SOC
PI WALTHAM
PA WALTHAM WOODS CENTER, 860 WINTER ST,, WALTHAM, MA 02451-1413 USA
SN 0028-4793
EI 1533-4406
J9 NEW ENGL J MED
JI N. Engl. J. Med.
PD MAR 2
PY 2017
VL 376
IS 9
BP 870
EP 875
DI 10.1056/NEJMcps1609391
PG 6
WC Medicine, General & Internal
SC General & Internal Medicine
GA EM9JK
UT WOS:000395627500012
ER
PT J
AU Sheshadri, A
Johansen, KL
AF Sheshadri, Anoop
Johansen, Kirsten L.
TI Prehabilitation for the Frail Patient Approaching ESRD
SO SEMINARS IN NEPHROLOGY
LA English
DT Review
DE Frailty; CKD; ESRD; prehabilitation; physical function; exercise
ID CHRONIC KIDNEY-DISEASE; STAGE RENAL-DISEASE; QUALITY-OF-LIFE; RECEIVING
MAINTENANCE HEMODIALYSIS; PHYSICAL-ACTIVITY; DIALYSIS PATIENTS; EXERCISE
PROGRAM; CONTROLLED-TRIAL; MUSCLE STRENGTH; PREDIALYSIS PATIENTS
AB Frailty is a distinct phenotype that is highly prevalent in chronic kidney disease (CKD) and appears to be more prevalent with decreasing glomerular filtration rate. Exercise training or intervention to increase physical activity may ameliorate poor physical functioning and frailty, and even may improve survival in patients with CKD. Although exercise interventions improve outcomes across the spectrum of CKD, including patients treated with dialysis, patients treated with dialysis face barriers to exercise that patients with predialysis CKD do not. Rehabilitation at earlier stages of CKD (or prehabilitation before dialysis) might be more beneficial than not addressing the decreasing physical functioning and low physical activity until patients are receiving dialysis. This review summarizes available literature on frailty in the CKD and end-stage renal disease population, including exercise interventions and the limited evidence for prehabilitation as a strategy. Published by Elsevier Inc.
C1 [Johansen, Kirsten L.] San Francisco VA Med Ctr, Nephrol Sect, 111J,4150 Clement St, San Francisco, CA 94121 USA.
Univ Calif San Francisco, San Francisco, CA 94143 USA.
RP Johansen, KL (reprint author), San Francisco VA Med Ctr, Nephrol Sect, 111J,4150 Clement St, San Francisco, CA 94121 USA.
EM Kirsten.johansen@ucsf.edu
FU NIDDK NIH HHS [K24 DK085153]
NR 102
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U1 0
U2 0
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0270-9295
EI 1558-4488
J9 SEMIN NEPHROL
JI Semin. Nephrol.
PD MAR
PY 2017
VL 37
IS 2
BP 159
EP 172
DI 10.1016/j.semnephrol.2016.12.006
PG 14
WC Urology & Nephrology
SC Urology & Nephrology
GA ES9CF
UT WOS:000399852900007
PM 28410650
ER
PT J
AU Brennan, MB
Hess, TM
Bartle, B
Cooper, JM
Kang, J
Huang, ES
Smith, M
Sohn, MW
Crnich, C
AF Brennan, Meghan B.
Hess, Timothy M.
Bartle, Brian
Cooper, Jennifer M.
Kang, Jonathan
Huang, Elbert S.
Smith, Maureen
Sohn, Min-Woong
Crnich, Christopher
TI Diabetic foot ulcer severity predicts mortality among veterans with type
2 diabetes
SO JOURNAL OF DIABETES AND ITS COMPLICATIONS
LA English
DT Article
DE Diabetes; Foot ulcer; Gangrene; Mortality; Vascular disease
ID EURODIALE; RISK; DISEASE
AB Aim: Diabetic foot ulcers are associated with an increased risk of death. We evaluated whether ulcer severity at presentation predicts mortality.
Methods: Patients from a national, retrospective, cohort of veterans with type 2 diabetes who developed incident diabetic foot ulcers between January 1, 2006 and September 1, 2010, were followed until death or the end of the study period, January 1, 2012. Ulcers were characterized as early stage, osteomyelitis, or gangrene at presentation. Cox proportional hazard regression identified independent predictors of death, controlling for comorbidities, laboratory parameters, and healthcare utilization.
Results: 66,323 veterans were included in the cohort and followed for a mean of 27.7 months: 1-, 2-, and 5-year survival rates were 80.80%, 69.01% and 28.64%, respectively. Compared to early stage ulcers, gangrene was associated with an increased risk of mortality (HR 1.70, 95% C11.57-1.83, p < 0.001). The magnitude of this effect was greater than diagnosed vascular disease, i.e., coronary artery disease, peripheral arterial disease, or stroke.
Conclusion: Initial diabetic foot ulcer severity is a more significant predictor of subsequent mortality than coronary artery disease, peripheral arterial disease, or stroke. Unrecognized or under-estimated vascular disease and/or sepsis secondary to gangrene should be explored as possible causal explanations. (C) 2017 Elsevier Inc. All rights reserved.
C1 [Brennan, Meghan B.; Hess, Timothy M.; Smith, Maureen; Crnich, Christopher] Univ Wisconsin, Sch Med & Publ Hlth, 1685 Highland Ave, Madison, WI 53705 USA.
[Brennan, Meghan B.; Hess, Timothy M.; Kang, Jonathan; Crnich, Christopher] William S Middleton Mem Vet Adm Med Ctr, 2500 Overlook Terrace, Madison, WI 53705 USA.
[Brennan, Meghan B.; Bartle, Brian; Huang, Elbert S.; Sohn, Min-Woong] Edward Hines Jr Vet Hosp, 5000 S 5th Ave, Hines, IL 60141 USA.
[Cooper, Jennifer M.; Huang, Elbert S.] Univ Chicago, Med Ctr, 5841 S Maryland Ave, Chicago, IL 60637 USA.
[Sohn, Min-Woong] Univ Virginia, Sch Med, 1215 Lee St, Charlottesville, VA 22908 USA.
RP Brennan, MB (reprint author), 1685 Highland Ave, Madison, WI 53705 USA.
EM mbbrennan@medicine.wisc.edu
FU Clinical and Translational Science Award (CSTA) program, through NIH
National Center for Advancing Translational Science (NCATS)
[UL1TR000427]; NIH [KL2TR000428, K24DK105340, P30DK092949]; AHRQ [R01
HS018542, R01 HS018368]
FX The project described was supported by the Clinical and Translational
Science Award (CSTA) program, through the NIH National Center for
Advancing Translational Science (NCATS), grant UL1TR000427. Additional
funding was through the NIH grant numbers KL2TR000428, K24DK105340, and
P30DK092949 and AHRQ grants R01 HS018542 and R01 HS018368. The content
is solely the responsibility of the authors and does not necessarily
represent the official views of the NIH, AHRQ or VA.
NR 11
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1056-8727
EI 1873-460X
J9 J DIABETES COMPLICAT
JI J. Diabetes Complications
PD MAR
PY 2017
VL 31
IS 3
BP 556
EP 561
DI 10.1016/j.jdiacomp.2016.11.020
PG 6
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA ES3NC
UT WOS:000399435300007
PM 27993523
ER
PT J
AU Patel, AM
Wang, V
Philipp, A
Yusin, JS
AF Patel, Anil M.
Wang, Vivian
Philipp, Ami
Yusin, Joseph S.
TI Underuse of allergy services for patients having systemic reactions to
Hymenoptera venom stings
SO ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY
LA English
DT Letter
ID EMERGENCY-DEPARTMENT VISITS; ANAPHYLAXIS; EPIDEMIOLOGY
C1 [Patel, Anil M.; Wang, Vivian; Philipp, Ami; Yusin, Joseph S.] VA Greater Los Angeles Healthcare Syst, Dept Allergy & Immunol, Los Angeles, CA 90073 USA.
RP Yusin, JS (reprint author), VA Greater Los Angeles Healthcare Syst, Dept Allergy & Immunol, Los Angeles, CA 90073 USA.
EM jsyusin@yahoo.com
NR 10
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1081-1206
EI 1534-4436
J9 ANN ALLERG ASTHMA IM
JI Ann. Allergy Asthma Immunol.
PD MAR
PY 2017
VL 118
IS 3
BP 366
EP 367
PG 3
WC Allergy; Immunology
SC Allergy; Immunology
GA ER6RT
UT WOS:000398935500023
PM 28073614
ER
PT J
AU Burge, SK
Ferrer, RL
Foster, EL
Becho, J
Talamantes, M
Wood, RC
Katerndahl, DA
AF Burge, Sandra K.
Ferrer, Robert L.
Foster, Erin L.
Becho, Johanna
Talamantes, Melissa
Wood, Robert C.
Katerndahl, David A.
TI Research or Intervention or Both? Women's Changes After Participation in
a Longitudinal Study About Intimate Partner Violence
SO FAMILIES SYSTEMS & HEALTH
LA English
DT Article
DE spouse abuse; battered women; domestic violence; longitudinal studies;
qualitative research
ID SURVIVORS; DYNAMICS
AB Introduction: The tensions between risk and benefit in research are particularly evident in studies about intimate partner violence. Recalling and relating traumatic experiences may deepen posttraumatic stress or relieve the burden of terrible events long borne in secret. In this article, we examine the effects of study participation in a longitudinal investigation of intimate partner violence using both qualitative and quantitative data. Method: Researchers enrolled 200 women in moderately violent intimate relationships and asked them to report about their relationships every day for 12 weeks. Daily, participants telephoned an automated survey and responded to 34 survey questions. They also completed baseline and end-of-study surveys and maintained telephone contact with 1 researcher weekly. Forty-2 participants completed qualitative end-of-study interviews to describe their relationships and their experiences in the study. Results: Over 12 weeks, participants showed improvements in coping strategies, hope, and mental health, and increased readiness to leave their partners. In qualitative interviews, women reported gaining insight, feeling better emotionally, making behavioral changes, finding comfort in daily surveys, learning resources for help, and taking action to improve their lives. Fourteen percent left their partners by end-of-study; 35% sought counseling. Discussion: The study's daily survey invited the participant to become more reflective about her relationship, which changed how she saw herself and her situation. The study methods also included weekly conversations with a compassionate researcher, allowing women to tell their stories. These 2 strategies may be incorporated into brief interventions for intimate partner violence in primary care settings.
C1 [Burge, Sandra K.; Ferrer, Robert L.; Wood, Robert C.; Katerndahl, David A.] Univ Texas Hlth Sci Ctr San Antonio, Dept Family & Community Med, 7703 Floyd Curl Dr,Mail Code 7795, San Antonio, TX 78229 USA.
[Foster, Erin L.] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA.
[Talamantes, Melissa] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
RP Burge, SK (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Family & Community Med, 7703 Floyd Curl Dr,Mail Code 7795, San Antonio, TX 78229 USA.
EM burge@uthscsa.edu
FU "Dynamics of Human Behavior" program, National Science Foundation
[0525026]
FX This study was funded with a grant from the "Dynamics of Human Behavior"
program, National Science Foundation, Award 0525026. Automated data
collection was provided by the University of Colorado, Department of
Family Medicine Information Services group. We thank Stephanie Mitchell,
Kelli Giacomini, and Wilson Pace for their invaluable assistance with
the Interactive Voice Response system. We also express appreciation to
Norma Cantu and Diandrea Garza for their commitment to screening and
enrolling women for this study.
NR 26
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U1 1
U2 1
PU EDUCATIONAL PUBLISHING FOUNDATION-AMERICAN PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST, NE, WASHINGTON, DC 20002-4242 USA
SN 1091-7527
EI 1939-0602
J9 FAM SYST HEALTH
JI Fam. Syst. Health
PD MAR
PY 2017
VL 35
IS 1
BP 25
EP 35
DI 10.1037/fsh0000246
PG 11
WC Health Care Sciences & Services; Family Studies; Public, Environmental &
Occupational Health
SC Health Care Sciences & Services; Family Studies; Public, Environmental &
Occupational Health
GA ER4OR
UT WOS:000398780300005
PM 28068119
ER
PT J
AU Vig, EK
Taylor, JS
O'Hare, AM
AF Vig, Elizabeth K.
Taylor, Janelle S.
O'Hare, Ann M.
TI Considering a Family Systems Approach to Surrogate Decision-Making
SO FAMILIES SYSTEMS & HEALTH
LA English
DT Editorial Material
C1 [Vig, Elizabeth K.] Vet Affairs Puget Sound Hlth Care Syst, Dept Geriatr & Extended Care, Seattle, WA 98108 USA.
[Vig, Elizabeth K.] Univ Washington, Dept Med, Seattle, WA 98195 USA.
[Taylor, Janelle S.] Univ Washington, Dept Anthropol, Seattle, WA 98195 USA.
[O'Hare, Ann M.] Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA 98108 USA.
[O'Hare, Ann M.] Univ Washington, Ctr Innovat Vet Ctr & Value Driven Care, Hosp & Specialty Med Serv, Seattle, WA 98195 USA.
[O'Hare, Ann M.] Univ Washington, Dept Med, Seattle, WA 98195 USA.
RP Vig, EK (reprint author), Vet Affairs Puget Sound Hlth Care Syst, Dept Geriatr & Extended Care, Seattle, WA 98108 USA.
EM vigster@uw.edu
NR 8
TC 0
Z9 0
U1 0
U2 0
PU EDUCATIONAL PUBLISHING FOUNDATION-AMERICAN PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST, NE, WASHINGTON, DC 20002-4242 USA
SN 1091-7527
EI 1939-0602
J9 FAM SYST HEALTH
JI Fam. Syst. Health
PD MAR
PY 2017
VL 35
IS 1
BP 85
EP 87
DI 10.1037/fsh0000255
PG 3
WC Health Care Sciences & Services; Family Studies; Public, Environmental &
Occupational Health
SC Health Care Sciences & Services; Family Studies; Public, Environmental &
Occupational Health
GA ER4OR
UT WOS:000398780300011
PM 28333517
ER
PT J
AU Kontos, AP
Van Cott, AC
Roberts, J
Pan, JW
Kelly, MB
McAllister-Deitrick, J
Hetherington, HP
AF Kontos, Anthony P.
Van Cott, Anne C.
Roberts, Jodilyn
Pan, Jullie W.
Kelly, Monique B.
McAllister-Deitrick, Jamie
Hetherington, Hoby P.
TI Clinical and Magnetic Resonance Spectroscopic Imaging Findings in
Veterans With Blast Mild Traumatic Brain Injury and Post-Traumatic
Stress Disorder
SO MILITARY MEDICINE
LA English
DT Article; Proceedings Paper
CT 5th Military Health System Research Symposium
CY AUG 17-21, 2015
CL Fort Lauderdale, FL
ID EXPLOSIVE BLAST; 7 T; AFGHANISTAN; HISTORY; ARRAYS; IRAQ; CARE
AB Objectives: To compare magnetic resonance spectroscopic imaging (MRSI) findings from the hippocampal regions of military veterans with blast-related mild traumatic brain injury (blast mTBI) and post-traumatic stress disorder (PTSD) to those with PTSD only; and to examine the relationship of MRSI findings to cognitive and neuromotor impairment. Methods: 35 military veterans-23 with blast mTBI and PTSD (blast mTBI/PTSD) and 12 with PTSD only participated in the study. Whole plane MRSI data including N-acetyl aspartate (NAA) and choline (Ch) were acquired at 7T for the hippocampus. Concurrent cognitive and neuromotor data were collected using established assessments. General linear models (GLMs) with Bonferroni correction were used to compare the two groups on NAA/Ch ratios across regions of the hippocampus. Spearman's correlations were used to examine correlations between NAA/Ch and cognitive and neuromotor impairment. Results: The NAA/Ch results for the left hippocampus were lower in the blast mTBI/PTSD group than the PTSD-only group. The blast mTBI/PTSD group also scored worse on the WAIS-IV-vocabulary. Significant correlations between NAA/Ch and neuromotor outcomes-including vestibular impairment-were supported. Conclusions: Combined MRSI and cognitive and neuromotor data may help inform more objective and accurate diagnoses and effective treatments for patients with blast mTBI and PTSD.
C1 [Kontos, Anthony P.; McAllister-Deitrick, Jamie] Univ Pittsburgh, Dept Orthopaed Surg, 3471 Fifth Ave,1010, Pittsburgh, PA 15213 USA.
[Van Cott, Anne C.; Roberts, Jodilyn; Kelly, Monique B.] VA Pittsburgh Healthcare Syst, Univ Dr C, Pittsburgh, PA 15240 USA.
[Van Cott, Anne C.; Pan, Jullie W.] Univ Pittsburgh, Dept Neurol, 811 Kaufmann Med Bldg,3471 Fifth Ave 810, Pittsburgh, PA 15213 USA.
[Hetherington, Hoby P.] Univ Pittsburgh, Magnet Resonance Res Ctr, 200 Lothrop St, Pittsburgh, PA 15213 USA.
RP Kontos, AP (reprint author), Univ Pittsburgh, Dept Orthopaed Surg, 3471 Fifth Ave,1010, Pittsburgh, PA 15213 USA.
FU National Institutes of Health/National Institute of Neurological
Disorders [Stroke-NIH-R01NS081772]; National Institute on Deafness and
Other Communication Disorders [1K01DC012332-01A1]; National Institutes
of Health/National Institute of Biomedical Imaging and Bioengineering
NIH [R01EB011639]
FX This research was supported in part by a grant to the University of
Pittsburgh to Dr. Hetherington and Dr. VanCott from the National
Institutes of Health/National Institute of Neurological Disorders and
Stroke-NIH-R01NS081772; and by a grant to the University of Pittsburgh
to Dr. Kontos from the National Institute on Deafness and Other
Communication Disorders (1K01DC012332-01A1); and a grant to Dr Jullie W.
Pan from the National Institutes of Health/National Institute of
Biomedical Imaging and Bioengineering NIH R01EB011639.
NR 27
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U1 0
U2 0
PU ASSOC MILITARY SURG US
PI BETHESDA
PA 9320 OLD GEORGETOWN RD, BETHESDA, MD 20814 USA
SN 0026-4075
EI 1930-613X
J9 MIL MED
JI Milit. Med.
PD MAR
PY 2017
VL 182
SU 1
BP 99
EP 104
DI 10.7205/MILMED-D-16-00177
PG 6
WC Medicine, General & Internal
SC General & Internal Medicine
GA ER6VN
UT WOS:000398947100017
PM 28291459
ER
PT J
AU Fung, CH
Martin, JL
Hays, RD
Patterson, ES
Aysola, R
Col, N
Mitchell, MN
Truong, C
Dzierzewski, JM
Jouldjian, S
Song, Y
Rodriguez, JC
Josephson, K
Alessi, C
AF Fung, Constance H.
Martin, Jennifer L.
Hays, Ron D.
Patterson, Emily S.
Aysola, Ravi
Col, Nananda
Mitchell, Michael N.
Truong, Cindy
Dzierzewski, Joseph M.
Jouldjian, Stella
Song, Yeonsu
Carlos Rodriguez, Juan
Josephson, Karen
Alessi, Cathy
TI Patient-Reported Usability of Positive Airway Pressure Equipment Is
Associated With Adherence in Older Adults
SO SLEEP
LA English
DT Article
DE sleep apnea; adherence; usability; predictive modeling.
ID SLEEP-APNEA; INTERNET; THERAPY; USERS; CARE
AB Study objectives: To examine the usability of positive airway pressure (PAP) devices and its association with PAP adherence among older adults with sleep-disordered breathing.
Methods: We mailed questionnaires to patients aged >= 65 years prescribed PAP therapy during the prior 36 months from two large healthcare systems. Survey participants completed the Usability of Sleep Apnea Equipment-Positive Airway Pressure (USE-PAP) questionnaire, which assessed the usability of their PAP device. Other questionnaire items included demographics and self-rated health. We also abstracted adherence data (mean nightly hours of PAP use available from one site) and interface type from the electronic health record.
Results: Five hundred sixty-four patients completed the survey (response rate = 33%). The mean USE-PAP score (0 = best to 100 = worst) was 20 (SD +/- 20). Mean duration of PAP use (available in 189 respondents) was 5.2 hours per night (SD +/- 2.0). In a nested regression model predicting nightly hours of PAP use, a 10-point (0.5 SD) increase in USE-PAP score corresponded to a 0.37 hour/night reduction in PAP use. The model including the USE-PAP score explained a significant proportion (R-2 = 15%) of the variation in nightly hours of PAP use above and beyond demographics, self-reported health, and interface type (R-2 = 12%).
Conclusions: Our results demonstrate that PAP usability varies among older patients and is associated with PAP adherence, above and beyond other predictors of adherence. These results support measuring and improving PAP usability to further improve PAP adherence for older patients.
C1 [Fung, Constance H.; Martin, Jennifer L.; Mitchell, Michael N.; Truong, Cindy; Dzierzewski, Joseph M.; Jouldjian, Stella; Song, Yeonsu; Josephson, Karen; Alessi, Cathy] VA Greater Los Angeles Healthcare Syst, Geriatr Res Educ & Clin Ctr, Los Angeles, CA USA.
[Fung, Constance H.; Martin, Jennifer L.; Hays, Ron D.; Aysola, Ravi; Song, Yeonsu; Carlos Rodriguez, Juan; Alessi, Cathy] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
[Patterson, Emily S.] Ohio State Univ, Sch Hlth & Rehabil Sci, Columbus, OH 43210 USA.
[Col, Nananda] Univ New England, Biddeford, ME USA.
[Dzierzewski, Joseph M.] Virginia Commonwealth Univ, Dept Psychol, Box 2018, Richmond, VA 23284 USA.
[Carlos Rodriguez, Juan] Pontificia Univ Catolica Chile, Santiago, Chile.
RP Fung, CH (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Geriatr Res Educ & Clin Ctr,VA Greater Los Angele, 16111 Plummer St,11E, North Hills, CA 91343 USA.
EM constance.fung@va.gov
FU VA Greater Los Angeles Healthcare System Sleep Center
FX We thank Michelle Zeidler, MD, MS and Silverio Santiago, MD from the VA
Greater Los Angeles Healthcare System Sleep Center for their support of
our study, and Sergio Martinez and Simone Vukelich for their help
abstracting data and preparing the survey mailings. We also thank the
UCLA Pulmonary/Sleep Clinic administrative staff for their support of
our project.
NR 22
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Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS INC
PI CARY
PA JOURNALS DEPT, 2001 EVANS RD, CARY, NC 27513 USA
SN 0161-8105
EI 1550-9109
J9 SLEEP
JI Sleep
PD MAR 1
PY 2017
VL 40
IS 3
DI 10.1093/sleep/zsx007
PG 7
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA ER6ND
UT WOS:000398921100024
ER
PT J
AU Katsiougiannis, S
Chia, D
Kim, Y
Singh, RP
Wong, DTW
AF Katsiougiannis, Stergios
Chia, David
Kim, Yong
Singh, Ram P.
Wong, David T. W.
TI Saliva exosomes from pancreatic tumor-bearing mice modulate NK cell
phenotype and antitumor cytotoxicity
SO FASEB JOURNAL
LA English
DT Article
DE extracellular vesicles; immune surveillance; cancer
ID NATURAL-KILLER-CELLS; EXTRACELLULAR VESICLES; CANCER EXOSOMES; EMERGING
ROLE; MARKERS; DIAGNOSTICS; METASTASIS; BIOMARKERS; INNATE
AB Tumor exosomes are emerging as antitumor immunity regulators; however, their effects on secondary exosome secretion by distal organs have not been explored. We have previously demonstrated that suppression of exosomes at the distal tumor site of pancreatic ductal adenocarcinoma (PDAC) ablated the development of salivary biomarker profile. Here, we explore the function of salivary exosomes from tumor-bearing mice in immune surveillance. We provide evidence that salivary exosomes from mice with PDA Cexhibit a suppressive effect that results in reduced tumor-killing capacity by NK cells. Salivary exosomes from mice with PDAC where pancreatic tumors were engineered to suppress exosome biogenesis failed to suppress NK cell cytotoxic potential against tumor cells, as opposed to salivary exosomes from mice with PDAC with normal tumor exosome biogenesis. These results reveal an important and previously unknown mechanism of antitumor immune regulation and provide new in sights into our understanding of the alterations of this biofluid during tumor development.
C1 [Katsiougiannis, Stergios; Kim, Yong; Wong, David T. W.] Univ Calif Los Angeles, Sch Dent, Ctr Oral Head & Neck Oncol Res, 10833 Le Conte Ave,Box 951668, Los Angeles, CA 90024 USA.
[Chia, David; Kim, Yong; Wong, David T. W.] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Los Angeles, CA 90024 USA.
[Kim, Yong] Univ Calif Los Angeles, Lab Stem Cell & Canc Epigenet Res, Los Angeles, CA USA.
[Chia, David] Univ Calif Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA USA.
[Singh, Ram P.] Univ Calif Los Angeles, David Geffen Sch Med, Div Rheumatol, Los Angeles, CA 90095 USA.
[Singh, Ram P.] Vet Affairs Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
RP Wong, DTW (reprint author), Univ Calif Los Angeles, Sch Dent, Ctr Oral Head & Neck Oncol Res, 10833 Le Conte Ave,Box 951668, Los Angeles, CA 90024 USA.
EM dwong@dentistry.ucla.edu
FU NCATS NIH HHS [UH2 TR000923]
NR 29
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Z9 0
U1 5
U2 5
PU FEDERATION AMER SOC EXP BIOL
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3998 USA
SN 0892-6638
EI 1530-6860
J9 FASEB J
JI Faseb J.
PD MAR
PY 2017
VL 31
IS 3
BP 998
EP +
DI 10.1096/fj.201600984R
PG 16
WC Biochemistry & Molecular Biology; Biology; Cell Biology
SC Biochemistry & Molecular Biology; Life Sciences & Biomedicine - Other
Topics; Cell Biology
GA EM9ZX
UT WOS:000395671200016
PM 27895106
ER
PT J
AU Marcuccilli, M
Chonchol, M
Jovanovich, A
AF Marcuccilli, Morgan
Chonchol, Michel
Jovanovich, Anna
TI Phosphate Binders and Targets Over Decades: Do We have it Right Now?
SO SEMINARS IN DIALYSIS
LA English
DT Article
ID CHRONIC KIDNEY-DISEASE; CORONARY-ARTERY CALCIFICATION; STAGE
RENAL-DISEASE; CHRONIC-HEMODIALYSIS PATIENTS; LEFT-VENTRICULAR
HYPERTROPHY; MINERAL BONE DISORDER; CARDIOVASCULAR-DISEASE; LANTHANUM
CARBONATE; PARATHYROID-HORMONE; CALCIUM-CARBONATE
AB In advanced renal disease, the kidney is unable to maintain phosphate balance due to decreased urinary excretion as well as the imbalance of the bone metabolic axis. It is well established that hyperphosphatemia is associated with increased cardiovascular events and mortality in patients with chronic kidney disease (CKD). However, there are no randomized controlled trials that demonstrate a clear benefit on hard outcomes in lowering serum phosphate levels to recommended targets in the CKD or dialysis population. In addition, while calcium-based phosphate binders have traditionally been the standard of care in the treatment of hyperphosphatemia, data regarding the increased risk of vascular mineralization continues to emerge. Clinicians continue to search for new phosphate-lowering therapies as well as investigate novel nutritional perspectives. The Kidney Disease: Improving Global Outcomes is currently revising the guidelines on phosphate goals in CKD. This review will outline the history of phosphate targets and phosphate binders, and explore innovative phosphate-lowering therapies. Based on current data, clinicians moving forward should continue to treat end-stage renal disease patients with hyperphosphatemia based on individual risk factors for vascular mineralization.
C1 [Marcuccilli, Morgan; Chonchol, Michel; Jovanovich, Anna] Hypertens Univ Colorado, Div Renal Dis, Denver, CO USA.
[Jovanovich, Anna] Denver VA Med Ctr, Denver, CO USA.
RP Chonchol, M (reprint author), Div Renal Dis & Hypertens, 12700,East 19th Ave C281, Aurora, CO 80045 USA.
EM michel.chonchol@ucdenver.edu
NR 60
TC 0
Z9 0
U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0894-0959
EI 1525-139X
J9 SEMIN DIALYSIS
JI Semin. Dial.
PD MAR-APR
PY 2017
VL 30
IS 2
SI SI
BP 134
EP 141
DI 10.1111/sdi.12568
PG 8
WC Urology & Nephrology
SC Urology & Nephrology
GA EM5HK
UT WOS:000395342400008
PM 28064444
ER
PT J
AU Baciewicz, AM
Lee, C
Ben-Ari, A
Kim, H
Lee, AT
AF Baciewicz, Anne M.
Lee, Calvin
Ben-Ari, Alon
Kim, Hojoong
Lee, Alex T.
TI Intravenous Tissue Plasminogen Activator Administration for Ischemic
Stroke 1 Hour After Epidural Catheter Removal: A Case Report
SO A & A CASE REPORTS
LA English
DT Article
ID ASSOCIATION; GUIDELINES; MEDICINE; SOCIETY
AB Anticoagulation after a recent neuraxial procedure poses risk for development of spinal hematoma. Clinical evidence supports prompt IV tissue plasminogen activator administration after onset of ischemic stroke. There is an absence of data regarding emergency fibrinolytic therapy for patients experiencing a stroke with recent neuraxial procedures, resulting in highly disparate, nonevidence-based guidelines. This report describes a patient who developed ischemic stroke when receiving postoperative epidural analgesia. Tissue plasminogen activator was emergently administered 1 hour after epidural catheter removal with a favorable recovery. The patient and his family reviewed the manuscript, and written consent to publish this case report was obtained from the patient.
C1 [Baciewicz, Anne M.] Univ Washington, Dept Pharm, VA Puget Sound Hlth Care Syst, Seattle, WA 98195 USA.
[Lee, Calvin] Univ Washington, Dept Anesthesiol & Pain Med, Seattle, WA 98195 USA.
[Ben-Ari, Alon; Lee, Alex T.] Univ Washington, Dept Anesthesiol & Pain Med, VA Puget Sound Hlth Care Syst, 1660 Columbian Way S-112-Anes, Seattle, WA 98108 USA.
[Kim, Hojoong] Univ Washington, Dept Neurol, VA Puget Sound Hlth Care Syst, Seattle, WA 98195 USA.
RP Lee, AT (reprint author), Univ Washington, Dept Anesthesiol & Pain Med, VA Puget Sound Hlth Care Syst, 1660 Columbian Way S-112-Anes, Seattle, WA 98108 USA.
EM alex.lee@va.gov
NR 9
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U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 2325-7237
J9 A A CASE REP
JI A A Case Rep.
PD MAR 1
PY 2017
VL 8
IS 5
BP 113
EP 115
DI 10.1213/XAA.0000000000000443
PG 3
WC Anesthesiology
SC Anesthesiology
GA EN3HQ
UT WOS:000395900000006
PM 28079666
ER
PT J
AU Katolik, A
Clark, NE
Tago, N
Montemayor, EJ
Hart, PJ
Damha, MJ
AF Katolik, Adam
Clark, Nathaniel E.
Tago, Nobuhiro
Montemayor, Eric J.
Hart, P. John
Damha, Masad J.
TI Fluorescent Branched RNAs for High-Throughput Analysis of Dbr1 Enzyme
Kinetics and Inhibition
SO ACS CHEMICAL BIOLOGY
LA English
DT Article
ID LARIAT-DEBRANCHING ENZYME; SOLID-PHASE SYNTHESIS; MANGANESE-DEPENDENT
PHOSPHODIESTERASE; TY1; OLIGORIBONUCLEOTIDES; RETROTRANSPOSITION;
MECHANISMS; LINKAGES; SEQUENCE; DESIGN
AB We have developed fluorescent 2',S' branched RNAs (bRNA) that permit real time monitoring of RNA lariat (intron) debranching enzyme (Dbrl) kinetics. These compounds contain fluorescein (FAM) on the 5' arm of the bRNA that is quenched by a dabcyl moiety on the 2 arm. Dbrl-mediated hydrolysis of the 2',S' linkage induces a large increase in fluorescence, providing a convenient assay for Dbrl hydrolysis. We show that unlabeled bRNAs with non-native 2',5'- phosphodiester linkages, such as phosphoramidate or phosphorothioate, can inhibit Dbrl-mediated debranching with IC50 values in the low nanomolar range. In addition to measuring kinetic parameters of the debranching enzyme, these probes can be used for high throughput screening (HTS) of chemical libraries with the aim of identifying Dbrl inhibitors, compounds that may be useful in treating neurodegenerative diseases and retroviral infections.
C1 [Katolik, Adam; Tago, Nobuhiro; Damha, Masad J.] McGill Univ, Dept Chem, 801 Sherbrooke St West, Montreal, PQ H3A 0B8, Canada.
[Clark, Nathaniel E.; Hart, P. John] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem & Struct Biol, 7703 Floyd Curl Dr, San Antonio, TX 78229 USA.
[Montemayor, Eric J.] Univ Wisconsin, Dept Biochem, 433 Babcock Dr, Madison, WI 53706 USA.
[Montemayor, Eric J.] Univ Wisconsin, Dept Biomol Chem, 433 Babcock Dr, Madison, WI 53706 USA.
[Hart, P. John] South Texas Vet Hlth Care Syst, Dept Vet Affairs, San Antonio, TX 78229 USA.
RP Damha, MJ (reprint author), McGill Univ, Dept Chem, 801 Sherbrooke St West, Montreal, PQ H3A 0B8, Canada.; Clark, NE; Hart, PJ (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem & Struct Biol, 7703 Floyd Curl Dr, San Antonio, TX 78229 USA.; Hart, PJ (reprint author), South Texas Vet Hlth Care Syst, Dept Vet Affairs, San Antonio, TX 78229 USA.
EM clarkn@uthscsa.edu; pjh@biochem.uthscsa.edu; masad.damha@mcgill.ca
FU National Sciences and Engineering Research Council of Canada; Department
of Veterans Affairs [1 I01 BX002580]; Robert A. Welch Foundation
[AQ-1399]; Judith and Jean Pape Adams Charitable Foundation; National
Science Foundation [DBI-0905865]; National Institutes of Health [T32
AG021890]; Strategic Young Researcher Overseas Visits Program for
Accelerating Brain Circulation from a Japan Society for the Promotion of
Science (JSPS)
FX This work was supported in part by grants from the National Sciences and
Engineering Research Council of Canada (to M.J.D.), Department of
Veterans Affairs (1 I01 BX002580, to PJ.H.), the Robert A. Welch
Foundation (AQ-1399, to PJ.H.), the Judith and Jean Pape Adams
Charitable Foundation (to PJ.H.), the National Science Foundation
(DBI-0905865, to E.J.M.), the National Institutes of Health (T32
AG021890, to N.E.C. and EJ.M.), and a Strategic Young Researcher
Overseas Visits Program for Accelerating Brain Circulation from a Japan
Society for the Promotion of Science (JSPS to N.T.).
NR 33
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U1 3
U2 3
PU AMER CHEMICAL SOC
PI WASHINGTON
PA 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1554-8929
EI 1554-8937
J9 ACS CHEM BIOL
JI ACS Chem. Biol.
PD MAR
PY 2017
VL 12
IS 3
BP 622
EP 627
DI 10.1021/acschembio.6b00971
PG 6
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA EP0LB
UT WOS:000397077700005
PM 28055181
ER
PT J
AU Lin, A
Brook, J
Grill, JD
Teng, E
AF Lin, Amy
Brook, Jenny
Grill, Joshua D.
Teng, Edmond
TI Participant-Informant Relationships Affect Quality of Life Ratings in
Incipient and Clinical Alzheimer Disease
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Article
DE Informant; study partner; quality of life; mild cognitive impairment;
Alzheimer disease
ID MILD COGNITIVE IMPAIRMENT; QOL-AD SCALE; CAREGIVER BURDEN; OLDER ADULTS;
DEMENTIA; PERSPECTIVES; PROGRESSION; DIAGNOSIS; VALIDITY; PEOPLE
AB Objective: Clinical trials in incipient and clinical Alzheimer disease (AD) often include informant-reported outcomes. Whereas informant reports in AD dementia may be modulated by the nature of participant-informant relationships, whether informant type affects reporting at earlier disease stages is less certain. We sought to determine the effects of participant-informant relationships on informant assessments of quality of life (QOL), functional abilities, and behavioral symptoms in individuals with normal cognition (NC), mild cognitive impairment (MCI), and mild-to-moderate AD dementia. Design: Cross-sectional. Setting: Easton Center for Alzheimer Disease Research at the University of California, Los Angeles. Participants: A total of 399 individuals who met criteria for NC (N = 100), MCI [amnestic (N = 125) and nonamnestic (N = 61)], and AD (N = 113). Participants were subdivided into groups based on informantparticipant relationships (spouse versus other). Measurements: We examined informant effects on the Quality of Life-Alzheimer's Disease (QOL-AD) scale, the Functional Activities Questionnaire (FAQ), and the Neuropsychiatric Inventory (NPI). Results: After adjustments for demographic and cognitive factors, spouse informants reported higher participant QOL in the amnestic MCI and AD groups than did other informants. No informant effects were seen on QOL-AD ratings in the nonamnestic MCI or NC groups or on the FAQ or NPI in the MCI andAD groups. Conclusions: Participant-informant relationships may modulate informant responses on subjective measures such as the QOL-AD in both incipient and clinical AD. Clinical trials that use informant measures may need to address these effects.
C1 [Lin, Amy] Univ Southern Calif, Keck Sch Med, Los Angeles, CA USA.
[Brook, Jenny] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
[Teng, Edmond] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA.
[Grill, Joshua D.] Univ Calif Irvine, Dept Psychiat & Human Behav, Inst Memory Impairments & Neurol Disorders, Irvine, CA 92717 USA.
[Teng, Edmond] Vet Affairs Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
RP Teng, E (reprint author), West Los Angeles VA Healthcare Ctr, Neurobehav Serv 116AF, 11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM eteng@mednet.ucla.edu
FU National Institute on Aging [T35 AG026736, P50 AG16570]; California
Alzheimer's Disease Centers; Sidell-Kagan Foundation
FX This research was supported by the National Institute on Aging (T35
AG026736 [UCLA Medical Student Training in Aging Research Program] and
P50 AG16570 [UCLA Alzheimer's Disease Research Center]), the California
Alzheimer's Disease Centers, and the Sidell-Kagan Foundation.
NR 39
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U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
BP 297
EP 307
DI 10.1016/j.jagp.2016.10.007
PG 11
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1FZ
UT WOS:000397132100015
PM 27818119
ER
PT J
AU Reese, PP
Bloom, RD
Trofe-Clark, J
Mussell, A
Leidy, D
Levsky, S
Zhu, JS
Yang, L
Wang, WL
Troxel, A
Feldman, HI
Volpp, K
AF Reese, Peter P.
Bloom, Roy D.
Trofe-Clark, Jennifer
Mussell, Adam
Leidy, Daniel
Levsky, Simona
Zhu, Jingsan
Yang, Lin
Wang, Wenli
Troxel, Andrea
Feldman, Harold I.
Volpp, Kevin
TI Automated Reminders and Physician Notification to Promote
Immunosuppression Adherence Among Kidney Transplant Recipients: A
Randomized Trial
SO AMERICAN JOURNAL OF KIDNEY DISEASES
LA English
DT Article
DE Kidney transplantation; kidney transplant recipient (KTR);
immunosuppression; tacrolimus; behavior change; adherence; compliance;
automated reminder; medication reminder; wireless pill bottle;
polypharmacy; end-stage renal disease (ESRD); tacrolimus trough level;
allograft loss; randomized controlled trial
ID PERCEIVED SOCIAL SUPPORT; MEDICATION ADHERENCE; ANTIRETROVIRAL THERAPY;
RENAL-TRANSPLANTATION; MULTIDIMENSIONAL SCALE; FINANCIAL INCENTIVES;
BLOOD-LEVELS; RISK-FACTOR; NONADHERENCE; REJECTION
AB Background: Immunosuppression nonadherence increases the risk for kidney transplant loss after transplantation. Wireless-enabled pill bottles have created the opportunity to monitor medication adherence in real time. Reminders may help patients with poor memory or organization. Provision of adherence data to providers may motivate patients to improve adherence and help providers identify adherence barriers.
Study Design: Randomized controlled trial.
Setting & Participants: Kidney transplant recipients (n = 120) at a single center.
Intervention: Participants were provided wireless pill bottles to store tacrolimus and record bottle openings. Participants were randomly assigned 1:1:1 to adherence monitoring with customized reminders (including alarms, texts, telephone calls, and/or e-mails), monitoring with customized reminders plus provider notification (every 2 weeks, providers received notification if adherence decreased to <90% during that period), or wireless pill bottle use alone (control).
Outcomes: The main outcome was bottle-measured tacrolimus adherence during the last 90 days of the 180-day trial. A secondary outcome was tacrolimus whole-blood concentrations at routine clinical visits.
Measurements: Adherence for the primary outcome was assessed via wireless pill bottle openings.
Results: Mean participant age was 50 years; 60% were men,. and 40% were black. Mean adherence was 78%, 88%, and 55% in the reminders, reminders-plus-notification, and control arms (P < 0.001 for comparison of each intervention to control). Mean tacrolimus levels were not significantly different between groups.
Limitations: The study did not assess clinical end points. Participants and study coordinators were not blinded to intervention arm.
Conclusions: Provider notification and customized reminders appear promising in helping patients achieve better medication adherence, but these strategies require evaluation in trials powered to detect differences in clinical outcomes. (C) 2016 by the National Kidney Foundation, Inc.
C1 [Reese, Peter P.; Bloom, Roy D.; Trofe-Clark, Jennifer; Feldman, Harold I.] Univ Penn, Renal Electrolyte & Hypertens Div, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Reese, Peter P.; Troxel, Andrea; Feldman, Harold I.] Univ Penn, Dept Biostat & Epidemiol, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Reese, Peter P.; Mussell, Adam; Leidy, Daniel; Troxel, Andrea; Feldman, Harold I.] Univ Penn, Perelman Sch Med, Ctr Clin Epidemiol & Biostat, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Reese, Peter P.; Zhu, Jingsan; Yang, Lin; Wang, Wenli; Troxel, Andrea; Volpp, Kevin] Univ Penn, Leonard Davis Inst Ctr Hlth Incent & Behav Econ, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Trofe-Clark, Jennifer] Hosp Univ Penn, Dept Pharm Serv, 3400 Spruce St, Philadelphia, PA 19104 USA.
[Levsky, Simona] Univ Penn, Sch Arts & Sci, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Volpp, Kevin] Perelman Sch Med, Dept Med, Philadelphia, PA USA.
[Volpp, Kevin] Perelman Sch Med, Med Eth & Hlth Policy, Philadelphia, PA USA.
[Volpp, Kevin] Univ Penn, Wharton Sch, Dept Hlth Care Management, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Volpp, Kevin] Cresencz Philadelphia Vet Affairs Med Ctr, Ctr Hlth Equ Res & Promot, Philadelphia, PA USA.
RP Reese, PP (reprint author), Univ Penn, Ctr Clin Epidemiol & Biostat, 917 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
EM peter.reese@uphs.upenn.edu
FU CVS Caremark; Merck, Sharpe, and Dohme; CVS Health; Humana; Weight
Watchers; Hawaii Medical Services Association; Vitality Institute;
Veloxis Pharma
FX The University of Pennsylvania has received research support from CVS
Caremark and Merck, Sharpe, and Dohme for other studies of medication
adherence, which provided salary support to Drs Reese and Volpp. Dr
Volpp is a principal at the behavioral economics consulting firm VAL
Health and has received consulting income and research support from CVS
Health and research support from Humana, Weight Watchers, the Hawaii
Medical Services Association, and the Vitality Institute (not related to
Vitality Inc, the manufacturer of the GlowCaps pill bottle). Dr Troxel
has received consulting income from VAL Health and research support from
the Vitality Institute, the Hawaii Medical Services Association, and
Weight Watchers. After the trial interventions were completed, the
University of Pennsylvania received research support from Veloxis
Pharma, which provided salary support for Dr Trofe-Clark; she also
received honorarium from Veloxis Pharma after this study was conducted.
The other authors declare that they have no other relevant financial
interests.
NR 58
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PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0272-6386
EI 1523-6838
J9 AM J KIDNEY DIS
JI Am. J. Kidney Dis.
PD MAR
PY 2017
VL 69
IS 3
BP 400
EP 409
DI 10.1053/j.ajkd.2016.10.017
PG 10
WC Urology & Nephrology
SC Urology & Nephrology
GA EM0ZV
UT WOS:000395047900013
PM 27940063
ER
PT J
AU Leung, LB
Escarce, JJ
AF Leung, Lucinda B.
Escarce, Jose J.
TI Consumer-Directed Health Plans: Do Doctors and Nurses Buy In?
SO AMERICAN JOURNAL OF MANAGED CARE
LA English
DT Article
ID CARE; SERVICES; COST
C1 [Leung, Lucinda B.] Vet Affairs Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Leung, Lucinda B.; Escarce, Jose J.] Univ Calif Los Angeles, Div Gen Internal Med & Hlth Serv Res, Los Angeles, CA USA.
RP Leung, LB (reprint author), UCLA Robert Wood Johnson Fdn, VA Clin Scholars Program, 10940 Wilshire Blvd,Ste 710, Los Angeles, CA 90024 USA.
EM lleung@mednet.ucla.edu
FU Robert Wood Johnson Foundation Clinical Scholars program; US Department
of Veterans Affairs
FX Support for this article was provided by the Robert Wood Johnson
Foundation Clinical Scholars program and the US Department of Veterans
Affairs. The views expressed in this article are those of the authors
and do not necessarily reflect the position or policy of the Department
of Veterans Affairs or the US government.
NR 16
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U1 0
U2 0
PU MANAGED CARE & HEALTHCARE COMMUNICATIONS LLC
PI PLAINSBORO
PA 666 PLAINSBORO RD, STE 300, PLAINSBORO, NJ 08536 USA
SN 1088-0224
J9 AM J MANAG CARE
JI Am. J. Manag. Care
PD MAR
PY 2017
VL 23
IS 3
PG 3
WC Health Care Sciences & Services; Health Policy & Services; Medicine,
General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EO0OP
UT WOS:000396398000004
ER
PT J
AU Govetto, A
Lalane, RA
Sarraf, D
Figueroa, MS
Hubschman, JP
AF Govetto, Andrea
Lalane, Robert A., III
Sarraf, David
Figueroa, Marta S.
Hubschman, Jean Pierre
TI Insights Into Epiretinal Membranes: Presence of Ectopic Inner Foveal
Layers and a New Optical Coherence Tomography. Staging Scheme
SO AMERICAN JOURNAL OF OPHTHALMOLOGY
LA English
DT Article
ID OUTER SEGMENT TIPS; PROGNOSTIC-FACTOR; VITREOMACULAR TRACTION; VISUAL
FUNCTION; SURGERY; METAMORPHOPSIA; ASSOCIATIONS; PREVALENCE; THICKNESS;
EYES
AB PURPOSE: To describe the presence of continuous ectopic inner foveal layers associated with epiretinal membranes (ERMs) and to present a new optical coherence tomography (OCT) staging system of ERMs.
DESIGN: Retrospective multicenter observational case series.
METHODS: Clinical charts and spectral-domain OCT images of 194 eyes of 172 consecutive patients diagnosed with ERMs were reviewed and analyzed.
RESULTS: The presence of continuous ectopic inner foveal layers was identified in 63 out of 194 eyes (32.5%) and this morphology was significantly associated with lower visual acuity. ERMs were divided into 4 stages. Stage 1 (43 out of 194 eyes, 22.1%) ERMs were mild and thin and a fovea! depression was present. Stage 2 (88 out of 194 eyes, 45.4%) ERMs were associated with widening of the outer nuclear layer and loss of the foveal depression. Stage 3 (51 out of 194 eyes, 26.3%) ERMs were associated with continuous ectopic inner foveal layers crossing the entire foveal area. In stages 1, 2, and 3 all retinal layers were clearly defined on OCT. Stage 4 ERMs (12 out of 194 eyes, 6.2%) were thick and associated with continuous ectopic inner foveal layers. In addition, retinal layers were disrupted. Visual acuity progressively declined from stage 1 through stage 4 (P < .001).
CONCLUSIONS: The presence of continuous ectopic inner foveal layers in ERMs is a newly described OCT finding associated with significant vision loss and is an essential element of a novel OCT-based grading scheme of ERMs that may influence visual prognosis. (C) 2016 Elsevier Inc. All rights reserved.
C1 [Govetto, Andrea; Lalane, Robert A., III; Hubschman, Jean Pierre] Univ Calif Los Angeles, Stein Eye Inst, Retina Div, 100 Stein Plaza, Los Angeles, CA 90095 USA.
[Sarraf, David] Univ Calif Los Angeles, Stein Eye Inst, Retinal Disorders & Ophthalm Genet Div, Los Angeles, CA USA.
[Sarraf, David] Greater Los Angeles VA Healthcare Ctr, Los Angeles, CA USA.
[Figueroa, Marta S.] Ramon y Cajal Univ Hosp, Dept Ophthalmol, Retina Div, Madrid, Spain.
RP Govetto, A (reprint author), Univ Calif Los Angeles, Stein Eye Inst, Retina Div, 100 Stein Plaza, Los Angeles, CA 90095 USA.
EM a.govetto@gmail.com
OI Govetto, Andrea/0000-0003-2192-810X
FU RESEARCH TO PRE vent Blindness (RPB), New York, New York, USA
FX THIS WORK WAS SUPPORTED BY AN UNRESTRICTED INSTITUTIONAL GRANT FROM
RESEARCH TO PRE vent Blindness (RPB), New York, New York, USA.
NR 39
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Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0002-9394
EI 1879-1891
J9 AM J OPHTHALMOL
JI Am. J. Ophthalmol.
PD MAR
PY 2017
VL 175
BP 99
EP 113
DI 10.1016/j.ajo.2016.12.006
PG 15
WC Ophthalmology
SC Ophthalmology
GA EN4IK
UT WOS:000395971000014
PM 27993592
ER
PT J
AU Feinstein, AJ
Shay, SG
Chang, E
Lewis, MS
Wang, MB
AF Feinstein, Aaron J.
Shay, Sophie G.
Chang, Elena
Lewis, Michael S.
Wang, Marilene B.
TI Treatment outcomes in veterans with HPV-positive head and neck cancer
SO AMERICAN JOURNAL OF OTOLARYNGOLOGY
LA English
DT Article
DE Squamous cell carcinoma; Human papilloma virus; Military veterans;
Surgery; Chemoradiation
ID SQUAMOUS-CELL CARCINOMAS; HUMAN-PAPILLOMAVIRUS INFECTION;
QUALITY-OF-LIFE; OROPHARYNGEAL CANCER; HEALTH-STATUS; SURVIVAL; TOBACCO;
POPULATION; ALCOHOL; SMOKING
AB Objectives: Head and neck squamous cell carcinoma (HNSCC) caused by the human papilloma virus (HPV) has an improved prognosis relative to HPV-negative tumors. Patients with HPV-positive disease may benefit from different treatment modalities in order to optimize survival and quality of life. We sought to investigate HPV-positive HNSCC within the military veteran population, and analyze the role of treatment modality in outcomes of patients with HPV-positive and HPV-negative tumors.
Methods: Patients diagnosed with HNSCC between January 1, 2010 and December 31, 2014 at one regional veterans health center were retrospectively examined. Pathologic specimens underwent testing for HPV subtype and p16 expression. Demographic and clinical factors, including treatment modality, were analyzed for their impact on the primary outcome of overall survival.
Results: There were 209 patients with primary tumor sites including larynx (25.4%), oral tongue (19.6%), oral cavity (13.4%), oropharynx (17.2%), tonsil (17.2%), unknown primary (2.9%), nasopharynx (1.9%), and multiple sites (2.4%). Patients had HPV-positive (n = 82, 392%), HPV-negative (ri = 89, 42.6%) or unknown HPV status (n = 38, 18.2%). Primary treatment modalities were chemoradiation (n = 124, 59.3%), surgery (n = 39, 18.7%), radiation therapy (n = 37, 17.7%), or no treatment (n = 9, 4.3%). Survival analysis with Cox proportional hazards model demonstrated significant associations with T classification (T4 3.61, P = 0.005), N classification (N3 3.52, P = 0.0159), M classification (Ml 2.8, P = 0.0209), and HPV status (HPV-positive 0.43, P = 0.0185), but no relation with primary treatment modality (primary surgery vs. primary chemoradiation 1.01, P = 0.9718).
Conclusion: HPV-positive HNSCC in the veteran population has a significantly improved prognosis relative to similarly staged patients with HPV-negative disease. This study demonstrates that the primary treatment modality- chemoradiation, radiation therapy, or surgery- does not impact overall survival among veterans with HPVpositive HNSCC.
C1 [Feinstein, Aaron J.; Shay, Sophie G.; Wang, Marilene B.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Head & Neck Surg, Los Angeles, CA 90095 USA.
[Feinstein, Aaron J.; Shay, Sophie G.; Wang, Marilene B.] Vet Affairs Greater Los Angeles Healthcare Syst, Dept Surg, Los Angeles, CA USA.
[Chang, Elena; Lewis, Michael S.] Vet Affairs Greater Los Angeles Healthcare Syst, Dept Pathol, Los Angeles, CA USA.
RP Wang, MB (reprint author), 200 UCLA Med Plaza Ste 550, Los Angeles, CA 90095 USA.
EM mbwang@ucla.edu
NR 27
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U1 0
U2 0
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0196-0709
EI 1532-818X
J9 AM J OTOLARYNG
JI Am. J. Otolaryngol.
PD MAR-APR
PY 2017
VL 38
IS 2
BP 188
EP 192
DI 10.1016/j.amjoto.2017.01.005
PG 5
WC Otorhinolaryngology
SC Otorhinolaryngology
GA EQ8KH
UT WOS:000398333800016
PM 28342482
ER
PT J
AU Matioc, AA
AF Matioc, Adrian A.
TI An Anesthesiologist's Perspective on the History of Basic Airway
Management The "Artisanal Anesthetic" Era: 1846 to 1904
SO ANESTHESIOLOGY
LA English
DT Article
ID INTUBATION; MEDICINE; SURGERY
AB This second installment of the history of basic airway management covers the early-artisanal-years of anesthesia from 1846 to 1904. Anesthesia was invented and practiced as a supporting specialty in the context of great surgical and medical advances. The current-day anesthesia provider tends to equate the history of airway management with the history of intubation, but for the first 58 yr after the introduction of ether anesthesia, airway management was provided by basic airway techniques with or without the use of a face mask. The jaw thrust and chin lift were described in the artisanal years and used primarily with inhalation anesthesia in the spontaneously breathing patient and less often with negative-pressure ventilation in the apneic victim. Positive-pressure ventilation and intubation stayed at the fringes of medical practice, and airway techniques and devices were developed by trial and error. At the beginning of the 20th century, airway management and anesthetic techniques lagged behind surgical requirements.
C1 [Matioc, Adrian A.] Univ Wisconsin Sch Med & Publ Hlth, Dept Anesthesiol, Madison, WI USA.
RP Matioc, AA (reprint author), William S Middleton Mem Vet Adm Med Ctr, 2500 Overlook Terrace,Room,A8030, Madison, WI 53705 USA.
EM aamatioc@wisc.edu
FU Paul M. Wood Fellowship at the Wood Library-Museum of Anesthesiology,
Schaumburg, Illinois
FX Support was provided by departmental sources and by a 2013 Paul M. Wood
Fellowship at the Wood Library-Museum of Anesthesiology, Schaumburg,
Illinois, awarded in my name for this topic.
NR 119
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U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0003-3022
EI 1528-1175
J9 ANESTHESIOLOGY
JI Anesthesiology
PD MAR
PY 2017
VL 126
IS 3
BP 394
EP 408
DI 10.1097/ALN.0000000000001508
PG 15
WC Anesthesiology
SC Anesthesiology
GA EO8DW
UT WOS:000396920200007
PM 28079564
ER
PT J
AU Myaskovsky, L
Gao, SS
Hausmann, LRM
Bornemann, KR
Burkitt, KH
Switzer, GE
Fine, MJ
Phillips, SL
Gater, D
Spungen, AM
Worobey, L
Boninger, ML
AF Myaskovsky, Larissa
Gao, Shasha
Hausmann, Leslie R. M.
Bornemann, Kellee R.
Burkitt, Kelly H.
Switzer, Galen E.
Fine, Michael J.
Phillips, Samuel. L.
Gater, David
Spungen, Ann M.
Worobey, Lynn
Boninger, Michael. L.
TI Quality and Equity in Wheelchairs Used by Veterans
SO ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
LA English
DT Article
DE Healthcare disparities; Rehabilitation; Spinal cord injuries;
Wheelchairs
ID SPINAL-CORD-INJURY; HEALTH-CARE; PERCEIVED DISCRIMINATION; OF-LIFE;
ASSISTIVE TECHNOLOGY; MANUAL WHEELCHAIRS; AFRICAN-AMERICAN;
PARTICIPATION; ASSOCIATION; DISPARITIES
AB Objectives: To assess in Veterans with spinal cord injury (SCI) or amputated limb (AL) the following: (1) patient demographics, medical factors, cultural and psychosocial characteristic by race; (2) wheelchair quality by race; and (3) the independent associations of patient race and the other factors with wheelchair quality.
Design: Cross-sectional cohort study.
Setting: Three Department of Veterans Affairs (VA) medical centers affiliated with academic medical centers.
Participants: Eligible participants were Veterans with SCI or ALs (N=516); 482 of them completed the interview. Analyses were restricted to white and African American participants. Because there was no variation in wheelchair quality among AL patients (n=42), they were excluded from all but descriptive analyses, leading to a final sample size of 421.
Interventions: Not applicable.
Main Outcome Measure: Wheelchair quality as defined by the Medicare Healthcare Common Procedure Coding System.
Results: We found race differences in many of our variables, but not in quality for manual (odds ratio [OR] = .67; 95% confidence interval [CI], .33-1.36) or power (OR=.82; 95% CI,.51-1.34) wheelchairs. Several factors including age (OR= .96; 95% CI, .93-.99) and income (OR=3.78; 95% CI, 1.43-9.97) were associated with wheelchair quality. There were no significant associations of cultural or psychosocial factors with wheelchair quality.
Conclusions: Although there were no racial differences in wheelchair quality, we found a significant association of older age and lower income with poorer wheelchair quality among Veterans. Efforts are needed to raise awareness of such disparities among VA wheelchair providers and to take steps to eliminate these disparities in prescription practice across VA sites. Published by Elsevier Inc. on behalf of the American Congress of Rehabilitation Medicine
C1 [Myaskovsky, Larissa; Gao, Shasha; Hausmann, Leslie R. M.; Bornemann, Kellee R.; Burkitt, Kelly H.; Switzer, Galen E.; Fine, Michael J.] Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Univ Dr 151C,Bldg 30, Pittsburgh, PA 15240 USA.
[Myaskovsky, Larissa; Hausmann, Leslie R. M.; Bornemann, Kellee R.; Switzer, Galen E.; Fine, Michael J.] Univ Pittsburgh, Sch Med, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15213 USA.
[Phillips, Samuel. L.] James A Haley Vet Hosp, Tampa, FL 33612 USA.
[Gater, David] Hunter Holmes McGuire Vet Affairs Med Ctr, Richmond, VA USA.
[Gater, David] Penn State Univ, Med Ctr, Hershey, PA USA.
[Spungen, Ann M.] James J Peters Vet Affairs Med Ctr, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY USA.
[Spungen, Ann M.] Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA.
[Spungen, Ann M.] Icahn Sch Med Mt Sinai, Dept Rehabil Med, New York, NY 10029 USA.
[Worobey, Lynn; Boninger, Michael. L.] Univ Pittsburgh, Sch Med, Dept Phys Med & Rehabil, Pittsburgh, PA USA.
[Worobey, Lynn; Boninger, Michael. L.] Vet Affairs Pittsburgh Healthcare Syst, Human Engn & Res Labs, Pittsburgh, PA USA.
RP Myaskovsky, L (reprint author), Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Univ Dr 151C,Bldg 30, Pittsburgh, PA 15240 USA.
EM larissa.myaskovsky@va.gov
FU Rehabilitation Research and Development Department of the Veterans
Affairs [871481]
FX Supported by the Rehabilitation Research and Development Department of
the Veterans Affairs (grant no. 871481).
NR 69
TC 0
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U1 1
U2 1
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0003-9993
EI 1532-821X
J9 ARCH PHYS MED REHAB
JI Arch. Phys. Med. Rehabil.
PD MAR
PY 2017
VL 98
IS 3
BP 442
EP 449
DI 10.1016/j.apmr.2016.09.116
PG 8
WC Rehabilitation; Sport Sciences
SC Rehabilitation; Sport Sciences
GA EN9CD
UT WOS:000396297400004
PM 27713075
ER
PT J
AU Vogelmeier, CF
Criner, GJ
Martinez, FJ
Anzueto, A
Barnes, PJ
Bourbeau, J
Celli, BR
Chen, RC
Decramer, M
Fabbri, LM
Frith, P
Halpin, DMG
Varela, MVL
Nishimura, M
Roche, N
Rodriuez-Roisin, R
Sin, DD
Singh, D
Stockley, R
Vestbo, J
Wedzicha, JA
Agusti, YA
AF Vogelmeier, Claus F.
Criner, Gerard J.
Martinez, Fernando J.
Anzueto, Antonio
Barnes, Peter J.
Bourbeau, Jean
Celli, Bartotome R.
Chen, Rongchang
Decramer, Marc
Fabbri, Leonardo M.
Frith, Peter
Halpin, David M. G.
Varela, M. Victorina Lopez
Nishimura, Masaharu
Roche, Nicolas
Rodriguez-Roisin, Roberto
Sin, Don D.
Singh, Dave
Stockley, Robert
Vestbo, Jorgen
Wedzicha, Jadwiga A.
Agusti, Y. Alvar
TI Global Strategy for the Diagnosis, Management, and Prevention of Chronic
Obstructive Lung Disease 2017 Report: GOLD Executive Summary
SO ARCHIVOS DE BRONCONEUMOLOGIA
LA Spanish
DT Article
DE Chronic obstructive pulmonary disease; COPD; diagnosis; COPD management;
COPD prevention
ID RANDOMIZED CONTROLLED-TRIAL; AIR-FLOW OBSTRUCTION; POSITIVE-PRESSURE
VENTILATION; PLACEBO-CONTROLLED TRIAL; QUALITY-OF-LIFE; INHALED
FLUTICASONE FUROATE; CHRONIC RESPIRATORY-DISEASE; VOLUME-REDUCTION
SURGERY; BONE-MINERAL DENSITY; REQUIRING MECHANICAL VENTILATION
AB This Executive Summary of the Global Strategy for the Diagnosis, Management, and Prevention of COPD (GOLD) 2017 Report focuses primarily on the revised and novel parts of the document. The most significant changes include; I) the assessment of COPD has been refined to separate the spirometric assessment from symptom evaluation. ABCD groups are now proposed to be derived exclusively from patient symptoms and their history of exacerbations; 2) for each of the groups A to D, escalation strategies for pharmacological treatments are proposed; 3) the concept of de-escalation of therapy is introduced in the treatment assessment scheme; 4) nonpharmacologic therapies are comprehensively presented and; 5) the importance of comorbid conditions in managing COPD is reviewed. (C) 2017 SEPAR. Published by Elsevier Espana, S.L.U. All rights reserved.
C1 [Vogelmeier, Claus F.] Univ Marburg, Miembro Ctr Aleman Invest Pulmonar DZL, Marburg, Germany.
[Agusti, Y. Alvar] Univ Barcelona, Hosp Clin, Ciberes, Barcelona, Spain.
[Anzueto, Antonio] Univ Texas Hlth Sci Ctr, South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Barnes, Peter J.] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, London, England.
[Bourbeau, Jean] McGill Univ, McGill Univ Hlth Ctr, Montreal, PQ, Canada.
[Celli, Bartotome R.] Brigham & Womens Hosp, Boston, MA USA.
[Chen, Rongchang] Primer Hosp Afiliado Univ Med Guangzhou, Inst Enfermedades Respiratorias Guangzhou, Lab Cent Estatal Enfermedades Respiratorias, Guangzhou, Peoples R China.
[Criner, Gerard J.] Temple Univ, Lewis Katz Sch Med, Philadelphia, PA USA.
[Decramer, Marc] Univ Louvain, Louvain, Belgium.
[Fabbri, Leonardo M.] Univ Modena & Reggio Emilia, Modena, Italy.
[Frith, Peter] Flinders Univ Fac Med, Bedford Pk, SA, Australia.
[Halpin, David M. G.] Royal Devon & Exeter Hosp, Exeter, Devon, England.
[Varela, M. Victorina Lopez] Univ Republ Montevideo, Montevideo, Uruguay.
[Martinez, Fernando J.] New York Presbyterian Hosp, Weil Cornell Med Ctr, New York, NY USA.
[Nishimura, Masaharu] Hokkaido Univ, Fac Med, Sapporo, Hokkaido, Japan.
[Roche, Nicolas] Univ Paris 05, Hop Cochin APHP, Paris, France.
[Rodriguez-Roisin, Roberto] Univ Barcelona, Hosp Clin, Inst Torax, Barcelona, Spain.
[Sin, Don D.] Univ British Columbia, St Pauls Hosp, Vancouver, BC, Canada.
[Singh, Dave; Vestbo, Jorgen] Univ Manchester, Manchester, Lancs, England.
[Stockley, Robert] Univ Hosp, Birmingham, W Midlands, England.
[Wedzicha, Jadwiga A.] Univ London Imperial Coll Sci Technol & Med, London, England.
RP Vogelmeier, CF (reprint author), Univ Marburg, Miembro Ctr Aleman Invest Pulmonar DZL, Marburg, Germany.
EM claus.vogelmeier@med.uni-marburg.de
FU Medical Research Council [G0800570, G1001365, G1001372]
NR 339
TC 0
Z9 0
U1 2
U2 2
PU ELSEVIER DOYMA SL
PI BARCELONA
PA TRAVESERA DE GARCIA, 17-21, BARCELONA, 08021, SPAIN
SN 0300-2896
EI 1579-2129
J9 ARCH BRONCONEUMOL
JI Arch. Bronconeumol.
PD MAR
PY 2017
VL 53
IS 3
BP 128
EP 149
DI 10.1016/j.arbres.2017.02.001
PG 22
WC Respiratory System
SC Respiratory System
GA EQ8KT
UT WOS:000398335000011
PM 28274597
ER
PT J
AU Wahl, E
Gross, A
Chernitskiy, V
Trupin, L
Gensler, L
Chaganti, K
Michaud, K
Katz, P
Yazdany, J
AF Wahl, Elizabeth
Gross, Andrew
Chernitskiy, Vladimir
Trupin, Laura
Gensler, Lianne
Chaganti, Krishna
Michaud, Kaleb
Katz, Patricia
Yazdany, Jinoos
TI Validity and Responsiveness of a 10-Item Patient-Reported Measure of
Physical Function in a Rheumatoid Arthritis Clinic Population
SO ARTHRITIS CARE & RESEARCH
LA English
DT Article
ID QUALITY-OF-LIFE; MINIMALLY IMPORTANT DIFFERENCE; ITEM RESPONSE THEORY;
DISEASE-ACTIVITY; SHORT-FORM; FUNCTION SCALES; HEALTH-STATUS;
RELIABILITY; OUTCOMES; VALIDATION
AB Objective: We assessed implementation of the 10-item Patient-Reported Outcomes Measurement Information System (PROMIS) physical function form (PF-10a) in routine practice in a racially and ethnically diverse population with rheumatoid arthritis (RA). Objectives were to determine feasibility of implementing PF-10a in the electronic health record (EHR) and PF-10a validity and longitudinal responsiveness.
Methods: Clinical and demographic data were abstracted from EHRs for all RA patients seen at a university-based rheumatology clinic between February 2013 and February 2015. We evaluated floor and ceiling (edge) effects and construct validity of PF-10a in a subgroup of patients with Health Assessment Questionnaire (HAQ) scores (n=189). We used linear mixed-effects models to assess responsiveness of PF-10a to longitudinal changes in the Clinical Disease Activity Index (CDAI) for patients in the entire clinical cohort, with both scores recorded on at least 2 encounters (n=326).
Results: Half of the patients were nonwhite, and 15% were non-English speakers. Over a 2-year period, PF10a was successfully implemented; 97% of patients and 89% of encounters had at least 1 measurement performed. PF-10a had fewer ceiling (defined as best) effects than the HAQ (8% versus 22%), and convergent validity was high (r=-0.85). PF-10a was sensitive to expected differences (older versus younger patients, more versus less active disease). Longitudinal changes in PF-10a were highly associated with changes in the CDAI score (P<0.0001).
Conclusion: PF-10a was feasible to implement in a diverse RA population. It strongly correlates with the HAQ but has fewer ceiling effects and is responsive to changes in RA disease activity, suggesting its validity for use in routine clinical practice.
C1 [Wahl, Elizabeth] Div Rheumatol, Dept Inter nal Med, VA Puget Sound Hlth Care Syst, 1660 S Columbian Way,Bldg 1,Room 219-D, Seattle, WA 98108 USA.
RP Wahl, E (reprint author), Div Rheumatol, Dept Inter nal Med, VA Puget Sound Hlth Care Syst, 1660 S Columbian Way,Bldg 1,Room 219-D, Seattle, WA 98108 USA.
EM elizabeth.wahl@va.gov
FU Veterans Affairs Quality Scholars Fellowship through the Veterans
Affairs Office of Academic Affiliations; NIH/National Institute of
Arthritis and Musculoskeletal and Skin Diseases [P60-AR-053308-01,
K23-AR-060259]; Rheumatology Research Foundation Investigator Award;
Innovative Research Grant; Russell/Engleman Rheumatology Research
Center; Robert L. Kroc Endowed Chair in Rheumatic and Connective Tissue
Diseases at the University of California, San Francisco
FX Dr. Wahl's work was supported by a Veterans Affairs Quality Scholars
Fellowship through the Veterans Affairs Office of Academic Affiliations.
Ms Trupin's and Dr. Katz's work was supported by the NIH/National
Institute of Arthritis and Musculoskeletal and Skin Diseases (grant
P60-AR-053308-01). Dr. Michaud's work was supported by a Rheumatology
Research Foundation Investigator Award and Innovative Research Grant.
Dr. Yazdany's work was supported by NIH/National Institute of Arthritis
and Musculoskeletal and Skin Diseases (grant K23-AR-060259), the
Russell/Engleman Rheumatology Research Center, and the Robert L. Kroc
Endowed Chair in Rheumatic and Connective Tissue Diseases at the
University of California, San Francisco.
NR 34
TC 0
Z9 0
U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2151-464X
EI 2151-4658
J9 ARTHRIT CARE RES
JI Arthritis Care Res.
PD MAR
PY 2017
VL 69
IS 3
BP 338
EP 346
DI 10.1002/acr.22956
PG 9
WC Rheumatology
SC Rheumatology
GA EM0DK
UT WOS:000394988800004
PM 27332620
ER
PT J
AU Ravenel, JG
Tanner, NT
Silvestri, GA
AF Ravenel, James G.
Tanner, Nichole T.
Silvestri, Gerard A.
TI Viewing All the Trees in the Forest The Importance of Reporting Abnormal
Findings on CT Scan When Screening for Lung Cancer
SO CHEST
LA English
DT Editorial Material
ID PULMONARY NODULES; CHEST PHYSICIANS; POLICY STATEMENT; PERFORMANCE;
COLLEGE; TRIAL
C1 [Ravenel, James G.] Ralph H Johnson Vet Affairs Hosp, Dept Radiol & Radiol Sci, Charleston, SC USA.
[Tanner, Nichole T.; Silvestri, Gerard A.] Ralph H Johnson Vet Affairs Hosp, Thorac Oncol Res Grp, Charleston, SC USA.
[Tanner, Nichole T.] Ralph H Johnson Vet Affairs Hosp, Hlth Equ & Rural Outreach Innovat Ctr, Charleston, SC USA.
RP Ravenel, JG (reprint author), Med Univ South Carolina, Dept Radiol & Radiol Sci, 96 Jonathan Lucas St,MSC 323, Charleston, SC 29425 USA.
EM ravenejg@musc.edu
NR 14
TC 0
Z9 0
U1 0
U2 0
PU AMER COLL CHEST PHYSICIANS
PI GLENVIEW
PA 2595 PATRIOT BLVD, GLENVIEW, IL 60026 USA
SN 0012-3692
J9 CHEST
JI Chest
PD MAR
PY 2017
VL 151
IS 3
BP 525
EP 526
DI 10.1016/j.chest.2016.10.053
PG 2
WC Critical Care Medicine; Respiratory System
SC General & Internal Medicine; Respiratory System
GA EP1TE
UT WOS:000397166400006
PM 28279269
ER
PT J
AU Jimenez-Torres, GJ
Weinstein, BL
Walker, CR
Fowler, JC
Ashford, P
Borckardt, JJ
Madan, A
AF Jimenez-Torres, G. Janice
Weinstein, Benjamin L.
Walker, Cory R.
Fowler, J. Christopher
Ashford, Philippa
Borckardt, Jeffrey J.
Madan, Alok
TI A study protocol for a single-blind, randomized controlled trial of
adjunctive transcranial direct current stimulation (tDCS) for chronic
pain among patients receiving specialized, inpatient multimodal pain
management
SO CONTEMPORARY CLINICAL TRIALS
LA English
DT Article
DE Chronic pain; Pain management; Transcranial direct current stimulation;
Somatic symptoms; Serious mental illness
ID DORSOLATERAL PREFRONTAL CORTEX; COGNITIVE-BEHAVIORAL THERAPY; COLD
PRESSOR TASK; COMMITMENT THERAPY; CLINICAL-TRIAL; PRIMARY-CARE;
EFFICACY; PERCEPTION; MINDFULNESS; ACCEPTANCE
AB Background: Available treatments for chronic pain (CP) are modestly effective or associated with iatrogenic harm. Transcranial direct current stimulation (tDCS) is a non-invasive brain stimulation technique that may be an effective, adjunctive treatment to non-opioid therapies. In this randomized contrortrial (RCI), we compare adjunctive active versus sham tDCS among patients in a multimodal inpatient pain management program. The primary objectives of the RCT are to improve pain tolerance and subjective pain experience.
Methods and design: Patients admitted to the Pain Management Program at The Menninger Clinic in Houston, Texas are eligible for this trial. Eighty-four participants will be randomized (1:1) into a single-blind, 2 x 12 (group x time) controlled trial. A battery-powered direct and constant current stimulator (Soterix Medical Inc. 2014) delivers anodal stimulation over the left dorsolateral prefrontal cortex (DLPFC) and cathodal stimulation over the right DLPFC. Active tDCS is applied by supplying a 2 mA current for 20 min/session over 10 sessions. Participants complete self-report and performance-based assessments on a weekly basis just prior to brain stimulation. Self-report assessMents are collected via Chronic Pain Tracker version 3.6, an iPad interfaced application. The performance-based pain tolerance task is completed through the cold presser task.
Discussion: Interventions with cross-symptomatic therapeutic potential are absolutely essential in the context of CP, in which psychiatric comorbidity is the norm. Modalities that can be used in tandem with evidence-based, non-opioid therapies have the potential to have a synergistic effect, resulting in increased effectiveness of what have been modestly effective treatments to date. (C) 2017 Elsevier Inc All rights reserved.
C1 [Jimenez-Torres, G. Janice; Weinstein, Benjamin L.; Walker, Cory R.; Fowler, J. Christopher; Ashford, Philippa; Madan, Alok] Menninger Clin, Houston, TX USA.
[Jimenez-Torres, G. Janice; Weinstein, Benjamin L.; Walker, Cory R.; Fowler, J. Christopher; Madan, Alok] Baylor Coll Med, Psychiat & Behav Sci, Houston, TX 77030 USA.
[Borckardt, Jeffrey J.] Med Univ South Carolina, Anesthesia & Perioperat Med, Charleston, SC USA.
[Borckardt, Jeffrey J.] Med Univ South Carolina, Psychiat & Behav Sci, Charleston, SC USA.
[Borckardt, Jeffrey J.] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA.
RP Madan, A (reprint author), 12301 South Main St, Houston, TX 77035 USA.
EM amadan@menninger.edu
FU Menninger Clinic Foundation, McNair Medical Institute; William and Ella
Owens Medical Research Foundation
FX This research was partially supported by the Menninger Clinic
Foundation, McNair Medical Institute, and the William and Ella Owens
Medical Research Foundation. Dr. Madan is a McNair Scholar. The study
follows the guidelines on good publication practices. The study sponsors
were not involved in any aspect of the research activities. Thus, the
authors were independent from study sponsors in the context of the
research. The authors have no other potential conflicts of interest to
disclose.
NR 82
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1551-7144
EI 1559-2030
J9 CONTEMP CLIN TRIALS
JI Contemp. Clin. Trials
PD MAR
PY 2017
VL 54
BP 36
EP 47
DI 10.1016/j.cct.2016.12.024
PG 12
WC Medicine, Research & Experimental; Pharmacology & Pharmacy
SC Research & Experimental Medicine; Pharmacology & Pharmacy
GA EL3YV
UT WOS:000394557500005
ER
PT J
AU Fan, Y
Lee, K
Wang, NS
He, JC
AF Fan, Ying
Lee, Kyung
Wang, Niansong
He, John Cijiang
TI The Role of Endoplasmic Reticulum Stress in Diabetic Nephropathy
SO CURRENT DIABETES REPORTS
LA English
DT Review
DE Diabetic nephropathy; Endoplasmic reticulum stress; Unfolded protein
response. Apoptosis; Reticulon-1 (RTN-1)
ID UNFOLDED PROTEIN RESPONSE; GLOMERULAR ENDOTHELIAL-CELLS; INDUCED
PODOCYTE APOPTOSIS; TUBULAR EPITHELIAL-CELLS; ACID-BINDING PROTEIN;
ER-STRESS; KIDNEY-DISEASE; MESENCHYMAL TRANSITION; PREMATURE SENESCENCE;
ASTRAGALOSIDE IV
AB Purpose of Review Diabetic nephropathy (DN) has become the leading cause of end-stage renal disease (ESRD) worldwide. Accumulating evidence suggests that endoplasmic reticulum (ER) stress plays a major role in the development and progression of DN. Recent findings suggested that many attributes of DN, such as hyperglycemia, proteinuria, and increased advanced glycation end products and free fatty acids, can all trigger unfolded protein response (UPR) in kidney cells. Herein, we review the current knowledge on the role of ER stress in the setting of kidney injury with a specific emphasis on DN.
Recent Findings As maladaptive ER stress response caused by excessively prolonged UPR will eventually cause cell death and increase kidney injury, several ER stress inhibitors have been shown to improve DN in animal models, albeit blocking both adaptive and maladaptive UPR. More recently, reticulon-1A (RTN1A), an ER-associated protein, was shown to be increased in both human and mouse diabetic kidneys. Its expression correlates with the progression of DN, and its polymorphisms are associated with kidney disease in people with diabetes. Increased RTN1A expression heightened the ER stress response and renal cell apoptosis, and conversely reduced RTN1A in renal cells decreased apoptosis and ameliorated kidney injury and DN progression, suggesting that RTN1A may be a novel target to specifically restrain the maladaptive UPR.
Summary These findings suggest that ER stress response in renal cells is a key driver of progression of DN and that the inhibition of the unchecked ER stress response in DN, such as by inhibition of RTN1A function, may be a promising therapeutic approach against DN.
C1 [Fan, Ying; Wang, Niansong] Shanghai Jiao Tong Univ, Affiliated Peoples Hosp 6, Shanghai, Peoples R China.
[Lee, Kyung; He, John Cijiang] Icahn Sch Med Mt Sinai, Div Nephrol, Dept Med, 1 Gustave L Levy Pl,Box 1243, New York, NY 10029 USA.
[He, John Cijiang] James J Peters VAMC, Renal Sect, Bronx, NY USA.
RP He, JC (reprint author), Icahn Sch Med Mt Sinai, Div Nephrol, Dept Med, 1 Gustave L Levy Pl,Box 1243, New York, NY 10029 USA.; He, JC (reprint author), James J Peters VAMC, Renal Sect, Bronx, NY USA.
EM cijiang.he@mssm.edu
FU National Natural Science Foundation of China [81400735, 81270824,
81670657]; Chinese Medical Association Funding [15020140602]; NIH [P30
DK079307, 1R01DK098126, 1R01DK109683, 1R01DK078897, 1R01DK088541,
P01-DK-56492]
FX Y.F. is supported by National Natural Science Foundation of China
(81400735) and Chinese Medical Association Funding (15020140602). K.L.
is supported by NIH P30 DK079307 and 1R01DK098126. N.W. is supported by
National Natural Science Foundation of China (81270824, 81670657).
J.C.H. is supported by NIH 1R01DK109683, 1R01DK078897, 1R01DK088541, and
P01-DK-56492.
NR 69
TC 0
Z9 0
U1 3
U2 3
PU CURRENT MEDICINE GROUP
PI PHILADELPHIA
PA 400 MARKET STREET, STE 700, PHILADELPHIA, PA 19106 USA
SN 1534-4827
EI 1539-0829
J9 CURR DIABETES REP
JI Curr. Diabetes Rep.
PD MAR
PY 2017
VL 17
IS 3
AR 17
DI 10.1007/s11892-017-0842-y
PG 7
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EO7KU
UT WOS:000396870400004
PM 28271468
ER
PT J
AU Correa, M
Fathi, R
Benoit, A
Dellavalle, R
AF Correa, Mark
Fathi, Ramin
Benoit, Anastasia
Dellavalle, Robert
TI Scalp Cyst Excision in an Unknown Previous Site of Neurosurgery: Issues
in Patient Safety in Dermatologic Surgery
SO DERMATOLOGIC SURGERY
LA English
DT Letter
C1 [Correa, Mark] Univ Florida, Coll Med, Gainesville, FL 32611 USA.
[Fathi, Ramin; Benoit, Anastasia] Univ Colorado, Sch Med, Dept Dermatol, Denver, CO 80202 USA.
[Dellavalle, Robert] Univ Colorado, Sch Med, Dept Dermatol, Denver VA Med Ctr, Denver, CO 80202 USA.
RP Correa, M (reprint author), Univ Florida, Coll Med, Gainesville, FL 32611 USA.
NR 5
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1076-0512
EI 1524-4725
J9 DERMATOL SURG
JI Dermatol. Surg.
PD MAR
PY 2017
VL 43
IS 3
BP 452
EP 454
PG 4
WC Dermatology; Surgery
SC Dermatology; Surgery
GA EQ4KZ
UT WOS:000398047200021
PM 27673489
ER
PT J
AU Sosenko, JM
Yu, L
Skyler, JS
Krischer, JP
Gottlieb, PA
Boulware, D
Miao, D
Palmer, JP
Steck, AK
AF Sosenko, Jay M.
Yu, Liping
Skyler, Jay S.
Krischer, Jeffrey P.
Gottlieb, Peter A.
Boulware, David
Miao, Dongmei
Palmer, Jerry P.
Steck, Andrea K.
TI The Use of Electrochemiluminescence Assays to Predict Autoantibody and
Glycemic Progression Toward Type 1 Diabetes in Individuals with Single
Autoantibodies
SO DIABETES TECHNOLOGY & THERAPEUTICS
LA English
DT Article
DE Type 1 diabetes; Autoantibodies; Hyperglycemia; Pediatrics
ID GLUTAMIC-ACID DECARBOXYLASE; IDENTIFY HIGH-RISK; RELATIVES; INSULIN;
CHILDREN
AB Background: Electrochemiluminescence (ECL) assays have shown promise for enhancing the prediction of type 1 diabetes (T1D) with autoantibodies. We thus studied relatives of T1D patients to determine whether ECL assays can be used to refine risk assessments for T1D among individuals either positive for single GADA or single mIAA autoantibodies.
Subjects and Methods: TrialNet Pathway to Prevention (PTP) study participants with either GADA or mIAA single autoantibodies were tested for ECL positivity during their participation in the TrialNet PTP study. Those ECL positive (ECL+) were compared with those ECL negative (ECL-) for conversion to multiple autoantibodies, 6-month glycemic progression (PS6M), and the progression to T1D.
Results: The progression to multiple autoantibodies was significantly higher for those GADA/ECL+ (n = 107) than those GADA/ECL-(n = 78) (P = 0.001) and for those mIAA/ECL+ (n = 24) than those mIAA/ECL-(n = 63) (P < 0.001). The hazard ratios with 95% confidence intervals were 3.42 (1.58-7.39; P < 0.01) for GADA and 8.15 (3.02-22.00; P < 0.001) for mIAA. GADA/ECL+ and mIAA/ECL+ participants had significantly higher PS6M values than their ECL-counterparts (P = 0.001 for GADA and P = 0.009 for mIAA). Of those GADA/ECL+, 14% progressed to T1D; of those mIAA/ECL+, 17% progressed to T1D. Only 1 individual (positive for GADA) of the 141 who was ECL-progressed to T1D (median follow-up: 5 years).
Conclusion: ECL measurements appear to have utility for natural history studies and prevention trials of individuals with single autoantibodies. Those ECL+ are at appreciable risk for developing multiple autoantibodies and for glycemic progression toward T1D, whereas those ECL-are at very low risk.
C1 [Sosenko, Jay M.; Skyler, Jay S.] Univ Miami, Miller Sch Med, Div Endocrinol, POB 016960 D1110, Miami, FL 33101 USA.
[Yu, Liping; Gottlieb, Peter A.; Miao, Dongmei; Steck, Andrea K.] Univ Colorado, Barbara Davis Ctr Childhood Diabet, Sch Med, Aurora, CO USA.
[Krischer, Jeffrey P.; Boulware, David] Univ S Florida, Div Informat & Biostat, Tampa, FL USA.
Univ Washington, VA Puget Sound Hlth Care Syst, Div Endocrinol Metab & Nutr, Seattle, WA USA.
RP Sosenko, JM (reprint author), Univ Miami, Miller Sch Med, Div Endocrinol, POB 016960 D1110, Miami, FL 33101 USA.
EM jsosenko@med.miami.edu
FU Type 1 Diabetes TrialNet Pathway to Prevention Study Group; National
Institutes of Health (NIH) through the National Institute of Diabetes
and Digestive and Kidney Diseases; National Institute of Allergy and
Infectious Diseases; Eunice Kennedy Shriver National Institute of Child
Health and Human Development; NIH [U01 DK061010, U01 DK061034, U01
DK061042, U01 DK061058, U01 DK085465, U01DK085453, U01DK085461,
U01DK085463, U01 DK085466, U01 DK085499, U01 DK085504, U01 DK085505,
U01DK085509, U01 DK103180, U01-DK103153, U01-DK085476, U01-DK103266];
Juvenile Diabetes Research Foundation International (JDRF)
FX The sponsor of the study was the Type 1 Diabetes TrialNet Pathway to
Prevention Study Group. Type 1 Diabetes TrialNet Pathway to Prevention
Study Group is a clinical trials network funded by the National
Institutes of Health (NIH) through the National Institute of Diabetes
and Digestive and Kidney Diseases, the National Institute of Allergy and
Infectious Diseases, and The Eunice Kennedy Shriver National Institute
of Child Health and Human Development through the cooperative
agreements. TrialNet is funded by NIH grants U01 DK061010, U01 DK061034,
U01 DK061042, U01 DK061058, U01 DK085465, U01DK085453, U01DK085461,
U01DK085463, U01 DK085466, U01 DK085499, U01 DK085504, U01 DK085505,
U01DK085509, U01 DK103180, U01-DK103153, U01-DK085476, U01-DK103266, and
the Juvenile Diabetes Research Foundation International (JDRF).
NR 14
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U2 1
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1520-9156
EI 1557-8593
J9 DIABETES TECHNOL THE
JI Diabetes Technol. Ther.
PD MAR
PY 2017
VL 19
IS 3
BP 183
EP 187
DI 10.1089/dia.2016.0243
PG 5
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EN8AP
UT WOS:000396223600008
PM 28177779
ER
PT J
AU Moyers, TB
Houck, J
Glynn, LH
Hallgren, KA
Manuel, JK
AF Moyers, Theresa B.
Houck, Jon
Glynn, Lisa H.
Hallgren, Kevin A.
Manuel, Jennifer K.
TI A randomized controlled trial to influence client language in substance
use disorder treatment
SO DRUG AND ALCOHOL DEPENDENCE
LA English
DT Article
DE Motivational interviewing; Counselor training; Client language;
Randomized controlled trial; Active mechanism; Technical component
ID BRIEF MOTIVATIONAL INTERVENTION; COMMITMENT LANGUAGE; DRINKING OUTCOMES;
SELF-PERSUASION; CHANGE TALK; METAANALYSIS; DISSONANCE; STRENGTH;
ALCOHOL; MATTERS
AB Background: Client language is hypothesized to be a mechanism of action in motivational interviewing (MI). Despite the association of change and sustain talk with substance treatment outcomes, it not known whether providers can intentionally influence this language as hypothesized.
Objective: This is a randomized controlled trial to investigate whether substance use providers can be trained to influence client language.
Methods: Treatment providers specializing in substance use disorders (n = 190) were randomly assigned to standard training in MI (MI-AU) or training emphasizing an influence of client language (MI-LEAF). Treatment sessions with actual clients were evaluated 3, 6 and 12 months after training by masked raters. Frequencies of client change and sustain talk were the outcome variables.
Results: Sustain talk, but not change talk, was significantly lower in clients whose providers had received the specialized training (b = -0.175, SE = 0.087, p=0.046, CI[-0.348 to 0.0021, d = -0.325). Mediation analyses supported a causal chain between a) training, b) providers' attempts to minimize sustain talk in treatment sessions via directive reflective listening and c) client sustain talk in the treatment session (kappa(2) = 0.0833, bootstrap SE = 0.0394, 95% CI [0.0148, 0.1691]).
Conclusions: With specialized training, providers can reduce the amount of opposition language their clients offer when considering a change in their substance use. Demonstrating that client language is under partial control of the provider supports the feasibility of clinical trials to investigate the impact of shaping client language on treatment outcomes. (C) 2017 Elsevier B.V. All rights reserved.
C1 [Moyers, Theresa B.; Houck, Jon] Univ New Mexico, Ctr Alcoholism Subst Abuse & Addict, MSC11 6280 1, Albuquerque, NM 87131 USA.
[Glynn, Lisa H.] VA Puget Sound Hlth Care Syst, Dept Anesthesiol, 1660 S Columbian Way, Seattle, WA 98108 USA.
[Hallgren, Kevin A.] Univ Washington, Dept Psychiat & Behav Sci, 1959 NE Pacific St, Seattle, WA 98195 USA.
[Manuel, Jennifer K.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Manuel, Jennifer K.] Univ Calif San Francisco, San Francisco, CA USA.
RP Moyers, TB (reprint author), Univ New Mexico, Ctr Alcoholism Subst Abuse & Addict, Dept Psychol, Albuquerque, NM 87106 USA.
EM tmoyers@unm.edu; jhouck@unm.edu; Lisa.glynn2@va.gov; khallgre@uw.edu;
jennifer.manuel@va.gov
FU National Institute on Drug Abuse [R01 DA 021227-01]
FX This research was funded by grant R01 DA 021227-01 from the National
Institute on Drug Abuse. No other contributions were made to this
project.
NR 34
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0376-8716
EI 1879-0046
J9 DRUG ALCOHOL DEPEN
JI Drug Alcohol Depend.
PD MAR 1
PY 2017
VL 172
BP 43
EP 50
DI 10.1016/j.drugalcdep.2016.11.036
PG 8
WC Substance Abuse; Psychiatry
SC Substance Abuse; Psychiatry
GA EM3LV
UT WOS:000395217500006
PM 28122270
ER
PT J
AU Riley, ED
Hsue, PY
Vittinghoff, E
Wu, AHB
Coffin, PO
Moore, PK
Lynch, KL
AF Riley, Elise D.
Hsue, Priscilla Y.
Vittinghoff, Eric
Wu, Alan H. B.
Coffin, Phillip O.
Moore, Peter K.
Lynch, Kara L.
TI Higher prevalence of detectable troponin I among cocaine-users without
known cardiovascular disease
SO DRUG AND ALCOHOL DEPENDENCE
LA English
DT Article
DE Cocaine; Benzoylecgonine; Cardiac injury; Troponin; cTnI
ID ACUTE MYOCARDIAL-INFARCTION; MORGAM BIOMARKER PROJECT; CRACK-COCAINE;
GENERAL-POPULATION; CORONARY-ARTERIES; RISK PREDICTION; HUMAN PLATELETS;
UNITED-STATES; SUBSTANCE USE; MORTALITY
AB Background: While cocaine use is an established risk factor for acute cardiovascular complications, associations between cocaine use and markers of cardiac injury outside of acute hospital presentation remain poorly characterized. We leveraged advances in cardiac troponin (cTnI) testing to assess low but clinically meaningful levels of cardiac injury among cocaine users and non-users.
Methods: We conducted a case control study comparing cTnI levels by the presence of cocaine among patients presenting for non-cardiac care in an urban safety net hospital. Samples were chosen sequentially among those for which urine drug screens were ordered by providers hospital-wide.
Results: During 2015, 14% of all hospital drug screens ordered were cocaine-positive. Among unique persons providing cocaine-positive (N = 100) and cocaine-negative (N = 100) samples, 37% were female, 45% were African-American and the median age was 51. Detectable cTnI (> 0.02 ng/mL) was observed in 21 samples (11%). It was more common in subjects using cocaine (Adjusted OR = 2.81; 95% CI = 1.03-7.65), but not other drugs. Moreover, there was a significant correlation between concentrations of cTnI and the cocaine metabolite, benzoylecgonine (Spearman Correlation = 0.34, p < 0.01).
Conclusions: Among urban safety net hospital patients, 11% had detectable cTnI, and cTnI concentration was significantly correlated with benzoylecgonine concentration. While these preliminary results require additional confirmation, they suggest the potential utility of considering cocaine use as more than just an episodic exposure leading to acute cardiac events. The consideration of cocaine use as an ongoing chronic exposure leading to subclinical cardiac injury may improve risk-stratification and patient outcomes in populations where cocaine use is high. (C) 2017 Elsevier B.V. All rights reserved.
C1 [Riley, Elise D.; Coffin, Phillip O.] Univ Calif San Francisco, Infect Dis & Global Hlth, Dept Med, Div HIV, San Francisco, CA 94143 USA.
[Hsue, Priscilla Y.] Univ Calif San Francisco, Dept Med, Div Cardiol, San Francisco, CA 94143 USA.
[Vittinghoff, Eric] Univ Calif San Francisco, Dept Epidemiol & Biostatist, San Francisco, CA 94143 USA.
[Wu, Alan H. B.; Lynch, Kara L.] Univ Calif San Francisco, San Francisco Gen Hosp, Dept Lab Med, San Francisco, CA 94143 USA.
[Coffin, Phillip O.] San Francisco Dept Publ Hlth, San Francisco, CA 94143 USA.
[Moore, Peter K.] Univ Calif San Francisco, Dept Med, Div Gen Internal Med, San Francisco, CA 94143 USA.
[Moore, Peter K.] San Francisco VA Med Ctr, Dept Med, Div Hosp Med, San Francisco, CA USA.
RP Riley, ED (reprint author), 1001 Potrero Ave,UCSF Mailbox 0874, San Francisco, CA 94143 USA.
EM elise.riley@ucsf.edu
FU National Institutes of Health [R01 DA037012, K24 DA039780]
FX This study was funded by the National Institutes of Health (R01 DA037012
and K24 DA039780). The National Institutes of Health and the National
Institute on Drug Abuse had no role in the design or conduct of the
study; the collection, management, analysis or interpretation of the
data; or the preparation, review or approval of the manuscript.
NR 56
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0376-8716
EI 1879-0046
J9 DRUG ALCOHOL DEPEN
JI Drug Alcohol Depend.
PD MAR 1
PY 2017
VL 172
BP 88
EP 93
DI 10.1016/j.drugalcdep.2016.11.039
PG 6
WC Substance Abuse; Psychiatry
SC Substance Abuse; Psychiatry
GA EM3LV
UT WOS:000395217500012
PM 28157591
ER
PT J
AU Marcum, ZA
Hanlon, JT
Murray, MD
AF Marcum, Zachary A.
Hanlon, Joseph T.
Murray, Michael D.
TI Improving Medication Adherence and Health Outcomes in Older Adults: An
Evidence-Based Review of Randomized Controlled Trials
SO DRUGS & AGING
LA English
DT Review
ID PHARMACIST INTERVENTION; ELDERLY-PATIENTS; PHARMACEUTICAL CARE;
BLOOD-PRESSURE; IMPACT; THERAPY; HOSPITALIZATIONS; HYPERTENSION;
POLYPHARMACY; METAANALYSIS
AB Background Poor medication adherence is a major public health problem in older adults often resulting in negative health outcomes.
Objective The objective of this review was to provide an updated summary of evidence from randomized controlled studies to determine whether interventions aimed at improving medication adherence also improve the health outcomes of older adults residing in community-based settings.
Methods Articles that assessed medication adherence interventions and related health outcomes in elderly individuals were identified through searches of MEDLINE (1970-June 2016), the Cochrane Database of Systematic Reviews (through to June 2016), and Google Scholar. Across the 12 included studies, interventions were grouped into three main categories: behavioral/educational (n = 3), pharmacist-led (n = 7), and reminder/simplification (n = 2).
Results Among the behavioral/educational intervention studies, two showed improvements in both adherence and related health outcomes, whereas one found no changes in adherence or health outcomes. Among the pharmacist-led studies, three showed improvements in both adherence and related health outcomes, while three reported no changes in adherence or health outcomes. One found an improvement in adherence but not health outcomes. Among the reminder/simplification studies, both studies reported improvements in adherence without a significant impact on related health outcomes.
Conclusion This evidence-based review of medication adherence interventions in older adults revealed promising strategies in the larger context of a largely mixed body of literature. Future patient-centered and multidisciplinary interventions should be developed and tested using evidence-based principles to improve medication adherence and health outcomes in older adults.
C1 [Marcum, Zachary A.] Univ Washington, Sch Pharm, Seattle, WA 98195 USA.
[Hanlon, Joseph T.] Univ Pittsburgh, Sch Med Geriatr Pharm & Publ Hlth, 3471 Fifth Ave,Suite 500, Pittsburgh, PA 15213 USA.
[Hanlon, Joseph T.] Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equ Res & Promot, Pittsburgh, PA 15240 USA.
[Hanlon, Joseph T.] Vet Affairs Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15240 USA.
[Murray, Michael D.] Purdue Univ, Coll Pharm, Indianapolis, IN USA.
[Murray, Michael D.] Regenstrief Inst Hlth Care, Indianapolis, IN USA.
RP Hanlon, JT (reprint author), Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equ Res & Promot, Pittsburgh, PA 15240 USA.; Hanlon, JT (reprint author), Vet Affairs Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15240 USA.
EM jth14@pitt.edu
FU Agency for Healthcare Research and Quality (AHRQ) [K12HS022982];
National Institutes of Health (NIH)/National Institute on Aging (NIA)
[P30AG024827, T32AG021885, U13AG047008]; AHRQ [R18HS023779]; Purdue
University (Indianapolis, IN, USA); Regenstrief Foundation
FX Dr. Marcum is supported by funding from the Agency for Healthcare
Research and Quality (AHRQ) (K12HS022982). Dr. Hanlon is supported by
funding from National Institutes of Health (NIH)/National Institute on
Aging (NIA) (P30AG024827, T32AG021885, U13AG047008) and AHRQ
(R18HS023779). Dr. Murray is supported by funding from an endowment on
medication safety from Purdue University (Indianapolis, IN, USA) and the
Regenstrief Foundation.
NR 37
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U1 3
U2 3
PU ADIS INT LTD
PI NORTHCOTE
PA 5 THE WAREHOUSE WAY, NORTHCOTE 0627, AUCKLAND, NEW ZEALAND
SN 1170-229X
EI 1179-1969
J9 DRUG AGING
JI Drugs Aging
PD MAR
PY 2017
VL 34
IS 3
BP 191
EP 201
DI 10.1007/s40266-016-0433-7
PG 11
WC Geriatrics & Gerontology; Pharmacology & Pharmacy
SC Geriatrics & Gerontology; Pharmacology & Pharmacy
GA EQ4KN
UT WOS:000398045900004
PM 28074410
ER
PT J
AU Brostow, DP
Petrik, ML
Starosta, AJ
Waldo, SW
AF Brostow, Diana P.
Petrik, Megan L.
Starosta, Amy J.
Waldo, Stephen W.
TI Depression in patients with peripheral arterial disease: A systematic
review
SO EUROPEAN JOURNAL OF CARDIOVASCULAR NURSING
LA English
DT Review
DE Depression; review; peripheral arterial disease; peripheral vascular
diseases
ID CORONARY-HEART-DISEASE; QUALITY-OF-LIFE; ANKLE-BRACHIAL INDEX;
LOWER-EXTREMITY REVASCULARIZATION; LEG SYMPTOMS; CARDIOVASCULAR-DISEASE;
FUNCTIONAL DECLINE; RISK-FACTORS; SMOKING-CESSATION; ANXIETY DISORDERS
AB Objectives: The association between cardiovascular disease and depression is well-established. Peripheral arterial disease arises from atherosclerosis like other cardiovascular disease, but unlike other cardiovascular disease, it impairs ambulation and lower extremity function. Given peripheral arterial disease's unique characteristics and underrepresentation in mental health research, we aimed to: (a) assess the prevalence of depression or depressive symptoms among peripheral arterial disease patients compared to coronary artery disease rates, (b) assess whether an independent association between peripheral arterial disease and depression exists, and (c) identify associated factors that may be targeted for intervention.
Design: This study was based on a systematic review.
Materials and methods: Electronic databases were searched to identify studies that examined peripheral arterial disease and depression or depressive symptoms. Methodological quality was assessed using the Newcastle-Ottawa Scale.
Results: We identified 28 studies. Prevalence of depression or depressive symptoms ranged from 11-48% in 12 cross-sectional studies, and from 3-36% in 16 longitudinal studies, which is comparable to reported coronary artery disease rates. Depressed peripheral arterial disease patients were more likely to be female, African American, and have more severe peripheral arterial disease symptoms and more compromised physical function compared to non-depressed patients. There is evidence to suggest that depression exerts a negative influence on walking ability and physical function independently of peripheral arterial disease.
Conclusions: There is a critical need to address depression in peripheral arterial disease patients, particularly those with characteristics that place them at increased risk. Vascular care providers appear to be the primary contact for assessing depressive symptoms, and once identified, integrated mental health providers may intervene to prevent the worsening of both depression and peripheral arterial disease.
C1 [Brostow, Diana P.; Waldo, Stephen W.] VA Eastern Colorado Healthcare Syst, 1055 Clermont St, Denver, CO 80220 USA.
[Petrik, Megan L.; Starosta, Amy J.] Denver VA Med Ctr, Rocky Mt Mental Illness Res Educ & Clin Ctr MIREC, Denver, CO USA.
[Petrik, Megan L.] Univ Minnesota, Sch Med, Dept Med, Minneapolis, MN 55455 USA.
[Starosta, Amy J.] Univ Colorado, Dept Psychiat, Boulder, CO 80309 USA.
RP Brostow, DP (reprint author), VA Eastern Colorado Healthcare Syst, 1055 Clermont St, Denver, CO 80220 USA.
EM Diana.Brostow@ucdenver.edu
FU Department of Veterans Affairs, Veterans Health Administration, Office
of Research and Development
FX This material is based upon work supported by the Department of Veterans
Affairs, Veterans Health Administration, Office of Research and
Development.
NR 77
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U1 5
U2 5
PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 1474-5151
EI 1873-1953
J9 EUR J CARDIOVASC NUR
JI Eur. J. Cardiovasc. Nurs.
PD MAR
PY 2017
VL 16
IS 3
BP 181
EP 193
DI 10.1177/1474515116687222
PG 13
WC Cardiac & Cardiovascular Systems; Nursing
SC Cardiovascular System & Cardiology; Nursing
GA EQ6GD
UT WOS:000398178900002
PM 28051339
ER
PT J
AU Mounessa, JS
Caravaglio, JV
Dellavalle, RP
AF Mounessa, Jessica S.
Caravaglio, Joseph Vincent
Dellavalle, Robert P.
TI Comparison of Regional and State Differences in Melanoma Rates in the
United States: 2003 vs 2013
SO JAMA DERMATOLOGY
LA English
DT Letter
C1 [Mounessa, Jessica S.; Dellavalle, Robert P.] Denver Vet Affairs Med Ctr, Dermatol Serv, 1055 Clermont St,POB 165, Denver, CO 80220 USA.
[Mounessa, Jessica S.; Dellavalle, Robert P.] Univ Colorado, Sch Med, Dept Dermatol, Aurora, CO USA.
[Caravaglio, Joseph Vincent] Univ Cent Florida, Coll Med, Dept Dermatol, Orlando, FL 32816 USA.
RP Dellavalle, RP (reprint author), Denver Vet Affairs Med Ctr, Dermatol Serv, 1055 Clermont St,POB 165, Denver, CO 80220 USA.
EM robert.dellavalle@ucdenver.edu
NR 4
TC 1
Z9 1
U1 0
U2 0
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6068
EI 2168-6084
J9 JAMA DERMATOL
JI JAMA Dermatol.
PD MAR 1
PY 2017
VL 153
IS 3
BP 345
EP 347
DI 10.1001/jamadermatol.2016.4625
PG 4
WC Dermatology
SC Dermatology
GA EN8JQ
UT WOS:000396247100029
PM 28030665
ER
PT J
AU Hall, DE
Arya, S
Schmid, KK
Carlson, MA
Lavedan, P
Bailey, TL
Purviance, G
Bockman, T
Lynch, TG
Johanning, JM
AF Hall, Daniel E.
Arya, Shipra
Schmid, Kendra K.
Carlson, Mark A.
Lavedan, Pierre
Bailey, Travis L.
Purviance, Georgia
Bockman, Tammy
Lynch, Thomas G.
Johanning, Jason M.
TI Association of a Frailty Screening Initiative With Postoperative
Survival at 30, 180, and 365 Days
SO JAMA SURGERY
LA English
DT Article
ID 30-DAY MORTALITY; DECISION-MAKING; SURGICAL CARE; QUALITY; RISK;
MORBIDITY; INDEX; PREDICTOR; OUTCOMES; SURGERY
AB IMPORTANCE As the US population ages, the number of operations performed on elderly patients will likely increase. Frailty predicts postoperative mortality and morbidity more than age alone, thus presenting opportunities to identify the highest-risk surgical patients and improve their outcomes.
OBJECTIVE To examine the effect of the Frailty Screening Initiative (FSI) on mortality and complications by comparing the surgical outcomes of a cohort of surgical patients treated before and after implementation of the FSI.
DESIGN, SETTING, AND PARTICIPANTS This single-site, facility-wide, prospective cohort quality improvement project studied all 9153 patients from a level 1b Veterans Affairs medical center who presented for major, elective, noncardiac surgery from October 1, 2007, to July 1, 2014.
INTERVENTIONS Assessment of preoperative frailty in all patients scheduled for elective surgery began in July 2011. Frailty was assessed with the Risk Analysis Index (RAI), and the records of all frail patients (RAI score, >= 21) were flagged for administrative review by the chief of surgery (or designee) before the scheduled operation. On the basis of this review, clinicians from surgery, anesthesia, critical care, and palliative care were notified of the patient's frailty and associated surgical risks; if indicated, perioperative plans were modified based on team input.
MAIN OUTCOMES AND MEASURES Postoperative mortality at 30, 180, and 365 days.
RESULTS From October 1, 2007, to July 1, 2014, a total of 9153 patients underwent surgery (mean [SD] age, 60.3 [13.5] years; female, 653 [7.1%]; and white, 7096 [79.8%]). Overall 30-day mortality decreased from 1.6%(84 of 5275 patients) to 0.7%(26 of 3878 patients, P <.001) after FSI implementation. Improvement was greatest among frail patients (12.2% [24 of 197 patients] to 3.8% [16 of 424 patients], P <.001), although mortality rates also decreased among the robust patients (1.2%[60 of 5078 patients] to 0.3%[10 of 3454 patients], P <.001). Themagnitude of improvement among frail patients increased at 180 (23.9%[47 of 197 patients] to 7.7%[30 of 389 patients], P <.001) and 365 days (34.5%[68 of 197 patients] to 11.7%[36 of 309 patients], P <.001). Multivariable models revealed improved survival after FSI implementation, controlling for age, frailty, and predicted mortality (adjusted odds ratio for 180-day survival, 2.87; 95% CI, 1.98-4.16).
CONCLUSIONS AND RELEVANCE Implementation of the FSI was associated with reduced mortality, suggesting the feasibility of widespread screening of patients preoperatively to identify frailty and the efficacy of system-level initiatives aimed at improving their surgical outcomes. Additional investigation is required to establish a causal connection.
C1 [Hall, Daniel E.] Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA USA.
[Hall, Daniel E.] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA.
[Arya, Shipra] Atlanta Vet Affairs Med Ctr, Atlanta, GA USA.
[Arya, Shipra] Emory Univ, Dept Surg, Div Vasc & Endovasc, Atlanta, GA 30322 USA.
[Schmid, Kendra K.] Univ Nebraska, Med Ctr, Dept Biostat, Omaha, NE USA.
[Carlson, Mark A.] Univ Nebraska, Med Ctr, Dept Genet Cell Biol & Anat, Omaha, NE USA.
[Carlson, Mark A.; Johanning, Jason M.] Univ Nebraska, Med Ctr, Dept Surg, Omaha, NE USA.
[Carlson, Mark A.; Bailey, Travis L.] VA Nebraska Western Iowa Hlth Care Syst, Omaha, NE USA.
[Lavedan, Pierre] VA Nebraska Western Iowa Hlth Care Syst, Dept Extended Care & Rehabil, Omaha, NE USA.
[Bailey, Travis L.] Univ Utah, Dept Orthopaed Surg, Salt Lake City, UT USA.
[Lynch, Thomas G.] Dept Vet Affairs Vet Hlth Adm, Off Hlth Operat & Management, Washington, DC USA.
[Lynch, Thomas G.] George Washington Univ, Dept Surg, Sch Med, Washington, DC USA.
RP Hall, DE (reprint author), UPMC Presbyterian, Ste 1264,200 Lothrop St, Pittsburgh, PA 15213 USA.
EM hallde@upmc.edu
FU US Department of Veterans Affairs, Veterans Health Administration,
Office of Research and Development, Health Services Research and
Development [CDA 08-281]
FX This investigation was supported by grant CDA 08-281 from the US
Department of Veterans Affairs, Veterans Health Administration, Office
of Research and Development, Health Services Research and Development
(Dr Hall).
NR 29
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U2 1
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6254
EI 2168-6262
J9 JAMA SURG
JI JAMA Surg.
PD MAR
PY 2017
VL 152
IS 3
DI 10.1001/jamasurg.2016.4219
PG 8
WC Surgery
SC Surgery
GA EQ5DI
UT WOS:000398101400007
PM 27902826
ER
PT J
AU Gros, DF
Szafranski, DD
Shead, SD
AF Gros, Daniel F.
Szafranski, Derek D.
Shead, Sarah D.
TI A real world dissemination and implementation of Transdiagnostic
Behavior Therapy (TBT) for veterans with affective disorders
SO JOURNAL OF ANXIETY DISORDERS
LA English
DT Article
DE Transdiagnostic Behavior Therapy; TBT; Dissemination; Implementation;
Veterans; Veterans Affairs Medical Center
ID SOMATIC ANXIETY STICSA; STATE-TRAIT INVENTORY; PRIMARY-CARE; PREVALENCE;
FEATURES; TRIAL
AB Dissemination and implementation of evidence-based psychotherapies is challenging in real world clinical settings. Transdiagnostic Behavior Therapy (TBT) for affective disorders was developed with dissemination and implementation in clinical settings in mind. The present study investigated a voluntary local dissemination and implementation effort, involving 28 providers participating in a four-hour training on TBT. Providers completed immediate (n = 22) and six-month follow-up (n = 12) training assessments and were encouraged to collect data on their TBT patients (delivery fidelity was not investigated). Findings demonstrated that providers endorsed learning of and interest in using TBT after the training. At six-months, 50% of providers reported using TBT with their patients and their perceived effectiveness of TBT to be very good to excellent. Submitted patient outcome data evidenced medium to large effect sizes. Together, these findings provide preliminary support for the effectiveness of a real world dissemination and implementation of TBT. Published by Elsevier Ltd.
C1 [Gros, Daniel F.; Szafranski, Derek D.; Shead, Sarah D.] Ralph H Johnson Vet Affairs Med Ctr, Mental Hlth Serv, Charleston, SC USA.
[Gros, Daniel F.; Szafranski, Derek D.] Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC USA.
RP Gros, DF (reprint author), Ralph H Johnson VAMC, Mental Hlth Serv 116, 109 Bee St, Charleston, SC 29401 USA.
EM grosd@musc.edu
FU Department of Veteran Affairs Clinical Sciences Research and Development
[CX000845]
FX This study is supported by Department of Veteran Affairs Clinical
Sciences Research and Development Career Development Award CX000845 (PI:
Gros). The views expressed in this article are those of the authors and
do not necessarily reflect the position or policy of the Department of
Veterans Affairs or the United States government. There are no conflicts
of interest to disclose. I would like to thank the providers within the
Ralph H. Johnson Veterans Affairs Medical Center for their participation
in this project.
NR 26
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U1 2
U2 2
PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0887-6185
EI 1873-7897
J9 J ANXIETY DISORD
JI J. Anxiety Disord.
PD MAR
PY 2017
VL 46
BP 72
EP 77
DI 10.1016/j.janxdis.2016.04.010
PG 6
WC Psychology, Clinical; Psychiatry
SC Psychology; Psychiatry
GA EO8VE
UT WOS:000396967800009
PM 27158076
ER
PT J
AU Marcum, ZA
Gellad, WF
AF Marcum, Zachary A.
Gellad, Walid F.
TI Improving Medication Adherence: Keep Your Eyes on the Prize
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Editorial Material
C1 [Marcum, Zachary A.] Univ Washington, Sch Pharm, Seattle, WA 98195 USA.
[Gellad, Walid F.] Univ Pittsburgh, Div Gen Internal Med, Pittsburgh, PA USA.
[Gellad, Walid F.] Univ Pittsburgh, Ctr Pharmaceut Policy & Prescribing, Pittsburgh, PA USA.
[Gellad, Walid F.] VA Pittsburgh Healthcare Syst, Univ Dr 151C, Pittsburgh, PA 15240 USA.
RP Gellad, WF (reprint author), VA Pittsburgh Healthcare Syst, Univ Dr 151C, Pittsburgh, PA 15240 USA.
EM Walid.gellad@pitt.edu
FU Agency for Healthcare Research and Quality (AHRQ) [K12HS022982]
FX Dr. Marcum is supported by funding from the Agency for Healthcare
Research and Quality (AHRQ; K12HS022982).
NR 10
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD MAR
PY 2017
VL 32
IS 3
BP 236
EP 237
DI 10.1007/s11606-016-3927-4
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EM2YI
UT WOS:000395181300003
PM 27848188
ER
PT J
AU Rollman, BL
Belnap, BH
Mazumdar, S
Abebe, KZ
Karp, JF
Lenze, EJ
Schulberg, HC
AF Rollman, Bruce L.
Belnap, Bea Herbeck
Mazumdar, Sati
Abebe, Kaleab Z.
Karp, Jordan F.
Lenze, Eric J.
Schulberg, Herbert C.
TI Telephone-Delivered Stepped Collaborative Care for Treating Anxiety in
Primary Care: A Randomized Controlled Trial
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Article
DE primary care; clinical trial; collaborative care; anxiety; depression;
mental health
ID COGNITIVE-BEHAVIORAL THERAPY; DISORDER SEVERITY SCALE; QUALITY-OF-CARE;
PANIC DISORDER; DEPRESSION; HEALTH; MANAGEMENT; VALIDITY; PROTOCOL;
IMPROVE
AB Collaborative care for depression is more effective in improving treatment outcomes than primary care physicians' (PCPs) usual care (UC). However, few trials of collaborative care have targeted anxiety.
To examine the impact and 12-month durability of a centralized, telephone-delivered, stepped collaborative care intervention (CC) for treating anxiety disorders across a network of primary care practices.
Randomized controlled trial with blinded outcome assessments.
A total of 329 patients aged 18-64 referred by their PCPs in response to an electronic medical record (EMR) prompt. They include 250 highly anxious patients randomized to either CC or to UC, and 79 moderately anxious patients who were triaged to a watchful waiting (WW) cohort and later randomized if their conditions clinically deteriorated.
Twelve months of telephone-delivered CC involving non-mental health professionals who provided patients with basic psycho-education, assessed preferences for guideline-based pharmacotherapy, monitored treatment responses, and informed PCPs of their patients' care preferences and progress via the EMR.
Mental health-related quality of life ([HRQoL]; SF-36 MCS); secondary outcomes: anxiety (Hamilton Anxiety Rating Scale [SIGH-A], Panic Disorder Severity Scale) and mood (PHQ-9).
At 12-month follow-up, highly anxious patients randomized to CC reported improved mental HRQoL (effect size [ES]: 0.38 [95 % CI: 0.13-0.63]; P = 0.003), anxiety (SIGH-A ES: 0.30 [0.05-0.55]; P = 0.02), and mood (ES: 0.45 [0.19-0.71] P = 0.001) versus UC. These improvements were sustained for 12 months among African-Americans (ES: 0.70-1.14) and men (ES: 0.43-0.93). Of the 79 WW patients, 29 % met severity criteria for randomization, and regardless of treatment assignment, WW patients reported fewer anxiety and mood symptoms and better mental HRQoL over the full 24-month follow-up period than highly anxious patients who were randomized at baseline.
Telephone-delivered, centralized, stepped CC improves mental HRQoL, anxiety and mood symptoms. These improvements were durable and particularly evident among those most anxious at baseline, and among African-Americans and men.
C1 [Rollman, Bruce L.; Belnap, Bea Herbeck; Abebe, Kaleab Z.] Univ Pittsburgh, Sch Med, Ctr Behav Hlth & Smart Technol, Div Gen Internal Med, Suite 600,230 McKee Pl, Pittsburgh, PA 15213 USA.
[Mazumdar, Sati] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Suite 600,230 McKee Pl, Pittsburgh, PA 15213 USA.
[Karp, Jordan F.] Univ Pittsburgh, Sch Med, Dept Psychiat, Suite 600,230 McKee Pl, Pittsburgh, PA 15213 USA.
[Karp, Jordan F.] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA USA.
[Lenze, Eric J.] Washington Univ, Sch Med, Dept Psychiat, Hlth Mind Lab, St Louis, MO 63110 USA.
[Schulberg, Herbert C.] Weill Cornell Med Coll, Dept Psychiat, White Plains, NY USA.
RP Rollman, BL (reprint author), Univ Pittsburgh, Sch Med, Ctr Behav Hlth & Smart Technol, Div Gen Internal Med, Suite 600,230 McKee Pl, Pittsburgh, PA 15213 USA.
EM rollmanbl@upmc.edu
FU National Institute of Mental Health [R01 MH09421, R01 MH093501]
FX All work described herein was supported by grants from the National
Institute of Mental Health (R01 MH09421 and R01 MH093501). The funding
source had no role in the design, conduct, or reporting of our study, or
in the preparation, review, or decision to submit this manuscript for
publication.
NR 41
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U1 1
U2 1
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD MAR
PY 2017
VL 32
IS 3
BP 245
EP 255
DI 10.1007/s11606-016-3873-1
PG 11
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EM2YI
UT WOS:000395181300008
PM 27714649
ER
PT J
AU Reddy, A
Huseman, TL
Canamucio, A
Marcus, SC
Asch, DA
Volpp, K
Long, JA
AF Reddy, Ashok
Huseman, Tiffany L.
Canamucio, Anne
Marcus, Steven C.
Asch, David A.
Volpp, Kevin
Long, Judith A.
TI Patient and Partner Feedback Reports to Improve Statin Medication
Adherence: A Randomized Control Trial
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Article
DE medication adherence; social force; social support; statins
ID MYOCARDIAL-INFARCTION; FINANCIAL INCENTIVES; THERAPY; MORTALITY; HEALTH
AB Simple nudges such as reminders and feedback reports to either a patient or a partner may facilitate improved medication adherence.
To test the impact of a pill bottle used to monitor adherence, deliver a daily alarm, and generate weekly medication adherence feedback reports on statin adherence.
Three-month, three-arm randomized clinical trial (ClinicalTrials.gov identifier: NCT02480530).
One hundred and twenty-six veterans with known coronary artery disease and poor adherence (medication possession ratio < 80 %).
Patients were randomized to one of three groups: (1) a control group (n = 36) that received a pill-monitoring device with no alarms or feedback; (2) an individual feedback group (n = 36) that received a daily alarm and a weekly medication adherence feedback report; and (3) a partner feedback group (n = 54) that received an alarm and a weekly feedback report that was shared with a friend, family member, or a peer. The intervention continued for 3 months, and participants were followed for an additional 3 months after the intervention period.
Adherence as measured by pill bottle. Secondary outcomes included change in LDL (mg/dl), patient activation, and social support.
During the 3-month intervention period, medication adherence was higher in both feedback arms than in the control arm (individual feedback group 89 %, partner feedback group 86 %, control group 67 %; p < 0.001 and = 0.001). At 6 months, there was no difference in medication adherence between either of the feedback groups and the control (individual feedback 60 %, partner feedback 52 %, control group 54 %; p = 0.75 and 0.97).
Daily alarms combined with individual or partner feedback reports improved statin medication adherence. While neither an individual feedback nor partner feedback strategy created a sustainable medication adherence habit, the intervention itself is relatively easy to implement and low cost.
C1 [Reddy, Ashok] Univ Washington, Sch Med, Div Gen Internal Med, 1959 NE Pacific St,Suite BB1240,Box 356526, Seattle, WA 98195 USA.
[Reddy, Ashok] UW Med Ctr Scholarship Patient Care Qual & Safety, Seattle, WA USA.
[Reddy, Ashok] Univ Washington, Sch Med, Dept Med, 1959 NE Pacific St,Suite BB1240,Box 356526, Seattle, WA 98195 USA.
[Huseman, Tiffany L.; Canamucio, Anne; Asch, David A.; Volpp, Kevin; Long, Judith A.] Philadelphia VA Med Ctr, VISN Ctr Evaluat PACT 4, Philadelphia, PA USA.
[Marcus, Steven C.] Univ Penn, Sch Social Policy & Practice, Philadelphia, PA 19104 USA.
[Asch, David A.; Volpp, Kevin; Long, Judith A.] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Asch, David A.; Volpp, Kevin; Long, Judith A.] Univ Penn, Leonard Davis Inst Hlth Econ, Philadelphia, PA 19104 USA.
RP Reddy, A (reprint author), Univ Washington, Sch Med, Dept Med, 1959 NE Pacific St,Suite BB1240,Box 356526, Seattle, WA 98195 USA.
EM reddya@uw.edu
FU Center for the Evaluation of Patient Aligned Care Teams at the
Philadelphia VA
FX This work was supported by a grant from the Center for the Evaluation of
Patient Aligned Care Teams at the Philadelphia VA.
NR 24
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U1 4
U2 4
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD MAR
PY 2017
VL 32
IS 3
BP 256
EP 261
DI 10.1007/s11606-016-3858-0
PG 6
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EM2YI
UT WOS:000395181300009
PM 27612487
ER
PT J
AU Payne, B
Brzezinski, WA
Clark, AV
Estrada, CA
Kraemer, RR
AF Payne, Brittany
Brzezinski, Walter A.
Clark, Amanda V.
Estrada, Carlos A.
Kraemer, Ryan R.
TI Lessons Learned from a Middle-Aged Man with Testicular Pain: Exercises
in Clinical Reasoning
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Article
DE clinical reasoning; cognitive error; testicular pain; self-reflection
ID POLYARTERITIS-NODOSA; DIAGNOSTIC ERRORS; STRATEGIES
C1 [Payne, Brittany; Kraemer, Ryan R.] Univ Alabama Birmingham, Tinsley Harrison Internal Med Residency Program, Birmingham, AL USA.
[Brzezinski, Walter A.] Med Univ South Carolina, Charleston, SC USA.
[Clark, Amanda V.] Louis Stokes Cleveland VA Med Ctr, Cleveland, OH USA.
[Clark, Amanda V.] Case Western Reserve Sch Med, Cleveland, OH USA.
[Estrada, Carlos A.; Kraemer, Ryan R.] Birmingham Vet Affairs Med Ctr, Birmingham, AL USA.
[Estrada, Carlos A.; Kraemer, Ryan R.] Univ Alabama Birmingham, 734 Fac Off Tower,510 20th St South, Birmingham, AL 35294 USA.
RP Kraemer, RR (reprint author), Univ Alabama Birmingham, 734 Fac Off Tower,510 20th St South, Birmingham, AL 35294 USA.
EM rkraemer@uabmc.edu
NR 15
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD MAR
PY 2017
VL 32
IS 3
BP 355
EP 359
DI 10.1007/s11606-016-3882-0
PG 5
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EM2YI
UT WOS:000395181300024
PM 27778213
ER
PT J
AU Hunt, SC
AF Hunt, Stephen C.
TI The Patient on the Long Journey Home
SO JOURNAL OF GENERAL INTERNAL MEDICINE
LA English
DT Editorial Material
C1 [Hunt, Stephen C.] Univ Washington, Dept Med, VA Puget Sound Hlth Care Syst, OEM Program, 1660 Columbian Way S, Seattle, WA 98108 USA.
RP Hunt, SC (reprint author), Univ Washington, Dept Med, VA Puget Sound Hlth Care Syst, OEM Program, 1660 Columbian Way S, Seattle, WA 98108 USA.
EM stephen.hunt@va.gov
NR 3
TC 0
Z9 0
U1 1
U2 1
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0884-8734
EI 1525-1497
J9 J GEN INTERN MED
JI J. Gen. Intern. Med.
PD MAR
PY 2017
VL 32
IS 3
BP 366
EP 367
DI 10.1007/s11606-016-3908-7
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EM2YI
UT WOS:000395181300029
PM 27844259
ER
PT J
AU Kwan, T
Floyd, CL
Kim, S
King, PH
AF Kwan, Thaddaeus
Floyd, Candace L.
Kim, Soojin
King, Peter H.
TI RNA Binding Protein Human Antigen R Is Translocated in Astrocytes
following Spinal Cord Injury and Promotes the Inflammatory Response
SO JOURNAL OF NEUROTRAUMA
LA English
DT Article
DE glial cell response to injury; inflammation; molecular biological
approaches; spinal cord injury
ID FACTOR-KAPPA-B; AMYOTROPHIC-LATERAL-SCLEROSIS; TRAUMATIC BRAIN-INJURY;
MESSENGER-RNA; HUR; EXPRESSION; CELLS; REGENERATION; MACROPHAGES;
ACTIVATION
AB Inflammation plays a prominent role in the events following traumatic injury to the central nervous system (CNS). The initial inflammatory response is driven by mediators such as tumor necrosis factor a and interleukin 1 beta, which are produced by activated astrocytes and microglia at the site of injury. These factors are regulated post-transcriptionally by RNA binding proteins (RBP) that interact with adenylate and uridylate-rich elements (ARE) in the 3'-untranslated region of the messenger RNA (mRNA). Human antigen R (HuR) is one of these RBPs and generally functions as a positive regulator of ARE-containing mRNAs. Here, we hypothesized that HuR plays an important role in the induction of cytokine and chemokines in astrocytes following traumatic injury. Using a mouse model of spinal cord injury, we found HuR to be extensively translocated to the cytoplasm in astrocytes at the level of injury, consistent with its activation. In an in vitro stretch injury model of CNS trauma, we observed a similar cytoplasmic shift of HuR in astrocytes and an attenuation of cytokine induction with HuR knockdown. RNA kinetics and luciferase assays suggested that the effect was more related to transcription than RNA destabilization. A small molecule inhibitor of HuR suppressed cytokine induction of injured astrocytes and reduced chemoattraction for neutrophils and microglia. In summary, HuR is activated in astrocytes in the early stages of CNS trauma and positively regulates the molecular response of key inflammatory mediators in astrocytes. Our findings suggest that HuR may be a therapeutic target in acute CNS trauma for blunting secondary tissue injury triggered by the inflammatory response.
C1 [Kwan, Thaddaeus; Kim, Soojin; King, Peter H.] Univ Alabama Birmingham, Dept Neurol, Birmingham, AL 35487 USA.
[Floyd, Candace L.] Univ Alabama Birmingham, Dept Phys Med & Rehabil, Birmingham, AL USA.
[King, Peter H.] Univ Alabama Birmingham, Dept Cell & Integrat Biol, Dept Dev & Integrat Biol, Birmingham, AL 35487 USA.
[King, Peter H.] Birmingham Vet Affairs Med Ctr, Birmingham, AL 35487 USA.
RP King, PH (reprint author), Univ Alabama Birmingham, Dept Neurol, Birmingham, AL 35487 USA.; King, PH (reprint author), Univ Alabama Birmingham, Dept Cell & Integrat Biol, Dept Dev & Integrat Biol, Birmingham, AL 35487 USA.; King, PH (reprint author), Birmingham Vet Affairs Med Ctr, Birmingham, AL 35487 USA.
EM phking@uabmc.edu
FU UAB Comprehensive Neuroscience Center
FX We wish to thank Terry Lewis, PhD, and the UAB Neuroscience Molecular
Detection Core Facility (P30 NS47466) for assistance with
immunohistochemistry, and Marion Spell and the UAB Center for AIDS
Research flow cytometry core for their assistance with FACS analysis.
This work was supported by a pilot grant from the UAB Comprehensive
Neuroscience Center.
NR 58
TC 0
Z9 0
U1 1
U2 1
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 0897-7151
EI 1557-9042
J9 J NEUROTRAUM
JI J. Neurotrauma
PD MAR
PY 2017
VL 34
IS 6
BP 1249
EP 1259
DI 10.1089/neu.2016.4757
PG 11
WC Critical Care Medicine; Clinical Neurology; Neurosciences
SC General & Internal Medicine; Neurosciences & Neurology
GA EN7ZR
UT WOS:000396221200012
PM 27852147
ER
PT J
AU Alexander, M
Courtois, F
AF Alexander, Marcalee
Courtois, Frederique
TI Blood Pressure during Sexual Activity after Spinal Cord Injury
Inaccurately Portrayed
SO JOURNAL OF NEUROTRAUMA
LA English
DT Letter
ID AUTONOMIC DYSREFLEXIA; CARDIOVASCULAR-RESPONSES; SPERM RETRIEVAL; MEN;
STIMULATION; EJACULATION
C1 [Alexander, Marcalee] Birmingham VA Med Ctr, Dept Rehabilitat Med, Birmingham, AL USA.
[Alexander, Marcalee] Univ Alabama Birmingham, Med Sch Birmingham, Dept Phys Med & Rehabil, Birmingham, AL USA.
[Alexander, Marcalee] Harvard Univ, Sch Med, Dept Phys Med & Rehabil, Boston, MA USA.
[Courtois, Frederique] Univ Quebec Montreal, Fac Sci Humaines, Dept Sexol, CP 8888,Succ,Ctr Ville, Montreal, PQ, Canada.
[Courtois, Frederique] Univ Quebec Montreal, Fac Sci Humaines, Dept Psychol, Montreal, PQ, Canada.
RP Courtois, F (reprint author), Univ Quebec Montreal, Fac Sci Humaines, Dept Sexol, CP 8888,Succ,Ctr Ville, Montreal, PQ, Canada.
EM courtois.frederique@uqam.ca
NR 11
TC 0
Z9 0
U1 0
U2 0
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 0897-7151
EI 1557-9042
J9 J NEUROTRAUM
JI J. Neurotrauma
PD MAR
PY 2017
VL 34
IS 6
BP 1289
EP 1290
DI 10.1089/neu.2016.4810
PG 2
WC Critical Care Medicine; Clinical Neurology; Neurosciences
SC General & Internal Medicine; Neurosciences & Neurology
GA EN7ZR
UT WOS:000396221200017
PM 27796188
ER
PT J
AU Rivera, JC
Amuan, ME
Morris, RM
Johnson, AE
Pugh, MJ
AF Rivera, Jessica C.
Amuan, Megan E.
Morris, Ruth M.
Johnson, Anthony E.
Pugh, Mary Jo
TI Arthritis, comorbidities, and care utilization in veterans of operations
enduring and Iraqi Freedom
SO JOURNAL OF ORTHOPAEDIC RESEARCH
LA English
DT Article
DE veterans health; military health; osteoarthritis; musculoskeletal health
care utilization; comorbid arthritis
ID MILITARY SERVICE MEMBERS; UNITED-STATES; HEALTH-CARE; OSTEOARTHRITIS;
POPULATION; PREVALENCE; DISEASE; FRACTURES; WOUNDS; INJURY
AB Veteran populations are known to have frequencies of arthritis higher than civilian populations. The aim of this study is to define the prevalence of arthritis among a cohort of veterans from ongoing U.S. military operations. A retrospective cohort study using Veterans Administration data sources for service connected disability, comorbidities, clinic utilization, and pharmacy utilization was conducted including veterans who deployed in service to operations in Afghanistan or Iraq, comparing veterans with a diagnosis of arthritis, arthritis plus back pain, and veterans with no pain diagnoses. The frequency of arthritis was 11.8%. Veterans with arthritis and arthritis plus back pain had greater frequencies of diabetes, hyperlipidemia, hypertension, and obesity compare to veterans with no pain diagnosis. Veterans with arthritis plus back pain had the highest pain clinic utilization and prescription use of opioids and anti-inflammatories. Veterans with no pain diagnosis had higher frequencies of diagnosis and clinic utilization for mental health disorders. Arthritis is prevalent among the latest generation of combat veterans and is associated with diabetes, obesity, and cardiovascular comorbidities. The need for arthritis care and associated comorbidities is expected to increase as the Veterans Administration and the civilian health care sector assumes care of these veterans. (c) 2016 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 35:682-687, 2017.
C1 [Rivera, Jessica C.] US Army Inst Surg Res, 3698 Chambers Pass, Jbsa Ft Sam Houston, TX 78234 USA.
[Rivera, Jessica C.; Johnson, Anthony E.] San Antonio Mil Med Ctr, Dept Orthopaed Surg, 3698 Chambers Pass, Jbsa Ft Sam Houston, TX 78234 USA.
[Amuan, Megan E.] Edith Nourse Roge Mem Vet Hosp, Bedford, MA USA.
[Morris, Ruth M.; Pugh, Mary Jo] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
RP Rivera, JC (reprint author), US Army Inst Surg Res, 3698 Chambers Pass, Jbsa Ft Sam Houston, TX 78234 USA.; Rivera, JC (reprint author), San Antonio Mil Med Ctr, Dept Orthopaed Surg, 3698 Chambers Pass, Jbsa Ft Sam Houston, TX 78234 USA.
EM jessica.c.rivera14.mil@mail.mil
NR 34
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0736-0266
EI 1554-527X
J9 J ORTHOP RES
JI J. Orthop. Res.
PD MAR
PY 2017
VL 35
IS 3
SI SI
BP 682
EP 687
DI 10.1002/jor.23323
PG 6
WC Orthopedics
SC Orthopedics
GA EP7YY
UT WOS:000397594300032
PM 27256517
ER
PT J
AU LeBlanc, ES
Rizzo, JH
Pedula, KL
Yaffe, K
Ensrud, KE
Cauley, J
Cawthon, PM
Cummings, S
Hillier, TA
AF LeBlanc, Erin S.
Rizzo, Joanne H.
Pedula, Kathryn L.
Yaffe, Kristine
Ensrud, Kristine E.
Cauley, Jane
Cawthon, Peggy M.
Cummings, Steven
Hillier, Teresa A.
CA Study Osteoporotic Fractures SOF R
TI Weight Trajectory over 20 Years and Likelihood of Mild Cognitive
Impairment or Dementia Among Older Women
SO JOURNAL OF THE AMERICAN GERIATRICS SOCIETY
LA English
DT Article
DE weight trajectory; dementia; cognitive dysfunction
ID BODY-MASS INDEX; INCIDENT ALZHEIMER-DISEASE; POPULATION-BASED COHORT;
MATTER VOLUME DEFICITS; CEREBRAL GRAY-MATTER; LATE-LIFE; RISK-FACTORS;
ANOREXIA-NERVOSA; CARDIOVASCULAR-HEALTH; POSTMENOPAUSAL WOMEN
AB ObjectivesThe association between weight change and cognition is controversial. We examined the association between 20-year weight change and cognitive function in late life.
DesignCohort study.
SettingStudy of Osteoporotic Fractures (SOF).
ParticipantsOne thousand two hundred eighty-nine older, community-dwelling women (mean baseline age 68 (65-81) and 88 (82-102) at cognitive testing).
MeasurementsStudy of Osteoporotic Fractures participants had body weight measured repeatedly over 20 years (mean 8 weights). Adjudicated cognitive status was classified as normal (n = 775) or mild cognitive impairment (MCI)/dementia (n = 514) at Year 20. Logistic models were used to evaluate whether absolute weight change, rate of weight loss per year, presence of abrupt, unrecovered weight loss, and weight variability were associated with MCI or dementia.
ResultsWomen with greater rate of weight loss over 20 years had increased chance of developing MCI or dementia. In age/education/clinic-adjusted base models, each 0.5 kg/yr decrease resulted in 30% increased odds of MCI/dementia (OR = 1.30 [95% CI: 1.14, 1.49]). After adjustment for age, education, clinic, depression, and walking speed, there was 17% (OR = 1.17 [95% CI: 1.02, 1.35]) increased odds of MCI/dementia for each 0.5 kg/yr decrease in weight. In base models, variability in weight was significant. Each 1% average deviation from each woman's predicted weight curve was associated with 11% increased odds of MCI/dementia (OR = 1.11 [95% CI: 1.04, 1.18]). The estimate was attenuated after full adjustment (OR = 1.06 [95% CI: 0.99, 1.14]). The presence of an abrupt weight decline was not associated with MCI/dementia.
ConclusionsRate of weight loss over 20 years was associated with development of MCI or dementia in women surviving past 80 years, suggesting that nutritional status, social-environmental factors, and/or adipose tissue function and structure may affect cognitive function with aging.
C1 [LeBlanc, Erin S.; Rizzo, Joanne H.; Pedula, Kathryn L.; Hillier, Teresa A.] Kaiser Permanente Northwest, Ctr Hlth Res, 3800 North Interstate Ave, Portland, OR 97227 USA.
[Yaffe, Kristine] Univ Calif San Francisco, Sch Med, Dept Psychiat, San Francisco, CA USA.
[Yaffe, Kristine] Univ Calif San Francisco, Sch Med, Dept Neurol, San Francisco, CA USA.
[Yaffe, Kristine] Univ Calif San Francisco, Sch Med, Dept Epidemiol & Biostat, San Francisco, CA USA.
[Yaffe, Kristine] San Francisco VA Med Ctr, San Francisco, CA USA.
[Ensrud, Kristine E.] Univ Minnesota, Dept Med, Univ Epidemiol & Community Hlth, Ctr Chron Dis Outcomes Res,VA Hlth Care Syst, Box 736 UMHC, Minneapolis, MN 55455 USA.
[Cauley, Jane] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA.
[Cawthon, Peggy M.; Cummings, Steven] Calif Pacific Med Ctr, Res Inst, San Francisco, CA USA.
[Hillier, Teresa A.] Kaiser Permanente Hawaii, Ctr Hlth Res, Honolulu, HI USA.
RP LeBlanc, ES (reprint author), Kaiser Permanente Northwest, Ctr Hlth Res, 3800 North Interstate Ave, Portland, OR 97227 USA.
EM erin.s.leblanc@kpchr.org
FU Amgen; Astrazeneca; Bristol Meyers Squibb; National Institutes of
Health; National Institute on Aging (NIA) [R01 ag005407, R01 ar35582,
R01 ar35583, R01 ar35584, R01 ag005394, R01 ag027574, R01 ag027576]
FX Dr. LeBlanc's institute has received research funding from Amgen,
Astrazeneca, and Bristol Meyers Squibb for unrelated projects on which
she was investigator.; The Study of Osteoporotic Fractures (SOF) is
supported by the National Institutes of Health. The National Institute
on Aging (NIA) provides support under the following grant numbers: R01
ag005407, R01 ar35582, R01 ar35583, R01 ar35584, R01 ag005394, R01
ag027574, and R01 ag027576.
NR 69
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0002-8614
EI 1532-5415
J9 J AM GERIATR SOC
JI J. Am. Geriatr. Soc.
PD MAR
PY 2017
VL 65
IS 3
BP 511
EP 519
DI 10.1111/jgs.14552
PG 9
WC Geriatrics & Gerontology; Gerontology
SC Geriatrics & Gerontology
GA EQ0XQ
UT WOS:000397794300014
PM 27991654
ER
PT J
AU Yoshikawa, TT
Norman, DC
AF Yoshikawa, Thomas T.
Norman, Dean C.
TI Geriatric Infectious Diseases: Current Concepts on Diagnosis and
Management
SO JOURNAL OF THE AMERICAN GERIATRICS SOCIETY
LA English
DT Article
DE infection; infectious disease; geriatric; aging; long-term care
ID CLOSTRIDIUM-DIFFICILE INFECTION; LONG-TERM-CARE; COMMUNITY-ACQUIRED
PNEUMONIA; URINARY-TRACT-INFECTION; NURSING-HOME RESIDENTS; FECAL
MICROBIOTA TRANSPLANTATION; CLINICAL-PRACTICE GUIDELINES; OLDER-ADULTS;
ASYMPTOMATIC BACTERIURIA; FUNCTIONAL STATUS
AB New information on infectious diseases in older adults has become available in the past 20years. In this review, in-depth discussions on the general problem of geriatric infectious diseases (epidemiology, pathogenesis, age-related host defenses, clinical manifestations, diagnostic approach); diagnosis and management of bacterial pneumonia, urinary tract infection, and Clostridium difficile infection; and the unique challenges of diagnosing and managing infections in a long-term care setting are presented.
C1 [Yoshikawa, Thomas T.] Dept Vet Affairs Greater Angeles Healthcare Syst, Los Angeles, CA USA.
[Yoshikawa, Thomas T.] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
[Norman, Dean C.] Dept Vet Affairs San Diego Healthcare Syst, San Diego, CA USA.
[Norman, Dean C.] Univ Calif Los Angeles, Los Angeles, CA USA.
RP Yoshikawa, TT (reprint author), VA Greater Los Angeles Healthcare Syst, 11300 Wilshire Blvd,Bldg 158-GRECC W 11G, Los Angeles, CA 90073 USA.
EM Toyoshikawa@cdrewu.edu
NR 97
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0002-8614
EI 1532-5415
J9 J AM GERIATR SOC
JI J. Am. Geriatr. Soc.
PD MAR
PY 2017
VL 65
IS 3
BP 631
EP 641
DI 10.1111/jgs.14731
PG 11
WC Geriatrics & Gerontology; Gerontology
SC Geriatrics & Gerontology
GA EQ0XQ
UT WOS:000397794300032
PM 28140454
ER
PT J
AU Cochran, G
Gordon, AJ
Lo-Ciganic, WH
Gellad, WF
Frazier, W
Lobo, C
Chang, CCH
Zheng, P
Donohue, JM
AF Cochran, Gerald
Gordon, Adam J.
Lo-Ciganic, Wei-Hsuan
Gellad, Walid F.
Frazier, Winfred
Lobo, Carroline
Chang, Chung-Chou H.
Zheng, Ping
Donohue, Julie M.
TI An Examination of Claims-based Predictors of Overdose from a Large
Medicaid Program
SO MEDICAL CARE
LA English
DT Article
DE opioid medication overdose; health claims; opioid medication misuse and
abuse
ID PRESCRIPTION OPIOID ABUSE; UNITED-STATES; CHRONIC PAIN; PRESCRIBING
PATTERNS; IDENTIFY PATIENTS; RISK; DEATHS; MISUSE; CARE; INTERVENTIONS
AB Background: Health systems may play an important role in identification of patients at-risk of opioid medication overdose. However, standard measures for identifying overdose risk in administrative data do not exist.
Objective: Examine the association between opioid medication overdose and 2 validated measures of nonmedical use of prescription opioids within claims data.
Research Design: A longitudinal retrospective cohort study that estimated associations between overdose and nonmedical use.
Subjects: Adult Pennsylvania Medicaid program 2007-2012 patients initiating opioid treatment who were: nondual eligible, without cancer diagnosis, and not in long-term care facilities or receiving hospice.
Measures: Overdose (International Classification of Disease, ninth edition, prescription opioid poisonings codes), opioid abuse (opioid use disorder diagnosis while possessing an opioid prescription), opioid misuse (a composite indicator of number of opioid prescribers, number of pharmacies, and days supplied), and dose exposure during opioid treatment episodes.
Results: A total of 372,347 Medicaid enrollees with 583,013 new opioid treatment episodes were included in the cohort. Opioid overdose was higher among those with abuse (1.5%) compared with those without (0.2%, P<0.001). Overdose was higher among those with probable (1.8%) and possible (0.9%) misuse compared with those without (0.2%, P<0.001). Abuse [adjusted rate ratio (ARR), 1.52; 95% confidence interval (CI), 1.10-2.10), probable misuse (ARR, 1.98; 95% CI, 1.46-2.67), and possible misuse (ARR, 1.76; 95% CI, 1.48-2.09) were associated with significantly more events of opioid medication overdose compared with those without.
Conclusions: Claims-based measures can be used by health systems to identify individuals at-risk of overdose who can be targeted for restrictions on opioid prescribing, dispensing, or referral to treatment.
C1 [Cochran, Gerald] Univ Pittsburgh, Sch Social Work, 4200 Forbes Ave,2117 CL, Pittsburgh, PA 15260 USA.
[Cochran, Gerald] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA USA.
[Cochran, Gerald; Gordon, Adam J.; Gellad, Walid F.; Donohue, Julie M.] Univ Pittsburgh, Ctr Pharmaceut Policy & Prescribing, Pittsburgh, PA USA.
[Gordon, Adam J.; Gellad, Walid F.] VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Gordon, Adam J.; Gellad, Walid F.; Frazier, Winfred] Univ Pittsburgh, Sch Med, Div Gen Internal Med, Pittsburgh, PA USA.
[Lo-Ciganic, Wei-Hsuan] Univ Arizona, Coll Pharm, Tucson, AZ 85721 USA.
[Lobo, Carroline; Chang, Chung-Chou H.; Zheng, Ping; Donohue, Julie M.] Univ Pittsburgh, Grad Sch Publ Hlth, Pittsburgh, PA USA.
[Chang, Chung-Chou H.] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA.
RP Cochran, G (reprint author), Univ Pittsburgh, Sch Social Work, 4200 Forbes Ave,2117 CL, Pittsburgh, PA 15260 USA.
EM gcochran@pitt.edu
FU Centers for Disease Control and Prevention [U01CE002496]
FX G.C., J.M.D, A.J.G., and W.F.G. are supported by a grant from the
Centers for Disease Control and Prevention (U01CE002496). The remaining
authors declare no conflict of interest.
NR 49
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U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0025-7079
EI 1537-1948
J9 MED CARE
JI Med. Care
PD MAR
PY 2017
VL 55
IS 3
BP 291
EP 298
PG 8
WC Health Care Sciences & Services; Health Policy & Services; Public,
Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EL3GD
UT WOS:000394506700013
PM 27984346
ER
PT J
AU Hernandez-Tejada, MA
Acierno, R
Sanchez-Carracedo, D
AF Hernandez-Tejada, Melba A.
Acierno, Ron
Sanchez-Carracedo, David
TI Addressing Dropout From Prolonged Exposure: Feasibility of Involving
Peers During Exposure Trials
SO MILITARY PSYCHOLOGY
LA English
DT Article
DE PTSD; peer; social support; dropout; Prolonged Exposure therapy
ID POSTTRAUMATIC-STRESS-DISORDER; PTSD TREATMENT; SERVICE; CARE
AB Posttraumatic stress disorder ( PTSD) is a significant problem for combat veterans. Fortunately, effective treatments, such as Prolonged Exposure ( PE), are available and widely disseminated in the Veterans Affairs ( VA) health-care system. Nonetheless, despite well-documented effectiveness, attrition remains high at approximately 30% across evidence-based interventions. Early studies indicated that dropout was largely related to stigma and logistical barriers ( e. g., travel time and cost). However, research demonstrates that eliminating these logistical and stigma-based barriers ( e. g., through home-based telemedicine) has little effect on dropout. We surveyed 82 veterans who dropped out of PE treatment regarding reasons for leaving treatment. Approximately half indicated that in vivo homework assignments caused significant problems, and when asked to consider the possibility of peer support during in vivo exposure assignments, 52% indicated that they would consider returning to treatment with such assistance. In response to this feedback, we constructed an in vivo therapy peer support program wherein peers are directly involved with in vivo exposure exercises. The following brief report presents the rationale for, outline of, and initial feasibility data supporting this program to enhance both return to, and completion of, exposure therapy treatment for PTSD.
C1 [Hernandez-Tejada, Melba A.; Sanchez-Carracedo, David] Univ Autonoma Barcelona, Dept Clin & Hlth Psychol, Barcelona, Spain.
[Hernandez-Tejada, Melba A.; Acierno, Ron] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA.
[Acierno, Ron] Med Univ South Carolina, Coll Nursing, 99 Jonathan Lucas St,MSC160, Charleston, SC 29425 USA.
RP Hernandez-Tejada, MA (reprint author), Med Univ South Carolina, Coll Nursing, 99 Jonathan Lucas St,MSC160, Charleston, SC 29425 USA.
EM hernanma@musc.edu
NR 17
TC 0
Z9 0
U1 1
U2 1
PU AMER PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST NE, WASHINGTON, DC 20002-4242 USA
SN 0899-5605
EI 1532-7876
J9 MIL PSYCHOL
JI Milit. Psychol.
PD MAR
PY 2017
VL 29
IS 2
BP 157
EP 163
DI 10.1037/mil0000137
PG 7
WC Psychology, Multidisciplinary
SC Psychology
GA EN5MR
UT WOS:000396050200006
ER
PT J
AU Rodriguez-Garcia, M
Shen, Z
Barr, FD
Boesch, AW
Ackerman, ME
Kappes, JC
Ochsenbauer, C
Wira, CR
AF Rodriguez-Garcia, M.
Shen, Z.
Barr, F. D.
Boesch, A. W.
Ackerman, M. E.
Kappes, J. C.
Ochsenbauer, C.
Wira, C. R.
TI Dendritic cells from the human female reproductive tract rapidly capture
and respond to HIV
SO MUCOSAL IMMUNOLOGY
LA English
DT Article
ID HUMAN-IMMUNODEFICIENCY-VIRUS; LEUKOCYTE PROTEASE INHIBITOR;
MENSTRUAL-CYCLE; PIGTAIL MACAQUES; LANGERHANS CELLS; EX-VIVO; INFECTION;
SUSCEPTIBILITY; SUBSETS; TYPE-1
AB Dendritic cells (DCs) throughout the female reproductive tract (FRT) were examined for phenotype, HIV capture ability and innate anti-HIV responses. Two main CD11c(+) DC subsets were identified: CD11b(+) and CD11b(low) DCs. CD11b(+)CD14(+) DCs were the most abundant throughout the tract. A majority of CD11c(+)CD14(+) cells corresponded to CD1c(+) myeloid DCs, whereas the rest lacked CD1c and CD163 expression (macrophage marker) and may represent monocyte-derived cells. In addition, we identified CD103(+) DCs, located exclusively in the endometrium, whereas DC-SIGN(+) DCs were broadly distributed throughout the FRT. Following exposure to GFP-labeled HIV particles, CD14(+) DC-SIGN(+) as well as CD14(+) DC-SIGN(-) cells captured virus, with similar to 30% of these cells representing CD1c(+) myeloid DCs. CD103(+) DCs lacked HIV capture ability. Exposure of FRT DCs to HIV induced secretion of CCL2, CCR5 ligands, interleukin (IL)-8, elafin, and secretory leukocyte peptidase inhibitor (SLPI) within 3 h of exposure, whereas classical pro-inflammatory molecules did not change and interferon-alpha 2 and IL-10 were undetectable. Furthermore, elafin and SLPI upregulation, but not CCL5, were suppressed by estradiol pre-treatment. Our results suggest that specific DC subsets in the FRT have the potential for capture and dissemination of HIV, exert antiviral responses and likely contribute to the recruitment of HIV-target cells through the secretion of innate immune molecules.
C1 [Rodriguez-Garcia, M.; Shen, Z.; Barr, F. D.; Wira, C. R.] Geisel Sch Med, Dept Physiol & Neurobiol, Lebanon, NH USA.
[Boesch, A. W.; Ackerman, M. E.] Dartmouth Coll, Thayer Sch Engn, Hanover, NH 03755 USA.
[Kappes, J. C.; Ochsenbauer, C.] Univ Alabama Birmingham, Dept Med, Res Serv Birmingham, Birmingham, AL USA.
[Kappes, J. C.; Ochsenbauer, C.] Univ Alabama Birmingham, UAB Ctr AIDS Res, Birmingham, AL USA.
[Kappes, J. C.] Birmingham Vet Affairs Med Ctr, Res Serv Birmingham, Birmingham, AL USA.
RP Rodriguez-Garcia, M (reprint author), Geisel Sch Med, Dept Physiol & Neurobiol, Lebanon, NH USA.
EM Marta.Rodriguez.Garcia@dartmouth.edu
FU NIH [AI102838, AI117739, CA73479, P30 AI27767]
FX We thank Dr John Fahey and Dr Yina Huang for critical comments and
suggestions. We thank Richard Rossoll for technical assistance and Dr
Rakesh Bakshi for help with preparing HIV-GFP VLPs. We thank the study
participants, Pathologists, Obstetrics, and Gynecology surgeons,
operating room nurses and support personnel at Dartmouth-Hitchcock
Medical Center. Flow cytometric analysis was carried out in DartLab, the
Immunoassay and Flow Cytometry Shared Resource at the Geisel School of
Medicine at Dartmouth. Study supported by NIH grants AI102838 and
AI117739 (CRW), CA73479 (JCK), and P30 AI27767 Birmingham Center for
AIDS Research-Virology Core (CO; JCK)
NR 67
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U1 4
U2 4
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 1933-0219
EI 1935-3456
J9 MUCOSAL IMMUNOL
JI Mucosal Immunol.
PD MAR
PY 2017
VL 10
IS 2
BP 531
EP 544
DI 10.1038/mi.2016.72
PG 14
WC Immunology
SC Immunology
GA EN1ZV
UT WOS:000395810000023
PM 27579858
ER
PT J
AU Chosich, J
Bradford, AP
Allshouse, AA
Reusch, JEB
Santoro, N
Schauer, IE
AF Chosich, Justin
Bradford, Andrew P.
Allshouse, Amanda A.
Reusch, Jane E. B.
Santoro, Nanette
Schauer, Irene E.
TI Acute Recapitulation of the Hyperinsulinemia and Hyperlipidemia
Characteristic of Metabolic Syndrome Suppresses Gonadotropins
SO OBESITY
LA English
DT Article
ID POLYCYSTIC OVARIAN SYNDROME; MUSCLE INSULIN-RESISTANCE; BODY-MASS INDEX;
LUTEINIZING-HORMONE; OBESE WOMEN; MENSTRUAL-CYCLE; LUTEAL-PHASE; INVERSE
RELATIONSHIP; FEMALE MICE; GLUCOSE
AB Objective: To determine the effect of lipid/heparin versus saline infusion, with or without concurrent euglycemic hyperinsulinemia, on serum follicle-stimulating hormone (FSH) and luteinizing hormone (LH). Obesity is associated with hyperlipidemia, insulin resistance, and relative hypogonadotropic hypogonadism. It was hypothesized that acutely elevated fatty acids and insulin would impair gonadotropin secretion.
Methods: Regularly cycling women and men without obesity underwent a crossover 6-hour infusion study over four visits. Participants received infusions of saline-control, lipid/heparin, insulin, and lipid/heparin plus insulin. Serum FSH and LH were measured by immunoassay.
Results: In women (n=10), infusion of lipid plus insulin significantly reduced LH, from 4.6 IU/L (3.7-5.4) ( mean [95% confidence interval]) to 3.3 IU/L (2.3-4.4); P=0.03, and FSH, from 3.9 IU/L (3.2-4.6) to 3.1 IU/L (2.3-3.8); P=0.03, compared to saline-control. Similarly, in men ( n=10), LH, 3.3 IU/L (2.4-4.1), and FSH, 2.1 IU/L (1.4-2.8), were significantly reduced after the combined infusion (2.2 [1.3-3.1] IU/L and 1.5 [0.8-2.1] IU/L; P=0.03, P=0.02, respectively). Neither lipid nor insulin alone significantly impacted gonadotropin levels compared to saline-control.
Conclusions: Hyperinsulinemia combined with elevated lipids acutely suppresses LH and FSH, providing a possible mechanism underlying the relative hypogonadotropic hypogonadism of obesity. Effects of insulin on the hypothalamic-pituitary-gonadal axis may be dependent on the concomitant metabolic environment.
C1 [Chosich, Justin; Bradford, Andrew P.; Santoro, Nanette] Univ Colorado, Sch Med, Dept Obstet & Gynecol, Aurora, CO 80045 USA.
[Allshouse, Amanda A.] Colorado Sch Publ Hlth, Dept Biostat & Informat, Aurora, CO USA.
[Reusch, Jane E. B.; Schauer, Irene E.] Univ Colorado, Sch Med, Dept Med, Div Endocrinol Metab & Diabet, Aurora, CO USA.
[Reusch, Jane E. B.; Schauer, Irene E.] Denver Vet Affairs Med Ctr, Endocrinol Sect, Denver, CO USA.
RP Santoro, N (reprint author), Univ Colorado, Sch Med, Dept Obstet & Gynecol, Aurora, CO 80045 USA.
EM nanette.santoro@ucdenver.edu
FU NIH [U54 HD058155, K23 DK091553, K12 HD057022, TL1 TR001081]
FX This work was supported by NIH grants U54 HD058155 (Jeffrey Pollard,
PI), K23 DK091553 (Irene E. Schauer, PI), K12 HD057022 (Judy
Regensteiner and Nanette Santoro, co-PIs), VA Merit Award (Jane E. B.
Reusch, PI), and TL1 TR001081 (Ron Sokol, PI).
NR 33
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U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1930-7381
EI 1930-739X
J9 OBESITY
JI Obesity
PD MAR
PY 2017
VL 25
IS 3
BP 553
EP 560
DI 10.1002/oby.21754
PG 8
WC Endocrinology & Metabolism; Nutrition & Dietetics
SC Endocrinology & Metabolism; Nutrition & Dietetics
GA EQ4IP
UT WOS:000398040000014
PM 28158916
ER
PT J
AU Hawkins, EJ
Malte, CA
Hagedorn, HJ
Berger, D
Frank, A
Lott, A
Achtmeyer, CE
Mariano, AJ
Saxon, AJ
AF Hawkins, Eric J.
Malte, Carol A.
Hagedorn, Hildi J.
Berger, Douglas
Frank, Anissa
Lott, Aline
Achtmeyer, Carol E.
Mariano, Anthony J.
Saxon, Andrew J.
TI Survey of Primary Care and Mental Health Prescribers' Perspectives on
Reducing Opioid and Benzodiazepine Co-Prescribing Among Veterans
SO PAIN MEDICINE
LA English
DT Article
DE Chronic Pain; Concurrent Opioid and Benzodiazepine Use; Primary Care;
Mental Health; Beliefs; Attitudes; High-Risk Conditions
ID POSTTRAUMATIC-STRESS-DISORDER; CHRONIC PAIN; GENERAL-PRACTITIONERS;
PARIHS FRAMEWORK; PHYSICIANS PERSPECTIVES; OLDER-ADULTS; US VETERANS;
IMPLEMENTATION; ATTITUDES; DOCTORS
AB Background. Due to the involvement of opioids and benzodiazepines in rising pharmaceutical overdoses, a reduction in coprescribing of these medications is a national priority, particularly among patients with substance use disorders and other high-risk conditions. However, little is known about primary care (PC) and mental health (MH) prescribers' perspectives on these medications and efforts being implemented to reduce coprescribing.
Design. An anonymous survey.
Setting. One multisite VA health care system.
Subjects. Participants were 55 PC and 31 MH prescribers.
Methods. Survey development was guided by the Promoting Action on Research Implementation in Health Services (PARIHS) conceptual framework. PC and MH prescribers of opioids or benzodiazepines were invited to complete an anonymous electronic survey. Responses were collapsed to highlight agreement, disagreement, and neutrality and summarized with means and percentages.
Results. Over 80% of both prescriber groups reported concern about concurrent use and > 75% strongly agreed with clinical practice guidelines (CPG) that recommend caution in coprescribing among patients with high-risk conditions. More than 40% of both prescriber groups indicated that coprescribing continues because of beliefs that patients appear stable without adverse events and tapering/discontinuation is too difficult. Over 70% of prescribers rated strategies for addressing patients who refuse to discontinue, more time with patients, and identification of high-risk patients as helpful in reducing coprescribing.
Conclusion. Despite strong agreement with CPGs, prescribers reported several barriers that contribute to coprescribing of opioids and benzodiazepines and challenge their ability to taper these medications. Multiple interventions are likely needed to reduce opioid and benzodiazepine coprescribing.
C1 [Hawkins, Eric J.; Malte, Carol A.; Frank, Anissa; Lott, Aline; Achtmeyer, Carol E.; Saxon, Andrew J.] Seattle Ctr Innovat Veteran Centered & Value Driv, Veteran Affairs VA Puget Sound Hlth Care Syst, HSR&D, Seattle, WA USA.
[Hawkins, Eric J.; Malte, Carol A.; Frank, Anissa; Lott, Aline; Achtmeyer, Carol E.; Saxon, Andrew J.] Ctr Excellence Substance Abuse Treatment & Educ, VA Puget Sound Hlth Care Syst Seattle, Div S116ATC, 1660 S Columbian Way, Seattle, WA 98108 USA.
[Hawkins, Eric J.; Hagedorn, Hildi J.] VA Qual Enhancement Res Initiat Substance Use Dis, Palo Alto, CA USA.
[Hawkins, Eric J.; Mariano, Anthony J.; Saxon, Andrew J.] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Hagedorn, Hildi J.] Minneapolis VA Hlth Care Syst, Minneapolis, MN USA.
[Berger, Douglas; Achtmeyer, Carol E.] Primary & Specialty Med Care Serv, VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Berger, Douglas] Univ Washington, Dept Med, Seattle, WA 98195 USA.
[Mariano, Anthony J.] VA Northwest Vet Integrated Serv Network VISN 20, VA Puget Sound Hlth Care Syst, Seattle, WA USA.
RP Hawkins, EJ (reprint author), Ctr Excellence Substance Abuse Treatment & Educ, VA Puget Sound Hlth Care Syst Seattle, Div S116ATC, 1660 S Columbian Way, Seattle, WA 98108 USA.
EM Eric.Hawkins@va.gov
FU U.S. Department of Veterans Affairs, Veterans Health Administration; VA
Center of Excellence in Substance Abuse Treatment Education; VA Health
Services Research and Development (HSR&D) Quality Enhancement Research
Initiative Rapid Response Project (RRP) [12-527]; Quality Enhancement
Research Initiative for Substance Use Disorders (SUD QUERI)
FX This material is based upon work supported by the U.S. Department of
Veterans Affairs, Veterans Health Administration, the VA Center of
Excellence in Substance Abuse Treatment & Education, the VA Health
Services Research and Development (HSR&D) Quality Enhancement Research
Initiative Rapid Response Project (RRP) # 12-527, and the Quality
Enhancement Research Initiative for Substance Use Disorders (SUD QUERI).
Supporting organizations had no further role in the study design; in the
collection, analysis and interpretation of data; in the writing of the
report; or in the decision to submit the paper for publication.
NR 58
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U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 1526-2375
EI 1526-4637
J9 PAIN MED
JI Pain Med.
PD MAR
PY 2017
VL 18
IS 3
BP 454
EP 467
DI 10.1093/pm/pnw140
PG 14
WC Medicine, General & Internal
SC General & Internal Medicine
GA EP0VE
UT WOS:000397104000009
PM 27558857
ER
PT J
AU Brellenthin, AG
Crombie, KM
Cook, DB
Sehgal, N
Koltyn, KF
AF Brellenthin, Angelique G.
Crombie, Kevin M.
Cook, Dane B.
Sehgal, Nalini
Koltyn, Kelli F.
TI Psychosocial Influences on Exercise-Induced Hypoalgesia
SO PAIN MEDICINE
LA English
DT Article
DE Sex; Family; Psychological; Exercise; Modulation; Catastrophizing
ID CONDITIONED PAIN MODULATION; ISOMETRIC-EXERCISE; SEX-DIFFERENCES;
POSTOPERATIVE PAIN; TEMPORAL SUMMATION; CATASTROPHIZING SCALE;
PSYCHOLOGICAL-FACTORS; QUESTIONNAIRE-III; FAMILY-HISTORY; BLOOD-PRESSURE
AB Objective. The purpose of this study was to examine psychosocial influences on exercise-induced hypoalgesia (EIH).
Design. Randomized controlled trial.
Setting. Clinical research unit in a hospital.
Subjects. Fifty-eight healthy men and women (mean age=21 +/- 3 years) participated in this study.
Methods. Participants were first asked to complete a series of baseline demographic and psychological questionnaires including the Pain Catastrophizing Scale, the Fear of Pain Questionnaire, and the Family Environment Scale. Following this, they were familiarized with both temporal summation of heat pain and pressure pain testing protocols. During their next session, participants completed the Profile of Mood States, rated the intensity of heat pulses, and indicated their pressure pain thresholds and ratings before and after three minutes of submaximal, isometric exercise. Situational catastrophizing was assessed at the end of the experimental session.
Results. Results indicated that experimental pain sensitivity was significantly reduced after exercise (P < 0.05). Men and women did not differ on any of the measured psychosocial variables (P > 0.05). Positive family environments predicted attenuated pain sensitivity and greater EIH, whereas negative and chronic pain-present family environments predicted worse pain and EIH outcomes. Situational catastrophizing and negative mood state also predicted worse pain and EIH outcomes and were additionally associated with increased ratings of perceived exertion and muscle pain during exercise.
Conclusions. This study provides preliminary evidence that psychosocial variables, such as the family environment and mood states, can affect both pain sensitivity and the ability to modulate pain through exercise-induced hypoalgesia.
C1 [Brellenthin, Angelique G.; Crombie, Kevin M.; Cook, Dane B.; Koltyn, Kelli F.] Univ Wisconsin Madison, Dept Kinesiol, Madison, WI USA.
[Sehgal, Nalini] Univ Wisconsin Madison, Dept Rehabil Med, Madison, WI USA.
[Cook, Dane B.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
RP Koltyn, KF (reprint author), Univ Wisconsin, 2000 Observ Dr, Madison, WI 53706 USA.
EM koltyn@education.wisc.edu
FU National Institutes of Health [R21AR057159, 1UL1RR025011]
FX This research was supported by National Institutes of Health grants
R21AR057159 and 1UL1RR025011.
NR 70
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U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 1526-2375
EI 1526-4637
J9 PAIN MED
JI Pain Med.
PD MAR
PY 2017
VL 18
IS 3
BP 538
EP 550
DI 10.1093/pm/pnw275
PG 13
WC Medicine, General & Internal
SC General & Internal Medicine
GA EP0VE
UT WOS:000397104000016
PM 28034985
ER
PT J
AU Glynn, SM
Marder, SR
Noordsy, DL
O'Keefe, C
Becker, DR
Drake, RE
Sugar, CA
AF Glynn, Shirley M.
Marder, Stephen R.
Noordsy, Douglas L.
O'Keefe, Christopher
Becker, Deborah R.
Drake, Robert E.
Sugar, Catherine A.
TI An RCT Evaluating the Effects of Skills Training and Medication Type on
Work Outcomes Among Patients With Schizophrenia
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID RANDOMIZED CONTROLLED-TRIALS; SEVERE MENTAL-ILLNESS; SUPPORTED
EMPLOYMENT; INDIVIDUAL PLACEMENT; WORKPLACE SKILLS; SCALE; MODEL
AB Objective: Although supported employment increases job acquisition for people with serious mental illness, data on participants' job tenure have been variable. This study evaluated the effects of a standardized work skills training program (the Workplace Fundamentals Module [WPFM]) on job tenure and other work outcomes among individuals receiving individual placement and support (IPS). The effects of two atypical antipsychotic medications on side effects were also tested. The primary hypothesis testedwas that participants in IPS plus WPFM would have increased job tenure compared with those enrolled in IPS only, and the secondary hypothesis was that different antipsychoticmedicationswould yield unique side effects.
Methods: A 232 randomized controlled trial compared work outcomes, including job tenure, of participants receiving IPS with or without WPFM for up to two years after obtaining a job. Participants were also randomly assigned to olanzapine or risperidone. Measures of work outcomes, clinical status, and medication side effects were collected.
Results: Among 107 participants, 63% obtained at least one job. WPFM did not increase job tenure (51.53 and 41.37 total weeks worked for IPS only and IPS plus WPFM, respectively) or affect other work outcomes. Participants on olanzapine experienced increased body mass index, whereas those on risperidone lost weight, but medications did not differentially affect clinical or job outcomes.
Conclusions: Clinic-based skills training did not improve work outcomes accruing from IPS. Risperidone, compared with olanzapine, may reduce body mass but has no differential effect on other work or clinical outcomes.
C1 [Glynn, Shirley M.; Marder, Stephen R.] US Dept Vet Affairs, Greater Los Angeles Healthcare Syst, Los Angeles, CA 90073 USA.
[Glynn, Shirley M.; Marder, Stephen R.; Sugar, Catherine A.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA.
[Noordsy, Douglas L.] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA USA.
[O'Keefe, Christopher] Southern New Hampshire Univ, Manchester, NH USA.
[Becker, Deborah R.; Drake, Robert E.] WESTAT Corp, Rockville Inst, Lebanon, NH USA.
[Sugar, Catherine A.] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Biostat, Los Angeles, CA 90024 USA.
[Noordsy, Douglas L.; O'Keefe, Christopher; Becker, Deborah R.; Drake, Robert E.] Dartmouth Coll, Geisel Sch Med, Dept Psychiat, Hanover, NH USA.
[Becker, Deborah R.; Drake, Robert E.] Dartmouth Coll, Geisel Sch Med, Dept Community & Family Med, Hanover, NH USA.
RP Glynn, SM (reprint author), US Dept Vet Affairs, Greater Los Angeles Healthcare Syst, Los Angeles, CA 90073 USA.; Glynn, SM (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA.
EM sglynn@ucla.edu
FU National Institute of Mental Health [5R0MH 041573-15]
FX This research was supported by a National Institute of Mental Health
grant (5R0MH 041573-15) to Dr. Marder. The authors thank the employment
specialists and staff who worked on the project and Jim Mintz, Ph.D.,
and Robert P. Liberman, M.D., for their contributions in the development
of the study.
NR 24
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U1 1
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PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD MAR 1
PY 2017
VL 68
IS 3
BP 271
EP 277
DI 10.1176/appi.ps.201500171
PG 7
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA EP0RB
UT WOS:000397093300012
PM 27799019
ER
PT J
AU Meyer, OL
Sisco, SM
Harvey, D
Zahodne, LB
Glymour, MM
Manly, JJ
Marsiske, M
AF Meyer, Oanh L.
Sisco, Shannon M.
Harvey, Danielle
Zahodne, Laura B.
Glymour, M. Maria
Manly, Jennifer J.
Marsiske, Michael
TI Neighborhood Predictors of Cognitive Training Outcomes and Trajectories
in ACTIVE
SO RESEARCH ON AGING
LA English
DT Article
DE neighborhood; cognition; cognitive training; plasticity; social
determinants
ID OLDER MEXICAN-AMERICANS; SOCIOECONOMIC-STATUS; AFRICAN-AMERICANS; HEALTH
CONSEQUENCES; URBAN NEIGHBORHOOD; ALZHEIMER-DISEASE; ETHNIC PATTERNS;
LATE-LIFE; ADULTS; CONTEXT
AB We examined the influence of neighborhood socioeconomic position (SEP), racial/ethnic composition, and living in a major city on cognitive trajectories and intervention outcomes. Data came from the Advanced Cognitive Training for Independent and Vital Elderly study (N = 2,438). Mixed effects analyses examined the associations between neighborhood variables and memory, reasoning, speed of processing, and everyday cognition, estimating differences in initial gains (potentially related to practice) and long-term rate of change over 10 years. The effect of reasoning training on initial gain was weaker for individuals in a major city. For everyday cognition, there was a stronger initial gain for memory-trained and control participants in areas with more racial/ethnic minorities and for speed-trained and control individuals in higher SEP areas. The racial/ethnic minority effect was no longer significant after adjustment for multiple comparisons. Neighborhood factors may be more important in practice-related improvement than in long-term change.
C1 [Meyer, Oanh L.] Univ Calif Davis, Sch Med, Sacramento, CA 95817 USA.
[Harvey, Danielle] Univ Calif Davis, Sch Med, Div Biostat Publ Hlth Sci, Sacramento, CA 95817 USA.
[Sisco, Shannon M.] US Dept Vet Affairs, Danville, IL USA.
[Zahodne, Laura B.] Columbia Univ, Dept Neurol, Cognit Neurosci Div, New York, NY USA.
[Manly, Jennifer J.] Columbia Univ, Neuropsychol, New York, NY USA.
[Glymour, M. Maria] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA.
[Marsiske, Michael] Univ Florida, Coll Publ Hlth & Hlth Profess, Dept Clin & Hlth Psychol, Gainesville, FL USA.
RP Meyer, OL (reprint author), Univ Calif Davis, Sch Med, Dept Neurol, Alzheimers Dis Ctr, 4860 Y St, Sacramento, CA 95817 USA.
EM olmeyer@ucdavis.edu
FU Advanced Psychometrics Methods in Cognitive Aging Research
[R13AG030995]; National Institutes of Health [P30AG010129, P30AG043097,
UL1 TR 000002]; National Institute on Aging; National Institute of
Nursing Research [U01NR04507, U01NR04508, U01AG14260, U01AG14282,
U01AG14263, U01AG14289, U01AG14276]
FX The author(s) disclosed receipt of the following financial support for
the research, authorship, and/or publication of this article: This work
was supported by the Advanced Psychometrics Methods in Cognitive Aging
Research (R13AG030995) and by National Institutes of Health grants to
the University of California, Davis Alzheimer's Disease Center
(P30AG010129), the Latino Aging Research Resource Center (P30AG043097),
and the Clinical and Translational Science Center (UL1 TR 000002). The
ACTIVE intervention trials were supported by grants from the National
Institute on Aging and the National Institute of Nursing Research to
Hebrew Senior Life (U01NR04507), Indiana University School of Medicine
(U01NR04508), Johns Hopkins University (U01AG14260), New England
Research Institutes (U01AG14282), Pennsylvania State University
(U01AG14263), the University of Alabama at Birmingham (U01AG14289), and
the University of Florida (U01AG14276).
NR 71
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PU SAGE PUBLICATIONS INC
PI THOUSAND OAKS
PA 2455 TELLER RD, THOUSAND OAKS, CA 91320 USA
SN 0164-0275
EI 1552-7573
J9 RES AGING
JI Res. Aging
PD MAR
PY 2017
VL 39
IS 3
BP 443
EP 467
DI 10.1177/0164027515618242
PG 25
WC Gerontology
SC Geriatrics & Gerontology
GA EN7RE
UT WOS:000396199100004
PM 26667987
ER
PT J
AU Ames, D
Tessier, J
Erickson, Z
Meyer, H
Baker, M
Gelberg, H
Arnold, I
Kwan, C
Chamberlin, V
Rosen, J
Shah, C
Hellemann, G
Lewis, M
Nguyen, C
Sachinvala, N
Amrami, B
Pierre, J
AF Ames, Donna
Tessier, Jillian
Erickson, Zachary
Meyer, Hilary
Baker, Matthew
Gelberg, Hollie
Arnold, Irina
Kwan, Crystal
Chamberlin, Valery
Rosen, Jennifer
Shah, Chandresh
Hellemann, Gerhard
Lewis, Melissa
Nguyen, Charles
Sachinvala, Neena
Amrami, Binyamin
Pierre, Joseph
TI THERAPEUTIC LIFESTYLE CHANGES (TLC) FOR ADULTS WITH SERIOUS MENTAL
ILLNESS
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Ames, Donna; Tessier, Jillian; Erickson, Zachary; Meyer, Hilary; Baker, Matthew; Gelberg, Hollie; Arnold, Irina; Kwan, Crystal; Chamberlin, Valery; Shah, Chandresh; Lewis, Melissa; Sachinvala, Neena; Amrami, Binyamin; Pierre, Joseph] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Ames, Donna; Gelberg, Hollie; Chamberlin, Valery; Hellemann, Gerhard; Sachinvala, Neena; Amrami, Binyamin; Pierre, Joseph] Univ Calif Los Angeles, Los Angeles, CA 90024 USA.
[Rosen, Jennifer] VA Northern Calif Healthcare Syst, Martinez, CA USA.
[Rosen, Jennifer] Univ Pacific, Sch Pharm, Stockton, CA 95211 USA.
[Rosen, Jennifer] Univ Southern Calif, Sch Pharm, Los Angeles, CA USA.
[Nguyen, Charles] VA Long Beach Healthcare Syst, Long Beach, CA USA.
[Amrami, Binyamin] Western Univ Hlth Sci, Pomona, CA USA.
FU US Department of Veterans Affairs Rehabilitation Research and
Development Merit Review Award
FX Research supported by US Department of Veterans Affairs Rehabilitation
Research and Development Merit Review Award.
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
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PY 2017
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GA EP1DS
UT WOS:000397126200581
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PT J
AU Buck, K
Leonhardt, B
George, S
James, A
Vohs, J
Lysaker, P
AF Buck, Kelly
Leonhardt, Bethany
George, Sunita
James, Alison
Vohs, Jenifer
Lysaker, Paul
TI METACOGNITIVE DEFICITS IN SCHIZOPHRENIA; COMPARISONS WITH BORDERLINE
PERSONALITY DISORDER AND SUBSTANCE USE DISORDER
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Buck, Kelly] VA Med Ctr, Indianapolis, IN USA.
[Leonhardt, Bethany; Vohs, Jenifer; Lysaker, Paul] Indiana Univ Sch Med, Indianapolis, IN 46202 USA.
[George, Sunita] Univ Indianapolis, Indianapolis, IN 46227 USA.
[James, Alison] San Francisco VA Med Ctr, San Francisco, CA USA.
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PU OXFORD UNIV PRESS
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J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA M42
BP S226
EP S226
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200608
ER
PT J
AU Dunn, W
Wynn, JK
Rassovsky, Y
Wu, A
Iacoboni, M
Hellemann, G
Green, MF
AF Dunn, Walter
Wynn, Jonathan K.
Rassovsky, Yuri
Wu, Allan
Iacoboni, Marco
Hellemann, Gerhard
Green, Michael F.
TI THE EFFECT OF BILATERAL TRANSCRANIAL DIRECT CURRENT STIMULATION ON TONE
MATCHING TASK PERFORMANCE AND MISMATCH NEGATIVITY IN SCHIZOPHRENIA
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 Univ Calif Los Angeles, VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Wynn, Jonathan K.] VISN 22 MIRECC, VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Wynn, Jonathan K.] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA.
[Rassovsky, Yuri] Bar Ilan Univ, Gonda Multidisciplinary Brain Res Ctr, Ramat Gan, Israel.
[Wu, Allan; Iacoboni, Marco; Hellemann, Gerhard; Green, Michael F.] Univ Calif Los Angeles, Los Angeles, CA 90024 USA.
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
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J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA SU103
BP S198
EP S198
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200535
ER
PT J
AU Ferri, J
Fryer, S
Roach, BJ
Loewy, R
Ford, JM
Mathalon, D
AF Ferri, Jamie
Fryer, Susanna
Roach, Brian J.
Loewy, Rachel
Ford, Judith M.
Mathalon, Daniel
TI THALAMIC DYSCONNECTIVITY IN INDIVIDUALS AT CLINICALLY HIGH RISK FOR
SCHIZOPHRENIA AND DURING EARLY ILLNESS
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Ferri, Jamie; Fryer, Susanna; Roach, Brian J.; Loewy, Rachel; Ford, Judith M.; Mathalon, Daniel] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Loewy, Rachel] San Francisco VA Med Ctr, San Francisco, CA USA.
NR 0
TC 0
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U1 0
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA 77
BP S44
EP S44
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200118
ER
PT J
AU Fryer, S
Townsend, JD
Ford, JM
Roach, BJ
Calhoun, VD
Pearlson, GD
Kiehl, KA
Srihari, VH
Woods, SW
McGlashan, TH
Mathalon, DH
AF Fryer, Susanna
Townsend, Jennifer D.
Ford, Judith M.
Roach, Brian J.
Calhoun, Vince D.
Pearlson, Godfrey D.
Kiehl, Kent A.
Srihari, Vinod H.
Woods, Scott W.
McGlashan, Thomas H.
Mathalon, Daniel H.
TI FMRI RESPONSE DURING ERROR PROCESSING IN CLINICAL HIGH RISK AND EARLY
ILLNESS SCHIZOPHRENIA
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Fryer, Susanna; Townsend, Jennifer D.; Ford, Judith M.; Roach, Brian J.; Mathalon, Daniel H.] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Townsend, Jennifer D.; Ford, Judith M.; Mathalon, Daniel H.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Calhoun, Vince D.; Kiehl, Kent A.] Mind Res Network, Daytona Beach, FL USA.
[Calhoun, Vince D.; Kiehl, Kent A.] Univ New Mexico, Albuquerque, NM 87131 USA.
[Pearlson, Godfrey D.] Yale Univ, Inst Living, Olin Neuropsychiat Res Ctr, New Haven, CT 06520 USA.
[Srihari, Vinod H.; Woods, Scott W.; McGlashan, Thomas H.] Yale Univ, Sch Med, New Haven, CT 06520 USA.
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA 76
BP S43
EP S44
PG 2
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200117
ER
PT J
AU Gelberg, H
Erickson, Z
Kwan, C
Arnold, I
Chamberlin, V
Rosen, J
Shah, C
Nguyen, C
Hellemann, G
Aragaki, D
Kunkel, C
Lewis, M
Sachinvala, N
Sonza, P
Baker, M
Mena, S
Meyer, H
Tessier, J
Pierre, J
Ames, D
AF Gelberg, Hollie
Erickson, Zachary
Kwan, Crystal
Arnold, Irina
Chamberlin, Valery
Rosen, Jennifer
Shah, Chandresh
Nguyen, Charles
Hellemann, Gerhard
Aragaki, Dixie
Kunkel, Charles
Lewis, Melissa
Sachinvala, Neena
Sonza, Patrick
Baker, Matthew
Mena, Shirley
Meyer, Hilary
Tessier, Jillian
Pierre, Joseph
Ames, Donna
TI BEHAVIORAL INTERVENTIONS FOR ANTIPSYCHOTIC MEDICATION-ASSOCIATED
OBESITY: A RANDOMIZED, CONTROLLED FOUR-SITE TRIAL
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Gelberg, Hollie; Erickson, Zachary; Kwan, Crystal; Arnold, Irina; Chamberlin, Valery; Shah, Chandresh; Aragaki, Dixie; Kunkel, Charles; Lewis, Melissa; Sachinvala, Neena; Sonza, Patrick; Baker, Matthew; Mena, Shirley; Meyer, Hilary; Tessier, Jillian; Pierre, Joseph; Ames, Donna] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Gelberg, Hollie; Chamberlin, Valery; Hellemann, Gerhard; Aragaki, Dixie; Kunkel, Charles; Sachinvala, Neena; Sonza, Patrick; Pierre, Joseph; Ames, Donna] Univ Calif Los Angeles, Los Angeles, CA 90024 USA.
[Rosen, Jennifer] VA Northern Calif Healthcare Syst, Mather, CA USA.
[Rosen, Jennifer] Univ Pacific, Sch Pharm, Stockton, CA 95211 USA.
[Rosen, Jennifer] Univ Southern Calif, Sch Pharm, Los Angeles, CA USA.
[Nguyen, Charles] VA Long Beach Healthcare Syst, Long Beach, CA USA.
FU US Department of Veterans Affairs Rehabilitation Research and
Development Merit Review Award
FX Research supported by US Department of Veterans Affairs Rehabilitation
Research and Development Merit Review Award.
NR 0
TC 0
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA SA15
BP S118
EP S118
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200319
ER
PT J
AU Greenberg, J
Wynn, JK
Lee, JH
Hellemann, G
Green, MF
AF Greenberg, Jared
Wynn, Jonathan K.
Lee, Junghee
Hellemann, Gerhard
Green, Michael F.
TI RESILIENCE IN HOMELESS VETERANS WITH AND WITHOUT A HISTORY OF PSYCHOSIS
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Greenberg, Jared] VA Greater Los Angeles Healthcare Syst VISN 22 MI, Los Angeles, CA USA.
[Wynn, Jonathan K.; Green, Michael F.] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Lee, Junghee] Univ Calif Los Angeles, Los Angeles, CA USA.
[Hellemann, Gerhard; Green, Michael F.] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA.
NR 1
TC 0
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PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
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J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA 95
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EP S51
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200136
ER
PT J
AU Horton, L
Haas, G
Stepp, S
AF Horton, Leslie
Haas, Gretchen
Stepp, Stephanie
TI CHILDHOOD SOCIAL AND EMOTIONAL FUNCTIONING DEFICITS IN A COMMUNITY
SAMPLE OF WOMEN WITH PSYCHOSIS
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Horton, Leslie] Univ Pittsburgh, Pittsburgh, PA 15260 USA.
[Haas, Gretchen] VA Pittsburgh Healthcare Syst, Med Res Serv, Pittsburgh, PA USA.
[Haas, Gretchen; Stepp, Stephanie] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15260 USA.
NR 0
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA M7
BP S213
EP S213
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200574
ER
PT J
AU Jacob, M
Ford, J
Roach, B
Calhoun, V
Mathalon, D
AF Jacob, Michael
Ford, Judith
Roach, Brian
Calhoun, Vince
Mathalon, Daniel
TI SEMANTIC PRIMING ABNORMALITIES IN SCHIZOPHRENIA: AN ERP-FMRI FUSION
STUDY
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Jacob, Michael; Ford, Judith; Mathalon, Daniel] UCSF, San Francisco, CA USA.
[Jacob, Michael; Ford, Judith; Mathalon, Daniel] San Francisco VA Med Ctr, San Francisco, CA USA.
[Roach, Brian] SFVAMC, San Francisco, CA USA.
[Calhoun, Vince] Univ New Mexico, Mind Res Network, Albuquerque, NM 87131 USA.
NR 0
TC 0
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
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J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA 145
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PG 2
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200206
ER
PT J
AU Jahshan, C
Wynn, JK
Dolinsky, M
Mathalon, D
Green, MF
AF Jahshan, Carol
Wynn, Jonathan K.
Dolinsky, Michelle
Mathalon, Daniel
Green, Michael F.
TI COGNITIVE CORRELATES OF VISUAL CORTICAL PLASTICITY IN SCHIZOPHRENIA
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Jahshan, Carol] Univ Calif Los Angeles, VA Greater Los Angeles Healthcare Syst, Los Angeles, CA 90024 USA.
[Wynn, Jonathan K.] VA Greater Los Angeles Healthcare Syst, VISN MIRECC 22, Los Angeles, CA USA.
[Dolinsky, Michelle] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Mathalon, Daniel] UCSF, San Francisco, CA USA.
[Mathalon, Daniel] SFVAMC, San Francisco, CA USA.
[Green, Michael F.] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA.
NR 0
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
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J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA SA70
BP S138
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PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200374
ER
PT J
AU James, A
Johannesen, J
Buck, K
Lysaker, P
AF James, Alison
Johannesen, Jason
Buck, Kelly
Lysaker, Paul
TI RELATIVELY MORE INTACT LEVELS OF SOCIAL COGNITION PREDICT FEWER
IMPAIRMENTS IN NEUROCOGNITION, METACOGNITION, AND HEALTHIER PERSONALITY
FUNCTIONING IN A SAMPLE WITH PROLONGED SCHIZOPHRENIA
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [James, Alison] UCSF, San Francisco, CA USA.
[James, Alison] San Francisco VA Med Ctr, San Francisco, CA USA.
[Johannesen, Jason] Yale Univ, New Haven, CT 06520 USA.
[Buck, Kelly; Lysaker, Paul] Roudebush VA Med Ctr, Indianapolis, IN USA.
[Lysaker, Paul] Indiana Univ Sch Med, Indianapolis, IN 46202 USA.
NR 0
TC 0
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
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J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA M121
BP S254
EP S255
PG 2
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200683
ER
PT J
AU Jimenez, A
Lee, JH
Wynn, JK
Horan, W
Iglesias, J
Hoy, J
Green, MF
AF Jimenez, Amy
Lee, Junghee
Wynn, Jonathan K.
Horan, William
Iglesias, Julio
Hoy, Jennifer
Green, Michael F.
TI THE ROLE OF PREFRONTAL CORTEX IN SELF-REFERENTIAL MEMORY RETRIEVAL IN
SCHIZOPHRENIA
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Jimenez, Amy] VA Greater Los Angeles Healthcare Syst Univ Calif, Los Angeles, CA USA.
[Lee, Junghee; Iglesias, Julio] Univ Calif Los Angeles, Los Angeles, CA USA.
[Wynn, Jonathan K.; Green, Michael F.] Univ Calif Los Angeles, VA Greater Los Angeles Healthcare Syst, Semel Inst Neurosci & Human Behav, Los Angeles, CA USA.
[Horan, William] Univ Calif Los Angeles, Semel Inst, Los Angeles, CA USA.
[Hoy, Jennifer] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA 56
BP S29
EP S29
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200077
ER
PT J
AU McCleery, A
Wynn, JK
Reavis, E
Kutasevich, E
Morales, J
Roach, BJ
Mathalon, D
Green, MF
AF McCleery, Amanda
Wynn, Jonathan K.
Reavis, Eric
Kutasevich, Eugene
Morales, Jaime
Roach, Brian J.
Mathalon, Daniel
Green, Michael F.
TI CORTICAL PLASTICITY IN SCHIZOPHRENIA: ASSOCIATIONS WITH COGNITION AND
COMMUNITY FUNCTIONING
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [McCleery, Amanda; Wynn, Jonathan K.; Reavis, Eric; Kutasevich, Eugene; Morales, Jaime; Green, Michael F.] Univ Calif Los Angeles, Los Angeles, CA USA.
[Roach, Brian J.; Mathalon, Daniel] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Mathalon, Daniel] San Francisco VA Med Ctr, San Francisco, CA USA.
FU VA Desert Pacific VISN 22 Mental Illness Research, Education, and
Clinical Center Pala grant; NIMH Career Development Award [K23MH108829]
FX This research was supported by a VA Desert Pacific VISN 22 Mental
Illness Research, Education, and Clinical Center Pala grant (PI:
McCleery). Dr. McCleery is supported by a NIMH Career Development Award
(K23MH108829).
NR 0
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA M72
BP S236
EP S236
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200635
ER
PT J
AU Ramsay, I
Fryer, S
Boos, A
Roach, BJ
Fisher, M
Loewy, R
Vinogradov, S
Mathalon, D
AF Ramsay, Ian
Fryer, Susanna
Boos, Alison
Roach, Brian J.
Fisher, Melissa
Loewy, Rachel
Vinogradov, Sophia
Mathalon, Daniel
TI TARGETED COGNITIVE TRAINING IS NEUROPROTECTIVE AGAINST THALAMIC VOLUME
LOSS IN EARLY SCHIZOPHRENIA
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Ramsay, Ian; Fisher, Melissa; Vinogradov, Sophia] Univ Minnesota, Minneapolis, MN 55455 USA.
[Fryer, Susanna; Roach, Brian J.; Loewy, Rachel; Mathalon, Daniel] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Boos, Alison] San Francisco VA Med Ctr, San Francisco, CA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA 90
BP S49
EP S49
PG 1
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200131
ER
PT J
AU Wynn, J
McCleery, A
Szewczyk, W
Kutasevich, E
Roach, BJ
Mathalon, D
Green, MF
AF Wynn, Jonathan
McCleery, Amanda
Szewczyk, Warren
Kutasevich, Eugene
Roach, Brian J.
Mathalon, Daniel
Green, Michael F.
TI DYSFUNCTIONAL PREDICTION ERROR CODING IN SCHIZOPHRENIA: TEST-RETEST
RELIABILITY OF AUDITORY MISMATCH NEGATIVITY AND REPETITION POSITIVITY
SO SCHIZOPHRENIA BULLETIN
LA English
DT Meeting Abstract
CT 16th International Congress on Schizophrenia Research (ICOSR)
CY MAR 24-28, 2017
CL San Diego, CA
SP Univ Maryland, Sch Med, Maryland Psychiat Res Ctr, Oxford Univ Press
C1 [Wynn, Jonathan] Univ Calif Los Angeles, VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[McCleery, Amanda; Szewczyk, Warren; Kutasevich, Eugene; Green, Michael F.] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA.
[Roach, Brian J.; Mathalon, Daniel] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Mathalon, Daniel] San Francisco VA Med Ctr, San Francisco, CA USA.
[Green, Michael F.] VA Greater Los Angeles Healthcare Syst, VISN MIRECC 22, Los Angeles, CA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
SU 1
MA SA68
BP S137
EP S138
PG 2
WC Psychiatry
SC Psychiatry
GA EP1DS
UT WOS:000397126200372
ER
PT J
AU Pop-Vicas, A
Musuuza, JS
Schmitz, M
Al-Niaimi, A
Safdar, N
AF Pop-Vicas, Aurora
Musuuza, Jackson S.
Schmitz, Michelle
Al-Niaimi, Ahmed
Safdar, Nasia
TI Incidence and risk factors for surgical site infection post-hysterectomy
in a tertiary care center
SO AMERICAN JOURNAL OF INFECTION CONTROL
LA English
DT Article
DE Post-surgical infection; Predictors
ID IMPROVEMENT PROJECT; ANTIMICROBIAL-PROPHYLAXIS; WOUND INFECTIONS;
UNITED-STATES; SURGERY; DURATION; CEFAZOLIN; COSTS; RATES; SSI
AB Background: Preoperative antibiotic prophylaxis and surgical technological advances have greatly reduced, but not totally eliminated surgical site infection (SSI) posthysterectomy. We aimed to identify risk factors for SSI posthysterectomy among women with a high prevalence of gynecologic malignancies, in a tertiary care setting where compliance with the Joint Commission's Surgical Care Improvement Project core measures is excellent.
Methods: The study was a matched case-control, 2 controls per case, matched on date of surgery. Study time was January 2, 2012-December 31, 2015. Procedures included abdominal and vaginal hysterectomies (open, laparoscopic, and robotic). SSI (superficial incisional or deep/organ/space) was defined as within 30 days postoperatively, per Centers for Disease Control and Prevention criteria. Statistical analysis included bivariate analysis and conditional logistic regression controlling for demographic and clinical variables, both patient-related and surgery-related, including detailed prophylactic antibiotic exposure.
Results: Of the total 1,531 hysterectomies performed, we identified 52 SSIs (3%), with 60% being deep incisional or organ/space infections. All case patients received appropriate preoperative antibiotics (timing, choice, and weight-based dosing). Bivariate analysis showed that higher median weight, higher median Charlson comorbidity index, immune suppressed state, American Society of Anesthesiologists score >= 3, prior surgery within 60 days, clindamycin/gentamicin prophylaxis, surgery involving the omentum or gastrointestinal tract, longer surgery duration, >= 4 surgeons present in the operating room, higher median blood loss, >= 7 catheters or invasive devices in the operating room, and higher median length of hospital stay increased SSI risk (P <.05 for all). Cefazolin preoperative prophylaxis, robot-assisted surgery, and laparoscopic surgery were protective (P <.05 for all). Duration of surgery was the only independent risk factor for SSI identified on multivariate analysis (odds ratio, 3.45; 95% confidence interval, 1.21-9.76; P =.02).
Conclusions: In our population of women with multimorbidity and hysterectomies largely due to underlying gynecologic malignancies, duration of surgery, presumed a marker of surgical complexity, is a significant SSI risk factor. The choice of preoperative antibiotic did not alter SSI risk in our study. (C) 2017 Association for Professionals in Infection Control and Epidemiology, Inc. Published by Elsevier Inc. All rights reserved.
C1 [Pop-Vicas, Aurora; Safdar, Nasia] Univ Wisconsin, Sch Med & Publ Hlth, Dept Med, Madison, WI USA.
[Musuuza, Jackson S.] Univ Wisconsin, Inst Clin & Translat Res, Madison, WI USA.
[Schmitz, Michelle; Safdar, Nasia] Univ Wisconsin Hosp & Clin, Dept Infect Control, Madison, WI 53792 USA.
[Al-Niaimi, Ahmed] Univ Wisconsin, Dept Obstet & Gynecol, Sch Med & Publ Hlth, Madison, WI 53706 USA.
[Safdar, Nasia] William S Middleton Mem Vet Adm Med Ctr, Dept Med, Madison, WI USA.
RP Pop-Vicas, A (reprint author), Univ Wisconsin, Sch Med & Publ Hlth, Div Infect Dis, 1685 Highland Ave,5th Fl, Madison, WI 53705 USA.
EM popvicas@medicine.wisc.edu
NR 31
TC 0
Z9 0
U1 1
U2 1
PU MOSBY-ELSEVIER
PI NEW YORK
PA 360 PARK AVENUE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0196-6553
EI 1527-3296
J9 AM J INFECT CONTROL
JI Am. J. Infect. Control
PD MAR 1
PY 2017
VL 45
IS 3
BP 284
EP 287
DI 10.1016/j.ajic.2016.10.008
PG 4
WC Public, Environmental & Occupational Health; Infectious Diseases
SC Public, Environmental & Occupational Health; Infectious Diseases
GA EQ4KU
UT WOS:000398046700013
PM 27938988
ER
PT J
AU Haefeli, J
Mabray, MC
Whetstone, WD
Dhall, SS
Pan, JZ
Upadhyayula, P
Manley, GT
Bresnahan, JC
Beattie, MS
Ferguson, AR
Talbott, JF
AF Haefeli, J.
Mabray, M. C.
Whetstone, W. D.
Dhall, S. S.
Pan, J. Z.
Upadhyayula, P.
Manley, G. T.
Bresnahan, J. C.
Beattie, M. S.
Ferguson, A. R.
Talbott, J. F.
TI Multivariate Analysis of MRI Biomarkers for Predicting Neurologic
Impairment in Cervical Spinal Cord Injury
SO AMERICAN JOURNAL OF NEURORADIOLOGY
LA English
DT Article
ID PRINCIPAL-COMPONENTS-ANALYSIS; OPTIMAL RADIOLOGIC METHOD; CANAL
COMPROMISE; REPRODUCIBLE METHOD; COMPRESSION; SEVERITY; RECOVERY;
TRAUMA; RELIABILITY; DAMAGE
AB BACKGROUND AND PURPOSE: Acute markers of spinal cord injury are essential for both diagnostic and prognostic purposes. The goal of this study was to assess the relationship between early MR imaging biomarkers after acute cervical spinal cord injury and to evaluate their predictive validity of neurologic impairment.
MATERIALS AND METHODS: We performed a retrospective cohort study of 95 patients with acute spinal cord injury and preoperative MR imaging within 24 hours of injury. The American Spinal Injury Association Impairment Scale was used as our primary outcome measure to define neurologic impairment. We assessed several MR imaging features of injury, including axial grade (Brain and Spinal Injury Center score), sagittal grade, length of injury, maximum canal compromise, and maximum spinal cord compression. Data-driven nonlinear principal component analysis was followed by correlation and optimal-scaled multiple variable regression to predict neurologic impairment.
RESULTS: Nonlinear principal component analysis identified 2 clusters of MR imaging variables related to 1) measures of intrinsic cord signal abnormality and 2) measures of extrinsic cord compression. Neurologic impairment was best accounted for by MR imaging measures of intrinsic cord signal abnormality, with axial grade representing the most accurate predictor of short-term impairment, even when correcting for surgical decompression and degree of cord compression.
CONCLUSIONS: This study demonstrates the utility of applying nonlinear principal component analysis for defining the relationship between MR imaging biomarkers in a complex clinical syndrome of cervical spinal cord injury. Of the assessed imaging biomarkers, the intrinsic measures of cord signal abnormality were most predictive of neurologic impairment in acute spinal cord injury, highlighting the value of axial T2 MR imaging.
C1 [Haefeli, J.; Dhall, S. S.; Upadhyayula, P.; Manley, G. T.; Bresnahan, J. C.; Beattie, M. S.; Ferguson, A. R.] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA USA.
[Mabray, M. C.; Talbott, J. F.] Univ Calif San Francisco, Dept Radiol & Biomed Imaging, San Francisco, CA 94143 USA.
[Whetstone, W. D.] Univ Calif San Francisco, Dept Emergency Med, San Francisco, CA 94143 USA.
[Pan, J. Z.] Univ Calif San Francisco, Dept Anesthesia & Perioperat Care, San Francisco, CA 94143 USA.
Zuckerberg San Francisco Gen Hosp, San Francisco, CA USA.
[Haefeli, J.; Whetstone, W. D.; Dhall, S. S.; Pan, J. Z.; Upadhyayula, P.; Manley, G. T.; Bresnahan, J. C.; Beattie, M. S.; Ferguson, A. R.; Talbott, J. F.] San Francisco VA Med Ctr, Brain & Spinal Injury Ctr, Weill Inst Neurosci, San Francisco, CA USA.
RP Ferguson, AR (reprint author), Zuckerberg San Francisco Gen Hosp, Dept Neurol Surg, Bldg 1,Room 101, San Francisco, CA 94110 USA.
EM adam.ferguson@ucsf.edu
FU Craig H. Neilsen Foundation; Wings for Life Foundation; Department of
Defense [SC120259]; National Institutes of Health T32 Fellowship
[5T32EB001631-10]; Craig H. Neilsen Foundation fellowship [313739];
[R01NS067092]; [R01NS088475]
FX This work was supported by R01NS067092 (A.R.F.), R01NS088475 (A.R.F.),
the Craig H. Neilsen Foundation (A.R.F., J.C.B.), Wings for Life
Foundation (A.R.F.), and Department of Defense grant SC120259 (M.S.B.,
J.C.B.). M.C.M. was supported by a National Institutes of Health T32
Fellowship, 5T32EB001631-10. J.H. was supported by a Craig H. Neilsen
Foundation fellowship (313739).
NR 42
TC 0
Z9 0
U1 0
U2 0
PU AMER SOC NEURORADIOLOGY
PI DENVILLE
PA PO BOX 3000, DENVILLE, NJ 07834-9349 USA
SN 0195-6108
EI 1936-959X
J9 AM J NEURORADIOL
JI Am. J. Neuroradiol.
PD MAR
PY 2017
VL 38
IS 3
BP 648
EP 655
DI 10.3174/ajnr.A5021
PG 8
WC Clinical Neurology; Neuroimaging; Radiology, Nuclear Medicine & Medical
Imaging
SC Neurosciences & Neurology; Radiology, Nuclear Medicine & Medical Imaging
GA EN6JB
UT WOS:000396109200040
PM 28007771
ER
PT J
AU Russell-Puleri, S
dela Paz, NG
Adams, D
Chattopadhyay, M
Cancel, L
Ebong, E
Orr, AW
Frangos, JA
Tarbell, JM
AF Russell-Puleri, Sparkle
dela Paz, Nathaniel G.
Adams, Diana
Chattopadhyay, Mitali
Cancel, Limary
Ebong, Eno
Orr, A. Wayne
Frangos, John A.
Tarbell, John M.
TI Fluid shear stress induces upregulation of COX-2 and PGI(2) release in
endothelial cells via a pathway involving PECAM-1, PI3K, FAK, and p38
SO AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
LA English
DT Article
DE prostaglandin I-2; cyclooxygenase-2; PECAM-1; integrins; shear stress;
glycocalyx; syndecan-4; primary cilia
ID FOCAL ADHESION KINASE; HEPARAN-SULFATE PROTEOGLYCAN; GENE-EXPRESSION;
CYCLOOXYGENASE-2 EXPRESSION; EXTRACELLULAR-MATRIX; SIGNAL-TRANSDUCTION;
HEMODYNAMIC FORCES; IN-VIVO; PROSTACYCLIN; INTEGRIN
AB Vascular endothelial cells play an important role in the regulation of vascular function in response to mechanical stimuli in both healthy and diseased states. Prostaglandin I-2 (PGI(2)) is an important antiatherogenic prostanoid and vasodilator produced in endothelial cells through the action of the cyclooxygenase (COX) isoenzymes COX-1 and COX-2. However, the mechanisms involved in sustained, shear-induced production of COX-2 and PGI(2) have not been elucidated but are determined in the present study. We used cultured endothelial cells exposed to steady fluid shear stress (FSS) of 10 dyn/cm(2) for 5 h to examine shear stress-induced induction of COX-2/PGI(2). Our results demonstrate the relationship between the mechanosensor platelet endothelial cell adhesion molecule-1 (PECAM-1) and the intracellular mechanoresponsive molecules phosphatidylinositol 3-kinase (PI3K), focal adhesion kinase (FAK), and mitogen-activated protein kinase p38 in the FSS induction of COX-2 expression and PGI2 release. Knockdown of PECAM-1 (small interference RNA) expression inhibited FSS-induced activation of alpha(5)beta(1)-integrin, upregulation of COX-2, and release of PGI(2) in both bovine aortic endothelial cells (BAECs) and human umbilical vein endothelial cells (HUVECs). Furthermore, inhibition of the PI3K pathway (LY294002) substantially inhibited FSS activation of alpha(5)beta(1)-integrin, upregulation of COX-2 gene and protein expression, and release of PGI(2) in BAECs. Inhibition of integrin-associated FAK (PF573228) and MAPK p38 (SB203580) also inhibited the shear-induced upregulation of COX-2. Finally, a PECAM-1(-/-) mouse model was characterized by reduced COX-2 immunostaining in the aorta and reduced plasma PGI(2) levels compared with wild-type mice, as well as complete inhibition of acute flow-induced PGI(2) release compared with wild-type animals.
NEW & NOTEWORTHY In this study we determined the major mechanotransduction pathway by which blood flow-driven shear stress activates cyclooxygenase-2 (COX-2) and prostaglandin I-2 (PGI(2)) release in endothelial cells. Our work has demonstrated for the first time that COX-2/PGI(2) mechanotransduction is mediated by the mechanosensor platelet endothelial cell adhesion molecule- 1 (PECAM-1).
C1 [Russell-Puleri, Sparkle; Cancel, Limary; Tarbell, John M.] CUNY City Coll, Dept Biomed Engn, Steinman Hall,Rm T-404B Convent Ave,140th St, New York, NY 10031 USA.
[dela Paz, Nathaniel G.; Adams, Diana; Frangos, John A.] La Jolla Bioengn Inst, La Jolla, CA USA.
[Chattopadhyay, Mitali] James J Peters Veteran Affairs Med Ctr, Bronx, NY USA.
[Ebong, Eno] Northeastern Univ, Dept Chem Engn, Boston, MA USA.
[Orr, A. Wayne] Louisiana State Univ, Dept Pathol, Shreveport, LA USA.
RP Tarbell, JM (reprint author), CUNY City Coll, Dept Biomed Engn, Steinman Hall,Rm T-404B Convent Ave,140th St, New York, NY 10031 USA.
EM jtarbell@ccny.cuny.edu
FU National Institutes of Health Research Supplement to Promote Diversity
in Health Related Research [PA-08-190]; National Heart, Lung, and Blood
Institute [R01-HL-094889, R37-HL-040696, R01-HL-098435, R01 HL133497]
FX This work was supported by the National Institutes of Health Research
Supplement to Promote Diversity in Health Related Research Grant
PA-08-190 (to S. Russell-Puleri) and the National Heart, Lung, and Blood
Institute Grants R01-HL-094889 (to J. M. Tarbell), MERIT Award
R37-HL-040696 (to J. A. Frangos), and R01-HL-098435 and R01 HL133497 (to
A. W. Orr).
NR 66
TC 0
Z9 0
U1 0
U2 0
PU AMER PHYSIOLOGICAL SOC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 0363-6135
EI 1522-1539
J9 AM J PHYSIOL-HEART C
JI Am. J. Physiol.-Heart Circul. Physiol.
PD MAR
PY 2017
VL 312
IS 3
BP H485
EP H500
DI 10.1152/ajpheart.00035.2016
PG 16
WC Cardiac & Cardiovascular Systems; Physiology; Peripheral Vascular
Disease
SC Cardiovascular System & Cardiology; Physiology
GA EQ1DC
UT WOS:000397808500015
PM 28011582
ER
PT J
AU Tanner, NT
Pastis, NJ
AF Tanner, Nichole T.
Pastis, Nicholas J.
TI Chronic Obstructive Pulmonary Disease as a Lung Cancer Risk: Worth Its
Weight in "GOLD"
SO ANNALS OF THE AMERICAN THORACIC SOCIETY
LA English
DT Editorial Material
C1 [Tanner, Nichole T.; Pastis, Nicholas J.] Med Univ South Carolina, Charleston, SC 29425 USA.
[Tanner, Nichole T.] Ralph H Johnson Vet Affairs Hosp, Charleston, SC USA.
RP Pastis, NJ (reprint author), Med Univ South Carolina Med, 96 Jonathan Lucas St,MSC 630, Charleston, SC 29425 USA.
EM pastisn@musc.edu
NR 0
TC 0
Z9 0
U1 0
U2 0
PU AMER THORACIC SOC
PI NEW YORK
PA 25 BROADWAY, 18 FL, NEW YORK, NY 10004 USA
SN 1546-3222
EI 2325-6621
J9 ANN AM THORAC SOC
JI Ann. Am. Thoracic Society
PD MAR
PY 2017
VL 14
IS 3
BP 309
EP 310
DI 10.1513/AnnalsATS.201701-008ED
PG 2
WC Respiratory System
SC Respiratory System
GA EP5PE
UT WOS:000397430100003
PM 28248590
ER
PT J
AU Horner, MD
Turner, TH
VanKirk, KK
Denning, JH
AF Horner, Michael David
Turner, Travis H.
VanKirk, Kathryn K.
Denning, John H.
TI An Intervention to Decrease the Occurrence of Invalid Data on
Neuropsychological Evaluation
SO ARCHIVES OF CLINICAL NEUROPSYCHOLOGY
LA English
DT Article
DE Neuropsychology; Neuropsychological assessment; Effort; Malingering;
Test performance; Behavioral economics
ID INADEQUATE EFFORT; COLLEGE SAMPLES; VALIDITY; PERFORMANCE; EXAGGERATION;
MALINGERERS; DETERRENCE; MILITARY; BELIEFS; INJURY
AB Objective: This study tested whether patients who were given a handout based on deterrence theory, immediately prior to evaluation, would provide invalid data less frequently than patients who were simply given an informational handout.
Method: All outpatients seen for clinical evaluation in a VA Neuropsychology Clinic were randomly given one of the two handouts immediately prior to evaluation. The "Intervention" handout emphasized the importance of trying one's hardest, explicitly listed consequences of valid and invalid responding and asked patients to sign and initial it. The "Control" handout provided general information about neuropsychological evaluation. Examiners were blinded to condition. Patients were excluded from analyses if they were diagnosed with major neurocognitive disorder or could not read the handout. Medical Symptom Validity Test (MSVT) was used to determine performance validity.
Results: Groups did not differ on age, education, or litigation status. For the entire sample (N = 251), there was no effect of handout on passing versus failing MSVT. However, among patients who were seeking disability benefits at the time of evaluation (n = 70), the Intervention handout was associated with lower frequency of failing MSVT than the Control handout.
Conclusions: This brief, theory-based, cost-free intervention was associated with lower frequency of invalid data among patients seeking disability benefits at the time of clinical evaluation. We suggest methodological modifications that might produce a more potent intervention that could be effective with additional subsets of patients.
C1 [Horner, Michael David; Turner, Travis H.; VanKirk, Kathryn K.; Denning, John H.] US Dept Vet Affairs, Ralph H Johnson Vet Affairs Med Ctr, Mental Hlth Serv, Charleston, SC USA.
[Horner, Michael David; Turner, Travis H.; VanKirk, Kathryn K.; Denning, John H.] Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC USA.
[Turner, Travis H.] Med Univ South Carolina, Dept Neurosci, Charleston, SC USA.
RP Horner, MD (reprint author), Ralph H Johnson VA Med Ctr, Mental Hlth Serv 116, 109 Bee St, Charleston, SC 29401 USA.
EM hornermd@musc.edu
FU National Academy of Neuropsychology clinical research grant
FX This work was supported by a National Academy of Neuropsychology
clinical research grant to MDH.
NR 35
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0887-6177
EI 1873-5843
J9 ARCH CLIN NEUROPSYCH
JI Arch. Clin. Neuropsychol.
PD MAR
PY 2017
VL 32
IS 2
BP 228
EP 237
DI 10.1093/arclin/acw094
PG 10
WC Psychology, Clinical; Psychology
SC Psychology
GA EQ4EG
UT WOS:000398026400008
PM 28365748
ER
PT J
AU Loebel, C
Szczesny, SE
Cosgrove, BD
Alini, M
Zenobi-Wong, M
Mauck, RL
Eglin, D
AF Loebel, Claudia
Szczesny, Spencer E.
Cosgrove, Brian D.
Alini, Mauro
Zenobi-Wong, Marcy
Mauck, Robert L.
Eglin, David
TI Cross-Linking Chemistry of Tyramine-Modified Hyaluronan Hydrogels Alters
Mesenchymal Stem Cell Early Attachment and Behavior
SO BIOMACROMOLECULES
LA English
DT Article
ID EXTRACELLULAR-MATRIX; FOCAL ADHESIONS; 3-DIMENSIONAL HYDROGELS;
STIFFENING HYDROGELS; SUBSTRATE STIFFNESS; TRACTION STRESSES; MECHANICAL
FORCE; ACID HYDROGELS; FATE; ELASTICITY
AB Given the significance of hydrogels as cell instructive materials, it is important to understand how differences in their chemical and physical properties are able to direct cell fate. For example, it remains unclear how different hydrogel cross-linking chemistries and gelation mechanisms influence cell behavior. Here, we report on hyaluronan-tyramine (HA-Tyr) hydrogels prepared either with enzymatic cross-linking using horseradish peroxidase and H2O2 or with visible light (500 nm) triggered gelation. We demonstrate that when hydrogels are polymerized to equivalent Young's moduli, the specific cross-linking chemistry of HA-Tyr hydrogels can have a substantial impact on mesenchymal stem cell (MSC) behavior. MSCs cultured on HA-Tyr hydrogels exhibit increased cell spread areas on enzymatically formed substrates relative to photo-cross-linked matrices. While enzymatically formed hydrogels led to MSCs exhibiting greater cell focal adhesion length, MSCs cultured on the photo-cross-linked matrices exhibited smaller cell spread area and shorter focal adhesion length but generated increased traction stress. These findings highlight the importance of understanding hydrogel cross-linking chemistries when the role of biophysical cues in regulating stem cell fate is investigated.
C1 [Loebel, Claudia; Alini, Mauro; Eglin, David] AO Res Inst Davos, Clavadelerstr 8, CH-7270 Davos, Switzerland.
[Loebel, Claudia; Zenobi-Wong, Marcy] ETH, Dept Hlth Sci & Technol, Cartilage Engn Regenerat, Otto Stern Weg 7, CH-8093 Zurich, Switzerland.
[Szczesny, Spencer E.; Cosgrove, Brian D.; Mauck, Robert L.] Univ Penn, Dept Orthopaed Surg, McKay Orthopaed Res Lab, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Loebel, Claudia; Szczesny, Spencer E.; Cosgrove, Brian D.; Mauck, Robert L.] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA.
[Szczesny, Spencer E.; Cosgrove, Brian D.; Mauck, Robert L.] Philadelphia VA Med Ctr, Translat Musculoskeletal Res Ctr, Philadelphia, PA 19104 USA.
RP Eglin, D (reprint author), AO Res Inst Davos, Clavadelerstr 8, CH-7270 Davos, Switzerland.
EM david.eglin@aofoundation.org
OI Szczesny, Spencer/0000-0002-7691-949X
FU European Science Foundation, COST Action NAMABIO [C11.0126]; European
Society for Biomaterials through the Racquel LeGeros Award
FX The authors thank Claire M. McLeod for technical support in AFM
measurements and Dr. Christoph Sprecher for helpful discussions
concerning image analysis and results. This work was financially
supported by the European Science Foundation, COST Action 1005 NAMABIO
(Grant No. C11.0126) and the European Society for Biomaterials through
the Racquel LeGeros Award 2015 (C.L.)
NR 64
TC 0
Z9 0
U1 5
U2 5
PU AMER CHEMICAL SOC
PI WASHINGTON
PA 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1525-7797
EI 1526-4602
J9 BIOMACROMOLECULES
JI Biomacromolecules
PD MAR
PY 2017
VL 18
IS 3
BP 855
EP 864
DI 10.1021/acs.biomac.6b01740
PG 10
WC Biochemistry & Molecular Biology; Chemistry, Organic; Polymer Science
SC Biochemistry & Molecular Biology; Chemistry; Polymer Science
GA EO0HT
UT WOS:000396379600020
PM 28146630
ER
PT J
AU Dougherty, RJ
Schultz, SA
Boots, EA
Ellingson, LD
Meyer, JD
Van Riper, S
Stegner, AJ
Edwards, DF
Oh, JM
Einerson, J
Korcarz, CE
Koscik, RL
Dowling, MN
Gallagher, CL
Carlsson, CM
Rowley, HA
Bendlin, BB
Asthana, S
Hermann, BP
Sager, MA
Stein, JH
Johnson, SC
Okonkwo, OC
Cook, DB
AF Dougherty, Ryan J.
Schultz, Stephanie A.
Boots, Elizabeth A.
Ellingson, Laura D.
Meyer, Jacob D.
Van Riper, Stephanie
Stegner, Aaron J.
Edwards, Dorothy F.
Oh, Jennifer M.
Einerson, Jean
Korcarz, Claudia E.
Koscik, Rebecca L.
Dowling, Maritza N.
Gallagher, Catherine L.
Carlsson, Cynthia M.
Rowley, Howard A.
Bendlin, Barbara B.
Asthana, Sanjay
Hermann, Bruce P.
Sager, Mark A.
Stein, James H.
Johnson, Sterling C.
Okonkwo, Ozioma C.
Cook, Dane B.
TI Relationships between cardiorespiratory fitness, hippocampal volume, and
episodic memory in a population at risk for Alzheimer's disease
SO BRAIN AND BEHAVIOR
LA English
DT Article
DE APOE-e4; cognition; exercise; family history; physical activity
ID MILD COGNITIVE IMPAIRMENT; AUTOMATED METHODS FREESURFER; RANDOMIZED
CONTROLLED-TRIAL; MAXIMAL AEROBIC CAPACITY; SURFACE-BASED ANALYSIS;
VERBAL-LEARNING TEST; PHYSICAL-ACTIVITY; OLDER-ADULTS; SEX-DIFFERENCES;
NORMATIVE DATA
AB Introduction: Cardiorespiratory fitness (CRF) has been shown to be related to brain health in older adults. In individuals at risk for developing Alzheimer's disease (AD), CRF may be a modifiable risk factor that could attenuate anticipated declines in brain volume and episodic memory. The objective of this study was to determine the association between CRF and both hippocampal volume and episodic memory in a cohort of cognitively healthy older adults with familial and/or genetic risk for Alzheimer's disease (AD).
Methods: Eighty-six enrollees from the Wisconsin Registry for Alzheimer's Prevention participated in this study. Participants performed a graded maximal exercise test, underwent a T-1 anatomical magnetic resonance imaging scan, and completed the Rey Auditory Verbal Learning Test (RAVLT).
Results: There were no significant relationships between CRF and HV or RAVLT memory scores for the entire sample. When the sample was explored on the basis of gender, CRF was significantly associated with hippocampal volume for women. For men, significant positive associations were observed between CRF and RAVLT memory scores.
Summary: These results suggest that CRF may be protective against both hippocampal volume and episodic memory decline in older adults at risk for AD, but that the relationships may be gender specific.
C1 [Dougherty, Ryan J.; Meyer, Jacob D.; Van Riper, Stephanie; Stegner, Aaron J.; Cook, Dane B.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
[Dougherty, Ryan J.; Boots, Elizabeth A.; Oh, Jennifer M.; Gallagher, Catherine L.; Carlsson, Cynthia M.; Bendlin, Barbara B.; Asthana, Sanjay; Johnson, Sterling C.; Okonkwo, Ozioma C.] Univ Wisconsin, Sch Educ, Dept Kinesiol, Madison, WI USA.
[Schultz, Stephanie A.; Van Riper, Stephanie; Stegner, Aaron J.; Edwards, Dorothy F.; Rowley, Howard A.; Cook, Dane B.] William S Middleton Mem Vet Adm Med Ctr, Geriatr Res Educ & Clin Ctr, Madison, WI USA.
[Schultz, Stephanie A.; Boots, Elizabeth A.; Edwards, Dorothy F.; Oh, Jennifer M.; Gallagher, Catherine L.; Carlsson, Cynthia M.; Bendlin, Barbara B.; Asthana, Sanjay; Hermann, Bruce P.; Sager, Mark A.; Johnson, Sterling C.; Okonkwo, Ozioma C.] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Alzheimers Dis Res Ctr, Madison, WI USA.
[Schultz, Stephanie A.; Boots, Elizabeth A.; Edwards, Dorothy F.; Oh, Jennifer M.; Koscik, Rebecca L.; Bendlin, Barbara B.; Hermann, Bruce P.; Sager, Mark A.; Johnson, Sterling C.; Okonkwo, Ozioma C.] Univ Wisconsin, Sch Med & Publ Hlth, Wisconsin Alzheimers Inst, Madison, WI USA.
[Ellingson, Laura D.] Iowa State Univ, Dept Kinesiol, Coll Human Sci, Ames, IA USA.
[Meyer, Jacob D.] Univ Wisconsin, Dept Family Med & Community Hlth, Madison, WI USA.
[Einerson, Jean; Korcarz, Claudia E.; Stein, James H.] Univ Wisconsin, Div Cardiol, Sch Med & Publ Hlth, Madison, WI USA.
[Dowling, Maritza N.] Univ Wisconsin, Dept Biostat & Med Informat, Sch Med & Publ Hlth, Madison, WI USA.
[Hermann, Bruce P.] Univ Wisconsin, Dept Neurol, Sch Med & Publ Hlth, Madison, WI 53706 USA.
RP Cook, DB (reprint author), Univ Wisconsin, Dept Kinesiol, Madison, WI 53706 USA.
EM dane.cook@wisc.edu
FU National Institute on Aging grants [K23 AG045957, R01 AG031790, R01
AG021155, R01 AG027161, P50 AG033514]; University of Wisconsin, Madison
[UL1RR025011]; Extendicare Foundation; Alzheimer's Association;
Wisconsin Alumni Research Foundation; Helen Bader Foundation;
Northwestern Mutual Foundation; Geriatric Research Education and
Clinical Center of the William S. Middleton Memorial Veterans Hospital,
Madison, WI; University of Wisconsin Department of Family Medicine and
Community Health [T32HP10010]
FX National Institute on Aging grants, Grant/Award Number: K23 AG045957,
R01 AG031790, R01 AG021155, R01 AG027161 and P50 AG033514; University of
Wisconsin, Madison, Grant/Award Number: UL1RR025011; Extendicare
Foundation; Alzheimer's Association; Wisconsin Alumni Research
Foundation; Helen Bader Foundation; Northwestern Mutual Foundation;
Geriatric Research Education and Clinical Center of the William S.
Middleton Memorial Veterans Hospital, Madison, WI; University of
Wisconsin Department of Family Medicine and Community Health,
Grant/Award Number: T32HP10010
NR 81
TC 0
Z9 0
U1 5
U2 5
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN, NJ 07030 USA
SN 2162-3279
J9 BRAIN BEHAV
JI Brain Behav.
PD MAR
PY 2017
VL 7
IS 3
DI 10.1002/brb3.625
PG 12
WC Behavioral Sciences; Neurosciences
SC Behavioral Sciences; Neurosciences & Neurology
GA EP7NJ
UT WOS:000397564200003
ER
PT J
AU Armstrong, EJ
Graham, L
Waldo, SW
Valle, JA
Maddox, TM
Hawn, MT
AF Armstrong, Ehrin J.
Graham, Laura
Waldo, Stephen W.
Valle, Javier A.
Maddox, Thomas M.
Hawn, Mary T.
TI Patient and Lesion-Specific Characteristics Predict Risk of Major
Adverse Cardiovascular Events Among Patients with Previous Percutaneous
Coronary Intervention Undergoing Noncardiac Surgery
SO CATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS
LA English
DT Article
DE percutaneous coronary intervention; surgery; operative risk
ID DRUG-ELUTING STENTS; ACUTE MYOCARDIAL-INFARCTION; CARDIAC EVENTS; ACUTE
CATHETERIZATION; HARMONIZING OUTCOMES; TRIAGE STRATEGY; BARE-METAL;
IMPLANTATION; REVASCULARIZATION; THROMBOSIS
AB Objectives: To identify predictors of major adverse cardiovascular outcomes (MACE) among patients with prior percutaneous coronary intervention (PCI) who require noncardiac surgery. Background: Patients with prior PCI who undergo noncardiac surgery have an increased risk of postoperative MACE, but few studies have examined the association of PCI lesion characteristics with subsequent operative risk. Methods: Patients were identified using the VA Clinical Assessment, Reporting, and Tracking (CART) program. Patients who underwent noncardiac surgery within 2 years after stent placement were linked to VA and non-VA surgical records. A multivariable logistic regression model was developed to identify predictors of postoperative MACE. Results: Among 12,621 patients with a history of prior PCI who underwent subsequent noncardiac surgery, 570 (4.5%) developed postoperative MACE. The median time from stent placement to surgery was 368 days (IQR 181-528). The strongest predictors of postoperative MACE were urgency of the operation, revised cardiac risk index, the indication for the prior PCI, and timing of the surgery after the PCI. Lesion characteristics independently associated with postoperative MACE included PCI to a distal (AOR 1.43, 95% CI 1.11-1.83) or ostial lesion (AOR 1.52, 95% CI 1.11-2.08), and lesion calcification (AOR 1.29, 95% CI 1.03-1.61), but stent length and target vessel were not independently associated with outcomes. Placement of a bare metal stent was also an independent predictor of MACE after noncardiac surgery (AOR 1.29, 95% CI 1.06-1.57). Conclusions: While patient and operative characteristics are the strongest predictors of MACE after noncardiac surgery, specific lesion characteristics including ostial or distal lesion location and calcification are novel risk factors for postoperative MACE. (C) 2016Wiley Periodicals, Inc.
C1 [Armstrong, Ehrin J.; Waldo, Stephen W.; Valle, Javier A.; Maddox, Thomas M.] Denver VA Med Ctr, Cardiol Sect, Aurora, CO USA.
[Armstrong, Ehrin J.; Waldo, Stephen W.; Valle, Javier A.; Maddox, Thomas M.] Univ Colorado, Sch Med, Aurora, CO USA.
[Graham, Laura; Hawn, Mary T.] Birmingham Vet Adm Hosp, Birmingham, AL USA.
[Hawn, Mary T.] Stanford Univ, Dept Surg, Stanford, CA 94305 USA.
RP Armstrong, EJ (reprint author), Denver VA Med Ctr, Med, 1055 Clermont St Denver, Denver, CO 80220 USA.
EM Ehrin.armstrong@gmail.com
FU Veterans Affairs Health Services Research and Development [IIR 09]
FX Veterans Affairs Health Services Research and Development; Contract
grant number: grant IIR 09
NR 25
TC 1
Z9 1
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1522-1946
EI 1522-726X
J9 CATHETER CARDIO INTE
JI Catheter. Cardiovasc. Interv.
PD MAR 1
PY 2017
VL 89
IS 4
BP 617
EP 627
DI 10.1002/ccd.26624
PG 11
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP3RV
UT WOS:000397300300012
PM 27315550
ER
PT J
AU Yim, CK
Barron, Y
Moore, S
Murtaugh, C
Lala, A
Aldridge, M
Goldstein, N
Gelfman, LP
AF Yim, Cindi K.
Barron, Yolanda
Moore, Stanley
Murtaugh, Chris
Lala, Anuradha
Aldridge, Melissa
Goldstein, Nathan
Gelfman, Laura P.
TI Hospice Enrollment in Patients With Advanced Heart Failure Decreases
Acute Medical Service Utilization
SO CIRCULATION-HEART FAILURE
LA English
DT Article
DE adult; caregiver; heart failure; hospice; Medicare
ID PALLIATIVE CARE; OF-LIFE; CANCER; MANAGEMENT; END; BENEFICIARIES;
CAREGIVERS; DIAGNOSIS; ASSOCIATION; DEPRESSION
AB Background-Patients with advanced heart failure (HF) enroll in hospice at low rates, and data on their acute medical service utilization after hospice enrollment is limited.
Methods and Results-We performed a descriptive analysis of Medicare fee-for-service beneficiaries, with at least one home health claim between July 1, 2009, and June 30, 2010, and at least 2 HF hospitalizations between July 1, 2009, and December 31, 2009, who subsequently enrolled in hospice between July 1, 2009, and December 31, 2009. We estimated panel-negative binomial models on a subset of beneficiaries to compare their acute medical service utilization before and after enrollment. Our sample size included 5073 beneficiaries: 55% were female, 45% were >= 85 years of age, 13% were non-white, and the mean comorbidity count was 2.38 (standard deviation 1.22). The median number of days between the second HF hospital discharge and hospice enrollment was 45. The median number of days enrolled in hospice was 15, and 39% of the beneficiaries died within 7 days of enrollment. During the study period, 11% of the beneficiaries disenrolled from hospice at least once. The adjusted mean number of hospital, intensive care unit, and emergency room admissions decreased from 2.56, 0.87, and 1.17 before hospice enrollment to 0.53, 0.19, and 0.76 after hospice enrollment.
Conclusions-Home health care Medicare beneficiaries with advanced HF who enrolled in hospice had lower acute medical service utilization after their enrollment. Their pattern of hospice use suggests that earlier referral and improved retention may benefit this population. Further research is necessary to understand hospice referral and palliative care needs of advanced HF patients.
C1 [Lala, Anuradha] Div Cardiol & Populat Hlth Sci & Policy, New York, NY USA.
[Aldridge, Melissa; Goldstein, Nathan; Gelfman, Laura P.] Icahn Sch Med Mt Sinai, Brookdale Dept Geriatr & Palliat Med, New York, NY 10029 USA.
[Yim, Cindi K.] Icahn Sch Med Mt Sinai, New York, NY 10029 USA.
[Barron, Yolanda; Murtaugh, Chris] Visiting Nurse Serv New, Ctr Home Care Policy & Res, New York, NY USA.
[Aldridge, Melissa; Gelfman, Laura P.] James J Peters VA Med Ctr, Geriatr Res Educ & Clin Ctr, Bronx, NY USA.
RP Gelfman, LP (reprint author), Icahn Sch Med Mt Sinai, Dept Geriatr & Palliat Med, One Gustave L Levy Pl,Box 1070, New York, NY 10029 USA.
EM laura.gelfman@mssm.edu
FU Medical Student Training in Aging Research (MSTAR); National Institute
on Aging (NIA) [1K23AG049930]; Mount Sinai Older Adults Independence
[P30AG028741]; Agency for Healthcare Research [R01HS020257]; American
Federation on Aging Research; National Palliative Care Research Center
FX C. K. Yim received support from the Medical Student Training in Aging
Research (MSTAR) Fellowship administered by American Federation for
Aging (AFAR) and National Institute on Aging (NIA). Dr Gelfman received
support from the National Institute on Aging (NIA; 1K23AG049930), The
Mount Sinai Older Adults Independence Center (P30AG028741), the American
Federation on Aging Research, and the National Palliative Care Research
Center. The core data set analyzed in this study was developed as part
of a project supported by grant number R01HS020257 from the Agency for
Healthcare Research and Quality.
NR 43
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1941-3289
EI 1941-3297
J9 CIRC-HEART FAIL
JI Circ.-Heart Fail.
PD MAR
PY 2017
VL 10
IS 3
AR e003335
DI 10.1161/CIRCHEARTFAILURE.116.003335
PG 7
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP7UN
UT WOS:000397582800008
ER
PT J
AU Saks, K
Amjadi, D
D'Souza, SL
AF Saks, Karen
Amjadi, Darius
D'Souza, Sharlene L.
TI Eosinophilic Cholecystitis and Enteritis Associated With Ampullary
Stenosis
SO CLINICAL GASTROENTEROLOGY AND HEPATOLOGY
LA English
DT Editorial Material
ID GASTROENTERITIS
C1 [Saks, Karen; Amjadi, Darius; D'Souza, Sharlene L.] Portland VA Med Ctr, Portland, OR 97210 USA.
RP Saks, K (reprint author), Portland VA Med Ctr, Portland, OR 97210 USA.
NR 7
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1542-3565
EI 1542-7714
J9 CLIN GASTROENTEROL H
JI Clin. Gastroenterol. Hepatol.
PD MAR
PY 2017
VL 15
IS 3
BP XXIII
EP XXIV
DI 10.1016/j.cgh.2016.11.008
PG 2
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EP2XK
UT WOS:000397246700002
PM 27840180
ER
PT J
AU Tamura, MK
Montez-Rath, ME
Hall, YN
Katz, R
O'Hare, AM
AF Tamura, Manjula Kurella
Montez-Rath, Maria E.
Hall, Yoshio N.
Katz, Ronit
O'Hare, Ann M.
TI Advance Directives and End-of-Life Care among Nursing Home Residents
Receiving Maintenance Dialysis
SO CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
LA English
DT Article
ID DECISION-MAKING; KIDNEY-DISEASE; HOSPITAL DEATH; QUALITY; INTERVENTION;
HEMODIALYSIS; ESRD
AB Background and objectives Little is known about the relation between the content of advance directives and downstream treatment decisions among patients receiving maintenance dialysis. In this study, we determined the prevalence of advance directives specifying treatment limitations and/or surrogate decision-makers in the last year of life and their association with end-of-life care among nursing home residents.
Design, setting, participants, & measurements Using national data from 2006 to 2007, we compared the content of advance directives among 30,716 nursing home residents receiving dialysis to 30,825 nursing home residents with other serious illnesses during the year before death. Among patients receiving dialysis, we linked the content of advance directives to Medicare claims to ascertain site of death and treatment intensity in the last month of life.
Results In the last year of life, 36% of nursing home residents receiving dialysis had a treatment-limiting directive, 22% had a surrogate decision-maker, and 13% had both in adjusted analyses. These estimates were 13%-27%, 5%-11%, and 6%-13% lower, respectively, than for decedents with other serious illnesses. For patients receiving dialysis who had both a treatment-limiting directive and surrogate decision-maker, the adjusted frequency of hospitalization, intensive care unit admission, intensive procedures, and inpatient death were lower by 13%, 17%, 13%, and 14%, respectively, and hospice use and dialysis discontinuation were 5% and 7% higher compared with patients receiving dialysis lacking both components.
Conclusions Among nursing home residents receiving dialysis, treatment-limiting directives and surrogates were associated with fewer intensive interventions and inpatient deaths, but were in place much less often than for nursing home residents with other serious illnesses.
C1 [Tamura, Manjula Kurella] Palo Alto Vet Affairs Hlth Care Syst, Geriatr Res & Educ Clin Ctr, Palo Alto, CA USA.
[Tamura, Manjula Kurella; Montez-Rath, Maria E.] Stanford Univ, Sch Med, Div Nephrol, Palo Alto, CA 94304 USA.
[Hall, Yoshio N.; Katz, Ronit; O'Hare, Ann M.] Grp Hlth Cooperat Puget Sound, Dept Med, Seattle, WA USA.
[Hall, Yoshio N.; Katz, Ronit; O'Hare, Ann M.] Univ Washington, Dept Med, Kidney Res Inst, Seattle, WA USA.
[O'Hare, Ann M.] Vet Affairs Puget Sound Hlth Care Syst, Dept Hosp & Specialty Med, Seattle, WA USA.
RP Tamura, MK (reprint author), Vet Affairs Palo Alto Hlth Care Syst, 3801 Miranda Ave, Palo Alto, CA 94304 USA.
EM mktamura@stanford.edu
FU National Institutes of Diabetes and Digestive and Kidney Diseases
[U01DK102150]
FX This work is supported by grant U01DK102150 from the National Institutes
of Diabetes and Digestive and Kidney Diseases.
NR 30
TC 1
Z9 1
U1 0
U2 0
PU AMER SOC NEPHROLOGY
PI WASHINGTON
PA 1725 I ST, NW STE 510, WASHINGTON, DC 20006 USA
SN 1555-9041
EI 1555-905X
J9 CLIN J AM SOC NEPHRO
JI Clin. J. Am. Soc. Nephrol.
PD MAR
PY 2017
VL 12
IS 3
BP 435
EP 442
DI 10.2215/CJN.07510716
PG 8
WC Urology & Nephrology
SC Urology & Nephrology
GA EO6SE
UT WOS:000396822000011
ER
PT J
AU Anderson, LJ
Albrecht, ED
Garcia, JM
AF Anderson, Lindsey J.
Albrecht, Eliette D.
Garcia, Jose M.
TI Update on Management of Cancer-Related Cachexia (vol 19, 2017)
SO CURRENT ONCOLOGY REPORTS
LA English
DT Correction
C1 [Anderson, Lindsey J.; Albrecht, Eliette D.; Garcia, Jose M.] VA Puget Sound Hlth Care Syst, Educ & Clin Ctr GRECC, Geriatr Res, Seattle, WA 98108 USA.
[Albrecht, Eliette D.] Yale Univ, New Haven, CT 06520 USA.
[Garcia, Jose M.] Univ Washington, Sch Med, Dept Med, Div Gerontol & Geriatr Med, Seattle, WA 98105 USA.
RP Garcia, JM (reprint author), VA Puget Sound Hlth Care Syst, Educ & Clin Ctr GRECC, Geriatr Res, Seattle, WA 98108 USA.; Garcia, JM (reprint author), Univ Washington, Sch Med, Dept Med, Div Gerontol & Geriatr Med, Seattle, WA 98105 USA.
EM lindsey.anderson5@va.gov; eliette.albrecht@yale.edu; jg77@uw.edu
NR 1
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1523-3790
EI 1534-6269
J9 CURR ONCOL REP
JI Curr. Oncol. Rep.
PD MAR
PY 2017
VL 19
IS 3
AR 22
DI 10.1007/s11912-017-0595-4
PG 1
WC Oncology
SC Oncology
GA EP2ZB
UT WOS:000397251100008
PM 28293870
ER
PT J
AU Wedzicha, JA
Miravitlles, M
Hurst, JR
Calverley, PMA
Albert, RK
Anzueto, A
Criner, GJ
Papi, A
Rabe, KF
Rigau, D
Sliwinski, P
Tonia, T
Vestbo, J
Wilson, KC
Krishnan, JA
AF Wedzicha, Jadwiga A.
Miravitlles, Marc
Hurst, John R.
Calverley, Peter M. A.
Albert, Richard K.
Anzueto, Antonio
Criner, Gerard J.
Papi, Alberto
Rabe, Klaus F.
Rigau, David
Sliwinski, Pawel
Tonia, Thomy
Vestbo, Jorgen
Wilson, Kevin C.
Krishnan, Jerry A.
TI Management of COPD exacerbations: a European Respiratory
Society/American Thoracic Society guideline
SO EUROPEAN RESPIRATORY JOURNAL
LA English
DT Article
ID OBSTRUCTIVE PULMONARY-DISEASE; RANDOMIZED CONTROLLED-TRIAL;
POSITIVE-PRESSURE VENTILATION; QUALITY-OF-LIFE; STANDARD MEDICAL
THERAPY; PLACEBO-CONTROLLED TRIAL; HEALTH-CARE UTILIZATION; NONINVASIVE
VENTILATION; HOSPITAL-CARE; REHABILITATION PROGRAM
AB This document provides clinical recommendations for treatment of chronic obstructive pulmonary disease (COPD) exacerbations.
Comprehensive evidence syntheses, including meta-analyses, were performed to summarise all available evidence relevant to the Task Force's questions. The evidence was appraised using the Grading of Recommendations, Assessment, Development and Evaluation approach and the results were summarised in evidence profiles. The evidence syntheses were discussed and recommendations formulated by a multidisciplinary Task Force of COPD experts.
After considering the balance of desirable and undesirable consequences, quality of evidence, feasibility, and acceptability of various interventions, the Task Force made: 1) a strong recommendation for noninvasive mechanical ventilation of patients with acute or acute-on-chronic respiratory failure; 2) conditional recommendations for oral corticosteroids in outpatients, oral rather than intravenous corticosteroids in hospitalised patients, antibiotic therapy, home-based management, and the initiation of pulmonary rehabilitation within 3 weeks after hospital discharge; and 3) a conditional recommendation against the initiation of pulmonary rehabilitation during hospitalisation.
The Task Force provided recommendations related to corticosteroid therapy, antibiotic therapy, noninvasive mechanical ventilation, home-based management, and early pulmonary rehabilitation in patients having a COPD exacerbation. These recommendations should be reconsidered as new evidence becomes available.
C1 [Wedzicha, Jadwiga A.] Imperial Coll London, Natl Heart & Lung Inst, Airways Dis Sect, London, England.
[Miravitlles, Marc] Hosp Univ Vall dHebron, Dept Pneumol, CIBER Enfermedades Resp CIBERES, Barcelona, Spain.
[Hurst, John R.] UCL, UCL Resp, London, England.
[Calverley, Peter M. A.] Univ Liverpool, Inst Ageing & Chron Dis, Liverpool, Merseyside, England.
[Albert, Richard K.] Univ Colorado, Dept Med, Aurora, CO USA.
[Anzueto, Antonio] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Anzueto, Antonio] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Criner, Gerard J.] Temple Univ, Lewis Katz Sch Med, Dept Thorac Med & Surg, Philadelphia, PA 19122 USA.
[Papi, Alberto] Univ Ferrara, Dept Med Sci, Resp Med, Ferrara, Italy.
[Rabe, Klaus F.] Univ Kiel, Dept Internal Med, Kiel, Germany.
[Rabe, Klaus F.] German Ctr Lung Res, LungenClin Grosshansdorf, Airway Res Ctr North, Grosshansdorf, Germany.
[Rigau, David] Iberoamer Cochrane Ctr, Barcelona, Spain.
[Sliwinski, Pawel] Inst TB & Lung Dis, Dept Resp Med 2, Warsaw, Poland.
[Tonia, Thomy] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland.
[Vestbo, Jorgen] Univ Manchester, Div Infect Immun & Resp Med, Manchester, Lancs, England.
[Wilson, Kevin C.] Boston Univ, Sch Med, Dept Med, Boston, MA 02118 USA.
[Krishnan, Jerry A.] Univ Illinois Hosp & Hlth Sci Syst, Chicago, IL USA.
RP Miravitlles, M (reprint author), Hosp Univ Vall dHebron, Dept Pneumol, Pg Vall dHebron 119-129, Barcelona 08035, Spain.
EM mmiravitlles@vhebron.net
OI PAPI, ALBERTO/0000-0002-6924-4500
NR 89
TC 0
Z9 0
U1 3
U2 3
PU EUROPEAN RESPIRATORY SOC JOURNALS LTD
PI SHEFFIELD
PA 442 GLOSSOP RD, SHEFFIELD S10 2PX, ENGLAND
SN 0903-1936
EI 1399-3003
J9 EUR RESPIR J
JI Eur. Resp. J.
PD MAR
PY 2017
VL 49
IS 3
AR 1600791
DI 10.1183/13993003.00791-2016
PG 16
WC Respiratory System
SC Respiratory System
GA EQ2WI
UT WOS:000397931500005
ER
PT J
AU Ialynytchev, A
Sear, AM
Williams, AR
Langland-Orban, B
Zhang, NH
AF Ialynytchev, Anna
Sear, Alan M.
Williams, Arthur R.
Langland-Orban, Barbara
Zhang, Nanhua
TI Factors associated with lumbar fusion surgery: a case-control study
SO EUROPEAN SPINE JOURNAL
LA English
DT Article
DE Lumbar fusion surgery; Spinal fusion surgery; Lower back surgery
ID UNITED-STATES TRENDS; SPINE SURGERY; BACK-PAIN; GUIDELINE; CHARGES
AB The objective of this study is to identify the demographic and payer factors that are associated with lumbar fusion surgery.
A case-control study was conducted utilizing a population of 38,092 patients from the 2010 Florida Agency for Health Care Administration (AHCA), USA hospital discharge data. The case population included 16,236 records with any of five ICD-9-CM principal procedure codes for initial lumbar fusion. The control group was comprised of 21,856 patients who were admitted for the same principal diagnoses as the cases, but who did not have initial fusion surgery. Logistic regression was used to analyze the association of age, gender, race and principal payer type with initial lumbar fusions. The interaction between age and payer was also examined, as payer type may moderate the association between age and lumbar fusion surgery.
Gender, race, principal payer and age were all found to be significantly associated with lumbar fusion surgery. The interaction of payer and age was also found to be significant. Being female was significantly associated with having a fusion (OR = 1.11, 95 % CI 1.07-1.16). The association between age and receiving surgery was greatest for the less than 20 age group (OR = 10.43, 95 % CI 8.74-12.45). Employees and dependents of Federal government agencies (Tricare, etc.) and patients with commercial insurance were significantly associated with surgery (OR = 1.48, 95 % CI 1.29-1.70 and OR = 1.12, 95 % CI 1.04-1.20, respectively). Patients insured through Medicaid (a social health care program for those with low incomes and limited resources), and the uninsured were negatively associated with surgery (OR = 0.53, 95 % CI 0.47-0.60 and OR = 0.52, 95 % CI 0.46-0.58, respectively).
Lumbar fusion surgery is not recommended in clinical practice guidelines for the top four principal diagnoses in this study. Yet, patients covered by certain types of insurance were found to be significantly associated with fusion surgery.
C1 [Ialynytchev, Anna; Sear, Alan M.; Langland-Orban, Barbara] Univ S Florida, Dept Hlth Policy & Management, 13201 Bruce B. Downs Blvd. MDC 56, Tampa, FL 33612 USA.
[Williams, Arthur R.] US Dept Vet Affairs, CINDRR, Tampa, FL 33637 USA.
[Williams, Arthur R.] George Mason Univ, Dept Hlth Adm & Policy, Fairfax, VA 22030 USA.
[Zhang, Nanhua] Cincinnati Childrens Hosp Med Ctr, Div Biostat & Epidemiol, 3333 Burnet Ave,MLC 5041, Cincinnati, OH 45229 USA.
[Zhang, Nanhua] Univ Cincinnati, Dept Pediat, Cincinnati, OH 45229 USA.
RP Ialynytchev, A (reprint author), Univ S Florida, Dept Hlth Policy & Management, 13201 Bruce B. Downs Blvd. MDC 56, Tampa, FL 33612 USA.
EM annai@mail.usf.edu
NR 24
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U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0940-6719
EI 1432-0932
J9 EUR SPINE J
JI Eur. Spine J.
PD MAR
PY 2017
VL 26
IS 3
BP 698
EP 707
DI 10.1007/s00586-016-4591-4
PG 10
WC Clinical Neurology; Orthopedics
SC Neurosciences & Neurology; Orthopedics
GA EN5JR
UT WOS:000396042000015
PM 27154167
ER
PT J
AU Persson, A
Back, SE
Killeen, TK
Brady, KT
Schwandt, ML
Heilig, M
Magnusson, A
AF Persson, Anna
Back, Sudie E.
Killeen, Therese K.
Brady, Kathleen T.
Schwandt, Melanie L.
Heilig, Markus
Magnusson, Asa
TI Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged
Exposure ( COPE): A Pilot Study in Alcohol-dependent Women
SO JOURNAL OF ADDICTION MEDICINE
LA English
DT Article
DE alcohol dependence; alcohol use disorder; integrated treatment; PTSD;
women
ID POSTTRAUMATIC-STRESS-DISORDER; NATIONAL EPIDEMIOLOGIC SURVEY;
INTERNATIONAL NEUROPSYCHIATRIC INTERVIEW; IDENTIFICATION TEST AUDIT;
PSYCHOMETRIC PROPERTIES; TRAUMA EXPOSURE; CONDITIONS-III; DRUG-USE;
DSM-IV; THERAPY
AB Objectives: Posttraumatic stress disorder (PTSD) and substance use disorders are highly comorbid. Effective treatments are largely lacking. This pilot study evaluated the safety and feasibility of a novel intervention, Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure (COPE), in preparation for a randomized controlled trial.
Methods: Twenty-two treatment-seeking women with current DSM-IV-TR PTSD and alcohol dependence (AD) were recruited. Participants received COPE. Safety and feasibility were evaluated, as were efficacy-related outcomes: PTSD and depression symptom severity, alcohol use, craving, and dependence severity.
Results: No adverse events occurred. COPE was implemented in routine clinical practice. Among the assessed women, 95.8% were eligible to participate. Treatment attendance and completion were higher than in previous studies. Post treatment, all efficacy-related outcomes, including PTSD and depression symptom severity, alcohol use, craving, and dependence severity, were significantly reduced.
Conclusions: COPE was safe and feasible to use. Concerns that trauma-focused, exposure-based therapy might promote relapse in this population appear unwarranted. Our findings provide initial evidence suggestive of COPE efficacy for comorbid PTSD and AD in women. These results provide a strong rationale for investigating the efficacy of COPE for comorbid PTSD and AD in women in a randomized controlled trial.
C1 [Persson, Anna; Magnusson, Asa] Karolinska Inst, Dept Clin Neurosci, Box 179 03, S-10401 Stockholm, Sweden.
[Persson, Anna; Magnusson, Asa] Stockholm Ctr Dependency Disorders, EWA Outpatient Unit, Stockholm, Sweden.
[Back, Sudie E.; Killeen, Therese K.; Brady, Kathleen T.] Med Univ South Carolina, Dept Psychiat, Charleston, SC 29425 USA.
[Back, Sudie E.; Brady, Kathleen T.] Ralph H Johnson Vet Affairs VA Med Ctr, Charleston, SC USA.
[Schwandt, Melanie L.] NIAAA, Lab Clin & Expt Studies, Bethesda, MD USA.
[Heilig, Markus] Linkoping Univ, Dept Clin & Expt Med, Linkoping, Sweden.
RP Magnusson, A (reprint author), Karolinska Inst, Dept Clin Neurosci, Box 179 03, S-10401 Stockholm, Sweden.; Magnusson, A (reprint author), Rosenlunds Hosp, Stockholm Ctr Dependency Disorders, EWA Outpatient Unit, Box 179 03, S-11895 Stockholm, Sweden.
EM asa.magnusson@ki.se
FU Swedish Society of Addiction Medicine; Systembolaget's Alcohol Research
Council; Soderstrom-Konigska Foundation
FX The work summarized herein was funded by grants from The Swedish Society
of Addiction Medicine, Systembolaget's Alcohol Research Council, and the
Soderstrom-Konigska Foundation. The above had no involvement in study
design, collection, analysis or interpretation of data, the writing of
the report, or the decision to submit the article for publication.
NR 40
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U2 1
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1932-0620
EI 1935-3227
J9 J ADDICT MED
JI J. Addict. Med.
PD MAR-APR
PY 2017
VL 11
IS 2
BP 119
EP 125
DI 10.1097/ADM.0000000000000286
PG 7
WC Substance Abuse
SC Substance Abuse
GA EP7ZE
UT WOS:000397594900009
PM 28079572
ER
PT J
AU Matsue, Y
ter Maaten, JM
Struck, J
Metra, M
O'Connor, CM
Ponikowski, P
Teerlink, JR
Cotter, G
Davison, B
Cleland, JG
Givertz, MM
Bloomfield, DM
Dittrich, HC
van Veldhuisen, DJ
van der Meer, P
Damman, K
Voors, AA
AF Matsue, Yuya
ter Maaten, Jozine M.
Struck, Joachim
Metra, Marco
O'Connor, Christopher M.
Ponikowski, Piotr
Teerlink, John R.
Cotter, Gad
Davison, Beth
Cleland, John G.
Givertz, Michael M.
Bloomfield, Daniel M.
Dittrich, Howard C.
van Veldhuisen, Dirk J.
van der Meer, Peter
Damman, Kevin
Voors, Adriaan A.
TI Clinical Correlates and Prognostic Value of Proenkephalin in Acute and
Chronic Heart Failure
SO JOURNAL OF CARDIAC FAILURE
LA English
DT Article
DE Renal function; heart failure; prognosis; enkephalin
ID RECEPTOR ANTAGONIST ROLOFYLLINE; GLOMERULAR-FILTRATION-RATE; BLOOD UREA
NITROGEN; ACUTE KIDNEY INJURY; RENAL-FUNCTION; MYOCARDIAL-INFARCTION;
VOLUME OVERLOAD; MORTALITY; CONGESTION; PROTECT
AB Background: Proenkephalin (pro-ENK) has emerged as a novel biomarker associated with both renal function and cardiac function. However, its clinical and prognostic value have not been well evaluated in symptomatic patients with heart failure.
Methods and Results: The association between pro-ENK and markers of renal function was evaluated in 95 patients with chronic heart failure who underwent renal hemodynamic measurements, including renal blood flow (RBF) and glomerular filtration rate (GFR) with the use of I-131-Hippuran and I-125-iothalainate clearances, respectively. The association between pro-ENK and clinical outcome in acute heart failure was assessed in another 1589 patients. Pro-ENK was strongly correlated with both RBF (P <.001) and GFR (P <.001), but not with renal tubular markers. In the acute heart failure cohort, pro-ENK was a predictor of death through 180 days, heart failure rehospitalization through 60 days, and death or cardiovascular or renal rehospitalization through day 60 in univariable analyses, but its predictive value was lost in a multivariable model when other renal markers were entered in the model. \ Conclusions: In patients with chronic and acute heart failure, pro-ENK is strongly associated with glomerular function, but not with tubular damage. Pro-ENK provides limited prognostic information in patients with acute heart failure on top of established renal markers.
C1 [Matsue, Yuya; ter Maaten, Jozine M.; van Veldhuisen, Dirk J.; van der Meer, Peter; Damman, Kevin; Voors, Adriaan A.] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands.
[Struck, Joachim] Sphingotec GmbH, Hennigsdorf, Germany.
[Metra, Marco] Univ Brescia, Brescia, Italy.
[O'Connor, Christopher M.] Inova Heart & Vasc Inst, Falls Church, VA USA.
[Ponikowski, Piotr] Med Univ, Clin Mil Hosp, Wroclaw, Poland.
[Teerlink, John R.] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Teerlink, John R.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Cotter, Gad; Davison, Beth] Momentum Res, Durham, NC USA.
[Cleland, John G.] Univ Hull, Kingston Upon Hull, Yorks, England.
[Givertz, Michael M.] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA.
[Bloomfield, Daniel M.] Merck Res Labs, Rahway, NJ USA.
[Dittrich, Howard C.] Univ Iowa, Carver Coll Med, Cardiovasc Res Ctr, Iowa City, IA USA.
RP Voors, AA (reprint author), Univ Med Ctr Groningen, Dept Cardiol, Hanzepl 1, NL-9713 GZ Groningen, Netherlands.
EM a.a.voors@umcg.nl
OI Matsue, Yuya/0000-0003-2456-8525
FU Novacardia
FX The PROTECT trial was supported by Novacardia, a subsidiary of Merck.
Alere, Singulex, and Sphingotec kindly provided assays and performed
biomarker measurements.
NR 22
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U2 0
PU CHURCHILL LIVINGSTONE INC MEDICAL PUBLISHERS
PI PHILADELPHIA
PA CURTIS CENTER, INDEPENDENCE SQUARE WEST, PHILADELPHIA, PA 19106-3399 USA
SN 1071-9164
EI 1532-8414
J9 J CARD FAIL
JI J. Card. Fail.
PD MAR
PY 2017
VL 23
IS 3
BP 231
EP 239
DI 10.1016/j.cardfail.2016.09.007
PG 9
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EQ4BR
UT WOS:000398018200006
PM 27663098
ER
PT J
AU Goodman, M
Hazlett, EA
AF Goodman, Marianne
Hazlett, Erin A.
TI Just What is "Dialectical" About Dialectical Behavior Therapy? Reply
SO JOURNAL OF CLINICAL PSYCHIATRY
LA English
DT Letter
ID EMOTION REGULATION; VETERANS
C1 [Goodman, Marianne; Hazlett, Erin A.] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.
[Goodman, Marianne; Hazlett, Erin A.] James J Peters VA Med Ctr, VISN Mental Illness Res Educ & Clin Ctr MIRECC 25, Bronx, NY USA.
[Goodman, Marianne] James J Peters VA Med Ctr, Outpatient Psychiat, Bronx, NY USA.
RP Goodman, M (reprint author), Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.; Goodman, M (reprint author), James J Peters VA Med Ctr, VISN Mental Illness Res Educ & Clin Ctr MIRECC 25, Bronx, NY USA.; Goodman, M (reprint author), James J Peters VA Med Ctr, Outpatient Psychiat, Bronx, NY USA.
EM marianne.goodman@va.gov
FU US Department of Defense [WX81XWH-09-1-0722]
FX The study discussed in this letter was supported by US Department of
Defense Grant WX81XWH-09-1-0722 (to Dr Goodman, principal investigator).
NR 4
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U1 0
U2 0
PU PHYSICIANS POSTGRADUATE PRESS
PI MEMPHIS
PA P O BOX 752870, MEMPHIS, TN 38175-2870 USA
SN 0160-6689
EI 1555-2101
J9 J CLIN PSYCHIAT
JI J. Clin. Psychiatry
PD MAR
PY 2017
VL 78
IS 3
BP E311
EP E311
DI 10.4088/JCP.16lr11394a
PG 1
WC Psychology, Clinical; Psychiatry
SC Psychology; Psychiatry
GA EQ3NE
UT WOS:000397978900013
PM 28394515
ER
PT J
AU Stephenson, KR
Simpson, TL
Martinez, ME
Kearney, DJ
AF Stephenson, Kyle R.
Simpson, Tracy L.
Martinez, Michelle E.
Kearney, David J.
TI Changes in Mindfulness and Posttraumatic Stress Disorder Symptoms Among
Veterans Enrolled in Mindfulness-Based Stress Reduction
SO JOURNAL OF CLINICAL PSYCHOLOGY
LA English
DT Article
DE posttraumatic stress disorder; mindfulness; veterans
ID RANDOMIZED CLINICAL-TRIAL; COGNITIVE-BEHAVIORAL THERAPY; EXPOSURE
THERAPY; MENTAL-HEALTH; SELF-REPORT; FUNCTIONAL IMPAIRMENT; PTSD;
PROGRAM; PARTICIPATION; MECHANISMS
AB Objectives: The current study assessed associations between changes in 5 facets of mindfulness (Acting With Awareness, Observing, Describing, Non-Reactivity, and Nonjudgment) and changes in 4 posttraumatic stress disorder (PTSD) symptom clusters (Re-Experiencing, Avoidance, Emotional Numbing, and Hyperarousal symptoms) among veterans participating in mindfulness-based stress reduction (MBSR). Method: Secondary analyses were performed with a combined data set consisting of 2 published and 2 unpublished trials of MBSR conducted at a large Veterans Affairs hospital. The combined sample included 113 veterans enrolled in MBSR who screened positive for PTSD and completed measures of mindfulness and PTSD symptoms before and after the 8-week intervention. Results: Increases in mindfulness were significantly associated with reduced PTSD symptoms. Increases in Acting With Awareness and Non-Reactivity were the facets of mindfulness most strongly and consistently associated with reduced PTSD symptoms. Increases in mindfulness were most strongly related to decreases in Hyperarousal and Emotional Numbing. Conclusions: These results extend previous research, provide preliminary support for changes in mindfulness as a viable mechanism of treatment, and have a number of potential practical and theoretical implications. (C) 2016 Wiley Periodicals, Inc.
C1 [Stephenson, Kyle R.; Simpson, Tracy L.; Martinez, Michelle E.; Kearney, David J.] Vet Affairs Puget Sound Healthcare Syst, 1660 South Columbian Way, Seattle, WA 98108 USA.
[Stephenson, Kyle R.] Willamette Univ, Dept Psychol, Salem, OR 97301 USA.
[Simpson, Tracy L.; Kearney, David J.] Univ Washington, Sch Med, Seattle, WA 98195 USA.
RP Kearney, DJ (reprint author), Vet Affairs Puget Sound Healthcare Syst, 1660 South Columbian Way, Seattle, WA 98108 USA.
EM david.kearney@va.gov
FU U.S. Department of Veterans Affairs, Office of Research and Development,
Clinical RD Program
FX The study was approved by the institutional review board at VA Puget
Sound Health Care System. This material is based upon work supported by
the U.S. Department of Veterans Affairs, Office of Research and
Development, Clinical R&D Program.
NR 54
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U1 5
U2 5
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0021-9762
EI 1097-4679
J9 J CLIN PSYCHOL
JI J. Clin. Psychol.
PD MAR
PY 2017
VL 73
IS 3
BP 201
EP 217
DI 10.1002/jclp.22323
PG 17
WC Psychology, Clinical
SC Psychology
GA EQ3UX
UT WOS:000397999900001
PM 27152480
ER
PT J
AU Pottiez, G
Yang, L
Stewart, T
Song, N
Aro, P
Galasko, DR
Quinn, JF
Peskind, ER
Shi, M
Zhang, J
AF Pottiez, Gwenael
Yang, Li
Stewart, Tessandra
Song, Ning
Aro, Patrick
Galasko, Douglas R.
Quinn, Joseph F.
Peskind, Elaine R.
Shi, Min
Zhang, Jing
TI Mass-Spectrometry-Based Method To Quantify in Parallel Tau and Amyloid
beta 1-42 in CSF for the Diagnosis of Alzheimer's Disease
SO JOURNAL OF PROTEOME RESEARCH
LA English
DT Article
DE Alzheimer's disease; mass spectrometry; SRM; diagnosis; biomarker;
cerebrospinal fluid; tau; amyloid beta; A beta(42)
ID MILD COGNITIVE IMPAIRMENT; HUMAN CEREBROSPINAL-FLUID; QUALITY-CONTROL
PROGRAM; QUANTIFICATION; BIOMARKERS; PROTEIN; ASSOCIATION; PLASMA;
BRAIN; BETA-AMYLOID((1-42))
AB Alzheimer's disease (AD), the most common form of dementia, afflicts about 50 million people worldwide. Currently, AD diagnosis is primarily based on psychological evaluation and can only be confirmed post-mortem. Reliable and objective biomarkers for prognosis and diagnosis have been sought for years. Together, tau and amyloid beta 1-42 (A beta(42)) in cerebrospinal fluid (CSF) have been shown to provide good diagnostic sensitivity and specificity. Additionally, phosphorylated forms of tau, such as tau pS181, have also shown promising results. However, the measurement of such markers currently relies on antibody-based immunoassays that have shown variability, leading to discrepant results across laboratories. To date, mass spectrometry methods developed to evaluate CSF tau and A,1342 are not compatible. We present in this article the development of a mass-spectrometry-based method of quantification for CSF tau and A beta(42) in parallel. The absolute concentrations of tau and A beta(42) we measured are on average 50 ng/mL (7-130 ng/mL) and 7.1 ng/mL (3-13 ng/mL), respectively. Analyses of CSF tau and A beta(42), in a cohort of patients with AD, mild cognitive impairment, and healthy controls (30 subjects), provide significant group differences evaluated with ROC curves (AUC(control-AD) and AUC((control-MCI)) = 1, AUC((MCI-AD))) = 0.76), with at least equivalent diagnostic utility to immunoassay measurements in the same sample set. Finally, a significant and negative correlation was found between the tau and A beta peptides ratio and the disease severity.
C1 [Pottiez, Gwenael; Yang, Li; Stewart, Tessandra; Song, Ning; Aro, Patrick; Shi, Min; Zhang, Jing] Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98104 USA.
[Galasko, Douglas R.] Univ Calif San Diego, Dept Neurosci, San Diego, CA 92093 USA.
[Quinn, Joseph F.] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97239 USA.
[Quinn, Joseph F.] Portland VA Med Ctr, Portland, OR 97239 USA.
[Peskind, Elaine R.] VA Puget Sound Hlth Care Syst, Northwest Network VISN 20, Mental Illness Res Educ & Clin Ctr, Seattle, WA 98108 USA.
[Peskind, Elaine R.] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Zhang, Jing] Peking Univ, Hlth Sci Ctr, Dept Pathol, Beijing 100083, Peoples R China.
[Zhang, Jing] Third Hosp, Beijing 100083, Peoples R China.
RP Zhang, J (reprint author), Univ Washington, Sch Med, Dept Pathol, Seattle, WA 98104 USA.; Zhang, J (reprint author), Peking Univ, Hlth Sci Ctr, Dept Pathol, Beijing 100083, Peoples R China.; Zhang, J (reprint author), Third Hosp, Beijing 100083, Peoples R China.
EM zhangj@uw.edu
FU National Institutes of Health (NIH) [U01 NS091272, U01 NS082137, P30
ES007033-8649, R01 ES016873, R01 ES019277, P50 AG05131]; University of
Washington's Proteomics Resource [UWPR95794]
FX We thank the participants for their generous donation of samples. This
study was supported by grants from the National Institutes of Health
(NIH) (U01 NS091272, U01 NS082137, P30 ES007033-8649, R01 ES016873, and
R01 ES019277 to J.Z. and P50 AG05131 to D.G.). It was also supported in
part by the University of Washington's Proteomics Resource (UWPR95794).
The content is solely the responsibility of the authors and does not
necessarily represent the official views of the NIH and other sponsors.
NR 38
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U1 7
U2 7
PU AMER CHEMICAL SOC
PI WASHINGTON
PA 1155 16TH ST, NW, WASHINGTON, DC 20036 USA
SN 1535-3893
EI 1535-3907
J9 J PROTEOME RES
JI J. Proteome Res.
PD MAR
PY 2017
VL 16
IS 3
BP 1228
EP 1238
DI 10.1021/acs.jproteome.6b00829
PG 11
WC Biochemical Research Methods
SC Biochemistry & Molecular Biology
GA EN0UO
UT WOS:000395726200010
PM 28112948
ER
PT J
AU Abbott, DE
Voils, CL
Fisher, DA
Greenberg, CC
Safdar, N
AF Abbott, Daniel E.
Voils, Corrine L.
Fisher, Deborah A.
Greenberg, Caprice C.
Safdar, Nasia
TI Socioeconomic disparities, financial toxicity, and opportunities for
enhanced system efficiencies for patients with cancer
SO JOURNAL OF SURGICAL ONCOLOGY
LA English
DT Review
DE cancer; financial toxicity; geographic disparity; socioeconomic
disparities; telehealth
ID AFRICAN-AMERICAN WOMEN; INFLUENCE MINORITY USE; LOW HEALTH LITERACY;
COLORECTAL-CANCER; BREAST-CANCER; RACIAL DISPARITIES; UNITED-STATES;
MEDICARE BENEFICIARIES; ADJUVANT BREAST; CARE REFORM
AB Cancer care continues to stress the US healthcare system with increases in life expectancy, cancer prevalence, and survivors' complex needs. These challenges are compounded by socioeconomic, racial, and cultural disparities that are associated with poor clinical outcomes. One innovative and resource-wise strategy to address this demand on the system is expanded use of telehealth. This paradigm has the potential to decrease healthcare and patient out-of-pocket costs and improve patient adherence to recommended treatment and/or surveillance.
C1 [Abbott, Daniel E.; Safdar, Nasia] William S Middleton Mem Vet Adm Med Ctr, Cincinnati, OH USA.
[Abbott, Daniel E.; Greenberg, Caprice C.] Univ Wisconsin, Sch Med & Publ Hlth, Dept Surg, Madison, WI USA.
[Voils, Corrine L.; Fisher, Deborah A.] Durham Vet Affairs Med Ctr, Durham, NC USA.
[Voils, Corrine L.; Fisher, Deborah A.] Duke Univ, Dept Med, Durham, NC USA.
[Safdar, Nasia] Univ Wisconsin, Dept Med, Sch Med & Publ Hlth, Madison, WI USA.
RP Abbott, DE (reprint author), Univ Wisconsin, Sch Med, Dept Surg, Surg, 600 Highland Ave,K4-742, Madison, WI 53792 USA.
EM abbott@surgery.wisc.edu
FU Department of Veterans Affairs; Research Career Scientist [RCS 14-443]
FX Department of Veterans Affairs; Research Career Scientist, Grant number:
RCS 14-443
NR 76
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Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0022-4790
EI 1096-9098
J9 J SURG ONCOL
JI J. Surg. Oncol.
PD MAR 1
PY 2017
VL 115
IS 3
BP 250
EP 256
DI 10.1002/jso.24528
PG 7
WC Oncology; Surgery
SC Oncology; Surgery
GA EP3JP
UT WOS:000397278900004
PM 28105638
ER
PT J
AU Ikonomidis, JS
Nadeau, EK
Akerman, AW
Stroud, RE
Mukherjee, R
Jones, JA
AF Ikonomidis, John S.
Nadeau, Elizabeth K.
Akerman, Adam W.
Stroud, Robert E.
Mukherjee, Rupak
Jones, Jeffrey A.
TI Regulation of membrane type-1 matrix metalloproteinase activity and
intracellular localization in clinical thoracic aortic aneurysms
SO JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY
LA English
DT Article
DE aneurysm; MT1-MMP; protein kinase C; remodeling; thoracic aorta
ID MARFAN-SYNDROME; TRANSMEMBRANE DOMAIN; EXTRACELLULAR-MATRIX; TISSUE
INHIBITOR; CELL INVASION; MURINE MODEL; MT1-MMP; ACTIVATION; EXPRESSION;
MMP-2
AB Objective: Membrane type-1 matrix metalloproteinase (MT1-MMP) is elevated during thoracic aortic aneurysm (TAA) development in mouse models, and plays an important role in the activation of matrix metalloproteinase (MMP)-2 and the release of matrix-bound transforming growth factor-b. In this study, we tested the hypothesis that MT1-MMP is subject to protein kinase C (PKC)-mediated regulation, which alters intracellular trafficking and activity with TAAs.
Methods: Levels of MMP-2, native and phosphorylated MT1-MMP, and PKC-d were measured in aortic tissue from patients with small TAAs (< 5 cm; n = 8) and large TAAs (> 6.5 cm; n = 8), and compared with values measured in normal controls (n = 8). Cellular localization of green fluorescent protein (GFP)-tagged MT1-MMP was assessed in aortic fibroblasts isolated from control and 4-week TAA mice. The effects of PKC-mediated phosphorylation on MT1-MMP cellular localization and function (active MMP-2 vs phospo-Smad2 abundance) were assessed after treatment with a PKC activator (phorbol-12-myristate-13-acetate [PMA], 100 nM) with and without a PKC-delta-specific inhibitor (rottlerin, 3 mM).
Results: Compared with controls, MT1-MMP abundance was increased in aortas from both TAA groups. Active MMP-2 was increased only in the large TAA group. The abundances of phosphorylated MT1-MMP and activated PKC-d were enhanced in the small TAA group compared with the large TAA group. MT1-MMP was localized on the plasma membrane in aortic fibroblasts from control mice and in endosomes from TAA mice. Treatment with PMA induced MT1-MMP-GFP internalization, enhanced phospho-Smad2, and reduced MMP-2 activation, whereas rottlerin pretreatment inhibited these effects.
Conclusions: Phosphorylation of MT1-MMP mediates its activity through directing cellular localization, shifting its role from MMP-2 activation to intracellular signaling. Thus, targeted inhibition of MT1-MMP may have therapeutic relevance as an approach to attenuating TAA development.
C1 [Ikonomidis, John S.; Nadeau, Elizabeth K.; Akerman, Adam W.; Stroud, Robert E.; Mukherjee, Rupak; Jones, Jeffrey A.] Med Univ South Carolina, Div Cardiothorac Surg, Charleston, SC 29425 USA.
[Mukherjee, Rupak; Jones, Jeffrey A.] Ralph H Johnson Vet Affairs Med Ctr, Res Serv, Charleston, SC USA.
RP Jones, JA (reprint author), Med Univ South Carolina, Div Cardiothorac Surg Res, Strom Thurmond Bldg,114 Doughty St,Suite 338, Charleston, SC 29425 USA.
EM jonesja@musc.edu
FU National Institutes of Health (NHLBI) [R01 HL102121]; Department of
Veterans Affairs (VA-ORD BLRD Merit) [I01BX000904]
FX This work was supported by grants from the National Institutes of Health
(NHLBI R01 HL102121, to J.S.I.) and the Department of Veterans Affairs
(VA-ORD BLR&D Merit I01BX000904, to J. A. J.).
NR 36
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U1 1
U2 1
PU MOSBY-ELSEVIER
PI NEW YORK
PA 360 PARK AVENUE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0022-5223
EI 1097-685X
J9 J THORAC CARDIOV SUR
JI J. Thorac. Cardiovasc. Surg.
PD MAR
PY 2017
VL 153
IS 3
BP 537
EP 546
DI 10.1016/j.jtcvs.2016.10.065
PG 10
WC Cardiac & Cardiovascular Systems; Respiratory System; Surgery
SC Cardiovascular System & Cardiology; Respiratory System; Surgery
GA EQ1PE
UT WOS:000397841200014
PM 27923483
ER
PT J
AU Allen, SR
Pascual, J
Martin, N
Reilly, P
Luckianow, G
Datner, E
Davis, KA
Kaplan, LJ
AF Allen, Steven R.
Pascual, Jose
Martin, Niels
Reilly, Patrick
Luckianow, Gina
Datner, Elizabeth
Davis, Kimberly A.
Kaplan, Lewis J.
TI A novel method of optimizing patient- and family-centered care in the
ICU
SO JOURNAL OF TRAUMA AND ACUTE CARE SURGERY
LA English
DT Article
DE Patient- and family-centered care; communication; satisfaction; quality
ID CRITICALLY-ILL PATIENTS; EVALUATION APACHE IV; LENGTH-OF-STAY;
CARDIOPULMONARY-RESUSCITATION; ACUTE PHYSIOLOGY; UNIT PATIENTS;
SATISFACTION; NEEDS; GUIDELINES; MORTALITY
AB BACKGROUND Patient- and family-centered care permeates critical care where there are often multiple teams involved in management. A method of facilitating information sharing to support shared decision making is essential in appropriately rendering care. This study sought to determine whether incorporating family members on rounds in the intensive care unit (ICU) improves patient and family knowledge and whether doing so improves team time management and satisfaction with the process.
METHODS A nonrandomized comparative before-and-after trial of incorporating family members on rounds (July to December 2009 vs January to July 2010) in a single quarternary center's surgical ICU assessed (1) family members' knowledge, (2) nurse's and physician's satisfaction with the intervention, (3) frequency and timing of family meetings, and (4) physician's workflow.
RESULTS Intensive care unit demographics and use were similar between time frames. Presurvey (n = 412 family members; 49 nurses) and postsurvey (n = 427 family members; 47 nurses) were coupled with presurvey (n = 5) and postsurvey (n = 6) physicians' informal feedback. Family knowledge of the clinical course and plans increased from 146 (35.4%) of 412 to 374 (87.6%) of 427 (p < 0.0001). Nurses were nearly uniformly satisfied with planned family interaction on rounds (presurvey: 9/49 [18.4%] vs postsurvey: 46/47 [97.9%]; p < 0.0001). Family meetings per week outside of rounds substantially decreased from a mean of 5.3 2.7 to 0.3 0.9; p < 0.001). Goals of therapy including end-of-life care became an element frequently discussed on rounds with families (presurvey: 9.4% +/- 4.7% vs postsurvey: 82.5% +/- 14.8%; p < 0.0001). One intensivist was dissatisfied with the process.
CONCLUSION Incorporating family members on rounds in the ICU improves communication and satisfaction and shifts the team's time away from family communication events outside of rounds, condensing most of those activities within the rounding structure. Critical care nurses and intensivists were principally satisfied with the process.
LEVEL OF EVIDENCE Therapeutic, level III.
C1 [Allen, Steven R.; Pascual, Jose; Martin, Niels; Reilly, Patrick; Datner, Elizabeth; Kaplan, Lewis J.] Univ Penn, Perelman Sch Med, 3900 Woodland Ave, Philadelphia, PA 19104 USA.
[Allen, Steven R.; Pascual, Jose; Datner, Elizabeth; Kaplan, Lewis J.] Philadelphia VA Med Ctr, Philadelphia, PA USA.
[Luckianow, Gina; Davis, Kimberly A.] Yale Sch Med, New Haven, CT USA.
RP Kaplan, LJ (reprint author), Univ Penn, Perelman Sch Med, Div Trauma Surg Crit Care & Emergency Surg, 3900 Woodland Ave, Philadelphia, PA 19104 USA.; Kaplan, LJ (reprint author), Corporal Michael J Crescenz VA Med Ctr, Surg Crit Care Sect, 3900 Woodland Ave, Philadelphia, PA 19104 USA.
EM Lewis.Kaplan@uphs.upenn.edu
NR 41
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U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 2163-0755
EI 2163-0763
J9 J TRAUMA ACUTE CARE
JI J. Trauma Acute Care Surg.
PD MAR
PY 2017
VL 82
IS 3
BP 582
EP 586
DI 10.1097/TA.0000000000001332
PG 5
WC Critical Care Medicine; Surgery
SC General & Internal Medicine; Surgery
GA EM8XV
UT WOS:000395595300020
PM 28030488
ER
PT J
AU Hammad, SM
Baker, NL
El Abiad, JM
Spassieva, SD
Pierce, JS
Rembiesa, B
Bielawski, J
Lopes-Virella, MF
Klein, RL
AF Hammad, Samar M.
Baker, Nathaniel L.
El Abiad, Jad M.
Spassieva, Stefanka D.
Pierce, Jason S.
Rembiesa, Barbara
Bielawski, Jacek
Lopes-Virella, Maria F.
Klein, Richard L.
CA DCCT EDIC Grp Investigators
TI Increased Plasma Levels of Select Deoxy-ceramide and Ceramide Species
are Associated with Increased Odds of Diabetic Neuropathy in Type 1
Diabetes: A Pilot Study
SO NEUROMOLECULAR MEDICINE
LA English
DT Article
DE Type 1 diabetes; Neuropathy; Deoxysphingolipid; Ceramide;
Deoxy-ceramide; Cysteine
ID HEREDITARY SENSORY NEUROPATHY; SERINE PALMITOYLTRANSFERASE; BIOPHYSICAL
PROPERTIES; PERIPHERAL NEUROPATHY; CHAIN LENGTH; SPHINGOLIPIDS; LONG;
1-DEOXYSPHINGOLIPIDS; MELLITUS; COMPLICATIONS
AB Plasma deoxy-sphingoid bases are elevated in type 2 diabetes patients and correlate with the stage of diabetic distal sensorimotor polyneuropathy; however, associations between deoxy-sphingolipids (DSL) and neuropathy in type 1 diabetes have not been examined. The primary aim of this exploratory pilot study was to assess the associations between multiple sphingolipid species including DSL and free amino acids and the presence of symptomatic neuropathy in a DCCT/EDIC type 1 diabetes subcohort. Using mass spectroscopy, plasma levels of DSL and free amino acids in DCCT/EDIC type 1 diabetes participants (n = 80), with and without symptoms of neuropathy, were investigated. Patient-determined neuropathy was based on 15-item self-administered questionnaire (Michigan Neuropathy Screening Instrument) developed to assess distal symmetrical peripheral neuropathy in diabetes. Patients who scored ae4, or reported inability to sense their feet during walking or to distinguish hot from cold water while bathing were considered neuropathic. Plasma levels of ceramide, sphingomyelin, hexosyl- and lactosylceramide species, and amino acids were measured and analyzed relative to neuropathy status in the patient. Deoxy-C24-ceramide, C24- and C26-ceramide were higher in patients with neuropathy than those without neuropathy. Cysteine was higher in patients with neuropathy. No differences in other sphingolipids or amino acids were detected. The covariate-adjusted Odds Ratios of positive patient-reported neuropathy was associated with increased levels of deoxy-C24-, and deoxy-C24:1-ceramide; C22-, C24-, and C26-ceramide; and cysteine. Plasma deoxy-ceramide and ceramide species may have potential diagnostic and prognostic significance in diabetic neuropathy.
C1 [Hammad, Samar M.; El Abiad, Jad M.] Med Univ South Carolina, Dept Regenerat Med & Cell Biol, 173 Ashley Ave,BSB 645,MSC 508, Charleston, SC 29425 USA.
[Baker, Nathaniel L.] Med Univ South Carolina, Dept Publ Hlth Sci, 173 Ashley Ave,BSB 645,MSC 508, Charleston, SC 29425 USA.
[Spassieva, Stefanka D.] Med Univ South Carolina, Div Hematol Oncol, Dept Med, 173 Ashley Ave,BSB 645,MSC 508, Charleston, SC 29425 USA.
[Pierce, Jason S.; Rembiesa, Barbara; Bielawski, Jacek] Med Univ South Carolina, Dept Biochem & Mol Biol, 173 Ashley Ave,BSB 645,MSC 508, Charleston, SC 29425 USA.
[Lopes-Virella, Maria F.; Klein, Richard L.] Ralph H Johnson Dept Vet Affairs Med Ctr, Res Serv, Charleston, SC USA.
[Klein, Richard L.] Med Univ South Carolina, Dept Med, Div Endocrinol Metab & Med Genet, 173 Ashley Ave,BSB 645,MSC 508, Charleston, SC 29425 USA.
RP Hammad, SM (reprint author), Med Univ South Carolina, Dept Regenerat Med & Cell Biol, 173 Ashley Ave,BSB 645,MSC 508, Charleston, SC 29425 USA.
EM hammadsm@musc.edu
FU NIDDK Diabetic Complications Consortium [DK076169]; National Institutes
of Health [P01-HL55782]; Department of Veterans Affairs Merit Review
Program; Lipidomics Shared Resource, Hollings Cancer Center [P30
CA138313]; Lipidomics Core in the SC Lipidomics and Pathobiology COBRE,
Department Biochemistry, MUSC [P20 RR017677]; National Institute of
Diabetes, Endocrinology and Metabolic Diseases of the National Institute
of Diabetes and Digestive and Kidney diseases (NIDDK); National
Institutes of Health; National Center for Research Resources through the
GCRC program; Genentech, Inc.; NIDDK
FX Financial support for this work was provided by the NIDDK Diabetic
Complications Consortium (DiaComp, www.diacomp.org), Grant DK076169
(RLK). This work was also supported by the National Institutes of Health
Grant P01-HL55782 (MLV). Additional funding was obtained from the
Department of Veterans Affairs Merit Review Program (MLV and RLK). The
contents of this manuscript do not represent the views of the Department
of Veterans Affairs or the United States Government. Sphingolipid
analyses were supported in part by the Lipidomics Shared Resource,
Hollings Cancer Center (P30 CA138313), and the Lipidomics Core in the SC
Lipidomics and Pathobiology COBRE, Department Biochemistry (P20
RR017677), MUSC. The DCCT/EDIC is sponsored through research contracts
from the National Institute of Diabetes, Endocrinology and Metabolic
Diseases of the National Institute of Diabetes and Digestive and Kidney
diseases (NIDDK) and the National Institutes of Health. Additional
support was provided by the National Center for Research Resources
through the GCRC program and by Genentech, Inc. through a cooperative
research and development agreement with the NIDDK.
NR 33
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U1 1
U2 1
PU HUMANA PRESS INC
PI TOTOWA
PA 999 RIVERVIEW DRIVE SUITE 208, TOTOWA, NJ 07512 USA
SN 1535-1084
EI 1559-1174
J9 NEUROMOL MED
JI Neuromol. Med.
PD MAR
PY 2017
VL 19
IS 1
BP 46
EP 56
DI 10.1007/s12017-016-8423-9
PG 11
WC Neurosciences
SC Neurosciences & Neurology
GA EN5EX
UT WOS:000396029500005
PM 27388466
ER
PT J
AU Gardner, RC
Langa, KM
Yaffe, K
AF Gardner, Raquel C.
Langa, Kenneth M.
Yaffe, Kristine
TI Subjective and objective cognitive function among older adults with a
history of traumatic brain injury: A population-based cohort study
SO PLOS MEDICINE
LA English
DT Article
ID TBI IDENTIFICATION METHOD; ALZHEIMERS-DISEASE; HEAD-INJURY; RISK-FACTOR;
DEMENTIA; RELIABILITY; ASSOCIATION; VETERANS; VALIDITY; HEALTH
AB Background
Traumatic brain injury (TBI) is extremely common across the lifespan and is an established risk factor for dementia. The cognitive profile of the large and growing population of older adults with prior TBI who do not have a diagnosis of dementia, however, has not been well described. Our aim was to describe the cognitive profile associated with prior TBI exposure among community-dwelling older adults without dementia-an understudied but potentially vulnerable population.
Methods and findings
In this population-based cohort study, we studied 984 community-dwelling older adults (age 51 y and older and their spouses) without dementia who had been randomly selected from respondents to the 2014 wave of the Health and Retirement Study to participate in a comprehensive TBI survey and who either reported no prior TBI (n = 737) or prior symptomatic TBI resulting in treatment in a hospital (n = 247). Mean time since first TBI was 38 +/- 19 y. Outcomes assessed included measures of global cognitive function, verbal episodic memory, semantic fluency, and calculation as well as a measure of subjective memory ("How would you rate your memory at the present time?"). We compared outcomes between the two TBI groups using regression models adjusting for demographics, medical comorbidities, and depression. Sensitivity analyses were performed stratified by TBI severity (no TBI, TBI without loss of consciousness [LOC], and TBI with LOC). Respondents with TBI were younger (mean age 64 +/- 10 y versus 68 +/- 11 y), were less likely to be female, and had higher prevalence of medical comorbidities and depression than respondents without TBI. Respondents with TBI did not perform significantly differently from respondents without TBI on any measure of objective cognitive function in either raw or adjusted models (fully adjusted: global cognitive function score 15.4 versus 15.2, p = 0.68; verbal episodic memory score 4.4 versus 4.3, p = 0.79; semantic fluency score 15.7 versus 14.0, p = 0.21; calculation impairment 22% versus 26%, risk ratio [RR] [95% CI] = 0.86 [0.67 +/- 1.11], p = 0.24). Sensitivity analyses stratified by TBI severity produced similar results. TBI was associated with significantly increased risk for subjective memory impairment in models adjusted for demographics and medical comorbidities (29% versus 24%; RR [95% CI]: 1.26 [1.02 +/- 1.57], p = 0.036). After further adjustment for active depression, however, risk for subjective memory impairment was no longer significant (RR [95% CI]: 1.18 [0.95 +/- 1.47], p = 0.13). Sensitivity analyses revealed that risk of subjective memory impairment was increased only among respondents with TBI with LOC and not among those with TBI without LOC. Furthermore, the risk of subjective memory impairment was significantly greater among those with TBI with LOC versus those without TBI even after adjustment for depression (RR [95% CI]: partially adjusted, 1.38 [1.09 +/- 1.74], p = 0.008; fully adjusted, 1.28 [1.01 +/- 1.61], p = 0.039).
Conclusions
In this population-based study of community-dwelling older adults without dementia, those with prior TBI with LOC were more likely to report subjective memory impairment compared to those without TBI even after adjustment for demographics, medical comorbidities, and active depression. Lack of greater objective cognitive impairment among those with versus without TBI may be due to poor sensitivity of the cognitive battery or survival bias, or may suggest that post-TBI cognitive impairment primarily affects executive function and processing speed, which were not rigorously assessed in this study. Our findings show that among community-dwelling non-demented older adults, history of TBI is common but may not preferentially impact cognitive domains of episodic memory, attention, working memory, verbal semantic fluency, or calculation.
C1 [Gardner, Raquel C.; Yaffe, Kristine] Univ Calif San Francisco, Dept Neurol, Memory & Aging Ctr, San Francisco, CA 94143 USA.
[Gardner, Raquel C.; Yaffe, Kristine] San Francisco VA Med Ctr, San Francisco, CA 94121 USA.
[Langa, Kenneth M.] Univ Michigan Hlth Syst, Div Gen Med, Ann Arbor, MI USA.
[Langa, Kenneth M.] Vet Affairs Ctr Practice Management & Outcomes Re, Ann Arbor, MI USA.
[Langa, Kenneth M.] Univ Michigan, Inst Social Res, Ann Arbor, MI USA.
[Langa, Kenneth M.] Univ Michigan, Inst Gerontol, Ann Arbor, MI 48109 USA.
[Langa, Kenneth M.] Univ Michigan, Inst Healthcare Policy & Innovat, Ann Arbor, MI 48109 USA.
[Yaffe, Kristine] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA.
[Yaffe, Kristine] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94143 USA.
RP Gardner, RC (reprint author), Univ Calif San Francisco, Dept Neurol, Memory & Aging Ctr, San Francisco, CA 94143 USA.; Gardner, RC (reprint author), San Francisco VA Med Ctr, San Francisco, CA 94121 USA.
EM raquel.gardner@ucsf.edu
FU National Institute of Neurological Disorders and Stroke [K23 NS095755];
National Institute on Aging [K24 AG031155, U01 AG009740]; American
Federation for Aging Research [K23 NS095755]; Weill Institute for
Neurosciences; Departments of Defense and Veterans Affairs
[W81XWH-12-1-0581, W81XWH-12-PHTBI-CENC]
FX This work was supported by the National Institute of Neurological
Disorders and Stroke (Beeson K23 NS095755 to RCG), National Institute on
Aging (K24 AG031155 to KY); the American Federation for Aging Research
(K23 NS095755 to RCG); the Weill Institute for Neurosciences (to RCG),
and the Departments of Defense and Veterans Affairs (W81XWH-12-1-0581
and W81XWH-12-PHTBI-CENC to KY). The Health and Retirement Study is
funded by the National Institute on Aging (U01 AG009740), and performed
at the Institute for Social Research, University of Michigan. The
funders had no role in study design, data collection and analysis,
decision to publish, or preparation of the manuscript.
NR 59
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U1 2
U2 2
PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1549-1676
J9 PLOS MED
JI PLos Med.
PD MAR
PY 2017
VL 14
IS 3
AR e1002246
DI 10.1371/journal.pmed.1002246
PG 16
WC Medicine, General & Internal
SC General & Internal Medicine
GA EQ2NJ
UT WOS:000397906100004
PM 28267747
ER
PT J
AU Fisher, M
Nahum, M
Howard, E
Rowlands, A
Brandrett, B
Kermott, A
Woolley, J
Vinogradov, S
AF Fisher, Melissa
Nahum, Mor
Howard, Elizabeth
Rowlands, Abby
Brandrett, Benjamin
Kermott, Amy
Woolley, Joshua
Vinogradov, Sophia
TI Supplementing Intensive Targeted Computerized Cognitive Training With
Social Cognitive Exercises for People With Schizophrenia: An Interim
Report
SO PSYCHIATRIC REHABILITATION JOURNAL
LA English
DT Article
DE cognitive remediation; emotion perception; motivation; neuroplasticity;
social cognition
ID NEUROCOGNITIVE DEFICITS; SCALE DEVELOPMENT; MENTAL-ILLNESS; VERBAL
MEMORY; NEURAL BASIS; MOTIVATION; REMEDIATION; PSYCHOSIS; ANHEDONIA;
PLEASURE
AB Objective: Individuals with schizophrenia demonstrate cognitive, social cognitive, and motivational deficits that contribute to impairment in real-world functioning. In the current study, we investigated the effects of supplementing computerized neurocognitive training with social cognitive exercises, as compared with neurocognitive training alone. Method: In this ongoing, double-blind, randomized controlled trial of 111 participants with psychosis, we compare the effects of supplementing intensive targeted cognitive training with social cognitive training exercises (TCT + SCT) with the effects of targeted cognitive training alone (TCT-only). Participants were assessed on cognition, symptoms, functional capacity, and functional outcomes, as well as social cognition and measures related to reward processing. Results: Both treatment groups showed significant improvement in multiple cognitive domains and improvement in functional capacity. However, as predicted, TCT + SCT group participants showed significant improvement in prosody identification and reward processing relative to TCT-only participants. Conclusions and Implications for Practice: Our findings indicate that supplementing intensive computerized cognitive training with social cognitive exercises in people with psychosis confers greater benefits in prosody identification and reward processing relative to cognitive training alone, even though both approaches drive significant improvements in cognition and functional capacity. Impairments in both prosody identification and reward processing have been associated with greater negative symptoms and poorer functional outcomes in schizophrenia, raising the possibility that this form of treatment may lead to better long-term outcomes than traditional cognitive training approaches. Follow-up assessments will determine whether results are durable and generalize over time to improvements in symptoms and functioning.
C1 [Fisher, Melissa] Univ Minnesota, Minneapolis, MN 55455 USA.
[Nahum, Mor] Posit Sci Inc, San Francisco, CA USA.
[Howard, Elizabeth; Rowlands, Abby; Brandrett, Benjamin; Kermott, Amy; Woolley, Joshua] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Howard, Elizabeth; Rowlands, Abby; Brandrett, Benjamin; Kermott, Amy; Woolley, Joshua] San Francisco VA Med Ctr, San Francisco, CA USA.
[Vinogradov, Sophia] Univ Minnesota, Minneapolis, MN 55455 USA.
[Vinogradov, Sophia] Univ Calif San Francisco, San Francisco, CA 94143 USA.
RP Vinogradov, S (reprint author), Univ Minnesota Med Sch, Dept Psychiat, F282-2A West,2450 Riverside Ave, Minneapolis, MN 55454 USA.
EM svinogra@umn.edu
FU PI on an NIMH SBIR grant
FX Fisher is a Co-Investigator on an NIMH SBIR grant to PositScience, and
does not hold any financial interest in the company. Nahum is a
consultant to PositScience, and the PI on an NIMH SBIR grant to
PositScience. She does not hold any financial interest in the company.
Vinogradov is a site PI on an NIMH SBIR grant to PositScience. She also
consults on the cognitive training software developed by PositScience.
Vinogradov does not hold a financial interest in the company.
NR 73
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U1 0
U2 0
PU CENTER PSYCHIATRIC REHABILITATION
PI BOSTON
PA BOSTON UNIV, 930 COMMONWEALTH AVE, BOSTON, MA 02215 USA
SN 1095-158X
EI 1559-3126
J9 PSYCHIATR REHABIL J
JI Psychiatr. Rehabil. J.
PD MAR
PY 2017
VL 40
IS 1
SI SI
BP 21
EP 32
DI 10.1037/pg0000244
PG 12
WC Psychiatry; Rehabilitation
SC Psychiatry; Rehabilitation
GA EQ4BN
UT WOS:000398017800004
PM 28368179
ER
PT J
AU Goldstein, LA
Dinh, J
Donalson, R
Hebenstreit, CL
Maguen, S
AF Goldstein, Lizabeth A.
Dinh, Julie
Donalson, Rosemary
Hebenstreit, Claire L.
Maguen, Shira
TI Impact of military trauma exposures on posttraumatic stress and
depression in female veterans
SO PSYCHIATRY RESEARCH
LA English
DT Article
DE Combat; Military sexual trauma; PTSD; Veterans; Women
ID MENTAL-HEALTH DIAGNOSES; WAR-I VETERANS; GENDER-DIFFERENCES; SEXUAL
ASSAULT; GULF-WAR; AFGHANISTAN VETERANS; RESILIENCE FACTORS; OEF/OIF
VETERANS; COMBAT EXPOSURE; WOMEN VETERANS
AB Previous research has demonstrated the deleterious effects of traumatic military experiences on symptoms of posttraumatic stress disorder (PTSD) and depression in female veterans. However, more research is needed to identify the unique predictors of distressing psychological symptoms when both combat-related and sexual trauma are considered, particularly as women's combat exposure in the military increases. Female veterans who had attended at least one appointment at a large Veterans Health Administration medical center were invited to complete questionnaires about traumatic military exposures and psychiatric symptoms. A total of 403 veterans responded, with 383 respondents' data used in analyses. Multiple regression analyses were conducted with trauma exposure items entered simultaneously to determine their association with symptoms of (1) PTSD and (2) depression. Sexual assault had the strongest relationship with both posttraumatic and depressive symptoms. Sexual assault, sexual harassment, feeling in danger of being killed, and seeing others killed/injured were associated with symptoms of PTSD, but only sexual assault and sexual harassment were associated with symptoms of depression, even when accounting for several aspects of combat exposure. Improving assessment for trauma exposure and developing treatments personalized to type of trauma experienced are important clinical research priorities as female service members' roles in the military expand.
C1 [Goldstein, Lizabeth A.; Dinh, Julie; Donalson, Rosemary; Hebenstreit, Claire L.; Maguen, Shira] San Francisco VA Med Ctr, 116P,4150 Clement St, San Francisco, CA 94121 USA.
[Goldstein, Lizabeth A.; Hebenstreit, Claire L.; Maguen, Shira] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA USA.
RP Goldstein, LA (reprint author), San Francisco VA Med Ctr, 116P,4150 Clement St, San Francisco, CA 94121 USA.
EM Lizabeth.Goldstein2@va.gov
FU Veterans Health and Integration Program (VEEP)
FX This research was supported by the Veterans Health and Integration
Program (VEEP; PI: Dr. Maguen). Writing of this manuscript was supported
by the Department of Veterans Affairs Office of Academic Affiliations,
Advanced Fellowship Program in Mental Illness Research and Treatment
(Dr. Goldstein) and Advanced Fellowship Program in Women's Health (Dr.
Hebenstreit). The funding sources did not have any role in the conduct
of the research or the preparation of this article.
NR 38
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U1 5
U2 5
PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 0165-1781
J9 PSYCHIAT RES
JI Psychiatry Res.
PD MAR
PY 2017
VL 249
BP 281
EP 285
DI 10.1016/j.psychres.2017.01.009
PG 5
WC Psychiatry
SC Psychiatry
GA EP4VI
UT WOS:000397377600043
PM 28135599
ER
PT J
AU Yuan, F
Xiong, GX
Cohen, NA
Cohen, AS
AF Yuan, Feng
Xiong, Guoxiang
Cohen, Noam A.
Cohen, Andakiva S.
TI Optimized Protocol of Methanol Treatment for Immunofluorescent Staining
in Fixed Brain Slices
SO APPLIED IMMUNOHISTOCHEMISTRY & MOLECULAR MORPHOLOGY
LA English
DT Article
DE brain ventricle; cilia; gamma-tubulin; beta-tubulin;
immunohistochemistry
ID IMMUNOHISTOCHEMISTRY; FIXATION; IMMUNOREACTIVITY; GUSTDUCIN; FORMALIN
AB We optimized methanol treatment in paraformaldehyde- fixed slices for immunofluorescent staining of ependymal basal bodies in brain ventricles. As 100% methanol induced severe deformations to the slices (including rolling and folding over), we tried to decrease methanol concentration. We found that 33.3% to 75% methanol could result in ideal immunostaining of basal bodies without inducing obvious deformations. Instead of treating slices at -20 degrees C (without proper cryoprotection measurements) as suggested in previous studies, we carried out methanol treatment at room temperature. Our modified protocol can not only raise immunostaining efficiency in tissue slices, it may also prevent potential freezing damages to the samples.
C1 [Yuan, Feng] Hosp Tongji Univ, Dept Orthoped, Shanghai, Peoples R China.
[Xiong, Guoxiang; Cohen, Andakiva S.] Univ Penn, Perelman Sch Med, Div Neurol, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA.
[Cohen, Noam A.] Univ Penn, Perelman Sch Med, Philadelphia Vet Affairs Med Ctr, Philadelphia, PA 19104 USA.
[Cohen, Noam A.] Univ Penn, Perelman Sch Med, Dept Otorhinolaryngol Head & Neck Surg, Philadelphia, PA 19104 USA.
[Cohen, Andakiva S.] Univ Penn, Perelman Sch Med, Dept Pediat, Philadelphia, PA 19104 USA.
RP Xiong, GX (reprint author), Childrens Hosp Philadelphia, Div Neurol, Philadelphia, PA 19104 USA.
EM xiong@email.chop.edu
FU NICHD NIH HHS [R37 HD059288]; NINDS NIH HHS [R01 NS069629]
NR 13
TC 1
Z9 1
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1541-2016
EI 1533-4058
J9 APPL IMMUNOHISTO M M
JI Appl. Immunohistochem.
PD MAR
PY 2017
VL 25
IS 3
BP 221
EP 224
PG 4
WC Anatomy & Morphology; Medical Laboratory Technology; Pathology
SC Anatomy & Morphology; Medical Laboratory Technology; Pathology
GA EN3VR
UT WOS:000395936500013
PM 26509907
ER
PT J
AU Campbell, SB
Renshaw, KD
Kashdan, TB
Curby, TW
Carter, SP
AF Campbell, Sarah B.
Renshaw, Keith D.
Kashdan, Todd B.
Curby, Timothy W.
Carter, Sarah P.
TI A Daily Diary Study of Posttraumatic Stress Symptoms and Romantic
Partner Accommodation
SO BEHAVIOR THERAPY
LA English
DT Article
DE PTSD; romantic relationships; accommodation; maintenance
ID SOCIAL SUPPORT; DISORDER; PTSD; VETERANS; EXPOSURE; OUTCOMES; THERAPY;
COMBAT; SCALE; COMMUNICATION
AB Little is known about the role of romantic partner symptom accommodation in PTSD symptom maintenance. To explore the bidirectional associations of posttraumatic stress disorder (PTSD) symptoms and romantic partner symptom accommodation over time, military servicemen (n = 64) with symptoms of PTSD and their cohabiting heterosexual civilian romantic partners (n = 64) completed a 2-week daily diary study. Cross-lagged, autoregressive models assessed the stability of men's PTSD symptoms and partners' accommodation, as well as the prospective associations of earlier PTSD symptoms with later accommodation and vice versa. Analyses used Bayesian estimation to provide point estimates (b) and Credible Intervals (CIs). In all models, PTSD symptoms (total and individual clusters) were highly stable (b = 0.91; CI: 0.88-0.95), and accommodation was moderately stable (b = 0.48; CI: 0.40-0.54). In all models, earlier PTSD symptoms (total and clusters) were significantly, positively associated with later accommodation (b = 0.04; CI: 0.02-0.07). In contrast, earlier accommodation was significantly associated only with later situational avoidance (b = 0.02; CI: 0.00-0.07). Thus, PTSD symptoms may lead to subsequent accommodating behaviors in romantic partners, but partner accommodation seems to contribute only to survivors' future situational avoidance symptoms. The findings reinforce the notion that PTSD symptoms have an impact on relationship behaviors, and that accommodation from partners may sustain avoidant behaviors in particular. Clinicians should attend to romantic partners' accommodating behaviors when working with survivors.
C1 [Campbell, Sarah B.; Renshaw, Keith D.; Kashdan, Todd B.; Curby, Timothy W.; Carter, Sarah P.] George Mason Univ, Fairfax, VA 22030 USA.
RP Campbell, SB (reprint author), VA Puget Sound Hlth Care Syst, Seattle Div, 1660 S Columbian Way,116MHC, Seattle, WA 98108 USA.
EM scampbep@gmu.edu
FU National Institute of Mental Health under Ruth L. Kirschstein National
Research Service Award [1F31MH098581-01A1]; International Society of
Traumatic Stress Studies; American Psychological Foundation
FX This research was supported in part by grants from the National
Institute of Mental Health under Ruth L. Kirschstein National Research
Service Award number 1F31MH098581-01A1, the International Society of
Traumatic Stress Studies, and the American Psychological Foundation
awarded to Sarah B. Campbell, M.A. The content is solely the
responsibility of the authors and does not necessarily represent the
official views of the National Institutes of Health.
NR 60
TC 0
Z9 0
U1 1
U2 1
PU ASSOC ADV BEHAVIOR THERAPY
PI NEW YORK
PA 305 7TH AVE #16A, NEW YORK, NY 10001-6008 USA
SN 0005-7894
EI 1878-1888
J9 BEHAV THER
JI Behav. Therapy
PD MAR
PY 2017
VL 48
IS 2
BP 222
EP 234
PG 13
WC Psychology, Clinical
SC Psychology
GA EO6KA
UT WOS:000396799700008
PM 28270332
ER
PT J
AU Knobloch-Fedders, LM
Caska-Wallace, C
Smith, TW
Renshaw, K
AF Knobloch-Fedders, Lynne M.
Caska-Wallace, Catherine
Smith, Timothy W.
Renshaw, Keith
TI Battling on the Home Front: Posttraumatic Stress Disorder and Conflict
Behavior Among Military Couples
SO BEHAVIOR THERAPY
LA English
DT Article
DE couples; PTSD; military; interpersonal behavior; Structural Analysis of
Social Behavior
ID ADMINISTERED PTSD SCALE; RELATIONSHIP QUALITY; COMBAT VETERANS;
STRUCTURAL-ANALYSIS; INTIMATE PARTNERS; DEPRESSION; SYMPTOMS; DISTRESS;
IMPACT; QUESTIONNAIRE
AB This study evaluated interpersonal behavior differences among male military service members with and without PTSD and their female partners. Couples (N= 64) completed a 17-minute videotaped conflict discussion, and their interaction behavior was coded using the circumplex-based Structural Analysis of Social Behavior model (SASB; Benjamin, 1979, 1987, 2000). Within couples, the behavior of partners was very similar. Compared to military couples without PTSD, couples with PTSD displayed more interpersonal hostility and control. Couples with PTSD also exhibited more sulking, blaming, and controlling behavior, and less affirming and connecting behavior, than couples without PTSD. Results advance our understanding of the relational impacts of PTSD on military service members and their partners, and underscore the value of couple-based interventions for PTSD in the context of relationship distress.
C1 [Knobloch-Fedders, Lynne M.] Northwestern Univ, Family Inst, Evanston, IL 60208 USA.
[Caska-Wallace, Catherine] Univ Washington, VA Puget Sound Hlth Care Syst, Mental Hlth Serv, Seattle Div, Seattle, WA 98195 USA.
[Smith, Timothy W.] Univ Utah, Salt Lake City, UT 84112 USA.
[Renshaw, Keith] George Mason Univ, Fairfax, VA 22030 USA.
RP Knobloch-Fedders, LM (reprint author), Northwestern Univ, Family Inst, Bette D Harris Ctr, 618 Lib Pl, Evanston, IL USA.
EM l-knobloch@northwestern.edu
FU American Psychological Association's Division 19 (Society for Military
Psychology) Member / Affiliate Member Research Grant Award; National
Institute of Mental Health grant [1F31MH091915-01A1]
FX This study was funded in part by the 2014 American Psychological
Association's Division 19 (Society for Military Psychology) Member /
Affiliate Member Research Grant Award, and by National Institute of
Mental Health grant 1F31MH091915-01A1.
NR 65
TC 0
Z9 0
U1 1
U2 1
PU ASSOC ADV BEHAVIOR THERAPY
PI NEW YORK
PA 305 7TH AVE #16A, NEW YORK, NY 10001-6008 USA
SN 0005-7894
EI 1878-1888
J9 BEHAV THER
JI Behav. Therapy
PD MAR
PY 2017
VL 48
IS 2
BP 247
EP 261
PG 15
WC Psychology, Clinical
SC Psychology
GA EO6KA
UT WOS:000396799700010
PM 28270334
ER
PT J
AU Askenazi, DJ
Heung, M
Connor, MJ
Basu, RK
Cerda, J
Doi, K
Koyner, JL
Bihorac, A
Golestaneh, L
Vijayan, A
Okusa, MD
Faubel, S
AF Askenazi, D. J.
Heung, Michael
Connor, Michael J., Jr.
Basu, Rajit K.
Cerda, Jorge
Doi, Kent
Koyner, Jay L.
Bihorac, Azra
Golestaneh, Ladan
Vijayan, Anitha
Okusa, Mark D.
Faubel, Sarah
CA Amer Soc
Nephrology Acute Kidney Injury Adv
TI Optimal Role of the Nephrologist in the Intensive Care Unit
SO BLOOD PURIFICATION
LA English
DT Article
DE Critical care nephrology; Quality Improvement; Acute kidney injury;
Education; Renal replacement therapy
ID ACUTE KIDNEY INJURY; RENAL-REPLACEMENT THERAPY; CRITICALLY-ILL PATIENTS;
CYCLE ARREST BIOMARKERS; FUROSEMIDE STRESS TEST; DIALYSIS FACILITY;
MEDICAL DIRECTOR; MORTALITY; AKI; SURGERY
AB As advances in Critical Care Medicine continue, critically ill patients are surviving despite the severity of their illness. The incidence of acute kidney injury (AKI) has increased, and its impact on clinical outcomes as well as medical expenditures has been established. The role, indications and technological advancements of renal replacement therapy (RRT) have evolved, allowing more effective therapies with less complications. With these changes, Critical Care Nephrology has become an established specialty, and ongoing collaborations between critical care physicians and nephrologist have improved education of multi-disciplinary team members and patient care in the ICU. Multidisciplinary programs to support these changes have been stablished in some hospitals to maximize the delivery of care, while other programs have continue to struggle in their ability to acquire the necessary resources to maximize outcomes, educate their staff, and develop quality initiatives to evaluate and drive improvements. Clearly, the role of the nephrologist in the ICU has evolved, and varies widely among institutions. This special article will provide insights that will hopefully optimize the role of the nephrologist as the leader of the acute care nephrology program, as clinician for critically ill patients, and as teacher for all members of the health care team. (C) 2016 S. Karger AG, Basel
C1 [Askenazi, D. J.] Univ Alabama Birmingham, Dept Pediat, Div Pediat Nephrol, ACC 516,1600 7th Ave South, Birmingham, AL 35233 USA.
[Heung, Michael] Univ Michigan, Dept Med, Div Nephrol, Ann Arbor, MI 48109 USA.
[Connor, Michael J., Jr.] Emory Univ, Dept Med, Div Renal Med, Atlanta, GA 30322 USA.
[Basu, Rajit K.] Cincinnati Childrens Hosp Ctr, Ctr Acute Care Nephrol, Cincinnati, OH USA.
[Cerda, Jorge] Albany Med Coll, Dept Med, Albany, NY 12208 USA.
[Koyner, Jay L.] Univ Chicago, Dept Med, Nephrol Sect, 5841 S Maryland Ave, Chicago, IL 60637 USA.
[Bihorac, Azra] Univ Florida, Dept Anesthesiol, Gainesville, FL USA.
[Golestaneh, Ladan] Albert Einstein Coll Med, Dept Clin Med, Div Nephrol, Bronx, NY 10467 USA.
[Vijayan, Anitha] Washington Univ, Div Nephrol, St Louis, MO USA.
[Okusa, Mark D.] Univ Virginia Hlth Syst, Div Nephrol, Charlottesville, VA USA.
[Faubel, Sarah] Univ Colorado, Dept Med, Denver, CO USA.
[Faubel, Sarah] Denver VA Med Ctr, Denver, CO USA.
[Doi, Kent] Tokyo Univ Hosp, Dept Emergency & Crit Care Med, Bunkyo Ku, Tokyo, Japan.
RP Askenazi, DJ (reprint author), Univ Alabama Birmingham, Dept Pediat, Div Pediat Nephrol, ACC 516,1600 7th Ave South, Birmingham, AL 35233 USA.
EM daskenazi@peds.uab.edu
OI Bihorac, Azra/0000-0002-5745-2863
FU NCATS NIH HHS [UL1 TR001417]; NIDDK NIH HHS [R01 DK103608]; NIGMS NIH
HHS [P50 GM111152, R01 GM110240]
NR 55
TC 0
Z9 0
U1 0
U2 0
PU KARGER
PI BASEL
PA ALLSCHWILERSTRASSE 10, CH-4009 BASEL, SWITZERLAND
SN 0253-5068
EI 1421-9735
J9 BLOOD PURIFICAT
JI Blood Purif.
PD MAR
PY 2017
VL 43
IS 1-3
BP 68
EP 77
DI 10.1159/000452317
PG 10
WC Hematology; Urology & Nephrology
SC Hematology; Urology & Nephrology
GA EN4AA
UT WOS:000395948100009
PM 27923227
ER
PT J
AU Garrido, MM
Prigerson, HG
Neupane, S
Penrod, JD
Johnson, CE
Boockvar, KS
AF Garrido, Melissa M.
Prigerson, Holly G.
Neupane, Suvam
Penrod, Joan D.
Johnson, Christopher E.
Boockvar, Kenneth S.
TI Mental Illness and Mental Healthcare Receipt among Hospitalized Veterans
with Serious Physical Illnesses
SO JOURNAL OF PALLIATIVE MEDICINE
LA English
DT Article
DE depression; hospitalized; mental health; veterans
ID OBSESSIVE-COMPULSIVE DISORDER; POSTTRAUMATIC-STRESS-DISORDER;
ADMINISTRATIVE DATA; PHARMACOLOGICAL-TREATMENT; PSYCHIATRIC COMORBIDITY;
ANXIETY DISORDERS; PALLIATIVE CARE; ADVANCED CANCER; HEART-FAILURE;
DEPRESSION
AB Background: Psychosocial distress among patients with limited life expectancy influences treatment decisions, treatment adherence, and physical health. Veterans may be at elevated risk of psychosocial distress at the end of life, and understanding their mental healthcare needs may help identify hospitalized patients to whom psychiatric services should be targeted. Objective: To examine mental illness prevalence and mental health treatment rates among a national sample of hospitalized veterans with serious physical illnesses. Design, Subjects, and Measurements: This was a retrospective study of 11,286 veterans hospitalized in a Veterans Health Administration acute care facility in fiscal year 2011 with diagnoses of advanced cancer, congestive heart failure, chronic obstructive pulmonary disease, and/or advanced HIV/AIDS. Prevalent and incident mental illness diagnoses during and before hospitalization and rates of psychotherapy and psychotropic use among patients with incident depression and anxiety were measured. Results: At least one-quarter of the patients in our sample had a mental illness or substance use disorder. The most common diagnoses at hospitalization were depression (11.4%), followed by alcohol abuse or dependence (5.5%), and post-traumatic stress disorder (4.9%). Of the 831 patients with incident past-year depression and 258 with incident past-year anxiety, nearly two-thirds received at least some psychotherapy or guideline-concordant medication within 90 days of diagnosis. Of 191 patients with incident depression and 47 with incident anxiety at time of hospitalization, fewer than half received mental healthcare before discharge. Conclusions: Many veterans hospitalized with serious physical illnesses have comorbid mental illnesses and may benefit from depression and anxiety treatment.
C1 [Garrido, Melissa M.; Penrod, Joan D.; Boockvar, Kenneth S.] James J Peters VA Med Ctr, GRECC, Bronx, NY USA.
[Garrido, Melissa M.; Neupane, Suvam; Penrod, Joan D.; Boockvar, Kenneth S.] Icahn Sch Med Mt Sinai, Brookdale Dept Geriatr & Palliat Med, New York, NY 10029 USA.
[Prigerson, Holly G.] Weill Cornell Med Coll, Cornell Ctr Res End Life Care, New York, NY USA.
[Johnson, Christopher E.] Univ Louisville, Dept Hlth Management & Syst Sci, Louisville, KY 40292 USA.
[Boockvar, Kenneth S.] Jewish Home Lifecare, New York, NY USA.
RP Garrido, MM (reprint author), James J Peters VA Med Ctr, GRECC 4A-17,130 W Kingsbridge Rd, Bronx, NY 10468 USA.
EM melissa.garrido@mssm.edu
FU VA HSRD [CDA 11-201/CDP 12-255]; NIH [CA197730, MH095378, MD007652];
American Federation for Aging Research
FX Dr. M.M.G. is supported by a career development award from VA HSR&D (CDA
11-201/CDP 12-255). Dr. H.G.P. is supported by the following NIH Grant
Nos.: CA197730, MH095378, and MD007652. Mr. S.N. is supported by the
American Federation for Aging Research.
NR 35
TC 0
Z9 0
U1 0
U2 0
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1096-6218
EI 1557-7740
J9 J PALLIAT MED
JI J. Palliat. Med.
PD MAR
PY 2017
VL 30
IS 3
BP 247
EP 252
DI 10.1089/jpm.2016.0261
PG 6
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA EM6FC
UT WOS:000395407200010
ER
PT J
AU Shatzel, JJ
Taylor, JA
AF Shatzel, Joseph J.
Taylor, Jason A.
TI Syndromes of Thrombotic Microangiopathy
SO MEDICAL CLINICS OF NORTH AMERICA
LA English
DT Article
DE Thrombotic thrombocytopenic purpura (TTP); Hemolytic uremic syndrome
(HUS); Microangiopathic hemolytic anemia (MAHA); Atypical hemolytic
uremic syndrome (aHUS); Pregnancy induced microangiopathic hemolytic
anemia; Transplant induced microangiopathic hemolytic anemia
ID HEMOLYTIC-UREMIC SYNDROME; VON-WILLEBRAND-FACTOR;
BONE-MARROW-TRANSPLANTATION; FACTOR-CLEAVING PROTEASE; THERAPEUTIC
PLASMA-EXCHANGE; STEM-CELL TRANSPLANTATION; ACUTE FATTY LIVER;
SINGLE-CENTER EXPERIENCE; SERUM LACTATE-DEHYDROGENASE; THROMBOCYTOPENIC
PURPURA
AB Thrombotic thrombocytopenia purpura (TTP) and the hemolytic uremic syndrome (HUS) are rare thrombotic microangiopathies that can be rapidly fatal. Although the acquired versions of TTP and HUS are generally highest on this broad differential, multiple rarer entities can produce a clinical picture similar to TTP/HUS, including microangiopathic hemolysis, renal failure, and neurologic compromise. More recent analysis has discovered a host of genetic factors that can produce microangiopathic hemolytic syndromes. This article discusses the current understanding of thrombotic microangiopathy and outlines the pathophysiology and causative agents associated with each distinct syndrome as well as the most accepted treatments.
C1 [Shatzel, Joseph J.] Oregon Hlth & Sci Univ, Knight Canc Inst, Div Hematol & Med Oncol, 3181 Southwest Sam Jackson Pk Rd, Portland, OR 97239 USA.
[Taylor, Jason A.] Oregon Hlth & Sci Univ, Portland VA Med Ctr, Hemophilia Ctr, Knight Canc Inst,Div Hematol & Med Oncol, 3181 Southwest Sam Jackson Pk Road,L586, Portland, OR 97239 USA.
RP Taylor, JA (reprint author), Oregon Hlth & Sci Univ, Portland VA Med Ctr, Hemophilia Ctr, Knight Canc Inst,Div Hematol & Med Oncol, 3181 Southwest Sam Jackson Pk Road,L586, Portland, OR 97239 USA.
EM taylojas@ohsu.edu
NR 183
TC 0
Z9 0
U1 1
U2 1
PU W B SAUNDERS CO-ELSEVIER INC
PI PHILADELPHIA
PA 1600 JOHN F KENNEDY BOULEVARD, STE 1800, PHILADELPHIA, PA 19103-2899 USA
SN 0025-7125
EI 1557-9859
J9 MED CLIN N AM
JI Med. Clin. N. Am.
PD MAR
PY 2017
VL 101
IS 2
BP 395
EP +
DI 10.1016/j.mcna.2016.09.010
PG 22
WC Medicine, General & Internal
SC General & Internal Medicine
GA EN7KD
UT WOS:000396180800011
ER
PT J
AU Church, LWP
Chopra, A
Judson, MA
AF Church, L. W. Preston
Chopra, Amit
Judson, Marc A.
TI Paradoxical Reactions and the Immune Reconstitution Inflammatory
Syndrome
SO MICROBIOLOGY SPECTRUM
LA English
DT Article
ID ACTIVE ANTIRETROVIRAL THERAPY; HUMAN-IMMUNODEFICIENCY-VIRUS;
MYCOBACTERIUM-AVIUM COMPLEX; HIV-INFECTED PATIENTS; KIDNEY-TRANSPLANT
RECIPIENT; OF-THE-LITERATURE; PULMONARY SARCOIDOSIS;
ACQUIRED-IMMUNODEFICIENCY; MILIARY TUBERCULOSIS; INTERFERON-GAMMA
AB In HIV-infected individuals, paradoxical reactions after the initiation of antiretroviral therapy (ART) are associated with a variety of underlying infections and have been called the immune reconstitution inflammatory syndrome (IRIS). In cases of IRIS associated with tuberculosis (TB), two distinct patterns of disease are recognized: (i) the progression of subclinical TB to clinical disease after the initiation of ART, referred to as unmasking, and (ii) the progression or appearance of new clinical and/or radiographic disease in patients with previously recognized TB after the initiation of ART, the classic or "paradoxical" TB-IRIS. IRIS can potentially occur in all granulomatous diseases, not just infectious ones. All granulomatous diseases are thought to result from interplay of inflammatory cells and mediators. One of the inflammatory cells thought to be integral to the development of the granuloma is the CD4 T lymphocyte. Therefore, HIV-infected patients with noninfectious granulomatous diseases such as sarcoidosis may also develop IRIS reactions. Here, we describe IRIS in HIV-infected patients with TB and sarcoidosis and review the basic clinical and immunological aspects of these phenomena.
C1 [Church, L. W. Preston] Ralph H Johnson VA Med Ctr, Charleston, SC 29425 USA.
[Chopra, Amit; Judson, Marc A.] Albany Med Coll, Div Pulm & Crit Care Med, Albany, NY 12208 USA.
RP Judson, MA (reprint author), Albany Med Coll, Div Pulm & Crit Care Med, Albany, NY 12208 USA.
EM judsonm@mail.amc.edu
NR 113
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Z9 0
U1 0
U2 0
PU AMER SOC MICROBIOLOGY
PI WASHINGTON
PA 1752 N ST NW, WASHINGTON, DC 20036-2904 USA
EI 2165-0497
J9 MICROBIOL SPECTR
JI Microbiol. Spectr.
PD MAR
PY 2017
VL 5
IS 2
AR UNSP TNMI7-0033-2016
DI 10.1128/microbiolspec.TNMI7-0033-2016
PG 15
WC Microbiology
SC Microbiology
GA EP3IE
UT WOS:000397275200004
ER
PT J
AU Bauman, WA
Krassioukov, A
Biering-Sorensen, F
AF Bauman, W. A.
Krassioukov, A.
Biering-Sorensen, F.
TI Version 2.0 of the international spinal cord injury endocrinology and
metabolic function basic data set
SO SPINAL CORD
LA English
DT Letter
C1 [Bauman, W. A.] James J Peters Vet Affairs Med Ctr, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY 10468 USA.
[Krassioukov, A.] Univ British Columbia, Int Collaborat Repair Discoveries ICORD, Div Phys Med & Rehabil,Auton Res Unit,Dept Med, Spinal Cord Program,GF Strong Rehabil Ctr, Vancouver, BC, Canada.
[Krassioukov, A.] Univ Western Ontario, London, ON, Canada.
[Biering-Sorensen, F.] Univ Copenhagen, Clin Spinal Cord Injuries, Rigshosp, Copenhagen, Denmark.
RP Bauman, WA (reprint author), James J Peters Vet Affairs Med Ctr, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY 10468 USA.
EM William.Bauman@va.gov
NR 4
TC 0
Z9 0
U1 0
U2 0
PU NATURE PUBLISHING GROUP
PI LONDON
PA MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
SN 1362-4393
EI 1476-5624
J9 SPINAL CORD
JI Spinal Cord
PD MAR
PY 2017
VL 55
IS 3
BP 327
EP 328
DI 10.1038/sc.2016.105
PG 2
WC Clinical Neurology; Rehabilitation
SC Neurosciences & Neurology; Rehabilitation
GA EN3RA
UT WOS:000395924400020
PM 27401128
ER
PT J
AU Johnson, TJ
Winger, DG
Hickey, RW
Switzer, GE
Miller, E
Nguyen, MB
Saladino, RA
Hausmann, LRM
AF Johnson, Tiffani J.
Winger, Daniel G.
Hickey, Robert W.
Switzer, Galen E.
Miller, Elizabeth
Nguyen, Margaret B.
Saladino, Richard A.
Hausmann, Leslie R. M.
TI Comparison of Physician Implicit Racial Bias Toward Adults Versus
Children
SO ACADEMIC PEDIATRICS
LA English
DT Article
DE implicit bias; pediatric health care disparities; physician implicit
attitudes; racial bias; racial disparities
ID ASSOCIATION TEST; ACHIEVEMENT GAP; EXPLICIT ATTITUDES;
AFRICAN-AMERICANS; UNCONSCIOUS RACE; MEDICAL-STUDENTS; DECISION-MAKING;
HEALTH-CARE; BLACK; STEREOTYPES
AB BACKGROUND AND OBJECTIVES: The general population and most physicians have implicit racial bias against black adults. Pediatricians also have implicit bias against black adults, albeit less than other specialties. There is no published research on the implicit racial attitudes of pediatricians or other physicians toward children. Our objectives were to compare implicit racial bias toward adults versus children among resident physicians working in a pediatric emergency department, and to assess whether bias varied by specialty (pediatrics, emergency medicine, or other), gender, race, age, and year of training.
METHODS: We measured implicit racial bias of residents before a pediatric emergency department shift using the Adult and Child Race Implicit Association Tests (IATs). Generalized linear models compared Adult and Child IAT scores and determined the association of participant demographics with Adult and Child IAT scores.
RESULTS: Among 91 residents, we found moderate pro-white/anti-black bias on both the Adult (mean = 0.49, standard deviation = 0.34) and Child Race IAT (mean = 0.55, standard deviation = 0.37). There was no significant difference between Adult and Child Race IAT scores (difference = 0.06, P = .15). Implicit bias was not associated with resident demographic characteristics, including specialty.
CONCLUSIONS: This is the first study demonstrating that resident physicians have implicit racial bias against black children, similar to levels of bias against black adults. Bias in our study did not vary by resident demographic characteristics, including specialty, suggesting that pediatric residents are as susceptible as other physicians to implicit bias. Future studies are needed to explore how physicians' implicit attitudes toward parents and children may impact inequities in pediatric health care.
C1 [Johnson, Tiffani J.; Hickey, Robert W.; Nguyen, Margaret B.; Saladino, Richard A.] Univ Pittsburgh, Div Pediat Emergency Med, Pittsburgh, PA USA.
[Miller, Elizabeth] Univ Pittsburgh, Div Adolescent & Young Adult Med, Pittsburgh, PA USA.
[Winger, Daniel G.] Univ Pittsburgh, Childrens Hosp Pittsburgh, Clin & Translat Sci Inst, Pittsburgh, PA USA.
[Switzer, Galen E.; Hausmann, Leslie R. M.] Univ Pittsburgh, Div Gen Internal Med, Pittsburgh, PA USA.
[Switzer, Galen E.; Hausmann, Leslie R. M.] Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA USA.
RP Johnson, TJ (reprint author), Childrens Hosp Philadelphia, PolicyLab, 3535 Market St,Room 1425, Philadelphia, PA 19104 USA.
EM johnsont6@email.chop.edu
FU RWJF [AMFDP 72430]; National Institutes of Health [UL 1-TR-000005];
[T32 HS 017587]; [K12 HL109009]
FX We thank Dennis Durbin, MD, MSCE, Children's Hospital of Philadelphia,
for his critical review of the manuscript. Supported in part by grants
T32 HS 017587, K12 HL109009, and RWJF AMFDP 72430 (to TJJ); and by the
National Institutes of Health through grant UL 1-TR-000005 to the
University of Pittsburgh Clinical and Translational Science Institute.
The sponsoring agencies had no role in the design and conduct of the
study; in the collection, management, analysis, and interpretation of
the data; or in the preparation, review, or approval of the manuscript.
The content of this article is solely the responsibility of the authors
and does not necessarily represent the official views of the sponsoring
agency.
NR 41
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U1 5
U2 5
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1876-2859
EI 1876-2867
J9 ACAD PEDIATR
JI Acad. Pediatr.
PD MAR
PY 2017
VL 17
IS 2
BP 120
EP 126
PG 7
WC Pediatrics
SC Pediatrics
GA EM9GB
UT WOS:000395618700004
PM 27620844
ER
PT J
AU Byers, AL
Lai, AX
Bruce, ML
AF Byers, Amy L.
Lai, Amy X.
Bruce, Martha L.
TI Timing of Mental Health Services Use: Reducing the Risk of Late-life
Suicidal Behavior
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Meeting Abstract
CT Annual Meeting of the American-Association-for-Geriatric-Psychiatry
(AAGP) on Integrated Geriatric Mental Health Care Through Innovation
CY MAR 24-27, 2017
CL Dallas, TX
SP Amer Assoc Geriatr Psychiat
C1 [Byers, Amy L.] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Byers, Amy L.; Lai, Amy X.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Bruce, Martha L.] Dartmouth Coll, Geisel Sch Med, Hanover, NH 03755 USA.
FU NIH [MD007019]
FX This work is supported by a NIH R01 grant (MD007019) that is
administered by the Northern California Institute for Research and
Education through resources from the San Francisco Veterans Affairs
Medical Center.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
SU S
MA NR 21
BP S135
EP S136
PG 2
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1IG
UT WOS:000397138000133
ER
PT J
AU Gebara, MA
DiNapoli, E
Kho, T
Karp, J
Gildengers, A
Butters, MA
Albert, S
Reynoldsiii, CF
AF Gebara, Marie Anne
DiNapoli, Elizabeth
Kho, Terry
Karp, Jordan
Gildengers, Ariel
Butters, Meryl A.
Albert, Stven
Reynoldsiii, Charles F.
TI Depression Prevention in Older Adults: Changes in Mood and Sleep
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Meeting Abstract
CT Annual Meeting of the American-Association-for-Geriatric-Psychiatry
(AAGP) on Integrated Geriatric Mental Health Care Through Innovation
CY MAR 24-27, 2017
CL Dallas, TX
SP Amer Assoc Geriatr Psychiat
C1 [Gebara, Marie Anne; DiNapoli, Elizabeth] VA Pittsburgh Healthcare Syst, Mental Illness Res Educ & Clin Ctr, Pittsburgh, PA USA.
[Gebara, Marie Anne; Kho, Terry; Karp, Jordan; Gildengers, Ariel; Butters, Meryl A.; Albert, Stven; Reynoldsiii, Charles F.] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA.
NR 0
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
SU S
MA EI 3
BP S64
EP S65
PG 2
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1IG
UT WOS:000397138000061
ER
PT J
AU Kasckow, J
Reynolds, CF
Karp, J
Chickering, S
Morse, J
AF Kasckow, John
Reynolds, Charles F., III
Karp, Jordan
Chickering, Sunita
Morse, Jennifer
TI Problem Solving Therapy Improves Social Problem Solving Skills in Older
Adults with Depression and Low Back Pain
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Meeting Abstract
CT Annual Meeting of the American-Association-for-Geriatric-Psychiatry
(AAGP) on Integrated Geriatric Mental Health Care Through Innovation
CY MAR 24-27, 2017
CL Dallas, TX
SP Amer Assoc Geriatr Psychiat
C1 [Kasckow, John; Reynolds, Charles F., III; Karp, Jordan; Chickering, Sunita] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA.
[Kasckow, John; Karp, Jordan] VA Pittsburgh Hlth Care Syst, Pittsburgh, PA USA.
[Morse, Jennifer] Chatham Univ, Pittsburgh, PA USA.
FU [AG033575]; [MH101371]
FX This research was funded by: AG033575 and MH101371.
NR 0
TC 0
Z9 0
U1 2
U2 2
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
SU S
MA NR 2
BP S116
EP S117
PG 2
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1IG
UT WOS:000397138000114
ER
PT J
AU Kasckow, J
Gebara, MA
Mulsant, BH
Lenze, E
AF Kasckow, John
Gebara, Marie Anne
Mulsant, Benoit H.
Lenze, Eric
TI ADVANCES IN PHARMACOTHERAPY OF LATE-LIFE DEPRESSION
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Meeting Abstract
CT Annual Meeting of the American-Association-for-Geriatric-Psychiatry
(AAGP) on Integrated Geriatric Mental Health Care Through Innovation
CY MAR 24-27, 2017
CL Dallas, TX
SP Amer Assoc Geriatr Psychiat
C1 [Kasckow, John] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA.
[Gebara, Marie Anne] VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Mulsant, Benoit H.; Lenze, Eric] Univ Toronto, Toronto, ON, Canada.
FU Bristol-Myers Squibb; Eli Lilli; NIH; CAMH Foundation; Lundbeck; Takeda
FX Bristol-Myers Squibb-Medications for a NIH-funded clinical trial; Eli
Lilli-Medications for a NIH-funded clinical trial; Pfizer-Medications
for a NIH-funded clinical trial; Capital Solution Design LLC-Software
used in study funded by CAMH Foundation; Lundbeck-co-funding for IISR;
Takeda-co-funding for IISR
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
SU S
MA 107
BP S7
EP S7
PG 1
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1IG
UT WOS:000397138000009
ER
PT J
AU Radue, RM
Boyle, LL
Welch, L
Eastman, A
Schroeder, R
Hermann, C
Barczi, S
AF Radue, Rebecca M.
Boyle, Lisa L.
Welch, Lauren
Eastman, Alexis
Schroeder, Rebecca
Hermann, Carol
Barczi, Steve
TI Interprofessional Learners' Performance in a Late Life Depression
Simulated-Patient Assessment: Preliminary Results From the GEAR-UP
Project
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Meeting Abstract
CT Annual Meeting of the American-Association-for-Geriatric-Psychiatry
(AAGP) on Integrated Geriatric Mental Health Care Through Innovation
CY MAR 24-27, 2017
CL Dallas, TX
SP Amer Assoc Geriatr Psychiat
C1 [Radue, Rebecca M.; Boyle, Lisa L.; Barczi, Steve] Univ Wisconsin, Madison, WI USA.
[Boyle, Lisa L.; Welch, Lauren; Eastman, Alexis; Schroeder, Rebecca; Hermann, Carol; Barczi, Steve] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
FU William S. Middleton Veterans Administration (VA) Geriatric Research,
Education and Clinical Center (GRECC) & University ofWisconsin (UW)
Department of Medicine, Madison, WI; Health Resources and Services
Administration (HRSA) of the U.S. Department of Health and Human
Services (HHS) [U1QHP28712]
FX This research was funded by: William S. Middleton Veterans
Administration (VA) Geriatric Research, Education and Clinical Center
(GRECC) & University ofWisconsin (UW) Department of Medicine, Madison,
WI-This project was supported by the Health Resources and Services
Administration (HRSA) of the U.S. Department of Health and Human
Services (HHS) under grant U1QHP28712 (Geriatrics Workforce Enhancement
Program). The information or content and conclusions contained herein
are those of the authors and should not be construed as the official
position or policy of, nor should any endorsements be inferred by HRSA,
HHS or the U.S. Government.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
SU S
MA EI 56
BP S113
EP S115
PG 3
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1IG
UT WOS:000397138000111
ER
PT J
AU Renn, BN
Ali, AA
Thielke, S
Catic, A
Martini, SR
Mitchell, BG
Kunik, M
AF Renn, Brenna N.
Ali, Ali Asghar
Thielke, Stephen
Catic, Angela
Martini, Sharyl R.
Mitchell, Brian G.
Kunik, Mark
TI A Review of Cholinesterase Inhibitor Discontinuation in Alzheimer's
Disease: Should Clinicians Ever Stop Treatment?
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Meeting Abstract
CT Annual Meeting of the American-Association-for-Geriatric-Psychiatry
(AAGP) on Integrated Geriatric Mental Health Care Through Innovation
CY MAR 24-27, 2017
CL Dallas, TX
SP Amer Assoc Geriatr Psychiat
C1 [Renn, Brenna N.; Thielke, Stephen] Univ Washington, Seattle, WA 98195 USA.
[Ali, Ali Asghar; Martini, Sharyl R.; Mitchell, Brian G.; Kunik, Mark] Baylor Coll Med, Houston, TX 77030 USA.
[Ali, Ali Asghar; Catic, Angela; Mitchell, Brian G.] Michael E DeBakey VA Med Ctr, Houston, TX USA.
[Thielke, Stephen] VA Puget Sound Healthcare Syst, Seattle, WA USA.
[Kunik, Mark] VA HSR&D Houston Ctr Innovat, Houston, TX USA.
NR 0
TC 0
Z9 0
U1 2
U2 2
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD MAR
PY 2017
VL 25
IS 3
SU S
MA EI 19
BP S80
EP S81
PG 2
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1IG
UT WOS:000397138000077
ER
PT J
AU Ahmad, I
Zelnick, LR
Robinson, NR
Hung, AM
Kestenbaum, B
Utzschneider, KM
Kahn, SE
de Boer, IH
AF Ahmad, Iram
Zelnick, Leila R.
Robinson, Nicole R.
Hung, Adriana M.
Kestenbaum, Bryan
Utzschneider, Kristina M.
Kahn, Steven E.
de Boer, Ian. H.
TI Chronic kidney disease and obesity bias surrogate estimates of insulin
sensitivity compared with the hyperinsulinemic euglycemic clamp
SO AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
LA English
DT Article
ID GLUCOSE-TOLERANCE TEST; RENAL-DISEASE; FATTY-ACIDS; RESISTANCE;
CLEARANCE; INDEX; HOMEOSTASIS; SECRETION; VALIDATION; METABOLISM
AB Insulin sensitivity can be measured by procedures such as the hyperinsulinemic euglycemic clamp or by using surrogate indices. Chronic kidney disease (CKD) and obesity may differentially affect these measurements because of changes in insulin kinetics and organ-specific effects on insulin sensitivity. In a cross-sectional study of 59 subjects with nondiabetic CKD [estimated glomerular filtration rate: (GFR) , 60 ml.min(-1.)1.73 m(2)] and 39 matched healthy controls, we quantified insulin sensitivity by clamp (SIclamp), oral glucose tolerance test, and fasting glucose and insulin. We compared surrogate insulin sensitivity indices to SIclamp using descriptive statistics, graphical analyses, correlation coefficients, and linear regression. Mean age was 62.6 yr; 48% of the participants were female, and 77% were Caucasian. Insulin sensitivity indices were 8-38% lower in participants with vs. without CKD and 13-59% lower in obese compared with nonobese participants. Correlations of surrogate indices with SIclamp did not differ significantly by CKD or obesity status. Adjusting for SIclamp in addition to demographic factors, Matsuda index was 15% lower in participants with vs. without CKD (P = 0.09) and 36% lower in participants with vs. without obesity (P = 0.0001), whereas 1/HOMA-IR was 23% lower in participants with vs. without CKD (P = 0.02) and 46% lower in participants with vs. without obesity (P = 0.0001). We conclude that CKD and obesity do not significantly alter correlations of surrogate insulin sensitivity indices with SIclamp, but they do bias surrogate measurements of insulin sensitivity toward lower values. This bias may be due to differences in insulin kinetics or organ-specific responses to insulin.
C1 [Ahmad, Iram; Utzschneider, Kristina M.; Kahn, Steven E.] Univ Washington, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA USA.
[Ahmad, Iram; Zelnick, Leila R.; Robinson, Nicole R.; Kestenbaum, Bryan; de Boer, Ian. H.] Univ Washington, Dept Med, Div Nephrol, Kidney Res Inst, Seattle, WA 98195 USA.
[Hung, Adriana M.] Vanderbilt Univ, Sch Med, Div Nephrol & Hypertens, Nashville, TN 37212 USA.
[Utzschneider, Kristina M.; Kahn, Steven E.; de Boer, Ian. H.] Vet Affairs Puget Sound Hlth Care Syst, Seattle, WA USA.
RP Ahmad, I (reprint author), Kidney Res Inst, 325 9th Ave,Box 359606, Seattle, WA 98104 USA.
EM iram@uw.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases
[R01-DK-087726]; Department of Veterans Affairs; National Institutes of
Health Grants [UL1-TR-000423, P01-DK-017047, P30-DK-035816,
R01-DK-088762, R01-DK-099199, T32-DK-007247]; unrestricted fund from the
Northwest Kidney Center
FX The SUGAR study was funded primarily by Grant no. R01-DK-087726 from the
National Institute of Diabetes and Digestive and Kidney Diseases.
Additional support came from the Department of Veterans Affairs,
National Institutes of Health Grants UL1-TR-000423, P01-DK-017047,
P30-DK-035816, R01-DK-088762, R01-DK-099199, and T32-DK-007247, and an
unrestricted fund from the Northwest Kidney Center.
NR 37
TC 0
Z9 0
U1 1
U2 1
PU AMER PHYSIOLOGICAL SOC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 0193-1849
EI 1522-1555
J9 AM J PHYSIOL-ENDOC M
JI Am. J. Physiol.-Endocrinol. Metab.
PD MAR
PY 2017
VL 312
IS 3
BP E175
EP E182
DI 10.1152/ajpendo.00394.2016
PG 8
WC Endocrinology & Metabolism; Physiology
SC Endocrinology & Metabolism; Physiology
GA EN1YD
UT WOS:000395805500005
PM 28073780
ER
PT J
AU Jaconis, M
Ana, EJS
Killeen, TK
Badour, CL
Back, SE
AF Jaconis, Maryanne
Ana, Elizabeth J. Santa
Killeen, Therese K.
Badour, Christal L.
Back, Sudie E.
TI Case-Series: Concurrent Treatment of PTSD and Alcohol Use Disorder via
Telehealth in a Female Iraq Veteran
SO AMERICAN JOURNAL ON ADDICTIONS
LA English
DT Article
ID POSTTRAUMATIC-STRESS-DISORDER; PROLONGED EXPOSURE THERAPY; DEPENDENCE
AB Background and Objectives: A growing literature provides evidence for the use of integrated treatments (e.g., Concurrent Treatment of PTSD and Substance Use Disorders Using Prolonged Exposure; COPE); however, no known studies have applied COPE via telehealth.
Method: COPE was delivered via telehealth to treat one black female veteran with combat trauma and alcohol use disorder.
Results: The patient demonstrated significant reductions in alcohol consumption and PTSD and depressive symptoms.
Conclusions and Scientific Significance: Although preliminary, findings demonstrate that integrated treatment via telehealth is feasible and effective, and may be useful for female veterans reluctant to seek services at male-dominated VAMCs.
C1 [Jaconis, Maryanne; Ana, Elizabeth J. Santa; Killeen, Therese K.; Back, Sudie E.] Med Univ South Carolina, Dept Psychiat & Behav Sci, Addict Sci Div, Charleston, SC USA.
[Jaconis, Maryanne] Univ Wyoming, Dept Psychol, Laramie, WY 82071 USA.
[Jaconis, Maryanne] VA Portland Hlth Care Syst, 3710 SW US Vet Hosp Rd,P3MHN, Portland, OR 97202 USA.
[Ana, Elizabeth J. Santa; Killeen, Therese K.; Back, Sudie E.] Ralph H Johnson VA Med Ctr, Charleston, SC USA.
[Badour, Christal L.] Univ Kentucky, Dept Psychol, Lexington, KY 40506 USA.
RP Jaconis, M (reprint author), VA Portland Hlth Care Syst, 3710 SW US Vet Hosp Rd,P3MHN, Portland, OR 97202 USA.
EM maryanne.jaconis@va.gov
FU NIDA [T32 DA007288]
FX This publication was supported by NIDA grant T32 DA007288 (Jaconis).
NR 11
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1055-0496
EI 1521-0391
J9 AM J ADDICTION
JI Am. J. Addict.
PD MAR
PY 2017
VL 26
IS 2
BP 112
EP 114
DI 10.1111/ajad.12481
PG 3
WC Substance Abuse
SC Substance Abuse
GA EP3QK
UT WOS:000397296600002
PM 28118514
ER
PT J
AU Capurso, NA
AF Capurso, Noah A.
TI Case-Series: Naltrexone for the Treatment of Comorbid Tobacco and
Pornography Addiction
SO AMERICAN JOURNAL ON ADDICTIONS
LA English
DT Article
ID SMOKING-CESSATION; CONTROLLED-TRIAL; ALCOHOL; AUGMENTATION; DISORDER;
BEHAVIOR
AB Background and Objectives: Co-occurring addictive disorders are common, however treatment strategies for this population have not been extensively studied. This is especially the case for behavioral addictions.
Methods: We present a patient (N = 1) with tobacco use disorder and problematic pornography use treated with naltrexone.
Results: Naltrexone treatment resulted in a decrease in pornography viewing and cigarette smoking, however had the adverse effect of anhedonia. A lower dose modestly impacted pornography viewing but not smoking.
Discussions and Conclusions: Relevant literature regarding co-occurring addictions as well as use of naltrexone is reviewed.
Scientific Significance: This report represents the first case of tobacco and pornography co-addiction in the literature and supports the assertion that treatment of one addictive disorder can benefit another in the dually addicted patient. The efficacy of naltrexone for smoking is notable as previous studies of naltrexone in smoking have been disappointing. This case suggests future treatment strategies for comorbid addictions.
C1 [Capurso, Noah A.] Yale Univ, Sch Med, Dept Psychiat, 300 George St,Suite 901, New Haven, CT 06520 USA.
[Capurso, Noah A.] VA Connecticut Healthcare Syst, US Dept Vet Affairs, West Haven, CT USA.
RP Capurso, NA (reprint author), Yale Univ, Sch Med, Dept Psychiat, 300 George St,Suite 901, New Haven, CT 06520 USA.
EM noah.capurso@yale.edu
NR 20
TC 0
Z9 0
U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1055-0496
EI 1521-0391
J9 AM J ADDICTION
JI Am. J. Addict.
PD MAR
PY 2017
VL 26
IS 2
BP 115
EP 117
DI 10.1111/ajad.12501
PG 3
WC Substance Abuse
SC Substance Abuse
GA EP3QK
UT WOS:000397296600003
PM 28106937
ER
PT J
AU Shields, RK
Chen, L
Cheng, SJ
Chavda, KD
Press, EG
Snyder, A
Pandey, R
Doi, Y
Kreiswirth, BN
Nguyen, MH
Clancy, CJ
AF Shields, Ryan K.
Chen, Liang
Cheng, Shaoji
Chavda, Kalyan D.
Press, Ellen G.
Snyder, Avin
Pandey, Ruchi
Doi, Yohei
Kreiswirth, Barry N.
Nguyen, M. Hong
Clancy, Cornelius J.
TI Emergence of Ceftazidime-Avibactam Resistance Due to Plasmid-Borne
bla(KPC-3) Mutations during Treatment of Carbapenem-Resistant Klebsiella
pneumoniae Infections
SO ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
LA English
DT Article
DE ceftazidime-avibactam; resistance; carbapenem-resistant
Enterobacteriaceae; Klebsiella pneumoniae; Klebsiella pneumoniae
carbapenemase,sequence type 258
ID SEQUENCE TYPE 258; BETA-LACTAMASE; US HOSPITALS; ENTEROBACTERIACEAE;
KPC; BACTEREMIA; MORTALITY; EVOLUTION; VARIANTS; THERAPY
AB Ceftazidime-avibactam is a novel beta lactam/ beta-lactamase inhibitor with activity against carbapenem-resistant Enterobacteriaceae (CRE) that produce Kleb-siella pneumoniae carbapenemase (KPC). We report the first cases of ceftazidimeavibactam resistance to develop during treatment of CRE infections and identify resistance mechanisms. Ceftazidime-avibactam-resistant K. pneumoniae emerged in three patients after ceftazidime-avibactam treatment for 10 to 19 days. Wholegenome sequencing (WGS) of longitudinal ceftazidime-avibactam-susceptible and -resistant K. pneumoniae isolates was used to identify potential resistance mechanisms. WGS identified mutations in plasmid-borne bla(KPC-3), which were not present in baseline isolates. bla(KPC-3) mutations emerged independently in isolates of a novel sequence type 258 sublineage and resulted in variant KPC-3 enzymes. The mutations were validated as resistance determinants by measuring MICs of ceftazidime-avibactam and other agents following targeted gene disruption in K. pneumoniae, plasmid transfer, and blaKPC cloning into competent Escherichia coli. In rank order, the impact of KPC-3 variants on ceftazidime-avibactam MICs was as follows: D179Y/T243M double substitution > D179Y > V240G. Remarkably, mutations reduced meropenem MICs >= 4-fold from baseline, restoring susceptibility in K. pneumoniae from two patients. Cefepime and ceftriaxone MICs were also reduced >= 4-fold against D179Y/T243M and D179Y variant isolates, but susceptibility was not restored. Reverse transcription-PCR revealed that expression of bla(KPC-3) encoding D179Y/T243M and D179Y variants was diminished compared to bla(KPC-3) expression in baseline isolates. In conclusion, the development of resistance-conferring bla(KPC-3) mutations in K. pneumoniae within 10 to 19 days of ceftazidime-avibactam exposure is troubling, but clinical impact may be ameliorated if carbapenem susceptibility is restored in certain isolates.
C1 [Shields, Ryan K.; Cheng, Shaoji; Press, Ellen G.; Snyder, Avin; Doi, Yohei; Nguyen, M. Hong; Clancy, Cornelius J.] Univ Pittsburgh, Dept Med, Pittsburgh, PA 15260 USA.
[Shields, Ryan K.; Nguyen, M. Hong; Clancy, Cornelius J.] Univ Pittsburgh, Med Ctr, XDR Pathogen Lab, Pittsburgh, PA 15260 USA.
[Chen, Liang; Chavda, Kalyan D.; Pandey, Ruchi; Kreiswirth, Barry N.] Rutgers State Univ, New Jersey Med Sch, Publ Hlth Res Inst, TB Ctr, Newark, NJ USA.
[Clancy, Cornelius J.] VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
RP Nguyen, MH (reprint author), Univ Pittsburgh, Dept Med, Pittsburgh, PA 15260 USA.; Nguyen, MH (reprint author), Univ Pittsburgh, Med Ctr, XDR Pathogen Lab, Pittsburgh, PA 15260 USA.
EM mhn5@pitt.edu
FU National Institutes of Health [K08AI114883, R21AI117338, R01AI090155,
UM1AI104681, R21AI111037]
FX This work was funded, in part, by grants from the National Institutes of
Health (K08AI114883 to R.K.S., R21AI117338 to L.C., R01AI090155 to
B.N.K., UM1AI104681 to M.H.N., and R21AI111037 to C.J.C.).
NR 41
TC 1
Z9 1
U1 1
U2 1
PU AMER SOC MICROBIOLOGY
PI WASHINGTON
PA 1752 N ST NW, WASHINGTON, DC 20036-2904 USA
SN 0066-4804
EI 1098-6596
J9 ANTIMICROB AGENTS CH
JI Antimicrob. Agents Chemother.
PD MAR
PY 2017
VL 61
IS 3
AR e02097-16
DI 10.1128/AAC.02097-16
PG 11
WC Microbiology; Pharmacology & Pharmacy
SC Microbiology; Pharmacology & Pharmacy
GA EL4QM
UT WOS:000394605900054
ER
PT J
AU Locke, FL
Pidala, J
Storer, B
Martin, PJ
Pulsipher, MA
Chauncey, TR
Jacobsen, N
Kroger, N
Walker, I
Light, S
Shaw, BE
Beato, F
Laport, GG
Nademanee, A
Keating, A
Socie, G
Anasetti, C
AF Locke, Frederick L.
Pidala, Joseph
Storer, Barry
Martin, Paul J.
Pulsipher, Michael A.
Chauncey, Thomas R.
Jacobsen, Niels
Kroeger, Nicolaus
Walker, Irwin
Light, Susan
Shaw, Bronwen E.
Beato, Francisca
Laport, Ginna G.
Nademanee, Auayporn
Keating, Armand
Socie, Gerard
Anasetti, Claudio
TI CD25 Blockade Delays Regulatory T Cell Reconstitution and Does Not
Prevent Graft-versus-Host Disease After Allogeneic Hematopoietic Cell
Transplantation
SO BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
LA English
DT Article
DE Antitumor immunity; Daclizumab; Regulatory T cells
ID BONE-MARROW-TRANSPLANTATION; STEROID-REFRACTORY ACUTE; PERIPHERAL-BLOOD;
MONOCLONAL-ANTIBODY; IMPROVED SURVIVAL; UNRELATED DONORS; STEM-CELLS;
DACLIZUMAB; IMMUNOTHERAPY; RECIPIENTS
AB Daclizumab, a humanized monoclonal antibody, binds CD25 and blocks formation of the IL-2 receptor on T cells. A study of daclizumab as acute graft-versus-host disease (GVHD) prophylaxis after unrelated bone marrow transplantation was conducted before the importance of CD25(+)FOXP3(+) regulatory T cells (Tregs) was recognized. Tregs can abrogate the onset of GVHD. The relation between Tregs and a graft-versus-malignancy effect is not fully understood. An international, multicenter, double-blind clinical trial randomized 210 adult or pediatric patients to receive 5 weekly doses of daclizumab at 0.3 mg/kg (n = 69) or 1.2 mg/kg (n = 76) or placebo (n = 65) after unrelated marrow transplantation for treatment of hematologic malignancies or severe aplas-, tic anemia. The risk of acute GVHD did not differ among the groups (P =.68). Long-terrri follow-up of clinical outcomes and correlative analysis of peripheral blood T cell phenotype suggested that the patients treated with daclizumab had an increased risk of chronic GVHD (hazard ratio [HR]. 1.49; 95% confidence interval [CI], 1.0 to 2.3; P =.08) and a decreased risk of relapse (HR, 0.57; 95% CI, 0.3 to 1.0; P =.05), but similar survival (HR, 0.89; 95% CI, 0.6 to 1.3; P =.53). T cells from a subset of patients (n = 107) were analyzed by flow cytometry. Compared with placebo, treatment with daclizumab decreased the proportion of Tregs among CD4 T cells at days 11-35 and increased the proportion of central memory cells among CD4 T cells at 1 year. Prophylactic administration of daclizumab does not prevent acute GVHD, but may increase the risk of chronic GVHD and decrease the risk of relapse. By delaying Treg reconstitution and promoting immunologic memory, anti-CD25 therapy may augment alloreactivity and antitumor immunity. (C) 2017 Published by Elsevier Inc. on behalf of the American Society for Blood and Marrow Transplantation.
C1 [Locke, Frederick L.; Pidala, Joseph; Beato, Francisca; Anasetti, Claudio] H Lee Moffitt Canc Ctr & Res Inst, Blood & Marrow Transplantat Program, Tampa, FL USA.
[Storer, Barry; Martin, Paul J.] Fred Hutchinson Canc Res Ctr, Div Clin Res, 1124 Columbia St, Seattle, WA 98104 USA.
[Martin, Paul J.; Chauncey, Thomas R.] Univ Washington, Dept Med, Div Oncol, Seattle, WA 98195 USA.
[Pulsipher, Michael A.] Univ Utah, Huntsman Canc Inst, Med Ctr, Blood & Marrow Transplant Program, Salt Lake City, UT 84112 USA.
[Chauncey, Thomas R.] VA Puget Sound Hlth Care Syst, Canc Care Div, Seattle, WA USA.
[Jacobsen, Niels] Rigshospitalet, Dept Hematol, Copenhagen, Denmark.
[Kroeger, Nicolaus] Univ Med Ctr Hamburg Eppendorf, Ctr Oncol, Dept Stem Cell Transplantat, Hamburg, Germany.
[Walker, Irwin] McMaster Univ, Dept Med, Hamilton, ON L8N 3Z5, Canada.
[Light, Susan] Hoffman La Roche, Nutley, NJ USA.
[Shaw, Bronwen E.] Royal Marsden Hosp, Haemato Oncol Unit, Downs Rd, Sutton SM2 5NG, Surrey, England.
[Laport, Ginna G.] Stanford Univ, Div Blood & Marrow Transplantat, Stanford, CA 94305 USA.
[Nademanee, Auayporn] Hematol Malignancies & Stem Cell Transplantat Ins, City Hope, Duarte, CA USA.
[Keating, Armand] Princess Margaret Hosp, Blood & Marrow Transplant Ctr, Dept Hematol, Toronto, ON M4X 1K9, Canada.
[Socie, Gerard] Hosp St Louis, Dept Hematol Transplantat, Paris, France.
RP Anasetti, C (reprint author), H Lee Moffitt Canc Ctr & Res Inst, Blood & Marrow Transplantat Program, Tampa, FL USA.
EM claudio.anasetti@moffitt.org
NR 46
TC 0
Z9 0
U1 2
U2 2
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1083-8791
EI 1523-6536
J9 BIOL BLOOD MARROW TR
JI Biol. Blood Marrow Transplant.
PD MAR
PY 2017
VL 23
IS 3
BP 405
EP 411
DI 10.1016/j.bbmt.2016.12.624
PG 7
WC Hematology; Immunology; Transplantation
SC Hematology; Immunology; Transplantation
GA EM5QL
UT WOS:000395367300006
PM 28007665
ER
PT J
AU Stewart, IJ
Sosnov, JA
Snow, BD
Batou, A
Howard, JT
Janak, JC
Bollinger, M
Chung, KK
AF Stewart, Ian J.
Sosnov, Jonathan A.
Snow, Brian D.
Batou, Augen
Howard, Jeffrey T.
Janak, Jud C.
Bollinger, Mary
Chung, Kevin K.
TI Hypertension after injury among burned combat veterans: A retrospective
cohort study
SO BURNS
LA English
DT Article
DE Burns; Hypertension; Acute kidney injury; War; Veterans
ID CARDIOVASCULAR-DISEASE; CHILDREN; SYSTEM; PREVALENCE; SURVIVORS; RISK
AB Background: The long-term health effects of burn are poorly understood. We sought to evaluate the relationship between burn and the subsequent development of hypertension.
Methods: Retrospective cohort study of patients admitted to our burn center from 2003 to 2010. Data collected included demographic variables, burn size, injury severity score, presence of inhalation injury, serum creatinine, need for renal replacement therapy, as well as days spent in the hospital, in the intensive care unit and on mechanical ventilation. Data for the subsequent diagnosis of hypertension was obtained from medical records. Cox proportional hazard regression models were performed to determine what factors were associated with hypertension.
Results: Of the 711 patients identified, 670 were included for analysis after exclusions. After adjustment, only age (HR 1.06 per one year increase, 95% confidence interval 1.03-1.08; p<0.001), percentage of total body surface area burned (HR 1.11 per 5% increase, 95% confidence interval 1.04-1.19; p=0.002) and acute kidney injury (HR 1.68, 95% confidence interval 1.05-2.69; p=0.03) were associated with hypertension.
Conclusion: Burn size is independently associated with the subsequent risk of hypertension in combat casualties. Clinical support for primary prevention techniques to reduce the incidence of hypertension specific to burn patients may be warranted. Published by Elsevier Ltd.
C1 [Stewart, Ian J.] David Grant USAF Med Ctr, Clin Invest Facil, 101 Bodin Circle, Travis AFB, CA 94535 USA.
[Stewart, Ian J.; Sosnov, Jonathan A.; Chung, Kevin K.] Uniformed Serv Univ Hlth Sci, 4301 Jones Bridge Rd, Bethesda, MD 20814 USA.
[Sosnov, Jonathan A.] San Antonio Mil Med Ctr, 3551 Roger Brooke Dr, Ft Sam Houston, TX 78219 USA.
[Snow, Brian D.] Wright Patterson Med Ctr, 4881 Sugar Maple Dr, Wright Patterson AFB, OH 45433 USA.
[Batou, Augen] Mike OCallaghan Fed Med Ctr, 4700 N Las Vegas Blvd, Nellis AFB, NV 89191 USA.
[Howard, Jeffrey T.; Janak, Jud C.; Chung, Kevin K.] US Army, Inst Surg Res, 3698 Chambers Rd, Ft Sam Houston, TX 78234 USA.
[Bollinger, Mary] South Texas Vet Hlth Care Syst, 7400 Merton Minter Blvd, San Antonio, TX 78229 USA.
RP Stewart, IJ (reprint author), David Grant USAF Med Ctr, 101 Bodin Circle, Travis AFB, CA 94535 USA.
EM ian.stewart@us.af.mil
NR 29
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U1 1
U2 1
PU ELSEVIER SCI LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
SN 0305-4179
EI 1879-1409
J9 BURNS
JI Burns
PD MAR
PY 2017
VL 43
IS 2
BP 290
EP 296
DI 10.1016/j.burns.2016.10.005
PG 7
WC Critical Care Medicine; Dermatology; Surgery
SC General & Internal Medicine; Dermatology; Surgery
GA EN2LI
UT WOS:000395841300006
PM 28029474
ER
PT J
AU Shen, H
Monto, A
AF Shen, H.
Monto, A.
TI Identifying Drug-Induced Liver Illness (DILI) with Computerized
Information Extraction: No More Dilly-Dallying
SO DIGESTIVE DISEASES AND SCIENCES
LA English
DT Editorial Material
C1 [Shen, H.; Monto, A.] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA.
[Shen, H.; Monto, A.] San Francisco VA Med Ctr, Med 111A, 4150 Clement St, San Francisco, CA 94121 USA.
RP Shen, H (reprint author), Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA.; Shen, H (reprint author), San Francisco VA Med Ctr, Med 111A, 4150 Clement St, San Francisco, CA 94121 USA.
EM Hui.Shen@ucsf.edu
NR 9
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Z9 0
U1 0
U2 0
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0163-2116
EI 1573-2568
J9 DIGEST DIS SCI
JI Dig. Dis. Sci.
PD MAR
PY 2017
VL 62
IS 3
BP 564
EP 566
DI 10.1007/s10620-016-4359-z
PG 3
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EL9YB
UT WOS:000394974900002
PM 27943016
ER
PT J
AU Fuller, G
Bolus, R
Whitman, C
Talley, J
Erder, MH
Joseph, A
Silberg, DG
Spiegel, B
AF Fuller, Garth
Bolus, Roger
Whitman, Cynthia
Talley, Jennifer
Erder, M. Haim
Joseph, Alain
Silberg, Debra G.
Spiegel, Brennan
TI PRISM, a Patient-Reported Outcome Instrument, Accurately Measures
Symptom Change in Refractory Gastroesophageal Reflux Disease
SO DIGESTIVE DISEASES AND SCIENCES
LA English
DT Article
DE Gastroesophageal reflux; Proton pump inhibitors; Patient-reported
outcomes; Qualitative research; Psychometrics; Validation studies; US
Food and Drug Administration
ID INFORMATION-SYSTEM PROMIS; PUMP INHIBITOR THERAPY; PRIMARY-CARE;
CLINICAL-TRIALS; QUESTIONNAIRE; RESPONDERS; PERSISTENT
AB Most patients with gastroesophageal reflux disease (GERD) experience relief following treatment with proton pump inhibitors (PPIs) (Vakil et al. in Am J Gastroenterol 101:1900-1920, 2006; Everhart and Ruhl in Gastroenterology 136:376-386, 2009). As many as 17-44% of patients, however, exhibit only partial response to therapy. Most extant GERD patient-reported outcome (PRO) instruments fail to meet development best practices as described by the FDA (Talley and Wiklund in Qual Life Res 14:21-33, 2005; Van Pinxteren et al. in Cochrane Database Syst Rev 18:CD002095, 2004; El-Serag et al. in Aliment Pharmacol Ther 32:720-737, 2010).
To develop and validate a PRO instrument for clinical trials involving patients with GERD who are PPI partial responders.
We prepared a systematic literature review, held patient focus groups, convened an expert panel, and conducted cognitive interviews to establish content validity. Eligible participants took PPI therapy for at least 8 weeks, had undergone an upper endoscopy, and scored at least 8 points on the GerdQ [6]. Qualitative data guided development of 26 draft items. Items were reviewed by expert panels and debriefed with patients. The resulting 21-item instrument underwent psychometric evaluation during a Phase IIB trial.
During the trial, confirmatory factor analysis (n = 220) resulted in a four-factor model displaying the highest goodness of fit. All domains had a high inter-item correlation (Cronbach's alpha > 0.8). Test-retest reliability and convergent validity were strong, with highly significant (p < 0.01) correlations between average weekly PRISM scores and severity anchors and significant (p < 0.05) correlations with anchor subscales. Cumulative distribution functions revealed significant differences between responders and non-responders.
Analysis in a clinical trial setting demonstrated strong psychometric properties suggesting validity of PRISM. Developed in line with FDA guidance on PROs, PRISM represents an important new outcome measure for patients with GERD with a partial response to PPI therapy.
C1 [Fuller, Garth; Bolus, Roger; Whitman, Cynthia; Talley, Jennifer; Spiegel, Brennan] CS CORE, 116 N Robertson Blvd Suite 400, Los Angeles, CA 90048 USA.
[Bolus, Roger; Spiegel, Brennan] UCLA Fielding Sch Publ Hlth, Los Angeles, CA 90095 USA.
[Erder, M. Haim; Silberg, Debra G.] MH Erder Hlth Econ Inc, Livingston, NJ USA.
[Joseph, Alain] Shire, Zahlerweg 10, CH-6300 Zug, Switzerland.
[Spiegel, Brennan] Cedars Sinai Med Ctr, Dept Med, Cedars Sinai Hlth Syst, Los Angeles, CA 90048 USA.
[Spiegel, Brennan] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA 90073 USA.
[Bolus, Roger] 1016 Quail Gardens Ct, Encinitas, CA 92024 USA.
[Whitman, Cynthia] 44 16th St, Hermosa Beach, CA 90254 USA.
RP Spiegel, B (reprint author), CS CORE, 116 N Robertson Blvd Suite 400, Los Angeles, CA 90048 USA.; Spiegel, B (reprint author), UCLA Fielding Sch Publ Hlth, Los Angeles, CA 90095 USA.; Spiegel, B (reprint author), Cedars Sinai Med Ctr, Dept Med, Cedars Sinai Hlth Syst, Los Angeles, CA 90048 USA.; Spiegel, B (reprint author), VA Greater Los Angeles Healthcare Syst, Los Angeles, CA 90073 USA.
EM garth.fuller@cshs.org; rbolus@netzero.net; cwhitman@psi.org;
Jennifer.Soares@cshs.org; hmerder@gmail.com; ajoseph@shire.com;
dsilberg@shire.com; brennan.spiegel@cshs.org
FU Shire-Movetis NV
FX Support for this study was provided by a research grant from
Shire-Movetis NV.
NR 23
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U1 0
U2 0
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0163-2116
EI 1573-2568
J9 DIGEST DIS SCI
JI Dig. Dis. Sci.
PD MAR
PY 2017
VL 62
IS 3
BP 593
EP 606
DI 10.1007/s10620-016-4440-7
PG 14
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EL9YB
UT WOS:000394974900008
PM 28116591
ER
PT J
AU Everett, CJ
Thompson, OM
Dismuke, CE
AF Everett, Charles J.
Thompson, Olivia M.
Dismuke, Clara E.
TI Exposure to DDT and diabetic nephropathy among Mexican Americans in the
1999-2004 National Health and Nutrition Examination Survey
SO ENVIRONMENTAL POLLUTION
LA English
DT Article
DE DDT (dichlorodiphenyltrichloroethane); DDE
(dichlorodiphenyldichloroethylene); Diabetes; Kidney disease
ID CHRONIC KIDNEY-DISEASE; ORGANOCHLORINE PESTICIDES; BREAST-CANCER;
ASSOCIATION; ACCULTURATION; POLYMORPHISM; PREVALENCE; HISPANICS; TRENDS;
WOMEN
AB Concentrations of the pesticide DDT (dichlorodiphenyltrichloroethane) and its metabolite DDE (dichlorodiphenyldichloroethylene), in the blood of Mexican Americans, were evaluated to determine their relationships with diabetes and diabetic nephropathy. The data were derived from the National Health and Nutrition Examination Survey (NHANES) 1999-2004 (unweighted N = 1,411, population estimate = 13,760,609). The sample included teens, 12-19 years old, which accounted for 19.8% of the data. The time of the study overlapped the banning of DDT in Mexico in the year 2000, and those participants born in Mexico were exposed to DDT before they immigrated to the US. We sought to better understand the relationship of DDT with diabetes in a race/ethnicity group prone to develop diabetes and exposed to DDT. In this study, nephropathy was defined as urinary albumin to creatinine ratio >30 mg/g, representing microalbuminuria and macroalbuminuria, and total diabetes was defined as diagnosed and undiagnosed diabetes (glycohemoglobin, A1c >= 6.5%). The proportion with the isomer p,p'-DDT >0.086 ng/g (above the maximum limit of detection) was 13.3% for Mexican Americans born in the US, and 36.9% for those born in Mexico. Levels of p,p'-DDT >0.086 ng/g were associated with total diabetes with nephropathy (odds ratio = 4.42, 95% CI 2.23-8.76), and with total diabetes without nephropathy (odds ratio = 2.02, 95% CI 1.19-3.44). The third quartile of p,p'-DDE (2.99-7.67 ng/g) and the fourth quartile of p,p'-DDE (>= 7.68 ng/g) were associated with diabetic nephropathy and had odds ratios of 5.32 (95% CI 1.05-26.87) and 14.95 (95% CI 2.96-75.48) compared to less than the median, respectively, whereas p,p'-DDE was not associated with total diabetes without nephropathy. The findings of this study differ from those of a prior investigation of the general adult US population in that there were more associations found with the Mexican Americans sample. Published by Elsevier Ltd.
C1 [Everett, Charles J.; Dismuke, Clara E.] US Dept Vet Affairs, Ralph H Johnson VA Med Ctr, Charleston, SC USA.
[Thompson, Olivia M.] Coll Charleston, Mayor Joseph P Riley Inst Livable Commun, Charleston, SC USA.
[Everett, Charles J.] Med Univ S Carolina, Dept Publ Hlth Sci, Charleston, SC USA.
[Everett, Charles J.; Dismuke, Clara E.] Ralph H Johnson VA Med Ctr, 109 Bee St,Mail Code 151, Charleston, SC 29401 USA.
RP Everett, CJ; Thompson, OM; Dismuke, CE (reprint author), Ralph H Johnson VA Med Ctr, 109 Bee St,Mail Code 151, Charleston, SC 29401 USA.
EM Charles.Everett@va.gov; thompsonom@cofc.edu; Clara.Dismuke@va.gov
NR 30
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Z9 0
U1 1
U2 1
PU ELSEVIER SCI LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
SN 0269-7491
EI 1873-6424
J9 ENVIRON POLLUT
JI Environ. Pollut.
PD MAR
PY 2017
VL 222
BP 132
EP 137
DI 10.1016/j.envPol.2016.12.069
PG 6
WC Environmental Sciences
SC Environmental Sciences & Ecology
GA EM5OJ
UT WOS:000395360900016
PM 28065571
ER
PT J
AU Winkelman, WD
Huang, AJ
Schembri, M
Rogers, RG
Richter, H
Myers, DL
Kraus, SR
Johnson, KC
Hess, R
Gregory, T
Bradley, CS
Arya, L
Brown, JS
Subak, LL
AF Winkelman, William D.
Huang, Alison J.
Schembri, Michael
Rogers, Rebecca G.
Richter, Holly
Myers, Deborah L.
Kraus, Stephen R.
Johnson, Karen C.
Hess, Rachel
Gregory, Tomas
Bradley, Catherine S.
Arya, Lily
Brown, Janette S.
Subak, Leslee L.
TI Modifiers of Response to Treatment With Fesoterodine for
Urgency-Predominant Urinary Incontinence in a Randomized Controlled
Trial
SO FEMALE PELVIC MEDICINE AND RECONSTRUCTIVE SURGERY
LA English
DT Article; Proceedings Paper
CT Annual Scientific Meeting of the American-Urogynecologic-Society (AUGS)
CY SEP 27-OCT 01, 2016
CL Denver, CO
SP Amer Urogynecol Soc
DE fesoterodine; predictors of treatment response; urgency urinary
incontinence
ID OVERACTIVE BLADDER; TOLERABILITY; EFFICACY; PLACEBO; SAFETY;
PHARMACOKINETICS; TOLTERODINE; SOLIFENACIN; PREVALENCE; VALIDATION
AB Objective: The aim of this studywas to identify clinical and demographic characteristics that moderate response to treatment with fesoterodine among women with a diagnosis of urgency-predominant urinary incontinence.
Methods: A multicenter, double-blinded, 12-week randomized controlled trial of pharmacologic therapy for urgency-predominant urinary incontinence in community-dwelling women diagnosed by the 3-item Incontinence Questionnaire (3IQ) was previously performed. Participants (N = 645) were randomized to fesoterodine therapy (4-8 mg daily; n = 322) or placebo (n = 323). Urinary incontinence was assessed by 3-day voiding diaries. In this secondary analysis, a "responder" was defined as reduction of 50% or greater in overall incontinence episode frequency compared with baseline. Clinical and demographic characteristics that may moderate treatment response were assessed by testing for interaction between characteristics and intervention in logit models of responders, adjusting for clinical site.
Results: Participants' ages were a mean of 56 (SD, 14) years, 68% were white race, and they had a mean of 3.9 (SD, 3.0) urgency incontinence episodes per day. There were no baseline differences in demographic, clinical, or incontinence characteristics between treatment and placebo groups or between responders and nonresponders. There was an increase in the proportion of responders to fesoterodine with increasing age (P = 0.04) and parity (0.04) and among married women (P = 0.03), but no effect modification was observed by race/ethnicity, body mass index, education, employment status, or alcohol or tobacco use.
Conclusions: In ambulatory women with urgency-predominant urinary incontinence, older age, being married, and higher parity significantly moderated and potentiated the effects of pharmacologic therapy on incontinence frequency. This study identifies certain populations who may have increased responsiveness to treatment with antimuscarinic therapy andmay be used to inform and guide future therapy.
C1 [Winkelman, William D.; Huang, Alison J.; Schembri, Michael; Brown, Janette S.; Subak, Leslee L.] Univ Calif San Francisco, Irene Betty Moore Womens Hosp, Dept Obstet Gynecol & Reprod Med, San Francisco, CA 94143 USA.
[Rogers, Rebecca G.] Univ New Mexico, Albuquerque, NM 87131 USA.
[Richter, Holly] Univ Alabama Birmingham, Birmingham, AL USA.
[Myers, Deborah L.] Brown Univ, Providence, RI 02912 USA.
[Kraus, Stephen R.] UT Hlth Sci Ctr, San Antonio, TX USA.
[Johnson, Karen C.] Univ Tennessee, Hlth Sci Ctr, Memphis, TN USA.
[Hess, Rachel] Univ Utah, Salt Lake City, UT USA.
[Gregory, Tomas] Oregon Hlth & Sci Univ, Portland, OR 97201 USA.
[Bradley, Catherine S.] Univ Iowa, Iowa City, IA USA.
[Arya, Lily] Univ Penn, Philadelphia, PA 19104 USA.
[Subak, Leslee L.] San Francisco VA Med Ctr, San Francisco, CA USA.
RP Subak, LL (reprint author), UCSF Womens Hlth Clin Res Ctr, 550 16th St,6th Floor, San Francisco, CA 94143 USA.
EM Leslee.Subak@ucsf.edu
FU Pfizer, Inc; NIDDK [K24 DK080775]; Astellas, Inc.; US National
Institutes of Health [RR024130, 1K23AG038335-01A1, 2K24DK080775-06];
Astellas
FX L.L.S., J.S.B., and A.J.H. have received a University of California San
Francisco research grant from Pfizer, Inc, to conduct research related
to urinary incontinence. Pfizer, Inc, provided funding for the study and
the study medication but did not provide other input into the design of
the study; collection, analysis, or interpretation of data; writing of
the report; or the decision to submit the paper for publication. L.L.S.
is additionally supported by NIDDK K24 DK080775. L.L.S. had full access
to all the data in the study and takes responsibility for the integrity
of the data and the accuracy of the data analysis. No manuscript
preparation assistance was provided by the study funders. L.L.S. and
A.J.H. receive investigator-initiated trial funding from Astellas, Inc.
A.J.H. was additionally supported by grants RR024130 and
1K23AG038335-01A1 and L.L.S. from 2K24DK080775-06 from the US National
Institutes of Health; however, the views expressed in this article do
not necessarily represent those of the National Institutes of Health. L.
A. has received a research grant from Pfizer, Inc. H.R. has received a
research grant and participated in a speaker's bureau for Pfizer, Inc;
received a research grant and participated in an advisory board for
Astellas; and served as a consultant for Uromedica and GlaxoSmithKline.
S.R.K. has served as a consultant for Pfizer, Inc, and Allergan and has
been a course director and teaching faculty member for Laborie. The
other authors declare that they have nothing to disclose.
NR 21
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U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 2151-8378
EI 2154-4212
J9 FEMALE PELVIC MED RE
JI Female Pelvic Med. Reconstr. Surg.
PD MAR-APR
PY 2017
VL 23
IS 2
BP 151
EP 156
DI 10.1097/SPV.0000000000000396
PG 6
WC Obstetrics & Gynecology
SC Obstetrics & Gynecology
GA EM8RX
UT WOS:000395579800017
PM 28118174
ER
PT J
AU Matsue, Y
van der Meer, P
Damman, K
Metra, M
O'Connor, CM
Ponikowski, P
Teerlink, JR
Cotter, G
Davison, B
Cleland, JG
Givertz, MM
Bloomfield, DM
Dittrich, HC
Gansevoort, RT
Bakker, SJL
van der Harst, P
Hillege, HL
van Veldhuisen, DJ
Voors, AA
AF Matsue, Yuya
van der Meer, Peter
Damman, Kevin
Metra, Marco
O'Connor, Christopher M.
Ponikowski, Piotr
Teerlink, John R.
Cotter, Gad
Davison, Beth
Cleland, John G.
Givertz, Michael M.
Bloomfield, Daniel M.
Dittrich, Howard C.
Gansevoort, Ron T.
Bakker, Stephan J. L.
van der Harst, Pim
Hillege, Hans L.
van Veldhuisen, Dirk J.
Voors, Adriaan A.
TI Blood urea nitrogen-to-creatinine ratio in the general population and in
patients with acute heart failure
SO HEART
LA English
DT Article
ID MUSCLE PROTEIN-SYNTHESIS; RECEPTOR ANTAGONIST ROLOFYLLINE;
RENAL-FUNCTION; NITROGEN/CREATININE RATIO; POSTABSORPTIVE STATE; VOLUME
OVERLOAD; MORTALITY; DYSFUNCTION; WOMEN; RISK
AB Objective The blood urea nitrogen-to-creatinine (BUN/creatinine) ratio has been proposed as a useful parameter in acute heart failure (AHF), but data on the normal range and the added value of the ratio compared with its separate components in patients with AHF are lacking. The aim of this study is to define the normal range of BUN/creatinine ratio and to investigate its clinical significance in patients with AHF.
Methods In 4484 subjects from the general population without cardiovascular comorbidities, we calculated agespecific and sex-specific normal values of the BUN/creatinine ratio, deriving a higher and lower than normal range of BUN/creatinine ratio (exceeding the 95% prediction intervals). Association of abnormal range to prognosis was tested in 2033 patients with AHF for the outcome of all-cause death through 180 days, death or cardiovascular or renal rehospitalisation through 60 days and heart failure (HF) rehospitalisation within 60 days.
Results In a cohort of patients with AHF, 482 (24.6%) and 28 (1.4%) patients with HF were classified into higher and lower than normal range groups, respectively. In Cox regression analysis, higher than normal range of BUN/creatinine ratio group was an independent predictor for all-cause death (HR: 1.86, 95% CI 1.29 to 2.66) and death or cardiovascular or renal rehospitalisation (HR: 1.37, 95% CI 1.03 to 1.82), but not for HF rehospitalisation (HR: 1.23, 95% CI 0.81 to 1.86) after adjustment for other prognostic factors including both creatinine and BUN.
Conclusions In patients with AHF, BUN/creatinine higher than age-specific and sex-specific normal range is associated with worse prognosis independently from both creatinine and BUN.
C1 [Matsue, Yuya; van der Meer, Peter; Damman, Kevin; van der Harst, Pim; Hillege, Hans L.; van Veldhuisen, Dirk J.; Voors, Adriaan A.] Univ Groningen, Univ Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands.
[Metra, Marco] Univ Brescia, Dept Expt & Clin Med, Brescia, Italy.
[O'Connor, Christopher M.] Inova Heart & Vasc Inst, Falls Church, VA USA.
[Ponikowski, Piotr] Med Univ, Clin Mil Hosp, Wroclaw, Poland.
[Teerlink, John R.] Univ Calif San Francisco, San Francisco Vet Affairs Med Ctr, San Francisco, CA 94143 USA.
[Cotter, Gad; Davison, Beth] Momentum Res, Durham, NC USA.
[Cleland, John G.] Imperial Coll, Royal Brompton Hosp, Natl Heart & Lung Inst, London, England.
[Cleland, John G.] Imperial Coll, Harefield Hosp, London, England.
[Givertz, Michael M.] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA.
[Bloomfield, Daniel M.] Merck Res Labs, Rahway, NJ USA.
[Dittrich, Howard C.] Univ Iowa, Carver Coll Med, Cardiovasc Res Ctr, Iowa City, IA USA.
[Gansevoort, Ron T.; Bakker, Stephan J. L.] Univ Groningen, Univ Med Ctr Groningen, Dept Nephrol, Groningen, Netherlands.
[Bakker, Stephan J. L.] Top Inst Food & Nutr, Wageningen, Netherlands.
[Hillege, Hans L.] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands.
RP Voors, AA (reprint author), Univ Med Ctr Groningen, Dept Cardiol, Hanzepl 1, NL-9713 GZ Groningen, Netherlands.
EM a.a.voors@umcg.nl
OI Matsue, Yuya/0000-0003-2456-8525
FU NovaCardia; Merck
FX The PROTECT trial was supported by NovaCardia, a subsidiary of Merck.
Alere, Singulex and Sphingotec kindly provided assays and performed
biomarker measurements.
NR 30
TC 0
Z9 0
U1 2
U2 2
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 1355-6037
EI 1468-201X
J9 HEART
JI Heart
PD MAR
PY 2017
VL 103
IS 6
DI 10.1136/heartjnl-2016-310112
PG 7
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EN0AI
UT WOS:000395672300004
ER
PT J
AU Noto, MJ
Becker, KW
Boyd, KL
Schmidt, AM
Skaar, EP
AF Noto, Michael J.
Becker, Kyle W.
Boyd, Kelli L.
Schmidt, Ann Marie
Skaar, Eric P.
TI RAGE-Mediated Suppression of Interleukin-10 Results in Enhanced
Mortality in a Murine Model of Acinetobacter baumannii Sepsis
SO INFECTION AND IMMUNITY
LA English
DT Article
DE Acinetobacter baumannii; IL-10; innate immunity; pneumonia; RAGE;
receptor for advanced glycation end products; sepsis
ID GLYCATION END-PRODUCTS; FACTOR-KAPPA-B; PNEUMOCOCCAL PNEUMONIA;
IMMUNE-RESPONSE; SEPTIC SHOCK; RECEPTOR; ACTIVATION; INFECTION;
PATHOGENESIS; MICE
AB The receptor for advanced glycation end products (RAGE) is a pattern recognition receptor capable of recognizing multiple pathogen-associated and dangerassociated molecular patterns that contributes to the initiation and potentiation of inflammation in many disease processes. During infection, RAGE functions to either exacerbate disease severity or enhance pathogen clearance depending on the pathogen studied. Acinetobacter baumannii is an opportunistic human pathogen capable of causing severe infections, including pneumonia and sepsis, in impaired hosts. The role of RAGE signaling in response to opportunistic bacterial infections is largely unknown. In murine models of A. baumannii pneumonia, RAGE signaling alters neither inflammation nor bacterial clearance. In contrast, RAGE(-/-) mice systemically infected with A. baumannii exhibit increased survival and reduced bacterial burdens in the liver and spleen. The increased survival of RAGE(-/-) mice is associated with increased circulating levels of the anti-inflammatory cytokine interleukin-10 (IL-10). Neutralization of IL-10 in RAGE(-/-) mice results in decreased survival during systemic A. baumannii infection that mirrors that of wild-type (WT) mice, and exogenous IL-10 administration to WT mice enhances survival in this model. These findings demonstrate the role for RAGE-dependent IL-10 suppression as a key modulator of mortality from Gram-negative sepsis.
C1 [Noto, Michael J.] Vanderbilt Univ, Ctr Med, Div Allergy Pulm & Crit Care Med, Dept Med, Nashville, TN 37232 USA.
[Becker, Kyle W.; Boyd, Kelli L.; Skaar, Eric P.] Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA.
[Schmidt, Ann Marie] NYU, Langone Med Ctr, New York, NY USA.
[Skaar, Eric P.] US Dept Vet Affairs, Tennessee Valley Healthcare Syst, Nashville, TN USA.
RP Skaar, EP (reprint author), Vanderbilt Univ, Med Ctr, Dept Pathol Microbiol & Immunol, Nashville, TN USA.; Skaar, EP (reprint author), US Dept Vet Affairs, Tennessee Valley Healthcare Syst, Nashville, TN USA.
EM eric.skaar@vanderbilt.edu
FU Department of Veterans Affairs Merit Award [INFB024-13F]; Cystic
Fibrosis Foundation [NOTO15D0]; National Institutes of Health
[2T32HL087738-06]; [5RO1AI101171]
FX We thank members of the Skaar laboratory for review of the manuscript.
This research was supported by Department of Veterans Affairs Merit
Award INFB024-13F and grant 5RO1AI101171 to E.P.S. and Cystic Fibrosis
Foundation award NOTO15D0 and National Institutes of Health grant
2T32HL087738-06 to M.J.N.E.P.S. is a Burroughs Wellcome Fellow in the
Pathogenesis of Infectious Diseases. We declare that we have no
conflicts of interest.
NR 50
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U1 0
U2 0
PU AMER SOC MICROBIOLOGY
PI WASHINGTON
PA 1752 N ST NW, WASHINGTON, DC 20036-2904 USA
SN 0019-9567
EI 1098-5522
J9 INFECT IMMUN
JI Infect. Immun.
PD MAR
PY 2017
VL 85
IS 3
AR e00954-16
DI 10.1128/IAI.00954-16
PG 9
WC Immunology; Infectious Diseases
SC Immunology; Infectious Diseases
GA EL4SU
UT WOS:000394612000016
ER
PT J
AU Okland, T
Karimkhani, C
Pederson, H
Boyers, LN
Sawyer, MD
Rove, KO
Kenny, MC
Steinberg, S
Naghavi, M
Dellavalle, RP
AF Okland, Tyler
Karimkhani, Chante
Pederson, Hannah
Boyers, Lindsay N.
Sawyer, Mark D.
Rove, Kyle O.
Kenny, McCabe C.
Steinberg, Steven
Naghavi, Mohsen
Dellavalle, Robert P.
TI Research prioritization of men's health and urologic diseases
SO INTERNATIONAL BRAZ J UROL
LA English
DT Article
DE Men's Health; Urologic Diseases; Neoplasms; Infertility; Male
ID SYSTEMATIC-REVIEWS; GLOBAL BURDEN; COCHRANE-DATABASE; RESEARCH GAPS;
TRIALS
AB Objectives: We sought to determine whether disease representation in the Cochrane Database of Systematic Reviews (CDSR) reflects disease burden, measured by the Global Burden of Disease (GBD) Study as disability-adjusted life-years (DALYs).
Materials and Methods: Two investigators performed independent assessment of ten men's health and urologic diseases (MHUDs) in CDSR for systematic review and protocol representation, which were compared with percentage of total 2010 DALYs for the ten conditions. Data were analyzed for correlation using Spearman rank analysis.
Results: Nine of ten MHUDs were represented by at least one CDSR review. There was a poor and statistically insignificant positive correlation between CDSR representation and disease burden (rho = 0.42, p = 0.23). CDSR representation was aligned with disease burden for three conditions, greater than disease burden for one condition, and less than disease burden for six conditions.
Conclusions: These results yield high-quality estimates to inform future research prioritization for MHUDs. While prioritization processes are complex and multi-faceted, disease burden should be strongly considered. Awareness of research priority setting has the potential to minimize research disparities on a global scale.
C1 [Okland, Tyler; Pederson, Hannah] Univ Colorado, Sch Med, Aurora, CO USA.
[Karimkhani, Chante] Columbia Univ, Coll Phys & Surg, New York, NY USA.
[Boyers, Lindsay N.] Georgetown Univ, Sch Med, Washington, DC USA.
[Sawyer, Mark D.; Steinberg, Steven] Eastern Colorado Hlth Care Syst, Urol Serv, US Dept Vet Affairs, Denver, CO USA.
[Rove, Kyle O.; Kenny, McCabe C.; Steinberg, Steven] Univ Colorado, Dept Urol, Anschutz Med Campus, Aurora, CO USA.
[Naghavi, Mohsen] Univ Washington, Inst Hlth Metr & Evaluat, Seattle, WA 98195 USA.
[Dellavalle, Robert P.] Univ Colorado, Dept Dermatol, Anschutz Med Campus, Aurora, CO USA.
[Dellavalle, Robert P.] Eastern Colorado Hlth Care Syst, Dermatol Serv, US Dept Vet, Denver, CO USA.
[Dellavalle, Robert P.] Univ Colorado, Dept Epidemiol, Colorado Sch Publ Hlth, Anschutz Med Campus, Aurora, CO USA.
RP Dellavalle, RP (reprint author), US Dept Vet Affairs, Med Ctr, Dermatol Serv, 1055 Clermont St,Box 165, Denver, CO 80220 USA.
EM robert.dellavalle@ucdenver.edu
FU Bill and Melinda Gates Foundation; CDC; National Institutes of Health
FX There was no direct funding to the current study. The Global Burden of
Disease study received funding from the Bill and Melinda Gates
Foundation (PI: Christopher J.L. Murray). Lindsay Boyers, Mark Sawyer,
and Robert Dellavalle are employees of the U.S. Department of Veterans
Affairs. The U.S. Department of Veterans Affairs had no role in the
design and execution of the study. Robert Dellavalle is supported by
grants from the CDC and National Institutes of Health. Tyler Okland,
Chante Karimkhani, Hannah Pederson, Lindsay Boyers, Mohsen Naghavi, and
Mark Sawyer report no relevant disclosures. Any opinions expressed
herein do not necessarily reflect the opinions of the CDC or the
Department of Veterans Affairs.
NR 15
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U2 0
PU BRAZILIAN SOC UROL
PI RIO DE JANEIRO
PA RUA BAMBINA, 153, RIO DE JANEIRO, 2251-050, BRAZIL
SN 1677-5538
EI 1677-6119
J9 INT BRAZ J UROL
JI Int. Braz J Urol
PD MAR-APR
PY 2017
VL 43
IS 2
BP 289
EP 303
DI 10.1590/S1677-5538.IBJU.2016.0047
PG 15
WC Urology & Nephrology
SC Urology & Nephrology
GA EN4UR
UT WOS:000396002900017
PM 28128909
ER
PT J
AU Halaney, DL
Sanyal, A
Nafissi, NA
Escobedo, D
Goros, M
Michalek, J
Acevedo, PJ
Perez, W
Escobar, GP
Feldman, MD
Han, HC
AF Halaney, David L.
Sanyal, Arnav
Nafissi, Navid A.
Escobedo, Daniel
Goros, Martin
Michalek, Joel
Acevedo, Pedro J.
Perez, William
Escobar, G. Patricia
Feldman, Marc D.
Han, Hai-Chao
TI The Effect of Trabeculae Carneae on Left Ventricular Diastolic
Compliance: Improvement in Compliance With Trabecular Cutting
SO JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME
LA English
DT Article
DE trabeculae carneae; LV compliance; wall stress; stiffness; hypertrophy;
surgery
ID NON-COMPACTION CARDIOMYOPATHY; DIFFERENT CARDIAC-DISEASES;
HEART-FAILURE; MAGNETIC-RESONANCE; EJECTION FRACTION; PAPILLARY-MUSCLES;
EUROPEAN-SOCIETY; OF-CARDIOLOGY; TASK-FORCE; QUANTIFICATION
AB The role of trabeculae carneae in modulating left ventricular (LV) diastolic compliance remains unclear. The objective of this study was to determine the contribution of trabeculae carneae to the LV diastolic compliance. LV pressure-volume compliance curves were measured in six human heart explants from patients with LV hypertrophy at baseline and following trabecular cutting. The effect of trabecular cutting was also analyzed with finite-element model (FEM) simulations. Our results demonstrated that LV compliance improved after trabecular cutting (p < 0.001). Finite-element simulations further demonstrated that stiffer trabeculae reduce LV compliance further, and that the presence of trabeculae reduced the wall stress in the apex. In conclusion, we demonstrate that integrity of the LV and trabeculae is important to maintain LV stiffness and loss in trabeculae leads to more LV compliance.
C1 [Halaney, David L.; Nafissi, Navid A.; Escobedo, Daniel; Escobar, G. Patricia; Feldman, Marc D.] Univ Texas Hlth Sci, Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA.
[Halaney, David L.; Escobedo, Daniel; Feldman, Marc D.] South Texas Vet Hlth Care Syst, Dept Vet Affairs, San Antonio, TX 78229 USA.
[Sanyal, Arnav; Han, Hai-Chao] Univ Texas San Antonio, Dept Mech Engn, San Antonio, TX 78249 USA.
[Goros, Martin; Michalek, Joel] Univ Texas Hlth Sci, Ctr San Antonio, Dept Epidemiol & Biostat, San Antonio, TX 78229 USA.
[Acevedo, Pedro J.] Univ Environm & Appl Sci UDCA, Dept Anat, Bogota, Colombia.
[Perez, William] Univ Republica, Fac Vet Med, Dept Anat, Montevideo 11200, Uruguay.
RP Feldman, MD (reprint author), Univ Texas Hlth Sci, Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA.; Feldman, MD (reprint author), South Texas Vet Hlth Care Syst, Dept Vet Affairs, San Antonio, TX 78229 USA.
OI Perez, William/0000-0002-9647-4731
FU South Texas Veterans Health Care System (VA Merit Grant, San Antonio,
TX); Janey and Dolph Briscoe Center for Cardiovascular Research (San
Antonio, TX); National Heart, Lung, and Blood Institute [HL095852];
Clayton Foundation; AHA National Innovation Award [15IRG23320009];
Office of the Vice President for Research of the University of Texas at
San Antonio
FX This work was supported by the South Texas Veterans Health Care System
(VA Merit Grant, San Antonio, TX), the Janey and Dolph Briscoe Center
for Cardiovascular Research (San Antonio, TX), Grant No. HL095852 from
the National Heart, Lung, and Blood Institute, the Clayton Foundation,
and an AHA National Innovation Award (15IRG23320009). This project was
also funded in part by the GREAT program from the Office of the Vice
President for Research of the University of Texas at San Antonio.
NR 41
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U1 1
U2 1
PU ASME
PI NEW YORK
PA TWO PARK AVE, NEW YORK, NY 10016-5990 USA
SN 0148-0731
EI 1528-8951
J9 J BIOMECH ENG-T ASME
JI J. Biomech. Eng.-Trans. ASME
PD MAR
PY 2017
VL 139
IS 3
AR 031012
DI 10.1115/1.4035585
PG 8
WC Biophysics; Engineering, Biomedical
SC Biophysics; Engineering
GA EM2XR
UT WOS:000395179600012
ER
PT J
AU Telfer, S
Kindig, MW
Sangeorzan, BJ
Ledoux, WR
AF Telfer, Scott
Kindig, Matthew W.
Sangeorzan, Bruce J.
Ledoux, William R.
TI Metatarsal Shape and Foot Type: A Geometric Morphometric Analysis
SO JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME
LA English
DT Article
DE foot type; bone morphology; pes planus; pes cavus; metatarsal
ID LOWER-LIMB KINEMATICS; PLANTAR PRESSURE; STATISTICAL SHAPE; FRAMINGHAM
FOOT; BONE MORPHOLOGY; CAVUS FOOT; PES PLANUS; WALKING; POSTURE;
DEFORMITY
AB Planus and cavus foot types have been associated with an increased risk of pain and disability. Improving our understanding of the geometric differences between bones in different foot types may provide insights into injury risk profiles and have implications for the design of musculoskeletal and finite-element models. In this study, we performed a geometric morphometric analysis on the geometry of metatarsal bones from 65 feet, segmented from computed tomography (CT) scans. These were categorized into four foot types: pes cavus, neutrally aligned, asymptomatic pes planus, and symptomatic pes planus. Generalized procrustes analysis (GPA) followed by permutation tests was used to determine significant shape differences associated with foot type and sex, and principal component analysis was used to find the modes of variation for each metatarsal. Significant shape differences were found between foot types for all the metatarsals (p < 0.01), most notably in the case of the second metatarsal which showed significant pairwise differences across all the foot types. Analysis of the principal components of variation showed pes cavus bones to have reduced cross-sectional areas in the sagittal and frontal planes. The first (p = 0.02) and fourth metatarsals (p = 0.003) were found to have significant sex-based differences, with first metatarsals from females shown to have reduced width, and fourth metatarsals from females shown to have reduced frontal and sagittal plane cross-sectional areas. Overall, these findings suggest that metatarsal bones have distinct morphological characteristics that are associated with foot type and sex, with implications for our understanding of anatomy and numerical modeling of the foot.
C1 [Telfer, Scott; Sangeorzan, Bruce J.; Ledoux, William R.] Univ Washington, Dept Orthopaed & Sports Med, Box 356500,1959 Northeasr Pacific St, Seattle, WA 98195 USA.
[Kindig, Matthew W.; Ledoux, William R.] VA Puget Sound, RR&D Ctr Excellence, Seattle, WA 98108 USA.
[Ledoux, William R.] Univ Washington, Dept Mech Engn, Seattle, WA 98195 USA.
RP Telfer, S (reprint author), Univ Washington, Dept Orthopaed & Sports Med, Box 356500,1959 Northeasr Pacific St, Seattle, WA 98195 USA.
EM telfers@uw.edu
NR 45
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Z9 0
U1 4
U2 4
PU ASME
PI NEW YORK
PA TWO PARK AVE, NEW YORK, NY 10016-5990 USA
SN 0148-0731
EI 1528-8951
J9 J BIOMECH ENG-T ASME
JI J. Biomech. Eng.-Trans. ASME
PD MAR
PY 2017
VL 139
IS 3
AR 031008
DI 10.1115/1.4035077
PG 8
WC Biophysics; Engineering, Biomedical
SC Biophysics; Engineering
GA EM2XR
UT WOS:000395179600008
ER
PT J
AU Ripley, B
Levin, D
Kelil, T
Hermsen, JL
Kim, S
Maki, JH
Wilson, GJ
AF Ripley, Beth
Levin, Dmitry
Kelil, Tatiana
Hermsen, Joshua L.
Kim, Sooah
Maki, Jeffrey H.
Wilson, Gregory J.
TI 3D Printing From MRI Data: Harnessing Strengths and Minimizing
Weaknesses
SO JOURNAL OF MAGNETIC RESONANCE IMAGING
LA English
DT Article
DE 3D printing; 3D printing; dditive manufacturing; MRI
ID 3-DIMENSIONAL PRINTERS; TEMPORAL BONE; LONG BONES; RECONSTRUCTION;
MODELS; ACCURACY; BRAIN; SEGMENTATION; REPLACEMENT; ANGIOGRAPHY
AB 3D printing facilitates the creation of accurate physical models of patient-specific anatomy from medical imaging datasets. While the majority of models to date are created from computed tomography (CT) data, there is increasing interest in creating models from other datasets, such as ultrasound and magnetic resonance imaging (MRI). MRI, in particular, holds great potential for 3D printing, given its excellent tissue characterization and lack of ionizing radiation. There are, however, challenges to 3D printing from MRI data as well. Here we review the basics of 3D printing, explore the current strengths and weaknesses of printing from MRI data as they pertain to model accuracy, and discuss considerations in the design of MRI sequences for 3D printing. Finally, we explore the future of 3D printing and MRI, including creative applications and new materials.
C1 [Ripley, Beth; Kim, Sooah; Maki, Jeffrey H.; Wilson, Gregory J.] Univ Washington, Dept Radiol, Seattle, WA 98195 USA.
[Levin, Dmitry] Univ Washington, Dept Med, Div Cardiol, Seattle, WA USA.
[Kelil, Tatiana] Harvard Med Sch, Brigham & Womens Hosp, Dept Radiol, Boston, MA USA.
[Hermsen, Joshua L.] Univ Washington, Dept Surg, Div Cardiothorac Surg, Seattle, WA 98195 USA.
[Ripley, Beth] VA Puget Sound Hlth Care Syst, Dept Radiol, Seattle, WA 98108 USA.
RP Ripley, B (reprint author), 1959 Pacific Ave NE, Seattle, WA 98195 USA.
NR 69
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Z9 0
U1 6
U2 6
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1053-1807
EI 1522-2586
J9 J MAGN RESON IMAGING
JI J. Magn. Reson. Imaging
PD MAR
PY 2017
VL 45
IS 3
BP 635
EP 645
DI 10.1002/jmri.25526
PG 11
WC Radiology, Nuclear Medicine & Medical Imaging
SC Radiology, Nuclear Medicine & Medical Imaging
GA EL4QF
UT WOS:000394605200001
PM 27875009
ER
PT J
AU Nguyen, KL
Yoshida, T
Han, F
Ayad, I
Reemtsen, BL
Salusky, IB
Satou, GM
Hu, P
Finn, JP
AF Nguyen, Kim-Lien
Yoshida, Takegawa
Han, Fei
Ayad, Ihab
Reemtsen, Brian L.
Salusky, Isidro B.
Satou, Gary M.
Hu, Peng
Finn, J. Paul
TI MRI With Ferumoxytol: A Single Center Experience of Safety Across the
Age Spectrum
SO JOURNAL OF MAGNETIC RESONANCE IMAGING
LA English
DT Article
ID AMBULATORY BLOOD-PRESSURE; IRON-DEFICIENCY ANEMIA; CHRONIC
KIDNEY-DISEASE; YOUNG-ADULTS; PHYSICOCHEMICAL PROPERTIES;
HEMODIALYSIS-PATIENTS; CONTRAST AGENTS; HIGH-RESOLUTION; UNITED-STATES;
POOL AGENT
AB Purpose: To summarize our single-center safety experience with the off-label use of ferumoxytol for magnetic resonance imaging (MRI) and to compare the effects of ferumoxytol on monitored physiologic indices in patients under anesthesia with those of gadofosveset trisodium.
Materials and Methods: Consecutive patients who underwent ferumoxytol-enhanced (FE) MRI exams were included. Adverse events (AEs) were classified according to the Common Terminology Criteria for Adverse Events v4.0. In a subgroup of patients examined under general anesthesia, recording of blood pressure, heart rate, oxygen saturation, and end-tidal CO2 was performed. A comparable group of 23 patients who underwent gadofosveset-enhanced (GE) MRI under anesthesia with similar monitoring was also analyzed.
Results: In all, 217 unique patients, ages 3 days to 94 years, underwent FE-MRI. No ferumoxytol-related severe, life-threatening, or fatal AEs occurred acutely or at follow-up. Two patients developed ferumoxytol-related nausea. Between-group (FE- vs. GE-MRI) comparisons showed no statistical difference in heart rate (P = 0.69, 95% confidence interval [CI] 96-113 bpm), mean arterial blood pressure (MAP) (P = 0.74, 95% CI 44-52 mmHg), oxygen saturation (P = 0.76, 95% CI 94-98%), and end-tidal CO2 (P = 0.73, 95% CI 31-37 mmHg). No significant change in MAP (P = 0.12, 95% CI 50-58 mmHg) or heart rate (P=0.25, 95% CI 91-105 bpm) was noted between slow infusion of ferumoxytol (n = 113) vs. bolus injection (n = 104).
Conclusion: In our single-center experience, no serious AEs occurred with the diagnostic use of ferumoxytol across a wide spectrum of age, renal function, and indications. Because of the limited sample size, firm conclusions cannot be drawn about the generalizability of our results. Thus, vigilance and monitoring are recommended to mitigate potential rare adverse reactions.
C1 [Nguyen, Kim-Lien; Yoshida, Takegawa; Han, Fei; Hu, Peng; Finn, J. Paul] Univ Calif Los Angeles, David Geffen Sch Med, Diagnost Cardiovasc Imaging Lab, Los Angeles, CA 90095 USA.
[Nguyen, Kim-Lien] Univ Calif Los Angeles, David Geffen Sch Med, Div Cardiol, Los Angeles, CA 90095 USA.
[Nguyen, Kim-Lien] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Yoshida, Takegawa; Han, Fei; Hu, Peng; Finn, J. Paul] Univ Calif Los Angeles, David Geffen Sch Med, Dept Radiol, Los Angeles, CA 90095 USA.
[Ayad, Ihab] Univ Calif Los Angeles, David Geffen Sch Med, Dept Anesthesiol, Los Angeles, CA 90095 USA.
[Salusky, Isidro B.; Satou, Gary M.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA.
[Reemtsen, Brian L.] Univ Calif Los Angeles, David Geffen Sch Med, Div Cardiothorac Surg, Los Angeles, CA 90095 USA.
RP Finn, JP (reprint author), Univ Calif Los Angeles, Dept Radiol Sci, Peter V Ueberroth Bldg Suite 3371, Los Angeles, CA 90095 USA.
EM pfinn@mednet.ucla.edu
OI Nguyen, Kim-Lien/0000-0002-8854-2976
FU National Heart, Lung, and Blood Institute [R01HL127153]; NIH/ National
Center for Advancing Translational Science (NCATS) CTSI [UL1TR000124]
FX Contract grant sponsor: National Heart, Lung, and Blood Institute;
contract grant number: R01HL127153; Contract grant sponsor: REDCap
hosting by the NIH/ National Center for Advancing Translational Science
(NCATS) CTSI; contract grant number: UL1TR000124.
NR 51
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U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1053-1807
EI 1522-2586
J9 J MAGN RESON IMAGING
JI J. Magn. Reson. Imaging
PD MAR
PY 2017
VL 45
IS 3
BP 804
EP 812
DI 10.1002/jmri.25412
PG 9
WC Radiology, Nuclear Medicine & Medical Imaging
SC Radiology, Nuclear Medicine & Medical Imaging
GA EL4QF
UT WOS:000394605200019
PM 27480885
ER
PT J
AU Rogal, S
Dew, MA
DiMartini, A
AF Rogal, Shari
Dew, Mary Amanda
DiMartini, Andrea
TI High-Dose Opioid Use and Liver Transplantation: An Underestimated
Problem?
SO LIVER TRANSPLANTATION
LA English
DT Editorial Material
ID KIDNEY-TRANSPLANTATION; CIRRHOSIS; PAIN
C1 [Rogal, Shari] VA Pittsburgh Healthcare Syst, Ctr Hlth Equ Res & Promot, Pittsburgh, PA USA.
[Rogal, Shari; DiMartini, Andrea] Univ Pittsburgh, Dept Surg, Pittsburgh, PA USA.
[Rogal, Shari] Univ Pittsburgh, Dept Gastroenterol Hepatol & Nutr, Pittsburgh, PA USA.
[Dew, Mary Amanda; DiMartini, Andrea] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA.
[Dew, Mary Amanda] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA.
[Dew, Mary Amanda] Univ Pittsburgh, Dept Epidemiol, Pittsburgh, PA 15261 USA.
[Dew, Mary Amanda] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15261 USA.
RP DiMartini, A (reprint author), Western Psychiat Inst & Clin, 3811 OHara St, Pittsburgh, PA 15213 USA.
EM dimartiniaf@upmc.edu
FU VA Pittsburgh Healthcare System
FX This material is the result of work supported with resources and the use
of facilities at the VA Pittsburgh Healthcare System. The views
expressed in this article are those of the authors and do not
necessarily reflect the position or policy of the Department of Veterans
Affairs.
NR 13
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U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1527-6465
EI 1527-6473
J9 LIVER TRANSPLANT
JI Liver Transplant.
PD MAR
PY 2017
VL 23
IS 3
BP 285
EP 287
DI 10.1002/lt.24731
PG 3
WC Gastroenterology & Hepatology; Surgery; Transplantation
SC Gastroenterology & Hepatology; Surgery; Transplantation
GA EM0BO
UT WOS:000394984000001
PM 28133898
ER
PT J
AU Han, CJ
Kohen, R
Jun, S
Jarrett, ME
Cain, KC
Burr, R
Heitkemper, MM
AF Han, Claire J.
Kohen, Ruth
Jun, Sangeun
Jarrett, Monica E.
Cain, Kevin C.
Burr, Robert
Heitkemper, Margaret M.
TI COMT Val158Met Polymorphism and Symptom Improvement Following a
Cognitively Focused Intervention for Irritable Bowel Syndrome
SO NURSING RESEARCH
LA English
DT Article
DE catechol-O-methyltransferase (COMT) polymorphism; cognitive behavioral
therapy; digestive signs and symptoms; irritable bowel syndrome;
self-management
ID SELF-MANAGEMENT; GASTROINTESTINAL SYMPTOMS; LIFE STRESS; WOMEN; TRIAL;
PAIN; ASSOCIATION; DISORDERS; GENOTYPE; BEHAVIOR
AB Background: Our nurse-delivered comprehensive self-management (CSM) program, a cognitive behavioral therapy intervention, is effective in reducing gastrointestinal and psychological distress symptoms in patients with irritable bowel syndrome (IBS). Findings from non-IBS studies indicate that the catechol-O-methyltransferase (COMT) Val158Met polymorphism may moderate the efficacy of cognitive behavioral therapy. It is unknown whether this COMT polymorphism is associated with symptom improvements in patients with IBS.
Objective: We tested whether this COMT Val158Met polymorphism influences the efficacy of our 2-month CSM intervention.
Methods: We analyzed data from two published randomized controlled trials of CSM. The combined European American sample included 149 women and 23 men with IBS (CSM, n = 111; usual care [UC], n = 61). The primary outcomes were daily reports of abdominal pain, depression, anxiety, and feeling stressed measured 3 and 6 months after randomization. Secondary outcomes were additional daily symptoms, retrospective psychological distress, IBS quality of life, and cognitive beliefs about IBS. The interaction between COMT Val158Met polymorphism and treatment group (CSM vs. UC) in a generalized estimating equation model tested the main objective.
Results: At 3 months, participants with at least one Val allele benefited more from CSM than did those with the Met/Met genotype (p =.01 for anxiety and feeling stressed, and p <.16 for abdominal pain and depression). The moderating effect of genotype was weaker at 6 months.
Discussion: Persons with at least one Val allele may benefit more from CSM than those homozygous for the Met allele. Future studies with larger and more racially diverse samples are needed to confirm these findings.
C1 [Han, Claire J.; Jarrett, Monica E.; Heitkemper, Margaret M.] Univ Washington, Dept Biobehav Nursing & Hlth Syst, Box 357266, Seattle, WA 98195 USA.
[Kohen, Ruth] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Kohen, Ruth] Vet Affairs Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Seattle, WA USA.
[Jun, Sangeun] Keimyung Univ, Coll Nursing, Daegu, South Korea.
[Cain, Kevin C.; Burr, Robert] Univ Washington, Dept Biostat, Seattle, WA 98195 USA.
[Cain, Kevin C.; Burr, Robert] Univ Washington, Off Nursing Res, Seattle, WA 98195 USA.
RP Heitkemper, MM (reprint author), Univ Washington, Dept Biobehav Nursing & Hlth Syst, Box 357266, Seattle, WA 98195 USA.
EM heit@u.washington.edu
FU National Institute of Nursing Research, National Institutes of Health,
USA [NR004142, P30 NR04001]
FX The authors acknowledge that this was not an industry-supported study.
The authors received no financial support for the research, authorship,
and/or publication of this article (secondary data analysis). Parent
studies were supported by National Institute of Nursing Research,
National Institutes of Health, USA (Grants NR004142 and P30 NR04001).
NR 39
TC 1
Z9 1
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0029-6562
EI 1538-9847
J9 NURS RES
JI Nurs. Res.
PD MAR-APR
PY 2017
VL 66
IS 2
BP 75
EP 84
DI 10.1097/NNR.0000000000000199
PG 10
WC Nursing
SC Nursing
GA EN1YF
UT WOS:000395805700358
PM 28252569
ER
PT J
AU Moriarty, H
Winter, L
Robinson, K
Piersol, C
Vause-Earland, T
Newhart, B
AF Moriarty, Helene
Winter, Laraine
Robinson, Keith
Piersol, Catherine
Vause-Earland, Tracey
Newhart, Brian
TI Randomized Controlled Trial of the Veterans' In-Home Program for
Veterans with TBI and Their Families: Report on Family Outcomes
SO NURSING RESEARCH
LA English
DT Meeting Abstract
C1 [Moriarty, Helene] Villanova Univ, Villanova, PA 19085 USA.
[Winter, Laraine; Robinson, Keith; Newhart, Brian] Philadelphia VA Med Ctr, Philadelphia, PA USA.
[Piersol, Catherine; Vause-Earland, Tracey] Thomas Jefferson Univ, Philadelphia, PA 19107 USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0029-6562
EI 1538-9847
J9 NURS RES
JI Nurs. Res.
PD MAR-APR
PY 2017
VL 66
IS 2
BP E70
EP E70
PG 1
WC Nursing
SC Nursing
GA EN1YF
UT WOS:000395805700179
ER
PT J
AU Moriarty, H
Winter, L
True, G
Robinson, K
Short, T
AF Moriarty, Helene
Winter, Laraine
True, Gala
Robinson, Keith
Short, Thomas
TI Community Reintegration in Military Veterans with Traumatic Brain
Injury: The Key Role of Depression as a Mediator
SO NURSING RESEARCH
LA English
DT Meeting Abstract
C1 [Moriarty, Helene] Villanova Univ, Villanova, PA 19085 USA.
[Winter, Laraine; True, Gala; Robinson, Keith] Philadelphia VA Med Ctr, Philadelphia, PA USA.
[Short, Thomas] West Chester Univ, W Chester, PA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0029-6562
EI 1538-9847
J9 NURS RES
JI Nurs. Res.
PD MAR-APR
PY 2017
VL 66
IS 2
BP E75
EP E75
PG 1
WC Nursing
SC Nursing
GA EN1YF
UT WOS:000395805700193
ER
PT J
AU Lu, Z
Li, Y
Brinson, CW
Kirkwood, KL
Lopes-Virella, MF
Huang, Y
AF Lu, Z.
Li, Y.
Brinson, C. W.
Kirkwood, K. L.
Lopes-Virella, M. F.
Huang, Y.
TI CD36 is upregulated in mice with periodontitis and metabolic syndrome
and involved in macrophage gene upregulation by palmitate
SO ORAL DISEASES
LA English
DT Article
DE CD36; metabolic syndrome; periodontitis; lipopolysaccharide
ID PORPHYROMONAS-GINGIVALIS LIPOPOLYSACCHARIDE; FATTY-ACID RECEPTORS; BONE
LOSS; INSULIN-RESISTANCE; ACTINOBACILLUS-ACTINOMYCETEMCOMITANS;
THERAPEUTIC TARGETS; CARDIOVASCULAR RISK; INFLAMMATION; ASSOCIATION;
ACTIVATION
AB BackgroundWe reported that high-fat diet (HFD)-induced metabolic syndrome (MetS) exacerbates lipopolysaccharide (LPS)-stimulated periodontitis and palmitate, the major saturated fatty acid in the HFD, amplified LPS-stimulated gene expression invitro. As CD36 is a major receptor for fatty acids, we investigated periodontal CD36 expression in mice with periodontitis and MetS, and the role of CD36 in inflammatory gene expression in macrophages stimulated by palmitate.
MethodsMetS and periodontitis were induced in mice by HFD and periodontal injection of LPS, respectively. The periodontal CD36 expression and its relationship with alveolar bone loss were studied using immunohistochemistry, real-time PCR, and correlation analysis. The role of CD36 in upregulation of inflammatory mediators by LPS and palmitate in macrophages was assessed using pharmacological inhibitor and small interfering RNA.
ResultsPeriodontal CD36 expression was higher in mice with both MetS and periodontitis than that in mice with periodontitis or MetS alone and was correlated with osteoclastogenesis and alveolar bone loss. In vitro studies showed that CD36 expression in macrophages was upregulated by LPS and palmitate, and targeting CD36 attenuated palmitate-enhanced gene expression.
ConclusionCD36 expression is upregulated in mice with periodontitis and MetS and involved in gene expression in macrophages stimulated by palmitate and LPS.
C1 [Lu, Z.; Li, Y.; Brinson, C. W.; Lopes-Virella, M. F.; Huang, Y.] Med Univ South Carolina, Div Endocrinol Diabet & Med Genet, Dept Med, Coll Med, Charleston, SC USA.
[Kirkwood, K. L.] Med Univ South Carolina, Dept Oral Hlth Sci, Coll Dent Med, Charleston, SC USA.
[Lopes-Virella, M. F.; Huang, Y.] Ralph H Johnson Vet Affairs Med Ctr, 114 Doughty St, Charleston, SC 29425 USA.
RP Huang, Y (reprint author), Ralph H Johnson Vet Affairs Med Ctr, 114 Doughty St, Charleston, SC 29425 USA.; Huang, Y (reprint author), Med Univ South Carolina, Dept Med, Div Endocrinol Diabet & Med Genet, 114 Doughty St, Charleston, SC 29425 USA.
EM huangyan@musc.edu
FU National Institutes of Health [DE016353]; Biomedical Laboratory Research
and Development Program of the Department of Veterans Affairs; National
Institute of General Medicine [P30 GM103331]
FX This work was supported by National Institutes of Health grant DE016353
and the Biomedical Laboratory Research and Development Program of the
Department of Veterans Affairs (to Y.H.). This project utilized
facilities, resources, and/or technical assistance of the Laboratory of
the Center for Oral Health Research that is supported by the National
Institute of General Medicine grant P30 GM103331.
NR 49
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U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1354-523X
EI 1601-0825
J9 ORAL DIS
JI Oral Dis.
PD MAR
PY 2017
VL 23
IS 2
BP 210
EP 218
DI 10.1111/odi.12596
PG 9
WC Dentistry, Oral Surgery & Medicine
SC Dentistry, Oral Surgery & Medicine
GA EL8ZM
UT WOS:000394908900010
PM 27753178
ER
PT J
AU Hooper, LG
Dieye, Y
Ndiaye, A
Diallo, A
Fan, VS
Neuzil, KM
Ortiz, JR
AF Hooper, Laura G.
Dieye, Yakou
Ndiaye, Assane
Diallo, Aldiouma
Fan, Vincent S.
Neuzil, Kathleen M.
Ortiz, Justin R.
TI Estimating Pediatric Asthma Prevalence in Rural Senegal: A
Cross-Sectional Survey
SO PEDIATRIC PULMONOLOGY
LA English
DT Article
DE children; Africa; Senegal; epidemiology; asthma; international health
ID CHILDHOOD ISAAC; BRONCHIAL HYPERRESPONSIVENESS; ATOPIC ECZEMA;
ALLERGIES; QUESTIONNAIRE; SYMPTOMS; CHILDREN; CHALLENGES; COUNTRIES;
SEVERITY
AB Rationale: In Senegal, the prevalence of childhood asthma and utilization of appropriate asthma therapies is unknown. Methodology: We used the International Study of Asthma and Allergies in Childhood (ISAAC) survey instrument to assess childhood respiratory health in rural Senegal. We interviewed the caregivers of children aged 5 through 8 years of age in the four largest Niakhar villages in August 2012. Results: We interviewed 1,103 primary caregivers for 1,513 children, representing 91% of all age-eligible children in the study area. Overall, 206 (14%) children had wheeze at any time in the past, 130 (9%) had wheeze within the past year, and only 41 (3%) reported a clinical diagnosis of asthma. Among children with wheeze within the past year, 81 (62%) had symptoms of severe asthma. Nocturnal cough was reported in 186 (14%) children who denied any history of wheezing illness. Only four (3%) children with wheeze in the past year had ever received bronchodilator therapy. Children with wheeze in the past year were significantly more likely to seek medical care for respiratory symptoms and to be perceived as less healthy than their peers. Children of lower socioeconomic status were significantly more likely to have wheeze. Conclusions: Nearly one in ten children in Niakhar, Senegal had symptoms suggestive of asthma; however, few children have a diagnosis of asthma or use appropriate therapies. This study highlights an opportunity to raise community awareness of asthma in rural Senegal and to increase access to appropriate medical therapies.. (C) 2016 Wiley Periodicals, Inc.
C1 [Hooper, Laura G.; Fan, Vincent S.; Neuzil, Kathleen M.; Ortiz, Justin R.] Univ Washington, Dept Med, 1959 NE Pacific St,Box 356522, Seattle, WA 98195 USA.
[Dieye, Yakou] PATH, Dakar, Senegal.
[Ndiaye, Assane; Diallo, Aldiouma] Inst Rech Dev, Dakar, Senegal.
[Fan, Vincent S.] VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Neuzil, Kathleen M.; Ortiz, Justin R.] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA.
[Neuzil, Kathleen M.; Ortiz, Justin R.] PATH, Seattle, WA USA.
RP Hooper, LG (reprint author), Univ Washington, Dept Med, 1959 NE Pacific St,Box 356522, Seattle, WA 98195 USA.
EM lghooper@u.washington.edu
NR 30
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U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 8755-6863
EI 1099-0496
J9 PEDIATR PULM
JI Pediatr. Pulmonol.
PD MAR
PY 2017
VL 52
IS 3
BP 303
EP 309
DI 10.1002/ppul.23545
PG 7
WC Pediatrics; Respiratory System
SC Pediatrics; Respiratory System
GA EL6GN
UT WOS:000394718500007
PM 27551858
ER
PT J
AU Gelman, A
Rosenfeld, EA
Nikolajski, C
Freedman, LR
Steinberg, JR
Borrero, S
AF Gelman, Amanda
Rosenfeld, Elian A.
Nikolajski, Cara
Freedman, Lori R.
Steinberg, Julia R.
Borrero, Sonya
TI Abortion Stigma Among Low-Income Women Obtaining Abortions in Western
Pennsylvania: A Qualitative Assessment
SO PERSPECTIVES ON SEXUAL AND REPRODUCTIVE HEALTH
LA English
DT Article
ID UNITED-STATES; RISK-FACTORS; ACCESS; US; PERSPECTIVES; DISCLOSURE;
MORTALITY; DECISIONS; PREGNANCY; OBSTACLES
AB CONTEXTAbortion stigma may cause psychological distress in women who are considering having an abortion or have had one. This phenomenon has been relatively underexplored in low-income women, who may already be at an increased risk for poor abortion-related outcomes because of difficulties accessing timely and safe abortion services.
METHODSA qualitative study conducted between 2010 and 2013 used semistructured interviews to explore pregnancy intentions among low-income women recruited from six reproductive health clinics in Western Pennsylvania. Transcripts from interviews with 19 participants who were planning to terminate a pregnancy or had had an abortion in the last two weeks were examined through content analysis to identify the range of attitudes they encountered that could contribute to or reflect abortion stigma, the sources of these attitudes and women's responses to them.
RESULTSWomen commonly reported that partners, family members and they themselves held antiabortion attitudes. Such attitudes communicated that abortion is morally reprehensible, a rejection of motherhood, rare and thus potentially deviant, detrimental to future fertility and an irresponsible choice. Women reacted to external and internal negative attitudes by distinguishing themselves from other women who obtain abortions, experiencing negative emotions, and concealing or delaying their abortions.
CONCLUSIONSWomen's reactions to antiabortion attitudes may perpetuate abortion stigma. Further research is needed to inform interventions to address abortion stigma and improve women's abortion experiences.
C1 [Gelman, Amanda] Univ Colorado, Internal Med, Aurora, CO USA.
[Rosenfeld, Elian A.] VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Nikolajski, Cara] Univ Pittsburgh, Ctr Res Hlth Care, Sch Med, Dept Gen Internal Med, Pittsburgh, PA 15260 USA.
[Freedman, Lori R.] Univ Calif San Francisco, Dept Obstet Gynecol & Reprod Sci, San Francisco, CA USA.
[Steinberg, Julia R.] Univ Maryland, Dept Family Sci, Sch Publ Hlth, College Pk, MD 20742 USA.
[Borrero, Sonya] Univ Pittsburgh, Med & Clin & Translat Sci, Sch Med, Pittsburgh, PA 15260 USA.
RP Borrero, S (reprint author), Univ Pittsburgh, Med & Clin & Translat Sci, Sch Med, Pittsburgh, PA 15260 USA.
EM borrerosp@upmc.edu
FU Eunice Kennedy Shriver National Institute of Child Health and Human
Development (NICHD), a component of the National Institutes of Health
(NIH) [1 R21 HD068736-01]; NICHD [K01 HD075834]
FX This study was funded by grant 1 R21 HD068736-01 from the Eunice Kennedy
Shriver National Institute of Child Health and Human Development
(NICHD), a component of the National Institutes of Health (NIH).
Additional support came from NICHD award K01 HD075834. The content of
this publication is the responsibility solely of the authors and does
not necessarily represent the official views of NICHD or NIH.
NR 48
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PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1538-6341
EI 1931-2393
J9 PERSPECT SEX REPRO H
JI Perspect. Sex Reprod. Health
PD MAR
PY 2017
VL 49
IS 1
BP 29
EP 36
DI 10.1363/psrh.12014
PG 8
WC Demography; Family Studies
SC Demography; Family Studies
GA EP6MS
UT WOS:000397494200003
PM 27984674
ER
PT J
AU Kreys, ED
Frei, CR
Villarreal, SM
Bollinger, MJ
Jones, X
Koeller, JM
AF Kreys, Eugene D.
Frei, Christopher R.
Villarreal, Sarah M.
Bollinger, Mary J.
Jones, Xavier
Koeller, Jim M.
TI Evaluation of Long-Term Chronic Myeloid Leukemia Treatment Practices
with Tyrosine Kinase Inhibitors in a National Cohort of Veterans
SO PHARMACOTHERAPY
LA English
DT Article
DE chronic myeloid leukemia; tyrosine kinase inhibitors; veterans;
treatment persistence; survival; long term
ID DIAGNOSED HYPERTENSIVE PATIENTS; CHRONIC-PHASE; FOLLOW-UP; CML PATIENTS;
IMATINIB; PERSISTENCE; DISCONTINUATION; PATTERNS; TRIAL; DASATINIB
AB STUDY OBJECTIVE To evaluate nationwide chronic myeloid leukemia (CML) treatment practices over an extended period and across multiple lines of tyrosine kinase inhibitor (TKI) therapy with imatinib, dasatinib, and nilotinib.
DESIGN Retrospective cohort study.
DATA SOURCE Veterans Health Administration (VHA) national database.
PATIENTS A total of 2873 VHA beneficiaries aged 18-89 years who had at least one encounter at any of the similar to 150 VHA hospitals and 800 VHA clinics, had a diagnosis code for CML, and filled at least one prescription for imatinib, nilotinib, or dasatinib between October 1, 2001, and September 30, 2010.
MEASUREMENT AND MAIN RESULTS The VHA database was used for the time period of October 1, 2000, to September 30, 2012, allowing for a 1-year observation period to identify CML treatments prior to study enrollment and a minimum of a 2-year follow-up period to assess study end points. Primary study end points included change in TKI treatment, gaps in TKI treatment, TKI treatment persistence, and patient survival. Persistence for each distinct line of treatment was defined as the time of continuous therapy, quantified by the number of days covered by the drug from treatment initiation until a 60-day gap in treatment was identified or a switch in treatment occurred. A Kaplan-Meier model was used to evaluate persistence and survival. Of the 2873 patients receiving first-line TKI treatment, 586 (20.4%) switched to a different TKI, constituting second-line treatment. Overall, 245 patients (8.5%) were switched again to third-line treatment. Only 4.4% of patients receiving first-line treatment experienced a gap in therapy of 60 or more days. First-line treatment persistence rates were 75%, 65%, and 55% for the first, second, and third years of treatment, respectively. Five-year survival with first-line treatment was 62%.
CONCLUSION In this national cohort of VHA patients, 1-year persistence of first-line TKI treatment was similar to that in prior studies. Five-year survival was comparable with that in other observational studies but was lower than that in prospective clinical trials. Persistence rates declined after the introduction of the new TKIs.
C1 [Kreys, Eugene D.] Calif Northstate Univ, Coll Pharm, Clin & Adm Sci, 9700 West Taron Dr, Elk Grove, CA 95757 USA.
[Frei, Christopher R.; Villarreal, Sarah M.; Koeller, Jim M.] Univ Texas Austin, Coll Pharm, Pharmacotherapy Div, Austin, TX 78712 USA.
[Frei, Christopher R.; Villarreal, Sarah M.; Koeller, Jim M.] Univ Texas Hlth Sci Ctr San Antonio, Sch Med, Pharmacotherapy Educ & Res Ctr, San Antonio, TX 78229 USA.
[Bollinger, Mary J.; Jones, Xavier] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
RP Kreys, ED (reprint author), Calif Northstate Univ, Coll Pharm, Clin & Adm Sci, 9700 West Taron Dr, Elk Grove, CA 95757 USA.
EM ekreys@cnsu.edu
FU Bristol-Myers Squibb
FX This study was funded by a grant from Bristol-Myers Squibb.
NR 40
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PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0277-0008
EI 1875-9114
J9 PHARMACOTHERAPY
JI Pharmacotherapy
PD MAR
PY 2017
VL 37
IS 3
BP 278
EP 286
DI 10.1002/phar.1893
PG 9
WC Pharmacology & Pharmacy
SC Pharmacology & Pharmacy
GA EP5JZ
UT WOS:000397416100003
PM 28052354
ER
PT J
AU Li, J
Echevarria, KL
Traugott, KA
AF Li, Julius
Echevarria, Kelly L.
Traugott, Kristi A.
TI beta-Lactam Therapy for Methicillin-Susceptible Staphylococcus aureus
Bacteremia: A Comparative Review of Cefazolin versus Antistaphylococcal
Penicillins
SO PHARMACOTHERAPY
LA English
DT Review
DE cefazolin; antistaphylococcal penicillins; methicillin-susceptible
Staphylococcus aureus; bacteremia
ID CLINICAL-PRACTICE GUIDELINES; INFECTIOUS-DISEASES SOCIETY; BLOOD-STREAM
INFECTIONS; BLAZ GENE TYPES; ANTIMICROBIAL THERAPY; ANTIBIOTIC-THERAPY;
TREATMENT FAILURE; IN-VIVO; NAFCILLIN; ENDOCARDITIS
AB Methicillin-susceptible Staphylococcus aureus (MSSA) bacteremia is associated with high morbidity and mortality. Traditionally, antistaphylococcal penicillins (ASPs) have been considered the agents of choice for the treatment of MSSA bacteremia. Vancomycin has been demonstrated to have poorer outcomes in several studies and is only recommended for patients with severe penicillin allergies. Although cefazolin is considered as an alternative to the ASPs for patients with nonsevere penicillin allergies, cefazolin offers several pharmacologic advantages over ASPs, such as more convenient dosing regimens, and antimicrobial stewardship programs are increasingly using cefazolin as the preferential agent for MSSA infections as part of cost-saving initiatives. Concerns about susceptibility to hydrolysis by type A beta-lactamases, particularly at high inocula seen in deep-seated infections such as endocarditis; selective pressures from unnecessary gram-negative coverage; and lack of comparative clinical data have precluded recommending cefazolin as a first-line therapy for MSSA bacteremia. Recent clinical studies, however, have suggested similar clinical efficacy but better tolerability, with lower rates of discontinuation due to adverse drug reactions, of cefazolin compared with ASPs. Other variables, such as adequate source control (e.g., intravascular catheter removal, debridement, or drainage) and enhanced pharmacodynamics through aggressive cefazolin dosing, may mitigate the role of cefazolin inoculum effect and factor into determining improved clinical outcomes. In this review, we highlight the utility of cefazolin versus ASPs in the treatment of MSSA bacteremia with a focus on clinical efficacy and safety.
C1 [Li, Julius] Ochsner Med Ctr, Dept Pharm, New Orleans, LA USA.
[Echevarria, Kelly L.] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Echevarria, Kelly L.; Traugott, Kristi A.] Univ Texas Austin, Coll Pharm, Austin, TX 78712 USA.
[Echevarria, Kelly L.; Traugott, Kristi A.] Univ Texas Hlth Sci Ctr San Antonio, Pharmacotherapy Educ & Res Ctr, Austin, TX USA.
[Traugott, Kristi A.] Univ Hlth Syst, Dept Pharm, San Antonio, TX USA.
RP Li, J (reprint author), Ochsner Med Ctr, 1514 Jefferson Highway, New Orleans, LA 70121 USA.
EM juli@ochsner.org
NR 55
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0277-0008
EI 1875-9114
J9 PHARMACOTHERAPY
JI Pharmacotherapy
PD MAR
PY 2017
VL 37
IS 3
BP 346
EP 360
DI 10.1002/phar.1892
PG 15
WC Pharmacology & Pharmacy
SC Pharmacology & Pharmacy
GA EP5JZ
UT WOS:000397416100009
PM 28035690
ER
PT J
AU Chi, YC
Rahkola, JT
Kendrick, AA
Holliday, MJ
Paukovich, N
Roberts, TS
Janoff, EN
Eisenmesser, EZ
AF Chi, Ying-Chih
Rahkola, Jeremy T.
Kendrick, Agnieszka A.
Holliday, Michael J.
Paukovich, Natasia
Roberts, Thomas S.
Janoff, Edward N.
Eisenmesser, Elan Z.
TI Streptococcus pneumoniae IgA1 protease: A metalloprotease that can
catalyze in a split manner in vitro
SO PROTEIN SCIENCE
LA English
DT Article
DE IgA1 protease; split protease; protease turnover; metalloprotease;
streptococcal pneumoniae
ID COMMUNITY-ACQUIRED PNEUMONIA; IMMUNOGLOBULIN A1 PROTEASE;
NEISSERIA-MENINGITIDIS; HAEMOPHILUS-INFLUENZAE; BACTERIAL-COLONIZATION;
BURDEN; ACTIVATION; PROTEINS; ENZYMES; ADULTS
AB IgA1 proteases (IgA1P) from diverse pathogenic bacteria specifically cleave human immunoglobulin A1 (IgA1) at the hinge region, thereby thwarting protective host immune responses. Streptococcus pneumoniae (S. pneumoniae) IgA1P shares no sequence conservation with serine or cysteine types of IgA1Ps or other known proteins, other than a conserved HExxH Zn-binding motif (1604-1608) found in metalloproteases. We have developed a novel expression system to produce the mature S. pneumoniae IgA1P and we have discovered that this form is both attached to the bacterial cell surface and released in its full form. Our data demonstrate that the S. pneumoniae IgA1P comprises two distinct regions that associate to form an active metalloprotease, the first such example of a metalloprotease that can be split in vitro and recombined to form an active enzyme. By capitalizing on this novel domain architecture, we show that the N-terminal region of S. pneumoniae IgA1P comprises the primary binding region for IgA1, although the C-terminal region of S. pneumoniae IgA1P is necessary for cleavage of IgA1. Our findings lend insight into the protein domain architecture of the S. pneumoniae IgA1P and function of this important virulence factor for S. pneumoniae infection.
C1 [Chi, Ying-Chih; Kendrick, Agnieszka A.; Holliday, Michael J.; Paukovich, Natasia; Roberts, Thomas S.; Eisenmesser, Elan Z.] Univ Colorado Denver, Dept Biochem, Aurora, CO USA.
[Chi, Ying-Chih; Kendrick, Agnieszka A.; Holliday, Michael J.; Paukovich, Natasia; Roberts, Thomas S.; Eisenmesser, Elan Z.] Univ Colorado Denver, Dept Mol Genet, Aurora, CO USA.
[Rahkola, Jeremy T.; Janoff, Edward N.] Univ Colorado Denver, Mucosal & Vaccine Res Program Colorado MAVRC, Aurora, CO USA.
[Rahkola, Jeremy T.; Janoff, Edward N.] Denver Vet Affairs Med Ctr, Denver, CO USA.
RP Eisenmesser, EZ (reprint author), 12801 East 17th Ave, Aurora, CO 80045 USA.
EM Elan.Eisenmesser@ucdenver.edu
FU NIH [AI092468, RO1GM107262, 108479]; University of Colorado Denver
Mucosal and Vaccine Research Program Colorado (MAVRC); Veterans Affairs
Research Service
FX Grant sponsor: NIH; Grant numbers: AI092468, RO1GM107262, 108479; Grant
sponsors: University of Colorado Denver Mucosal and Vaccine Research
Program Colorado (MAVRC) and Veterans Affairs Research Service.
NR 28
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U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0961-8368
EI 1469-896X
J9 PROTEIN SCI
JI Protein Sci.
PD MAR
PY 2017
VL 26
IS 3
BP 600
EP 610
DI 10.1002/pro.3110
PG 11
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA EM0EX
UT WOS:000394992700019
PM 28028839
ER
PT J
AU Alexander, EK
Pearce, EN
Brent, GA
Brown, RS
Chen, H
Dosiou, C
Grobman, WA
Laurberg, P
Lazarus, JH
Mandel, SJ
Peeters, RP
Sullivan, S
AF Alexander, Erik K.
Pearce, Elizabeth N.
Brent, Gregory A.
Brown, Rosalind S.
Chen, Herbert
Dosiou, Chrysoula
Grobman, William A.
Laurberg, Peter
Lazarus, John H.
Mandel, Susan J.
Peeters, Robin P.
Sullivan, Scott
TI 2017 Guidelines of the American Thyroid Association for the Diagnosis
and Management of Thyroid Disease During Pregnancy and the Postpartum
SO THYROID
LA English
DT Article
DE pregnancy; thyroid and pregnancy; thyroid function tests; postpartum
thyroiditis
ID IN-VITRO FERTILIZATION; HUMAN CHORIONIC-GONADOTROPIN; MILD IODINE
DEFICIENCY; STIMULATING HORMONE-LEVELS; ANTITHYROID DRUG-THERAPY;
ANTIBODY-POSITIVE WOMEN; FINE-NEEDLE-ASPIRATION; HYPOTHYROIDISM
COMPLICATING PREGNANCY; MATERNAL SUBCLINICAL HYPOTHYROIDISM; TRANSIENT
CONGENITAL HYPOTHYROIDISM
AB Background: Thyroid disease in pregnancy is a common clinical problem. Since the guidelines for the management of these disorders by the American Thyroid Association (ATA) were first published in 2011, significant clinical and scientific advances have occurred in the field. The aim of these guidelines is to inform clinicians, patients, researchers, and health policy makers on published evidence relating to the diagnosis and management of thyroid disease in women during pregnancy, preconception, and the postpartum period.
Methods: The specific clinical questions addressed in these guidelines were based on prior versions of the guidelines, stakeholder input, and input of task force members. Task force panel members were educated on knowledge synthesis methods, including electronic database searching, review and selection of relevant citations, and critical appraisal of selected studies. Published English language articles were eligible for inclusion. The American College of Physicians Guideline Grading System was used for critical appraisal of evidence and grading strength of recommendations. The guideline task force had complete editorial independence from the ATA. Competing interests of guideline task force members were regularly updated, managed, and communicated to the ATA and task force members.
Results: The revised guidelines for the management of thyroid disease in pregnancy include recommendations regarding the interpretation of thyroid function tests in pregnancy, iodine nutrition, thyroid autoantibodies and pregnancy complications, thyroid considerations in infertile women, hypothyroidism in pregnancy, thyrotoxicosis in pregnancy, thyroid nodules and cancer in pregnant women, fetal and neonatal considerations, thyroid disease and lactation, screening for thyroid dysfunction in pregnancy, and directions for future research.
Conclusions: We have developed evidence-based recommendations to inform clinical decision-making in the management of thyroid disease in pregnant and postpartum women. While all care must be individualized, such recommendations provide, in our opinion, optimal care paradigms for patients with these disorders.
C1 [Alexander, Erik K.] Brigham & Womens Hosp, Div Endocrinol Diabet & Hypertens, 75 Francis St, Boston, MA 02115 USA.
[Alexander, Erik K.] Harvard Med Sch, Boston, MA USA.
[Pearce, Elizabeth N.] Boston Univ, Sch Med, Sect Endocrinol Diabet & Nutr, 88 East Newton St,H3600, Boston, MA 02118 USA.
[Brent, Gregory A.] VA Greater Los Angeles Healthcare Syst, Dept Med, Los Angeles, CA USA.
[Brent, Gregory A.] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
[Brown, Rosalind S.] Harvard Med Sch, Boston Childrens Hosp, Div Endocrinol, Boston, MA USA.
[Chen, Herbert] Univ Alabama Birmingham, Dept Surg, Birmingham, AL 35294 USA.
[Dosiou, Chrysoula] Stanford Univ, Div Endocrinol, Sch Med, Stanford, CA 94305 USA.
[Grobman, William A.] Northwestern Univ, Dept Obstet & Gynecol, Chicago, IL 60611 USA.
[Laurberg, Peter] Aalborg Univ Hosp, Dept Endocrinol, Aalborg, Denmark.
[Laurberg, Peter] Aalborg Univ Hosp, Dept Clin Med, Aalborg, Denmark.
[Lazarus, John H.] Cardiff Univ, Inst Mol Med, Cardiff, S Glam, Wales.
[Mandel, Susan J.] Univ Penn, Perelman Sch Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA.
[Peeters, Robin P.] Erasmus MC, Dept Internal Med, Rotterdam, Netherlands.
[Peeters, Robin P.] Erasmus MC, Rotterdam Thyroid Ctr, Rotterdam, Netherlands.
[Sullivan, Scott] Med Univ South Carolina, Dept Obstet & Gynecol, Charleston, SC USA.
RP Pearce, EN (reprint author), Boston Univ, Sch Med, Sect Endocrinol Diabet & Nutr, 88 East Newton St,H3600, Boston, MA 02118 USA.
EM elizabeth.pearce@bmc.org
FU ATA
FX The task force wishes to thank Ms. Bobbi Smith, Executive Director, ATA,
and the rest of the ATA staff for their constant help and support, as
well as Ms. Sheri Slaughter for her substantial assistance in compiling
meeting notes, updating drafts, and final manuscript preparation. We
thank Dr. Tim I. Korevaar (Erasmus University, the Netherlands) for his
help in compiling Tables 4-7. We would like to thank the ATA members who
responded to our survey in preparation for this iteration of the
guidelines as well as manuscript review prior to journal submission.
These guidelines were funded by the ATA without support from any
commercial sources. The following groups reviewed and endorsed the final
document: American Association of Clinical Endocrinologists (AACE);
American Radium Society (ARS); Brazilian Society of Head and Neck
Surgery (BSHNS); Graves' Disease and Thyroid Foundation; International
Association of Endocrine Surgeons (IAES); Japan Thyroid Association; The
Endocrine Society of Australia (ESA); ThyCa: Thyroid Cancer Survivors'
Association, Inc.; and the Thyroid Federation International. The
Pediatric Endocrine Society affirms the value of these guidelines.
NR 613
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U1 4
U2 4
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1050-7256
EI 1557-9077
J9 THYROID
JI Thyroid
PD MAR
PY 2017
VL 27
IS 3
BP 315
EP +
DI 10.1089/thy.2016.0457
PG 76
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EN1QS
UT WOS:000395785500003
PM 28056690
ER
PT J
AU Jensen, DM
Eklund, S
Persson, T
Ahlbom, H
Stuart, R
Barkun, AN
Kuipers, EJ
Mossner, J
Lau, JY
Sung, JJ
Kilhamn, J
Lind, T
AF Jensen, Dennis M.
Eklund, Stefan
Persson, Tore
Ahlbom, Henrik
Stuart, Robert
Barkun, Alan N.
Kuipers, Ernest J.
Mossner, Joachim
Lau, James Y.
Sung, Joseph J.
Kilhamn, Jan
Lind, Tore
TI Reassessment of Rebleeding Risk of Forrest IB (Oozing) Peptic Ulcer
Bleeding in a Large International Randomized Trial
SO AMERICAN JOURNAL OF GASTROENTEROLOGY
LA English
DT Article
ID ADRENALINE INJECTION; HEATER PROBE; MANAGEMENT; HEMOSTASIS; HEMORRHAGE
AB OBJECTIVES: Our aims were to assess risks of early rebleeding after successful endoscopic hemostasis for Forrest oozing (FIB) peptic ulcer bleeding (PUBs) compared with other stigmata of recent hemorrhage (SRH).
METHODS: These were post hoc multivariable analyses of a large, international, double-blind study (NCT00251979) of patients randomized to high-dose intravenous (IV) esomeprazole (PPI) or placebo for 72 h. Rebleeding rates of patients with PUB SRH treated with either PPI or placebo after successful endoscopic hemostasis were also compared.
RESULTS: For patients treated with placebo for 72 h after successful endoscopic hemostasis, rebleed rates by SRH were spurting arterial bleeding (FIA) 22.5%, adherent clot (FIIB) 17.6%, non-bleeding visible vessel (FIIA) 11.3%, and oozing bleeding (FIB) 4.9%. Compared with FIB patients, FIA, FIIB, and FIIA had significantly greater risks of rebleeding with odds ratios (95% CI's) from 2.61 (1.05, 6.52) for FIIA to 6.66 (2.19, 20.26) for FIA. After hemostasis, PUB rebleeding rates for FIB patients at 72 h were similar with esomeprazole (5.4%) and placebo (4.9%), whereas rebleed rates for all other major SRH (FIA, FIIA, FIIB) were lower for PPI than placebo, but the treatment by SRH interaction test was not statistically significant.
CONCLUSIONS: After successful endoscopic hemostasis, FIB patients had very low PUB rebleeding rates irrespective of PPI or placebo treatment. This implies that after successful endoscopic hemostasis the prognostic classification of FIB ulcers as a high-risk SRH and the recommendation to treat these with high-dose IV PPI's should be re-evaluated.
C1 [Jensen, Dennis M.] Univ Calif Los Angeles, David Geffen Sch Med, CURE Digest Dis Res Ctr, Los Angeles, CA 90095 USA.
[Jensen, Dennis M.] UCLA & Vet Adm, Div Gastroenterol, Los Angeles, CA USA.
[Eklund, Stefan; Persson, Tore; Ahlbom, Henrik; Kilhamn, Jan; Lind, Tore] AstraZeneca R & D, Molndal, Sweden.
[Stuart, Robert] Glasgow Royal Infirm, Dept Surg, Glasgow, Lanark, Scotland.
[Barkun, Alan N.] McGill Univ, Div Gastroenterol, Montreal, PQ, Canada.
[Kuipers, Ernest J.] Erasmus MC Univ Med Ctr, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands.
[Kuipers, Ernest J.] Erasmus MC Univ Med Ctr, Dept Internal Med, Rotterdam, Netherlands.
[Mossner, Joachim] Univ Hosp Leipzig, Dept Internal Med Neurol & Dermatol, Div Gastroenterol & Rheumatol, Berlin, Germany.
[Lau, James Y.; Sung, Joseph J.] Chinese Univ Hong Kong, Inst Digest Dis, Hong Kong, Hong Kong, Peoples R China.
RP Jensen, DM (reprint author), VA Greater Los Angeles Healthcare Syst, CURE Digest Dis Res Ctr, Rm 318 Blgd 115,11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM djensen@mednet.ucla.edu
FU Astra-Zeneca; VA Clinical Merit Review Grant [CLIN -013-07F]; NIH-NIDDK
CURE:DDRC grant [41301]
FX The data analysis was funded in part by Astra-Zeneca. This was through
support of the biostatisticians (Henrik Ahlbom and Tore Persson). Dennis
Jensen was funded by a VA Clinical Merit Review Grant (CLIN -013-07F)
and also by NIH-NIDDK CURE:DDRC grant 41301(Human Studies Core).
NR 19
TC 0
Z9 0
U1 1
U2 1
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 0002-9270
EI 1572-0241
J9 AM J GASTROENTEROL
JI Am. J. Gastroenterol.
PD MAR
PY 2017
VL 112
IS 3
BP 441
EP 446
DI 10.1038/ajg.2016.582
PG 6
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EP3XA
UT WOS:000397313800013
PM 28094314
ER
PT J
AU Baker, JF
Conaghan, PG
Emery, P
Baker, DG
Ostergaard, M
AF Baker, Joshua F.
Conaghan, Philip G.
Emery, Paul
Baker, Daniel G.
Ostergaard, Mikkel
TI Relationship of patient-reported outcomes with MRI measures in
rheumatoid arthritis
SO ANNALS OF THE RHEUMATIC DISEASES
LA English
DT Article
ID NECROSIS-FACTOR-ALPHA; DISEASE-ACTIVITY; METHOTREXATE THERAPY;
RADIOGRAPHIC PROGRESSION; JOINT DAMAGE; DOUBLE-BLIND; GO-FORWARD;
PHASE-III; GOLIMUMAB; ANTIBODY
AB Purpose We assessed whether MRI measures of synovitis, osteitis and bone erosion were associated with patient-reported outcomes (PROs) in a longitudinal clinical trial setting among patients with rheumatoid arthritis (RA).
Methods This longitudinal cohort of 291 patients with RA was derived from the MRI substudy of the GO-BEFORE randomised controlled trial of golimumab among methotrexate-naive patients. Correlations between RAMRIS scores (synovitis, osteitis, bone erosion) and physical function (Health Assessment Questionnaire (HAQ)), pain and global patient scores were determined at 0, 12, 24 and 52 weeks. Correlations between interval changes were also assessed. Multivariable regression models using robust generalised estimating equations evaluated associations over all time-points and their relationship to other clinical disease activity measures.
Results Greater synovitis, osteitis and bone erosion scores were positively associated with HAQ at all time-points (all p<0.05) and with pain and patient global scores at 24 and 52 weeks. Over all visits, synovitis was associated with HAQ, pain and patient global scores (p <= 0.03) independent of clinical disease activity measures. Improvements in synovitis and bone erosion were also associated with improvements in PROs. Less improvement in synovitis and progression in MRI erosion at 52 weeks were both independently associated with worsening in all PROs at 52 weeks while progression on X-ray was not associated. Similar associations were observed across treatment groups.
Conclusions MRI measures of inflammation and structural damage correlate independently with physical function, pain and patient global assessments. These observations support the validity of MRI biomarkers.
C1 [Baker, Joshua F.] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA USA.
[Baker, Joshua F.] Univ Penn, Sch Med, Philadelphia, PA 19104 USA.
[Baker, Joshua F.] Univ Penn, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA.
[Conaghan, Philip G.; Emery, Paul] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Leeds, W Yorkshire, England.
[Conaghan, Philip G.; Emery, Paul] NIHR Leeds Musculoskeletal Biomed Res Unit, Leeds, W Yorkshire, England.
[Baker, Daniel G.] Janssen Res & Dev LLC, Horsham, PA USA.
[Ostergaard, Mikkel] Ctr Rheumatol & Spine Dis, Copenhagen Ctr Arthrit Res, Glostrup, Denmark.
[Ostergaard, Mikkel] Univ Copenhagen, Fac Hlth & Med Sci, Dept Clin Med, Copenhagen, Denmark.
RP Baker, JF (reprint author), Hosp Univ Penn, Div Rheumatol, Dept Med, 5 White Bldg,3600 Spruce St, Philadelphia, PA 19104 USA.
EM bakerjo@uphs.upenn.edu
FU Veterans Affairs Clinical Science Research and Development Career
Development Award [IK2 CX000955]
FX JFB is supported by a Veterans Affairs Clinical Science Research and
Development Career Development Award (IK2 CX000955).
NR 23
TC 1
Z9 1
U1 1
U2 1
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 0003-4967
EI 1468-2060
J9 ANN RHEUM DIS
JI Ann. Rheum. Dis.
PD MAR
PY 2017
VL 76
IS 3
BP 486
EP 490
DI 10.1136/annrheumdis-2016-209463
PG 5
WC Rheumatology
SC Rheumatology
GA EL3IR
UT WOS:000394513300005
PM 27432355
ER
PT J
AU Munroe, ME
Young, KA
Kamen, DL
Guthridge, JM
Niewold, TB
Costenbader, KH
Weisman, MH
Ishimori, ML
Wallace, DJ
Gilkeson, GS
Karp, DR
Harley, JB
Norris, JM
James, JA
AF Munroe, Melissa E.
Young, Kendra A.
Kamen, Diane L.
Guthridge, Joel M.
Niewold, Timothy B.
Costenbader, Karen H.
Weisman, Michael H.
Ishimori, Mariko L.
Wallace, Daniel J.
Gilkeson, Gary S.
Karp, David R.
Harley, John B.
Norris, Jill M.
James, Judith A.
TI Discerning Risk of Disease Transition in Relatives of Systemic Lupus
Erythematosus Patients Utilizing Soluble Mediators and Clinical Features
SO ARTHRITIS & RHEUMATOLOGY
LA English
DT Article
ID REGULATORY T-CELLS; 1ST-DEGREE RELATIVES; REVISED CRITERIA;
UNITED-STATES; CLASSIFICATION; AUTOANTIBODIES; PREVALENCE; FAMILIES;
HYDROXYCHLOROQUINE; DYSREGULATION
AB Objective. Systemic lupus erythematosus (SLE) and other autoimmune diseases cause significant morbidity. Identifying populations at risk of developing SLE is essential for curtailing irreversible inflammatory damage. The aim of this study was to identify factors associated with transition to classified disease that would inform our understanding of the risk of SLE.
Methods. Previously identified blood relatives of patients with SLE, who had <4 American College of Rheumatology (ACR) classification criteria for SLE at baseline, were enrolled in this follow-up study (n=409 unaffected relatives). Participants provided detailed family, demographic, and clinical information, including the SLE-specific portion of the Connective Tissue Disease Screening Questionnaire (SLE-CSQ). Serum and plasma samples were tested for the presence of lupus-associated autoantibodies and 52 soluble mediators. Generalized estimating equations (GEEs) were applied to identify factors predictive of disease transition.
Results. Of the 409 unaffected relatives of SLE patients, 45 (11%) had transitioned to classified SLE at follow-up (mean time to follow-up 6.4 years). Relatives who transitioned to SLE displayed more lupus-associated autoantibody specificities and higher SLE-CSQ scores (P<0.0001) at baseline than did relatives who did not transition. Importantly, those who had developed SLE during the follow-up period also had elevated baseline plasma levels of inflammatory mediators, including B lymphocyte stimulator, stem cell factor (SCF), and interferon-associated chemokines (P <= 0.02), with concurrent decreases in the levels of regulatory mediators, transforming growth factor (TGF), and interleukin-10 (P <= 0.03). GEE analyses revealed that baseline SLE-CSQ scores or ACR scores (number of ACR criteria satisfied) and plasma levels of SCF and TGF, but not autoantibodies, were significant and independent predictors of SLE transition (P <= 0.03).
Conclusion. Preclinical alterations in levels of soluble mediators may predict transition to classified disease in relatives of SLE patients. Thus, immune perturbations precede SLE classification and can help identify high-risk relatives for rheumatology referral and potential enrollment in prevention trials.
C1 [Munroe, Melissa E.; Guthridge, Joel M.; James, Judith A.] Oklahoma Med Res Fdn, 825 NE 13th St, Oklahoma City, OK 73104 USA.
[Young, Kendra A.; Norris, Jill M.] Colorado Sch Publ Hlth, Aurora, CO USA.
[Kamen, Diane L.; Gilkeson, Gary S.] Med Univ South Carolina, Charleston, SC USA.
[Niewold, Timothy B.] Mayo Clin, Rochester, MN USA.
[Costenbader, Karen H.] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA.
[Weisman, Michael H.; Ishimori, Mariko L.; Wallace, Daniel J.] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA.
[Karp, David R.] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA.
[Harley, John B.] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA.
[Harley, John B.] US Dept Vet Affairs, Med Ctr, Cincinnati, OH USA.
[James, Judith A.] Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA.
RP James, JA (reprint author), Oklahoma Med Res Fdn, Arthrit & Clin Immunol, 825 NE 13th St, Oklahoma City, OK 73104 USA.
EM jamesj@omrf.org
OI Munroe, Melissa/0000-0002-6933-9745
FU NIH (National Institute of Allergy and Infectious Diseases grant)
[U01-AI-101934, R01-AI-024717, U19-AI- 082714]; NIH (National Institute
of General Medical Sciences grant) [U54-GM-104938, P30-GM-103510]; NIH
(National Institute of Arthritis and Musculoskeletal and Skin Diseases
grant) [P30-AR-053483, RC1-AR-058554, U34-AR-067392]; Office of Research
on Women's Health [U1-9AI-082714]; Department of Veterans Affairs
FX Supported by the NIH (National Institute of Allergy and Infectious
Diseases grants U01-AI-101934, R01-AI-024717, and U19-AI- 082714,
National Institute of General Medical Sciences grants U54-GM-104938 and
P30-GM-103510, and National Institute of Arthritis and Musculoskeletal
and Skin Diseases grants P30-AR-053483, RC1-AR-058554, and
U34-AR-067392), the Office of Research on Women's Health (partial
funding provided to the Autoimmunity Center of Excellence, grant
U1-9AI-082714), and the Department of Veterans Affairs.
NR 49
TC 1
Z9 1
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2326-5191
EI 2326-5205
J9 ARTHRITIS RHEUMATOL
JI Arthritis Rheumatol.
PD MAR
PY 2017
VL 69
IS 3
BP 630
EP 642
DI 10.1002/art.40004
PG 13
WC Rheumatology
SC Rheumatology
GA EM0VF
UT WOS:000395035100019
PM 27863174
ER
PT J
AU Godfrey, KM
Herbert, M
Strachan, E
Mostoufi, S
Crofford, LJ
Buchwald, D
Poeschla, B
Succop, A
Afari, N
AF Godfrey, Kathryn M.
Herbert, Matthew
Strachan, Eric
Mostoufi, Sheeva
Crofford, Leslie J.
Buchwald, Dedra
Poeschla, Brian
Succop, Annemarie
Afari, Niloofar
TI Dexamethasone-suppressed Salivary Cortisol and Pain Sensitivity in
Female Twins
SO CLINICAL JOURNAL OF PAIN
LA English
DT Article
DE salivary cortisol; dexamethasone; HPA axis; pain sensitivity; cold
pressor; genetics
ID NOXIOUS INHIBITORY CONTROLS; ADRENAL STRESS AXIS;
INDIVIDUAL-DIFFERENCES; FIBROMYALGIA PATIENTS; PSYCHOLOGICAL STRESS;
MODULATORY INFLUENCE; POSTOPERATIVE PAIN; HEALTHY-SUBJECTS; PERCEPTION;
ZYGOSITY
AB Objectives: Hypothalamic-pituitary-adrenal (HPA) axis dysregulation is associated with chronic pain. Studying pain sensitivity and the HPA axis could elucidate the role of stress in chronic pain development, which might be influenced by familial factors, including genes.
Methods: Associations between pain sensitivity and salivary cortisol and familial confounding in these associations were examined in 88 female, community-based twin pairs (75% monozygotic, mean age 29 y). Cortisol was assessed after 0.25mg dexamethasone (DEX), recovery from 0.25mg DEX, and after 0.5mg DEX. Cold pressor task (CPT) pain ratings were obtained at threshold and at tolerance. Conditioned pain modulation (CPM) was examined using thermal heat as the testing stimulus and hot water as the conditioning stimulus. Generalized estimating equation models were used and adjusted for baseline pain rating, age, and other relevant covariates.
Results: After controlling for baseline cortisol, greater cortisol suppression following DEX administration and lower recovery cortisol levels were associated with higher pain ratings at tolerance during the CPT (Bs = -2.42 to -17.82; Ps = 0.031 to < 0.001) as well as with reduced CPM (Bs = -0.92 to -1.68; Ps = 0.003 to 0.046). Interestingly, familial confounding was evident in the CPT and CPM during recovery from DEX administration, but not immediately following DEX administration.
Discussion: These findings contribute to understanding possible mechanisms underlying chronic pain by demonstrating that HPA axis response to negative feedback is related to pain sensitivity.
C1 [Godfrey, Kathryn M.] Univ Calif San Diego, San Diego State Univ Univ Calif San Diego Joint D, San Diego, CA 92103 USA.
[Godfrey, Kathryn M.; Herbert, Matthew; Afari, Niloofar] Univ Calif San Diego, VA Ctr Excellence Stress & Mental Hlth, San Diego, CA 92103 USA.
[Afari, Niloofar] Univ Calif San Diego, Dept Psychiat, 9500 Gilman Dr,0737, San Diego, CA 92103 USA.
[Strachan, Eric; Poeschla, Brian] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Succop, Annemarie] Univ Washington, Dept Epidemiol & Med, Seattle, WA 98195 USA.
[Mostoufi, Sheeva] VA Puget Sound Healthcare Syst, Seattle Div, Seattle, WA USA.
[Buchwald, Dedra] Washington State Univ, Elson S Floyd Coll Med, Seattle, WA USA.
[Buchwald, Dedra] Washington State Univ, Elson S Floyd Coll Med, Spokane, WA USA.
[Crofford, Leslie J.] Vanderbilt Univ, Dept Med, Div Rheumatol & Immunol, Nashville, TN USA.
RP Afari, N (reprint author), Univ Calif San Diego, Dept Psychiat, 9500 Gilman Dr,0737, San Diego, CA 92103 USA.
EM nafari@ucsd.edu
FU National Institutes of Health, Bethesda, MD [R01AR051524, UL1RR025014,
KL2RR025015, TL1RR025016, UL1RR033173, UL1TR000117, U01DK082325];
Veterans Administration Center of Excellence for Stress and Mental
Health, San Diego, CA
FX This research was supported by National Institutes of Health award
R01AR051524 (N.A.) Bethesda, MD. Portions of this research were
conducted at the University of Washington Institutes of Translational
Health Sciences, which is supported by National Institutes of Health
awards UL1RR025014, KL2RR025015, and TL1RR025016, Bethesda, MD. Cortisol
assays were conducted at the University of Kentucky Center for Clinical
and Translational Science, which is supported by the National Institutes
of Health awards UL1RR033173 and UL1TR000117, Bethesda, MD. N.A. also is
supported by the Veterans Administration Center of Excellence for Stress
and Mental Health, San Diego, CA. N.A., E.S., and D.B. are supported in
part by National Institutes of Health award U01DK082325, Bethesda, MD.
The authors declare no conflict of interest.
NR 54
TC 0
Z9 0
U1 2
U2 2
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0749-8047
EI 1536-5409
J9 CLIN J PAIN
JI Clin. J. Pain
PD MAR
PY 2017
VL 33
IS 3
BP 246
EP 253
DI 10.1097/AJP.0000000000000398
PG 8
WC Anesthesiology; Clinical Neurology
SC Anesthesiology; Neurosciences & Neurology
GA EL1CR
UT WOS:000394358600008
PM 27275736
ER
PT J
AU Ahuja, SK
Manoharan, MS
Harper, NL
Jimenez, F
Hobson, BD
Martinez, H
Ingale, P
Liu, YG
Carrillo, A
Lou, Z
Kellog, DL
Ahuja, SS
Rather, CG
Esch, RE
Ramirez, DA
Clark, RA
Nadeau, K
Andrews, CP
Jacobs, RL
He, WJ
AF Ahuja, Sunil K.
Manoharan, Muthu Saravanan
Harper, Nathan L.
Jimenez, Fabio
Hobson, Benjamin D.
Martinez, Hernan
Ingale, Puraskar
Liu, Ya-Guang
Carrillo, Andrew
Lou, Zheng
Kellog, Dean L.
Ahuja, Seema S.
Rather, Cynthia G.
Esch, Robert E.
Ramirez, Daniel A.
Clark, Robert A.
Nadeau, Kari
Andrews, Charles P.
Jacobs, Robert L.
He, Weijing
TI Preservation of epithelial cell barrier function and muted inflammation
in resistance to allergic rhinoconjunctivitis from house dust mite
challenge
SO JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
LA English
DT Article
DE Allergen challenge chamber; house dust mites; rhino-conjunctivitis; RNA
sequencing; epithelial barrier
ID GENOME-WIDE ASSOCIATION; LARGE GENE LISTS; ATOPIC-DERMATITIS;
SUSCEPTIBILITY LOCI; SKIN BARRIER; SENSITIZATION; EXPOSURE; FILAGGRIN;
CHAMBER; POLLEN
AB Background: An emerging paradigm holds that resistance to the development of allergic diseases, including allergic rhinoconjunctivitis, relates to an intact epithelial/epidermal barrier during early childhood. Conceivably, the immunologic and genomic footprint of this resistance is preserved in nonatopic, nonallergic adults and is unmasked during exposure to an aeroallergen.
Objective: The aim of this study was to obtain direct support of the epithelial/epidermal barrier model for allergic rhinoconjunctivitis.
Methods: Twenty-three adults allergic to house dust mites (HDMs) (M+) and 15 nonsensitive, nonallergic (M-) participants completed 3-hour exposures to aerosolized HDM (Dermatophagoides pteronyssinus) powder on 4 consecutive days in an allergen challenge chamber. We analyzed: (1) peripheral blood leukocyte levels and immune responses; and (2) RNA sequencing-derived expression profiles of nasal cells, before and after HDM exposure.
Results: On HDM challenge: (1) onlyM+ persons developed allergic rhinoconjunctivitis symptoms; and (2) peripheral blood leukocyte levels/responses and gene expression patterns in nasal cells were largely concordant between M+ and M- participants; gross differences in these parameters were not observed at baseline (pre-exposure). Two key differences were observed. First, peripheral blood CD4(+) and CD8(+) T-cell activation levels initially decreased in M- participants versus increased in M+ participants. Second, in M-compared with M+ participants, genes that promoted epidermal/epithelial barrier function (eg, filament- aggregating protein [filaggrin]) versus inflammation (eg, chemokines) and innate immunity (interferon) were upregulated versus muted, respectively.
Conclusion: An imprint of resistance to HDM challenge in nonatopic, nonallergic adults was muted T-cell activation in the peripheral blood and inflammatory response in the nasal compartment, coupled with upregulation of genes that promote epidermal/epithelial cell barrier function.
C1 [Ahuja, Sunil K.; Manoharan, Muthu Saravanan; Harper, Nathan L.; Jimenez, Fabio; Martinez, Hernan; Ingale, Puraskar; Liu, Ya-Guang; Carrillo, Andrew; Lou, Zheng; Ahuja, Seema S.; Clark, Robert A.; He, Weijing] South Texas Vet Hlth Care Syst, Vet Adm Ctr Personalized Med, San Antonio, TX USA.
[Ahuja, Sunil K.; Manoharan, Muthu Saravanan; Harper, Nathan L.; Jimenez, Fabio; Martinez, Hernan; Ingale, Puraskar; Liu, Ya-Guang; Carrillo, Andrew; Lou, Zheng; Kellog, Dean L.; Ahuja, Seema S.; Clark, Robert A.; He, Weijing] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA.
[Ahuja, Sunil K.] Univ Texas Hlth Sci Ctr San Antonio, Dept Microbiol & Immunol, San Antonio, TX 78229 USA.
[Ahuja, Sunil K.] Univ Texas Hlth Sci Ctr San Antonio, Dept Biochem, San Antonio, TX 78229 USA.
[Harper, Nathan L.; Jimenez, Fabio; Martinez, Hernan] Fdn Advancing Vet Hlth Res, San Antonio, TX USA.
[Hobson, Benjamin D.; Nadeau, Kari] Stanford Univ, Dept Pediat, Stanford, CA 94305 USA.
[Hobson, Benjamin D.; Nadeau, Kari] Stanford Univ, Sch Med, Sean N Parker Ctr Allergy Res, Stanford, CA USA.
[Rather, Cynthia G.; Ramirez, Daniel A.; Andrews, Charles P.; Jacobs, Robert L.] Biogen Res Chamber, San Antonio, TX USA.
[Esch, Robert E.] Lenoir Rhyne Univ, Sch Nat Sci, Hickory, NC USA.
[Nadeau, Kari] Stanford Hosp, Lucile Packard Childrens Hosp, Div Allergy Immunol & Rheumatol, Stanford, CA USA.
RP Ahuja, SK (reprint author), 7400 Merton Minter Blvd,Room W200, San Antonio, TX 78229 USA.
EM ahujas@uthscsa.edu
OI Ingale, Puraskar/0000-0003-2769-878X
FU Doris Duke Distinguished Clinical Scientist Award; Burroughs Wellcome
Clinical Scientist in Transitional Research Award; Max and Minnie
Tomerlin Senior Scholar Voelcker Award; Center for Personalized Medicine
South Texas Veterans Health Care System [CX00875-01A1]; National
Institutes of Health Clinical and Translational Science Award
[UL1-TR001120]; Sean N. Parker Center for Food Allergy Research
FX Supported by a the Doris Duke Distinguished Clinical Scientist Award, a
Burroughs Wellcome Clinical Scientist in Transitional Research Award, a
Max and Minnie Tomerlin Senior Scholar Voelcker Award, and a grant from
the Center for Personalized Medicine (CX00875-01A1) at the South Texas
Veterans Health Care System (S.K.A.); by a National Institutes of Health
Clinical and Translational Science Award (UL1-TR001120; R.A.C.); and by
the Sean N. Parker Center for Food Allergy Research (K.N.).
NR 43
TC 1
Z9 1
U1 2
U2 2
PU MOSBY-ELSEVIER
PI NEW YORK
PA 360 PARK AVENUE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0091-6749
EI 1097-6825
J9 J ALLERGY CLIN IMMUN
JI J. Allergy Clin. Immunol.
PD MAR
PY 2017
VL 139
IS 3
BP 844
EP 854
DI 10.1016/j.jaci.2016.08.019
PG 11
WC Allergy; Immunology
SC Allergy; Immunology
GA EP3QC
UT WOS:000397295800017
PM 27658763
ER
PT J
AU Williams, BA
Ibinson, JW
Ezaru, CS
Rakesh, H
Mangione, MP
AF Williams, Brian A.
Ibinson, James W.
Ezaru, Catalin S.
Rakesh, Hulimangala
Mangione, Michael P.
TI Translational Interpretations of Combined
Bupivacaine-Clonidine-Buprenorphine-Dexamethasone
SO REGIONAL ANESTHESIA AND PAIN MEDICINE
LA English
DT Letter
ID PERIPHERAL-NERVE BLOCKS; ANALGESIA
C1 [Williams, Brian A.] Univ Pittsburgh, Sch Med, Dept Anesthesiol, Pittsburgh, PA 15261 USA.
Vet Affairs Pittsburgh Healthcare Syst, Surg Serv Line, Pittsburgh, PA USA.
RP Williams, BA (reprint author), Univ Pittsburgh, Sch Med, Dept Anesthesiol, Pittsburgh, PA 15261 USA.
NR 6
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1098-7339
EI 1532-8651
J9 REGION ANESTH PAIN M
JI Region. Anesth. Pain Med.
PD MAR-APR
PY 2017
VL 42
IS 2
BP 271
EP 272
PG 3
WC Anesthesiology
SC Anesthesiology
GA EL3JE
UT WOS:000394514600020
PM 28207646
ER
PT J
AU Wong, LL
Lacar, L
Roytman, M
Orloff, SL
AF Wong, L. L.
Lacar, L.
Roytman, M.
Orloff, S. L.
TI Urgent Liver Transplantation for Dietary Supplements: An
Under-Recognized Problem
SO TRANSPLANTATION PROCEEDINGS
LA English
DT Article
ID OXYELITE PRO; HEPATOTOXICITY; HEPATITIS; FAILURE; INJURY; ACID
AB Background. The recent outbreak of acute liver failure caused by herbal/dietary supplements (HDS) in Hawaii prompted evaluation of those patients who underwent emergency liver transplantation (LT) for HDS in the United States.
Methods. We queried the Scientific Registry of Transplant Recipients (2003-2015) to identify patients who underwent urgent LT for acute hepatic necrosis (AHN) and identified those with HDS use. This group of patients was then characterized.
Results. Of 2408 adult cases, 625 were characterized as a drug-induced liver injury. The majority of cases (n = 300) were due to acetaminophen toxicity, but the fourth highest category was due to HDS (n = 21). Of these 21 cases caused by HDS, 13 did not list the specific agent responsible, mean age was 36 years, and all cases occurred after 2007. There probably are more cases because 25% of all LT cases in the study did not list a specific reason for liver failure and 20% of all drug-induced liver failure did not list a specific drug.
Conclusions. Herbal/supplement use is the fourth most common cause of drug-induced AHN requiring LT, albeit an underestimation of the problem. Detailed questioning of patients and their support systems regarding herbal/supplement use and better reporting are imperative to further define this problem and identify products that have the potential to lead to liver failure.
C1 [Wong, L. L.] Univ Hawaii, John A Burns Sch Med, Dept Surg, Honolulu, HI 96822 USA.
[Lacar, L.] Univ Hawaii, Honolulu, HI 96822 USA.
[Roytman, M.] Queens Med Ctr, Liver Ctr, Honolulu, HI USA.
[Orloff, S. L.] Oregon Hlth & Sci Univ, Div Abdominal Organ Transplantat Hepatobiliary Su, Portland VA Med Ctr, Portland, OR 97201 USA.
RP Wong, LL (reprint author), 550 South Beretania St,Suite 403, Honolulu, HI 96813 USA.
EM hepatoma@aol.com
NR 15
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U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0041-1345
EI 1873-2623
J9 TRANSPL P
JI Transplant. Proc.
PD MAR
PY 2017
VL 49
IS 2
BP 322
EP 325
DI 10.1016/j.transproceed.2016.11.041
PG 4
WC Immunology; Surgery; Transplantation
SC Immunology; Surgery; Transplantation
GA EL9GC
UT WOS:000394927300014
PM 28219592
ER
PT J
AU Lam, CA
Sherbourne, C
Gelberg, L
Lee, ML
Huynh, AK
Chu, KR
Strauss, JL
Metzger, ME
Post, EP
Rubenstein, LV
Farmer, MM
AF Lam, Christine A.
Sherbourne, Cathy
Gelberg, Lillian
Lee, Martin L.
Huynh, Alexis K.
Chu, Karen
Strauss, Jennifer L.
Metzger, Maureen E.
Post, Edward P.
Rubenstein, Lisa V.
Farmer, Melissa M.
TI Differences in Depression Care for Men and Women among Veterans with and
without Psychiatric Comorlbidities
SO WOMENS HEALTH ISSUES
LA English
DT Article
ID QUALITY-OF-CARE; VA HEALTH-CARE; DISORDERS; SERVICES; DISPARITIES;
RESOURCES
AB Background: Depression is common among primary care patients, affecting more women than men. Women veterans are an extreme but growing minority among patients seeking care from the Department of Veterans Affairs (VA), an organization historically designed to serve men. Little is known about gender differences in depression care quality within the VA primary care population.
Purpose: This works assesses the gender differences in depression care among veterans using longitudinal electronic measures.
Methods: We undertook a cross-sectional study of all veteran VA primary care users with a new episode of depression from federal fiscal year 2010, covering nine geographically diverse regions. We assessed the quality of depression care based on receipt of minimally appropriate depression treatment within 1 year of a new episode of depression and on receipt of depression-related follow-up visits within 180 days. Minimally appropriate treatment and follow-up were operationalized as meeting or exceeding a minimally appropriate threshold for care, based on national quality measures and expert panel consensus. Regression models were used to produce predicted probabilities for each process outcome accounting for the presence or absence of other psychiatric comorbidities. All models were adjusted for model covariates and clinic clusters (404 sites).
Main Findings: In 2010, 110,603 veterans with a primary care visit had a new episode of depression; 10,094 (9%) were women. In multivariate analyses, women had modest yet significantly higher rates of minimally appropriate depression treatment than men, whether patients had depression only (79% of women vs. 76% of men; p < .001) or depression along with other psychiatric comorbidities (92% of women vs. 91% or men; p < .001). There were no significant gender
C1 [Lam, Christine A.; Lee, Martin L.; Huynh, Alexis K.; Chu, Karen; Rubenstein, Lisa V.; Farmer, Melissa M.] VA Greater Los Angeles Healthcare Syst, VA HSR&D Ctr Study Healthcare Innovat Implementat, Sepulveda, CA USA.
[Lam, Christine A.; Farmer, Melissa M.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA.
[Sherbourne, Cathy; Rubenstein, Lisa V.] RAND Corp, Santa Monica, CA USA.
[Gelberg, Lillian] Univ Calif Los Angeles, David Geffen Sch Med, Dept Family Med, Los Angeles, CA 90095 USA.
[Gelberg, Lillian; Rubenstein, Lisa V.] Univ Calif Los Angeles, Dept Hlth Policy & Management, Fielding Sch Publ Hlth, Los Angeles, CA USA.
[Sherbourne, Cathy] VA Greater Los Angeles Healthcare Syst, Off Healthcare Transformat & Innovat, Los Angeles, CA USA.
[Lee, Martin L.] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Biostat, Los Angeles, CA USA.
[Strauss, Jennifer L.] Mental Hlth Serv, Dept Vet Affairs, Washington, DC USA.
[Strauss, Jennifer L.] Duke Univ, Med Ctr, Dept Psychiat, Durham, NC 27710 USA.
[Metzger, Maureen E.; Post, Edward P.] VA Ann Arbor, VA HSR&D Ctr Clin Management Res, Ann Arbor, MI USA.
[Post, Edward P.] Univ Michigan, Sch Med, Ann Arbor, MI USA.
RP Lam, CA (reprint author), VA Greater Los Angeles Healthcare Syst GLA, 11301 Wilshire Blvd,111G, Los Angeles, CA 90073 USA.
EM Christine.Lam@va.gov
FU VA Health Services Research Development [IIR 11-326]; VA Quality
Scholars advanced fellowship program
FX Funding Statement: Funding for this research was supported by a grant
from VA Health Services Research & Development (Project #IIR 11-326; PI:
Farmer). Dr. Lam is supported by the VA Quality Scholars advanced
fellowship program. The views expressed in the manuscript are solely
those of the authors, and do not necessarily represent the views of the
U.S. Department of Veterans Affairs or the United States government. The
authors declare that they do not have conflicts of interest.
NR 38
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PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1049-3867
EI 1878-4321
J9 WOMEN HEALTH ISS
JI Womens Health Iss.
PD MAR-APR
PY 2017
VL 27
IS 2
BP 206
EP 213
DI 10.1016/j.whi.2016.11.001
PG 8
WC Public, Environmental & Occupational Health; Women's Studies
SC Public, Environmental & Occupational Health; Women's Studies
GA EO1FA
UT WOS:000396442600013
PM 28007391
ER
PT J
AU Chuang, E
Brunner, J
Mak, S
Hamilton, AB
Canelo, I
Darling, J
Rubenstein, LV
Yano, EM
AF Chuang, Emmeline
Brunner, Julian
Mak, Selene
Hamilton, Alison B.
Canelo, Ismelda
Darling, Jill
Rubenstein, Lisa V.
Yano, Elizabeth M.
TI Challenges with Implementing a Patient-Centered Medical Home Model for
Women Veterans
SO WOMENS HEALTH ISSUES
LA English
DT Article
ID PRIMARY-CARE CLINICS; SPECIALTY CARE; HEALTH-CARE; SATISFACTION;
EXPERIENCES; CONTINUITY; PHYSICIANS; ACCESS; TRIAL
AB Background: The Veterans Health Administration (VA) Patient Aligned Care Team (PACT) initiative aims to ensure that all patients receive care consistent with medical home principles. Women veterans' unique care needs and minority status within the VA pose challenges to delivery of equitable, comprehensive primary care for this population. Currently, little is known about whether and/or how PACT should be tailored to better meet women veterans' needs.
Methods: In 2014, we conducted semistructured interviews with 73 primary care providers and staff to examine facilitators and barriers encountered in providing PACT-principled care to women veterans. Respondents were located in eight VA medical centers in eight different states across the United States.
Results: Respondents perceived PACT as improving continuity of care for patients and as increasing ability of nursing staff to practice at the top of their license. However, the implementation of core medical home features and team huddles was inconsistent and varied both within and across medical centers. Short staffing, inclusion of part-time providers on teams, balancing performance requirements for continuity and same-day access, and space constraints were identified as ongoing barriers to PACT implementation. Challenges unique to care of women veterans included a higher prevalence of psychosocial needs, the need for specialized training of primary care personnel, and short staffing owing to additional sharing of primary care support staff with specialist providers.
Conclusion: Providers and staff face unique challenges in delivering comprehensive primary care to women veterans that may require special policy, practice, and management action if benefits of PACT are to be fully realized for this population. (C) 2016 Jacobs Institute of Women's Health. Published by Elsevier Inc.
C1 [Chuang, Emmeline; Brunner, Julian; Mak, Selene; Rubenstein, Lisa V.; Yano, Elizabeth M.] Univ Calif Los Angeles, Dept Hlth Policy & Management, Fielding Sch Publ Hlth, 650 Charles E Young Dr South, Los Angeles, CA 90095 USA.
[Hamilton, Alison B.; Canelo, Ismelda; Darling, Jill; Rubenstein, Lisa V.; Yano, Elizabeth M.] VA Greater Los Angeles Hlth Care Syst, HSR&D Ctr Study Healthcare Innovat Implementat &, Los Angeles, CA USA.
RP Chuang, E (reprint author), Univ Calif Los Angeles, Dept Hlth Policy & Management, Fielding Sch Publ Hlth, 650 Charles E Young Dr South, Los Angeles, CA 90095 USA.
EM emchuang@ucla.edu
OI Chuang, Emmeline/0000-0001-9227-3273
FU VA HSRD Service; Veterans Health Administration through the CREATE
initiative [CRE 12-026]; VA HSRD Center for the Study of Healthcare
Innovation, Implementation, Policy [CIN 13-417]; VA HSR& D Senior
Research Career Scientist Award [RCS 05-195]
FX The authors thank Eva Selski and Anneka Oishi for their assistance in
coordinating interviews and Philip Pantoja for pulling the sample file
used to recruit participants. We are also grateful for all of the
primary care providers and staff that participated in this study.
Support for this research was provided by VA HSR&D Service, Veterans
Health Administration through the CREATE initiative (CRE 12-026) and the
VA HSRD Center for the Study of Healthcare Innovation, Implementation, &
Policy (CIN 13-417). Dr. Yano's effort was funded by a VA HSR& D Senior
Research Career Scientist Award (Project #RCS 05-195). The views
expressed within this study are solely those of the authors and do not
necessarily represent the views of the Department of Veterans Affairs or
the U. S. government.
NR 29
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U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1049-3867
EI 1878-4321
J9 WOMEN HEALTH ISS
JI Womens Health Iss.
PD MAR-APR
PY 2017
VL 27
IS 2
BP 214
EP 220
DI 10.1016/j.whi.2016.11.005
PG 7
WC Public, Environmental & Occupational Health; Women's Studies
SC Public, Environmental & Occupational Health; Women's Studies
GA EO1FA
UT WOS:000396442600014
PM 28063848
ER
PT J
AU Meredith, LS
Wang, Y
Okunogbe, A
Bergman, AA
Canelo, IA
Darling, JE
Yano, EM
AF Meredith, Lisa S.
Wang, Yan
Okunogbe, Adeyemi
Bergman, Alicia A.
Canelo, Ismelda A.
Darling, Jill E.
Yano, Elizabeth M.
TI Attitudes, Practices, and Experiences with Implementing a
Patient-Centered Medical Home for Women Veterans
SO WOMENS HEALTH ISSUES
LA English
DT Article
ID PRIMARY-CARE; HEALTH
AB Background: Despite the growing demand for health care among women veterans in the Veterans Health Administration (VHA), little is known about the perspectives of primary care providers (PCPs) and other primary care staff about the care they provide to women veterans. We sought to understand whether barriers to, attitudes about, and practices in caring for women veterans were associated with two measures of implementation of the VHA patient-centered medical home for women veterans (self-efficacy and satisfaction).
Methods: We administered a cross-sectional survey by Internet from September 8, 2014, through April 27, 2015 (and by mail from December 16, 2014, through June 18, 2015) to all PCPs and affiliated primary care staff in 12 VHA medical centers. We used descriptive and bivariate analyses to characterize their barriers, attitudes, and practices regarding care for women veterans; and ordinary least squares regression to identify associations with satisfaction and self-efficacy regarding medical home implementation for women veterans among members of a VHA patient-centered medical home teamlet for women patients.
Results: Of 775 surveys sent, 288 were completed (94 PCPs and 194 staff) for a response rate of 37% (33% for PCPs; 39% for staff). On average, providers had one female patient for every five patients in their panels. Lower perceived barriers, higher gender-sensitive attitudes, and being a PCP were significantly associated with satisfaction and self-efficacy of patient-centered medical home for women patients.
Conclusions: Training efforts focused on eliminating perceived barriers and strengthening positive attitudes toward women may be more successful than changing women's health practice characteristics alone. (Cd) 2016 Jacobs Institute of Women's Health. Published by Elsevier Inc.
C1 [Meredith, Lisa S.; Wang, Yan; Okunogbe, Adeyemi] RAND Corp, 1776 Main St, Santa Monica, CA 90407 USA.
[Meredith, Lisa S.; Bergman, Alicia A.; Canelo, Ismelda A.; Darling, Jill E.; Yano, Elizabeth M.] VA Greater Los Angeles Healthcare Syst, VA HSR&D Ctr Healthcare Innovat Implementat & Pol, Sepulveda, CA USA.
[Wang, Yan; Okunogbe, Adeyemi] Pardee RAND Grad Sch, Santa Monica, CA USA.
[Darling, Jill E.] USC Ctr Econ & Social Res, Los Angeles, CA USA.
[Yano, Elizabeth M.] Univ Calif Los Angeles, Dept Hlth Policy & Management, Fielding Sch Publ Hlth, Los Angeles, CA USA.
RP Meredith, LS (reprint author), RAND Corp, 1776 Main St, Santa Monica, CA 90407 USA.
EM lisa_meredith@rand.org
FU VA HSRD Service [CRE 12-026, CIN 13-417]; VA HSR&D Senior Research
Career Scientist Award [RCS 05-195]
FX This study was funded by the VA HSR&D Service (Projects # CRE 12-026 and
# CIN 13-417). Dr. Yano's time was covered by a VA HSR&D Senior Research
Career Scientist Award (Project # RCS 05-195). The authors thank Andy
Lanto for data management assistance at the VA. We also thank Rosie
Velasquez at RAND for help with the manuscript formatting. Finally, we
thank Dr. Chloe Bird for providing a quality review of the draft
manuscript.
NR 25
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U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1049-3867
EI 1878-4321
J9 WOMEN HEALTH ISS
JI Womens Health Iss.
PD MAR-APR
PY 2017
VL 27
IS 2
BP 221
EP 227
DI 10.1016/j.whi.2016.11.008
PG 7
WC Public, Environmental & Occupational Health; Women's Studies
SC Public, Environmental & Occupational Health; Women's Studies
GA EO1FA
UT WOS:000396442600015
PM 28087130
ER
PT J
AU Mansh, M
Ing, L
Dimon, M
Celli, A
Mauro, TM
Arron, ST
AF Mansh, M.
Ing, L.
Dimon, M.
Celli, A.
Mauro, T. M.
Arron, S. T.
TI Voriconazole exposure regulates distinct cell-cycle and terminal
differentiation pathways in primary human keratinocytes
SO BRITISH JOURNAL OF DERMATOLOGY
LA English
DT Letter
ID UP-REGULATION; FOXM1; CANCER; TRANSPLANTATION; PROPHYLAXIS; CARCINOMA
C1 [Mansh, M.] Univ Minnesota, Dept Dermatol, Minneapolis, MN 55455 USA.
[Ing, L.; Dimon, M.; Celli, A.; Mauro, T. M.; Arron, S. T.] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA.
[Celli, A.; Mauro, T. M.; Arron, S. T.] San Francisco VA Med Ctr, Dermatol Serv, San Francisco, CA 94121 USA.
RP Arron, ST (reprint author), Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94143 USA.; Arron, ST (reprint author), San Francisco VA Med Ctr, Dermatol Serv, San Francisco, CA 94121 USA.
EM sarah.arron@ucsf.edu
FU Stanford University Medical Scholars Research Grant; American Skin
Association Research Grant Targeting Skin Cancer; National Institutes of
Health [R01 AR051930]; Research Service of the United States Department
of Veterans Affairs; Nina Ireland Lung Disease Program at the University
of California, San Francisco
FX This work was supported by the Stanford University Medical Scholars
Research Grant and American Skin Association Research Grant Targeting
Skin Cancer (to M.M.); the National Institutes of Health (R01 AR051930)
and the Research Service of the United States Department of Veterans
Affairs (to T.M.M.); and the Nina Ireland Lung Disease Program at the
University of California, San Francisco (to. S.T.A).
NR 15
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Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0007-0963
EI 1365-2133
J9 BRIT J DERMATOL
JI Br. J. Dermatol.
PD MAR
PY 2017
VL 176
IS 3
BP 816
EP 820
DI 10.1111/bjd.14838
PG 5
WC Dermatology
SC Dermatology
GA EO4ZW
UT WOS:000396703800047
PM 27373453
ER
PT J
AU Goldberg, DS
Taddei, TH
Serper, M
Mehta, R
Dieperink, E
Aytaman, A
Baytarian, M
Fox, R
Hunt, K
Pedrosa, M
Pocha, C
Valderrama, A
Kaplan, DE
AF Goldberg, David S.
Taddei, Tamar H.
Serper, Marina
Mehta, Rajni
Dieperink, Eric
Aytaman, Ayse
Baytarian, Michelle
Fox, Rena
Hunt, Kristel
Pedrosa, Marcos
Pocha, Christine
Valderrama, Adriana
Kaplan, David E.
TI Identifying Barriers to Hepatocellular Carcinoma Surveillance in a
National Sample of Patients With Cirrhosis
SO HEPATOLOGY
LA English
DT Article
ID UNITED-STATES; COMPETING RISKS; VETERANS; SURVIVAL; CARE; CANCER;
POPULATION; DIAGNOSIS; DISEASE; RATES
AB Hepatocellular carcinoma (HCC) is a leading cause of morbidity and mortality in cirrhosis patients. This provides an opportunity to target the highest-risk population, yet surveillance rates in the United States and Europe range from 10% to 40%. The goal of this study was to identify barriers to HCC surveillance, using data from the Veterans Health Administration, the largest provider of liver-related health care in the United States. We included all patients 75 years of age or younger who were diagnosed with cirrhosis from January 1, 2008, until December 31, 2010. The primary outcome was a continuous measure of the percentage of time up-to-date with HCC surveillance (PTUDS) based on abdominal ultrasound (secondary outcomes included computed tomography and magnetic resonance imaging). Among 26,577 patients with cirrhosis (median follow-up = 4.7 years), the mean PTUDS was 17.8 +/- 21.5% (ultrasounds) and 23.3 +/- 24.1% when any liver imaging modality was included. The strongest predictor of increased PTUDS was the number of visits to a specialist (gastroenterologist/hepatologist and/or infectious diseases) in the first year after cirrhosis diagnosis; the association between visits to a primary care physician and increasing surveillance was very small. Increasing distance to the closest Veterans Administration center was associated with decreased PTUDS. There was an inverse association between ultrasound lead time (difference between the date an ultrasound was ordered and requested exam date) and the odds of it being performed: odds ratio = 0.77, 95% confidence interval 0.72-0.82 when ordered> 180 days ahead of time; odds ratio = 0.90, 95% confidence interval 0.85-0.94 if lead time 91-180 days. Conclusions: The responsibility for suboptimal surveillance rests with patients, providers, and the overall health care system; several measures can be implemented to potentially increase HCC surveillance, including increasing patient-specialist visits and minimizing appointment lead time.
C1 [Goldberg, David S.; Serper, Marina; Kaplan, David E.] Univ Penn, Div Gastroenterol, Philadelphia, PA USA.
[Goldberg, David S.] Univ Penn, Dept Biostat & Epidemiol, Philadelphia, PA USA.
[Taddei, Tamar H.; Mehta, Rajni] VA Connecticut Healthcare Syst, West Haven, CT USA.
[Dieperink, Eric] Minneapolis VA Hlth Care Syst, Minneapolis, MN USA.
[Aytaman, Ayse] VA New York Harbor Hlth Care Syst, Brooklyn, NY USA.
[Baytarian, Michelle] Boston MA Healthcare Syst, Boston, MA USA.
[Fox, Rena] San Francisco VA Med Ctr, San Francisco, CA USA.
[Hunt, Kristel] James J Peters VA Med Ctr, Bronx, NY USA.
[Pocha, Christine] Univ Bern, Bern, Switzerland.
[Valderrama, Adriana] Bayer HealthCare Pharmaceut, Whippany, NJ USA.
[Kaplan, David E.] Corporal Michael J Crescenz VA Med Ctr, Philadelphia, PA USA.
RP Kaplan, DE (reprint author), Univ Penn, Dept Med, Blockley Hall,423 Guardian Dr Room 730, Philadelphia, PA 19104 USA.
EM david.goldberg@uphs.upenn.edu
OI Kaplan, David E./0000-0002-3839-336X
FU Bayer Healthcare Pharmaceuticals; VA HIV, Hepatitis and Public Health
Pathogens Programs in the Office of Public Health/Clinical Public
Health; Health Resources and Services Administration [234-2005-37011C]
FX Supported by unrestricted research funds from Bayer Healthcare
Pharmaceuticals and the VA HIV, Hepatitis and Public Health Pathogens
Programs in the Office of Public Health/Clinical Public Health and in
part by the Health Resources and Services Administration (contract
234-2005-37011C).
NR 31
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U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0270-9139
EI 1527-3350
J9 HEPATOLOGY
JI Hepatology
PD MAR
PY 2017
VL 65
IS 3
BP 864
EP 874
DI 10.1002/hep.28765
PG 11
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EP3SF
UT WOS:000397301300012
PM 27531119
ER
PT J
AU Shively, SB
Edgerton, SL
Iacono, D
Purohit, DP
Qu, BX
Haroutunian, V
Davis, KL
Diaz-Arrastia, R
Perl, DP
AF Shively, Sharon B.
Edgerton, Sarah L.
Iacono, Diego
Purohit, Dushyant P.
Qu, Bao-Xi
Haroutunian, Vahram
Davis, Kenneth L.
Diaz-Arrastia, Ramon
Perl, Daniel P.
TI Localized cortical chronic traumatic encephalopathy pathology after
single, severe axonal injury in human brain
SO ACTA NEUROPATHOLOGICA
LA English
DT Article
DE Traumatic brain injury; Chronic traumatic encephalopathy; Axonal injury;
Tau; Neurofibrillary tangle; beta-Amyloid plaque
ID AMYLOID PROTEIN DEPOSITION; APOLIPOPROTEIN-E EPSILON-4; HEAD-INJURY;
ALZHEIMERS-DISEASE; NEURODEGENERATIVE DISEASES; BETA-PROTEIN;
WHITE-MATTER; RISK; DEGENERATION; ASSOCIATION
AB Chronic traumatic encephalopathy (CTE) is a neurodegenerative disease associated with repetitive mild impact traumatic brain injury from contact sports. Recently, a consensus panel defined the pathognomonic lesion for CTE as accumulations of abnormally hyperphosphorylated tau (p-tau) in neurons (neurofibrillary tangles), astrocytes and cell processes distributed around small blood vessels at sulcal depths in irregular patterns within the cortex. The pathophysiological mechanism for this lesion is unknown. Moreover, a subset of CTE cases harbors cortical beta-amyloid plaques. In this study, we analyzed postmortem brain tissues from five institutionalized patients with schizophrenia and history of surgical leucotomy with subsequent survival of at least another 40 years. Because leucotomy involves severing axons bilaterally in prefrontal cortex, this surgical procedure represents a human model of single traumatic brain injury with severe axonal damage and no external impact. We examined cortical tissues at the leucotomy site and at both prefrontal cortex rostral and frontal cortex caudal to the leucotomy site. For comparison, we analyzed brain tissues at equivalent neuroanatomical sites from non-leucotomized patients with schizophrenia, matched in age and gender. All five leucotomy cases revealed severe white matter damage with dense astrogliosis at the axotomy site and also neurofibrillary tangles and p-tau immunoreactive neurites in the overlying gray matter. Four cases displayed p-tau immunoreactivity in neurons, astrocytes and cell processes encompassing blood vessels at cortical sulcal depths in irregular patterns, similar to CTE. The three cases with apolipoprotein E epsilon 4 haplotype showed scattered beta-amyloid plaques in the overlying gray matter, but not the two cases with apolipoprotein E epsilon 3/3 genotype. Brain tissue samples from prefrontal cortex rostral and frontal cortex caudal to the leucotomy site, and all cortical samples from the non-leucotomized patients, showed minimal p-tau and beta-amyloid pathology. These findings suggest that chronic axonal damage contributes to the unique pathology of CTE over time.
C1 [Shively, Sharon B.; Iacono, Diego; Perl, Daniel P.] Uniformed Serv Univ Hlth Sci, F Edward Hebert Sch Med, Dept Pathol, 4301 Jones Bridge Rd, Bethesda, MD 20814 USA.
[Shively, Sharon B.; Edgerton, Sarah L.; Iacono, Diego; Qu, Bao-Xi; Diaz-Arrastia, Ramon; Perl, Daniel P.] Ctr Neurosci & Regenerat Med, 4301 Jones Bridge Rd, Bethesda, MD 20814 USA.
[Shively, Sharon B.; Edgerton, Sarah L.; Iacono, Diego] Henry M Jackson Fdn Adv Mil Med, 6720 Rockledge Dr, Bethesda, MD 20817 USA.
[Purohit, Dushyant P.] Icahn Sch Med Mt Sinai, Dept Pathol, 1468 Madison Ave, New York, NY 10029 USA.
[Qu, Bao-Xi; Diaz-Arrastia, Ramon] Uniformed Serv Univ Hlth Sci, F Edward Hebert Sch Med, Dept Neurol, 4301 Jones Bridge Rd, Bethesda, MD 20814 USA.
[Haroutunian, Vahram; Davis, Kenneth L.] Icahn Sch Med Mt Sinai, Dept Psychiat, 1 Gustave L Levy Pl, New York, NY 10029 USA.
[Haroutunian, Vahram] Icahn Sch Med Mt Sinai, Dept Neurosci, 1 Gustave L Levy Pl, New York, NY 10029 USA.
[Haroutunian, Vahram] James J Peters Vet Affairs Med Ctr, Mental Illness Res Educ & Clin Ctr, 130 West Kingsbridge Rd, Bronx, NY 10468 USA.
[Davis, Kenneth L.] Icahn Sch Med Mt Sinai, Dept Pharmacol Sci, 1 Gustave L Levy Pl, New York, NY 10029 USA.
RP Perl, DP (reprint author), Uniformed Serv Univ Hlth Sci, F Edward Hebert Sch Med, Dept Pathol, 4301 Jones Bridge Rd, Bethesda, MD 20814 USA.; Perl, DP (reprint author), Ctr Neurosci & Regenerat Med, 4301 Jones Bridge Rd, Bethesda, MD 20814 USA.
EM daniel.perl@usuhs.edu
FU Defense Health Program of the United States Department of Defense;
National Institutes of Health [MH45212, MH064673]
FX This study was funded by the Defense Health Program of the United States
Department of Defense and the National Institutes of Health (grants
MH45212, MH064673). This study utilized neuropathology core facilities
of Center for Neuroscience and Regenerative Medicine and Uniformed
Services University of the Health Sciences within the United States
Department of Defense. The authors wish to thank Dr. Peter Davies for
the generous gift of CP13 and PHF1 antibodies. We also thank Drs.
Charles Rice, Arthur Kellermann, Yvonne Maadox and Regina Armstrong for
their continuous encouragement and support, and Patricia Lee for her
technical expertise. The cases were obtained from tissue archives of the
Pilgrim Psychiatric Center Brain Bank in West Brentwood, NY. The
opinions expressed herein are those of the authors and are not
necessarily representative of those of the Uniformed Services University
of the Health Sciences, the Department of Defense; or, the United States
Army, Navy or Air Force.
NR 50
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U1 1
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PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0001-6322
EI 1432-0533
J9 ACTA NEUROPATHOL
JI Acta Neuropathol.
PD MAR
PY 2017
VL 133
IS 3
BP 353
EP 366
DI 10.1007/s00401-016-1649-7
PG 14
WC Clinical Neurology; Neurosciences; Pathology
SC Neurosciences & Neurology; Pathology
GA EL9ST
UT WOS:000394961100002
PM 27885490
ER
PT J
AU Finlay, AK
Stimmel, M
Blue-Howells, J
Rosenthal, J
McGuire, J
Binswanger, I
Smelson, D
Harris, AHS
Frayne, SM
Bowe, T
Timko, C
AF Finlay, Andrea K.
Stimmel, Matthew
Blue-Howells, Jessica
Rosenthal, Joel
McGuire, Jim
Binswanger, Ingrid
Smelson, David
Harris, Alex H. S.
Frayne, Susan M.
Bowe, Tom
Timko, Christine
TI Use of Veterans Health Administration Mental Health and Substance Use
Disorder Treatment After Exiting Prison: The Health Care for Reentry
Veterans Program
SO ADMINISTRATION AND POLICY IN MENTAL HEALTH AND MENTAL HEALTH SERVICES
RESEARCH
LA English
DT Article
DE Veterans health; Prisoners; Mental disorders; Substance use disorders;
Mental health services; United States Department of Veterans Affairs
ID RANDOMIZED CLINICAL-TRIAL; JUSTICE-INVOLVED VETERANS; INCARCERATED
VETERANS; FEDERAL PRISONS; DRUG-USE; RISK; MAINTENANCE; RELEASE;
INTERVENTION; HOMELESSNESS
AB The Veterans Health Administration (VA) Health Care for Reentry Veterans (HCRV) program links veterans exiting prison with treatment. Among veterans served by HCRV, national VA clinical data were used to describe contact with VA health care, and mental health and substance use disorder diagnoses and treatment use. Of veterans seen for an HCRV outreach visit, 56 % had contact with VA health care. Prevalence of mental health disorders was 57 %; of whom 77 % entered mental health treatment within a month of diagnosis. Prevalence of substance use disorders was 49 %; of whom 37 % entered substance use disorder treatment within a month of diagnosis. For veterans exiting prison, increasing access to VA health care, especially for rural veterans, and for substance use disorder treatment, are important quality improvement targets.
C1 [Finlay, Andrea K.; Harris, Alex H. S.; Frayne, Susan M.; Bowe, Tom; Timko, Christine] VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat Ci2i, 795 Willow Rd, Menlo Pk, CA 94025 USA.
[Stimmel, Matthew; Rosenthal, Joel; McGuire, Jim] Dept Vet Affairs, Vet Justice Programs, 795 Willow Rd, Menlo Pk, CA 94025 USA.
[Blue-Howells, Jessica] VA Greater Los Angeles Healthcare Syst, Dept Vet Affairs, Vet Justice Programs, 11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
[Binswanger, Ingrid] Kaiser Permanente Inst Hlth Res, 10065 E Harvard Ave,Suite 300, Denver, CO 80231 USA.
[Binswanger, Ingrid] Univ Colorado, Sch Med, Div Gen Internal Med, 12631 E 17th Ave, Aurora, CO 80045 USA.
[Smelson, David] Edith Nourse Rogers Mem Vet Hosp, Natl Ctr Homelessness Vet, 200 Springs Rd, Bedford, MA 01730 USA.
[Smelson, David] Univ Massachusetts, Sch Med, Dept Psychiat, 55 N Lake Ave, Worcester, MA 01655 USA.
[Frayne, Susan M.] VA Palo Alto Hlth Care Syst, Med Serv, Womens Hlth Serv, 3801 Miranda Ave, Palo Alto, CA 94304 USA.
[Frayne, Susan M.] Stanford Univ, Sch Med, Div Gen Med Disciplines, 1265 Welch Rd, Stanford, CA 94305 USA.
[Timko, Christine] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, 401 Quarry Rd, Stanford, CA 94305 USA.
RP Finlay, AK (reprint author), VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat Ci2i, 795 Willow Rd, Menlo Pk, CA 94025 USA.
EM andrea.finlay@va.gov; matthew.stimmel@va.gov;
jessica.blue-howells@va.gov; joel.rosenthal@va.gov;
jimfmcguire@yahoo.com; ingrid.a.binswanger@kp.org;
david.smelson@umassmed.edu; alexander.harris2@va.gov;
susan.frayne@va.gov; thomas.bowe@va.gov; ctimko@stanford.edu
FU Department of Veterans Affairs (VA) Substance Use Disorder Quality
Enhancement Research Initiative [SUD-QLP59-045]; VA Health Services
Research and Development (HSRD) [CDA 13-279]; VA HSRD [RCS 00-001, RCS
14-132]; VA National Center on Homelessness Among Veterans
FX This work was supported by the Department of Veterans Affairs (VA)
Substance Use Disorder Quality Enhancement Research Initiative
(SUD-QLP59-045). Dr. Finlay was supported by a VA Health Services
Research and Development (HSR&D) Career Development Award (CDA 13-279).
Dr. Timko was funded as a Senior Research Career Scientist (RCS 00-001)
in VA HSR&D. Dr. Harris was funded as a Research Career Scientist (RCS
14-132) in VA HSR&D. A portion of this work was also supported by the VA
National Center on Homelessness Among Veterans.
NR 40
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0894-587X
EI 1573-3289
J9 ADM POLICY MENT HLTH
JI Adm. Policy. Ment. Health
PD MAR
PY 2017
VL 44
IS 2
BP 177
EP 187
DI 10.1007/s10488-015-0708-z
PG 11
WC Health Policy & Services; Public, Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EL1EV
UT WOS:000394364200004
PM 26687114
ER
PT J
AU Kelly, K
Mejia, A
Suhasini, AN
Lin, AP
Kuhn, J
Karnad, AB
Weitman, S
Aguiar, RCT
AF Kelly, Kevin
Mejia, Alex
Suhasini, Avvaru N.
Lin, An-Ping
Kuhn, John
Karnad, Anand B.
Weitman, Steven
Aguiar, Ricardo C. T.
TI Safety and Pharmacodynamics of the PDE4 Inhibitor Roflumilast in
Advanced B-cell Malignancies
SO CLINICAL CANCER RESEARCH
LA English
DT Article
ID CHRONIC LYMPHOCYTIC-LEUKEMIA; CYCLIC-NUCLEOTIDE PHOSPHODIESTERASE; ACUTE
LYMPHOBLASTIC-LEUKEMIA; GENE-EXPRESSION; IN-VITRO; TARGETING BTK;
T-CELLS; LYMPHOMA; IBRUTINIB; RECEPTOR
AB Purpose: In this study, we aimed to validate our extensive preclinical data on phosphodiesterase 4 (PDE4) as actionable target in B-cell malignancies. Our specific objectives were to determine the safety, pharmacokinetics, and pharmacodynamics (PI3K/AKT activity), as well as to capture any potential antitumor activity of the PDE4 inhibitor roflumilast in combination with prednisone in patients with advanced B-cell malignancies.
Experimental Design: Single-center, exploratory phase Ib open-label, nonrandomized study. Roflumilast (500 mcg PO) was given daily for 21 days with prednisone on days 8 to 14. Additional 21-day cycles were started if patients tolerated cycle 1 and had at least stable disease.
Results: Ten patients, median age 65 years with an average of three prior therapies, were enrolled. The median number of cycles administered was 4 (range, 1-13). Treatment was well tolerated; the most common >= grade 2 treatment-related adverse events were fatigue, anorexia (>= 25%), and transient >= grade 2 neutropenia (30%). Treatment with roflumilast as a single agent significantly suppressed PI3K activity in the 77% of patients evaluated; on average, patients with PI3K/AKT suppression stayed in trial for 156 days (49-315) versus 91 days (28-139 days) for those without this biomarker response. Six of the nine evaluable patients (66%) had partial response or stable disease. The median number of days in trial was 105 days (range, 28-315).
Conclusions: Repurposing the PDE4 inhibitor roflumilast for treatment of B-cell malignancies is safe, suppresses the oncogenic PI3K/AKT kinases, and may be clinically active. (C)2016 AACR.
C1 [Kelly, Kevin; Mejia, Alex; Suhasini, Avvaru N.; Lin, An-Ping; Karnad, Anand B.; Aguiar, Ricardo C. T.] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Hematol & Med Oncol, San Antonio, TX 78229 USA.
[Kelly, Kevin; Mejia, Alex; Karnad, Anand B.; Weitman, Steven; Aguiar, Ricardo C. T.] Univ Texas Hlth Sci Ctr San Antonio, Canc Res & Therapy Ctr, Inst Drug Dev, San Antonio, TX 78229 USA.
[Kuhn, John] Univ Texas Hlth Sci Ctr San Antonio, Coll Pharm, San Antonio, TX 78229 USA.
[Kuhn, John] UT Austin, Austin, TX USA.
[Weitman, Steven] Univ Texas Hlth Sci Ctr San Antonio, Dept Pediat, San Antonio, TX 78229 USA.
[Aguiar, Ricardo C. T.] Univ Texas Hlth Sci Ctr San Antonio, Greehey Childrens Canc Res Inst, San Antonio, TX 78229 USA.
[Aguiar, Ricardo C. T.] Audie Murphy VA Hosp, South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Kelly, Kevin] Univ Southern Calif, Los Angeles, CA USA.
RP Aguiar, RCT (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Med, 7703 Floyd Curl Dr, San Antonio, TX 78229 USA.
EM aguiarr@uthscsa.edu
FU CTRC pilot award; CPRIT awards [RP110200, RP150277]; William and Ella
Owens Medical Research Foundation; Cancer Center support [P30 CA054174]
FX This study was supported by a CTRC pilot award to S. Weitman, CPRIT
awards RP110200 and RP150277 and a grant from the William and Ella Owens
Medical Research Foundation, all to R.C.T. Aguiar, and Cancer Center
support grant P30 CA054174.
NR 48
TC 0
Z9 0
U1 2
U2 2
PU AMER ASSOC CANCER RESEARCH
PI PHILADELPHIA
PA 615 CHESTNUT ST, 17TH FLOOR, PHILADELPHIA, PA 19106-4404 USA
SN 1078-0432
EI 1557-3265
J9 CLIN CANCER RES
JI Clin. Cancer Res.
PD MAR 1
PY 2017
VL 23
IS 5
BP 1186
EP 1192
DI 10.1158/1078-0432.CCR-16-1207
PG 7
WC Oncology
SC Oncology
GA EN4ZO
UT WOS:000396015600009
PM 27542768
ER
PT J
AU Foley, TM
Payne, SN
Pasch, CA
Yueh, AE
Van De Hey, DR
Korkos, DP
Clipson, L
Maher, ME
Matkowskyj, KA
Newton, MA
Deming, DA
AF Foley, Tyler M.
Payne, Susan N.
Pasch, Cheri A.
Yueh, Alex E.
Van De Hey, Dana R.
Korkos, Demetra P.
Clipson, Linda
Maher, Molly E.
Matkowskyj, Kristina A.
Newton, Michael A.
Deming, Dustin A.
TI Dual PI3K/mTOR Inhibition in Colorectal Cancers with APC and PIK3CA
Mutations
SO MOLECULAR CANCER RESEARCH
LA English
DT Article
ID ADVANCED SOLID TUMORS; I PI3K INHIBITOR; PHASE-I; COLON TUMORS; MTOR;
PATHWAY; RAPAMYCIN; 1ST-IN-HUMAN; TRANSFORMATION; TUMORIGENESIS
AB Therapeutic targeting of the PI3K pathway is an active area of research in multiple cancer types, including breast and endometrial cancers. This pathway is commonly altered in cancer and plays an integral role in numerous vital cellular functions. Mutations in the PIK3CA gene, resulting in a constitutively active form of PI3K, often occur in colorectal cancer, though the population of patients who would benefit from targeting this pathway has yet to be identified. In human colorectal cancers, PIK3CA mutations most commonly occur concomitantly with loss of adenomatous polyposis coli (APC). Here, treatment strategies are investigated that target the PI3K pathway in colon cancers with mutations in APC and PIK3CA. Colorectal cancer spheroids with Apc and Pik3ca mutations were generated and characterized confirming that these cultures represent the tumors from which they were derived. Pan and alpha isomer-specific PI3K inhibitors did not induce a significant treatment response, whereas the dual PI3K/mTOR inhibitors BEZ235 and LY3023414 induced a dramatic treatment response through decreased cellular proliferation and increased differentiation. The significant treatment responses were confirmed in mice with Apc and Pik3ca-mutant colon cancers as measured using endoscopy with a reduction in median lumen occlusion of 53% with BEZ235 and a 24% reduction with LY3023414 compared with an increase of 53% in controls (P < 0.001 and P = 0.03, respectively). This response was also confirmed with F-18-FDG microPET/CT imaging.
Implications: Spheroid models and transgenic mice suggest that dual PI3K/mTOR inhibition is a potential treatment strategy for APC and PIK3CA-mutant colorectal cancers. Thus, further clinical studies of dual PI3K/mTOR inhibitors are warranted in colorectal cancers with these mutations. (C) 2016 AACR.
C1 [Foley, Tyler M.; Yueh, Alex E.; Van De Hey, Dana R.; Korkos, Demetra P.; Maher, Molly E.; Deming, Dustin A.] Univ Wisconsin, Dept Med, Div Hematol & Oncol, Madison, WI USA.
[Payne, Susan N.; Pasch, Cheri A.; Matkowskyj, Kristina A.; Deming, Dustin A.] Univ Wisconsin, Carbone Canc Ctr, Madison, WI USA.
[Clipson, Linda; Deming, Dustin A.] Univ Wisconsin, McArdle Lab Canc Res, Dept Oncol, 1400 Univ Ave, Madison, WI 53706 USA.
[Matkowskyj, Kristina A.] Univ Wisconsin, Dept Pathol & Lab Med, Madison, WI USA.
[Matkowskyj, Kristina A.; Deming, Dustin A.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
[Newton, Michael A.] Univ Wisconsin, Dept Stat, Madison, WI 53706 USA.
[Newton, Michael A.] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI USA.
RP Deming, DA (reprint author), Univ Wisconsin, 1111 Highland Ave, Madison, WI 53705 USA.
EM ddeming@medicine.wisc.edu
FU UW Carbone Cancer Center; UW Department of Medicine; UW School of
Medicine and Public Health; UW Graduate School through the Wisconsin
Alumni Research Foundation; Funk Out Cancer [P30 CA014520]; UWCCC
Experimental Therapeutics pilot award
FX This project was supported by start-up funds (D.A. Deming) from the UW
Carbone Cancer Center, UW Department of Medicine, UW School of Medicine
and Public Health, and the UW Graduate School through the Wisconsin
Alumni Research Foundation, Funk Out Cancer, P30 CA014520 (Core Grant,
University of Wisconsin Carbone Cancer Center), and UWCCC Experimental
Therapeutics pilot award. LY3023414 was provided by Eli Lilly and Co.
NR 47
TC 0
Z9 0
U1 3
U2 3
PU AMER ASSOC CANCER RESEARCH
PI PHILADELPHIA
PA 615 CHESTNUT ST, 17TH FLOOR, PHILADELPHIA, PA 19106-4404 USA
SN 1541-7786
EI 1557-3125
J9 MOL CANCER RES
JI Mol. Cancer Res.
PD MAR
PY 2017
VL 15
IS 3
BP 317
EP 327
DI 10.1158/1541-7786.MCR-16-0256-T
PG 11
WC Oncology; Cell Biology
SC Oncology; Cell Biology
GA EN5CY
UT WOS:000396024400008
ER
PT J
AU Post, RM
Altshuler, LL
Kupka, R
McElroy, SL
Frye, MA
Rowe, M
Grunze, H
Suppes, T
Keck, PE
Leverich, GS
Nolen, WA
AF Post, Robert M.
Altshuler, Lori L.
Kupka, Ralph
McElroy, Susan L.
Frye, Mark A.
Rowe, Michael
Grunze, Heinz
Suppes, Trisha
Keck, Paul E., Jr.
Leverich, Gabriele S.
Nolen, Willem A.
TI More childhood onset bipolar disorder in the United States than Canada
or Europe: Implications for treatment and prevention
SO NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS
LA English
DT Review
DE Childhood onset bipolar disorder; Depression; Substance abuse; Genetics;
Epigenetics; Cohort effect; Assortative mating; Childhood adversity;
Early intervention; Primary and secondary prevention
ID AGE-OF-ONSET; COMORBIDITY SURVEY REPLICATION; PSYCHIATRIC-DISORDERS;
MENTAL-DISORDERS; HIGH-RISK; SPECTRUM DISORDERS; MOOD-DISORDERS;
I-DISORDER; FAMILIAL AGGREGATION; ILLNESS PROGRESSION
AB Evidence of a high or increasing incidence of childhood onset bipolar disorder in the United States (US) has been viewed skeptically. Here we review evidence that childhood onsets of bipolar disorder are more common in the US than in Europe, treatment delays are longer, and illness course is more adverse and difficult. Epidemiological data and studies of offspring at high risk also support these findings.
In our cohort of outpatients with bipolar disorder, two of the major vulnerability factors for early onset - genetics and environmental adversity in childhood - were also greater in the US than in Europe. An increased familial loading for multiple psychiatric disorders was apparent in 4 generations of the family members of the patients from the US, and that familial burden was linked to early onset bipolar disorder. Since both early onset and treatment delay are risk factors for a poor outcome in adulthood, new clinical, research, and public health initiatives are needed to begin to address and ameliorate this ongoing and potentially devastating clinical situation. (C) 2017 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.orgilicensesiby-nc-nd/4.0/).
C1 [Post, Robert M.; Rowe, Michael; Leverich, Gabriele S.] Bipolar Collaborat Network, Bethesda, MD USA.
[Post, Robert M.] George Washington Univ, Dept Psychiat & Behav Sci, Washington, DC USA.
[Altshuler, Lori L.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA.
[Altshuler, Lori L.] West Angeles Healthcare Ctr, VA Greater Angeles Healthcare Syst, Dept Psychiat, Los Angeles, CA USA.
[Kupka, Ralph; Keck, Paul E., Jr.] Univ Cincinnati, Coll Med, Dept Psychiat & Behav Neurosci, Cincinnati, OH USA.
[McElroy, Susan L.; Keck, Paul E., Jr.] Lindner Ctr HOPE, Mason, OH USA.
[McElroy, Susan L.] Univ Cincinnati, Biol Psychiat Program, Coll Med, Cincinnati, OH USA.
[Frye, Mark A.] Mayo Clin, Dept Psychiat, Rochester, MI USA.
[Grunze, Heinz] Paracelsius Med Univ, Salzburg, Austria.
[Suppes, Trisha] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Palo Alto, CA 94304 USA.
[Suppes, Trisha] VA Palo Alto Hlth Care Syst, Palo Alto, CA USA.
[Nolen, Willem A.] Univ Groningen, Univ Med Ctr, Groningen, Netherlands.
RP Post, RM (reprint author), George Washington Univ, Bipolar Collaborat Network, Clin Prof Psychiat, Sch Med, 5415W Cedar Lane,Suite 201-B, Bethesda, MD 20814 USA.
EM robert.post@speakeasy.net
NR 113
TC 1
Z9 1
U1 2
U2 2
PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0149-7634
EI 1873-7528
J9 NEUROSCI BIOBEHAV R
JI Neurosci. Biobehav. Rev.
PD MAR
PY 2017
VL 74
BP 204
EP 213
DI 10.1016/j.neubiorev.2017.01.022
PN A
PG 10
WC Behavioral Sciences; Neurosciences
SC Behavioral Sciences; Neurosciences & Neurology
GA EM9BF
UT WOS:000395605200013
PM 28119069
ER
PT J
AU McDonough, CM
Ni, PS
Peterik, K
Marfeo, EE
Marino, ME
Meterko, M
Rasch, EK
Brandt, DE
Jette, AM
Chan, L
AF McDonough, Christine M.
Ni, Pengsheng
Peterik, Kara
Marfeo, Elizabeth E.
Marino, Molly E.
Meterko, Mark
Rasch, Elizabeth K.
Brandt, Diane E.
Jette, Alan M.
Chan, Leighton
TI Improving measures of work-related physical functioning
SO QUALITY OF LIFE RESEARCH
LA English
DT Article
DE Disability evaluation; Work disability; Questionnaires
ID BEHAVIORAL HEALTH FUNCTION; FUNCTION INSTRUMENT; DISABILITY; INDEX; DIF;
IRT
AB To expand content of the physical function domain of the Work Disability Functional Assessment Battery (WD-FAB), developed for the US Social Security Administration's (SSA) disability determination process.
Newly developed questions were administered to 3532 recent SSA applicants for work disability benefits and 2025 US adults. Factor analyses and item response theory (IRT) methods were used to calibrate and link the new items to the existing WD-FAB, and computer-adaptive test simulations were conducted.
Factor and IRT analyses supported integration of 44 new items into three existing WD-FAB scales and the addition of a new 11-item scale (Community Mobility). The final physical function domain consisting of: Basic Mobility (56 items), Upper Body Function (34 items), Fine Motor Function (45 items), and Community Mobility (11 items) demonstrated acceptable psychometric properties.
The WD-FAB offers an important tool for enhancement of work disability determination. The FAB could provide relevant information about work-related functioning for initial assessment of claimants; identifying denied applicants who may benefit from interventions to improve work and health outcomes; enhancing periodic review of work disability beneficiaries; and assessing outcomes for policies, programs and services targeting people with work disability.
C1 [McDonough, Christine M.; Ni, Pengsheng; Peterik, Kara; Marfeo, Elizabeth E.; Marino, Molly E.; Meterko, Mark; Jette, Alan M.] Boston Univ, Sch Publ Hlth, Hlth & Disabil Res Inst, 715 Albany St,T5W, Boston, MA 02118 USA.
[McDonough, Christine M.] Geisel Sch Med Dartmouth, Dept Orthopaed Surg, Hanover, NH 03755 USA.
[Marfeo, Elizabeth E.] Tufts Univ, Medford, MA 02155 USA.
[Meterko, Mark] US Dept Vet Affairs, Ctr Healthcare Org & Implementat Res, Boston, MA USA.
[Rasch, Elizabeth K.; Brandt, Diane E.; Chan, Leighton] NIH, Dept Rehabil Med, Bethesda, MD 20892 USA.
RP McDonough, CM (reprint author), Boston Univ, Sch Publ Hlth, Hlth & Disabil Res Inst, 715 Albany St,T5W, Boston, MA 02118 USA.; McDonough, CM (reprint author), Geisel Sch Med Dartmouth, Dept Orthopaed Surg, Hanover, NH 03755 USA.
EM cmm@bu.edu
FU Social Security Administration-National Institutes of Health Interagency
Agreements under the National Institutes of Health [HHSN269200900004C,
HHSN269201000011C, HHSN269201100009I, HHSN269201200005C]; National
Institutes of Health Intramural Research Program
FX This study was supported by Social Security Administration-National
Institutes of Health Interagency Agreements under the National
Institutes of Health (Contract Nos. HHSN269200900004C,
HHSN269201000011C, HHSN269201100009I, HHSN269201200005C), and by the
National Institutes of Health Intramural Research Program.
NR 24
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER
PI DORDRECHT
PA VAN GODEWIJCKSTRAAT 30, 3311 GZ DORDRECHT, NETHERLANDS
SN 0962-9343
EI 1573-2649
J9 QUAL LIFE RES
JI Qual. Life Res.
PD MAR
PY 2017
VL 26
IS 3
BP 789
EP 798
DI 10.1007/s11136-016-1477-1
PG 10
WC Health Care Sciences & Services; Health Policy & Services; Public,
Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EL1DX
UT WOS:000394361800025
PM 28005243
ER
PT J
AU Rhoads, JP
Lukens, JR
Wilhelm, AJ
Moore, JL
Mendez-Fernandez, Y
Kanneganti, TD
Major, AS
AF Rhoads, Jillian P.
Lukens, John R.
Wilhelm, Ashley J.
Moore, Jared L.
Mendez-Fernandez, Yanice
Kanneganti, Thirumala-Devi
Major, Amy S.
TI Oxidized Low-Density Lipoprotein Immune Complex Priming of the Nlrp3
Inflammasome Involves TLR and Fc gamma R Cooperation and Is Dependent on
CARD9
SO JOURNAL OF IMMUNOLOGY
LA English
DT Article
ID SYSTEMIC-LUPUS-ERYTHEMATOSUS; TOLL-LIKE RECEPTOR; RHEUMATOID-ARTHRITIS;
CITRULLINATED FIBRINOGEN; DIABETES-MELLITUS; DENDRITIC CELLS; DEFICIENT
MICE; HOST-DEFENSE; MODIFIED LDL; ACTIVATION
AB Oxidized low-density lipoprotein (oxLDL) is known to activate inflammatory responses in a variety of cells, especially macrophages and dendritic cells. Interestingly, much of the oxLDL in circulation is complexed to Abs, and these resulting immune complexes (ICs) are a prominent feature of chronic inflammatory disease, such as atherosclerosis, type-2 diabetes, systemic lupus erythematosus, and rheumatoid arthritis. Levels of oxLDL ICs often correlate with disease severity, and studies demonstrated that oxLDL ICs elicit potent inflammatory responses in macrophages. In this article, we show that bone marrow-derived dendritic cells (BMDCs) incubated with oxLDL ICs for 24 h secrete significantly more IL-1 beta compared with BMDCs treated with free oxLDL, whereas there was no difference in levels of TNF-alpha or IL-6. Treatment of BMDCs with oxLDL ICs increased expression of inflammasomerelated genes Il1a, Il1b, and Nlrp3, and pretreatment with a caspase 1 inhibitor decreased IL-1b secretion in response to oxLDL ICs. This inflammasome priming was due to oxLDL IC signaling via multiple receptors, because inhibition of CD36, TLR4, and FcgR significantly decreased IL-1 beta secretion in response to oxLDL ICs. Signaling through these receptors converged on the adaptor protein CARD9, a component of the CARD9-Bcl10-MALT1 signalosome complex involved in NF-kappa B translocation. Finally, oxLDL IC-mediated IL-1 beta production resulted in increased Th17 polarization and cytokine secretion. Collectively, these data demonstrate that oxLDL ICs induce inflammasome activation through a separate and more robust mechanism than oxLDL alone and that these ICs may be immunomodulatory in chronic disease and not just biomarkers of severity.
C1 [Rhoads, Jillian P.; Moore, Jared L.; Major, Amy S.] US Dept Vet Affairs, Tennessee Valley Healthcare Syst, Nashville, TN 37212 USA.
[Rhoads, Jillian P.; Major, Amy S.] Vanderbilt Univ, Dept Pathol Microbiol & Immunol, Nashville, TN 37232 USA.
[Lukens, John R.] Univ Virginia, Dept Neurosci, Ctr Brain Immunol & Glia, Charlottesville, VA 22908 USA.
[Wilhelm, Ashley J.; Moore, Jared L.; Major, Amy S.] Vanderbilt Univ Sch Med, Dept Med, Div Rheumatol, Nashville, TN 37232 USA.
[Mendez-Fernandez, Yanice] Trevecca Nazarene Univ, Dept Biol, Nashville, TN 37210 USA.
[Kanneganti, Thirumala-Devi] St Jude Childrens Res Hosp, Dept Immunol, Memphis, TN 38105 USA.
RP Major, AS (reprint author), Vanderbilt Univ, 1161 21st Ave South,T-3113 MCN, Nashville, TN 37232 USA.
EM amy.major@vanderbilt.edu
FU Lupus Research Institute; National Institutes of Health [R21AR066971,
T32 AR059039, F31 HL128040]; Veterans Administration [I01BX002968]
FX This work was supported by grants from the Lupus Research Institute, the
National Institutes of Health (Grant R21AR066971), and the Veterans
Administration (Grant I01BX002968) (all to A.S.M.). J.P.R. was supported
by National Institutes of Health Grants T32 AR059039 and F31 HL128040.
NR 46
TC 0
Z9 0
U1 0
U2 0
PU AMER ASSOC IMMUNOLOGISTS
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 0022-1767
EI 1550-6606
J9 J IMMUNOL
JI J. Immunol.
PD MAR 1
PY 2017
VL 198
IS 5
BP 2105
EP 2114
DI 10.4049/jimmunol.1601563
PG 10
WC Immunology
SC Immunology
GA EN3JE
UT WOS:000395904000035
PM 28130494
ER
PT J
AU Guille, C
Barth, KS
Mateus, J
McCauley, JL
Brady, KT
AF Guille, Constance
Barth, Kelly S.
Mateus, Julio
McCauley, Jenna L.
Brady, Kathleen T.
TI Treatment of Prescription Opioid Use Disorder in Pregnant Women
SO AMERICAN JOURNAL OF PSYCHIATRY
LA English
DT Editorial Material
ID METHADONE-MAINTENANCE TREATMENT; NEONATAL OUTCOMES; UNITED-STATES;
ABSTINENCE SYNDROME; ABUSE; DETOXIFICATION; POPULATION; PREDICTORS;
RETENTION; HMO
C1 [Guille, Constance] Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA.
Med Univ South Carolina, Dept Obstet & Gynecol, Charleston, SC USA.
Ralph H Johnson VA Med Ctr, Charleston, SC USA.
RP Guille, C (reprint author), Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC 29425 USA.
EM guille@musc.edu
FU National Institute on Drug Abuse [1K23DA039318-01, 1K23 DA039328-01A1,
1K23 DA036566-01A1]; [R25 DA020537]; [UL1 TR00006205S1]; [P50
DA016511]; [U10 DA01372]; [K12 HD055885]
FX Dr. Guille (1K23DA039318-01), Dr. Barth (1K23 DA039328-01A1), and Dr.
McCauley (1K23 DA036566-01A1) are funded by the National Institute on
Drug Abuse. Dr. Brady is funded by grants R25 DA020537, UL1
TR00006205S1, P50 DA016511, U10 DA01372, and K12 HD055885.
NR 35
TC 0
Z9 0
U1 2
U2 2
PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 0002-953X
EI 1535-7228
J9 AM J PSYCHIAT
JI Am. J. Psychiat.
PD MAR 1
PY 2017
VL 174
IS 3
BP 208
EP 214
DI 10.1176/appi.ajp.2016.16060710
PG 7
WC Psychiatry
SC Psychiatry
GA EO4KV
UT WOS:000396664700006
PM 28245688
ER
PT J
AU Altshuler, LL
Sugar, CA
McElroy, SL
Calimlim, B
Gitlin, M
Keck, PE
Aquino-Elias, A
Martens, BE
Fischer, G
English, TL
Roach, J
Suppes, T
AF Altshuler, Lori L.
Sugar, Catherine A.
McElroy, Susan L.
Calimlim, Brian
Gitlin, Michael
Keck, Paul E., Jr.
Aquino-Elias, Ana
Martens, Brian E.
Fischer, Grace
English, Teri L.
Roach, Janine
Suppes, Trisha
TI Switch Rates During Acute Treatment for Bipolar II Depression With
Lithium, Sertraline, or the Two Combined: A Randomized Double-Blind
Comparison
SO AMERICAN JOURNAL OF PSYCHIATRY
LA English
DT Article
ID TERM FLUOXETINE MONOTHERAPY; NOS MAJOR DEPRESSION; MOOD CONVERSION RATE;
PLACEBO-SUBSTITUTION; SUICIDAL-BEHAVIOR; DISORDER; ANTIDEPRESSANT;
EFFICACY; MANIA; COMBINATION
AB Objective: The authors compared medication-induced mood switch risk (primary outcome), as well as treatment response and side effects (secondary outcomes) with three acute-phase treatments for bipolar II depression.
Method: In a 16-week, double-blind, multisite comparison study, 142 participants with bipolar II depression were randomly assigned to receive lithium monotherapy (N=49), sertraline monotherapy (N=45), or combination treatment with lithium and sertraline (N=48). At each visit, mood was assessed using standardized rating scales. Rates of switch were compared, as were rates of treatment response and the presence and severity of treatment-emergent side effects.
Results: Twenty participants (14%) experienced a switch during the study period (hypomania, N=17; severe hypomania, N=3). Switch rates did not differ among the three treatment groups, even after accounting for dropout. No patient had a manic switch or was hospitalized for a switch. Most switches occurred within the first 5 weeks of treatment. The treatment response rate for the overall sample was 62.7% (N=89), without significant differences between groups after accounting for dropout. The lithium/sertraline combination group had a significantly higher overall dropout rate than the monotherapy groups but did not have an accelerated time to response.
Conclusions: Lithium monotherapy, sertraline monotherapy, and lithium/sertraline combination therapy were associated with similar switch and treatment response rates in participants with bipolar II depression. The dropout rate was higher in the lithium/sertraline combination treatment group, without any treatment acceleration advantage.
C1 [Suppes, Trisha] Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA.
Univ Calif Los Angeles, Jane & Terry Semel Inst Neurosci & Human Behav, Los Angeles, CA USA.
VA Greater Los Angeles Healthcare Syst, Dept Psychiat, West Los Angeles Healthcare Ctr, Los Angeles, CA USA.
Univ Calif Los Angeles, Sch Publ Hlth, Dept Biostat, Los Angeles, CA 90024 USA.
Lindner Ctr HOPE, Mason, OH USA.
Univ Cincinnati, Coll Med, Dept Psychiat & Behav Neurosci, Cincinnati, OH USA.
Stanford Univ, Dept Psychiat & Biobehav Sci, Sch Med, Stanford, CA USA.
VA Palo Alto Hlth Care Syst, Palo Alto, CA USA.
Olive View UCLA Med Ctr, Dept Psychiat, 14445 Olive View Dr, Sylmar, CA 91342 USA.
RP Suppes, T (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA.
EM tsuppes@stanford.edu
FU NIMH [5R01MH074707, 5R01MH074929, 5R01MH074928]; Elan; NIMH; Pathway
Genomics; Stanley Medical Research Institute; Sunovion Pharmaceuticals;
VA Cooperative Studies Program; Alkermes; Forest; Marriott Foundation;
Naurex; Orexigen Therapeutics; Shire; Sunovion; Takeda
FX Supported by a collaborative R01 grant by the NIMH: 5R01MH074707 (to Dr.
Altshuler at UCLA Medical Center and VA Greater Los Angeles Healthcare
System), 5R01MH074929 (to Dr. McElroy at University of Cincinnati
College of Medicine and the Lindner Center of HOPE), and 5R01MH074928
(to Dr. Suppes at the University of Texas Southwestern Medical Center,
Dallas, and the VA Palo Alto Health Care System, Palo Alto).; Dr.
McElroy is a consultant to or scientific advisory board member for
Bracket, Hoffmann-La Roche, MedAvante, Myriad, Naurex, NovoNordisk,
Shire, and Sunovion; she is a principal or co-investigator on studies
sponsored by Alkermes, Forest, the Marriott Foundation, Naurex, NIMH,
Orexigen Therapeutics, Shire, Sunovion, and Takeda; she is an inventor
on U.S. patent no. 6,323,236 B2 (Use of Sulfamate Derivatives for
Treating Impulse Control Disorders) and, along with the patent's
assignee, University of Cincinnati, has received payments from Johnson &
Johnson, which has exclusive rights under thepatent. Dr. Gitlin has been
on speakers bureaus for and received honoraria and travel expenses from
Bristol-Myers Squibb and Otsuka. Dr. Keck is a co-inventor on U.S.
patent no. 6,387,956 (a method of treating obsessive-compulsive spectrum
disorder that includes administering an effectiveamountof tramadol), for
which he has received no financial benefit. Dr. Suppes has received
research funding from Elan, NIMH, Pathway Genomics, Stanley Medical
Research Institute, Sunovion Pharmaceuticals, and the VA Cooperative
Studies Program; has served as a consultant or an advisory board member
for A/S H. Lundbeck, Merck, and Sunovion Pharmaceuticals; and has
received royalties from Jones & Bartlett and UpToDate. The other authors
report no financial relationships with commercial interests.
NR 43
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PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 0002-953X
EI 1535-7228
J9 AM J PSYCHIAT
JI Am. J. Psychiat.
PD MAR 1
PY 2017
VL 174
IS 3
BP 266
EP 276
DI 10.1176/appi.ajp.2016.15040558
PG 11
WC Psychiatry
SC Psychiatry
GA EO4KV
UT WOS:000396664700013
PM 28135846
ER
PT J
AU Bates, DW
Sheikh, A
Asch, DA
AF Bates, David W.
Sheikh, Aziz
Asch, David A.
TI Innovative Environments In Health Care: Where And How New Approaches To
Care Are Succeeding
SO HEALTH AFFAIRS
LA English
DT Article
ID CENTERS
AB Organizations seeking to create innovative environments in health care need to pay attention to a number of factors. These include making available sufficient resources, notably money and physical space, but also coordination and consultation regarding intellectual property and licensing; enabling access to engineers, software developers, and behavioral scientists; making providers and patients available to innovators; having a sufficiently long-term view; and insulating the innovation group from operational demands. If there is a single essential key to success, it is making innovation a strategic priority. Academic health systems are enormous generators of innovation in the form of generalizable research in biomedical sciences. Typically, much of that innovation is externally supported, and little is directed to improving care processes internally. In industries other than health care, organizations invest their own funds in research and development to promote innovation, and this investment is seen as a metric for a firm's commitment to its future. Increased investment in care-process innovation is long overdue.
C1 [Bates, David W.] Brigham & Womens Hosp, Div Gen Internal Med, 75 Francis St, Boston, MA 02115 USA.
[Sheikh, Aziz] Univ Edinburgh, Ctr Populat Hlth, Primary Care Res & Dev, Edinburgh, Midlothian, Scotland.
[Asch, David A.] Univ Penn, Ctr Hlth Care Innovat, Philadelphia, PA 19104 USA.
[Asch, David A.] Univ Penn, Wharton Sch, Philadelphia, PA 19104 USA.
[Asch, David A.] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Asch, David A.] Philadelphia Vet Affairs Med Ctr, Ctr Hlth Equ Res & Promot, Philadelphia, PA USA.
RP Bates, DW (reprint author), Brigham & Womens Hosp, Div Gen Internal Med, 75 Francis St, Boston, MA 02115 USA.
EM dbates@partners.org
FU QPID, Inc.; Center for Digital Innovation (Negev), Ltd.
FX David Bates is a co-inventor on Patent No. 6029138, held by Brigham and
Women's Hospital, on the use of decision support software for medical
management, licensed to the Medicalis Corporation, a privately held
company. He holds a minority equity position in Medicalis, which
develops web-based decision support for ordering radiology tests. He
serves on the board for SEA Medical Systems, which makes intravenous
pump technology. He consults for EarlySense, which makes patient safety
monitoring systems. He receives equity and cash compensation from QPID,
Inc., a company focused on intelligence systems for electronic health
records. He receives cash compensation from the Center for Digital
Innovation (Negev), Ltd., which is a not-for-profit incubator for health
information technology start-ups. He receives equity from Enelgy, which
makes software to support evidence-based clinical decisions. He receives
equity from ValeraHealth, which makes software to help patients with
chronic diseases. He receives equity from Intensix, which makes software
to support clinical decision making in intensive care. He receives
equity from MDClone which takes clinical data and produces deidentified
versions of it. His financial interests have been reviewed by Brigham
and Women's Hospital and Partners HealthCare System in accordance with
their institutional policies. David Asch is a partner and part owner of
VAL Health, a behavioral economics consulting firm.
NR 22
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U1 5
U2 5
PU PROJECT HOPE
PI BETHESDA
PA 7500 OLD GEORGETOWN RD, STE 600, BETHESDA, MD 20814-6133 USA
SN 0278-2715
J9 HEALTH AFFAIR
JI Health Aff.
PD MAR
PY 2017
VL 36
IS 3
BP 400
EP 407
DI 10.1377/hlthaff.2016.1311
PG 8
WC Health Care Sciences & Services; Health Policy & Services
SC Health Care Sciences & Services
GA EN9RS
UT WOS:000396337900005
PM 28264940
ER
PT J
AU Hare, SM
Ford, JM
Ahmadi, A
Damaraju, E
Belger, A
Bustillo, J
Lee, HJ
Mathalon, DH
Mueller, BA
Preda, A
van Erp, TGM
Potkin, SG
Calhoun, VD
Turner, JA
AF Hare, Stephanie M.
Ford, Judith M.
Ahmadi, Aral
Damaraju, Eswar
Belger, Aysenil
Bustillo, Juan
Lee, Hyo Jong
Mathalon, Daniel H.
Mueller, Bryon A.
Preda, Adrian
van Erp, Theo G. M.
Potkin, Steven G.
Calhoun, Vince D.
Turner, Jessica A.
CA Functional Imaging Biomedical Info
TI Modality-Dependent Impact of Hallucinations on Low-Frequency
Fluctuations in Schizophrenia
SO SCHIZOPHRENIA BULLETIN
LA English
DT Article
DE hallucinations; hippocampus; ALFF; rest ing-state; fMRI
ID AUDITORY VERBAL HALLUCINATIONS; STATE FUNCTIONAL CONNECTIVITY; VISUAL
HALLUCINATIONS; AMPLITUDE; OSCILLATIONS; DISEASE; GYRUS; FMRI; MRI
AB Prior resting-state functional magnetic resonance imaging (fMRI) analyses have identified patterns of functional connectivity associated with hallucinations in schizophrenia (Sz). In this study, we performed an analysis of the mean amplitude of low-frequency fluctuations (ALFF) to compare resting state spontaneous low-frequency fluctuations in patients with Sz who report experiencing hallucinations impacting different sensory modalities. By exploring dynamics across 2 low-frequency passbands (slow-4 and slow-5), we assessed the impact of hallucination modality and frequency range on spatial ALFF variation. Drawing from a sample of Sz and healthy controls studied as part of the Functional Imaging Biomedical Informatics Research Network (FBIRN), we replicated prior findings showing that patients with Sz have decreased ALFF in the posterior brain in comparison to controls. Remarkably, we found that patients that endorsed visual hallucinations did not show this pattern of reduced ALFF in the back of the brain. These patients also had elevated ALFF in the left hippocampus in comparison to patients that endorsed auditory (but not visual) hallucinations. Moreover, left hippocampal ALFF across all the cases was related to reported hallucination severity in both the auditory and visual domains, and not overall positive symptoms. This supports the hypothesis that dynamic changes in the ALFF in the hippocampus underlie severity of hallucinations that impact different sensory modalities.
C1 [Hare, Stephanie M.; Turner, Jessica A.] Georgia State Univ, Inst Neurosci, POB 5030, Atlanta, GA 30302 USA.
[Ford, Judith M.; Mathalon, Daniel H.] Univ Calif San Francisco, Dept Psychiat, San Francisco VA Med Ctr, San Francisco, CA USA.
[Ahmadi, Aral; Turner, Jessica A.] Georgia State Univ, Dept Psychol, Univ Plaza, Atlanta, GA 30303 USA.
[Damaraju, Eswar; Calhoun, Vince D.; Turner, Jessica A.] Mind Res Network, Albuquerque, NM USA.
[Belger, Aysenil] Univ N Carolina, Dept Psychiat, Chapel Hill, NC USA.
[Belger, Aysenil] Univ N Carolina, Dept Psychol, Chapel Hill, NC USA.
[Bustillo, Juan] Univ New Mexico, Dept Psychiat, Albuquerque, NM 87131 USA.
[Lee, Hyo Jong] Chonbuk Natl Univ, Dept Comp Sci & Engn, Jeonju, South Korea.
[Mueller, Bryon A.] Univ Minnesota, Dept Psychiat, Minneapolis, MN 55455 USA.
[Preda, Adrian; van Erp, Theo G. M.; Potkin, Steven G.; Functional Imaging Biomedical Info] Univ Calif Irvine, Dept Psychiat & Human Behav, Irvine, CA 92717 USA.
[Calhoun, Vince D.] Univ New Mexico, Dept Elect & Comp Engn, Albuquerque, NM 87131 USA.
RP Hare, SM (reprint author), Georgia State Univ, Inst Neurosci, POB 5030, Atlanta, GA 30302 USA.
EM share1@student.gsu.edu
FU National Institutes of Health [U24 RR021992]; Georgia State University
FX This work was supported by awards from National Institutes of Health,
U24 RR021992 to the Functional Imaging Biomedical Informatics Research
Network (FBIRN, http://www.birncommunity.org), and an internal 2CI
Fellowship from Georgia State University to S.M.H.
NR 30
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U1 3
U2 3
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0586-7614
EI 1745-1701
J9 SCHIZOPHRENIA BULL
JI Schizophr. Bull.
PD MAR
PY 2017
VL 43
IS 2
BP 389
EP 396
DI 10.1093/schbul/sbw093
PG 8
WC Psychiatry
SC Psychiatry
GA EO6FG
UT WOS:000396786800019
PM 27421792
ER
PT J
AU Mathew, AR
Hogarth, L
Leventhal, AM
Cook, JW
Hitsman, B
AF Mathew, Amanda R.
Hogarth, Lee
Leventhal, Adam M.
Cook, Jessica W.
Hitsman, Brian
TI Cigarette smoking and depression comorbidity: systematic review and
proposed theoretical model
SO ADDICTION
LA English
DT Review
DE Depression; nicotine dependence; review; smoking; smoking cessation;
treatment
ID TREATMENT-SEEKING SMOKERS; COGNITIVE-BEHAVIORAL TREATMENT; TOBACCO
WITHDRAWAL SYNDROME; NEGATIVE AFFECT; MAJOR DEPRESSION;
PSYCHIATRIC-DISORDERS; NICOTINE DEPENDENCE; RANDOMIZED-TRIAL;
MENTAL-ILLNESS; UNITED-STATES
AB Background and Aims Despite decades of research on co-occurring smoking and depression, cessation rates remain consistently lower for depressed smokers than for smokers in the general population, highlighting the need for theory-driven models of smoking and depression. This paper provides a systematic review with a particular focus upon psychological states that disproportionately motivate smoking in depression, and frame an incentive learning theory account of smoking-depression co-occurrence. Methods We searched PubMed, Scopus, PsychINFO and CINAHL to December 2014, which yielded 852 papers. Using pre-established eligibility criteria, we identified papers focused on clinical issues and motivational mechanisms underlying smoking in established, adult smokers (i.e. maintenance, quit attempts and cessation/relapse) with elevated symptoms of depression. Two reviewers determined independently whether papers met review criteria. We included 297 papers in qualitative synthesis. Results Our review identified three primary mechanisms that underlie persistent smoking among depressed smokers: low positive affect, high negative affect and cognitive impairment. We propose a novel application of incentive learning theory which posits that depressed smokers experience greater increases in the expected value of smoking in the face of these three motivational states, which promotes goal-directed choice of smoking behavior over alternative actions. Conclusions The incentive learning theory accounts for current evidence on how depression primes smoking behavior and provides a unique framework for conceptualizing psychological mechanisms of smoking maintenance among depressed smokers. Treatment should focus upon correcting adverse internal states and beliefs about the high value of smoking in those states to improve cessation outcomes for depressed smokers.
C1 [Mathew, Amanda R.; Hitsman, Brian] Northwestern Univ, Dept Prevent Med, Feinberg Sch Med, 680 North Lake Shore Dr,Suite 1400, Chicago, IL 60611 USA.
[Hogarth, Lee] Univ Exeter, Sch Psychol, Exeter, Devon, England.
[Leventhal, Adam M.] Univ Southern Calif, Keck Sch Med, Dept Prevent Med, Los Angeles, CA USA.
[Leventhal, Adam M.] Univ Southern Calif, Keck Sch Med, Dept Psychol, Los Angeles, CA USA.
[Cook, Jessica W.] Univ Wisconsin Madison, Sch Med & Publ Hlth, Madison, WI USA.
[Cook, Jessica W.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
RP Mathew, AR (reprint author), Northwestern Univ, Dept Prevent Med, Feinberg Sch Med, 680 North Lake Shore Dr,Suite 1400, Chicago, IL 60611 USA.
EM amanda.mathew@northwestern.edu
FU National Cancer Institute; National Institute on Drug Abuse of the
United States National Institutes of Health [F32DA036947, R01CA184211];
US Department of Veterans Affairs [101CX00056]
FX This work is supported by the National Cancer Institute and National
Institute on Drug Abuse of the United States National Institutes of
Health (Grant Numbers F32DA036947 and R01CA184211). J.W.C. is supported
by Merit Review Award 101CX00056 from the US Department of Veterans
Affairs. We thank Dr Robert West for feedback on an earlier draft of
this manuscript.
NR 158
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U1 8
U2 8
PU WILEY-BLACKWELL
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0965-2140
EI 1360-0443
J9 ADDICTION
JI Addiction
PD MAR
PY 2017
VL 112
IS 3
BP 401
EP 412
DI 10.1111/add.13604
PG 12
WC Substance Abuse; Psychiatry
SC Substance Abuse; Psychiatry
GA EK5TG
UT WOS:000393988200008
PM 27628300
ER
PT J
AU Vogelmeier, CF
Criner, GJ
Martinez, FJ
Anzueto, A
Barnes, PJ
Bourbeau, J
Celli, BR
Chen, RC
Decramer, M
Fabbri, LM
Frith, P
Halpin, DMG
Varela, MVL
Nishimura, M
Roche, N
Rodriguez-Roisin, R
Sin, DD
Singh, D
Stockley, R
Vestbo, J
Wedzicha, JA
Agusti, A
AF Vogelmeier, Claus F.
Criner, Gerard J.
Martinez, Fernando J.
Anzueto, Antonio
Barnes, Peter J.
Bourbeau, Jean
Celli, Bartolome R.
Chen, Rongchang
Decramer, Marc
Fabbri, Leonardo M.
Frith, Peter
Halpin, David M. G.
Varela, M. Victorina Lopez
Nishimura, Masaharu
Roche, Nicolas
Rodriguez-Roisin, Roberto
Sin, Don D.
Singh, Dave
Stockley, Robert
Vestbo, Jurgen
Wedzicha, Jadwiga A.
Agusti, Alvar
TI Global Strategy for the Diagnosis, Management, and Prevention of Chronic
Obstructive Lung Disease 2017 Report
SO AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
LA English
DT Article
DE chronic obstructive pulmonary disease; COPD diagnosis; COPD management;
COPD prevention
ID RANDOMIZED CONTROLLED-TRIAL; AIR-FLOW OBSTRUCTION; POSITIVE-PRESSURE
VENTILATION; PLACEBO-CONTROLLED TRIAL; QUALITY-OF-LIFE; INHALED
FLUTICASONE FUROATE; CHRONIC RESPIRATORY-DISEASE; BONE-MINERAL DENSITY;
REQUIRING MECHANICAL VENTILATION; GASTROESOPHAGEAL-REFLUX DISEASE
AB This Executive Summary of the Global Strategy for the Diagnosis, Management, and Prevention of COPD, Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2017 report focuses primarily on the revised and novel parts of the document. The most significant changes include: (1) the assessment of chronic obstructive pulmonary disease has been refined to separate the spirometric assessment from symptom evaluation. ABCD groups are now proposed to be derived exclusively from patient symptoms and their history of exacerbations; (2) for each of the groups A to D, escalation strategies for pharmacologic treatments are proposed; (3) the concept of deescalation of therapy is introduced in the treatment assessment scheme; (4) nonpharmacologic therapies are comprehensively presented; and (5) the importance of comorbid conditions in managing chronic obstructive pulmonary disease is reviewed.
C1 [Vogelmeier, Claus F.] Univ Marburg, German Ctr Lung Res DZL, Marburg, Germany.
[Criner, Gerard J.] Temple Univ, Lewis Katz Sch Med, Philadelphia, PA 19122 USA.
[Martinez, Fernando J.] New York Presbyterian Hosp, Weill Cornell Med Ctr, New York, NY USA.
[Anzueto, Antonio] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Anzueto, Antonio] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Barnes, Peter J.; Wedzicha, Jadwiga A.] Imperial Coll, Natl Heart & Lung Inst, London, England.
[Bourbeau, Jean] McGill Univ, Ctr Hlth, Montreal, PQ, Canada.
[Celli, Bartolome R.] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA.
[Chen, Rongchang] Guangzhou Med Univ, Affiliated Hosp 1, Guangzhou Inst Resp Dis, State Key Lab Resp Dis, Guangzhou, Guangdong, Peoples R China.
[Decramer, Marc] Univ Leuven, Leuven, Belgium.
[Fabbri, Leonardo M.] Univ Modena & Reggio Emilia, Modena, Italy.
[Frith, Peter] Flinders Univ S Australia, Fac Med, Bedford Pk, SA, Australia.
[Halpin, David M. G.] Royal Devon & Exeter Hosp, Exeter, Devon, England.
[Varela, M. Victorina Lopez] Univ Republica, Hosp Maciel, Montevideo, Uruguay.
[Nishimura, Masaharu] Hokkaido Univ, Sch Med, Sapporo, Hokkaido, Japan.
[Roche, Nicolas] Univ Paris 05, Hop Cochin, AP HP, Paris, France.
[Rodriguez-Roisin, Roberto] Univ Barcelona, Hosp Clin, Thorax Inst, Barcelona, Spain.
[Sin, Don D.] Univ British Columbia, St Pauls Hosp, Vancouver, BC, Canada.
[Singh, Dave; Vestbo, Jurgen] Univ Manchester, Manchester, Lancs, England.
[Stockley, Robert] Univ Hosp, Birmingham, W Midlands, England.
[Agusti, Alvar] Univ Barcelona, Hosp Clin, Ctr Invest Biomed Red Enfermedade Resp, Barcelona, Spain.
RP Vogelmeier, CF (reprint author), Univ Marburg, Dept Med Pulm & Crit Care Med, Baldingerstr, D-35043 Marburg, Germany.
EM claus.vogelmeier@med.uni-marburg.de
FU Medical Research Council [G0800570, G1001365, G1001372]
NR 339
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U1 8
U2 8
PU AMER THORACIC SOC
PI NEW YORK
PA 25 BROADWAY, 18 FL, NEW YORK, NY 10004 USA
SN 1073-449X
EI 1535-4970
J9 AM J RESP CRIT CARE
JI Am. J. Respir. Crit. Care Med.
PD MAR 1
PY 2017
VL 195
IS 5
BP 557
EP 582
DI 10.1164/rccm.201701-0218PP
PG 26
WC Critical Care Medicine; Respiratory System
SC General & Internal Medicine; Respiratory System
GA EM5ND
UT WOS:000395357400007
PM 28128970
ER
PT J
AU Kaz, AM
Wong, CJ
Varadan, V
Willis, JE
Chak, A
Grady, WM
AF Kaz, Andrew M.
Wong, Chao-Jen
Varadan, Vinay
Willis, Joseph E.
Chak, Amitabh
Grady, William M.
TI Global DNA methylation patterns in Barrett's esophagus, dysplastic
Barrett's, and esophageal adenocarcinoma are associated with BMI,
gender, and tobacco use (vol 8, 111, 2016)
SO CLINICAL EPIGENETICS
LA English
DT Correction
C1 [Kaz, Andrew M.] VA Puget Sound Hlth Care Syst, Gastroenterol Sect, Seattle, WA 98108 USA.
[Kaz, Andrew M.; Wong, Chao-Jen; Grady, William M.] Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA.
[Kaz, Andrew M.; Grady, William M.] Univ Washington, Sch Med, Seattle, WA 98195 USA.
[Varadan, Vinay; Chak, Amitabh] Case Western Reserve Univ, Case Comprehens Canc Ctr, Cleveland, OH 44106 USA.
[Willis, Joseph E.] Case Western Reserve Univ, Sch Med, Dept Pathol, Cleveland, OH 44106 USA.
[Chak, Amitabh] Case Western Reserve Univ, Sch Med, Div Gastroenterol, Cleveland, OH 44106 USA.
RP Kaz, AM (reprint author), VA Puget Sound Hlth Care Syst, Gastroenterol Sect, Seattle, WA 98108 USA.; Kaz, AM (reprint author), Fred Hutchinson Canc Res Ctr, Div Clin Res, Seattle, WA 98109 USA.; Kaz, AM (reprint author), Univ Washington, Sch Med, Seattle, WA 98195 USA.
EM Andrew.Kaz@va.gov
FU DeGregorio Family Foundation; Price Family Foundation
FX Following publication of this article [1], it has come to our attention
that the following publication should have acknowledged the DeGregorio
Family Foundation and the Price Family Foundation as providing funding
for the studies and for supporting the work.
NR 1
TC 0
Z9 0
U1 3
U2 3
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1868-7083
J9 CLIN EPIGENETICS
JI Clin. Epigenetics
PD MAR 1
PY 2017
VL 9
AR 23
DI 10.1186/s13148-017-0324-8
PG 1
WC Oncology
SC Oncology
GA EM5HI
UT WOS:000395342200001
PM 28265303
ER
PT J
AU Bartunek, J
Terzic, A
Davison, BA
Filippatos, GS
Radovanovic, S
Beleslin, B
Merkely, B
Musialek, P
Wojakowski, W
Andreka, P
Horvath, IG
Katz, A
Dolatabadi, D
El Nakadi, B
Arandjelovic, A
Edes, I
Seferovic, PM
Obradovic, S
Vanderheyden, M
Jagic, N
Petrov, I
Atar, S
Halabi, M
Gelev, VL
Shochat, MK
Kasprzak, JD
Sanz-Ruiz, R
Heyndrickx, GR
Nyolczas, N
Legrand, V
Guedes, A
Heyse, A
Moccetti, T
Fernandez-Aviles, F
Jimenez-Quevedo, P
Bayes-Genis, A
Hernandez-Garcia, JM
Ribichini, F
Gruchala, M
Waldman, SA
Teerlink, JR
Gersh, BJ
Povsic, TJ
Henry, TD
Metra, M
Hajjar, RJ
Tendera, M
Behfar, A
Alexandre, B
Seron, A
Stough, WG
Sherman, W
Cotter, G
Wijns, W
AF Bartunek, Jozef
Terzic, Andre
Davison, Beth A.
Filippatos, Gerasimos S.
Radovanovic, Slavica
Beleslin, Branko
Merkely, Bela
Musialek, Piotr
Wojakowski, Wojciech
Andreka, Peter
Horvath, Ivan G.
Katz, Amos
Dolatabadi, Dariouch
El Nakadi, Badih
Arandjelovic, Aleksandra
Edes, Istvan
Seferovic, Petar M.
Obradovic, Slobodan
Vanderheyden, Marc
Jagic, Nikola
Petrov, Ivo
Atar, Shaul
Halabi, Majdi
Gelev, Valeri L.
Shochat, Michael K.
Kasprzak, Jaroslaw D.
Sanz-Ruiz, Ricardo
Heyndrickx, Guy R.
Nyolczas, Noemi
Legrand, Victor
Guedes, Antoine
Heyse, Alex
Moccetti, Tiziano
Fernandez-Aviles, Francisco
Jimenez-Quevedo, Pilar
Bayes-Genis, Antoni
Maria Hernandez-Garcia, Jose
Ribichini, Flavio
Gruchala, Marcin
Waldman, Scott A.
Teerlink, John R.
Gersh, Bernard J.
Povsic, Thomas J.
Henry, Timothy D.
Metra, Marco
Hajjar, Roger J.
Tendera, Michal
Behfar, Atta
Alexandre, Bertrand
Seron, Aymeric
Stough, Wendy Gattis
Sherman, Warren
Cotter, Gad
Wijns, William
CA CHART Program
TI Cardiopoietic cell therapy for advanced ischaemic heart failure: results
at 39 weeks of the prospective, randomized, double blind,
sham-controlled CHART-1 clinical trial
SO EUROPEAN HEART JOURNAL
LA English
DT Article
DE Regenerative medicine; Cardiopoiesis; Cardiovascular disease; Stem cell;
Target population; Disease severity; Marker; Precision medicine
ID MESENCHYMAL STEM-CELLS; BONE-MARROW; REGENERATIVE MEDICINE; DISEASE;
PREDICTORS; MORTALITY; DELIVERY; OUTCOMES
AB Aims Cardiopoietic cells, produced through cardiogenic conditioning of patients' mesenchymal stem cells, have shown preliminary efficacy. The Congestive Heart Failure Cardiopoietic Regenerative Therapy (CHART-1) trial aimed to validate cardiopoiesis-based biotherapy in a larger heart failure cohort.
Methods and results This multinational, randomized, double-blind, sham-controlled study was conducted in 39 hospitals. Patients with symptomatic ischaemic heart failure on guideline-directed therapy (n= 484) were screened; n = 348 underwent bone marrow harvest and mesenchymal stem cell expansion. Those achieving> 24 million mesenchymal stem cells (n= 315) were randomized to cardiopoietic cells delivered endomyocardially with a retention-enhanced catheter (n= 157) or sham procedure (n= 158). Procedures were performed as randomized in 271 patients (n = 120 cardiopoietic cells, n= 151 sham). The primary efficacy endpoint was a Finkelstein-Schoenfeld hierarchical composite (all-cause mortality, worsening heart failure, Minnesota Living with Heart Failure Questionnaire score, 6-min walk distance, left ventricular end-systolic volume, and ejection fraction) at 39 weeks. The primary outcome was neutral (Mann-Whitney estimator 0.54, 95% confidence interval [CI] 0.47-0.61 [value> 0.5 favours cell treatment], P = 0.27). Exploratory analyses suggested a benefit of cell treatment on the primary composite in patients with baseline left ventricular end-diastolic volume 200-370mL (60% of patients) (Mann-Whitney estimator 0.61, 95% CI 0.52-0.70, P = 0.015). No difference was observed in serious adverse events. One (0.9%) cardiopoietic cell patient and 9 (5.4%) sham patients experienced aborted or sudden cardiac death.
Conclusion The primary endpoint was neutral, with safety demonstrated across the cohort. Further evaluation of cardiopoietic cell therapy in patients with elevated end-diastolic volume is warranted.
C1 [Bartunek, Jozef; Vanderheyden, Marc; Heyndrickx, Guy R.; Wijns, William] Onze Lieve Vrouwziekenhuis OLV Hosp, Ctr Cardiovasc, Moorselbaan 164, B-9300 Aalst, Belgium.
[Terzic, Andre; Gersh, Bernard J.; Behfar, Atta] Mayo Clin, Ctr Regenerat Med, Dept Cardiovasc Dis, 200 First St SW, Rochester, MI USA.
[Davison, Beth A.; Cotter, Gad] Momentum Res Inc, Durham, NC USA.
[Filippatos, Gerasimos S.] Univ Athens, Attikon Univ Hosp, Sch Med, Athens, Greece.
[Radovanovic, Slavica] Univ Hosp, Ctr Bezanijska Kosa, Belgrade, Serbia.
[Beleslin, Branko] Univ Belgrade, Sch Med, Cardiol Clin, Clin Ctr Serbia, Belgrade, Serbia.
[Merkely, Bela] Semmelweis Univ, Heart & Vasc Ctr, Budapest, Hungary.
[Musialek, Piotr] Jagiellonian Univ, John Paul Hosp 2, Dept Cardiac & Vasc Dis, Krakow, Poland.
[Wojakowski, Wojciech; Tendera, Michal] Med Univ Silesia, Div Cardiol 3, Katowice, Poland.
[Andreka, Peter] Gottsegen Gyorgy Hungarian Inst Cardiol, Budapest, Hungary.
[Horvath, Ivan G.] Univ Pecs, Inst Heart, Pecs, Hungary.
[Katz, Amos] Ben Gurion Univ Negev, Israel Fac Hlth Sci, Barzilai Med Ctr, Dept Cardiol, Beer Sheva, Israel.
[Dolatabadi, Dariouch; El Nakadi, Badih] Ctr Hosp Univ Charleroi, Div Cardiol, Charleroi, Belgium.
[Arandjelovic, Aleksandra] Clin Hosp Zvezdara, Dept Cardiol, Belgrade, Serbia.
[Edes, Istvan] Univ Debrecen, Dept Cardiol, Debrecen, Hungary.
[Seferovic, Petar M.] Univ Belgrade, Med Ctr, Sch Med, Belgrade, Serbia.
[Obradovic, Slobodan] Univ Def, Mil Med Acad, Sch Med, Clin Emergency Med, Belgrade, Serbia.
[Jagic, Nikola] Clin Ctr Kragujevac, Kragujevac, Serbia.
[Petrov, Ivo; Gelev, Valeri L.] Univ Sofia, City Clin Heart & Vasc Inst, Dept Cardiol Angiol & Electrophysiol, Sofia, Bulgaria.
[Atar, Shaul] Galilee Med Ctr, Dept Cardiol, Nahariyya, Israel.
[Atar, Shaul; Halabi, Majdi] Bar Ilan Univ, Fac Med Galilee, Safed, Israel.
[Shochat, Michael K.] Inst Heart, Hillel Yaffe Med Ctr, Hadera Rappaport Sch Med, Haifa, Israel.
[Kasprzak, Jaroslaw D.] Med Univ Lodz, Dept Cardiol, Lodz, Poland.
[Sanz-Ruiz, Ricardo; Fernandez-Aviles, Francisco] Univ Gregorio Maranon, Gen Hosp, Madrid, Spain.
[Nyolczas, Noemi] Med Ctr, Hungarian Def Forces, Budapest, Hungary.
[Legrand, Victor] Ctr Hosp Univ Liege, Dept Cardiol, Liege, Belgium.
[Guedes, Antoine] Catholic Univ Louvain, Dept Cardiol, CHU UcL Namur, Yvoir, Belgium.
[Heyse, Alex] AZ Glorieux, Dept Cardiol, Ronse, Belgium.
[Moccetti, Tiziano] Cardioctr Ticino, Lugano, Switzerland.
[Jimenez-Quevedo, Pilar] Hosp Clin San Carlos, Dept Cardiol, Madrid, Spain.
[Bayes-Genis, Antoni] Univ Autonoma Barcelona, Hosp Univ Germans Trias & Pujol, Barcelona, Spain.
[Maria Hernandez-Garcia, Jose] Hosp Clinico Univ Virgen Victoria, Malaga, Spain.
[Ribichini, Flavio] Univ Verona, Dept Cardiol, I-37100 Verona, Italy.
[Arandjelovic, Aleksandra; Gruchala, Marcin] Med Univ Gdansk, Dept Cardiol, Gdansk, Poland.
[Waldman, Scott A.] Thomas Jefferson Univ, Sidney Kimmel Med Coll, Philadelphia, PA USA.
[Teerlink, John R.] Univ Calif San Francisco & Sect Cardiol, San Francisco Vet Affairs Med Ctr, Sch Med, San Francisco, CA USA.
[Povsic, Thomas J.] Duke Clin Res Inst & Duke Med, Durham, NC USA.
[Henry, Timothy D.] Cedars Sinai Heart Inst, Los Angeles, CA USA.
[Metra, Marco] Univ & Spedali Civili, Dept Med & Surg Specialties Radiol Sci & Publ Hlt, Cardiol, Brescia, Italy.
[Hajjar, Roger J.] Mt Sinai Sch Med, New York, NY USA.
[Alexandre, Bertrand; Seron, Aymeric; Sherman, Warren] Celyad, Mont St Guibert, Belgium.
[Stough, Wendy Gattis] Campbell Univ Coll Pharm & Hlth Sci, Dept Clin Res & Pharm Practice, Cary, NC USA.
[Wijns, William] Natl Univ Ireland Galway & Saolta Univ Healthcare, Lambe Inst Translat Med & Curam, Galway, Ireland.
RP Bartunek, J (reprint author), Onze Lieve Vrouwziekenhuis OLV Hosp, Ctr Cardiovasc, Moorselbaan 164, B-9300 Aalst, Belgium.; Terzic, A (reprint author), Mayo Clin, Ctr Regenerat Med, Dept Cardiovasc Dis, 200 First St SW, Rochester, MI USA.
EM jozef.bartunek@olvz-aalst.be; terzic.andre@mayo.edu
FU Celyad, SA (Mont-Saint-Guibert, Belgium); Walloon Region (Belgium)
[DG06]
FX This work was supported by Celyad, SA (Mont-Saint-Guibert, Belgium).
Celyad has received research grants from the Walloon Region (Belgium,
DG06 funding).
NR 32
TC 3
Z9 3
U1 5
U2 5
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0195-668X
EI 1522-9645
J9 EUR HEART J
JI Eur. Heart J.
PD MAR 1
PY 2017
VL 38
IS 9
BP 648
EP 660
DI 10.1093/eurheartj/ehw543
PG 13
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EO2EU
UT WOS:000396510200008
PM 28025189
ER
PT J
AU Sonnenberg, A
AF Sonnenberg, Amnon
TI Cry wolf and inflate medical urgency to expedite consult resolution
through gastrointestinal endoscopy
SO EUROPEAN JOURNAL OF GASTROENTEROLOGY & HEPATOLOGY
LA English
DT Article
DE alarm symptoms; clinical practice; decision analysis; gastrointestinal
endoscopy; health economics
ID GAME-THEORETICAL APPROACH; PERSONAL VIEW
AB Background and aims To expedite a consult resolution, referring physicians sometimes inflate the urgency and need for endoscopic workup. The aim of the present decision analysis was to study the impact of inflationary indication on the expected benefits to gastroenterologists and referring physicians.
Methods The study aims were pursued in terms of game theory and medical decision analysis using decision trees. Different outcomes associated with true versus false urgent indication in immediate versus delayed endoscopy were ranked according to different preference schemes of gastroenterologists versus referring physicians.
Results The decision analysis shows that inflating the urgency of indication for endoscopy reduces the benefit from the perspective of gastroenterologists and referring physicians alike. Raising the level of false urgent indications results in a lost opportunity for immediate endoscopy among patients with true urgent indications and, thus, diminishes the overall benefit of endoscopy. By comparison, all other influences play only a marginal role. For referring physicians, the small benefit of expediting nonurgent endoscopies by exaggerated claims does not compensate for the concomitant loss of truly needed endoscopy slots. For gastroenterologists, a small benefit derived from delaying endoscopies in patients with false urgent endoscopies rapidly wears off as inflationary indications become common practice.
Conclusion An underlying communication problem between referring physicians and gastroenterologists needs to be resolved by educating referring physicians about the operative exigencies of endoscopy units and about the true appearance of alarm symptoms in common digestive diseases. Copyright (C) 2017 Wolters Kluwer Health, Inc. All rights reserved.
C1 [Sonnenberg, Amnon] Oregon Hlth & Sci Univ, Div Gastroenterol Hepatol, Portland VA Med Ctr, Portland, OR 97201 USA.
RP Sonnenberg, A (reprint author), Portland VA Med Ctr, P3-GI,3710 SW US Vet Hosp Rd, Portland, OR 97239 USA.
EM sonnenbe@ohsu.edu
NR 18
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0954-691X
EI 1473-5687
J9 EUR J GASTROEN HEPAT
JI Eur. J. Gastroenterol. Hepatol.
PD MAR
PY 2017
VL 29
IS 3
BP 360
EP 365
DI 10.1097/MEG.0000000000000796
PG 6
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EK2QZ
UT WOS:000393773100019
PM 27861253
ER
PT J
AU Kinsinger, LS
Anderson, C
Kim, J
Larson, M
Chan, SH
King, HA
Rice, KL
Slatore, CG
Tanner, NT
Pittman, K
Monte, RJ
McNeil, RB
Grubber, JM
Kelley, MJ
Provenzale, D
Datta, SK
Sperber, NS
Barnes, LK
Abbott, DH
Sims, KJ
Whitley, RL
Wu, RR
Jackson, GL
AF Kinsinger, Linda S.
Anderson, Charles
Kim, Jane
Larson, Martha
Chan, Stephanie H.
King, Heather A.
Rice, Kathryn L.
Slatore, Christopher G.
Tanner, Nichole T.
Pittman, Kathleen
Monte, Robert J.
McNeil, Rebecca B.
Grubber, Janet M.
Kelley, Michael J.
Provenzale, Dawn
Datta, Santanu K.
Sperber, Nina S.
Barnes, Lottie K.
Abbott, David H.
Sims, Kellie J.
Whitley, Richard L.
Wu, R. Ryanne
Jackson, George L.
TI Implementation of Lung Cancer Screening in the Veterans Health
Administration
SO JAMA INTERNAL MEDICINE
LA English
DT Article
ID DOSE COMPUTED-TOMOGRAPHY; FLEISCHNER-SOCIETY; CHEST PHYSICIANS; POLICY
STATEMENT; CARE-SYSTEM; TRIAL; CT; MANAGEMENT; PROGRAMS; COLLEGE
AB IMPORTANCE The US Preventive Services Task Force recommends annual lung cancer screening (LCS) with low-dose computed tomography for current and former heavy smokers aged 55 to 80 years. There is little published experience regarding implementing this recommendation in clinical practice.
OBJECTIVES To describe organizational-and patient-level experiences with implementing an LCS program in selected Veterans Health Administration (VHA) hospitals and to estimate the number of VHA patients who may be candidates for LCS.
DESIGN, SETTING, AND PARTICIPANTS This clinical demonstration projectwas conducted at 8 academic VHA hospitals among 93 033 primary care patients who were assessed on screening criteria; 2106 patients underwent LCS between July 1, 2013, and June 30, 2015.
INTERVENTIONS Implementation Guide and support, full-time LCS coordinators, electronic tools, tracking database, patient education materials, and radiologic and nodule follow-up guidelines.
MAIN OUTCOMES AND MEASURES Description of implementation processes; percentages of patients who agreed to undergo LCS, had positive findings on results of low-dose computed tomographic scans (nodules to be tracked or suspicious findings), were found to have lung cancer, or had incidental findings; and estimated number of VHA patients who met the criteria for LCS.
RESULTS Of the 4246 patients who met the criteria for LCS, 2452 (57.7%) agreed to undergo screening and 2106 (2028 men and 78 women; mean [SD] age, 64.9 [5.1] years) underwent LCS. Wide variation in processes and patient experiences occurred among the 8 sites. Of the 2106 patients screened, 1257 (59.7%) had nodules; 1184 of these patients (56.2%) required tracking, 42 (2.0%) required further evaluation but the findings were not cancer, and 31 (1.5%) had lung cancer. A variety of incidental findings, such as emphysema, other pulmonary abnormalities, and coronary artery calcification, were noted on the scans of 857 patients (40.7%).
CONCLUSIONS AND RELEVANCE It is estimated that nearly 900 000 of a population of 6.7 million VHA patients met the criteria for LCS. Implementation of LCS in the VHA will likely lead to large numbers of patients eligible for LCS and will require substantial clinical effort for both patients and staff.
C1 [Kinsinger, Linda S.; Kim, Jane; Larson, Martha; Chan, Stephanie H.; Pittman, Kathleen] Vet Hlth Adm, Natl Ctr Hlth Promot & Dis Prevent, 3022 Croasdaile Dr,Ste 200, Durham, NC 27705 USA.
[Anderson, Charles] Vet Hlth Adm, Natl Radiol Program Off, Durham, NC USA.
[King, Heather A.; McNeil, Rebecca B.; Provenzale, Dawn; Datta, Santanu K.; Sperber, Nina S.; Barnes, Lottie K.; Abbott, David H.; Sims, Kellie J.; Whitley, Richard L.; Wu, R. Ryanne; Jackson, George L.] Durham Vet Affairs Hlth Serv Res & Dev, Ctr Innovat, Durham, NC USA.
[King, Heather A.; McNeil, Rebecca B.; Grubber, Janet M.; Kelley, Michael J.; Provenzale, Dawn; Datta, Santanu K.; Sperber, Nina S.; Wu, R. Ryanne; Jackson, George L.] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA.
[Rice, Kathryn L.] Minneapolis Vet Affairs Healthcare Syst, Dept Med, Minneapolis, MN USA.
[Slatore, Christopher G.] Vet Affairs Portland Hlth Care Syst, Dept Med, Portland, OR USA.
[Tanner, Nichole T.] Ralph H Johnson Vet Affairs Med Ctr, Dept Med, Charleston, SC USA.
[Monte, Robert J.] Pittsburgh Vet Engn Resource Ctr, Pittsburgh, PA USA.
[Kelley, Michael J.] Vet Hlth Adm, Natl Oncol Program, Durham, NC USA.
RP Kinsinger, LS (reprint author), Vet Hlth Adm, Natl Ctr Hlth Promot & Dis Prevent, 3022 Croasdaile Dr,Ste 200, Durham, NC 27705 USA.
EM lkinsinger@mac.com
FU Veterans Health Administration
FX The Veterans Health Administration Lung Cancer Screening Demonstration
Project was funded by the Veterans Health Administration.
NR 32
TC 1
Z9 1
U1 2
U2 2
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6106
EI 2168-6114
J9 JAMA INTERN MED
JI JAMA Intern. Med.
PD MAR 1
PY 2017
VL 177
IS 3
BP 399
EP 406
DI 10.1001/jamainternmed.2016.9022
PG 8
WC Medicine, General & Internal
SC General & Internal Medicine
GA EN7RX
UT WOS:000396201000024
PM 28135352
ER
PT J
AU Adams, MA
Prenovost, KM
Dominitz, JA
Kerr, EA
Krein, SL
Saini, SD
Rubenstein, JH
AF Adams, Megan A.
Prenovost, Katherine M.
Dominitz, Jason A.
Kerr, Eve A.
Krein, Sarah L.
Saini, Sameer D.
Rubenstein, Joel H.
TI National Trends in Use of Monitored Anesthesia Care for Outpatient
Gastrointestinal Endoscopy in the Veterans Health Administration
SO JAMA INTERNAL MEDICINE
LA English
DT Editorial Material
ID COLONOSCOPY
C1 [Adams, Megan A.; Prenovost, Katherine M.; Kerr, Eve A.; Krein, Sarah L.; Saini, Sameer D.; Rubenstein, Joel H.] VA Ann Arbor Healthcare Syst, Dept Vet Affairs, Ctr Clin Management Res, Ann Arbor, MI USA.
[Adams, Megan A.; Kerr, Eve A.; Krein, Sarah L.; Saini, Sameer D.; Rubenstein, Joel H.] Univ Michigan Hlth Syst, Dept Internal Med, Ann Arbor, MI USA.
[Dominitz, Jason A.] VA Puget Sound Hlth Care Syst, Dept Vet Affairs, Seattle, WA USA.
[Dominitz, Jason A.] Univ Washington, Sch Med, Div Gastroenterol, Seattle, WA USA.
RP Adams, MA (reprint author), Univ Michigan, Dept Internal Med, Div Gastroenterol, 2215 Fuller Rd,Gastroenterol 3-D, Ann Arbor, MI 48105 USA.
EM meganada@med.umich.edu
FU National Institutes of Health [5 T32 DK 62708-12]; VA Health Services
Research and Development Research Career Scientist Award [RCS 11-222];
Veterans Health Administration's Office of Informatics and Analytics
FX Dr Adams was supported by National Institutes of Health 5 T32 DK
62708-12 during this research. Dr Krein is supported by a VA Health
Services Research and Development Research Career Scientist Award (RCS
11-222). This study was also supported by the Veterans Health
Administration's Office of Informatics and Analytics.
NR 7
TC 1
Z9 1
U1 0
U2 0
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6106
EI 2168-6114
J9 JAMA INTERN MED
JI JAMA Intern. Med.
PD MAR 1
PY 2017
VL 177
IS 3
BP 436
EP 438
DI 10.1001/jamainternmed.2016.8566
PG 4
WC Medicine, General & Internal
SC General & Internal Medicine
GA EN7RX
UT WOS:000396201000035
PM 28114670
ER
PT J
AU Germeroth, LJ
Carpenter, MJ
Baker, NL
Froeliger, B
LaRowe, SD
Saladin, ME
AF Germeroth, Lisa J.
Carpenter, Matthew J.
Baker, Nathaniel L.
Froeliger, Brett
LaRowe, Steven D.
Saladin, Michael E.
TI Effect of a Brief Memory Updating Intervention on Smoking Behavior A
Randomized Clinical Trial
SO JAMA PSYCHIATRY
LA English
DT Article
ID CONDITIONED PLACE PREFERENCE; POST-RETRIEVAL EXTINCTION; CUE REACTIVITY;
FEAR MEMORIES; DRUG-ADDICTION; ERASING FEAR; RECONSOLIDATION; RELAPSE;
PROPRANOLOL; CESSATION
AB IMPORTANCE Recent research on addiction-related memory processes suggests that protracted extinction training following brief cue-elicited memory retrieval (ie, retrieval-extinction [R-E] training) can attenuate/ eradicate the ability of cues to elicit learned behaviors. One study reported that cue-elicited craving among detoxified heroin addicts was substantially attenuated following R-E training and through 6-month follow-up.
OBJECTIVE To build on these impressive findings by examining whether R-E training could attenuate smoking-related craving and behavior.
DESIGN, SETTING, AND PARTICIPANTS This prospective, mixed-design, human laboratory randomized clinical trial took place between December 2013 and September 2015. Participants were recruited in Charleston, South Carolina. Study sessions took place at the Medical University of South Carolina. The participants were 168 screened volunteer smokers, of whom 88 were randomized; 72 of these 88 participants (81.8%) attended all the follow-up sessions through 1 month. The primary eligibility criteria were current nicotine dependence (DSM criteria), smoking 10 or more cigarettes per day, and a willingness to attempt smoking cessation.
INTERVENTIONS Participants were randomly assigned to receive either smoking-related memory retrieval followed by extinction training (the R-E group) or nonsmoking-related retrieval followed by extinction training (the NR-E group).
MAIN OUTCOMES AND MEASURES Primary outcomes were cue-elicited craving and physiological responding to familiar and novel cues in the R-E group vs the NR-E group over a 1-month follow-up period. Secondary outcomes were smoking-related behaviors.
RESULTS A total of 44 participants were randomly assigned to the R-E group (mean age, 48.3 years; 72.7% male); a total of 44 participants were randomly assigned to the NR-E group, with 43 attending at least 1 training session (mean age, 46.7 years; 55.8% male). The mean craving response to both familiar and novel smoking cues was significantly lower for participants in the R-E group than for participants in the NR-E group at 1-month follow-up (for both cue types: t(1225) = 2.1, P =.04, d = 0.44, and Delta = 0.47 [95% CI, 0.04-0.90]). The mean numbers of cigarettes smoked per day at 2 weeks and 1-month were significantly lower for the R-E group than for the NR-E group (treatment main effect: F-1.68 = 5.4, P =.02, d = 0.50, and Delta = 2.4 [95% CI, 0.4-4.5]). Significant differences in physiological responses, urine cotinine level, number of days abstinent, lapse, and relapse were not observed between groups (all between P =.06 and .75).
CONCLUSIONS AND RELEVANCE Retrieval-extinction training substantially attenuated craving to both familiar and novel smoking cues and reduced the number of cigarettes smoked per day by participants 1 month after treatment relative to extinction training alone. Between-group differences were not observed for physiological responses, cotinine level, number of days abstinent, relapse, or lapse. In summary, R-E training is a brief behavioral treatment that targets smoking-related memories and has the potential to enhance relapse prevention. Copyright 2017 American Medical Association. All rights reserved.
C1 [Germeroth, Lisa J.; Saladin, Michael E.] Med Univ South Carolina, Dept Hlth Sci & Res, 77 President St, Charleston, SC 29425 USA.
[Germeroth, Lisa J.; Carpenter, Matthew J.; Froeliger, Brett; LaRowe, Steven D.; Saladin, Michael E.] Med Univ South Carolina, Dept Psychiat & Behav Sci, Charleston, SC USA.
[Carpenter, Matthew J.] Med Univ South Carolina, Hollings Canc Ctr, Charleston, SC USA.
[Baker, Nathaniel L.] Med Univ South Carolina, Dept Publ Hlth Sci, Charleston, SC USA.
[Froeliger, Brett] Med Univ South Carolina, Dept Neurosci, Charleston, SC USA.
[LaRowe, Steven D.] Ralph H Johnson VA Med Ctr, Mental Hlth Serv Line, Charleston, SC USA.
RP Saladin, ME (reprint author), Med Univ South Carolina, Dept Hlth Sci & Res, 77 President St, Charleston, SC 29425 USA.
EM saladinm@musc.edu
FU National Institute on Drug Abuse [5R21DA035993-02]; Medical University
of South Carolina, through National Institutes of Health [UL1 RR029882,
UL1 TR000062]; South Carolina Clinical and Translational Research
Institute
FX This research was funded by National Institute on Drug Abuse grant
5R21DA035993-02 (Dr Saladin, principal investigator), South Carolina
Clinical and Translational Research Institute, with an academic home at
the Medical University of South Carolina, through National Institutes of
Health grants UL1 RR029882 and UL1 TR000062.
NR 74
TC 0
Z9 0
U1 3
U2 3
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-622X
EI 2168-6238
J9 JAMA PSYCHIAT
JI JAMA Psychiatry
PD MAR 1
PY 2017
VL 74
IS 3
BP 214
EP 223
DI 10.1001/jamapsychiatry.2016.3148
PG 10
WC Psychiatry
SC Psychiatry
GA EN5LP
UT WOS:000396047300004
PM 28146243
ER
PT J
AU Karimkhani, C
Wanga, V
Naghavi, P
Dellavalle, RP
Naghavi, M
AF Karimkhani, Chante
Wanga, Valentine
Naghavi, Paria
Dellavalle, Robert P.
Naghavi, Mohsen
TI Global burden of cutaneous leishmaniasis
SO LANCET INFECTIOUS DISEASES
LA English
DT Letter
C1 [Karimkhani, Chante] Case Western Reserve Univ, Univ Hosp Case Med Ctr, Cleveland, OH 44113 USA.
[Wanga, Valentine; Naghavi, Paria; Naghavi, Mohsen] Univ Washington, Inst Hlth Metr & Evaluat, Seattle, WA 98195 USA.
[Dellavalle, Robert P.] Univ Colorado, Dept Dermatol, Anschutz Med Campus, Aurora, CO USA.
[Dellavalle, Robert P.] US Dept Vet Affairs, Dermatol Serv, Eastern Colorado Hlth Care Syst, Denver, CO USA.
[Dellavalle, Robert P.] Colorado Sch Publ Hlth, Dept Epidemiol, Aurora, CO USA.
RP Karimkhani, C (reprint author), Case Western Reserve Univ, Univ Hosp Case Med Ctr, Cleveland, OH 44113 USA.
EM ck2525@caa.columbia.edu
NR 5
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCI LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND
SN 1473-3099
EI 1474-4457
J9 LANCET INFECT DIS
JI Lancet Infect. Dis.
PD MAR
PY 2017
VL 17
IS 3
BP 264
EP 264
PG 1
WC Infectious Diseases
SC Infectious Diseases
GA EL6KX
UT WOS:000394732600024
PM 28244391
ER
PT J
AU Trampush, JW
Yang, MLZ
Yu, J
Knowles, E
Davies, G
Liewald, DC
Starr, JM
Djurovic, S
Melle, I
Sundet, K
Christoforou, A
Reinvang, I
DeRosse, P
Lundervold, AJ
Steen, VM
Espeseth, T
Raikkonen, K
Widen, E
Palotie, A
Eriksson, JG
Giegling, I
Konte, B
Roussos, P
Giakoumaki, S
Burdick, KE
Payton, A
Ollier, W
Horan, M
Chiba-Falek, O
Attix, DK
Need, AC
Cirulli, ET
Voineskos, AN
Stefanis, NC
Avramopoulos, D
Hatzimanolis, A
Arking, DE
Smyrnis, N
Bilder, RM
Freimer, NA
Cannon, TD
London, E
Poldrack, RA
Sabb, FW
Congdon, E
Conley, ED
Scult, MA
Dickinson, D
Straub, RE
Donohoe, G
Morris, D
Corvin, A
Gill, M
Hariri, AR
Weinberger, DR
Pendleton, N
Bitsios, P
Rujescu, D
Lahti, J
Le Hellard, S
Keller, MC
Andreassen, OA
Deary, IJ
Glahn, DC
Malhotra, AK
Lencz, T
AF Trampush, J. W.
Yang, M. L. Z.
Yu, J.
Knowles, E.
Davies, G.
Liewald, D. C.
Starr, J. M.
Djurovic, S.
Melle, I.
Sundet, K.
Christoforou, A.
Reinvang, I.
DeRosse, P.
Lundervold, A. J.
Steen, V. M.
Espeseth, T.
Raikkonen, K.
Widen, E.
Palotie, A.
Eriksson, J. G.
Giegling, I.
Konte, B.
Roussos, P.
Giakoumaki, S.
Burdick, K. E.
Payton, A.
Ollier, W.
Horan, M.
Chiba-Falek, O.
Attix, D. K.
Need, A. C.
Cirulli, E. T.
Voineskos, A. N.
Stefanis, N. C.
Avramopoulos, D.
Hatzimanolis, A.
Arking, D. E.
Smyrnis, N.
Bilder, R. M.
Freimer, N. A.
Cannon, T. D.
London, E.
Poldrack, R. A.
Sabb, F. W.
Congdon, E.
Conley, E. D.
Scult, M. A.
Dickinson, D.
Straub, R. E.
Donohoe, G.
Morris, D.
Corvin, A.
Gill, M.
Hariri, A. R.
Weinberger, D. R.
Pendleton, N.
Bitsios, P.
Rujescu, D.
Lahti, J.
Le Hellard, S.
Keller, M. C.
Andreassen, O. A.
Deary, I. J.
Glahn, D. C.
Malhotra, A. K.
Lencz, T.
TI GWAS meta-analysis reveals novel loci and genetic correlates for general
cognitive function: a report from the COGENT consortium
SO MOLECULAR PSYCHIATRY
LA English
DT Article
ID GENOME-WIDE ASSOCIATION; SCOTTISH MENTAL SURVEY; UK BIOBANK N=112151;
EDUCATIONAL-ATTAINMENT; INTELLECTUAL DISABILITY; DEVELOPMENTAL DELAY;
EXECUTIVE FUNCTION; HUMAN INTELLIGENCE; PROVIDES INSIGHTS; ABILITY
AB The complex nature of human cognition has resulted in cognitive genomics lagging behind many other fields in terms of gene discovery using genome-wide association study (GWAS) methods. In an attempt to overcome these barriers, the current study utilized GWAS meta-analysis to examine the association of common genetic variation (similar to 8M single-nucleotide polymorphisms (SNP) with minor allele frequency >= 1%) to general cognitive function in a sample of 35 298 healthy individuals of European ancestry across 24 cohorts in the Cognitive Genomics Consortium (COGENT). In addition, we utilized individual SNP lookups and polygenic score analyses to identify genetic overlap with other relevant neurobehavioral phenotypes. Our primary GWAS meta-analysis identified two novel SNP loci (top SNPs: rs76114856 in the CENPO gene on chromosome 2 and rs6669072 near LOC105378853 on chromosome 1) associated with cognitive performance at the genome-wide significance level (P<5x10(-8)). Gene-based analysis identified an additional three Bonferroni-corrected significant loci at chromosomes 17q21.31, 17p13.1 and 1p13.3. Altogether, common variation across the genome resulted in a conservatively estimated SNP heritability of 21.5% (s.e. = 0.01%) for general cognitive function. Integration with prior GWAS of cognitive performance and educational attainment yielded several additional significant loci. Finally, we found robust polygenic correlations between cognitive performance and educational attainment, several psychiatric disorders, birth length/weight and smoking behavior, as well as a novel genetic association to the personality trait of openness. These data provide new insight into the genetics of neurocognitive function with relevance to understanding the pathophysiology of neuropsychiatric illness.
C1 [Trampush, J. W.; Yu, J.; DeRosse, P.; Lencz, T.] Zucker Hillside Hosp, Div Psychiat Res, 75-59 263rd St, Glen Oaks, NY 11004 USA.
[Yang, M. L. Z.] Inst Mental Hlth, Singapore, Singapore.
[Yu, J.; DeRosse, P.; Malhotra, A. K.; Lencz, T.] Feinstein Inst Med Res, Ctr Psychiat Neurosci, Manhasset, NY USA.
[Knowles, E.] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA.
[Davies, G.; Starr, J. M.; Deary, I. J.] Univ Edinburgh, Ctr Cognit Ageing & Cognit Epidemiol, Edinburgh, Midlothian, Scotland.
[Davies, G.; Liewald, D. C.; Deary, I. J.] Univ Edinburgh, Dept Psychol, Edinburgh, Midlothian, Scotland.
[Starr, J. M.] Univ Edinburgh, Alzheimer Scotland Dementia Res Ctr, Edinburgh, Midlothian, Scotland.
[Djurovic, S.] Univ Bergen, Oslo Univ Hosp, Dept Med Genet, Oslo, Norway.
[Djurovic, S.; Melle, I.; Christoforou, A.; Le Hellard, S.] Univ Bergen, KG Jebsen Ctr Psychosis Res, NORMENT, Bergen, Norway.
[Melle, I.; Sundet, K.; Espeseth, T.] Oslo Univ Hosp, Div Mental Hlth & Addict, Oslo, Norway.
[Sundet, K.; Espeseth, T.] Univ Oslo, Dept Psychol, Oslo, Norway.
[Christoforou, A.] Haukeland Hosp, Ctr Med Genet & Mol Med, Dr Einar Martens Res Grp Biol Psychiat, Bergen, Norway.
[Lundervold, A. J.] Univ Bergen, Dept Biol & Med Psychol, Bergen, Norway.
[Raikkonen, K.] Univ Helsinki, Inst Behav Sci, Helsinki, Finland.
[Widen, E.; Palotie, A.] Univ Helsinki, Inst Mol Med Finland FIMM, Helsinki, Finland.
[Palotie, A.] Wellcome Trust Genome Campus, Wellcome Trust Sanger Inst, Cambridge, England.
[Palotie, A.] Univ Helsinki, Dept Med Genet, Helsinki, Finland.
[Palotie, A.] Univ Cent Hosp, Helsinki, Finland.
[Eriksson, J. G.] Natl Inst Hlth & Welf, Helsinki, Finland.
[Eriksson, J. G.] Univ Helsinki, Dept Gen Practice & Primary Hlth Care, Helsinki, Finland.
[Eriksson, J. G.] Univ Helsinki, Unit Gen Practice, Cent Hosp, Helsinki, Finland.
[Eriksson, J. G.] Folkhalsan Res Ctr, Helsinki, Finland.
[Giegling, I.; Konte, B.; Rujescu, D.] Martin Luther Univ Halle Wittenberg, Dept Psychiat, Halle, Germany.
[Roussos, P.; Burdick, K. E.] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.
[Roussos, P.; Burdick, K. E.] Icahn Sch Med Mt Sinai, Dept Genet & Genom Sci, New York, NY 10029 USA.
[Roussos, P.; Burdick, K. E.] Icahn Sch Med Mt Sinai, Inst Multiscale Biol, New York, NY 10029 USA.
[Roussos, P.] James J Peters VA Med Ctr, Mental Illness Res Educ & Clin Ctr VISN 3, Bronx, NY USA.
[Giakoumaki, S.] Univ Crete, Dept Psychol, Rethimnon, Greece.
[Payton, A.] Univ Manchester, Manchester Acad Hlth Sci Ctr, Manchester Ctr Audiol & Deafness, Manchester, Lancs, England.
[Payton, A.] Univ Manchester, Sch Biol Sci, Div Evolut & Genom Sci, Manchester, Lancs, England.
[Ollier, W.] Univ Manchester, Inst Populat Hlth, Ctr Integrated Genom Med Res, Manchester, Lancs, England.
[Horan, M.] Univ Manchester, Inst Brain Behav & Mental Hlth, Manchester Med Sch, Manchester, Lancs, England.
[Chiba-Falek, O.; Attix, D. K.] Duke Univ, Med Ctr, Div Neurol, Bryan Alzheimers Dis Res Ctr, Durham, NC 27710 USA.
[Chiba-Falek, O.; Attix, D. K.] Duke Univ, Med Ctr, Ctr Genom & Computat Biol, Durham, NC USA.
[Attix, D. K.] Duke Univ, Med Ctr, Dept Neurol Psychiat & Behav Sci, Div Med Psychol, Durham, NC USA.
[Need, A. C.] Imperial Coll, Dept Med, Div Brain Sci, London, England.
[Cirulli, E. T.] Duke Univ, Sch Med, Ctr Appl Genom & Precis Med, Durham, NC USA.
[Voineskos, A. N.] Univ Toronto, Ctr Addict & Mental Hlth, Campbell Family Mental Hlth Inst, Toronto, ON, Canada.
[Stefanis, N. C.; Hatzimanolis, A.] Univ Athens, Sch Med, Eginit Hosp, Dept Psychiat, Athens, Greece.
[Stefanis, N. C.; Hatzimanolis, A.] Univ Mental Hlth Res Inst, Athens, Greece.
[Stefanis, N. C.; Hatzimanolis, A.] Theodor Theohari Cozzika Fdn, Neurobiol Res Inst, Athens, Greece.
[Avramopoulos, D.] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21205 USA.
[Avramopoulos, D.; Arking, D. E.] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21205 USA.
[Avramopoulos, D.; Arking, D. E.] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD USA.
[Bilder, R. M.; Freimer, N. A.; London, E.] Univ Calif Los Angeles, Semel Inst Neurosci & Human Behav, Los Angeles, CA USA.
[Cannon, T. D.] Yale Univ, Dept Psychol, New Haven, CT USA.
[Poldrack, R. A.] Stanford Univ, Dept Psychol, Palo Alto, CA 94304 USA.
[Sabb, F. W.] Univ Oregon, Robert & Beverly Lewis Ctr Neuroimaging, Eugene, OR 97403 USA.
[Conley, E. D.] 23andMe Inc, Mountain View, CA USA.
[Scult, M. A.; Hariri, A. R.] Duke Univ, Neurogenet Lab, Dept Psychol & Neurosci, Durham, NC USA.
[Congdon, E.; Dickinson, D.] NIMH, Clin & Translat Neurosci Branch, Intramural Res Program, NIH, Bethesda, MD 20892 USA.
[Straub, R. E.; Weinberger, D. R.] Johns Hopkins Univ, Lieber Inst Brain Dev, Med Campus, Baltimore, MD USA.
[Donohoe, G.] Natl Univ Ireland, Dept Psychol, Galway, Ireland.
[Morris, D.; Corvin, A.; Gill, M.] Trinity Coll Dublin, Trinity Coll Inst Neurosci, Neuropsychiat Genet Res Grp, Dept Psychiat, Dublin, Ireland.
[Bitsios, P.] Univ Crete, Fac Med, Dept Psychiat & Behav Sci, Iraklion, Greece.
[Rujescu, D.; Lahti, J.] Univ Helsinki, Helsinki Collegium Adv Studies, Helsinki, Finland.
[Keller, M. C.] Univ Colorado, Inst Behav Genet, Boulder, CO 80309 USA.
[Andreassen, O. A.] Univ Oslo, Inst Clin Med, Oslo, Norway.
[Malhotra, A. K.; Lencz, T.] Hofstra Northwell Sch Med, Dept Psychiat, Hempstead, NY USA.
RP Lencz, T (reprint author), Zucker Hillside Hosp, Div Psychiat Res, 75-59 263rd St, Glen Oaks, NY 11004 USA.
EM tlencz@northwell.edu
RI Bilder, Robert/A-8894-2008
OI Bilder, Robert/0000-0001-5085-7852; Sundet, Kjetil/0000-0003-2850-3673;
Payton, Antony/0000-0003-0335-152X; Scult, Matthew/0000-0001-5554-8186;
Le Hellard, Stephanie/0000-0002-8085-051X
FU National Institutes of Health [R01MH079800, P50 MH080173, R01 MH080912,
K23 MH077807, K01 MH085812, R01 DA033369, R01 AG049789]; Research
Council of Norway; South-East Norway Health Authority; KG Jebsen
Foundation; Research Council of Norway [154313/V50, 177458/V50]; Bergen
Research Foundation; University of Bergen; Research Council of Norway
(FUGE, Psykisk Helse); Helse Vest RHF and Dr Einar Martens Fund; Academy
of Finland; Finnish Diabetes Research Society; Folkhalsan Research
Foundation; Novo Nordisk Foundation; Finska Lakaresallskapet; Signe and
Ane Gyllenberg Foundation; University of Helsinki; Ministry of
Education; Ahokas Foundation; Emil Aaltonen Foundation; Disconnected
Mind project; UK Biotechnology and Biological Sciences Research Council
(BBSRC) [BB/F019394/1]; Medical Research Council; Biotechnology and
Biological Sciences Research Council [MR/K026992/1]; CAMH Foundation;
Canadian Institutes of Health Research; National Institute of Mental
Health of the National Institutes of Health [K01MH098126]; Ellison
Medical Foundation New Scholar award [AG-NS-0441-08]; NIH [UL1DE019580,
PL1MH083271, RL1MH083269, RL1DA024853, PL1NS062410]; National Institute
of Mental Health research [R01MH085018, R01MH092515]; National Science
Foundation Graduate Research Fellowship; Science Foundation Ireland
[12/IP/1670, 12/IP/1359, 08/IN. 1/B1916]
FX This work has been supported by grants from the National Institutes of
Health (R01MH079800 and P50 MH080173 to AKM; R01 MH080912 to DCG; K23
MH077807 to KEB; K01 MH085812 to MCK). Data collection for the TOP
cohort was supported by the Research Council of Norway, South-East
Norway Health Authority and KG Jebsen Foundation. The NCNG study was
supported by Research Council of Norway Grants 154313/V50 and
177458/V50. The NCNG GWAS was financed by grants from the Bergen
Research Foundation, the University of Bergen, the Research Council of
Norway (FUGE, Psykisk Helse), Helse Vest RHF and Dr Einar Martens Fund.
The Helsinki Birth Cohort Study has been supported by grants from the
Academy of Finland, the Finnish Diabetes Research Society, Folkhalsan
Research Foundation, Novo Nordisk Foundation, Finska Lakaresallskapet,
Signe and Ane Gyllenberg Foundation, University of Helsinki, Ministry of
Education, Ahokas Foundation, Emil Aaltonen Foundation. For the LBC1936
cohort, phenotype collection was supported by The Disconnected Mind
project. Genotyping was funded by the UK Biotechnology and Biological
Sciences Research Council (BBSRC grant no. BB/F019394/1). The work was
undertaken by The University of Edinburgh Centre for Cognitive Ageing
and Cognitive Epidemiology, part of the cross council Lifelong Health
and Wellbeing Initiative, which is funded by the Medical Research
Council and the Biotechnology and Biological Sciences Research Council
(MR/K026992/1). The CAMH work was supported by the CAMH Foundation and
the Canadian Institutes of Health Research. The Duke Cognition Cohort
(DCC) acknowledges K Linney, JM McEvoy, P Hunt, V Dixon, T Pennuto, K
Cornett, D Swilling, L Phillips, M Silver, J Covington, N Walley, J
Dawson, H Onabanjo, P Nicoletti, A Wagoner, J Elmore, L Bevan, J Hunkin
and R Wilson for recruitment and testing of subjects. DCC also
acknowledges the Ellison Medical Foundation New Scholar award
AG-NS-0441-08 for partial funding of this study as well as the National
Institute of Mental Health of the National Institutes of Health under
award number K01MH098126. The UCLA Consortium for Neuropsychiatric
Phenomics (CNP) study acknowledges the following sources of funding from
the NIH: Grants UL1DE019580 and PL1MH083271 (RMB), RL1MH083269 (TDC),
RL1DA024853 (EL) and PL1NS062410. The ASPIS study was supported by
National Institute of Mental Health research grants R01MH085018 and
R01MH092515 to Dr Dimitrios Avramopoulos. Support for the Duke
Neurogenetics Study was provided the National Institutes of Health (R01
DA033369 and R01 AG049789 to ARH) and by a National Science Foundation
Graduate Research Fellowship to MAS. Recruitment, genotyping and
analysis of the TCD healthy control samples were supported by Science
Foundation Ireland (grants 12/IP/1670, 12/IP/1359 and 08/IN. 1/B1916).
NR 73
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PU NATURE PUBLISHING GROUP
PI LONDON
PA MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
SN 1359-4184
EI 1476-5578
J9 MOL PSYCHIATR
JI Mol. Psychiatr.
PD MAR
PY 2017
VL 22
IS 3
BP 336
EP 345
DI 10.1038/mp.2016.244
PG 10
WC Biochemistry & Molecular Biology; Neurosciences; Psychiatry
SC Biochemistry & Molecular Biology; Neurosciences & Neurology; Psychiatry
GA EL3RQ
UT WOS:000394537100003
PM 28093568
ER
PT J
AU Cirnigliaro, CM
Myslinski, MJ
La Fountaine, MF
Kirshblum, SC
Forrest, GF
Bauman, WA
AF Cirnigliaro, C. M.
Myslinski, M. J.
La Fountaine, M. F.
Kirshblum, S. C.
Forrest, G. F.
Bauman, W. A.
TI Bone loss at the distal femur and proximal tibia in persons with spinal
cord injury: imaging approaches, risk of fracture, and potential
treatment options
SO OSTEOPOROSIS INTERNATIONAL
LA English
DT Review
DE Distal femur; Dual energy x-ray absorptiometry; Peripheral quantitative
computed tomography; Proximal tibia; Quantitative computed tomography;
Spinal cord injury
ID QUANTITATIVE COMPUTED-TOMOGRAPHY; ENERGY X-RAY; LOWER-EXTREMITY
FRACTURES; FUNCTIONAL ELECTRICAL-STIMULATION; LONG-TERM CHANGES; MINERAL
DENSITY; TRABECULAR BONE; INDUCED OSTEOPOROSIS; CANDIDATE BIOMARKER;
PARAPLEGIC PATIENTS
AB Persons with spinal cord injury (SCI) undergo immediate unloading of the skeleton and, as a result, have severe bone loss below the level of lesion associated with increased risk of long-bone fractures. The pattern of bone loss in individuals with SCI differs from other forms of secondary osteoporosis because the skeleton above the level of lesion remains unaffected, while marked bone loss occurs in the regions of neurological impairment. Striking demineralization of the trabecular epiphyses of the distal femur (supracondylar) and proximal tibia occurs, with the knee region being highly vulnerable to fracture because many accidents occur while sitting in a wheelchair, making the knee region the first point of contact to any applied force. To quantify bone mineral density (BMD) at the knee, dual energy x-ray absorptiometry (DXA) and/or computed tomography (CT) bone densitometry are routinely employed in the clinical and research settings. A detailed review of imaging methods to acquire and quantify BMD at the distal femur and proximal tibia has not been performed to date but, if available, would serve as a reference for clinicians and researchers. This article will discuss the risk of fracture at the knee in persons with SCI, imaging methods to acquire and quantify BMD at the distal femur and proximal tibia, and treatment options available for prophylaxis against or reversal of osteoporosis in individuals with SCI.
C1 [Cirnigliaro, C. M.; La Fountaine, M. F.; Bauman, W. A.] James J Peters Vet Affairs Med Ctr, Dept Vet Affairs Rehabil Res & Dev Serv, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY 10468 USA.
[Myslinski, M. J.] Rutgers New Jersey Med Sch, Dept Phys Therapy, Sch Hlth Related Profess, Newark, NJ USA.
[La Fountaine, M. F.] Seton Hall Univ, Sch Hlth & Med Sci, Dept Phys Therapy, S Orange, NJ 07079 USA.
[La Fountaine, M. F.] Seton Hall Univ, Inst Adv Study Rehabil & Sports Sci, Sch Hlth & Med Sci, S Orange, NJ 07079 USA.
[Kirshblum, S. C.] Kessler Inst Rehabil, W Orange, NJ USA.
[Kirshblum, S. C.; Forrest, G. F.] Rutgers New Jersey Med Sch, Dept Phys Med & Rehabil, Newark, NJ USA.
[Forrest, G. F.] Kessler Fdn, W Orange, NJ USA.
[Bauman, W. A.] Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA.
[Bauman, W. A.] Icahn Sch Med Mt Sinai, Dept Rehabil Med, New York, NY 10029 USA.
RP Bauman, WA (reprint author), James J Peters Vet Affairs Med Ctr, Dept Vet Affairs Rehabil Res & Dev Serv, Natl Ctr Med Consequences Spinal Cord Injury, Bronx, NY 10468 USA.; Bauman, WA (reprint author), Icahn Sch Med Mt Sinai, Dept Med, New York, NY 10029 USA.; Bauman, WA (reprint author), Icahn Sch Med Mt Sinai, Dept Rehabil Med, New York, NY 10029 USA.
EM william.bauman@va.gov
FU Veterans Affairs Rehabilitation Research and Development Service
[B9212-C, B2020-C]; James J. Peters VA Medical Center
FX Veterans Affairs Rehabilitation Research and Development Service
(#B9212-C, B2020-C) and the James J. Peters VA Medical Center.
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PU SPRINGER LONDON LTD
PI LONDON
PA 236 GRAYS INN RD, 6TH FLOOR, LONDON WC1X 8HL, ENGLAND
SN 0937-941X
EI 1433-2965
J9 OSTEOPOROSIS INT
JI Osteoporosis Int.
PD MAR
PY 2017
VL 28
IS 3
BP 747
EP 765
DI 10.1007/s00198-016-3798-x
PG 19
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EK9QC
UT WOS:000394258000002
PM 27921146
ER
PT J
AU Abderhalden, L
Weaver, FM
Bethel, M
Demirtas, H
Burns, S
Svircev, J
Hoenig, H
Lyles, K
Miskevics, S
Carbone, LD
AF Abderhalden, L.
Weaver, F. M.
Bethel, M.
Demirtas, H.
Burns, S.
Svircev, J.
Hoenig, H.
Lyles, K.
Miskevics, S.
Carbone, L. D.
TI Dual-energy X-ray absorptiometry and fracture prediction in patients
with spinal cord injuries and disorders
SO OSTEOPOROSIS INTERNATIONAL
LA English
DT Article
DE Dual-energy X-ray absorptiometry; Fractures; Osteoporosis; Spinal cord
injury
ID BONE-MINERAL DENSITY; QUANTITATIVE COMPUTED-TOMOGRAPHY; LOWER-EXTREMITY
FRACTURES; LUMBAR SPINE; RELIABLE METHOD; RISK-FACTORS; OSTEOPOROSIS;
WOMEN; INDIVIDUALS; MEN
AB Low T-scores at the hip predict incident fractures in persons with a SCI. Introduction Persons with a spinal cord injury (SCI) have substantial morbidity and mortality following osteoporotic fractures. The objective of this study was to determine whether dual-energy X-ray absorptiometry (DXA) measurements predict osteoporotic fractures in this population. Methods A retrospective historical analysis that includes patients (n = 552) with a SCI of at least 2 years duration who had a DXA performed and were in the VA Spinal Cord Disorders Registry from fiscal year (FY) 2002-2012 was performed. Results The majority of persons (n = 455, 82%) had a diagnosis of osteoporosis or osteopenia, with almost half having osteoporosis. BMD and T-scores at the lumbar spine were not significantly associated with osteoporotic fractures (p > 0.48) for both. In multivariable analyses, osteopenia (OR = 4.75 95% CI 1.2317.64) or osteoporosis (OR = 4.31, 95% CI 1.15-16.23) compared with normal BMD was significantly associated with fractures and higher T-scores at the hip were inversely associated with fractures (OR 0.73 (95% CI 0.57-0.92)). There was no significant association of T-scores or World Health Organization (WHO) classification with incident fractures in those with complete SCI (p > 0.15 for both). Conclusion The majority (over 80%) of individuals with a SCI have osteopenia or osteoporosis. DXA-derived measurements at the hip, but not the lumbar spine, predict fracture risk in persons with a SCI. WHO-derived bone density categoriesmay be useful in classifying fracture risk in persons with a SCI.
C1 [Abderhalden, L.; Weaver, F. M.] Edward J Hines Jr VA Hosp, Ctr Innovat Complex Chron Healthcare, 5000 S 5th Ave,POB 1033, Hines, IL USA.
[Abderhalden, L.; Demirtas, H.] Univ Illinois, Sch Publ Hlth, Dept Epidemiol & Biostat, Chicago, IL USA.
[Weaver, F. M.; Miskevics, S.] Loyola Univ, Stritch Sch Med, Publ Hlth Sci, 2160 S 1st Ave, Maywood, IL 60153 USA.
[Bethel, M.; Carbone, L. D.] Charlie Norwood Vet Affairs Med Ctr, 950 15th St,6D-155, Augusta, GA 30912 USA.
[Bethel, M.; Carbone, L. D.] Augusta Univ, Dept Med, Med Coll Georgia, Augusta, GA 30912 USA.
[Burns, S.; Svircev, J.] VA Puget Sound Hlth Care Syst, Seattle Div, 1660 S Columbian Way, Seattle, WA USA.
[Burns, S.; Svircev, J.] Univ Washington, Dept Rehabil Med, Seattle, WA 98195 USA.
[Hoenig, H.] Durham VA Med Ctr, 508 Fulton St, Durham, NC USA.
[Lyles, K.] Duke Univ, Durham, NC USA.
[Lyles, K.] VA Med Ctr, Durham, NC USA.
[Lyles, K.] Carolinas Ctr Med Excellence, Cary, NC USA.
RP Carbone, LD (reprint author), Charlie Norwood Vet Affairs Med Ctr, 950 15th St,6D-155, Augusta, GA 30912 USA.; Carbone, LD (reprint author), Augusta Univ, Dept Med, Med Coll Georgia, Augusta, GA 30912 USA.
EM lcarbone@gru.edu
FU Department of Veterans Affairs, Veterans Health Administration, Health
Services Research and Development [IIR 11-103-3]
FX We would like to acknowledge Kristen Swindells, MHSA, for her editorial
assistance with this manuscript. This work was supported by the
Department of Veterans Affairs, Veterans Health Administration, Health
Services Research and Development IIR 11-103-3. The contents do not
represent the views of the Department of Veterans Affairs or the United
States Government.
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PU SPRINGER LONDON LTD
PI LONDON
PA 236 GRAYS INN RD, 6TH FLOOR, LONDON WC1X 8HL, ENGLAND
SN 0937-941X
EI 1433-2965
J9 OSTEOPOROSIS INT
JI Osteoporosis Int.
PD MAR
PY 2017
VL 28
IS 3
BP 925
EP 934
DI 10.1007/s00198-016-3841-y
PG 10
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EK9QC
UT WOS:000394258000020
PM 27924381
ER
PT J
AU Carlson, SW
Yan, H
Dixon, CE
AF Carlson, Shaun W.
Yan, Hong
Dixon, C. Edward
TI Lithium increases hippocampal SNARE protein abundance after traumatic
brain injury
SO EXPERIMENTAL NEUROLOGY
LA English
DT Article
DE Traumatic brain injury; Synapse; SNARE; Hippocampus; Cognition; Vesicle
ID CONTROLLED CORTICAL IMPACT; SYNAPTIC VESICLE DOCKING; CYSTEINE STRING
PROTEIN; REDUCED EVOKED RELEASE; IN-VITRO; RAT-BRAIN; NEUROTROPHIC
FACTOR; MESSENGER-RNA; KNOCKOUT MICE; CSP-ALPHA
AB Rodent models of traumatic brain injury (TBI) reproduce secondary injury sequela and cognitive impairments observed in patients afflicted by a TBI. Impaired neurotransmission has been reported in the weeks following experimental TBI, and may be a contributor to behavioral dysfunction. The soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complex, the machinery facilitating vesicular docking and fusion, is a highly-conserved mechanism important for neurotransmission. Following TBI, there is a reduction in both the formation of the SNARE complex and the abundance of multiple SNARE proteins, including the chaperone protein cysteine string protein alpha (CSP alpha). Treatment with lithium in na ve rats reportedly increases the expression of CSPa. In the context of TBI, brain-injured rats treated with lithium exhibit improved outcome in published reports, but the mechanisms underlying the improvement are poorly understood. The current study evaluated the effect of lithium administration on the abundance of SNARE proteins and SNARE complex formation, hemispheric tissue loss, and neurobehavioral performance following controlled cortical impact (CCI). Sprague Dawley rats were subjected to CCI or sham injury, and treated daily with lithium chloride or vehicle for up to 14 days. Administration of lithium after TBI modestly improved spatial memory at 14 days post-injury. Semi-quantitative immunoblot analysis of hippocampal lysates revealed that treatment with lithium attenuated reductions in key SNARE proteins and SNARE complex formation at multiple time points post-injury. These findings highlight that treatment with lithium increased the abundance of synaptic proteins that facilitate neurotransmission and may contribute to improved cognitive function after TBI. Published by Elsevier Inc.
C1 Univ Pittsburgh, Dept Neurosurg, Safar Ctr Resuscitat Res, Pittsburgh, PA USA.
VA Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
RP Dixon, CE (reprint author), Safar Ctr Resuscitat Res, Dept Neurosurg, 3434 Fifth Ave, Pittsburgh, PA 15260 USA.
EM dixoec@upmc.edu
FU National Institutes of Health [NIH-NS40125, NIH-NS060672,
1-F32NS090748]; VA Healthcare System [VAI01RX001127]; Walter L. Copeland
Fund of The Pittsburgh Foundation [UN2014-73618]
FX This work was supported by the National Institutes of Health
[NIH-NS40125 (CED), NIH-NS060672 (CED), 1-F32NS090748 (SWC)] the VA
Healthcare System [VAI01RX001127 (CED)] and The Walter L. Copeland Fund
of The Pittsburgh Foundation [UN2014-73618 (SWC)].
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PU ACADEMIC PRESS INC ELSEVIER SCIENCE
PI SAN DIEGO
PA 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA
SN 0014-4886
EI 1090-2430
J9 EXP NEUROL
JI Exp. Neurol.
PD MAR
PY 2017
VL 289
BP 55
EP 63
DI 10.1016/j.expneurol.2016.12.006
PG 9
WC Neurosciences
SC Neurosciences & Neurology
GA EJ9JF
UT WOS:000393541700006
PM 28011122
ER
PT J
AU Graham, SH
AF Graham, Steven H.
TI Introduction to special issue: Neurovascular aging-A driving force for
neurological dysfunction in stroke and neurodegenerative diseases
SO AGEING RESEARCH REVIEWS
LA English
DT Editorial Material
ID CHRONIC CEREBRAL HYPOPERFUSION; ALZHEIMERS-DISEASE; BRAIN ISCHEMIA;
PROTEIN AGGREGATION; OLDER PERSONS; DEMENTIA; DISORDERS; AUTOPHAGY;
STRESS; RISK
C1 [Graham, Steven H.] Univ Pittsburgh, Dept Neurol, VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15260 USA.
RP Graham, SH (reprint author), Univ Pittsburgh, Dept Neurol, VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15260 USA.
EM Steven.Graham@va.gov
NR 26
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U2 4
PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 1
EP 2
DI 10.1016/j.arr.2016.10.002
PG 2
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100001
PM 27793608
ER
PT J
AU Yin, Y
Sun, G
Li, E
Kiselyov, K
Sun, DD
AF Yin, Yan
Sun, George
Li, Eric
Kiselyov, Kiri
Sun, Dandan
TI ER stress and impaired autophagy flux in neuronal degeneration and brain
injury
SO AGEING RESEARCH REVIEWS
LA English
DT Review
DE Autophagy; Brain aging; Docosahexaenoic acid; Lysosome; Stroke;
Traumatic brain injury
ID ENDOPLASMIC-RETICULUM STRESS; POLYUNSATURATED FATTY-ACIDS; UNFOLDED
PROTEIN RESPONSE; LONG-CHAIN OMEGA-3-FATTY-ACIDS; FOCAL
CEREBRAL-ISCHEMIA; CELL-DEATH MECHANISMS; DOUBLE-EDGED-SWORD; TRAUMATIC
BRAIN; DOCOSAHEXAENOIC ACID; ALZHEIMERS-DISEASE
AB Autophagy is a highly controlled lysosome-mediated function in eukaryotic cells to eliminate damaged or aged long-lived proteins and organelles. It is required for restoring cellular homeostasis in cell survival under multiple stresses. Autophagy is known to be a double-edged sword because too much activation or inhibition of autophagy can disrupt homeostatic degradation of protein and organelles within the brain and play a role in neuronal cell death. Many factors affect autophagy flux function in the brain, including endoplasmic reticulum (ER) stress, oxidative stress, and aging. Newly emerged research indicates that altered autophagy flux functionality is involved in neurodegeneration of the aged brain, chronic neurological diseases, and after traumatic and ischemic brain injuries. In search to identify neuroprotective agents that may reduce oxidative stress and stimulate autophagy, one particular neuroprotective agent docosahexaenoic acid (DHA) presents unique functions in reducing ER and oxidative stress and modulating autophagy. This review will summarize the recent findings on changes of autophagy in aging, neurodegenerative diseases, and brain injury after trauma or ischemic strokes. Discussion of DHA functions is focused on modulating ER stress and autophagy in regard to its neuroprotection and anti-tumor functions. (C) 2016 Elsevier B.V. All rights reserved.
C1 [Yin, Yan] Dalian Med Univ, Hosp 2, Dept Neurol, Dalian 116023, Peoples R China.
[Yin, Yan; Sun, George; Li, Eric; Sun, Dandan] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA.
[Kiselyov, Kiri] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15213 USA.
[Sun, Dandan] Vet Affairs Pittsburgh Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15213 USA.
RP Yin, Y (reprint author), Dalian Med Univ, Hosp 2, Dept Neurol, Dalian 116023, Peoples R China.; Sun, DD (reprint author), Univ Pittsburgh, Med Ctr, Dept Neurol, S-598 South Biomed Sci Tower,3500 Terrace St, Pittsburgh, PA 15213 USA.
EM yanyin1208@126.com; sund@upmc.edu
OI Yin, Yan/0000-0002-5982-7462
FU National Institutes of Health [R01 NS038118, NS048216, NS089051];
Veteran Affairs Merit Award [I01BX002891]; Chinese Dalian Municipal
Science and Technology Plan Project [2014E14SF186]; Dalian Municipal
Medical Training Project
FX This work was supported in part by the National Institutes of Health R01
NS038118, NS048216, and NS089051, and Veteran Affairs Merit Award
I01BX002891 (D.S); the Chinese Dalian Municipal Science and Technology
Plan Project 2014E14SF186 (Y.Y.), and Dalian Municipal Medical Training
Project (Y.Y).
NR 175
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 3
EP 14
DI 10.1016/j.arr.2016.08.008
PG 12
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100002
PM 27594375
ER
PT J
AU Graham, SH
Liu, H
AF Graham, Steven H.
Liu, Hao
TI Life and death in the trash heap: The ubiquitin proteasome pathway and
UCHL1 in brain aging, neurodegenerative disease and cerebral Ischemia
SO AGEING RESEARCH REVIEWS
LA English
DT Review
DE Ubiquitin; Ubiquitin proteasome pathway (UPP); Neurodegenerative
disease; Ubiquitin carboxy-terminal hydrolase L1(UCHL1); Cerebral
ischemia; Aging
ID TERMINAL HYDROLASE L1; MEDIATED K63-LINKED POLYUBIQUITINATION;
AMYLOID-BETA-PROTEIN; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE;
ALPHA-SYNUCLEIN; 15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2);
CYCLOPENTENONE PROSTAGLANDINS; HUNTINGTONS-DISEASE; OXIDATIVE STRESS
AB The ubiquitin proteasome pathway (UPP) is essential for removing abnormal proteins and preventing accumulation of potentially toxic proteins within the neuron. UPP dysfunction occurs with normal aging and is associated with abnormal accumulation of protein aggregates within neurons in neurodegenerative diseases. Ischemia disrupts UPP function and thus may contribute to UPP dysfunction seen in the aging brain and in neurodegenerative diseases. Ubiquitin carboxy-terminal hydrolase L1 (UCHL1), an important component of the UPP in the neuron, is covalently modified and its activity inhibited by reactive lipids produced after ischemia. As a result, degradation of toxic proteins is impaired which may exacerbate neuronal function and cell death in stroke and neurodegenerative diseases. Preserving or restoring UCHL1 activity may be an effective therapeutic strategy in stroke and neurodegenerative diseases. Published by Elsevier B.V.
C1 [Graham, Steven H.; Liu, Hao] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA USA.
[Graham, Steven H.; Liu, Hao] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA.
RP Graham, SH (reprint author), Geriatr Res Educ & Clin Ctr, Off Res & Dev, Res Off Bldg 30,Mail Code 151,Univ Dr, Pittsburgh, PA 15240 USA.
EM Steven.Graham@va.gov
OI Graham, Steven/0000-0002-1718-2547
FU National Institutes of Health NINDS [R01NS37549]
FX This work was supported by the National Institutes of Health NINDS
R01NS37549, 2015 (SHG). The authors thank Marie Rose for figure
preparation and editorial assistance.
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PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 30
EP 38
DI 10.1016/j.arr.2016.09.011
PG 9
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100004
PM 27702698
ER
PT J
AU Wang, Y
Ji, XM
Leak, RK
Chen, FH
Cao, GD
AF Wang, Yuan
Ji, Xunming
Leak, Rehana K.
Chen, Fenghua
Cao, Guodong
TI Stem cell therapies in age-related neurodegenerative diseases and stroke
SO AGEING RESEARCH REVIEWS
LA English
DT Review
DE Aging; Stem cell; Neurodegenerative diseases; Stroke; Plasticity;
Self-renew
ID MARROW MONONUCLEAR-CELLS; CENTRAL-NERVOUS-SYSTEM; ISCHEMIC BRAIN-INJURY;
TRANSIENT CEREBRAL-ISCHEMIA; MESENCHYMAL STROMAL CELLS; AMYLOID-BETA
DEPOSITION; UMBILICAL-CORD BLOOD; ADULT BONE-MARROW; ALZHEIMERS-DISEASE;
PARKINSONS-DISEASE
AB Aging, a complex process associated with various structural, functional and metabolic changes in the brain, is an important risk factor for neurodegenerative diseases and stroke. These diseases share similar neuropathological changes, such as the formation of misfolded proteins, oxidative stress, loss of neurons and synapses, dysfunction of the neurovascular unit (NVU), reduction of self-repair capacity, and motor and/or cognitive deficiencies. In addition to gray matter dysfunction, the plasticity and repair capacity of white matter also decrease with aging and contribute to neurodegenerative diseases. Aging not only renders patients more susceptible to these disorders, but also attenuates their self-repair capabilities. In addition, low drug responsiveness and intolerable side effects are major challenges in the prevention and treatment of senile diseases. Thus, stem cell therapies characterized by cellular plasticity and the ability to self-renew may be a promising strategy for aging-related brain disorders. Here, we review the common pathophysiological changes, treatments, and the promises and limitations of stem cell therapies in age-related neurodegenerative diseases and stroke. Published by Elsevier B.V.
C1 [Wang, Yuan] Capital Univ Med, Xuanwu Hosp, Dept Neurol, Beijing 100053, Peoples R China.
[Ji, Xunming] Capital Univ Med, Xuanwu Hosp, Dept Neurosurg, Beijing 100053, Peoples R China.
[Leak, Rehana K.] Duquesne Univ, Div Pharmaceut Sci, Pittsburgh, PA 15282 USA.
[Chen, Fenghua; Cao, Guodong] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15260 USA.
[Cao, Guodong] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15240 USA.
RP Cao, GD (reprint author), VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15240 USA.
EM caog@upmc.edu
FU National Institutes of Health/NINDS [NS079345]; VA Merit Review grants
[BX002346]; Chinese 12th Five science and technology support program
[2013BAI07B01]
FX This project was supported by National Institutes of Health/NINDS grants
NS079345 (to G. C.), VA Merit Review grants BX002346 (to G. C.), and
Chinese 12th Five science and technology support program2013BAI07B01 (to
X. J).
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 39
EP 50
DI 10.1016/j.arr.2016.11.002
PG 12
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100005
PM 27876573
ER
PT J
AU Ikonomovic, MD
Mi, ZP
Abrahamson, EE
AF Ikonomovic, Milos D.
Mi, Zhiping
Abrahamson, Eric E.
TI Disordered APP metabolism and neurovasculature in trauma and aging:
Combined risks for chronic neurodegenerative disorders
SO AGEING RESEARCH REVIEWS
LA English
DT Review
DE Aging; Alzheimer's disease; Amyloid-beta; Brain trauma;
Neurodegeneration; Neurovascular unit
ID AMYLOID-PRECURSOR-PROTEIN; BLOOD-BRAIN-BARRIER; SEVERE HEAD-INJURY;
PRECLINICAL ALZHEIMERS-DISEASE; MILD COGNITIVE IMPAIRMENT; TRANSGENIC
MOUSE MODEL; PITTSBURGH COMPOUND-B; A-BETA PEPTIDE; AXONAL INJURY;
NITRIC-OXIDE
AB Traumatic brain injury (TBI), advanced age, and cerebral vascular disease are factors conferring increased risk for late onset Alzheimer's disease (AD). These conditions are also related pathologically through multiple interacting mechanisms. The hallmark pathology of AD consists of pathological aggregates of amyloid-beta (A beta) peptides and tau proteins. These molecules are also involved in neuropathology of several other chronic neurodegenerative diseases, and are under intense investigation in the aftermath of TBI as potential contributors to the risk for developing AD and chronic traumatic encephalopathy (CTE). The pathology of TBI is complex and dependent on injury severity, age-at-injury, and length of time between injury and neuropathological evaluation. In addition, the mechanisms influencing pathology and recovery after TBI likely involve genetic/epigenetic factors as well as additional disorders or comorbid states related to age and central and peripheral vascular health. In this regard, dysfunction of the aging neurovascular system could be an important link between TBI and chronic neurodegenerative diseases, either as a precipitating event or related to accumulation of AD-like pathology which is amplified in the context of aging. Thus with advanced age and vascular dysfunction, TBI can trigger self-propagating cycles of neuronal injury, pathological protein aggregation, and synaptic loss resulting in chronic neurodegenerative disease. In this review we discuss evidence supporting TBI and aging as dual, interacting risk factors for AD, and the role of A beta and cerebral vascular dysfunction in this relationship. Evidence is discussed that A beta is involved in cyto- and synapto-toxicity after severe TBI, and that its chronic effects are potentiated by aging and impaired cerebral vascular function. From a therapeutic perspective, we emphasize that in the fields of TBI- and aging-related neurodegeneration protective strategies should include preservation of neurovascular function. Published by Elsevier B.V.
C1 [Ikonomovic, Milos D.; Mi, Zhiping; Abrahamson, Eric E.] VA Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15213 USA.
[Ikonomovic, Milos D.; Mi, Zhiping; Abrahamson, Eric E.] Univ Pittsburgh, Sch Med, Dept Neurol, Pittsburgh, PA 15213 USA.
[Ikonomovic, Milos D.] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15213 USA.
RP Ikonomovic, MD (reprint author), Univ Pittsburgh, Sch Med, Thomas Detre Hall WPIC,Room 1421,3811 OHara St, Pittsburgh, PA 15213 USA.
EM ikonomovicmd@upmc.edu
FU Veterans Affairs grants [1I01RX000511, 1I01RX000952, 1I01RX001778]; NIA
[AG014449, AG05133]; NINDS [NS30318]
FX This work was supported by Veterans Affairs grants 1I01RX000511,
1I01RX000952, 1I01RX001778, NIA grants AG014449 and AG05133, and NINDS
grant NS30318.
NR 202
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 51
EP 63
DI 10.1016/j.arr.2016.11.003
PG 13
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100006
PM 27829172
ER
PT J
AU Liu, H
Yang, YY
Xia, YG
Zhu, W
Leak, RK
Wei, ZS
Wang, JY
Hu, XM
AF Liu, Huan
Yang, Yuanyuan
Xia, Yuguo
Zhu, Wen
Leak, Rehana K.
Wei, Zhishuo
Wang, Jianyi
Hu, Xiaoming
TI Aging of cerebral white matter
SO AGEING RESEARCH REVIEWS
LA English
DT Review
DE Aging; White matter; Stroke; Traumatic brain injury; Neurodegeneration;
Myelin; Axon
ID TRAUMATIC BRAIN-INJURY; MILD COGNITIVE IMPAIRMENT; EARLY
HUNTINGTONS-DISEASE; AGE-RELATED-CHANGES; EXPERIMENTAL INTRACEREBRAL
HEMORRHAGE; REMITTING MULTIPLE-SCLEROSIS; SPORADIC PARKINSONS-DISEASE;
A-BETA ACCUMULATION; ALZHEIMERS-DISEASE; DIFFUSION TENSOR
AB White matter (WM) occupies a large volume of the human cerebrum and is mainly composed of myelinated axons and myelin-producing glial cells. The myelinated axons within WM are the structural foundation for efficient neurotransmission between cortical and subcortical areas. Similar to neuron enriched gray matter areas, WM undergoes a series of changes during the process of aging. WM malfunction can induce serious neurobehavioral and cognitive impairments. Thus, age-related changes in WM may contribute to the functional decline observed in the elderly. In addition, aged WM becomes more susceptible to neurological disorders, such as stroke, traumatic brain injury (TBI), and neurodegeneration. In this review, we summarize the structural and functional alterations of WM in natural aging and speculate on the underlying mechanisms. We also discuss how age-related WM changes influence the progression of various brain disorders, including ischemic and hemorrhagic stroke, TBI, Alzheimer's disease, and Parkinson's disease. Although the physiology of WM is still poorly understood relative to gray matter, WM is a rational therapeutic target for a number of neurological and psychiatric conditions. (C) 2016 Elsevier B.V. All rights reserved.
C1 [Liu, Huan; Yang, Yuanyuan; Xia, Yuguo; Zhu, Wen; Wei, Zhishuo; Wang, Jianyi; Hu, Xiaoming] Univ Pittsburgh, Pittsburgh Inst Brain Disorders & Recovery, Dept Neurol, Sch Med, Pittsburgh, PA 15213 USA.
[Hu, Xiaoming] Vet Affairs Pittsburgh Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15261 USA.
[Liu, Huan; Yang, Yuanyuan; Xia, Yuguo; Wang, Jianyi] Cent S Univ, Xiangya Sch Med, Changsha, Hunan, Peoples R China.
[Leak, Rehana K.] Duquesne Univ, Div Pharmaceut Sci, Pittsburgh, PA 15282 USA.
RP Hu, XM (reprint author), Univ Pittsburgh, Sch Med, Dept Neurol, 200 Lothrop St,SBST 506, Pittsburgh, PA 15213 USA.
EM hux2@upmc.edu
FU NIH from NIH/National Institute of neurological disorders and stroke
(NINDS) [NS094573, NS092618]; American Heart Association
[13SDCG14570025]
FX This work was supported by the NIH grants from NIH/National Institute of
neurological disorders and stroke (NINDS) (NS094573 and NS092618 to
X.H), and the American Heart Association (13SDCG14570025 to X. H).
NR 200
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PU ELSEVIER IRELAND LTD
PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 64
EP 76
DI 10.1016/j.arr.2016.11.006
PG 13
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100007
PM 27865980
ER
PT J
AU Cai, W
Zhang, K
Li, PY
Zhu, L
Xu, J
Yang, BY
Hu, XM
Lu, ZQ
Chen, J
AF Cai, Wei
Zhang, Kai
Li, Peiying
Zhu, Ling
Xu, Jing
Yang, Boyu
Hu, Xiaoming
Lu, Zhengqi
Chen, Jun
TI Dysfunction of the neurovascular unit in ischemic stroke and
neurodegenerative diseases: An aging effect
SO AGEING RESEARCH REVIEWS
LA English
DT Review
DE Aging; Neurovascular unit; Vulnerability; Ischemic stroke;
Neurodegeneration
ID BLOOD-BRAIN-BARRIER; ALZHEIMERS-DISEASE; PARKINSONS-DISEASE;
CEREBRAL-ISCHEMIA; OXIDATIVE STRESS; MICROGLIA/MACROPHAGE POLARIZATION;
ENDOPLASMIC-RETICULUM; ALPHA-SYNUCLEIN; DENTATE GYRUS; MICROGLIA
AB Current understanding on the mechanisms of brain injury and neurodegeneration highlights an appreciation of multicellular interactions within the neurovascular unit (NVU), which include the evolution of blood-brain barrier (BBB) damage, neuronal cell death or degeneration, glial reaction, and immune cell infiltration. Aging is an important factor that influences the integrity of the NVU. The age-related physiological or pathological changes in the cellular components of the NVU have been shown to increase the vulnerability of the NVU to ischemia/reperfusion injury or neurodegeneration, and to result in deteriorated brain damage. This review describes the impacts of aging on each NVU component and discusses the mechanisms by which aging increases NVU sensitivity to stroke and neurodegenerative diseases. Prophylactic or therapeutic perspectives that may delay or diminish aging and thus prevent the incidence of these neurological disorders will also be reviewed. (C) 2016 Elsevier B.V. All rights reserved.
C1 [Cai, Wei; Zhang, Kai; Zhu, Ling; Xu, Jing; Yang, Boyu; Hu, Xiaoming; Chen, Jun] Vet Affairs Pittsburgh Hlth Care Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15261 USA.
[Cai, Wei; Lu, Zhengqi] Sun Yat Sen Univ, Dept Neurol, Affiliated Hosp 3, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China.
[Li, Peiying; Zhu, Ling] Shanghai Jiao Tong Univ, Renji Hosp, Dept Anesthesiol, Sch Med, Shanghai 200127, Peoples R China.
[Cai, Wei; Zhang, Kai; Li, Peiying; Zhu, Ling; Xu, Jing; Yang, Boyu; Hu, Xiaoming; Chen, Jun] Univ Pittsburgh, Pittsburgh Inst Brain Disorders & Recovery, Sch Med, Pittsburgh, PA 15213 USA.
RP Lu, ZQ (reprint author), Sun Yat Sen Univ, Dept Neurol, Affiliated Hosp 3, 600 Tianhe Rd, Guangzhou 510630, Guangdong, Peoples R China.; Chen, J (reprint author), Univ Pittsburgh, Sch Med, Dept Neurol, 200 Lothrop St,SBST 506, Pittsburgh, PA 15213 USA.
EM lzq1828@aliyun.com; chenj2@upmc.edu
FU VA merit grants [I01BX002495, I01RX000420]; NIH [NS095671, NS089534,
NS45048]; U.S. Department of Veterans Affairs Senior Research Career
Scientist Award
FX This work was supported by VA merit grants (I01BX002495 and I01RX000420
to Jun Chen), NIH grants (NS095671, NS089534 and NS45048 to Jun Chen);
and the U.S. Department of Veterans Affairs Senior Research Career
Scientist Award (to Jun Chen).
NR 133
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PI CLARE
PA ELSEVIER HOUSE, BROOKVALE PLAZA, EAST PARK SHANNON, CO, CLARE, 00000,
IRELAND
SN 1568-1637
EI 1872-9649
J9 AGEING RES REV
JI Ageing Res. Rev.
PD MAR
PY 2017
VL 34
SI SI
BP 77
EP 87
DI 10.1016/j.arr.2016.09.006
PG 11
WC Cell Biology; Geriatrics & Gerontology
SC Cell Biology; Geriatrics & Gerontology
GA EJ9FN
UT WOS:000393532100008
PM 27697546
ER
PT J
AU Rief, JJ
Hamm, ME
Zickmund, SL
Nikolajski, C
Lesky, D
Hess, R
Fischer, GS
Weimer, M
Clark, S
Zieth, C
Roberts, MS
AF Rief, John J.
Hamm, Megan E.
Zickmund, Susan L.
Nikolajski, Cara
Lesky, Dan
Hess, Rachel
Fischer, Gary S.
Weimer, Melissa
Clark, Sunday
Zieth, Caroline
Roberts, Mark S.
TI Using Health Information Technology to Foster Engagement: Patients'
Experiences with an Active Patient Health Record
SO HEALTH COMMUNICATION
LA English
DT Article
ID DIABETES SELF-MANAGEMENT; IMPROVING PRIMARY-CARE; CHRONIC ILLNESS CARE;
PERSONAL HEALTH; COLLABORATIVE MANAGEMENT; ACTIVATION MEASURE;
DECISION-MAKING; CHRONIC DISEASE; HEART-FAILURE; E-MAIL
AB Personal health records (PHRs) typically employ "passive" communication strategies, such as non-personalized medical text, rather than direct patient engagement in care. Currently there is a call for more active PHRs that directly engage patients in an effort to improve their health by offering elements such as personalized medical information, health coaches, and secure messaging with primary care providers. As part of a randomized clinical trial comparing "passive" with "active" PHRs, we explore patients' experiences with using an "active" PHR known as HealthTrak. The "passive" elements of this PHR included problem lists, medication lists, information about patient allergies and immunizations, medical and surgical histories, lab test results, health reminders, and secure messaging. The active arm included all of these elements and added personalized alerts delivered through the secure messaging platform to patients for services coming due based on various demographic features (including age and sex) and chronic medical conditions. Our participants were part of the larger clinical trial and were eligible if they had been randomized to the active PHR arm, one that included regular personalized alerts. We conducted focus group discussions on the benefits of this active PHR for patients who are at risk for cardiovascular disease. Forty-one patients agreed to participate and were organized into five separate focus group sessions. Three main themes emerged from the qualitatively analyzed focus groups: participants reported that the active PHR promoted better communication with providers; enabled them to more effectively partner with their providers; and helped them become more proactive about tracking their health information. In conclusion, patients reported improved communication, partnership with their providers, and a sense of self-management, thus adding insights for PHR designers hoping to address low adoption rates and other patient barriers to the development and use of the technology.
C1 [Rief, John J.] Duquesne Univ, Dept Commun & Rhetor Studies, 600 Forbes Ave, Pittsburgh, PA 15282 USA.
[Hamm, Megan E.] Univ Pittsburgh, Qualitat Evaluat & Stakeholder Engagement Serv, Ctr Res Hlth Care, Pittsburgh, PA 15260 USA.
[Zickmund, Susan L.] Univ Pittsburgh, Sch Med, Ctr Hlth Equ Res & Promot,Dept Med, VA Pittsburgh Healthcare Syst,Div Gen Internal Me, Pittsburgh, PA 15260 USA.
[Nikolajski, Cara; Weimer, Melissa; Zieth, Caroline] Univ Pittsburgh, Ctr Res Hlth Care, Pittsburgh, PA 15260 USA.
[Lesky, Dan] Univ Pittsburgh, Sch Med, Pittsburgh, PA 15260 USA.
[Hess, Rachel] Univ Utah, Dept Populat Hlth Sci, Salt Lake City, UT 84112 USA.
[Hess, Rachel] Univ Utah, Dept Internal Med, Salt Lake City, UT 84112 USA.
[Fischer, Gary S.; Roberts, Mark S.] Univ Pittsburgh, Sch Med, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15260 USA.
[Clark, Sunday] Weill Cornell Med Coll, Dept Emergency Med, New York, NY USA.
[Roberts, Mark S.] Univ Pittsburgh, Sch Publ Hlth, Dept Hlth Policy & Management, Pittsburgh, PA 15260 USA.
RP Rief, JJ (reprint author), Duquesne Univ, Dept Commun & Rhetor Studies, 600 Forbes Ave, Pittsburgh, PA 15282 USA.
EM riefj@duq.edu
FU National Institute of Health's Agency for Healthcare Research and
Quality (AHRQ) [1R18HS018167-01]; AHRQ [T32HS017587]
FX This work and material are supported by funding from the National
Institute of Health's Agency for Healthcare Research and Quality (AHRQ)
(grant number 1R18HS018167-01). In addition, during the completion of
this manuscript, the corresponding author, John J. Rief, was supported
by a postdoctoral fellowship funded by the AHRQ (grant number
T32HS017587). The content is solely the responsibility of the authors
and does not necessarily represent the views of the AHRQ.
NR 70
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PU ROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD
PI ABINGDON
PA 2-4 PARK SQUARE, MILTON PARK, ABINGDON OX14 4RN, OXON, ENGLAND
SN 1041-0236
EI 1532-7027
J9 HEALTH COMMUN
JI Health Commun.
PD MAR
PY 2017
VL 32
IS 3
BP 310
EP 319
DI 10.1080/10410236.2016.1138378
PG 10
WC Communication; Health Policy & Services
SC Communication; Health Care Sciences & Services
GA EI9PE
UT WOS:000392839800006
PM 27223684
ER
PT J
AU Abboud, S
Kim, SK
Jacoby, S
Mooney-Doyle, K
Waite, T
Froh, E
Sefcik, JS
Kim, H
Sowicz, TJ
Kelly, TA
Kagan, S
AF Abboud, Sarah
Kim, Su Kyung
Jacoby, Sara
Mooney-Doyle, Kim
Waite, Terease
Froh, Elizabeth
Sefcik, Justine S.
Kim, Hyejin
Sowicz, Timothy Joseph
Kelly, Terri-Ann
Kagan, Sarah
TI Co-creation of a pedagogical space to support qualitative inquiry: An
advanced qualitative collective
SO NURSE EDUCATION TODAY
LA English
DT Article
AB Background: Situated in a research-intensive School of Nursing, the Advanced Qualitative Collective (AQC) provides an innovative educational forum for the study of qualitative research by doctoral and postdoctoral scholars. This long-standing collective is guided by a faculty facilitator using a collaborative co-learning approach to address individual and group needs, from the conception of research projects through dissemination of completed qualitative research. This article describes the dynamics of the AQC and the ways a co-created pedagogical entity supports professional development among its diverse members. The informal, participatory style, and dynamic content used by the AQC resists a course structure typical of doctoral education in health sciences, and promotes engagement and self-direction. The AQC provides opportunities for members to examine theoretical frameworks and methodologies rarely addressed within a positivism-dominant learning environment while simultaneously serving as an alternative exemplar for the pedagogy of research. (C) 2016 Elsevier Ltd. All rights reserved.
C1 [Abboud, Sarah] Univ Illinois, Coll Nursing, Chicago, IL USA.
[Kim, Su Kyung] Univ Penn, Sch Med, Philadelphia, PA 19104 USA.
[Jacoby, Sara] Univ Penn, Sch Med, Penn Injury Sci Ctr, Philadelphia, PA 19104 USA.
[Mooney-Doyle, Kim; Waite, Terease; Sefcik, Justine S.; Kim, Hyejin; Kelly, Terri-Ann] Univ Penn, Sch Nursing, Philadelphia, PA 19104 USA.
[Froh, Elizabeth] Univ Penn, Sch Nursing, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA.
[Sowicz, Timothy Joseph] VA Pittsburgh Healthcare Syst, Interdisciplinary Addict Program Educ & Res VIPER, Pittsburgh, PA USA.
[Kagan, Sarah] Univ Penn, Sch Nursing, Gerontol Nursing, Philadelphia, PA 19104 USA.
RP Abboud, S (reprint author), Univ Illinois, Coll Nursing, Dept Women Children & Family Hlth Sci, 845 S Damen Ave,Off 618, Chicago, IL 60607 USA.
EM abbouds@uic.edu
FU Ruth L. Kirschstein NRSA T32 funding [T32NR007100, T32NR009356,
1F31NR013847-01A1, 5F31NR013599-03]; NRSA Individual F31 funding [F31 NR
015693]
FX Sarah Abboud, Kim Mooney-Doyle, and Terri-Ann Kelly were on a Ruth L.
Kirschstein NRSA T32 funding (T32NR007100); Justine S. Sefcik was on a
Ruth L. Kirschstein NRSA T32 funding (T32NR009356) and NRSA Individual
F31 funding (F31 NR 015693); Terease Waite was on Ruth L. Kirschstein
NRSA Individual F31 funding (1F31NR013847-01A1); Sara Jacoby was on Ruth
L. Kirschstein NRSA Individual F31 funding (5F31NR013599-03), all at the
University of Pennsylvania School of Nursing.
NR 12
TC 0
Z9 0
U1 10
U2 10
PU CHURCHILL LIVINGSTONE
PI EDINBURGH
PA JOURNAL PRODUCTION DEPT, ROBERT STEVENSON HOUSE, 1-3 BAXTERS PLACE,
LEITH WALK, EDINBURGH EH1 3AF, MIDLOTHIAN, SCOTLAND
SN 0260-6917
EI 1532-2793
J9 NURS EDUC TODAY
JI Nurse Educ. Today
PD MAR
PY 2017
VL 50
BP 8
EP 11
DI 10.1016/j.nedt.2016.12.001
PG 4
WC Education, Scientific Disciplines; Nursing
SC Education & Educational Research; Nursing
GA EJ2CK
UT WOS:000393017300002
PM 28002756
ER
PT J
AU Miller, MB
Van Reen, E
Barker, DH
Roane, BM
Borsari, B
McGeary, JE
Seifer, R
Carskadon, MA
AF Miller, Mary Beth
Van Reen, Eliza
Barker, David H.
Roane, Brandy M.
Borsari, Brian
McGeary, John E.
Seifer, Ronald
Carskadon, Mary A.
TI The impact of sleep and psychiatric symptoms on alcohol consequences
among young adults
SO ADDICTIVE BEHAVIORS
LA English
DT Article
DE Binge drinking; Heavy episodic drinking; Mental health; College students
ID COLLEGE-STUDENTS; USE DISORDERS; SUBSTANCE USE; BINGE DRINKING; QUALITY
INDEX; MENTAL-HEALTH; POOR SLEEP; DEPRESSION; ANXIETY; QUESTIONNAIRE
AB Objective: Independent lines of research have documented links between psychiatric symptoms and poor sleep quality, psychiatric symptoms and alcohol use, and alcohol use and poor sleep quality. The current study examined the synergistic effect of poor sleep quality and psychiatric symptoms on alcohol-related consequences in heavy-drinking young adults.
Method: Matriculating college students reporting at least one heavy drinking episode over the first nine weeks of the semester (N= 385, 52% female) were categorized as experiencing 'good' (n = 280) versus 'poor' sleep quality (n = 105) and screening 'positive' (n = 203) or 'negative' (n = 182) for a psychiatric disorder. Sleep quality was assessed using the Pittsburgh Sleep Quality Index; psychiatric diagnosis was assessed using the Psychiatric Diagnostic Screening Questionnaire; and alcohol-related consequences were assessed" using the Brief Young Adult Alcohol Consequences Questionnaire. General linear models were used to examine the main effects and interaction between sleep quality and psychiatric symptoms on alcohol-related consequences.
Results: Sleep quality moderated the association between psychiatric screen and alcohol-related consequences among heavy-drinking college students, such that psychiatric symptoms were associated with more alcohol-related consequences in the context of poor sleep quality.
Conclusions: The combination of poor sleep quality and psychiatric symptoms is associated with increased alcohol -related consequences among heavy-drinking college students. Given the significant interaction between these symptoms, healthcare providers are encouraged to screen for the presence of sleep and psychiatric disorders among heavy-drinking young adults and to provide empirically-supported treatments as appropriate. (C) 2016 Elsevier Ltd. All rights reserved.
C1 [Miller, Mary Beth] Brown Univ, Sch Publ Hlth, Dept Behav & Social Sci, Ctr Alcohol & Addict Studies, Box G-S121-4, Providence, RI 02912 USA.
[Van Reen, Eliza; Barker, David H.; Roane, Brandy M.; Seifer, Ronald; Carskadon, Mary A.] Brown Univ, Sleep Sci Res Lab, 300 Duncan Dr, Providence, RI 02906 USA.
[Van Reen, Eliza; Barker, David H.; Roane, Brandy M.; McGeary, John E.; Seifer, Ronald; Carskadon, Mary A.] Brown Univ, Warren Alpert Med Sch, Dept Psychiat & Human Behav, 1 Hoppin St,Coro West Suite 204, Providence, RI 02903 USA.
[Roane, Brandy M.] Univ North Texas, Hlth Sci Ctr, 3500 Camp Bowie Blvd, Ft Worth, TX 76107 USA.
[Borsari, Brian] San Francisco VA Med Ctr, 4150 Clement St, San Francisco, CA 94121 USA.
[McGeary, John E.] Providence VA Med Ctr, 830 Chalkstone Ave, Providence, RI 02908 USA.
[Carskadon, Mary A.] Univ South Australia, Sch Psychol Social Work & Social Policy, Adelaide, SA, Australia.
EM millerme04@gmail.com
FU National Institutes of Health [MH079179, T32-AA007459, K23-MH102131];
National Institute of Drug Abuse [R01-DA033425]
FX This research was supported by grant numbers MH079179 (PI: Mary
Carskadon), T32-AA007459 (PI: Peter Monti), and K23-MH102131 (PI: David
Barker) at the National Institutes of Health. Brian Borsari's
contribution to this manuscript was supported by the National Institute
of Drug Abuse grant R01-DA033425. The contents of this manuscript do not
represent the views of the National Institutes of Health, the Department
of Veterans Affairs, or the United States Government.
NR 45
TC 0
Z9 0
U1 21
U2 21
PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0306-4603
EI 1873-6327
J9 ADDICT BEHAV
JI Addict. Behav.
PD MAR
PY 2017
VL 66
BP 138
EP 144
DI 10.1016/j.addbeh.2016.11.023
PG 7
WC Psychology, Clinical; Substance Abuse
SC Psychology; Substance Abuse
GA EI7NG
UT WOS:000392684300023
PM 27940388
ER
PT J
AU Williams, EM
Walker, RJ
Faith, T
Egede, LE
AF Williams, Edith M.
Walker, Rebekah J.
Faith, Trevor
Egede, Leonard E.
TI The impact of arthritis and joint pain on individual healthcare
expenditures: findings from the Medical Expenditure Panel Survey (MEPS),
2011
SO ARTHRITIS RESEARCH & THERAPY
LA English
DT Article
DE Joint pain; Arthritis; Healthcare cost; Medical expenditures; MEPS;
Functional limitations
ID SYSTEMIC-LUPUS-ERYTHEMATOSUS; RHEUMATOID-ARTHRITIS;
ANKYLOSING-SPONDYLITIS; WORK PRODUCTIVITY; UNITED-STATES; OLDER-ADULTS;
DISABILITY; COSTS; BURDEN; DETERMINANTS
AB Background: Joint pain, including back pain, and arthritis are common conditions in the United States, affecting more than 100 million individuals and costing upwards of $200 billion each year. Although activity limitations associated with these disorders impose a substantial economic burden, this relationship has not been explored in a large U.S. cohort.
Methods: In this study, we used the Medical Expenditures Panel Survey to investigate whether functional limitations explain the difference in medical expenditures between patients with arthritis and joint pain and those without. We used sequential explanatory linear models to investigate this relationship and accounted for various covariates.
Results: Unadjusted mean expenditures were $10,587 for those with joint pain or arthritis, compared with $3813 for those without. In a fully adjusted model accounting also for functional limitations, those with joint pain or arthritis paid $1638 more than those without, a statistically significant difference.
Conclusions: The growing economic and public health burden of arthritis and joint pain, as well as the corresponding complications of functional, activity, and sensory limitations, calls for an interdisciplinary approach and heightened awareness among providers to identify strategies that meet the needs of high-risk patients in order to prevent and delay disease progression.
C1 [Williams, Edith M.; Faith, Trevor] Med Univ South Carolina, Dept Publ Hlth Sci, 135 Cannon St,Suite CS303, Charleston, SC 29425 USA.
[Williams, Edith M.; Walker, Rebekah J.; Egede, Leonard E.] Med Univ South Carolina, Ctr Hlth Dispar Res, 135 Rutledge Ave,Room 280H, Charleston, SC 29425 USA.
[Walker, Rebekah J.; Egede, Leonard E.] Med Univ South Carolina, Div Gen Internal Med & Geriatr, Dept Med, 96 Jonathan Lucas St,Suite 803, Charleston, SC 29425 USA.
[Walker, Rebekah J.; Egede, Leonard E.] HEROIC, Ralph H Johnson Vet Affairs Med Ctr, 109 Bee St, Charleston, SC 29401 USA.
RP Egede, LE (reprint author), Med Univ South Carolina, Ctr Hlth Dispar Res, 135 Rutledge Ave,Room 280H, Charleston, SC 29425 USA.; Egede, LE (reprint author), Med Univ South Carolina, Div Gen Internal Med & Geriatr, Dept Med, 96 Jonathan Lucas St,Suite 803, Charleston, SC 29425 USA.; Egede, LE (reprint author), HEROIC, Ralph H Johnson Vet Affairs Med Ctr, 109 Bee St, Charleston, SC 29401 USA.
EM legede@musc.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases
[K24DK093699]
FX This study was supported by the National Institute of Diabetes and
Digestive and Kidney Diseases (grant K24DK093699 [to principal
investigator LEE]).
NR 33
TC 0
Z9 0
U1 0
U2 0
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1478-6354
EI 1478-6362
J9 ARTHRITIS RES THER
JI Arthritis Res. Ther.
PD FEB 28
PY 2017
VL 19
AR 38
DI 10.1186/s13075-017-1230-3
PG 8
WC Rheumatology
SC Rheumatology
GA EN8UM
UT WOS:000396275300002
PM 28245879
ER
PT J
AU Abdallah, CG
Wrocklage, KM
Averill, CL
Akiki, T
Schweinsburg, B
Roy, A
Martini, B
Southwick, SM
Krystal, JH
Scott, JC
AF Abdallah, C. G.
Wrocklage, K. M.
Averill, C. L.
Akiki, T.
Schweinsburg, B.
Roy, A.
Martini, B.
Southwick, S. M.
Krystal, J. H.
Scott, J. C.
TI Anterior hippocampal dysconnectivity in posttraumatic stress disorder: a
dimensional and multimodal approach
SO TRANSLATIONAL PSYCHIATRY
LA English
DT Article
ID ADMINISTERED PTSD SCALE; FUNCTIONAL CONNECTIVITY; BRAIN NETWORKS;
PREFRONTAL CORTEX; SCHIZOPHRENIA; MODEL; NEUROBIOLOGY; METAANALYSIS;
KETAMINE; ANXIETY
AB The anterior hippocampus (aHPC) has a central role in the regulation of anxiety-related behavior, stress response, emotional memory and fear. However, little is known about the presence and extent of aHPC abnormalities in posttraumatic stress disorder (PTSD). In this study, we used a multimodal approach, along with graph-based measures of global brain connectivity (GBC) termed functional GBC with global signal regression (f-GBCr) and diffusion GBC (d-GBC), in combat-exposed US Veterans with and without PTSD. Seed-based aHPC anatomical connectivity analyses were also performed. A whole-brain voxel-wise data-driven investigation revealed a significant association between elevated PTSD symptoms and reduced medial temporal f-GBCr, particularly in the aHPC. Similarly, aHPC d-GBC negatively correlated with PTSD severity. Both functional and anatomical aHPC dysconnectivity measures remained significant after controlling for hippocampal volume, age, gender, intelligence, education, combat severity, depression, anxiety, medication status, traumatic brain injury and alcohol/substance comorbidities. Depression-like PTSD dimensions were associated with reduced connectivity in the ventromedial and dorsolateral prefrontal cortex. In contrast, hyperarousal symptoms were positively correlated with ventromedial and dorsolateral prefrontal connectivity. We believe the findings provide first evidence of functional and anatomical dysconnectivity in the aHPC of veterans with high PTSD symptomatology. The data support the putative utility of aHPC connectivity as a measure of overall PTSD severity. Moreover, prefrontal global connectivity may be of clinical value as a brain biomarker to potentially distinguish between PTSD subgroups.
C1 [Abdallah, C. G.; Wrocklage, K. M.; Averill, C. L.; Akiki, T.; Schweinsburg, B.; Roy, A.; Martini, B.; Southwick, S. M.; Krystal, J. H.] US Dept Vet Affairs, Clin Neurosci Div, VA Natl Ctr PTSD, West Haven, CT 06516 USA.
[Abdallah, C. G.; Wrocklage, K. M.; Averill, C. L.; Akiki, T.; Schweinsburg, B.; Roy, A.; Martini, B.; Southwick, S. M.; Krystal, J. H.] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA.
[Scott, J. C.] Univ Penn, Perelman Sch Med, Dept Psychiat, Philadelphia, PA 19104 USA.
[Scott, J. C.] Philadelphia VA Med Ctr, Mental Illness Res Educ & Clin Ctr VISN4, Philadelphia, PA USA.
RP Abdallah, CG (reprint author), US Dept Vet Affairs, Clin Neurosci Div, VA Natl Ctr PTSD, West Haven, CT 06516 USA.; Abdallah, CG (reprint author), Yale Univ, Sch Med, Dept Psychiat, 950 Campbell Ave,151E, West Haven, CT 06516 USA.
EM chadi.abdallah@yale.edu
FU U.S. Department of Veterans Affairs National Center for PTSD and NIH
[MH-101498]; Department of Veterans Affairs Career Development Award
[IK2CX000772]
FX The authors thank the Veterans who participated in this study for their
invaluable contribution. Funding support was provided by the U.S.
Department of Veterans Affairs National Center for PTSD and NIH
(MH-101498). Dr. Scott's participation was supported by a Department of
Veterans Affairs Career Development Award (IK2CX000772). The content is
solely the responsibility of the authors and does not necessarily
represent the official views of the sponsors. The sponsors had no role
in the design and conduct of the study; collection, management,
analysis, and interpretation of the data; and preparation, review, or
approval of the manuscript.
NR 52
TC 0
Z9 0
U1 1
U2 1
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 2158-3188
J9 TRANSL PSYCHIAT
JI Transl. Psychiatr.
PD FEB 28
PY 2017
VL 7
AR e1045
DI 10.1038/tp.2017.12
PG 7
WC Psychiatry
SC Psychiatry
GA EP2LT
UT WOS:000397215300002
PM 28244983
ER
PT J
AU Yuan, HF
He, ML
Cheng, F
Bai, R
da Silva, SR
Aguiar, RCT
Gao, SJ
AF Yuan, Hongfeng
He, Meilan
Cheng, Fan
Bai, Rosemary
da Silva, Suzane Ramos
Aguiar, Ricardo C. T.
Gao, Shou-Jiang
TI Tenovin-6 inhibits proliferation and survival of diffuse large B-cell
lymphoma cells by blocking autophagy
SO ONCOTARGET
LA English
DT Article
DE tenovin-6; diffuse large B-cell lymphoma; autophagy; sirtuins; p53
ID CHRONIC LYMPHOCYTIC-LEUKEMIA; STEM-CELLS; LYSOSOME FUSION;
CANCER-THERAPY; C-MYC; ACTIVATION; SIRT1; P53; APOPTOSIS; DEATH
AB Diffuse large B-cell lymphoma (DLBCL) is one of the most aggressive non-Hodgkin lymphomas. It is curable but one-third of cases are refractory to therapy or relapse after initial response highlighting the urgent need for developing novel therapeutic approaches. Targeting sirtuins, particularly SIRT1 by genetic approaches or using pharmaceutical inhibitor tenovin-6, has shown promising therapeutic potential in various hematopoietic malignancies. However, it remains unknown whether these approaches are effective for DLBCL. In this study, we have found that tenovin-6 potently inhibits the proliferation and survival of DLBCL cells. Surprisingly, specific knockdown of SIRT1/2/3 has no effect on DLBCL. Mechanistically, tenovin-6 increases the level of microtubule-associated protein 1 light chain 3B (LC3B)-II in a SIRT1/2/3- and p53-independent manner in DLBCL cell lines. Tenovin-6-mediated increase of LC3B-II is through inhibition of classical autophagy pathway. Furthermore, inhibition of the autophagy pathway by using other inhibitors or by knocking down key genes in the pathway impairs cell proliferation and survival of DLBCL cells. These results indicate that targeting the autophagic pathway could be a novel therapeutic strategy for DLBCL and that precaution should be taken to interpret data where tenovin-6 was used as an inhibitor of sirtuins.
C1 [Yuan, Hongfeng; He, Meilan; Cheng, Fan; Bai, Rosemary; da Silva, Suzane Ramos; Gao, Shou-Jiang] Univ Southern Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA USA.
[Aguiar, Ricardo C. T.] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, San Antonio, TX 78229 USA.
[Aguiar, Ricardo C. T.] Univ Texas Hlth Sci Ctr San Antonio, Canc Therapy & Res Ctr, San Antonio, TX 78229 USA.
[Aguiar, Ricardo C. T.] South Texas Vet Hlth Care Syst, Audie Murphy VA Hosp, San Antonio, TX USA.
RP Gao, SJ (reprint author), Univ Southern Calif, Keck Sch Med, Dept Mol Microbiol & Immunol, Los Angeles, CA USA.
EM shoujiag@usc.edu
FU NIH [CA096512, CA124332, CA132637, CA177377, CA213275, DE025465,
CA197153]; CPRIT [RP140452, RP150277]; VA Merit Award [I01-BX001882]
FX This work was supported by grants from NIH (CA096512, CA124332,
CA132637, CA177377, CA213275, DE025465 and CA197153) to S-J Gao; RCT
Aguiar was supported by grants from the CPRIT (RP140452 and RP150277)
and a VA Merit Award (I01-BX001882).
NR 64
TC 0
Z9 0
U1 0
U2 0
PU IMPACT JOURNALS LLC
PI ORCHARD PARK
PA 6666 E QUAKER ST, STE 1, ORCHARD PARK, NY 14127 USA
SN 1949-2553
J9 ONCOTARGET
JI Oncotarget
PD FEB 28
PY 2017
VL 8
IS 9
BP 14912
EP 14924
DI 10.18632/oncotarget.14741
PG 13
WC Oncology; Cell Biology
SC Oncology; Cell Biology
GA EN4YV
UT WOS:000396013700057
PM 28118604
ER
PT J
AU Rosset, EM
Trombetta-eSilva, J
Hepfer, G
Yao, H
Bradshaw, AD
AF Rosset, Emilie Moore
Trombetta-eSilva, Jessica
Hepfer, Glenn
Yao, Hai
Bradshaw, Amy Dodd
TI SPARC and the N-propeptide of collagen I influence fibroblast
proliferation and collagen assembly in the periodontal ligament
SO PLOS ONE
LA English
DT Article
ID EPITHELIAL-CELL RESTS; EXTRACELLULAR-MATRIX; MECHANICAL STRENGTH;
GLOBULAR DOMAIN; NULL MICE; MALASSEZ; PROCOLLAGEN; EXPRESSION;
CATARACTOGENESIS; PROTEINASE
AB The periodontal ligament (PDL) is a fibrous connective tissue that anchors tooth cementum into alveolar bone. Secreted protein acidic and rich in cysteine (SPARC) is a collagen-binding matricellular protein known to influence collagen fiber assembly in the PDL. In contrast, functional properties of the N-propeptide of collagen I, encoded in exon 2 of the COL1A1 gene, are poorly understood. In this study, the PDL of collagen I exon 2-deleted (wt/ko), SPARC-null (ko/wt), and double transgenic (ko/ko) mice were evaluated in terms of cellularity, collagen area, fiber morphology, and extraction force and compared to WT (wt/wt) mice. Picro sirius red staining indicated a decrease in total PDL collagen content in each of the transgenic mice compared to WT at 1 and 3 month age points. At 12 months, only SPARCn-ull (ko/wt) and double-null PDL demonstrated less total collagen versus WT. Likewise, an increase in thin PDL collagen fibers was observed at 1 and 3 months in each transgenic, with increases only in SPARC-null and double-null mice at 12 months. The force required for tooth extraction was significantly reduced in SPARC-null versus exon 2-deleted and WT mice, whereas double-null mice demonstrated further decreases in force required for tooth extraction. The number of proliferating fibroblasts and number and size of epithelial rests of Malassez were increased in each transgenic versus WT with double-null PDL exhibiting highest levels of proliferation and rests of Malassez at 1 month of age. Consistent with increases in PDL collagen in exon-2 deleted mice, with age, numbers of rests decreased at 12 months in this genotype. These results demonstrate for the first time a functional role of the N-propeptide in regulating collagen fiber assembly and cell behavior and suggest that SPARC and the N-propeptide of collagen I have distinct activities in regulating collagen fiber assembly and fibroblast function.
C1 [Rosset, Emilie Moore; Trombetta-eSilva, Jessica; Yao, Hai; Bradshaw, Amy Dodd] Med Univ South Carolina, Dept Oral Hlth Sci, Charleston, SC 29425 USA.
[Hepfer, Glenn; Yao, Hai] Clemson Univ, Dept Bioengn, Clemson, SC USA.
[Bradshaw, Amy Dodd] Med Univ South Carolina, Dept Med, Gazes Cardiac Res Inst, Div Cardiol, Charleston, SC USA.
[Bradshaw, Amy Dodd] Ralph H Johnson Dept Vet Affairs Med Ctr, Charleston, SC USA.
RP Rosset, EM (reprint author), Med Univ South Carolina, Dept Oral Hlth Sci, Charleston, SC 29425 USA.
EM rosset@musc.edu
NR 25
TC 0
Z9 0
U1 2
U2 2
PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1932-6203
J9 PLOS ONE
JI PLoS One
PD FEB 28
PY 2017
VL 12
IS 2
AR e0173209
DI 10.1371/journal.pone.0173209
PG 15
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EN4LY
UT WOS:000395980200059
PM 28245286
ER
PT J
AU Toro-Tobon, D
Agosto, S
Ahmadi, S
Koops, M
Bruder, JM
AF Toro-Tobon, David
Agosto, Sarimar
Ahmadi, Sara
Koops, Maureen
Bruder, Jan M.
TI Chronic Myeloid Leukemia Associated Hypercalcemia: A Case Report and
Literature Review
SO AMERICAN JOURNAL OF CASE REPORTS
LA English
DT Article
DE Case Reports; Hypercalcemia; Leukemia; Myelogenous; Chronic; BCR-ABL
Positive
ID CHRONIC MYELOGENOUS LEUKEMIA; ACUTE LYMPHOBLASTIC-LEUKEMIA;
HORMONE-RELATED PROTEIN; ACCELERATED PHASE; BONE-RESORPTION; BLAST
CRISIS; MALIGNANCY; TRANSFORMATION; MACROPHAGES; CANCER
AB Objective: Rare co-existance of disease or pathology
Background: Hypercalcemia associated with chronic myeloid leukemia (CML) is an ominous sign. Although rare, several cases have been reported and multiple pathophysiologic mechanisms have been independently proposed. We present a patient case and a literature review of the clinical presentation and mechanisms of CML-associated hypercalcemia.
Case Report: A 58-year-old male with a past medical history of CML diagnosed six years earlier, presented to the emergency department with one week of acute confusion, disorientation, polyuria, and polydipsia. On physical examination, we observed tachycardia, altered mental status, and dehydration. Blood analysis revealed leukocytosis, thrombocytosis, and marked hypercalcemia (18.6 mg/dL). His chest CT scan showed diffuse lytic lesions and bone destruction concerning for diffuse bone marrow involvement. The patient was diagnosed with hypercalcemia in the context of a CML blast phase. Treatment with hydration, calcitonin, and zoledronic acid lead to control of his symptoms and normalization of his serum calcium levels. After discharged, the patient was maintained on palliative treatment and zoledronic acid management without new episodes of hypercalcemia. However, eight months later, the patient died.
Conclusions: Evidence from the literature demonstrates a highly variable clinical presentation of CML-associated hypercalcemia, commonly occurring during an accelerated or a blast phase, and associated with poor survival. Multiple mechanisms could be involved and are not exclusive of each other. Better understanding of the pathophysiologic mechanisms involved in CML-associated hypercalcemia could lead to improvement in clinical and laboratory evaluation of these patients and be the foundation for the development of better management strategies and possibly target-directed therapy to positively improve prognosis.
C1 [Toro-Tobon, David] CES Univ, Dept Med, Medellin, Colombia.
[Agosto, Sarimar; Ahmadi, Sara; Koops, Maureen; Bruder, Jan M.] Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Endocrinol, San Antonio, TX 78229 USA.
[Koops, Maureen] South Texas Vet Hlth Care Syst, Dept Endocrinol, San Antonio, TX USA.
RP Bruder, JM (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Med, Div Endocrinol, San Antonio, TX 78229 USA.
EM Bruder@uthscsa.edu
OI Toro-Tobon, David/0000-0003-1910-4144
NR 26
TC 0
Z9 0
U1 1
U2 1
PU INT SCIENTIFIC LITERATURE, INC
PI SMITHTOWN
PA 361 FOREST LANE, SMITHTOWN, NY 11787 USA
SN 1941-5923
J9 AM J CASE REP
JI Am. J. Case Rep.
PD FEB 27
PY 2017
VL 18
BP 203
EP 207
DI 10.12659/AJCR.902467
PG 5
WC Medicine, General & Internal
SC General & Internal Medicine
GA EO5SL
UT WOS:000396753000001
PM 28239141
ER
PT J
AU Armstrong, EJ
Graham, LA
Waldo, SW
Valle, JA
Maddox, TM
Hawn, MT
AF Armstrong, Ehrin J.
Graham, Laura A.
Waldo, Stephen W.
Valle, Javier A.
Maddox, Thomas M.
Hawn, Mary T.
TI Incomplete Revascularization Is Associated With an Increased Risk for
Major Adverse Cardiovascular Events Among Patients Undergoing Noncardiac
Surgery
SO JACC-CARDIOVASCULAR INTERVENTIONS
LA English
DT Article
DE ischemia; operative risk; percutaneous coronary intervention; surgery
ID PERCUTANEOUS CORONARY INTERVENTION; RESIDUAL SYNTAX SCORE;
ARTERY-DISEASE; MYOCARDIAL-INFARCTION; STENT IMPLANTATION;
VASCULAR-SURGERY; OUTCOMES; QUANTIFICATION; COMPLETENESS; PREVENTION
AB OBJECTIVES The aim of this study was to determine whether incomplete revascularization is associated with a higher risk for major adverse cardiovascular events (MACE) and myocardial infarction (MI) among patients undergoing noncardiac surgery.
BACKGROUND Patients with coronary artery disease and prior percutaneous coronary intervention (PCI) frequently undergo noncardiac surgery. These patients may have had PCI either on all obstructive lesions (i.e., complete revascularization) or only on some (i.e., incomplete revascularization).
METHODS Patients were identified using the Veterans Affairs Clinical Assessment, Reporting, and Tracking program. Veterans Affairs and non-Veterans Affairs surgical records were used to link patients who underwent noncardiac surgery within 2 years after stent placement. Incomplete revascularization was defined as a residual stenosis of >= 50% in the left main coronary artery or >= 70% in another major epicardial coronary artery on the basis of operator visual estimate.
RESULTS In total, 4,332 patients (34.7%) had incomplete revascularization. A total of 567 MACE occurred within 1 month post-operatively. Patients with incomplete revascularization had an unadjusted 19% increased odds of postoperative MACE, compared with those with complete revascularization (odds ratio: 1.19; 95% confidence interval [CI]: 1.00 to 1.41). Among the MACE components, post-operative MI appears to contribute the most, with a 37% increased risk for post-operative MI among patients with incomplete revascularization (odds ratio: 1.37; 95% CI: 1.10 to 1.70). After adjustment, there was a significant interaction between time from PCI and outcomes after noncardiac surgery; incomplete revascularization was associated with significantly increased risk for post-operative MI primarily if surgery was performed within 6 weeks after PCI (adjusted odds ratio: 1.84; 95% CI: 1.04 to 2.38). The number of vessels with incomplete revascularization was also associated with an increased risk for post-operative MI: for each additional vessel with incomplete revascularization, there was a 17% increased odds of post-operative MI.
CONCLUSIONS Incomplete revascularization among patients with coronary artery disease is associated with an increased risk for MI after noncardiac surgery. (J Am Coll Cardiol Intv 2017; 10: 329-38) Published by Elsevier on behalf of the American College of Cardiology Foundation.
C1 [Armstrong, Ehrin J.; Waldo, Stephen W.; Valle, Javier A.; Maddox, Thomas M.] Denver VA Med Ctr, Sect Cardiol, Boulder, CO USA.
[Armstrong, Ehrin J.; Waldo, Stephen W.; Valle, Javier A.; Maddox, Thomas M.] Univ Colorado, Sch Med, Boulder, CO 80309 USA.
[Graham, Laura A.] Birmingham VA Med Ctr, Birmingham, AL USA.
[Hawn, Mary T.] Stanford Univ, Dept Surg, Stanford, CA USA.
RP Armstrong, EJ (reprint author), Denver VA Med Ctr, 1055 Clermont St, Denver, CO 80220 USA.
EM ehrin.armstrong@gmail.com
FU Veterans Affairs Health Services Research Development [IIR 09-347];
Merck Pharmaceuticals; Veterans Affairs Career Development Award
FX From the Section of Cardiology, Denver VA Medical Center and University
of Colorado School of Medicine, Aurora, Colorado; Birmingham VA Medical
Center, Birmingham, Alabama; and the Department of Surgery, Stanford
University, Stanford, California. This study was supported by Veterans
Affairs Health Services Research & Development (grant IIR 09-347). The
opinions expressed are those of the authors and not necessarily those of
the U.S. Department of Veterans Affairs or the U.S. government. Dr.
Armstrong is a consultant for Abbott Vascular, Boston Scientific,
Medtronic, Merck, Pfizer, and Spectranetics. Dr. Waldo has received
investigator-initiated research support from Merck Pharmaceuticals. Dr.
Maddox is supported by a Veterans Affairs Career Development Award. All
other authors have reported that they have no relationships relevant to
the contents of this paper to disclose.
NR 22
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PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1936-8798
EI 1876-7605
J9 JACC-CARDIOVASC INTE
JI JACC-Cardiovasc. Interv.
PD FEB 27
PY 2017
VL 10
IS 4
BP 329
EP 338
DI 10.1016/j.jcin.2016.11.001
PG 10
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP2QC
UT WOS:000397227200007
PM 28161261
ER
PT J
AU Athalye, VR
Ganguly, K
Costa, RM
Carmena, JM
AF Athalye, Vivek R.
Ganguly, Karunesh
Costa, Rui M.
Carmena, Jose M.
TI Emergence of Coordinated Neural Dynamics Underlies Neuroprosthetic
Learning and Skillful Control
SO NEURON
LA English
DT Article
ID BRAIN-MACHINE INTERFACES; MOTOR CORTEX; CORTICOSTRIATAL PLASTICITY;
NETWORK REORGANIZATION; VARIABILITY; ADAPTATION; TASK; NEURONS; DESIGN;
MODULATION
AB During motor learning, movements and underlying neural activity initially exhibit large trial-to-trial variability that decreases over learning. However, it is unclear how task-relevant neural populations coordinate to explore and consolidate activity patterns. Exploration and consolidation could happen for each neuron independently, across the population jointly, or both. We disambiguated among these possibilities by investigating how subjects learned de novo to control a brain-machine interface using neurons from motor cortex. We decomposed population activity into the sum of private and shared signals, which produce uncorrelated and correlated neural variance, respectively, and examined how these signals' evolution causally shapes behavior. We found that initially large trial-to-trial movement and private neural variability reduce over learning. Concomitantly, task-relevant shared variance increases, consolidating a manifold containing consistent neural trajectories that generate refined control. These results suggest that motor cortex acquires skillful control by leveraging both independent and coordinated variance to explore and consolidate neural patterns.
C1 [Athalye, Vivek R.; Carmena, Jose M.] Univ Calif Berkeley, Dept Elect Engn & Comp Engn, Berkeley, CA 94720 USA.
[Carmena, Jose M.] Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA.
[Carmena, Jose M.] Univ Calif Berkeley, UC Berkeley UCSF Joint Grad Program Bioengn, Berkeley, CA 94720 USA.
[Ganguly, Karunesh] San Francisco VA Med Ctr, Neurol & Rehabil Serv, San Francisco, CA 94121 USA.
[Ganguly, Karunesh] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA.
[Athalye, Vivek R.; Costa, Rui M.] Champalimaud Ctr Unknown, Champalimaud Neurosci Programme, Ave Brasilia, P-1400038 Lisbon, Portugal.
[Costa, Rui M.] Columbia Univ, Zuckerman Mind Brain Behav Inst, Dept Neurosci, New York, NY 10032 USA.
RP Carmena, JM (reprint author), Univ Calif Berkeley, Dept Elect Engn & Comp Engn, Berkeley, CA 94720 USA.; Carmena, JM (reprint author), Univ Calif Berkeley, Helen Wills Neurosci Inst, Berkeley, CA 94720 USA.; Carmena, JM (reprint author), Univ Calif Berkeley, UC Berkeley UCSF Joint Grad Program Bioengn, Berkeley, CA 94720 USA.; Costa, RM (reprint author), Champalimaud Ctr Unknown, Champalimaud Neurosci Programme, Ave Brasilia, P-1400038 Lisbon, Portugal.; Costa, RM (reprint author), Columbia Univ, Zuckerman Mind Brain Behav Inst, Dept Neurosci, New York, NY 10032 USA.
EM rui.costa@neuro.fchampalimaud.org; jcarmena@berkeley.edu
FU National Science Foundation Graduate Research Fellowship; ERA-NET;
European Research Council [COG 617142]; Howard Hughes Medical Institute
[IEC 55007415]; National Science Foundation [CBET-0954243, EFRI-M3C
1137267]; Office of Naval Research [N00014-15-1-2312]
FX We thank A. Motiwala, D. Kobaks, J. Semedo, P. Khanna, and S. Gowda for
helpful discussions, and R. Neely and S. Santacruz for manuscript
comments. We also thank the reviewers for helpful comments and
constructive suggestions. This work was supported by the National
Science Foundation Graduate Research Fellowship to V.R.A.; grants from
ERA-NET, European Research Council (COG 617142), and Howard Hughes
Medical Institute (IEC 55007415) to R.M.C.; and grants from the National
Science Foundation (CBET-0954243 and EFRI-M3C 1137267) and Office of
Naval Research (N00014-15-1-2312) to J.M.C.
NR 51
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U1 2
U2 2
PU CELL PRESS
PI CAMBRIDGE
PA 600 TECHNOLOGY SQUARE, 5TH FLOOR, CAMBRIDGE, MA 02139 USA
SN 0896-6273
EI 1097-4199
J9 NEURON
JI Neuron
PD FEB 22
PY 2017
VL 93
IS 4
BP 955
EP +
DI 10.1016/j.neuron.2017.01.016
PG 21
WC Neurosciences
SC Neurosciences & Neurology
GA EO1AE
UT WOS:000396429100022
PM 28190641
ER
PT J
AU Emens, JS
AF Emens, Jonathan S.
TI Circadian Rhythms: The Price of Electric Light
SO CURRENT BIOLOGY
LA English
DT Editorial Material
ID SLEEP; TIME
C1 [Emens, Jonathan S.] Oregon Hlth & Sci Univ, Oregon Inst Occupat Hlth Sci, Portland VA Med Ctr, Dept Psychiat, Portland, OR 97239 USA.
[Emens, Jonathan S.] Oregon Hlth & Sci Univ, Oregon Inst Occupat Hlth Sci, Portland VA Med Ctr, Dept Med, Portland, OR 97239 USA.
RP Emens, JS (reprint author), Oregon Hlth & Sci Univ, Oregon Inst Occupat Hlth Sci, Portland VA Med Ctr, Dept Psychiat, Portland, OR 97239 USA.; Emens, JS (reprint author), Oregon Hlth & Sci Univ, Oregon Inst Occupat Hlth Sci, Portland VA Med Ctr, Dept Med, Portland, OR 97239 USA.
EM emensj@ohsu.edu
NR 15
TC 0
Z9 0
U1 5
U2 5
PU CELL PRESS
PI CAMBRIDGE
PA 600 TECHNOLOGY SQUARE, 5TH FLOOR, CAMBRIDGE, MA 02139 USA
SN 0960-9822
EI 1879-0445
J9 CURR BIOL
JI Curr. Biol.
PD FEB 20
PY 2017
VL 27
IS 4
BP R144
EP R145
DI 10.1016/j.cub.2017.01.014
PG 2
WC Biochemistry & Molecular Biology; Cell Biology
SC Biochemistry & Molecular Biology; Cell Biology
GA EL6IF
UT WOS:000394724600009
PM 28222291
ER
PT J
AU McNamara, RK
Szeszko, PR
Smesny, S
Ikuta, T
Derosse, P
Vaz, FM
Milleit, B
Hipler, UC
Wiegand, C
Hesse, J
Amminger, GP
Malhotra, AK
Peters, BD
AF McNamara, Robert K.
Szeszko, Philip R.
Smesny, Stefan
Ikuta, Toshikazu
Derosse, Pamela
Vaz, Frederic M.
Milleit, Berko
Hipler, Uta-Christina
Wiegand, Cornelia
Hesse, Jana
Amminger, G. Paul
Malhotra, Anil K.
Peters, Bart D.
TI POLYUNSATURATED FATTY ACID BIOSTATUS, PHOSPHOLIPASE A(2) ACTIVITY AND
BRAIN WHITE MATTER MICROSTRUCTURE ACROSS ADOLESCENCE
SO NEUROSCIENCE
LA English
DT Article
DE white matter; myelin; polyunsaturated fatty acids; phospholipase;
adolescence; development
ID ARACHIDONIC-ACID; NERVOUS-SYSTEM; SCHIZOPHRENIA; DIFFUSION; ADULTHOOD;
RECEPTOR; CELLS; AGE; METABOLISM; CHILDHOOD
AB Adolescence is a period of major brain white matter (WM) changes, and membrane lipid metabolism likely plays a critical role in brain WM myelination. Long -chain polyunsaturated fatty acids (LC-PUFAs) are essential components of cell membranes including oligodendrocytes, and LC-PUFA release and turnover in membranes is regulated by phospholipase A(2) enzymes. To investigate the role of membrane lipid metabolism in healthy WM myelination across adolescence, the present study examined the relationship between membrane LC-PUFA biostatus, phospholipase A(2) activity, and brain WM microstructure in healthy subjects aged 9-20 years (n = 30). Diffusion tensor imaging (DTI) was performed to measure average fractional anisotropy (FA) and diffusivity (indices sensitive to WM myelination) of nine major cerebral WM tracts. Blood samples were collected to measure erythrocyte membrane fatty acid concentrations and plasma intracellular phospholipase A(2) activity (inPLA(2)). Plasma inPLA(2) activity showed a significant U-curved association with WM radial diffusivity, and an inverted U-curved association with WM FA, independent of age. A significant positive linear correlation was observed between docosahexaenoic acid concentration and axial diffusivity in the corpus callosum. These findings suggest that there may be optimal physiological inPLA(2) activity levels associated with healthy WM myelination in late childhood and adolescence. Myelination may be mediated by cleavage of docosahexaenoic acid from membrane phospholipids by inPLA(2). These findings have implications for our understanding of the role of LC-PUFA homeostasis in myelin related neurodevelopmental disorders. (C) 2016 IBRO. Published by Elsevier Ltd. All rights reserved.
C1 [McNamara, Robert K.] Univ Cincinnati, Coll Med, Dept Psychiat, Cincinnati, OH 45219 USA.
[Szeszko, Philip R.; Ikuta, Toshikazu; Derosse, Pamela; Malhotra, Anil K.; Peters, Bart D.] Zucker Hillside Hosp, Div Psychiat Res, Glen Oaks, NY 11004 USA.
[Szeszko, Philip R.; Ikuta, Toshikazu; Derosse, Pamela; Malhotra, Anil K.; Peters, Bart D.] Feinstein Inst Med Res, Ctr Psychiat Neurosci, Manhasset, NY 11030 USA.
[Smesny, Stefan] Univ Hosp Jena, Dept Psychiat, D-07743 Jena, Germany.
[Vaz, Frederic M.] Acad Med Ctr, Lab Genet Metab Dis, NL-1105 AZ Amsterdam, Netherlands.
[Milleit, Berko; Hipler, Uta-Christina; Wiegand, Cornelia; Hesse, Jana] Univ Hosp Jena, Dept Dermatol, Erfurter Str 35, D-07743 Jena, Germany.
[Amminger, G. Paul] Orygen, Parkville, Vic, Australia.
[Amminger, G. Paul] Univ Melbourne, Ctr Youth Mental Hlth, Parkville, Vic 3052, Australia.
[Szeszko, Philip R.] James J Peters Vet Adm Med Ctr, Bronx, NY 10468 USA.
[Szeszko, Philip R.] Icahn Sch Med Mt Sinai, New York, NY 10029 USA.
[Ikuta, Toshikazu] Univ Mississippi, Dept Commun Sci & Disorders, University, MS 38677 USA.
RP Peters, BD (reprint author), Vrije Univ Amsterdam, Dept Child & Adolescent Psychiat, Med Ctr, NL-1105 AZ Amsterdam, Netherlands.; Peters, BD (reprint author), Arkin Youth & Family, Baarsjesweg 224, NL-1058 AA Amsterdam, Netherlands.
EM mcnamar@ucmail.uc.edu; philip.szeszko@mssm.edu;
stefan.smesny@med.uni-jena.de; tikuta@umail.iu.edu; pderosse@NSHS.edu;
f.m.vaz@amc.uva.nl; berko.milleit@med.uni-jena.de;
christina.hipler@med.uni-jena.de; C.Wiegand@med.uni-jena.de;
jana.hesse@med.uni-jena.de; amminger@unimelb.edu.au; amalhotra@nshs.edu;
petersbart@hotmail.com
OI Ikuta, Toshikazu/0000-0003-0848-302X
FU National Institutes of Health [R01 MH076995, DK097599]; NSLIJ Research
Institute General Clinical Research Center [M01 RR018535]; Advanced
Center for Intervention and Services Research [P30 MH090590]; Center for
Intervention Development and Applied Research [P50 MH080173]; NARSAD
grant from the Brain and Behavior Research Foundation
FX Funding for this study was supported in part by grants from the National
Institutes of Health to Dr. Szeszko (R01 MH076995), to Dr. McNamara
(DK097599), the NSLIJ Research Institute General Clinical Research
Center (M01 RR018535), an Advanced Center for Intervention and Services
Research (P30 MH090590) and a Center for Intervention Development and
Applied Research (P50 MH080173 to Dr. Malhotra), and by a NARSAD grant
from the Brain and Behavior Research Foundation to Dr. Peters (2013).
The funding sources had no further role in study design; in the
collection, analysis and interpretation of data; in the writing of the
report; and in the decision to submit the paper for publication.
NR 59
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PU PERGAMON-ELSEVIER SCIENCE LTD
PI OXFORD
PA THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND
SN 0306-4522
EI 1873-7544
J9 NEUROSCIENCE
JI Neuroscience
PD FEB 20
PY 2017
VL 343
BP 423
EP 433
DI 10.1016/j.neuroscience.2016.12.007
PG 11
WC Neurosciences
SC Neurosciences & Neurology
GA EJ5PB
UT WOS:000393269100040
PM 27998778
ER
PT J
AU Haefeli, J
Ferguson, AR
Bingham, D
Orr, A
Won, SJ
Lam, TI
Shi, J
Hawley, S
Liu, JL
Swanson, RA
Massa, SM
AF Haefeli, Jenny
Ferguson, Adam R.
Bingham, Deborah
Orr, Adrienne
Won, Seok Joon
Lam, Tina I.
Shi, Jian
Hawley, Sarah
Liu, Jialing
Swanson, Raymond A.
Massa, Stephen M.
TI A data-driven approach for evaluating multi-modal therapy in traumatic
brain injury
SO SCIENTIFIC REPORTS
LA English
DT Article
ID SPINAL-CORD-INJURY; PRINCIPAL-COMPONENTS-ANALYSIS; VOLUNTARY EXERCISE;
MINOCYCLINE; PLASTICITY; RAT; NEUROGENESIS; IMPROVEMENT; STABILITY;
MICROGLIA
AB Combination therapies targeting multiple recovery mechanisms have the potential for additive or synergistic effects, but experimental design and analyses of multimodal therapeutic trials are challenging. To address this problem, we developed a data-driven approach to integrate and analyze raw source data from separate pre-clinical studies and evaluated interactions between four treatments following traumatic brain injury. Histologic and behavioral outcomes were measured in 202 rats treated with combinations of an anti-inflammatory agent (minocycline), a neurotrophic agent (LM11A-31), and physical therapy consisting of assisted exercise with or without botulinum toxin-induced limb constraint. Data was curated and analyzed in a linked workflow involving non-linear principal component analysis followed by hypothesis testing with a linear mixed model. Results revealed significant benefits of the neurotrophic agent LM11A-31 on learning and memory outcomes after traumatic brain injury. In addition, modulations of LM11A-31 effects by co-administration of minocycline and by the type of physical therapy applied reached statistical significance. These results suggest a combinatorial effect of drug and physical therapy interventions that was not evident by univariate analysis. The study designs and analytic techniques applied here form a structured, unbiased, internally validated workflow that may be applied to other combinatorial studies, both in animals and humans.
C1 [Haefeli, Jenny; Ferguson, Adam R.; Liu, Jialing] Univ Calif San Francisco, Dept Neurol Surg, BASIC, San Francisco, CA USA.
[Ferguson, Adam R.; Bingham, Deborah; Orr, Adrienne; Won, Seok Joon; Lam, Tina I.; Shi, Jian; Hawley, Sarah; Liu, Jialing; Swanson, Raymond A.; Massa, Stephen M.] San Francisco VA Med Ctr, San Francisco, CA 94121 USA.
[Won, Seok Joon; Lam, Tina I.; Shi, Jian; Swanson, Raymond A.; Massa, Stephen M.] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA.
RP Massa, SM (reprint author), San Francisco VA Med Ctr, San Francisco, CA 94121 USA.; Massa, SM (reprint author), Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA.
EM Stephen.Massa@ucsf.edu
FU Department of Veterans Affairs Research Enhancement Award Program Grant;
Craig H. Neilsen Foundation; NIH [R01NS067092, R01NS088475]; VA Merit
Reviews [I01BX000267, I01RX000655]
FX The authors thank Dr. Frank Longo, Stanford University, for the generous
provision of part of the LM11A-31 used in these studies. This work was
funded by a Department of Veterans Affairs Research Enhancement Award
Program Grant (RAS), the Craig H. Neilsen Foundation
(http://chnfoundation.org/) (JH and ARF), NIH R01NS067092 (ARF),
R01NS088475 (ARF) (https://grants.nih.gov/grants/oer.htm), and VA Merit
Reviews (http://www.research.va.gov/) I01BX000267 (SMM) and I01RX000655
(JL). The funders had no role in study design, data collection and
analysis, decision to publish, or preparation of the manuscript.
NR 54
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PU NATURE PUBLISHING GROUP
PI LONDON
PA MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
SN 2045-2322
J9 SCI REP-UK
JI Sci Rep
PD FEB 16
PY 2017
VL 7
AR 42474
DI 10.1038/srep42474
PG 10
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EK9CB
UT WOS:000394220400001
PM 28205533
ER
PT J
AU Xie, JX
Glorioso, TJ
Dattilo, PB
Aggarwal, V
Ho, PM
Baron, AE
Donaldson, D
Armstrong, EJ
Klein, A
Giri, J
Tsai, TT
AF Xie, Joe X.
Glorioso, Thomas J.
Dattilo, Philip B.
Aggarwal, Vikas
Ho, P. Michael
Baron, Anna E.
Donaldson, Darcy
Armstrong, Ehrin J.
Klein, Andrew
Giri, Jay
Tsai, Thomas T.
TI Effect of Chronic Kidney Disease on Mortality in Patients Who Underwent
Lower Extremity Peripheral Vascular Intervention
SO AMERICAN JOURNAL OF CARDIOLOGY
LA English
DT Article
ID PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY; GLOMERULAR-FILTRATION-RATE;
ALL-CAUSE MORTALITY; ARTERIAL-DISEASE; CARDIOVASCULAR-DISEASE;
RENAL-INSUFFICIENCY; CARDIAC-CATHETERIZATION; UNITED-STATES;
RISK-FACTOR; HEART
AB It is known that chronic kidney disease (CKD) is associated with increased postoperative morbidity and mortality in patients with peripheral artery disease who underwent lower extremity surgical revascularization; however, outcomes after peripheral vascular intervention (PVI) are less well established. This study sought to determine the impact of CKD on adverse outcomes in patients with peripheral artery disease who underwent PVI. Using data from the Veteran Affairs Clinical Assessment, Reporting, and Tracking System Program, we identified a cohort of 755 patients who underwent lower extremity PVI from June 2005 to August 2010 at 33 sites. The outcomes of interest were mortality, progression to dialysis, myocardial infarction, limb amputation, and stroke. Kaplan-Meier survival analysis and Cox proportional hazard frailty models assessed the association between CKD and adverse outcomes. Of the patients who underwent lower extremity PVI, 201 patients (27%) had CKD. The presence of CKD was associated with decreased survival (5-year survival probability of CKD compared with non-CKD: 49.9% [41.6% to 59.9%] vs 80.1% [76.2% to 84.1]), which persisted after risk adjustment (BR 1.57; 95% confidence interval 1.13 to 2.19). In addition, there was a significant association between CKD and progression to dialysis (HR 6.62; 95% confidence interval 2.25 to 19.43). In contrast, there was no association between CKD and re-hospitalization for myocardial infarction, limb amputation, or stroke. In conclusion, CKD is present in 1 of 4 patients who underwent PVI and is associated with increased risk of mortality and progression to dialysis. (C) 2016 Elsevier Inc. All rights reserved.
C1 [Xie, Joe X.; Dattilo, Philip B.; Aggarwal, Vikas; Tsai, Thomas T.] Univ Colorado, Dept Med, Sch Med, Aurora, CO 80045 USA.
[Glorioso, Thomas J.; Ho, P. Michael; Baron, Anna E.; Donaldson, Darcy; Armstrong, Ehrin J.; Tsai, Thomas T.] VA Eastern Colorado Hlth Care Syst, Div Cardiol, Denver, CO 80220 USA.
[Klein, Andrew] St Louis Univ, Med Ctr, Div Cardiol, St Louis, MO 63110 USA.
[Giri, Jay] Philadelphia VA Med Ctr, Div Cardiol, Philadelphia, PA USA.
[Tsai, Thomas T.] Kaiser Permanente Colorado, Inst Hlth Res, Denver, CO 80247 USA.
RP Tsai, TT (reprint author), Univ Colorado, Dept Med, Sch Med, Aurora, CO 80045 USA.; Tsai, TT (reprint author), VA Eastern Colorado Hlth Care Syst, Div Cardiol, Denver, CO 80220 USA.; Tsai, TT (reprint author), Kaiser Permanente Colorado, Inst Hlth Res, Denver, CO 80247 USA.
EM thomas.tsai@coloradooutcomes.org
FU VHA HSR&D grant, Denver, Colorado [RRP 09-120]
FX This work was supported by a VHA HSR&D grant (RRP 09-120, Treatment and
Outcomes among Veterans with Peripheral Arterial Disease), Denver,
Colorado.
NR 29
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U1 0
U2 0
PU EXCERPTA MEDICA INC-ELSEVIER SCIENCE INC
PI BRIDGEWATER
PA 685 ROUTE 202-206 STE 3, BRIDGEWATER, NJ 08807 USA
SN 0002-9149
EI 1879-1913
J9 AM J CARDIOL
JI Am. J. Cardiol.
PD FEB 15
PY 2017
VL 119
IS 4
BP 669
EP 674
DI 10.1016/j.amjcard.2016.10.053
PG 6
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EL6IJ
UT WOS:000394725100026
PM 28027725
ER
PT J
AU Cline, MM
Yumul, JC
Hysa, L
Murra, D
Garvin, GG
Cook, DG
Ladiges, WC
Minoshimaa, S
Cross, DJ
AF Cline, Marcella M.
Yumul, Josh C.
Hysa, Lisa
Murra, Dalia
Garvin, Gregory G.
Cook, David G.
Ladiges, Warren C.
Minoshimaa, Satoshi
Cross, Donna J.
TI Novel application of a Radial Water Tread maze can distinguish cognitive
deficits in mice with traumatic brain injury
SO BRAIN RESEARCH
LA English
DT Article
DE Traumatic brain injury; Cognitive testing; Behavioral testing; Water
maze; Controlled-cortical impact
ID CONTROLLED CORTICAL IMPACT; CIRCULAR MAZE; MOUSE MODEL; RAT; TASKS;
PERFORMANCE; IMPAIRMENT; RESPONSES; SEARCH
AB Introduction: The use of forced-swim, rat-validated cognition tests in mouse models of traumatic brain injury (TBI) raises methodological concerns; such models are vulnerable to a number of confounding factors including impaired motor function and stress-induced non-compliance (failure to swim). This study evaluated the ability of a Radial Water Tread (RWT) maze, designed specifically for mice, that requires no swimming to distinguish mice with controlled cortical impact (CCI) induced TBI and Sham controls.
Methods: Ten-week-old, male C57BL6/J mice were randomly assigned to receive either Sham (n = 14) or CCI surgeries (n = 15). Mice were tested for sensorimotor deficits via Gridwalk test and Noldus CatWalk gait analysis at I and 32 days post-injury. Mice received RWT testing at either 11 days (early time point) or 35 days (late time point) post-injury.
Results: Compared to Sham-treated animals, CCI-induced TBI resulted in significant impairment in RWT maze performance. Additionally, CCI injured mice displayed significant deficits on the Gridwalk test at both I day and 32 days post-injury, and impairment in the CatWalk task at 1 day, but not 32 days, compared to Shams.
Conclusions: The Radial Water Tread maze capitalizes on the natural tendency of mice to avoid open areas in favor of hugging the edges of an apparatus (thigmotaxis), and replaces a forced-swim model with water shallow enough that the animal is not required to swim, but aversive enough to motivate escape. Our findings indicate the RWT task is a sensitive species-appropriate behavioral test for evaluating spatial memory impairment in a mouse model of TBI. (C) 2016 Elsevier B.V. All rights reserved.
C1 [Cline, Marcella M.; Yumul, Josh C.; Hysa, Lisa; Murra, Dalia; Garvin, Gregory G.; Minoshimaa, Satoshi; Cross, Donna J.] Univ Washington, Dept Radiol, Seattle, WA USA.
[Ladiges, Warren C.] Univ Washington, Dept Comparat Med, Seattle, WA USA.
[Garvin, Gregory G.; Minoshimaa, Satoshi; Cross, Donna J.] Univ Utah, Dept Radiol, 30 North 1900 East 1A71, Salt Lake City, UT 84132 USA.
[Cook, David G.] Univ Washington, Dept Pharmacol, Seattle, WA USA.
[Cook, David G.] VA Puget Sound Hlth Care Syst, Geriatr Res Educ & Clin Ctr GRECC, Seattle, WA USA.
RP Cross, DJ (reprint author), Univ Utah, Dept Radiol, 30 North 1900 East 1A71, Salt Lake City, UT 84132 USA.
EM donna.cross@hsc.utah.edu
OI Cline, Marcella/0000-0002-9590-3725
FU Institute for Translational Health Sciences [UL1TR000423]; University of
Washington Center on Human Development and Disability; University of
Washington Animal Behavior Core and Brain Imaging Core; Department of
Veterans Affairs Office of Research and Development Medical Research
Service; University of Washington Friends of Alzheimer's Research; UW
Royalty Research Fund
FX This research was supported a by the Institute for Translational Health
Sciences pilot project grant opportunity (UL1TR000423), the University
of Washington Center on Human Development and Disability, University of
Washington Animal Behavior Core and Brain Imaging Core, the Department
of Veterans Affairs Office of Research and Development Medical Research
Service (DGC), University of Washington Friends of Alzheimer's Research
(DGC), and the UW Royalty Research Fund (DGC). We also thank Toby Cole
for his assistance with this project.
NR 32
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 0006-8993
EI 1872-6240
J9 BRAIN RES
JI Brain Res.
PD FEB 15
PY 2017
VL 1657
BP 140
EP 147
DI 10.1016/j.brainres.2016.11.027
PG 8
WC Neurosciences
SC Neurosciences & Neurology
GA EL9DI
UT WOS:000394919200015
PM 27923635
ER
PT J
AU Walker, RH
Danek, A
AF Walker, Ruth H.
Danek, Adrian
TI Response to "Neuroacanthocytosis: A case with unusual clinical features
and novel response to treatment" by Wu et al
SO JOURNAL OF THE NEUROLOGICAL SCIENCES
LA English
DT Letter
DE Neuroacanthocytosis; Chorea
ID HARP
C1 [Walker, Ruth H.] James J Peters Vet Affairs Med Ctr, Dept Neurol, Bronx, NY 10468 USA.
[Walker, Ruth H.] Mt Sinai Sch Med, New York, NY USA.
[Danek, Adrian] Univ Munich, Neurol Klin & Poliklin, Munich, Germany.
RP Walker, RH (reprint author), James J Peters Vet Affairs Med Ctr, Dept Neurol 127, Bronx, NY 10468 USA.
EM ruth.walker@mssm.edu
NR 8
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 0022-510X
EI 1878-5883
J9 J NEUROL SCI
JI J. Neurol. Sci.
PD FEB 15
PY 2017
VL 373
BP 347
EP 347
DI 10.1016/j.jns.2016.12.004
PG 1
WC Clinical Neurology; Neurosciences
SC Neurosciences & Neurology
GA EK8US
UT WOS:000394200700079
PM 27955933
ER
PT J
AU Price, RB
Lane, S
Gates, K
Kraynak, TE
Horner, MS
Thase, ME
Siegle, GJ
AF Price, Rebecca B.
Lane, Stephanie
Gates, Kathleen
Kraynak, Thomas E.
Horner, Michelle S.
Thase, Michael E.
Siegle, Greg J.
TI Parsing Heterogeneity in the Brain Connectivity of Depressed and Healthy
Adults During Positive Mood
SO BIOLOGICAL PSYCHIATRY
LA English
DT Article
DE Community detection; Depression; fMRI; Neural network connectivity;
Positive mood; S-GIMME
ID DEFAULT-MODE NETWORK; MAJOR DEPRESSION; FUNCTIONAL CONNECTIVITY;
EMOTIONAL INFORMATION; DISORDER; FMRI; INDIVIDUALS; METAANALYSIS;
HYPOTHESIS; RETRIEVAL
AB BACKGROUND: There is well-known heterogeneity in affective mechanisms in depression that may extend to positive affect. We used data-driven parsing of neural connectivity to reveal subgroups present across depressed and healthy individuals during positive processing, informing targets for mechanistic intervention.
METHODS: Ninety-two individuals (68 depressed patients, 24 never-depressed control subjects) completed a sustained positive mood induction during functional magnetic resonance imaging. Directed functional connectivity paths within a depression-relevant network were characterized using Group Iterative Multiple Model Estimation (GIMME), a method shown to accurately recover the direction and presence of connectivity paths in individual participants. During model selection, individuals were clustered using community detection on neural connectivity estimates. Subgroups were externally tested across multiple levels of analysis.
RESULTS: Two connectivity-based subgroups emerged: subgroup A, characterized by weaker connectivity overall, and subgroup B, exhibiting hyperconnectivity (relative to subgroup A), particularly among ventral affective regions. Subgroup predicted diagnostic status (subgroup B contained 81% of patients; 50% of control subjects; chi(2) = 8.6, p = .003) and default mode network connectivity during a separate resting-state task. Among patients, subgroup B members had higher self-reported symptoms, lower sustained positive mood during the induction, and higher negative bias on a reaction-time task. Symptom-based depression subgroups did not predict these external variables.
CONCLUSIONS: Neural connectivity-based categorization travels with diagnostic category and is clinically predictive, but not clinically deterministic. Both patients and control subjects showed heterogeneous, and overlapping, profiles. The larger and more severely affected patient subgroup was characterized by ventrally driven hyperconnectivity during positive processing. Data-driven parsing suggests heterogeneous substrates of depression and possible resilience in control subjects in spite of biological overlap.
C1 [Price, Rebecca B.; Siegle, Greg J.] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA.
[Kraynak, Thomas E.] Univ Pittsburgh, Dept Psychol, Pittsburgh, PA 15260 USA.
[Thase, Michael E.] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Thase, Michael E.] Philadelphia Vet Affairs Med Ctr, Philadelphia, PA USA.
[Lane, Stephanie; Gates, Kathleen] Univ N Carolina, Chapel Hill, NC USA.
Johns Hopkins Sch Med, Baltimore, MD USA.
RP Price, RB (reprint author), Univ Pittsburgh, Western Psychiat Inst & Clin, 3811 OHara St, Pittsburgh, PA 15213 USA.
EM rebecca.price@stanfordalumni.org
FU National Institute of Biomedical Imaging and Bioengineering
[R21EB015573]; National Institutes of Health [MH074807, MH082998,
MH58356, MH58397, MH69618]; Pittsburgh Foundation; Emmerling Fund;
National Institutes of Health Career Development Award [K23MH100259];
Alkermes; Shire US Inc; Allergan; AstraZeneca; BristolMyers Squibb
Company; Cerecor, Inc; Eli Lilly Co; Forest Laboratories; Gerson Lehrman
Group; Fabre-Kramer Pharmaceuticals, Inc.; GlaxoSmithKline; Guidepoint
Global; H. Lundbeck A/S; MedAvante, Inc.; Merck and Co. Inc.; Moksha8;
Naurex, Inc.; Neuronetics, Inc.; Novartis; Ortho-McNeil Pharmaceuticals;
Otsuka; Pamlab; LLC; Pfizer; Sunovion Pharmaceuticals, Inc.; Trius
Therapeutical, Inc.; Takeda
FX This research was supported by Grant No. R21EB015573 from the National
Institute of Biomedical Imaging and Bioengineering (to KG); Grant Nos.
MH074807, MH082998, MH58356, MH58397, and MH69618 from the National
Institutes of Health; the Pittsburgh Foundation; and the Emmerling Fund.
NR 56
TC 2
Z9 2
U1 2
U2 2
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0006-3223
EI 1873-2402
J9 BIOL PSYCHIAT
JI Biol. Psychiatry
PD FEB 15
PY 2017
VL 81
IS 4
BP 347
EP 357
DI 10.1016/j.biopsych.2016.06.023
PG 11
WC Neurosciences; Psychiatry
SC Neurosciences & Neurology; Psychiatry
GA EO9MT
UT WOS:000397013500014
PM 27712830
ER
PT J
AU Babic, JT
Sofjan, A
Babin, M
Echevarria, K
Ikwuagwu, JO
Lam, WYM
Aitken, SL
Perez, KK
AF Babic, Jessica T.
Sofjan, Amelia
Babin, Margaret
Echevarria, Kelly
Ikwuagwu, Judy O.
Lam, Wai-Ying M.
Aitken, Samuel L.
Perez, Katherine K.
TI Significant publications on infectious diseases pharmacotherapy in 2015
SO AMERICAN JOURNAL OF HEALTH-SYSTEM PHARMACY
LA English
DT Article
DE antiinfective agents; communicable diseases; drug therapy; microbiology;
publications; therapeutic use
ID SUSCEPTIBLE STAPHYLOCOCCUS-AUREUS; BLOOD-STREAM INFECTIONS;
CLINICAL-PRACTICE GUIDELINES; RESISTANT ENTEROCOCCAL BACTEREMIA;
COMBINATION ANTIFUNGAL THERAPY; TENOFOVIR DISOPROXIL FUMARATE;
RANDOMIZED CONTROLLED-TRIAL; CRITICALLY-ILL PATIENTS; INVASIVE
ASPERGILLOSIS; HIV-1 INFECTION
AB Purpose. The most important articles on infectious diseases (ID) pharmacotherapy published in the peer-reviewed literature in 2015, as nominated and selected by panels of pharmacists and others with ID expertise, are summarized.
Summary. Members of the Houston Infectious Diseases Network were asked to nominate articles published in prominent peer-reviewed journals in 2015 that were thought to have a major impact in the field of ID pharmacotherapy. A list of 55 nominated articles on general ID-related topics and 10 articles specifically related to human immunodeficiency virus (HIV) infection or acquired immunodeficiency syndrome (AIDS) was compiled. In a national online survey, members of the Society of Infectious Diseases Pharmacists (SIDP) were asked to select from the list 10 general ID articles believed to have made a significant contribution to the field of ID pharmacotherapy and 1 article contributing to HIV/AIDS pharmacotherapy. Of the 361 SIDP members surveyed, 153 (42%) and 76 (21%) participated in the selection of general ID-related articles and. HIV/AIDS-related articles, respectively. The 11 highest-ranked publications (10 general ID-related articles and 1 HIV/AIDS-related article) are summarized here.
Conclusion. With the growing number of significant ID-related publications each year, it can be challenging to stay current with the literature. This review of important ID pharmacotherapy publications in 2015 may be helpful in identifying key articles and lessening this burden.
C1 [Babic, Jessica T.] Univ Houston, Coll Pharm, CHI St Lukes Hlth Baylor St Lukes Med Ctr, Houston, TX 77030 USA.
[Sofjan, Amelia] Univ Houston, Coll Pharm, Dept Pharm Practice & Translat Res, Houston, TX 77030 USA.
[Babin, Margaret] Tomball Reg Med Ctr, Tomball, TX USA.
[Echevarria, Kelly] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Ikwuagwu, Judy O.] Houston Methodist Hosp Pharm Serv, Houston, TX USA.
[Lam, Wai-Ying M.] Univ Texas Med Branch, Galveston, TX 77555 USA.
[Aitken, Samuel L.] Univ Texas MD Anderson Canc Ctr, Div Pharm, Houston, TX 77030 USA.
[Aitken, Samuel L.] UTHlth McGovern Med Sch, Ctr Antimicrobial Resistance & Microbial Gen, Houston, TX USA.
[Perez, Katherine K.] Houston Methodist Hosp, Dept Pathol & Genom Med, Houston, TX USA.
[Perez, Katherine K.] Houston Methodist Hosp, Dept Pharm, Houston, TX USA.
RP Perez, KK (reprint author), Houston Methodist Hosp, Dept Pathol & Genom Med, Houston, TX USA.; Perez, KK (reprint author), Houston Methodist Hosp, Dept Pharm, Houston, TX USA.
EM kkperez@houstonmethodist.org
NR 89
TC 0
Z9 0
U1 0
U2 0
PU AMER SOC HEALTH-SYSTEM PHARMACISTS
PI BETHESDA
PA 7272 WISCONSIN AVE, BETHESDA, MD 20814 USA
SN 1079-2082
EI 1535-2900
J9 AM J HEALTH-SYST PH
JI Am. J. Health-Syst. Pharm.
PD FEB 15
PY 2017
VL 74
IS 4
BP 238
EP 252
DI 10.2146/ajhp160090
PG 15
WC Pharmacology & Pharmacy
SC Pharmacology & Pharmacy
GA EK4XG
UT WOS:000393930600013
PM 28082303
ER
PT J
AU Almoguera, B
Vazquez, L
Mentch, F
Connolly, J
Pacheco, JA
Sundaresan, AS
Peissig, PL
Linneman, JG
McCarty, CA
Crosslin, D
Carrell, DS
Lingren, T
Namjou-Khales, B
Harley, JB
Larson, E
Jarvik, GP
Brilliant, M
Williams, MS
Kullo, LJ
Hysinger, EB
Sleiman, PMA
Hakonarson, H
AF Almoguera, Berta
Vazquez, Lyam
Mentch, Frank
Connolly, John
Pacheco, Jennifer A.
Sundaresan, Agnes S.
Peissig, Peggy L.
Linneman, James G.
McCarty, Catherine A.
Crosslin, David
Carrell, David S.
Lingren, Todd
Namjou-Khales, Bahram
Harley, John B.
Larson, Eric
Jarvik, Gail P.
Brilliant, Murray
Williams, Marc S.
Kullo, Lftikhar J.
Hysinger, Erik B.
Sleiman, Patrick M. A.
Hakonarson, Hakon
TI Identification of Four Novel Loci in Asthma in European American and
African American Populations
SO AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE
LA English
DT Article
DE asthma; genetics; genome-wide association study
ID GENOME-WIDE ASSOCIATION; VARIANTS; SUSCEPTIBILITY; EXPRESSION; CARE;
RISK; INFLAMMATION; DISPARITIES; COMPONENTS; CHILDREN
AB Rationale: Despite significant advances in knowledge of the genetic architecture of asthma, specific contributors to the variability in the burden between populations remain uncovered.
Objectives: To identify additional genetic susceptibility factors of asthma in European American and African American populations.
Methods: A phenotyping algorithm mining electronic medical records was developed and validated to recruit cases with asthma and control subjects from the Electronic Medical Records and Genomics network. Genome-wide association analyses were performed in pediatric and adult asthma cases and control subjects with European American and African American ancestry followed by metaanalysis. Nominally significant results were reanalyzed conditioning on allergy status.
Measurements and Main Results: The validation of the algorithm yielded an average of 95.8% positive predictive values for both cases and control subjects. The algorithm accrued 21,644 subjects (65.83% European American and 34.17% African American). We identified four novel population-specific associations with asthma after metaanalyses: loci 6p21.31, 9p21.2, and 10q21.3 in the European American population, and the PTGES gene in African Americans. TEK at 9p21.2, which encodes TIE2, has been shown to be involved in remodeling the airway wall in asthma, and the association remained significant after conditioning by allergy. PTGES, which encodes the prostaglandin E synthase, has also been linked to asthma, where deficient Prostaglandin E-2 synthesis has been associated with airway remodeling.
Conclusions: This study adds to understanding of the genetic architecture of asthma in European Americans and African Americans and reinforces the need to study populations of diverse ethnic backgrounds to identify shared and unique genetic predictors of asthma.
C1 [Almoguera, Berta; Vazquez, Lyam; Mentch, Frank; Connolly, John; Hysinger, Erik B.; Sleiman, Patrick M. A.; Hakonarson, Hakon] Childrens Hosp Philadelphia, Ctr Appl Genom, Philadelphia, PA 19104 USA.
[Pacheco, Jennifer A.] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA.
[Sundaresan, Agnes S.; Williams, Marc S.] Geisinger Hlth Syst, Danville, PA USA.
[Peissig, Peggy L.; Linneman, James G.; Brilliant, Murray] Marshfield Clin Res Fdn, Marshfield, WI USA.
[McCarty, Catherine A.] Essentia Inst Rural Hlth, Duluth, MN USA.
[Crosslin, David; Jarvik, Gail P.] Univ Washington, Med Ctr, Seattle, WA 98195 USA.
[Carrell, David S.; Larson, Eric] Grp Hlth Res Inst, Seattle, WA USA.
[Lingren, Todd; Namjou-Khales, Bahram; Harley, John B.] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA.
[Harley, John B.] US Dept Vet Affairs, Med Ctr, Cincinnati, OH USA.
[Kullo, Lftikhar J.] Mayo Clin, Rochester, MN USA.
[Sleiman, Patrick M. A.; Hakonarson, Hakon] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA.
RP Sleiman, PMA (reprint author), Childrens Hosp Philadelphia, Ctr Appl Genom, Leonard Madlyn Abramson Res Ctr, 3615 Civ Ctr Blvd,Suite 1216E, Philadelphia, PA 19104 USA.
EM sleimanp@email.chop.edu
FU U.S. Department of Veterans Affairs; Electronic Medical Records and
Genomics network
FX The authors thank all patients and control subjects for their
participation in the study. They also thank the U.S. Department of
Veterans Affairs and the Electronic Medical Records and Genomics network
and co-directors, Teri Manolio and Rongling Li, for their support.
NR 49
TC 1
Z9 1
U1 9
U2 9
PU AMER THORACIC SOC
PI NEW YORK
PA 25 BROADWAY, 18 FL, NEW YORK, NY 10004 USA
SN 1073-449X
EI 1535-4970
J9 AM J RESP CRIT CARE
JI Am. J. Respir. Crit. Care Med.
PD FEB 15
PY 2017
VL 195
IS 4
BP 456
EP 463
DI 10.1164/rccm.201604-0861OC
PG 8
WC Critical Care Medicine; Respiratory System
SC General & Internal Medicine; Respiratory System
GA EK1ZD
UT WOS:000393725700011
PM 27611488
ER
PT J
AU McKinney, B
Ding, Y
Lewis, DA
Sweet, RA
AF McKinney, B.
Ding, Y.
Lewis, D. A.
Sweet, R. A.
TI DNA methylation as a putative mechanism for reduced dendritic spine
density in the superior temporal gyrus of subjects with schizophrenia
SO TRANSLATIONAL PSYCHIATRY
LA English
DT Article
ID BIPOLAR DISORDER; HUMAN BRAIN; NEUROPSYCHIATRIC DISORDERS;
PSYCHIATRIC-DISORDERS; AUDITORY-CORTEX; GENE-EXPRESSION; FRONTAL-CORTEX;
SAP97 GENE; RISK; POSTMORTEM
AB Reduced dendritic spine density (DSD) in cortical layer 3 of the superior temporal gyrus (STG), and multiple other brain regions, is consistently observed in postmortem studies of schizophrenia (SZ). Elucidating the molecular mechanisms of this intermediate phenotype holds promise for understanding SZ pathophysiology, identifying SZ treatment targets and developing animal models. DNA methylation (DNAm), the addition of a methyl group to a cytosine nucleotide, regulates gene transcription and is a strong candidate for such a mechanism. We tested the hypothesis that DNAm correlates with DSD in the human STG and that this relationship is disrupted in SZ. We used the Illumina Infinium Human Methylation 450 Beadchip Array to quantify DNAm on a genome-wide scale in the postmortem STG from 22 SZ subjects and matched non-psychiatric control (NPC) subjects; DSD measures were available for 17 of the 22 subject pairs. We found DNAm to correlate with DSD at more sites than expected by chance in NPC, but not SZ, subjects. In addition, we show that the slopes of the linear DNAm-DSD correlations differed between SZ and NPC subjects at more sites than expected by chance. From these data, we identified 2 candidate genes for mediating DSD abnormalities in SZ: brain-specific angiogenesis inhibitor 1-associated protein 2 (BAIAP2) and discs large, Drosophila, homolog of, 1 (DLG1). Together, these data suggest that altered DNAm in SZ may be a mechanism for SZ-related DSD reductions.
C1 [McKinney, B.; Lewis, D. A.; Sweet, R. A.] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA.
[McKinney, B.; Lewis, D. A.; Sweet, R. A.] Univ Pittsburgh, Translat Neurosci Program, Pittsburgh, PA USA.
[Ding, Y.] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15261 USA.
[Lewis, D. A.] Univ Pittsburgh, Dept Neurosci, Pittsburgh, PA USA.
[Sweet, R. A.] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15260 USA.
[Sweet, R. A.] VA Pittsburgh Healthcare Syst, Mental Illness Res Educ & Clin Ctr, Pittsburgh, PA USA.
RP Sweet, RA (reprint author), MIRECC, Dept Psychiat Neurol & VISN 4, Biomed Sci Tower,Room W-1645,3811 OHara St, Pittsburgh, PA 15213 USA.
EM sweetra@upmc.edu
OI McKinney, Brandon/0000-0002-0663-7569
FU NIH [RO1 MH071533, RO3 MH108849, T32 MH016804, KL2 TR001856]
FX This work was supported by NIH Grants RO1 MH071533 (RAS), RO3 MH108849
(YD), T32 MH016804 (BCM), and KL2 TR001856 (BCM). The content is solely
the responsibility of the authors and does not necessarily represent the
official views of the National Institutes of Health, the Department of
Veterans Affairs, or the United States Government.
NR 72
TC 0
Z9 0
U1 2
U2 2
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 2158-3188
J9 TRANSL PSYCHIAT
JI Transl. Psychiatr.
PD FEB 14
PY 2017
VL 7
AR e1032
DI 10.1038/tp.2016.297
PG 8
WC Psychiatry
SC Psychiatry
GA EP2LG
UT WOS:000397214000005
PM 28195572
ER
PT J
AU Atkinson, TM
Giraud, GD
Togioka, BM
Jones, DB
Cigarroa, JE
AF Atkinson, Tamara M.
Giraud, George D.
Togioka, Brandon M.
Jones, Daniel B.
Cigarroa, Joaquin E.
TI Cardiovascular and Ventilatory Consequences of Laparoscopic Surgery
SO CIRCULATION
LA English
DT Article
DE cardiovascular complications; surgery
ID CARBON-DIOXIDE PNEUMOPERITONEUM; IMPROVEMENT PROGRAM DATABASE;
INTRA-ABDOMINAL PRESSURE; NONCARDIAC SURGERY; HEMODYNAMIC-CHANGES;
CARDIAC RISK; TRANSESOPHAGEAL ECHOCARDIOGRAPHY; INTRAABDOMINAL PRESSURE;
FONTAN PHYSIOLOGY; AMERICAN-COLLEGE
AB Although laparoscopic surgery accounts for >2 million surgical procedures every year, the current preoperative risk scores and guidelines do not adequately assess the risks of laparoscopy. In general, laparoscopic procedures have a lower risk of morbidity and mortality compared with operations requiring a midline laparotomy. During laparoscopic surgery, carbon dioxide insufflation may produce significant hemodynamic and ventilatory consequences such as increased intraabdominal pressure and hypercarbia. Hemodynamic insults secondary to increased intraabdominal pressure include increased afterload and preload and decreased cardiac output, whereas ventilatory consequences include increased airway pressures, hypercarbia, and decreased pulmonary compliance. Hemodynamic effects are accentuated in patients with cardiovascular disease such as congestive heart failure, ischemic heart disease, valvular heart disease, pulmonary hypertension, and congenital heart disease. Prevention of cardiovascular complications may be accomplished through a sound understanding of the hemodynamic and physiological consequences of laparoscopic surgery as well as a defined operative plan generated by a multidisciplinary team involving the preoperative consultant, anesthesiologist, and surgeon.
C1 [Atkinson, Tamara M.; Giraud, George D.] Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, Portland, OR 97201 USA.
[Togioka, Brandon M.] Oregon Hlth & Sci Univ, Dept Anesthesiol & Perioperat Med, Portland, OR 97201 USA.
[Atkinson, Tamara M.; Giraud, George D.] Portland VA Med Ctr, Div Cardiol, Portland, OR USA.
[Jones, Daniel B.] Harvard Univ, Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA.
RP Cigarroa, JE (reprint author), Oregon Hlth & Sci Univ, Knight Cardiovasc Inst, Cardiovasc Div, UHN 62,3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
EM Cigarroa@ohsu.edu
NR 68
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 0009-7322
EI 1524-4539
J9 CIRCULATION
JI Circulation
PD FEB 14
PY 2017
VL 135
IS 7
BP 700
EP 710
DI 10.1161/CIRCULATIONAHA.116.023262
PG 11
WC Cardiac & Cardiovascular Systems; Peripheral Vascular Disease
SC Cardiovascular System & Cardiology
GA EK5XB
UT WOS:000393998400015
PM 28193800
ER
PT J
AU Shi, YJ
Jiang, XY
Zhang, LL
Pu, HJ
Hu, XM
Zhang, WT
Cai, W
Gao, YQ
Leak, RK
Keep, RF
Bennett, MVL
Chen, J
AF Shi, Yejie
Jiang, Xiaoyan
Zhang, Lili
Pu, Hongjian
Hu, Xiaoming
Zhang, Wenting
Cai, Wei
Gao, Yanqin
Leak, Rehana K.
Keep, Richard F.
Bennett, Michael V. L.
Chen, Jun
TI Endothelium-targeted overexpression of heat shock protein 27 ameliorates
blood-brain barrier disruption after ischemic brain injury
SO PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF
AMERICA
LA English
DT Article
DE endothelial cell; stress fiber; tight junction; neuroinflammation; HSP27
ID FOCAL CEREBRAL-ISCHEMIA; STRESS FIBERS; ACTIN POLYMERIZATION; SIGNALING
PATHWAY; NEURONAL INJURY; HSP27 PROTECTS; CELL-DEATH; STROKE;
MATRIX-METALLOPROTEINASE-9; INHIBITOR
AB The damage borne by the endothelial cells (ECs) forming the blood-brain barrier (BBB) during ischemic stroke and other neurological conditions disrupts the structure and function of the neurovascular unit and contributes to poor patient outcomes. We recently reported that structural aberrations in brain microvascular ECs-namely, uncontrolled actin polymerization and subsequent disassembly of junctional proteins, are a possible cause of the early onset BBB breach that arises within 30-60 min of reperfusion after transient focal ischemia. Here, we investigated the role of heat shock protein 27 (HSP27) as a direct inhibitor of actin polymerization and protectant against BBB disruption after ischemia/reperfusion (I/R). Using in vivo and in vitro models, we found that targeted overexpression of HSP27 specifically within ECs-but not within neurons-ameliorated BBB impairment 1-24 h after I/R. Mechanistically, HSP27 suppressed I/R-induced aberrant actin polymerization, stress fiber formation, and junctional protein translocation in brain microvascular ECs, independent of its protective actions against cell death. By preserving BBB integrity after I/R, EC-targeted HSP27 overexpression attenuated the infiltration of potentially destructive neutrophils and macrophages into brain parenchyma, thereby improving long-term stroke outcome. Notably, early poststroke administration of HSP27 attached to a cell-penetrating transduction domain (TAT-HSP27) rapidly elevated HSP27 levels in brain microvessels and ameliorated I/R-induced BBB disruption and subsequent neurological deficits. Thus, the present study demonstrates that HSP27 can function at the EC level to preserve BBB integrity after I/R brain injury. HSP27 may be a therapeutic agent for ischemic stroke and other neurological conditions involving BBB breakdown.
C1 [Shi, Yejie; Jiang, Xiaoyan; Hu, Xiaoming; Zhang, Wenting; Gao, Yanqin; Bennett, Michael V. L.; Chen, Jun] Fudan Univ, State Key Lab Med Neurobiol, Inst Brain Sci, Shanghai 200032, Peoples R China.
[Shi, Yejie; Jiang, Xiaoyan; Hu, Xiaoming; Zhang, Wenting; Gao, Yanqin; Bennett, Michael V. L.; Chen, Jun] Fudan Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200032, Peoples R China.
[Shi, Yejie; Zhang, Lili; Hu, Xiaoming; Chen, Jun] Vet Affairs Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15261 USA.
[Shi, Yejie; Jiang, Xiaoyan; Zhang, Lili; Pu, Hongjian; Hu, Xiaoming; Cai, Wei; Gao, Yanqin; Chen, Jun] Univ Pittsburgh, Pittsburgh Inst Brain Disorders & Recovery, Pittsburgh, PA 15213 USA.
[Shi, Yejie; Jiang, Xiaoyan; Zhang, Lili; Pu, Hongjian; Hu, Xiaoming; Cai, Wei; Gao, Yanqin; Chen, Jun] Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA.
[Leak, Rehana K.] Duquesne Univ, Mylan Sch Pharm, Div Pharmaceut Sci, Pittsburgh, PA 15282 USA.
[Keep, Richard F.] Univ Michigan, Depat Neurosurg, Ann Arbor, MI 48109 USA.
[Bennett, Michael V. L.] Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10461 USA.
RP Bennett, MVL; Chen, J (reprint author), Fudan Univ, State Key Lab Med Neurobiol, Inst Brain Sci, Shanghai 200032, Peoples R China.; Bennett, MVL; Chen, J (reprint author), Fudan Univ, Collaborat Innovat Ctr Brain Sci, Shanghai 200032, Peoples R China.; Chen, J (reprint author), Vet Affairs Pittsburgh Healthcare Syst, Geriatr Res Educ & Clin Ctr, Pittsburgh, PA 15261 USA.; Chen, J (reprint author), Univ Pittsburgh, Pittsburgh Inst Brain Disorders & Recovery, Pittsburgh, PA 15213 USA.; Chen, J (reprint author), Univ Pittsburgh, Dept Neurol, Pittsburgh, PA 15213 USA.; Bennett, MVL (reprint author), Albert Einstein Coll Med, Dominick P Purpura Dept Neurosci, Bronx, NY 10461 USA.
EM michael.bennett@einstein.yu.edu; chenj2@upmc.edu
OI Shi, Yejie/0000-0001-7502-9201
FU US Department of Veterans Affairs (VA) Merit Review [BX002495]; NIH
[NS089534, NS045048, NS056118, NS036736, NS095029]; Chinese Natural
Science Foundation [81571285]; Shanghai Municipal Science and Technology
Commission Support Program [14431907002]; American Heart Association
[15POST22260011]; VA Senior Research Career Scientist Award; State
Administration of Foreign Experts Affairs, China [GDW20133100069]
FX This project was supported by US Department of Veterans Affairs (VA)
Merit Review BX002495 (to J.C.); NIH Grants NS089534, NS045048, and
NS056118 (to J.C.) and NS036736 and NS095029 (to M.V.L.B. and J.C.);
Chinese Natural Science Foundation Grant 81571285 (to Y.G.); the
Shanghai Municipal Science and Technology Commission Support Program
14431907002 (to Y.G.); and American Heart Association Grant
15POST22260011 (to Y.S.). J.C. is the Richard King Mellon Professor of
Neurology and a recipient of the VA Senior Research Career Scientist
Award. M.V.L.B. is the Sylvia and Robert S. Olnick Professor of
Neuroscience and a recipient of the High-End Distinguished Professorship
GDW20133100069 from the State Administration of Foreign Experts Affairs,
China.
NR 50
TC 0
Z9 0
U1 3
U2 3
PU NATL ACAD SCIENCES
PI WASHINGTON
PA 2101 CONSTITUTION AVE NW, WASHINGTON, DC 20418 USA
SN 0027-8424
J9 P NATL ACAD SCI USA
JI Proc. Natl. Acad. Sci. U. S. A.
PD FEB 14
PY 2017
VL 114
IS 7
BP E1243
EP E1252
DI 10.1073/pnas.1621174114
PG 10
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EK5TR
UT WOS:000393989300025
PM 28137866
ER
PT J
AU Kondapalli, AV
Jeon-Slaughter, H
Armstrong, E
Shammas, NW
Shammas, A
Prasad, A
Cawich, I
Rodriguez, G
Abu-Fadel, M
Brilakis, ES
Banerjee, S
AF Kondapalli, Ananya V.
Jeon-Slaughter, Haekyung
Armstrong, Ehrin
Shammas, Nicolas W.
Shammas, Andrew
Prasad, Anand
Cawich, Ian
Rodriguez, Gerardo
Abu-Fadel, Mazen
Brilakis, Emmanouil S.
Banerjee, Subhash
TI Comparative Assessment of Subintimal versus Intraluminal Crossing of
Infrainguinal Chronic Total Occlusion Lesions
SO JACC-CARDIOVASCULAR INTERVENTIONS
LA English
DT Meeting Abstract
C1 [Kondapalli, Ananya V.; Jeon-Slaughter, Haekyung; Banerjee, Subhash] Univ Texas Southwestern Med Ctr, Dallas, TX USA.
[Armstrong, Ehrin] Denver VA Med Ctr, Denver, CO USA.
[Shammas, Nicolas W.; Shammas, Andrew] Univ Iowa, Davenport, IA USA.
[Prasad, Anand] UT Hlth San Antonio, San Antonio, TX USA.
[Cawich, Ian; Rodriguez, Gerardo] Arkansas Heart Hosp, Little Rock, AR USA.
[Abu-Fadel, Mazen] Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA.
[Brilakis, Emmanouil S.] Minneapolis Heart Inst, Minneapolis, MN USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1936-8798
EI 1876-7605
J9 JACC-CARDIOVASC INTE
JI JACC-Cardiovasc. Interv.
PD FEB 13
PY 2017
VL 10
IS 3
SU S
MA CRT-300.20
BP S44
EP S44
PG 1
WC Cardiac & Cardiovascular Systems
SC Cardiovascular System & Cardiology
GA EP2MJ
UT WOS:000397217000124
ER
PT J
AU Quinones, AR
Nagel, CL
Newsom, JT
Huguet, N
Sheridan, P
Thielke, SM
AF Quinones, Ana R.
Nagel, Corey L.
Newsom, Jason T.
Huguet, Nathalie
Sheridan, Paige
Thielke, Stephen M.
TI Racial and ethnic differences in smoking changes after chronic disease
diagnosis among middle-aged and older adults in the United States
SO BMC GERIATRICS
LA English
DT Article
DE Racial/ethnic disparities; Smoking; Behavior change; Chronic disease;
Disease management
ID SELF-REPORTED HYPERTENSION; CARDIAC REHABILITATION; AFRICAN-AMERICAN;
HEALTH BEHAVIOR; CESSATION; SMOKERS; LIFE; VALIDITY; MENTHOL; BLACKS
AB Background: Middle-aged and older Americans from underrepresented racial and ethnic backgrounds are at risk for greater chronic disease morbidity than their white counterparts. Cigarette smoking increases the severity of chronic illness, worsens physical functioning, and impairs the successful management of symptoms. As a result, it is important to understand whether smoking behaviors change after the onset of a chronic condition. We assessed the racial/ethnic differences in smoking behavior change after onset of chronic diseases among middle-aged and older adults in the US.
Methods: We use longitudinal data from the Health and Retirement Study (HRS 1992-2010) to examine changes in smoking status and quantity of cigarettes smoked after a new heart disease, diabetes, cancer, stroke, or lung disease diagnosis among smokers.
Results: The percentage of middle-aged and older smokers who quit after a new diagnosis varied by racial/ethnic group and disease: for white smokers, the percentage ranged from 14% after diabetes diagnosis to 32% after cancer diagnosis; for black smokers, the percentage ranged from 15% after lung disease diagnosis to 40% after heart disease diagnosis; the percentage of Latino smokers who quit was only statistically significant after stoke, where 38% quit. In logistic models, black (OR = 0.43, 95% CI: 0.19-0.99) and Latino (OR = 0.26, 95% CI: 0.11-0.65) older adults were less likely to continue smoking relative to white older adults after a stroke, and Latinos were more likely to continue smoking relative to black older adults after heart disease onset (OR = 2.69, 95% CI [1.05-6.95]). In models evaluating changes in the number of cigarettes smoked after a new diagnosis, black older adults smoked significantly fewer cigarettes than whites after a new diagnosis of diabetes, heart disease, stroke or cancer, and Latino older adults smoked significantly fewer cigarettes compared to white older adults after newly diagnosed diabetes and heart disease. Relative to black older adults, Latinos smoked significantly fewer cigarettes after newly diagnosed diabetes.
Conclusions: A large majority of middle-aged and older smokers continued to smoke after diagnosis with a major chronic disease. Black participants demonstrated the largest reductions in smoking behavior. These findings have important implications for tailoring secondary prevention efforts for older adults.
C1 [Quinones, Ana R.; Nagel, Corey L.; Sheridan, Paige] Oregon Hlth & Sci Univ, OHSU PSU Sch Publ Hlth, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
[Quinones, Ana R.] Oregon Hlth & Sci Univ, Portland VA Med Ctr, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
[Nagel, Corey L.] Oregon Hlth & Sci Univ, Sch Nursing, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
[Newsom, Jason T.] Portland State Univ, Dept Psychol, POB 751, Portland, OR 97207 USA.
[Huguet, Nathalie] Oregon Hlth & Sci Univ, Dept Family Med, Portland, OR 97201 USA.
[Thielke, Stephen M.] Puget Sound VA Med Ctr, Geriatr Res Educ & Clin Ctr, 1660 South Columbian Way, Seattle, WA 98108 USA.
[Thielke, Stephen M.] Univ Washington, Psychiat & Behav Sci, 1959 Pacific Ave, Seattle, WA 98195 USA.
RP Quinones, AR (reprint author), Oregon Hlth & Sci Univ, OHSU PSU Sch Publ Hlth, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.; Quinones, AR (reprint author), Oregon Hlth & Sci Univ, Portland VA Med Ctr, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
EM quinones@ohsu.edu
FU National Institutes of Health, National Institute on Aging
[R01-AG034211]; American Diabetes Association [ADA 7-13-CD-08];
Mentoring Researchers in Latino Health Disparities at San Diego State
University program (NIH/NHLBI) [R25HL105430]
FX This research was supported by a grant from the National Institutes of
Health, National Institute on Aging (R01-AG034211, Newsom PI). Dr.
Quinones is supported by the American Diabetes Association (ADA
7-13-CD-08, Quinones PI) and the Mentoring Researchers in Latino Health
Disparities at San Diego State University program (NIH/NHLBI
R25HL105430, Elder PI). The content is solely the responsibility of the
authors and does not necessarily represent the official views of the
National Institutes of Health or the American Diabetes Association.
NR 36
TC 0
Z9 0
U1 1
U2 1
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1471-2318
J9 BMC GERIATR
JI BMC Geriatr.
PD FEB 8
PY 2017
VL 17
AR 48
DI 10.1186/s12877-017-0438-z
PG 9
WC Geriatrics & Gerontology; Gerontology
SC Geriatrics & Gerontology
GA EP5WO
UT WOS:000397449900003
PM 28178927
ER
PT J
AU Thorpe, JM
Thorpe, CT
Gellad, WF
Good, CB
Hanlon, JT
Mor, MK
Pleis, JR
Schleiden, LJ
Van Houtven, CH
AF Thorpe, Joshua M.
Thorpe, Carolyn T.
Gellad, Walid F.
Good, Chester B.
Hanlon, Joseph T.
Mor, Maria K.
Pleis, John R.
Schleiden, Loren J.
Van Houtven, Courtney Harold
TI Dual Health Care System Use and High-Risk Prescribing in Patients With
Dementia
SO ANNALS OF INTERNAL MEDICINE
LA English
DT Article
ID OF-VETERANS-AFFAIRS; ANTIPSYCHOTIC-DRUG TREATMENT; OLDER-ADULTS;
ANTICHOLINERGIC BURDEN; ALZHEIMER-DISEASE; CONTROLLED-TRIAL; MEDICARE;
MEDICATIONS; VA; INFORMATION
AB Background: Recent federal policy changes attempt to expand veterans' access to providers outside the Department of Veterans Affairs (VA). Receipt of prescription medications across unconnected systems of care may increase the risk for unsafe prescribing, particularly in persons with dementia.
Objective: To investigate the association between dual health care system use and potentially unsafe medication (PUM) prescribing.
Design: Retrospective cohort study.
Setting: National VA outpatient care facilities in 2010.
Participants: 75 829 veterans with dementia who were continuously enrolled in Medicare from 2007 to 2010; 80% were VA-only users, and 20% were VA-Medicare Part D (dual) users.
Measurements: Augmented inverse propensity weighting was used to estimate the effect of dual-system versus VA-only prescribing on 4 indicators of PUM prescribing in 2010: any exposure to Healthcare Effectiveness Data and Information Set (HEDIS) high-risk medication in older adults (PUM-HEDIS), any daily exposure to prescriptions with a cumulative Anticholinergic Cognitive Burden (ACB) score of 3 or higher (PUM-ACB), any antipsychotic prescription (PUM-antipsychotic), and any PUM exposure (any-PUM). The annual number of days of each PUM exposure was also examined.
Results: Compared with VA-only users, dual users had more than double the odds of exposure to any-PUM (odds ratio [OR], 2.2 [95% CI, 2.2 to 2.3]), PUM-HEDIS (OR, 2.4 [CI, 2.2 to 2.8]), and PUM-ACB (OR, 2.1 [CI, 2.0 to 2.2]). The odds of PUM-antipsychotic exposure were also greater in dual users (OR, 1.5 [CI, 1.4 to 1.6]). Dual users had an adjusted average of 44.1 additional days of any-PUM exposure (CI, 37.2 to 45.0 days).
Limitation: Observational study design of veteran outpatients only.
Conclusion: Among veterans with dementia, rates of PUM prescribing are significantly higher among dual-system users than with VA-only users.
C1 Vet Affairs Pittsburgh Healthcare Syst, Ctr Hlth Equ Res & Promot, Pittsburgh, PA USA.
Durham Vet Affairs Med Ctr, Ctr Hlth Serv Res Primary Care, Durham, NC USA.
[Thorpe, Joshua M.; Thorpe, Carolyn T.; Gellad, Walid F.; Good, Chester B.; Hanlon, Joseph T.; Pleis, John R.; Schleiden, Loren J.] Vet Affairs Pittsburgh Healthcare Syst, Univ Dr 151C, Pittsburgh, PA 15240 USA.
[Van Houtven, Courtney Harold] US Dept Vet Affairs, Durham Vet Affairs Med Ctr, 508 Fulton St, Durham, NC 27705 USA.
RP Thorpe, JM (reprint author), Vet Affairs Pittsburgh Healthcare Syst, Univ Dr 151C, Pittsburgh, PA 15240 USA.
EM Joshua.Thorpe@va.gov
FU U.S. Department of Veterans Affairs, Health Services Research &
Development Merit Award [IIR 12-379]
FX By the U.S. Department of Veterans Affairs, Health Services Research &
Development Merit Award (IIR 12-379; all authors).
NR 44
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U1 2
U2 2
PU AMER COLL PHYSICIANS
PI PHILADELPHIA
PA INDEPENDENCE MALL WEST 6TH AND RACE ST, PHILADELPHIA, PA 19106-1572 USA
SN 0003-4819
EI 1539-3704
J9 ANN INTERN MED
JI Ann. Intern. Med.
PD FEB 7
PY 2017
VL 166
IS 3
BP 157
EP +
DI 10.7326/M16-0551
PG 15
WC Medicine, General & Internal
SC General & Internal Medicine
GA EL7DL
UT WOS:000394781200004
PM 27919104
ER
PT J
AU Mayr, FB
Talisa, VB
Balakumar, V
Chang, CCH
Fine, M
Yende, S
AF Mayr, Florian B.
Talisa, Victor B.
Balakumar, Vikram
Chang, Chung-Chou H.
Fine, Michael
Yende, Sachin
TI Proportion and Cost of Unplanned 30-Day Readmissions After Sepsis
Compared With Other Medical Conditions
SO JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
LA English
DT Letter
ID UNITED-STATES; EPIDEMIOLOGY
C1 [Mayr, Florian B.; Fine, Michael; Yende, Sachin] VA Pittsburgh Healthcare Syst, Ctr Hlth Equ Res & Promot, Univ Dr C, Pittsburgh, PA 15240 USA.
[Talisa, Victor B.; Chang, Chung-Chou H.] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Biostat, Pittsburgh, PA 15261 USA.
[Balakumar, Vikram] Univ Pittsburgh, Clin Res Invest & Syst Modeling Acute Illness Ctr, Pittsburgh, PA USA.
RP Yende, S (reprint author), VA Pittsburgh Healthcare Syst, Ctr Hlth Equ Res & Promot, Univ Dr C, Pittsburgh, PA 15240 USA.
EM yendes@upmc.edu
FU National Institute of General Medical Sciences [R01GM097471,
R34GM107650]
FX Dr Yende was supported by grants R01GM097471 and R34GM107650 from the
National Institute of General Medical Sciences.
NR 3
TC 0
Z9 0
U1 0
U2 0
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 0098-7484
EI 1538-3598
J9 JAMA-J AM MED ASSOC
JI JAMA-J. Am. Med. Assoc.
PD FEB 7
PY 2017
VL 317
IS 5
BP 530
EP 531
DI 10.1001/jama.2016.20468
PG 2
WC Medicine, General & Internal
SC General & Internal Medicine
GA EJ9RN
UT WOS:000393564200023
PM 28114505
ER
PT J
AU Khawaja, AM
Wang, GQ
Cutter, GR
Szaflarski, JP
AF Khawaja, Ayaz M.
Wang, Guoqiao
Cutter, Gary R.
Szaflarski, Jerzy P.
TI Continuous Electroencephalography (cEEG) Monitoring and Outcomes of
Critically Ill Patients
SO MEDICAL SCIENCE MONITOR
LA English
DT Article
DE Anticonvulsants; Electroencephalography; Intensive Care Units; Patient
Outcome Assessment; Seizures
ID INTENSIVE-CARE-UNIT; CONTINUOUS EEG; CONSENSUS STATEMENT; STATUS
EPILEPTICUS; INTRACEREBRAL HEMORRHAGE; SEIZURES; SCALE; STROKE; ADULTS;
CHILDREN
AB Background: It is not clear whether performing continuous EEG (cEEG) in critically ill patients during intensive care unit (ICU) treatment affects outcomes at discharge.
Material/Methods: We prospectively matched 234 patients who received cEEG (cases) by admission diagnosis and sex to 234 patients who did not receive cEEG (controls) and followed them until discharge. Patients admitted due to seizures were excluded. The primary measures of outcome were Glasgow Coma Scale at Discharge (GCSD) and disposition at discharge, and the secondary measures of outcome were AED modifications, Glasgow Outcomes Scale, and Modified-Rankin Scale. These outcomes were compared between the cases and controls.
Results: Some differences in primary outcome measures between the groups emerged on univariate analyses, but these differences were small and not significant after controlling for covariates. Cases had longer ICU stays (p=0.002) and lower admission GCS (p=0.01) but similar GCSD (p=0.10). Of the secondary outcome measures, the mean (SD) number of AED modifications for cases was 2.2 +/- 3.1 compared to 0.4 +/- 0.8 for controls (p<0.0001); 170 (72.6%) cases had at least 1 AED modification compared to only 56 (24.1%) of the controls (p<0.0001).
Conclusions: Performing cEEG did not improve discharge outcome but it significantly influenced AED prescription patterns. Further studies assessing long-term outcomes are needed to better define the role of cEEG in this patient population.
C1 [Khawaja, Ayaz M.; Szaflarski, Jerzy P.] Univ Alabama Birmingham UAB Hosp, Dept Neurol, Birmingham, AL 35294 USA.
[Khawaja, Ayaz M.] Birmingham Vet Affairs Med Ctr, Dept Neurol, Birmingham, AL 35233 USA.
[Wang, Guoqiao; Cutter, Gary R.] UAB, Dept Biostat, Birmingham, AL USA.
[Szaflarski, Jerzy P.] UAB, Epilepsy Ctr, Birmingham, AL USA.
RP Khawaja, AM (reprint author), Univ Alabama Birmingham UAB Hosp, Dept Neurol, Birmingham, AL 35294 USA.; Khawaja, AM (reprint author), Birmingham Vet Affairs Med Ctr, Dept Neurol, Birmingham, AL 35233 USA.
EM dr.ayazmk@gmail.com
FU UAB Epilepsy Center
FX This study was supported in part by funds from the UAB Epilepsy Center
NR 32
TC 0
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U1 0
U2 0
PU INT SCIENTIFIC LITERATURE, INC
PI SMITHTOWN
PA 361 FOREST LANE, SMITHTOWN, NY 11787 USA
SN 1643-3750
J9 MED SCI MONITOR
JI Med. Sci. Monitor
PD FEB 4
PY 2017
VL 23
BP 649
EP 658
DI 10.12659/MSM.900826
PG 10
WC Medicine, Research & Experimental
SC Research & Experimental Medicine
GA EJ5BQ
UT WOS:000393231900002
PM 28160596
ER
PT J
AU Dang, BN
Westbrook, RA
Njue, SM
Giordano, TP
AF Dang, Bich N.
Westbrook, Robert A.
Njue, Sarah M.
Giordano, Thomas P.
TI Building trust and rapport early in the new doctor-patient relationship:
a longitudinal qualitative study
SO BMC MEDICAL EDUCATION
LA English
DT Article
DE Patient satisfaction; Patient-centered care; Patient preference;
Physician-patient relations; Patient engagement; Health communication;
HIV infection; Retention in care; Qualitative studies; Longitudinal
studies
ID PRIMARY-CARE; COMMUNICATION-SKILLS; META-ANALYSIS; REASSURANCE; CANCER;
PHYSICIANS; HEALTH; DECISIONS; STIGMA; AGENDA
AB Background: New patients are a particularly vulnerable population because they are at high risk of missing a subsequent visit or dropping out of care completely. However, few data exist on what new patients value in the beginning of a relationship with a new provider. Persons with HIV infection may be an ideal population to study the drivers of a positive initial patient-provider relationship, as it is a chronic and serious condition that requires a reliable, ongoing relationship with a provider. Informed by patients' real experiences, this study aims to identify what patients see as the most critical elements for building trust and rapport from the outset.
Methods: We conducted longitudinal, in-person interviews with 21 patients new to the HIV clinic at the Michael E. DeBakey Veterans Affairs Medical Center in Houston, Texas, from August 2013 to March 2015. Patients were interviewed across three time points: once before their first provider visit, a second time within two weeks after the first visit, and a third time at 6 to 12 months after the first provider visit.
Results: We conducted 61 h of patient interviews. The mean age was 53 years; 52% were non-Hispanic white, 23% were non-Hispanic black and 19% were Hispanic. Patients described significant anxiety and vulnerability not just from HIV itself, but also in starting a relationship as a new patient to a new provider. Our analysis of these experiences revealed five actions providers can take to reduce their patients' anxiety and build trust early in the first visit: 1) provide reassurance to patients, 2) tell patients it's okay to ask questions, 3) show patients their lab results and explain what they mean, 4) avoid language and behaviors that are judgmental of patients, and 5) ask patients what they want [i.e., treatment goals and preferences].
Conclusions: Our study incorporates direct input from patients and highlights the unique psychological challenges that patients face in seeking care from a new provider. The actionable opportunities cited by patients have the potential to mitigate patients' feelings of anxiety and vulnerability, and thereby improve their overall health care experience.
C1 [Dang, Bich N.; Njue, Sarah M.; Giordano, Thomas P.] VA Ctr, Innovat Qual Effectiveness & Safety IQuESt, Houston, TX USA.
[Dang, Bich N.; Njue, Sarah M.; Giordano, Thomas P.] Michael E DeBakey Vet Affairs Med Ctr 152, 2002 Holcombe Blvd, Houston, TX 77030 USA.
[Dang, Bich N.; Westbrook, Robert A.; Giordano, Thomas P.] Baylor Coll Med, Dept Med, Houston, TX USA.
[Westbrook, Robert A.] Rice Univ, Jesse H Jones Grad Sch Business, Houston, TX USA.
RP Dang, BN (reprint author), VA Ctr, Innovat Qual Effectiveness & Safety IQuESt, Houston, TX USA.; Dang, BN (reprint author), Michael E DeBakey Vet Affairs Med Ctr 152, 2002 Holcombe Blvd, Houston, TX 77030 USA.; Dang, BN (reprint author), Baylor Coll Med, Dept Med, Houston, TX USA.
EM bndang@bcm.edu
FU National Institutes of Health; Baylor College of Medicine Chao
Physician-Scientist Award
FX Dr. Dang is a current recipient of the K23 Mentored Patient-Oriented
Research Career Development Award from the National Institutes of
Health. This study was supported by the Baylor College of Medicine Chao
Physician-Scientist Award, and the facilities and resources of the
Houston VA Center for Innovations in Quality, Effectiveness and Safety
(HFP90-020).
NR 55
TC 0
Z9 0
U1 15
U2 15
PU BIOMED CENTRAL LTD
PI LONDON
PA 236 GRAYS INN RD, FLOOR 6, LONDON WC1X 8HL, ENGLAND
SN 1472-6920
J9 BMC MED EDUC
JI BMC Med. Educ.
PD FEB 2
PY 2017
VL 17
AR 32
DI 10.1186/s12909-017-0868-5
PG 10
WC Education & Educational Research; Education, Scientific Disciplines
SC Education & Educational Research
GA EP5PR
UT WOS:000397431400003
PM 28148254
ER
PT J
AU Prabhakaran, A
Dhaliwal, G
Schilf, CRJ
Caughey, GH
Pile, J
AF Prabhakaran, Anbazhagan
Dhaliwal, Gurpreet
Schilf, Christopher Robert-James
Caughey, George H.
Pile, James
TI A Shocking Diagnosis
SO JOURNAL OF HOSPITAL MEDICINE
LA English
DT Editorial Material
ID ADVANCED SYSTEMIC MASTOCYTOSIS; KIT MUTATION; MAST-CELLS; DISORDERS;
IMATINIB; NETWORK
C1 [Prabhakaran, Anbazhagan; Schilf, Christopher Robert-James] Cleveland Clin, Med Inst, M2 Annex,9500 Euclid Ave, Cleveland, OH 44195 USA.
[Dhaliwal, Gurpreet; Caughey, George H.] Univ Calif San Francisco, Dept Med, San Francisco, CA USA.
[Dhaliwal, Gurpreet; Caughey, George H.] San Francisco VA Med Ctr, Med Serv, San Francisco, CA USA.
[Pile, James] Case Western Reserve Univ, Dept Med, MetroHlth Med Ctr, Cleveland, OH 44106 USA.
RP Prabhakaran, A (reprint author), Cleveland Clin, Med Inst, M2 Annex,9500 Euclid Ave, Cleveland, OH 44195 USA.
EM prabhak@ccf.org
NR 15
TC 0
Z9 0
U1 0
U2 0
PU FRONTLINE MEDICAL COMMUNICATIONS
PI THE WOODLANDS
PA WRIGHTS MEDIA, 2407 TIMBERLOCH PLACE, SUITE B, THE WOODLANDS, TX 77386
USA
SN 1553-5592
EI 1553-5606
J9 J HOSP MED
JI J. Hosp. Med.
PD FEB
PY 2017
VL 12
IS 2
BP 104
EP 108
DI 10.12788/jhm.2690
PG 5
WC Medicine, General & Internal
SC General & Internal Medicine
GA ES5KK
UT WOS:000399577300008
PM 28182807
ER
PT J
AU Russell, DW
Genschmer, K
Szul, T
Jackson, P
Blalock, J
AF Russell, D. W.
Genschmer, K.
Szul, T.
Jackson, P.
Blalock, J.
TI NEUTROPHIL STIMULATION INCREASES CAPACITY TO DEGRADE THE MATRIKINE
PROLINE-GLYCINE-PROLINE VIA EXOSOMES
SO JOURNAL OF INVESTIGATIVE MEDICINE
LA English
DT Meeting Abstract
CT Southern Regional Meeting of the
American-Federation-for-Medical-Research (AFMR)
CY FEB 11-13, 2017
CL New Orleans, LA
SP Amer Federat Med Res
C1 [Russell, D. W.; Genschmer, K.; Szul, T.; Jackson, P.; Blalock, J.] Univ Alabama Birmingham, Hoover, AL USA.
[Russell, D. W.; Genschmer, K.; Szul, T.; Jackson, P.; Blalock, J.] Univ Alabama Birmingham, Lung Hlth Ctr, Birmingham, AL USA.
[Blalock, J.] Birmingham Vet Affairs Med Ctr, Birmingham, AL USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 1081-5589
EI 1708-8267
J9 J INVEST MED
JI J. Invest. Med.
PD FEB
PY 2017
VL 65
IS 2
MA 537
BP 614
EP 615
DI 10.1136/jim-2016-000393.540
PG 2
WC Medicine, General & Internal; Medicine, Research & Experimental
SC General & Internal Medicine; Research & Experimental Medicine
GA ER6BZ
UT WOS:000398891000554
ER
PT J
AU Thorlacius, L
Ingram, JR
Garg, A
Villumsen, B
Esmann, S
Kirby, JS
Gottlieb, AB
Merola, JF
Dellavalle, R
Christensen, R
Jemec, GBE
AF Thorlacius, Linnea
Ingram, John R.
Garg, Amit
Villumsen, Bente
Esmann, Solveig
Kirby, Joslyn S.
Gottlieb, Alice B.
Merola, Joseph F.
Dellavalle, Robert
Christensen, Robin
Jemec, Gregor B. E.
TI Protocol for the development of a core domain set for hidradenitis
suppurativa trial outcomes
SO BMJ OPEN
LA English
DT Article
ID CLINICAL-TRIALS; SYSTEMATIC REVIEWS; PREVALENCE; QUALITY; OMERACT;
IMPROVE
AB Introduction: Randomised controlled trials (RCTs) should have well-defined primary and secondary outcomes to answer questions generated by the main hypotheses. However, for the chronic, inflammatory skin disease hidradenitis suppurativa (HS), the reported outcome measures are numerous and diverse. A recent systematic review found a total of 30 outcome measure instruments in 12 RCTs. This use of a broad range of outcome measures can increase difficulties in interpretation and comparison of results and may potentially obstruct appropriate evidence synthesis by causing reporting bias. One strategy for dealing with these problems is to develop a core outcome set (COS). A COS is a list of outcomes that are meant as mandatory and should be measured and reported in all clinical trials. The aim of this study is to develop a COS for the management of HS.
Method and analysis: An international steering group of researchers, clinicians and a patient research partner will guide the COS development. 6 stakeholder groups are involved: patients, dermatologists, surgeons, nurses, industry representatives and drug regulatory authorities. A 1: 1 ratio of patients: healthcare professionals is aimed for. The initial list of candidate items will be obtained by combining three data sets: (1) a systematic review of the literature, (2) US and Danish qualitative interview studies involving patients with HS and (3) an online healthcare professional (HCP) item generation survey. To reach consensus on the COS, 4 anonymous online Delphi rounds are then planned together with 2 face-to-face consensus meetings (1 in Europe and 1 in the USA) to ensure global representation.
Ethics and dissemination: The study will be performed according to the Helsinki declaration. All results from the study, including inconclusive or negative results, will be published in peer-reviewed indexed journals. The study will involve different stakeholder groups to ensure that the developed COS will be suitable and well accepted.
C1 [Thorlacius, Linnea; Esmann, Solveig; Jemec, Gregor B. E.] Zealand Univ Hosp, Dept Dermatol, Roskilde, Denmark.
[Thorlacius, Linnea; Esmann, Solveig; Jemec, Gregor B. E.] Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark.
[Thorlacius, Linnea; Christensen, Robin] Bispebjerg & Frederiksberg Hosp, Musculoskeletal Stat Unit, Parker Inst, Copenhagen, Denmark.
[Ingram, John R.] Cardiff Univ, Inst Infect & Immun, Dept Dermatol & Wound Healing, Cardiff, Wales.
[Garg, Amit] Hofstra Northwell Sch Med, Dept Dermatol, New York, NY USA.
[Villumsen, Bente] Patients Assoc HS Denmark, Copenhagen, Denmark.
[Kirby, Joslyn S.] Penn State Hershey Med Ctr, Dept Dermatol, Hershey, PA USA.
[Gottlieb, Alice B.] New York Med Coll, Dept Dermatol, Valhalla, NY 10595 USA.
[Merola, Joseph F.] Harvard Med Sch, Boston, MA USA.
[Merola, Joseph F.] Brigham & Womens Hosp, Div Rheumatol, Dept Dermatol, 75 Francis St, Boston, MA 02115 USA.
[Merola, Joseph F.] Brigham & Womens Hosp, Dept Med, Div Rheumatol, 75 Francis St, Boston, MA 02115 USA.
[Dellavalle, Robert] US Dept Vet Affairs, Med Ctr, Dermatol Serv, Denver, CO USA.
RP Thorlacius, L (reprint author), Zealand Univ Hosp, Dept Dermatol, Roskilde, Denmark.; Thorlacius, L (reprint author), Univ Copenhagen, Fac Hlth Sci, Copenhagen, Denmark.; Thorlacius, L (reprint author), Bispebjerg & Frederiksberg Hosp, Musculoskeletal Stat Unit, Parker Inst, Copenhagen, Denmark.
EM linneath@gmail.com
FU IDEOM; Department of Dermatology, Zealand University Hospital; Region
Zealand Research Foundation; Oak Foundation; Health Research Fellowship
from Health and Care Research Wales
FX This work is supported by grants from IDEOM and The Department of
Dermatology, Zealand University Hospital. LT is supported by the Region
Zealand Research Foundation. Musculoskeletal Statistics Unit, The Parker
Institute (RC), is supported by grants from the Oak Foundation. JRI is
supported by a Health Research Fellowship from Health and Care Research
Wales.
NR 24
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PU BMJ PUBLISHING GROUP
PI LONDON
PA BRITISH MED ASSOC HOUSE, TAVISTOCK SQUARE, LONDON WC1H 9JR, ENGLAND
SN 2044-6055
J9 BMJ OPEN
JI BMJ Open
PD FEB
PY 2017
VL 7
IS 2
AR e014733
DI 10.1136/bmjopen-2016-014733
PG 8
WC Medicine, General & Internal
SC General & Internal Medicine
GA EQ2BD
UT WOS:000397872400149
PM 28219961
ER
PT J
AU Vandenberg, AE
Vaughan, CP
Stevens, M
Hastings, SN
Powers, J
Markland, A
Hwang, U
Hung, W
Echt, KV
AF Vandenberg, Ann E.
Vaughan, Camille P.
Stevens, Melissa
Hastings, Susan N.
Powers, James
Markland, Alayne
Hwang, Ula
Hung, William
Echt, Katharina V.
TI Improving geriatric prescribing in the ED: a qualitative study of
facilitators and barriers to clinical decision support tool use
SO INTERNATIONAL JOURNAL FOR QUALITY IN HEALTH CARE
LA English
DT Article
DE quality improvement; quality management, qualitative methods; general
methodology, appropriateness, under-use and over-use appropriate
healthcare, elderly; specific populations, emergency care; setting of
care
ID EMERGENCY-DEPARTMENT; CONTROLLED-TRIAL; OLDER-ADULTS; SYSTEMS; CARE
AB Quality problem or issue: Clinical decision support (CDS) may improve prescribing for older adults in the Emergency Department (ED) if adopted by providers.
Initial assessment: Existing prescribing order entry processes were mapped at an initial Veterans Administration Medical Center site, demonstrating cognitive burden, effort and safety concerns.
Choice of solution: Geriatric order sets incorporating 2012 Beers guidelines and including geriatric prescribing advice and prepopulated order options were developed.
Implementation: Geriatric order sets were implemented at two sites as part of the multicomponent 'Enhancing Quality of Prescribing Practices for Older Veterans Discharged from the Emergency Department' quality improvement initiative.
Evaluation: Facilitators and barriers to order sets use at the two sites were evaluated. Phone interviews were conducted with two provider groups (n = 20), those 'EQUiPPED' with the interventions (n = 10, 5 at each site) and Comparison providerswho were only exposed to order sets through a clickable option on the ED order menu within the patient's medical record (n = 10, 5 at each site). All providers were asked about order set 'use' and 'usefulness'. Users (n = 11) were asked about 'usability'.
Lessons learned: Order set adopters described 'usefulness' in terms of 'safety' and 'efficiency', whereas order set consultants and order set non-users described 'usefulness' in terms of 'information' or 'training'. Provider 'autonomy', 'comfort' level with existing tools, and 'learning curve' were stated as barriers to use.
Conclusions: Quantifying efficiency advantages and communicating safety benefit over preexisting practices and tools may improve adoption of CDS in ED and in other settings of care.
C1 [Vandenberg, Ann E.; Vaughan, Camille P.; Stevens, Melissa; Markland, Alayne; Echt, Katharina V.] Birmingham Atlanta VA GRECC, Atlanta VA Med Ctr, 1670 Clairmont Rd, Decatur, GA 30033 USA.
[Vandenberg, Ann E.; Vaughan, Camille P.; Stevens, Melissa; Markland, Alayne; Echt, Katharina V.] Birmingham Atlanta VA GRECC, Birmingham VA Med Ctr, 700 S 19th St, Birmingham, AL 35233 USA.
[Vandenberg, Ann E.; Vaughan, Camille P.; Stevens, Melissa; Echt, Katharina V.] Emory Univ, Dept Med, 201 Dowman Dr, Atlanta, GA 30322 USA.
[Hastings, Susan N.] Durham VA GRECC & HSR&D Ctr, Durham VA Med Ctr, 508 Fulton St, Durham, NC 27705 USA.
[Hastings, Susan N.] Duke Univ, Ctr Study Aging, Med Ctr 3710, Durham, NC 27710 USA.
[Hastings, Susan N.] Duke Univ, Dept Med, Med Ctr 3710, Durham, NC 27710 USA.
[Powers, James] Tennessee Valley Healthcare Syst, Tennessee Valley VA GRECC, 1310 24th Ave S, Nashville, TN 37212 USA.
[Powers, James] Vanderbilt Univ, Div Geriatr, Dept Med, Sch Med, 7159 Vanderbilt Med Ctr East, Nashville, TN 37232 USA.
[Markland, Alayne] Univ Alabama Birmingham, Dept Med, 1720 2nd Ave South, Birmingham, AL 35294 USA.
[Hwang, Ula; Hung, William] James J Peters VA Med Ctr GRECC, GRECC, 130 West Kingsbridge Rd,4A-17, Bronx, NY 10468 USA.
[Hwang, Ula] Icahn Sch Med Mt Sinai, Dept Emergency Med, 1428 Madison Ave, New York, NY 10029 USA.
[Hwang, Ula] Icahn Sch Med Mt Sinai, Dept Geriatr & Palliat, 1428 Madison Ave, New York, NY 10029 USA.
[Hung, William] Icahn Sch Med Mt Sinai, Dept Geriatr & Palliat Med, 1428 Madison Ave, New York, NY 10029 USA.
RP Vandenberg, AE (reprint author), Emory Univ, Div Gen Med & Geriatr, Wesley Woods Hlth Ctr, 1841 Clifton Rd NE,Rm 546, Atlanta, GA 30329 USA.
EM avanden@emory.edu
FU Department of Veterans Affairs Office of Geriatrics and Extended Care
T-21 Initiative [G508-1, G521-5]; John A. Hartford Foundation Center of
Excellence in Geriatric Medicine Pilot Project; John A. Hartford
Foundation Center of Excellence in Geriatric Psychiatry Collaborative
Pilot Project
FX This work was supported by the Department of Veterans Affairs Office of
Geriatrics and Extended Care T-21 Initiative [G508-1, G521-5] and John
A. Hartford Foundation Centers of Excellence in Geriatric Medicine and
Geriatric Psychiatry Collaborative Pilot Projects.
NR 20
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PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 1353-4505
EI 1464-3677
J9 INT J QUAL HEALTH C
JI Int. J. Qual. Health Care
PD FEB
PY 2017
VL 29
IS 1
BP 117
EP 123
DI 10.1093/intqhc/mzw129
PG 7
WC Health Care Sciences & Services; Health Policy & Services
SC Health Care Sciences & Services
GA EQ9DN
UT WOS:000398384600018
PM 27852639
ER
PT J
AU Hong, SN
Dunn, JCY
Stelzner, M
Martiin, MG
AF Hong, Sung Noh
Dunn, James C. Y.
Stelzner, Matthias
Martin, Martin G.
TI Concise Review: The Potential Use of Intestinal Stem Cells to Treat
Patients with Intestinal Failure
SO STEM CELLS TRANSLATIONAL MEDICINE
LA English
DT Review
DE Intestinal failure; Congenital diarrhea; Microvillus inclusion disease;
Congenital tufting enteropathy; Intestinal stem cell
ID MOUSE SMALL-INTESTINE; IN-VITRO; TUMOR-SUPPRESSOR; GENE-THERAPY; WNT
RECEPTORS; GROUND-STATE; SELF-RENEWAL; HUMAN COLON; EPITHELIUM; CRYPT
AB Intestinal failure is a rare life-threatening condition that results in the inability to maintain normal growth and hydration status by enteral nutrition alone. Although parenteral nutrition and whole organ allogeneic transplantation have improved the survival of these patients, current therapies are associated with a high risk for morbidity and mortality. Development of methods to propagate adult human intestinal stem cells (ISCs) and pluripotent stem cells raises the possibility of using stem cell-based therapy for patients with monogenic and polygenic forms of intestinal failure. Organoids have demonstrated the capacity to proliferate indefinitely and differentiate into the various cellular lineages of the gut. Genome-editing techniques, including the overexpression of the corrected form of the defective gene, or the use of CRISPR (clustered regularly interspaced short palindromic repeats)/Cas9 to selectively correct the monogenic disease-causing variant within the stem cell, make autologous ISC transplantation a feasible approach. However, numerous techniques still need to be further optimized, including more robust ex vivo ISC expansion, native ISC ablation, and engraftment protocols. Large-animal models can to be used to develop such techniques and protocols and to establish the safety of autologous ISC transplantation because outcomes in such models can be extrapolated more readily to humans.
C1 [Hong, Sung Noh; Martin, Martin G.] Univ Calif Los Angeles, Dept Pediat, Div Gastroenterol & Nutr, Mattel Childrens Hosp, 10833 LeConte Ave,Box 951752, Los Angeles, CA 90095 USA.
[Hong, Sung Noh; Martin, Martin G.] Univ Calif Los Angeles, David Geffen Sch Med, 10833 LeConte Ave,Box 951752, Los Angeles, CA 90095 USA.
[Hong, Sung Noh] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Med, Seoul, South Korea.
[Dunn, James C. Y.] Univ Calif Los Angeles, David Geffen Sch Med, Div Pediat Surg, Dept Surg, Los Angeles, CA 90095 USA.
[Stelzner, Matthias] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA.
[Stelzner, Matthias] Vet Adm Greater Los Angeles Hlth Syst, Dept Surg, Los Angeles, CA USA.
RP Martiin, MG (reprint author), Univ Calif Los Angeles, Dept Pediat, Div Gastroenterol & Nutr, Mattel Childrens Hosp, 10833 LeConte Ave,Box 951752, Los Angeles, CA 90095 USA.; Martiin, MG (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, 10833 LeConte Ave,Box 951752, Los Angeles, CA 90095 USA.
EM mmartin@mednet.ucla.edu
FU Intestinal Stem Cell Consortium - National Institute of Diabetes and
Digestive and Kidney Diseases; National Institute of Allergy and
Infectious Diseases [DK085535]; California Institute of Regenerative
Medicine [RT2-01985]
FX This work was supported by grants from the Intestinal Stem Cell
Consortium, a collaborative research project funded by the National
Institute of Diabetes and Digestive and Kidney Diseases and the National
Institute of Allergy and Infectious Diseases (DK085535), and the
California Institute of Regenerative Medicine (RT2-01985).
NR 95
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U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2157-6564
EI 2157-6580
J9 STEM CELL TRANSL MED
JI Stem Cells Transl. Med.
PD FEB
PY 2017
VL 6
IS 2
BP 666
EP 676
DI 10.5966/sctm.2016-0153
PG 11
WC Cell & Tissue Engineering
SC Cell Biology
GA EQ6NK
UT WOS:000398198500029
PM 28191783
ER
PT J
AU Shieh, Y
Hu, D
Huntsman, S
Ma, L
Gard, CC
Leung, JWT
Tice, JA
Cummings, SR
Kerlikowske, K
Ziv, E
AF Shieh, Y.
Hu, D.
Huntsman, S.
Ma, L.
Gard, C. C.
Leung, J. W. T.
Tice, J. A.
Cummings, S. R.
Kerlikowske, K.
Ziv, E.
TI A model with polygenic risk score and mammographic density predicts
interval cancers
SO CANCER RESEARCH
LA English
DT Meeting Abstract
CT San Antonio Breast Cancer Symposium
CY DEC 06-10, 2016
CL San Antonio, TX
C1 Univ Calif San Francisco, San Francisco, CA 94143 USA.
New Mexico State Univ, Las Cruces, NM 88003 USA.
Univ Texas MD Anderson Canc Ctr, Houston, TX USA.
San Francisco Coordinating Ctr, San Francisco, CA USA.
San Francisco VA Med Ctr, San Francisco, CA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU AMER ASSOC CANCER RESEARCH
PI PHILADELPHIA
PA 615 CHESTNUT ST, 17TH FLOOR, PHILADELPHIA, PA 19106-4404 USA
SN 0008-5472
EI 1538-7445
J9 CANCER RES
JI Cancer Res.
PD FEB
PY 2017
VL 77
SU 4
MA P5-09-05
DI 10.1158/1538-7445.SABCS16-P5-09-05
PG 2
WC Oncology
SC Oncology
GA EQ3UP
UT WOS:000397999002104
ER
PT J
AU Miravitlles, M
Anzueto, A
AF Miravitlles, Marc
Anzueto, Antonio
TI A new two-step algorithm for the treatment of COPD
SO EUROPEAN RESPIRATORY JOURNAL
LA English
DT Letter
ID OBSTRUCTIVE PULMONARY-DISEASE; DOUBLE-BLIND; EXACERBATIONS; TIOTROPIUM;
GLYCOPYRRONIUM; SALMETEROL; EFFICACY
C1 [Miravitlles, Marc] Hosp Univ Vall Hebron, Ctr Invest Biomed & Red Enfermedades Resp CIBERES, Dept Pneumol, Barcelona, Spain.
[Anzueto, Antonio] Univ Texas Hlth Sci Ctr San Antonio, Sch Med, Div Pulm Dis & Crit Care Med, San Antonio, TX 78229 USA.
[Anzueto, Antonio] Audie L Murphy Mem VA Hosp, South Texas Vet Hlth Care Syst, San Antonio, TX USA.
RP Miravitlles, M (reprint author), Hosp Univ Vall Hebron, Dept Pneumol, P Vall Hebron 119-129, ES-08035 Barcelona, Spain.
EM mmiravitlles@vhebron.net
NR 15
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PU EUROPEAN RESPIRATORY SOC JOURNALS LTD
PI SHEFFIELD
PA 442 GLOSSOP RD, SHEFFIELD S10 2PX, ENGLAND
SN 0903-1936
EI 1399-3003
J9 EUR RESPIR J
JI Eur. Resp. J.
PD FEB
PY 2017
VL 49
IS 2
AR 1602200
DI 10.1183/13993003.02200-2016
PG 3
WC Respiratory System
SC Respiratory System
GA EQ1VQ
UT WOS:000397858100035
ER
PT J
AU Ornstein, KA
Aldridge, MD
Garrido, MM
Gorges, R
Bollens-Lund, E
Siu, AL
Langa, KM
Kelley, AS
AF Ornstein, Katherine A.
Aldridge, Melissa D.
Garrido, Melissa M.
Gorges, Rebecca
Bollens-Lund, Evan
Siu, Albert L.
Langa, Kenneth M.
Kelley, Amy S.
TI The Use of Life-Sustaining Procedures in the Last Month of Life Is
Associated With More Depressive Symptoms in Surviving Spouses
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Article
DE Caregiving; end-of-life care; life-sustaining procedures; bereavement
ID INTENSIVE-CARE-UNIT; POSTTRAUMATIC STRESS; REGIONAL-VARIATIONS;
FAMILY-MEMBERS; OLDER-ADULTS; MEDICARE BENEFICIARIES; ADVANCE
DIRECTIVES; DECISION-MAKING; SERIOUS ILLNESS; END
AB Context. Family caregivers of individuals with serious illness who undergo intensive life-sustaining medical procedures at the end of life may be at risk of negative consequences including depression.
Objectives. The objective of this study was to determine the association between patients' use of life-sustaining procedures at the end of life and depressive symptoms in their surviving spouses.
Methods. We used data from the Health and Retirement Study, a longitudinal survey of U. S. residents, linked to Medicare claims data. We included married Medicare beneficiaries aged 65 years and older who died between 2000 and 2011 (n = 1258) and their surviving spouses. The use of life-sustaining procedures (i. e., intubation/mechanical ventilation, tracheostomy, gastrostomy tube insertion, enteral/parenteral nutrition, and cardiopulmonary resuscitation) in the last month of life was measured via claims data. Using propensity score matching, we compared change in depressive symptoms of surviving spouses.
Results. Eighteen percent of decedents underwent one or more life-sustaining procedures in the last month of life. Those whose spouses underwent life-sustaining procedures had a 0.32-point increase in depressive symptoms after death (scale range = 0-8) and a greater likelihood of clinically significant depression (odds ratio = 1.51) compared with a matched sample of spouses of those who did not have procedures (P < 0.05).
Conclusion. Surviving spouses of those who undergo intensive life-sustaining procedures at the end of life experience a greater magnitude of increase in depressive symptoms than those whose spouses do not undergo such procedures. Further study of the circumstances and decision making surrounding these procedures is needed to understand their relationship with survivors' negative mental health consequences and how best to provide appropriate support. (C) 2016 American Academy of Hospice and Palliative Medicine. Published by Elsevier Inc. All rights reserved.
C1 [Ornstein, Katherine A.; Aldridge, Melissa D.; Garrido, Melissa M.; Bollens-Lund, Evan; Siu, Albert L.; Kelley, Amy S.] Icahn Sch Med Mt Sinai, Dept Geriatr & Palliat Med, New York, NY 10029 USA.
[Ornstein, Katherine A.] Icahn Sch Med Mt Sinai, Inst Translat Epidemiol, New York, NY 10029 USA.
[Aldridge, Melissa D.; Garrido, Melissa M.; Siu, Albert L.; Kelley, Amy S.] James J Peters Vet Affairs Med Ctr, Bronx, NY USA.
[Gorges, Rebecca] Univ Chicago, Harris Sch Publ Policy, Chicago, IL 60637 USA.
[Langa, Kenneth M.] Univ Michigan, Vet Affairs Ctr Clin Management Res, Inst Social Res, Inst Healthcare Policy & Innovat,Dept Internal Me, Ann Arbor, MI 48109 USA.
RP Ornstein, KA (reprint author), Icahn Sch Med Mt Sinai, Dept Geriatr & Palliat Med, New York, NY 10029 USA.
EM katherine.ornstein@mssm.edu
OI Garrido, Melissa/0000-0002-8986-3536
FU NIA [U01AG009740, K01AG047923, 1K23AG040774]; American Federation for
Aging Research; VA HSRD CDA [11-201/CDP 12-255]
FX The HRS (Health and Retirement Study) is sponsored by the NIA
(U01AG009740) and is conducted by the Institute for Social Research,
University of Michigan. The study investigators were supported by the
NIA K01AG047923 to Dr. Ornstein; NIA 1K23AG040774 and the American
Federation for Aging Research to Dr. Kelley; and VA HSR&D CDA 11-201/CDP
12-255 to Dr. Garrido. Funding sources had no role in the design,
conduct, and analysis of this study or in the decision to submit the
manuscript for publication. The authors declare no conflicts of
interest.
NR 47
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U2 2
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
BP 178
EP +
DI 10.1016/j.jpainsymman.2016.08.023
PG 11
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300007
PM 27864126
ER
PT J
AU Sanchez-Reilly, S
AF Sanchez-Reilly, Sandra
TI The Effects of Cognitive Impairment in Older Cancer Patients
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Editorial Material
C1 [Sanchez-Reilly, Sandra] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Sanchez-Reilly, Sandra] South Texas Vet Hlth Care Syst, San Antonio, TX 78229 USA.
RP Sanchez-Reilly, S (reprint author), Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.; Sanchez-Reilly, S (reprint author), South Texas Vet Hlth Care Syst, San Antonio, TX 78229 USA.
NR 2
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
BP 295
EP 296
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300023
ER
PT J
AU Sudore, R
You, J
Korfage, I
Rietjens, J
Le, G
Heyland, D
AF Sudore, Rebecca
You, John
Korfage, Ida
Rietjens, Judith
Le, Gem
Heyland, Daren
TI Prioritizing Outcomes for Advance Care Planning Research: Consensus from
a Multidisciplinary, International Delphi Panel
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Sudore, Rebecca] San Francisco VA Med Ctr, San Francisco, CA USA.
[Sudore, Rebecca; Le, Gem] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[You, John] McMaster Univ, Hamilton, ON, Canada.
[Korfage, Ida; Rietjens, Judith] Erasmus Univ, Med Ctr, Rotterdam, Netherlands.
[Heyland, Daren] Queens Univ, Kingston, ON, Canada.
NR 0
TC 0
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U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA TH307A
BP 316
EP 317
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300060
ER
PT J
AU Sudore, R
Boscardin, J
Barnes, D
AF Sudore, Rebecca
Boscardin, John
Barnes, Deborah
TI A Patient-Facing Advance Care Planning (ACP) Website Called PREPARE
Increases ACP Documentation and Engagement in a Randomized Trial of
Diverse Older Primary Care Patients at a VA Medical Center
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Sudore, Rebecca] San Francisco VA Med Ctr, San Francisco, CA USA.
[Sudore, Rebecca; Boscardin, John; Barnes, Deborah] Univ Calif San Francisco, San Francisco, CA 94143 USA.
NR 0
TC 0
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U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA TH307B
BP 317
EP 318
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300061
ER
PT J
AU Sudore, R
Heyland, D
Barnes, D
Howard, M
Fassbender, K
Robinson, C
Boscardin, J
You, J
AF Sudore, Rebecca
Heyland, Daren
Barnes, Deborah
Howard, Michelle
Fassbender, Konrad
Robinson, Carole
Boscardin, John
You, John
TI Measuring Advance Care Planning: Optimizing the Advance Care Planning
Engagement Survey
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Sudore, Rebecca] San Francisco VA Med Ctr, San Francisco, CA USA.
[Sudore, Rebecca; Barnes, Deborah; Boscardin, John] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Heyland, Daren] Queens Univ, Kingston, ON, Canada.
[Howard, Michelle; You, John] McMaster Univ, Hamilton, ON, Canada.
[Fassbender, Konrad] Covenant Hlth Palliat Inst, Edmonton, AB, Canada.
[Robinson, Carole] Univ British Columbia, Kelowna, BC, Canada.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA TH307C
BP 318
EP 318
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300062
ER
PT J
AU Zapata, C
Wistar, E
Horton, C
Lum, H
Sudore, R
AF Zapata, Carly
Wistar, Emily
Horton, Claire
Lum, Hillary
Sudore, Rebecca
TI Using A Video-Based Advance Care Planning (ACP) Website to Facilitate
Group Visits for Diverse Older Adults in Primary Care Is Feasible And
Improves ACP Engagement
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Zapata, Carly; Wistar, Emily; Horton, Claire; Sudore, Rebecca] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Lum, Hillary] Univ Colorado, Aurora, CO USA.
[Lum, Hillary] Eastern Colorado GRECC, Aurora, CO USA.
[Sudore, Rebecca] San Francisco VA Med Ctr, San Francisco, CA USA.
NR 0
TC 0
Z9 0
U1 1
U2 1
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA TH307D
BP 318
EP 319
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300063
ER
PT J
AU Lum, H
Garner, K
Antoni, C
AF Lum, Hillary
Garner, Kimberly
Antoni, Charlie
TI "I Heard Something from Another Veteran'': How to Use Group Visits to
Engage Patients in Advance Care Planning
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Lum, Hillary] Univ Colorado, Aurora, CO USA.
[Lum, Hillary] VA Eastern Colorado, Aurora, CO USA.
[Garner, Kimberly] US Dept Vet Affairs, Little Rock, AR USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA TH319
BP 324
EP 324
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300074
ER
PT J
AU Bekelman, D
Allen, L
Hattler, B
Havranek, E
Fairclough, D
McBryde, C
Meek, P
AF Bekelman, David
Allen, Larry
Hattler, Brack
Havranek, Edward
Fairclough, Diane
McBryde, Connor
Meek, Paula
TI Primary Results from the Collaborative Care to Alleviate Symptoms and
Adjust to Illness in Heart Failure (CASA) Randomized Clinical Trial
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Bekelman, David; McBryde, Connor] Univ Colorado, Denver, CO 80202 USA.
[Allen, Larry] Univ Colorado, Sch Med, Aurora, CO USA.
[Hattler, Brack] Denver VA Med Ctr, Denver, CO USA.
[Havranek, Edward] Denver Hlth Med Ctr, Denver, CO USA.
[Fairclough, Diane; Meek, Paula] Univ Colorado, Aurora, CO USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA TH321D
BP 328
EP 329
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300082
ER
PT J
AU Franklin, J
Painter, J
Cooke, K
Schluep, J
AF Franklin, John
Painter, John
Cooke, Kelly
Schluep, John
TI Moral Injury: Invisible Wounds of Combat
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Franklin, John; Painter, John] Ralph H Johnson VA Med Ctr, Charleston, SC USA.
[Cooke, Kelly] ProHlth Care, Waukesha, WI USA.
[Schluep, John] First Congregat Church Tallmadge, Tallmadge, OH USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA SA517
BP 400
EP 401
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300218
ER
PT J
AU Williams, B
Bailey, FA
Goode, P
Burgio, K
AF Williams, Beverly
Bailey, F. Amos
Goode, Patricia
Burgio, Kathryn
TI ''Just Knowing That I Was Going to Be Questioned About His Last Days'':
Bereaved Next-Of-Kin's Pre-Interview Cognitive and Affective Work (S703)
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Williams, Beverly] Univ Alabama Birmingham, Birmingham VA Med Ctr, Birmingham, AL USA.
[Bailey, F. Amos] Univ Colorado, Anschutz Med Campus, Aurora, CO USA.
[Goode, Patricia] Univ Alabama Birmingham, Birmingham, AL USA.
[Burgio, Kathryn] Birmingham VA Med Ctr, Birmingham, AL USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
BP 411
EP 411
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300235
ER
PT J
AU Ubhayakar, N
Prommer, E
Steckart, MJ
AF Ubhayakar, Nitin
Prommer, Eric
Steckart, M. Jillisa
TI Palliative Care Consultation from the Emergency Department: Rationale
and Patient Characteristics in a Veteran Population
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Ubhayakar, Nitin] Vet Affairs Greater Los Angeles Healthcare, Los Angeles, CA USA.
[Prommer, Eric] Greater Los Angeles Healthcare, Los Angeles, CA USA.
[Steckart, M. Jillisa] Univ Calif Los Angeles, David Geffen Sch Med, Vet Affairs Greater Los Angeles Healthcare, Los Angeles, CA 90095 USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S728
BP 424
EP 425
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300260
ER
PT J
AU Sudore, R
Lum, H
You, J
Hanson, L
Meier, D
Pantilat, S
Matlock, DD
Rietjens, J
Korfage, IJ
Ritchie, C
Kutner, JS
Teno, JM
Thomas, J
Heyland, DK
AF Sudore, Rebecca
Lum, Hillary
You, John
Hanson, Laura
Meier, Diane
Pantilat, Steven
Matlock, Daniel D.
Rietjens, Judith
Korfage, Ida J.
Ritchie, Christine
Kutner, Jean S.
Teno, Joan M.
Thomas, Judy
Heyland, Daren K.
TI Proactive Outpatient Palliative Care Consultations for Persons with
Advanced Cancer: What's in the "Special Sauce''?
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Sudore, Rebecca] San Francisco VA Med Ctr, San Francisco, CA USA.
[Sudore, Rebecca; Pantilat, Steven; Ritchie, Christine] Univ Calif San Francisco, San Francisco, CA 94143 USA.
[Lum, Hillary] Univ Colorado, Aurora, CO USA.
[Lum, Hillary] Eastern Colorado GRECC, Aurora, CO USA.
[You, John] McMaster Univ, Hamilton, ON, Canada.
[Hanson, Laura] Univ N Carolina, Chapel Hill, NC USA.
[Meier, Diane] Icahn Sch Med Mt Sinai, New York, NY 10029 USA.
[Matlock, Daniel D.; Kutner, Jean S.] Univ Colorado, Sch Med, Aurora, CO USA.
[Rietjens, Judith; Korfage, Ida J.] Erasmus Univ, Med Ctr, Rotterdam, Netherlands.
[Teno, Joan M.] Univ Washington, Seattle, WA 98195 USA.
[Thomas, Judy] Coalit Compassionate Care Calif, Sacramento, CA USA.
[Heyland, Daren K.] Queens Univ, Kingston, ON, Canada.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S739
BP 431
EP 432
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300272
ER
PT J
AU Huang, CHS
Kvale, E
Bailey, FA
Goode, P
Burgio, K
AF Huang, Chao-Hui Sylvia
Kvale, Elizabeth
Bailey, F. Amos
Goode, Patricia
Burgio, Kathryn
TI Association Between Mental Health Diagnoses and Process of Care at the
End Of Life: Findings from the BEACON Trial
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Huang, Chao-Hui Sylvia; Goode, Patricia] Univ Alabama Birmingham, Birmingham, AL USA.
[Kvale, Elizabeth] Univ Alabama Birmingham, Birmingham Ctrat & Support Care, Birmingham, AL USA.
[Bailey, F. Amos] Univ Colorado, Anschutz Med Campus, Aurora, CO USA.
[Burgio, Kathryn] Birmingham VA Med Ctr, Birmingham, AL USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S771
BP 449
EP 449
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300303
ER
PT J
AU Hansen, L
Dieckmann, N
Chang, M
Naugler, W
Kolbeck, K
AF Hansen, Lissi
Dieckmann, Nathan
Chang, Michael
Naugler, Willscott
Kolbeck, Kenneth
TI Symptom Distress in Patients with Advanced Hepatocellular Carcinoma
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Hansen, Lissi; Dieckmann, Nathan; Naugler, Willscott; Kolbeck, Kenneth] Oregon Hlth & Sci Univ, Portland, OR 97201 USA.
[Chang, Michael] Portland VA Med Ctr, Portland, VA USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S781
BP 455
EP 455
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300313
ER
PT J
AU Brown, LM
Sawey, K
Liu, R
Baday, YI
Lee, S
Healy, J
Shah, R
Sanchez-Reilly, S
AF Brown, Lisa -Marie
Sawey, Kathryn
Liu, Rosemary
Baday, Yiressy Izaguirre
Lee, Shuko
Healy, Jennifer
Shah, Ronak
Sanchez-Reilly, Sandra
TI Do You Really Know What Palliative Care Is? Developing an Electronic
Palliative Care Information Card
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Brown, Lisa -Marie; Liu, Rosemary; Healy, Jennifer; Shah, Ronak; Sanchez-Reilly, Sandra] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX USA.
[Sawey, Kathryn] Univ Hosp New Braunfels, New Braunfels, TX USA.
[Baday, Yiressy Izaguirre] Univ Texas Hlth Sci Ctr San Antonio, Ctr VA Hosp, San Antonio, TX USA.
[Lee, Shuko] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S784
BP 456
EP 457
PG 2
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300316
ER
PT J
AU Khan, H
Lee, S
Carretero, E
San-Chez-Reilly, S
AF Khan, Huma
Lee, Shuko
Carretero, Edgar
San-Chez-Reilly, Sandra
TI Serving Those Who Served: The Unique Benefit of Inpatient Hospice at the
VA
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Khan, Huma; San-Chez-Reilly, Sandra] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Lee, Shuko; Carretero, Edgar] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S783
BP 456
EP 456
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300315
ER
PT J
AU Haverhals, L
Manheim, C
Levy, C
AF Haverhals, Leah
Manheim, Chelsea
Levy, Cali
TI Navigating Multiple Systems to Ensure Delivery of Concurrent Care to US
Veterans with Cancer
SO JOURNAL OF PAIN AND SYMPTOM MANAGEMENT
LA English
DT Meeting Abstract
CT Annual Assembly of the
American-Academy-of-Hospice-and-Palliative-Medicine and the
Hospice-and-Palliative-Nurses-Association
CY FEB 22-25, 2017
CL Phoenix, AZ
SP Amer Acad Hospice & Palliat Med, Hosp & Palliat Nurses Assoc
C1 [Haverhals, Leah] Denver VA Med Ctr, Denver, CO USA.
[Manheim, Chelsea] VA Eastern Colorado Hlth Care Syst, Denver, CO USA.
[Levy, Cali] Univ Colorado, Denver, CO 80202 USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 0885-3924
EI 1873-6513
J9 J PAIN SYMPTOM MANAG
JI J. Pain Symptom Manage.
PD FEB
PY 2017
VL 53
IS 2
MA S806
BP 469
EP 469
PG 1
WC Health Care Sciences & Services; Medicine, General & Internal; Clinical
Neurology
SC Health Care Sciences & Services; General & Internal Medicine;
Neurosciences & Neurology
GA EP1AR
UT WOS:000397118300338
ER
PT J
AU Rodriguez, HR
Dobalian, A
AF Rodriguez, Heather R.
Dobalian, Aram
TI PROVIDER AND ADMINISTRATOR EXPERIENCES WITH PROVIDING HIV TREATMENT AND
PREVENTION SERVICES IN RURAL AREAS
SO AIDS EDUCATION AND PREVENTION
LA English
DT Article
ID MENTAL-HEALTH; UNITED-STATES; MEDICAL-CARE; DEEP SOUTH; INFECTED
PERSONS; CASE-MANAGEMENT; ADULTS; INTERVENTION; FACILITATORS; PHYSICIANS
AB Using Andersen's behavioral model of health services use, this study analyzes data from 62 semistructured interviews of providers and administrators at health clinics and social service agencies in rural Florida. Andersen's model addresses predisposing, enabling, and need factors that influence health services use. ATLASti was used to code all interviews and to extract HIV-related themes. The aim of this study was to: (1) add a new dimension to the literature on HIV care services in rural areas, (2) reveal factors that impact ability to provide care to PLWH in rural areas, and (3) suggest ways in which providers and administrators may address any unmet health care needs of PLWH. Respondents perceived systems factors to be more important determinants of access to care for individuals living with HIV and supported ongoing trainings that would increase staff understanding of the needs of people living with HIV.
C1 [Rodriguez, Heather R.] Cent Connecticut State Univ, Dept Sociol, 1615 Stanley St,SSH 317-03, New Britain, CT 06050 USA.
[Dobalian, Aram] US Dept Vet Affairs, Vet Emergency Management Evaluat Ctr, Washington, DC USA.
[Dobalian, Aram] Univ Calif Los Angeles, Fielding Sch Publ Hlth, Dept Hlth Policy & Management, Los Angeles, CA 90024 USA.
RP Rodriguez, HR (reprint author), Cent Connecticut State Univ, Dept Sociol, 1615 Stanley St,SSH 317-03, New Britain, CT 06050 USA.
EM hrodriguez@ccsu.edu
FU Agency for Healthcare Research and Quality [U01HS14355]; Department of
Veterans Affairs, Veterans Health Administration, Office of Patient Care
Services
FX This work was supported by grant U01HS14355 from the Agency for
Healthcare Research and Quality. Dr Dobalian is supported by the
Department of Veterans Affairs, Veterans Health Administration, Office
of Patient Care Services. The views expressed in this article are those
of the authors and do not necessarily reflect the position or policy of
the Department of Veterans Affairs or the U.S. government.
NR 37
TC 0
Z9 0
U1 0
U2 0
PU GUILFORD PUBLICATIONS INC
PI NEW YORK
PA 370 SEVENTH AVE, SUITE 1200, NEW YORK, NY 10001-1020 USA
SN 0899-9546
EI 1943-2755
J9 AIDS EDUC PREV
JI Aids Educ. Prev.
PD FEB
PY 2017
VL 29
IS 1
BP 77
EP 91
PG 15
WC Education & Educational Research; Public, Environmental & Occupational
Health
SC Education & Educational Research; Public, Environmental & Occupational
Health
GA EM3QP
UT WOS:000395230000007
PM 28195782
ER
PT J
AU Wu, CK
Shlipak, MG
Stawski, RS
Peralta, CA
Psaty, BM
Harris, TB
Satterfield, S
Shiroma, EJ
Newman, AB
Odden, MC
AF Wu, Chenkai
Shlipak, Michael G.
Stawski, Robert S.
Peralta, Carmen A.
Psaty, Bruce M.
Harris, Tamara B.
Satterfield, Suzanne
Shiroma, Eric J.
Newman, Anne B.
Odden, Michelle C.
CA Hlth ABC Study
TI Visit-to-Visit Blood Pressure Variability and Mortality and
Cardiovascular Outcomes Among Older Adults: The Health, Aging, and Body
Composition Study
SO AMERICAN JOURNAL OF HYPERTENSION
LA English
DT Article
DE blood pressure; blood pressure variability; hypertension; mortality;
stroke; myocardial infarction; aged
ID ALL-CAUSE MORTALITY; CORONARY-HEART-DISEASE; LONG-TERM;
PROGNOSTIC-SIGNIFICANCE; EPISODIC HYPERTENSION; MYOCARDIAL-INFARCTION;
METAANALYSIS; ASSOCIATION; STROKE; RISK
AB BACKGROUND
Level of blood pressure (BP) is strongly associated with cardiovascular (CV) events and mortality. However, it is questionable whether mean BP can fully capture BP-related vascular risk. Increasing attention has been given to the value of visit-to-visit BP variability.
METHODS
We examined the association of visit-to-visit BP variability with mortality, incident myocardial infarction (MI), and incident stroke among 1,877 well-functioning elders in the Health, Aging, and Body Composition Study. We defined visit-to-visit diastolic BP (DBP) and systolic BP (SBP) variability as the root-mean-square error of person-specific linear regression of BP as a function of time. Alternatively, we counted the number of considerable BP increases and decreases (separately; 10 mm Hg for DBP and 20 mm Hg for SBP) between consecutive visits for each individual.
RESULTS
Over an average follow-up of 8.5 years, 623 deaths (207 from CV disease), 153 MIs, and 156 strokes occurred. The median visit-to-visit DBP and SBP variability was 4.96 mmHg and 8.53 mmHg, respectively. After multivariable adjustment, visit-to-visit DBP variability was related to higher all-cause (hazard ratio (HR) = 1.18 per 1 SD, 95% confidence interval (CI) = 1.01-1.37) and CV mortality (HR = 1.35, 95% CI = 1.051.73). Additionally, individuals having more considerable decreases of DBP (>= 10mm Hg between 2 consecutive visits) had higher risk of allcause (HR = 1.13, 95% CI = 0.99-1.28) and CV mortality (HR = 1.30, 95% CI = 1.05-1.61); considerable increases of SBP (>= 20 mm Hg) were associated with higher risk of all-cause (HR = 1.18, 95% CI = 1.03-1.36) and CV mortality (HR = 1.37, 95% CI = 1.08-1.74).
CONCLUSIONS
Visit-to-visit DBP variability and considerable changes in DBP and SBP were risk factors for mortality in the elderly.
C1 [Wu, Chenkai; Odden, Michelle C.] Oregon State Univ, Sch Biol & Populat Hlth Sci, Corvallis, OR 97331 USA.
[Shlipak, Michael G.; Peralta, Carmen A.] Univ Calif San Francisco, Dept Med, San Francisco, CA USA.
[Shlipak, Michael G.; Peralta, Carmen A.] San Francisco VA Med Ctr, Kidney Hlth Res Collaborat, Dept Med, San Francisco, CA USA.
[Stawski, Robert S.] Oregon State Univ, Sch Social & Human Hlth Sci, Corvallis, OR 97331 USA.
[Psaty, Bruce M.] Univ Washington, Cardiovasc Hlth Res Unit, Seattle, WA 98195 USA.
[Psaty, Bruce M.] Univ Washington, Dept Med, Seattle, WA USA.
[Psaty, Bruce M.] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA.
[Psaty, Bruce M.] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA.
[Psaty, Bruce M.] Grp Hlth Cooperat Puget Sound, Grp Hlth Res Inst, Seattle, WA USA.
[Harris, Tamara B.] NIA, Intramural Res Program, Lab Epidemiol & Populat Sci, Bethesda, MD 20892 USA.
[Satterfield, Suzanne] Univ Tennessee, Hlth Sci Ctr, Dept Prevent Med, Memphis, TN USA.
[Shiroma, Eric J.] Harvard Med Sch, Brigham & Womens Hosp, Dept Med, Div Prevent Med, Boston, MA USA.
[Newman, Anne B.] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA.
RP Wu, CK (reprint author), Oregon State Univ, Sch Biol & Populat Hlth Sci, Corvallis, OR 97331 USA.
EM wuche@oregonstate.edu
FU National Institute on Aging (NIA) [N01-AG-6-2101, N01-AG-6-2103,
N01-AG-6-2106]; NIA [R01-AG028050]; NINR [R01-NR012459]; Intramural
Research Program of the NIH, National Institute on Aging; National
Institute on Aging [K01AG039387, R01AG46206]
FX The Health ABC Study was supported by National Institute on Aging (NIA)
Contracts N01-AG-6-2101; N01-AG-6-2103; N01-AG-6-2106; NIA grant
R01-AG028050, and NINR grant R01-NR012459, and in part by the Intramural
Research Program of the NIH, National Institute on Aging. Additional
support for this research was provided by National Institute on Aging
(K01AG039387, R01AG46206).
NR 33
TC 0
Z9 0
U1 2
U2 2
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0895-7061
EI 1941-7225
J9 AM J HYPERTENS
JI Am. J. Hypertens.
PD FEB
PY 2017
VL 30
IS 2
BP 151
EP 158
DI 10.1093/ajh/hpw106
PG 8
WC Peripheral Vascular Disease
SC Cardiovascular System & Cardiology
GA EO9QV
UT WOS:000397024100010
PM 27600581
ER
PT J
AU Doshi, JA
Lim, R
Li, PX
Young, PP
Lawnicki, VF
Troxel, AB
Volpp, KG
AF Doshi, Jalpa A.
Lim, Raymond
Li, Pengxiang
Young, Peinie P.
Lawnicki, Victor F.
Troxel, Andrea B.
Volpp, Kevin G.
TI Synchronized Prescription Refills and Medication Adherence: A
Retrospective Claims Analysis
SO AMERICAN JOURNAL OF MANAGED CARE
LA English
DT Article
ID ORDER PHARMACY USE; PERSISTENCE; USERS
AB OBJECTIVES: Medication adherence is often suboptimal, especially among patients on multiple chronic medications. We examined the association between synchronized medication refill schedules-which typically reduce organizational effort and logistical demands-and adherence.
STUDY DESIGN: Retrospective study among patients enrolled in Medicare Advantage prescription drug plans.
METHODS: We used 2012 pharmacy, medical, and enrollment data linked with consumer meta-data for Medicare patients filling 2 or more maintenance prescriptions for antihypertensives, lipid-lowering agents, antidiabetic agents, antidepressants, and/or antiosteoporotic agents. Medication adherence for the year was measured using the proportion of days covered (PDC) at the drug class level. Patients were deemed adherent if drug class PDC was = 0.80. Outcomes were compared between 1: 1 propensity score-matched patients on synchronized versus nonsynchronized refill schedules for maintenance medications.
RESULTS: The synchronized refill group showed better adherence than the control group, although the magnitude of effects varied by drug class and specific outcome measure. Mean PDC scores ranged from 0.02 higher for antihypertensives to 0.07 higher for antidepressants in the synchronized refill group relative to the control group (P <. 01). Further, compared with the control group, a larger proportion of synchronized refill group members were deemed adherent, ranging from 6 percentage points higher for antihypertensives to 15 percentage points higher for lipid-lowering agents (P <. 01). Differences between the synchronized and control groups were larger among exclusive users of retail versus mail order pharmacies for maintenance medications.
CONCLUSIONS: Synchronized medication refill schedules were associated with better medication adherence, particularly for patients filling maintenance medications exclusively at retail pharmacies.
C1 [Doshi, Jalpa A.; Lim, Raymond; Li, Pengxiang; Volpp, Kevin G.] Univ Penn, Dept Med, Philadelphia, PA 19104 USA.
[Lim, Raymond; Volpp, Kevin G.] Univ Penn, Dept Med Eth, Philadelphia, PA 19104 USA.
[Volpp, Kevin G.] Univ Penn, Dept Hlth Care Management, Philadelphia, PA 19104 USA.
[Doshi, Jalpa A.; Troxel, Andrea B.; Volpp, Kevin G.] Univ Penn, Leonard Davis Inst Hlth Econ, Ctr Hlth Incent & Behav Econ, Philadelphia, PA 19104 USA.
[Young, Peinie P.] Fuse Innovat Lab Cardinal Hlth, Dublin, OH USA.
[Lawnicki, Victor F.] Humana Inc, Louisville, KY USA.
[Troxel, Andrea B.] NYU, Dept Populat Hlth, New York, NY USA.
[Volpp, Kevin G.] Philadelphia Vet Affairs Med Ctr, Ctr Hlth Equ Res & Promot, Philadelphia, PA USA.
RP Doshi, JA (reprint author), Univ Penn, Med, 1223 Blockley Hall, Philadelphia, PA 19104 USA.; Doshi, JA (reprint author), Univ Penn, Ctr Evidence Based Practice, Econ Evaluat Unit, 1223 Blockley Hall, Philadelphia, PA 19104 USA.; Doshi, JA (reprint author), Univ Penn, Ctr Hlth Incent & Behav Econ, Value Based Insurance Design Initiat, 1223 Blockley Hall, Philadelphia, PA 19104 USA.
EM jdoshi@mail.med.upenn.edu
FU Humana, Inc.
FX Humana, Inc.
NR 18
TC 0
Z9 0
U1 1
U2 1
PU MANAGED CARE & HEALTHCARE COMMUNICATIONS LLC
PI PLAINSBORO
PA 666 PLAINSBORO RD, STE 300, PLAINSBORO, NJ 08536 USA
SN 1088-0224
J9 AM J MANAG CARE
JI Am. J. Manag. Care
PD FEB
PY 2017
VL 23
IS 2
BP 98
EP +
PG 28
WC Health Care Sciences & Services; Health Policy & Services; Medicine,
General & Internal
SC Health Care Sciences & Services; General & Internal Medicine
GA EO0OJ
UT WOS:000396397400008
PM 28245653
ER
PT J
AU Chen, JJ
Wu, PT
Middlekauff, HR
Nguyen, KL
AF Chen, Joseph J.
Wu, Pei-Tzu
Middlekauff, Holly R.
Nguyen, Kim-Lien
TI Aerobic exercise in anthracycline-induced cardiotoxicity: a systematic
review of current evidence and future directions
SO AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY
LA English
DT Review
DE aerobic exercise; anthracyclines; cancer; cardiotoxicity
ID SUBCLINICAL CARDIAC DYSFUNCTION; AMERICAN-HEART-ASSOCIATION;
CHILDHOOD-CANCER SURVIVORS; DOX-INDUCED CARDIOTOXICITY; BREAST-CANCER;
DOXORUBICIN CARDIOTOXICITY; PHYSICAL-ACTIVITY; SPORTS-MEDICINE;
CARDIOVASCULAR EVENTS; INDUCED CARDIOMYOCYTE
AB Cancer and cardiovascular disease are major causes of morbidity and mortality worldwide. Older cancer patients often wrestle with underlying heart disease during cancer therapy, whereas childhood cancer survivors are living long enough to face long-term unintended cardiac consequences of cancer therapies, including anthracyclines. Although effective and widely used, particularly in the pediatric population, anthracycline-related side effects including dose-dependent association with cardiac dysfunction limit their usage. Currently, there is only one United States Food and Drug Administration-approved drug, dexrazoxane, available for the prevention and mitigation of cardiotoxicity related to anthracycline therapy. While aerobic exercise has been shown to reduce cardiovascular complications in multiple diseases, its role as a therapeutic approach to mitigate cardiovascular consequences of cancer therapy is in its infancy. This systematic review aims to summarize how aerobic exercise can help to alleviate unintended cardiotoxic side effects and identify gaps in need of further research. While published work supports the benefits of aerobic exercise, additional clinical investigations are warranted to determine the effects of different exercise modalities, timing, and duration to identify optimal aerobic training regimens for reducing cardiovascular complications, particularly late cardiac effects, in cancer survivors exposed to anthracyclines.
C1 [Chen, Joseph J.; Wu, Pei-Tzu; Middlekauff, Holly R.; Nguyen, Kim-Lien] Univ Calif Los Angeles, David Geffen Sch Med, Div Cardiol, Los Angeles, CA 90024 USA.
[Chen, Joseph J.; Wu, Pei-Tzu; Nguyen, Kim-Lien] Vet Affairs Greater Los Angeles Healthcare Syst, Div Cardiol, Los Angeles, CA USA.
RP Nguyen, KL (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, VA Greater Los Angeles Healthcare Syst, 11301 Wilshire Blvd,MC 111E, Los Angeles, CA 90024 USA.
EM kimliennguyen@mednet.ucla.edu
FU Jonsson Comprehensive Cancer Center Foundation; National Center for
Advancing Translational Sciences Clinical and Translational Sciences
Institute [UL1TR000124]
FX This work was supported by a pilot grant from the Jonsson Comprehensive
Cancer Center Foundation and National Center for Advancing Translational
Sciences Clinical and Translational Sciences Institute grant
UL1TR000124.
NR 62
TC 0
Z9 0
U1 2
U2 2
PU AMER PHYSIOLOGICAL SOC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814 USA
SN 0363-6135
EI 1522-1539
J9 AM J PHYSIOL-HEART C
JI Am. J. Physiol.-Heart Circul. Physiol.
PD FEB
PY 2017
VL 312
IS 2
BP H213
EP H222
DI 10.1152/ajpheart.00646.2016
PG 10
WC Cardiac & Cardiovascular Systems; Physiology; Peripheral Vascular
Disease
SC Cardiovascular System & Cardiology; Physiology
GA EN1VF
UT WOS:000395797600003
PM 27923793
ER
PT J
AU Pagani-Estevez, GL
Swetz, KM
McGoon, MD
Frantz, RP
Tointon, SK
Karnyski, AM
Durst, LA
Watson, JC
AF Pagani-Estevez, Gabriel L.
Swetz, Keith M.
McGoon, Michael D.
Frantz, Robert P.
Tointon, Susan K.
Karnyski, Ann M.
Durst, Louise A.
Watson, James C.
TI Characterization of Prostacyclin-associated Leg Pain in Patients with
Pulmonary Arterial Hypertension
SO ANNALS OF THE AMERICAN THORACIC SOCIETY
LA English
DT Article
AB Rationale: Prostacyclinassociated leg pain is a potentially debilitating adverse effect of prostacyclin therapy for patients with pulmonary arterial hypertension (PAH). However, to our knowledge, this entity has not been systematically studied.
Objectives: To characterize the clinical features and metabolic risk factors for prostacyclinassociated leg pain.
Methods: At one academic medical center, we assembled and analyzed a case series of patients with PAH and prostacyclin-associated leg pain.
Measurements and Main Results: Over a period of 2 years, we identified 11 patients with PAH and prostacyclinassociated leg pain who agreed to participate in this study. Subjects underwent a standardized clinical evaluation, electrodiagnostic assessment, and serologic screen for metabolic causes of peripheral neuropathy. All 11 patients were female; their mean (SD) age was 50 (+/- 9) years; their median (interquartile range) PAH duration was 56 (20-96) months; and their prostacyclin therapy duration was a median (interquartile range) of 20 (14-36) months. All patients reported leg pain beginning soon after prostacyclin initiation and varying with dose. All described a neuropathic pain in a symmetric, distal, stocking distribution. Neurologic examination revealed a sensory, small-fiber, predominantly peripheral neuropathy in seven (78%) patients. Results of autonomic reflex testing and thermoregulatory sweat testing were abnormal in 82% and 90% of patients, respectively, suggesting smallfiber neuropathy. Serologic evaluation identified a new, previously unrecognized contributor to neuropathy in eight (73%) patients, including vitamin B-12 deficiency in six (55%), uncompensated hypothyroidism in three (27%), and diabetes mellitus in one (9%).
Conclusions: Chronic prostacyclin-associated leg pain is associated with a small-fiber neuropathy. Treatable metabolic contributors (vitamin B12 deficiency, thyroid dysfunction, or diabetes) appear to be common possible "second hits" that may be underrecognized. We recommend screening for possible metabolic contributors in patients who have otherwise unexplained leg pain in the setting of PAH and current or anticipated prostacyclin therapy.
C1 [Pagani-Estevez, Gabriel L.; Watson, James C.] Mayo Clin, Dept Neurol, 200 First St SW, Rochester, MN 55905 USA.
[McGoon, Michael D.; Frantz, Robert P.; Tointon, Susan K.; Karnyski, Ann M.] Mayo Clin, Dept Med, Cardiovasc Div, Rochester, MN USA.
[Watson, James C.] Mayo Clin, Pain Div, Dept Anesthesiol, Rochester, MN USA.
[Swetz, Keith M.] Univ Alabama Birmingham, Sch Med, Ctr Palliat & Support Care, Birmingham, AL USA.
[Swetz, Keith M.; Durst, Louise A.] Birmingham VA Med Ctr, Birmingham, AL USA.
RP Watson, JC (reprint author), Mayo Clin, Dept Neurol, 200 First St SW, Rochester, MN 55905 USA.
EM watson.james@mayo.edu
NR 0
TC 0
Z9 0
U1 1
U2 1
PU AMER THORACIC SOC
PI NEW YORK
PA 25 BROADWAY, 18 FL, NEW YORK, NY 10004 USA
SN 1546-3222
EI 2325-6621
J9 ANN AM THORAC SOC
JI Ann. Am. Thoracic Society
PD FEB
PY 2017
VL 14
IS 2
BP 206
EP 212
DI 10.1513/AnnalsATS.201609-674OC
PG 7
WC Respiratory System
SC Respiratory System
GA EP5OK
UT WOS:000397428000011
PM 27898216
ER
PT J
AU Parsons, EC
Mattox, EA
Beste, LA
Au, DH
Young, BA
Chang, MF
Palen, BN
AF Parsons, Elizabeth C.
Mattox, Elizabeth A.
Beste, Lauren A.
Au, David H.
Young, Bessie A.
Chang, Michael F.
Palen, Brian N.
TI Development of a Sleep Telementorship Program for Rural Department of
Veterans Affairs Primary Care Providers: Sleep Veterans Affairs
Extension for Community Healthcare Outcomes
SO ANNALS OF THE AMERICAN THORACIC SOCIETY
LA English
DT Article
AB Rationale: Primary care providers (PCPs) frequently encounter sleep complaints, especially in regions with limited specialty care access.
Objectives: The U.S. Department of Veterans Affairs Extension for Community Healthcare Outcomes (VA-ECHO) program (based on Project ECHO) has successfully provided rural PCP education in subspecialty areas, including hepatitis C. Wedescribe the feasibility of an ECHO program for sleep medicine.
Methods: ECHO creates a virtual learning community through video-teleconferencing, combining didactics with individualized clinical case review. We invited multidisciplinary providers to attend up to 10 stand-alone, 1-hour sessions. Invitees completed a needs assessment, which guided curriculum development. After program completion, we examined participant characteristics and self-reported changes in practice and comfort with managing sleep complaints. We surveyed participation barriers among invitees with low/no attendance.
Measurements and Main Results: Of the 39 program participants, 38% worked in rural healthcare. Participants included nurse practitioners (26%), registered nurses (21%), and physicians (15%). Seventeen (44%) completed the summative program evaluation. Respondents anticipated practice change from the program, especially in patient education about sleep disorders (93% of respondents). Respondents reported improved comfort managing sleep complaints, especially sleep-disordered breathing, insomnia, and sleep in post-traumatic stress disorder (80% of respondents each). A follow-up survey of program invitees who attended zero to two sessions reported scheduling conflicts (62%) and lack of protected time (52%) as major participation barriers.
Conclusions: Participants in a pilot sleep medicine VA-ECHO program report practice change and increased comfort managing common sleep complaints. Future work is needed to identify objective measures of return on investment and address participation barriers.
C1 [Parsons, Elizabeth C.; Mattox, Elizabeth A.; Au, David H.; Palen, Brian N.] Vet Affairs Puget Sound Hlth Care Syst, Pulm & Crit Care Sect, Seattle, WA USA.
[Young, Bessie A.] Vet Affairs Puget Sound Hlth Care Syst, Nephrol Sect, Hosp & Specialty Med, Seattle, WA USA.
[Beste, Lauren A.] Vet Affairs Puget Sound Hlth Care Syst, Gen Med Serv, Seattle, WA USA.
[Beste, Lauren A.; Au, David H.; Young, Bessie A.] Vet Affairs Puget Sound Hlth Care Syst, Hlth Serv Res & Dev Ctr Innovat, Seattle, WA USA.
[Parsons, Elizabeth C.; Au, David H.; Palen, Brian N.] Univ Washington, Div Pulm & Crit Care, Seattle, WA 98195 USA.
[Beste, Lauren A.] Univ Washington, Div Gen Internal Med, Seattle, WA 98195 USA.
[Young, Bessie A.] Univ Washington, Div Nephrol, Seattle, WA 98195 USA.
[Young, Bessie A.] Univ Washington, Kidney Res Inst, Seattle, WA 98195 USA.
[Chang, Michael F.] Vet Affairs Portland Hlth Care Syst, Gastroenterol & Hepatol Serv, Portland, OR USA.
[Chang, Michael F.] Oregon Hlth & Sci Univ, Div Gastroenterol & Hepatol, Portland, OR 97201 USA.
RP Parsons, EC (reprint author), 1660 South Columbian Way,S-111 PULM, Seattle, WA 98108 USA.
EM elizabeth.parsons@va.gov
FU U.S. Department of Veterans Affairs' (VA) Veterans Health Administration
Office of Patient Care Services, Specialty Care Services program office;
VA Office of Rural Health; VA Northwest Health Network (VISN 20); VA
Portland Health Care System (Portland, OR); Boise VA Medical Center
(Boise, ID)
FX Supported in part through funding by the U.S. Department of Veterans
Affairs' (VA) Veterans Health Administration Office of Patient Care
Services, Specialty Care Services program office, the VA Office of Rural
Health, and the VA Northwest Health Network (VISN 20). This material is
the result of work supported with resources and use of the facilities at
the VA Puget Sound Health Care System (Seattle, WA), the VA Portland
Health Care System (Portland, OR), and Boise VA Medical Center (Boise,
ID).
NR 0
TC 0
Z9 0
U1 0
U2 0
PU AMER THORACIC SOC
PI NEW YORK
PA 25 BROADWAY, 18 FL, NEW YORK, NY 10004 USA
SN 1546-3222
EI 2325-6621
J9 ANN AM THORAC SOC
JI Ann. Am. Thoracic Society
PD FEB
PY 2017
VL 14
IS 2
BP 267
EP 274
DI 10.1513/AnnalsATS.201605-361BC
PG 8
WC Respiratory System
SC Respiratory System
GA EP5OK
UT WOS:000397428000019
PM 27977293
ER
PT J
AU Ovsiowitz, RS
Pangarkar, S
AF Ovsiowitz, Rebecca S.
Pangarkar, Sanjog
TI Morel-Lavalle lesion
SO APPLIED RADIOLOGY
LA English
DT Editorial Material
C1 [Ovsiowitz, Rebecca S.; Pangarkar, Sanjog] Greater Los Angeles VA Med Ctr, Inpatient Pain Serv, Los Angeles, CA 90073 USA.
[Ovsiowitz, Rebecca S.; Pangarkar, Sanjog] Univ Calif Los Angeles, David Geffen Sch Med, Med, Los Angeles, CA 90095 USA.
RP Ovsiowitz, RS (reprint author), Greater Los Angeles VA Med Ctr, Inpatient Pain Serv, Los Angeles, CA 90073 USA.; Ovsiowitz, RS (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Med, Los Angeles, CA 90095 USA.
NR 4
TC 0
Z9 0
U1 0
U2 0
PU ANDERSON PUBLISHING, INC
PI SCOTCH PLAINS
PA 180 GLENSIDE AVE, SCOTCH PLAINS, NJ 07076 USA
SN 0160-9963
EI 1879-2898
J9 APPL RADIOL
JI Appl. Radiol.
PD FEB
PY 2017
VL 46
IS 2
BP 38
EP 39
PG 2
WC Radiology, Nuclear Medicine & Medical Imaging
SC Radiology, Nuclear Medicine & Medical Imaging
GA EP4HA
UT WOS:000397340400006
ER
PT J
AU Lee, S
Huang, EJ
AF Lee, Sebum
Huang, Eric J.
TI Modeling ALS and FTD with iPSC-derived neurons
SO BRAIN RESEARCH
LA English
DT Review
DE Induced pluripotent stem cells (iPSCs); Amyotrophic lateral sclerosis
(ALS); Frontotemporal dementia (FM); Frontotemporal lobar degeneration
(FTLD)
ID AMYOTROPHIC-LATERAL-SCLEROSIS; PLURIPOTENT STEM-CELLS; FRONTOTEMPORAL
LOBAR DEGENERATION; HEXANUCLEOTIDE REPEAT EXPANSION; MYOTONIC-DYSTROPHY;
MOTOR-NEURONS; NEURODEGENERATIVE DISEASES; BASOPHILIC INCLUSIONS;
GENETIC CORRECTION; FUS MUTATIONS
AB Recent advances in genetics and neuropathology support the idea that amyotrophic lateral sclerosis (ALS) and frontotemporal lobar dementia (FTD) are two ends of a disease spectrum. Although several animal models have been developed to investigate the pathogenesis and disease progression in ALS and FTD, there are significant limitations that hamper our ability to connect these models with the neurodegenerative processes in human diseases. With the technical breakthrough in reprogramming biology, it is now possible to generate patient-specific induced pluripotent stem cells (iPSCs) and disease-relevant neuron subtypes. This review provides a comprehensive summary of studies that use iPSC-derived neurons to model ALS and FTD. We discuss the unique capabilities of iPSC-derived neurons that capture some key features of ALS and FTD, and underscore their potential roles in drug discovery. There are, however, several critical caveats that require improvements before iPSC-derived neurons can become highly effective disease models. Published by Elsevier B.V.
C1 [Lee, Sebum; Huang, Eric J.] Univ Calif San Francisco, Dept Pathol, 505 Parnassus Ave, San Francisco, CA 94143 USA.
[Huang, Eric J.] San Francisco VA Med Ctr, Pathol Serv 113B, 505 Parnassus Ave, San Francisco, CA 94143 USA.
RP Huang, EJ (reprint author), Univ Calif San Francisco, Dept Pathol, 505 Parnassus Ave, San Francisco, CA 94143 USA.
EM eric.huang2@ucsf.edu
FU National Institute of Health [0D011915]; Veterans Administrations BLR&D
Merit Review Award [I01 BX0011-8]; Pilot Award [I21 BX1625]; Muscular
Dystrophy Association [217592]; Consortium for Frontotemporal Dementia
Research (CFR)
FX We thank Dr. Bruce Miller (UCSF Memory & Aging Center), Dr. Fen-Biao Gao
(University of Massachusetts) and Dr. Yadong Huang (Gladstone Institute
of Neurological Disease & UCSF) for many insightful discussions. Our
research on ALS and FTD disease mechanism and pathogenesis has been
supported by grants from the National Institute of Health (0D011915),
Veterans Administrations BLR&D Merit Review Award (I01 BX0011-8) and
Pilot Award (I21 BX1625), Muscular Dystrophy Association (Research Grant
#217592), and the Consortium for Frontotemporal Dementia Research (CFR).
NR 72
TC 1
Z9 1
U1 0
U2 0
PU ELSEVIER SCIENCE BV
PI AMSTERDAM
PA PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS
SN 0006-8993
EI 1872-6240
J9 BRAIN RES
JI Brain Res.
PD FEB 1
PY 2017
VL 1656
SI SI
BP 88
EP 97
DI 10.1016/j.brainres.2015.10.003
PG 10
WC Neurosciences
SC Neurosciences & Neurology
GA EK8RE
UT WOS:000394190500011
PM 26462653
ER
PT J
AU Richards, KA
Cesario, S
Lim, AH
Best, SL
Deeren, SM
Bushman, W
Safdar, N
AF Richards, Kyle A.
Cesario, Stacy
Lim, Amy H.
Best, Sara L.
Deeren, Susan M.
Bushman, Wade
Safdar, Nasia
TI Utility of routine urinalysis and urine culture testing in an ambulatory
urology clinic: a quality improvement initiative in a Veterans
healthcare facility
SO CANADIAN JOURNAL OF UROLOGY
LA English
DT Article
DE quality control; quality improvement; urine; urine assay; urinary tract
infection
ID INFECTIOUS-DISEASES-SOCIETY; ASYMPTOMATIC BACTERIURIA; PRACTICE
GUIDELINES; TRACT-INFECTION; AMERICA; DIAGNOSIS; ADULTS
AB Introduction: Urinalysis (UA) and urine culture (UCx) are commonly performed tests in the urology clinic. Many of these urine studies are performed prior to the patient visit may not always be indicated, thus contributing to unintended consequences such as antibiotic use and costs without enhancing patient care. Our objective was to perform a quality improvement initiative aimed to assess the utility of routine UA/UCx.
Materials and methods: The practice pattern at our site's Veteran Affairs (VA) urology clinic prior to 2014 was to obtain routine UA/UCx on most clinic visits prior to patient evaluation. Starting in 2014, we designed an intervention whereby our nurse practitioner triaged all new patient referrals and selectively ordered UA/UCx. We performed multivariable logistic regression to assess for predictors of obtaining UA or UCx.
Results: A total of 1308 patients were seen in January March 2013 and 1456 in June-August 2014 and were included in this analysis. Fewer patients in 2014 received UA (59.8% versus 70.0%, p < 0.001) and UCx (49.6% versus 64.2%, p < 0.001). There was a decreased odds of obtaining UA in 2014 (OR 0.52, p < 0.001) as well as a decreased odds of obtaining UCx in 2014 (OR0.38, p < 0.001) on multivariable logistic regression. The results of UA/UCx only rarely resulted in change of management in either cohort (3%). Selective ordering resulted in an estimated cost savings of $4915.08/month in UCx costs alone.
Conclusions: Our quality improvement initiatives reduced rates of UA/UCx testing when providers assess patients prior to ordering these tests. The implication of this initiative is significant cost savings for the healthcare system.
C1 [Richards, Kyle A.; Cesario, Stacy; Lim, Amy H.; Best, Sara L.; Deeren, Susan M.; Bushman, Wade] William S Middleton Mem Vet Adm Med Ctr, Dept Urol, Madison, WI 53705 USA.
[Richards, Kyle A.; Best, Sara L.; Bushman, Wade] Univ Wisconsin Madison, Dept Urol, 1685 Highland Ave, Madison, WI 53705 USA.
[Safdar, Nasia] Univ Wisconsin Madison, Dept Med, Madison, WI USA.
RP Richards, KA (reprint author), Univ Wisconsin Madison, Dept Urol, 1685 Highland Ave, Madison, WI 53705 USA.
FU VA; VAMERIT award
FX This material is the result of work supported with resources and the use
of facilities at the William S. Memorial Veterans Hospital. Dr. Safdar
is supported by a VA funded Patient Safety Center of Inquiry and a
VAMERIT award. The contents do not represent the views of the U. S.
Department of Veterans Affairs or the United States Government.
NR 18
TC 0
Z9 0
U1 1
U2 1
PU CANADIAN J UROLOGY
PI ST LAURENT
PA 2330 WARD ST, STE 604, ST LAURENT, QUEBEC H4M 2V6, CANADA
SN 1195-9479
J9 CAN J UROL
JI Can. J. Urol.
PD FEB
PY 2017
VL 24
IS 1
BP 8627
EP 8633
PG 7
WC Urology & Nephrology
SC Urology & Nephrology
GA EM5MQ
UT WOS:000395356100004
PM 28263127
ER
PT J
AU Morris, BJ
Klausner, JD
Krieger, JN
Willcox, BJ
Crouse, PD
Pollock, N
AF Morris, Brian J.
Klausner, Jeffrey D.
Krieger, John N.
Willcox, Bradley J.
Crouse, Pierre D.
Pollock, Neil
TI Reply by Authors - Re: Canadian Pediatrics Society position statement on
newborn circumcision: a risk-benefit analysis revisited
SO CANADIAN JOURNAL OF UROLOGY
LA English
DT Letter
ID HUMAN-PAPILLOMAVIRUS INFECTION; URINARY-TRACT-INFECTIONS;
PROSTATE-CANCER; FEMALE PARTNERS; MEN; COLONIZATION; PREVALENCE;
PREVENTION; CLEARANCE; SYPHILIS
C1 [Morris, Brian J.] Univ Sydney, Sch Med Sci, Bldg F13, Sydney, NSW 2006, Australia.
[Morris, Brian J.] Univ Sydney, Bosch Inst, Sydney, NSW, Australia.
[Klausner, Jeffrey D.] Univ Calif Los Angeles, David Geffen Sch Med, Div Infect Dis, Los Angeles, CA 90095 USA.
[Klausner, Jeffrey D.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA USA.
[Krieger, John N.] Univ Washington, Sch Med, VA Puget Sound Hlth Care Syst, Urol Sect, Seattle, WA USA.
[Willcox, Bradley J.] Univ Hawaii, Kuakini Med Ctr, Dept Res, Honolulu, HI 96822 USA.
[Crouse, Pierre D.] Intramed Med Ctr, Calgary, AB, Canada.
[Pollock, Neil] Univ British Columbia, Pollodc Clin, Vancouver, BC V5Z 1M9, Canada.
[Pollock, Neil] Univ British Columbia, New Westminster & Fac Med, Vancouver, BC V5Z 1M9, Canada.
RP Morris, BJ (reprint author), Univ Sydney, Sch Med Sci, Bldg F13, Sydney, NSW 2006, Australia.
NR 38
TC 0
Z9 0
U1 0
U2 0
PU CANADIAN J UROLOGY
PI ST LAURENT
PA 2330 WARD ST, STE 604, ST LAURENT, QUEBEC H4M 2V6, CANADA
SN 1195-9479
J9 CAN J UROL
JI Can. J. Urol.
PD FEB
PY 2017
VL 24
IS 1
BP 8687
EP 8692
PG 6
WC Urology & Nephrology
SC Urology & Nephrology
GA EM5MQ
UT WOS:000395356100017
PM 28263140
ER
PT J
AU Ho, SB
Monto, A
Peyton, A
Kaplan, DE
Byrne, S
Moon, S
Copans, A
Rossaro, L
Roy, A
Le, H
Dvory-Sobol, H
Zhu, YN
Brainard, DM
Guyer, W
Shaikh, O
Fuchs, M
Morgan, TR
AF Ho, Samuel B.
Monto, Alexander
Peyton, Adam
Kaplan, David E.
Byrne, Sean
Moon, Scott
Copans, Amanda
Rossaro, Lorenzo
Roy, Anupma
Le, Hadley
Dvory-Sobol, Hadas
Zhu, Yanni
Brainard, Diana M.
Guyer, William
Shaikh, Obaid
Fuchs, Michael
Morgan, Timothy R.
CA VALOR Study Team
TI Efficacy of Sofosbuvir Plus Ribavirin in Veterans With Hepatitis C Virus
Genotype 2 Infection, Compensated Cirrhosis, and Multiple Comorbidities
SO CLINICAL GASTROENTEROLOGY AND HEPATOLOGY
LA English
DT Article
DE VA; DAA; NS5B Inhibitor; Substance Abuse; Clinical Trial
ID PSYCHIATRIC-ILLNESS; US VETERANS; VELPATASVIR; PREVALENCE; OUTCOMES;
THERAPY; AFFAIRS; ALPHA; CARE
AB BACKGROUND & AIMS: We conducted a phase 4, open-label study with limited exclusion criteria to evaluate the safety and efficacy of sofosbuvir and ribavirin in veterans with hepatitis C virus genotype 2 infection, and compensated cirrhosis. This population is often excluded from clinical studies.
METHODS: We performed a prospective study of treatment-naive (n = 47) and treatment-experienced (n = 19) patients with chronic hepatitis C virus genotype 2 infection and compensated cirrhosis at 15 Department of Veterans Affairs sites. All subjects were given sofosbuvir (400 mg, once daily) plus ribavirin (1000-1200 mg/day) in divided doses for 12 weeks. Patients with major psychiatric diseases or alcohol or substance use disorders were not excluded. The primary endpoint was sustained virologic response 12 weeks after therapy.
RESULTS: Fifty- two patients achieved a sustained virologic response 12 weeks after therapy (79%; 95% confidence interval, 67%-88%); 16 of these patients were treatment experienced (84%; 95% confidence interval, 60%-97%) and 36 were treatment naive (77%; 95% confidence interval, 62%-88%). All patients had at least 1 comorbidity. Thirty-five percent had depression, 24% had posttraumatic stress disorder, and 30% had anxiety disorder. In addition, 29% had current substance use. Of the 7 patients (11%) who discontinued the study treatment prematurely, 3 did so because of adverse events. The most common adverse events were fatigue, anemia, nausea, and headache. Serious adverse events occurred in 8 patients. Only 2 of the serious adverse events (anemia and nausea) were considered to be related to study treatment.
CONCLUSIONS: In a phase 4 study, 12 weeks treatment with sofosbuvir and ribavirin led to a sustained virologic response 12 weeks after therapy in almost 80% of veterans with hepatitis C virus genotype 2 infection, compensated cirrhosis, and multiple comorbidities, regardless of their treatment history. ClinicalTrials. gov, Number: NCT02128542
C1 [Ho, Samuel B.] Vet Affairs San Diego Healthcare Syst, San Diego, CA USA.
[Monto, Alexander] San Francisco Vet Affairs Healthcare Syst, San Francisco, CA USA.
[Peyton, Adam] Miami Vet Affairs Healthcare Syst, Miami, FL USA.
[Kaplan, David E.] Corporal Michael J Crescenz Vet Affairs Med Ctr, Philadelphia, PA USA.
[Byrne, Sean; Moon, Scott; Copans, Amanda; Rossaro, Lorenzo; Roy, Anupma; Le, Hadley; Dvory-Sobol, Hadas; Zhu, Yanni; Brainard, Diana M.; Guyer, William] Gilead Sci, Foster City, CA USA.
[Shaikh, Obaid] Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Fuchs, Michael] Richmond Vet Affairs Med Ctr, Richmond, VA USA.
[Morgan, Timothy R.] Vet Affairs Long Beach Healthcare Syst, Long Beach, CA USA.
RP Ho, SB (reprint author), Vet Affairs San Diego Healthcare Syst, San Diego, CA USA.
EM samuel.ho2@va.gov
FU Gilead Sciences, Inc.
FX Funding for this study was provided by Gilead Sciences, Inc.
NR 20
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Z9 1
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1542-3565
EI 1542-7714
J9 CLIN GASTROENTEROL H
JI Clin. Gastroenterol. Hepatol.
PD FEB
PY 2017
VL 15
IS 2
BP 282
EP 288
DI 10.1016/j.cgh.2016.05.024
PG 7
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EP2XH
UT WOS:000397246400022
PM 27237429
ER
PT J
AU Scott, JL
Wirth, JR
EuDaly, JG
Gilkeson, GS
Cunningham, MA
AF Scott, Jennifer L.
Wirth, Jena R.
EuDaly, Jackie G.
Gilkeson, Gary S.
Cunningham, Melissa A.
TI Plasmacytoid dendritic cell distribution and maturation are altered in
lupus prone mice prior to the onset of clinical disease
SO CLINICAL IMMUNOLOGY
LA English
DT Article
DE Rodent; Dendritic cells; Autoimmunity; Systemic lupus erythematosus
ID I INTERFERON; PDC-TREM; SIGLEC-H; RECEPTOR; ERYTHEMATOSUS; ALPHA;
AUTOIMMUNITY; EXPRESSION; ANTIGEN-2; IMMUNITY
AB Plasmacytoid dendritic cells (pDCs) and their production of type I interferons (IFN) are key pathogenic mediators of systemic lupus erythematosus (SLE). Despite the key role of pDCs in SLE, the mechanism by which pDCs promote disease is not well understood. The first objective for this study was to assess the number and maturation state of pDCs in pre-disease NZM2410 lupus prone mice compared to control mice. Second, we sought to identify mechanisms responsible for the alteration in pDCs in NZM mice prior to onset of clinical disease. We compared the number and percent of pDCs in the spleens and bone marrow (BM) of pre-disease NZM24010 (NZM) mice to C57BL/6 (B6) control mice. In the spleens of pre-disease NZM mice, pDC percent and number were increased. This increase occurs in parallel with a decrease in BM pDC number and percent in the NZM mice. The decrease in BM pDC number suggests the increase in spleen pDCs is a result of altered pDC distribution and not increased production of pDCs in the BM. To determine if pDC developmental potential is altered in lupus prone mice, we cultured BM from NZM and B6 mice in vitro. We found a reduced percentage/number of pDCs developing from the BM of NZM mice compared to B6 mice, which further supports that the increase in pDC number is a result of altered pDC distribution rather than increased pDC production. To better characterize the pDC population, we compared the percentage of mature pDCs in the spleens and BM of NZM mice to controls. In the NZM mice, there is a dramatic reduction in the number of mature pDCs in the BM of NZM mice, suggesting that mature pDCs exit the BM at a higher rate/earlier maturation time compared to healthy mice. We conclude that pDCs contribution to disease pathogenesis in NZM mice may include the alteration of pDC distribution to increase the number of pDCs in the spleen prior to disease onset. (C) 2016 Published by Elsevier Inc.
C1 [Scott, Jennifer L.] Med Univ South Carolina, Coll Grad Studies, Dept Microbiol & Immunol, 173 Ashley Ave,BSB 203, Charleston, SC 29425 USA.
[Wirth, Jena R.; EuDaly, Jackie G.; Gilkeson, Gary S.; Cunningham, Melissa A.] Med Univ South Carolina, Div Rheumatol & Immunol, Dept Med, 96 Jonathan Lucas St,Suite 816, Charleston, SC 29425 USA.
[Gilkeson, Gary S.] Ralph H Johnson Vet Affairs Med Ctr, Med Res Serv, 109 Bee St, Charleston, SC 29401 USA.
RP Cunningham, MA (reprint author), Med Univ South Carolina, Dept Med, 96 Jonathan Lucas St,Suite 912, Charleston, SC 29425 USA.
EM ScottJL@musc.edu; WirthJ@musc.edu; Eudalyjg@musc.edu; Gilkeson@musc.edu;
Cunnima@musc.edu
FU VA merit review grant [BX000470]; NIH grant [UT1 TR000062]; American
Association of Immunology careers in Immunology Fellowship
FX This work was funded by the VA merit review grant BX000470, the NIH
grant UT1 TR000062, and American Association of Immunology careers in
Immunology Fellowship.
NR 24
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U2 0
PU ACADEMIC PRESS INC ELSEVIER SCIENCE
PI SAN DIEGO
PA 525 B ST, STE 1900, SAN DIEGO, CA 92101-4495 USA
SN 1521-6616
EI 1521-7035
J9 CLIN IMMUNOL
JI Clin. Immunol.
PD FEB
PY 2017
VL 175
BP 109
EP 114
DI 10.1016/j.clim.2016.12.009
PG 6
WC Immunology
SC Immunology
GA EN4FG
UT WOS:000395962800014
PM 28041989
ER
PT J
AU Shaw, PA
Yancy, WS
Wesby, L
Ulrich, V
Troxel, AB
Huffman, D
Foster, GD
Volpp, K
AF Shaw, Pamela A.
Yancy, William S., Jr.
Wesby, Lisa
Ulrich, Victoria
Troxel, Andrea B.
Huffman, David
Foster, Gary D.
Volpp, Kevin
TI The design and conduct of Keep It Off: An online randomized trial of
financial incentives for weight-loss maintenance
SO CLINICAL TRIALS
LA English
DT Article
DE Behavioral economics; financial incentive; obesity; pragmatic trial;
randomized trial; weight-loss maintenance
ID LOW-CARBOHYDRATE; UNITED-STATES; RISK-FACTORS; OBESITY; OVERWEIGHT;
METAANALYSIS; PREVALENCE; PREVENTION; DIETS
AB Background Obesity continues to be a serious public health challenge. Rates are increasing worldwide, with nearly 70% of the US adults overweight or obese, leading to increased clinical and economic burden. While successful approaches for achieving weight loss have been identified, techniques for long-term maintenance of initial weight loss have largely been unsuccessful. Financial incentive interventions have been shown in several settings to be successful in motivating participants to adopt healthy behaviors.
Purpose Keep It Off is a three-arm randomized controlled trial that compares the efficacy of a lottery-based incentive, traditional direct payment incentive, and control of daily feedback without any incentive for weight-loss maintenance. This design allows comparison of a traditional direct payment incentive with one based on behavioral economic principles that consider the underlying psychology of decision-making.
Methods Participants were randomized in a 2:1 ratio for each active arm relative to control, with a targeted 188 participants in total. Eligible participants were those aged 30-80 who lost at least 11lb (5kg) during the first 4months of participation in Weight Watchers, a national weight-loss program, with whom we partnered. The interventions lasted 6months (Phase I); participants were followed for an additional 6months without intervention (Phase II). The primary outcome is weight change from baseline to the end of Phase I, with the change at the end of Phase II a key secondary endpoint. Keep It Off is a pragmatic trial that recruited, consented, enrolled, and followed patients electronically. Participants were provided a wireless weight scale that electronically transmitted daily self-monitored weights. Weights were verified every 3months at a Weight Watchers center local to the participant and electronically transmitted.
Results Using the study web-based platform, we integrated recruitment, enrollment, and follow-up procedures into a digital platform that required little staff effort to implement and manage. We randomized 191 participants in less than 1year. We describe the design of Keep It Off and implementation of enrollment.
Lessons Learned We demonstrated that our pragmatic design was successful in rapid accrual of participants in a trial of interventions to maintain weight loss.
Limitations Despite the nationwide reach of Weight Watchers, the generalizability of study findings may be limited by the characteristics of its members. The interventions under study are appropriate for settings where an entity, such as an employer or health insurance company, could offer them as a benefit.
Conclusions Keep It Off was implemented and conducted with minimal staff effort. This study has the potential to identify a practical and effective weight-loss maintenance strategy.
C1 [Shaw, Pamela A.; Troxel, Andrea B.] Univ Penn, Perelman Sch Med, Dept Biostat & Epidemiol, 606 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
[Shaw, Pamela A.; Wesby, Lisa; Ulrich, Victoria; Troxel, Andrea B.; Huffman, David; Volpp, Kevin] Univ Penn, Leonard Davis Inst Hlth Econ, Perelman Sch Med, Ctr Hlth Incent & Behav Econ, Philadelphia, PA 19104 USA.
[Shaw, Pamela A.; Wesby, Lisa; Ulrich, Victoria; Troxel, Andrea B.] Univ Penn, Perelman Sch Med, Ctr Clin Epidemiol & Biostat, Philadelphia, PA 19104 USA.
[Yancy, William S., Jr.] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA.
[Yancy, William S., Jr.] US Dept Vet Affairs, Ctr Hlth Serv Res Primary Care, Durham, NC USA.
[Huffman, David] Univ Oxford, Dept Econ, Oxford, England.
[Foster, Gary D.] Weight Watchers Int, Dept Sci & Innovat, New York, NY USA.
[Foster, Gary D.] Temple Univ, Ctr Obes Res & Educ, Philadelphia, PA USA.
[Volpp, Kevin] Philadelphia Vet Affairs Med Ctr, Ctr Hlth Equ Res & Promot, Philadelphia, PA USA.
[Volpp, Kevin] Univ Penn, Dept Med, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Volpp, Kevin] Univ Penn, Wharton Sch, Dept Hlth Care Syst, Philadelphia, PA 19104 USA.
RP Shaw, PA (reprint author), Univ Penn, Perelman Sch Med, Dept Biostat & Epidemiol, 606 Blockley Hall,423 Guardian Dr, Philadelphia, PA 19104 USA.
EM shawp@mail.med.upenn.edu
FU National Institute on Aging of the National Institutes of Health
[R01-AG045045]
FX This study was sponsored by the National Institute on Aging of the
National Institutes of Health under award no. R01-AG045045 (Volpp and
Yancy, MPIs).
NR 34
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U1 1
U2 1
PU SAGE PUBLICATIONS LTD
PI LONDON
PA 1 OLIVERS YARD, 55 CITY ROAD, LONDON EC1Y 1SP, ENGLAND
SN 1740-7745
EI 1740-7753
J9 CLIN TRIALS
JI Clin. Trials
PD FEB
PY 2017
VL 14
IS 1
BP 29
EP 36
DI 10.1177/1740774516669679
PG 8
WC Medicine, Research & Experimental
SC Research & Experimental Medicine
GA EL5HR
UT WOS:000394652700003
PM 27646508
ER
PT J
AU Reyes, S
Varagic, J
Ahmad, S
VonCannon, J
Kon, ND
Wang, H
Groban, L
Cheng, CP
Dell'Italia, LJ
Ferrario, CM
AF Reyes, Santiago
Varagic, Jasmina
Ahmad, Sarfaraz
VonCannon, Jessica
Kon, Neal D.
Wang, Hao
Groban, Leanne
Cheng, Che Ping
Dell'Italia, Louis J.
Ferrario, Carlos M.
TI Novel Cardiac Intracrine Mechanisms Based on Ang-(1-12)/ Chymase Axis
Require a Revision of Therapeutic Approaches in Human Heart Disease
SO CURRENT HYPERTENSION REPORTS
LA English
DT Review
DE Intracrine; Angiotensin-(1-12); Chymase; Cardiomyocyte;
Angiotensin-converting enzyme inhibitor; Angiotensin receptor blockers
ID ANGIOTENSIN-CONVERTING-ENZYME; HIGH-RISK PATIENTS; LEFT-VENTRICULAR
DYSFUNCTION; RANDOMIZED CONTROLLED-TRIAL; HIGH CARDIOVASCULAR RISK;
CORONARY-ARTERY-DISEASE; II-RECEPTOR BLOCKERS; BLOOD-PRESSURE;
MYOCARDIAL-INFARCTION; FORMING PATHWAYS
AB Purpose of the Review Drugs targeting the renin-angiotensin system (RAS), namely angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor blockers, are the most commonly prescribed drugs for patients with or at risk for cardiovascular events. However, new treatment strategies aimed at mitigating the rise of the heart failure pandemic are warranted because clinical trials show that RAS blockers have limited benefits in halting disease progression. The main goal of this review is to put forward the concept of an intracrine RAS signaling through the novel angiotensin-(1-12)/chymase axis as the main source of deleterious angiotensin II (Ang II) in cardiac maladaptive remodeling leading to heart failure (HF).
Recent Findings Expanding traditional knowledge, Ang II can be produced in tissues independently from the circulatory renin-angiotensin system. In the heart, angiotensin-(1-12) [Ang-(1-12)], a recently discovered derivative of angiotensinogen, is a precursor of Ang II, and chymase rather than ACE is the main enzyme contributing to the direct production of Ang II from Ang-(1-12). The Ang-(1-12)/chymase axis is an independent intracrine pathway accounting for the trophic, contractile, and pro-arrhythmic Ang II actions in the human heart. Ang-(1-12) expression and chymase activity have been found elevated in the left atrial appendage of heart disease subjects, suggesting a pivotal role of this axis in the progression of HF.
Summary Recent meta-analysis of large clinical trials on the use of ACE inhibitors and angiotensin receptor blockers in cardiovascular disease has demonstrated an imbalance between patients that significantly benefit from these therapeutic agents and those that remain at risk for heart disease progression. Looking to find an explanation, detailed investigation on the RAS has unveiled a previously unrecognized complexity of substrates and enzymes in tissues ultimately associated with the production of Ang II that may explain the shortcomings of ACE inhibition and angiotensin receptor blockade. Discovery of the Ang-(1-12)/chymase axis in human hearts, capable of producing Ang II independently from the circulatory RAS, has led to the notion that a tissue-delimited RAS signaling in an intracrine fashion may account for the deleterious effects of Ang II in the heart, contributing to the transition from maladaptive cardiac remodeling to heart failure. Targeting intracellular RAS signaling may improve current therapies aimed at reducing the burden of heart failure.
C1 [Reyes, Santiago; Varagic, Jasmina; Ahmad, Sarfaraz; VonCannon, Jessica; Ferrario, Carlos M.] Wake Forest Univ Hlth Sci, Dept Gen Surg, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Varagic, Jasmina; VonCannon, Jessica; Groban, Leanne] Wake Forest Univ Hlth Sci, Cardiovasc Sci Ctr, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Kon, Neal D.] Wake Forest Univ Hlth Sci, Dept Cardiothorac Surg, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Wang, Hao; Groban, Leanne] Wake Forest Univ Hlth Sci, Dept Anesthesiol, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Wang, Hao] Wake Forest Univ Hlth Sci, Dept Internal Med Mol Med, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Cheng, Che Ping] Wake Forest Univ Hlth Sci, Dept Internal Med Cardiovasc Med, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Dell'Italia, Louis J.] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL USA.
[Dell'Italia, Louis J.] Univ Alabama Birmingham, Dept Microbiol & Physiol, Birmingham, AL USA.
[Dell'Italia, Louis J.] Univ Alabama Birmingham, Dept Med, Div Cardiovasc Dis, Birmingham, AL USA.
[Dell'Italia, Louis J.] Birmingham Vet Affairs Med Ctr, Dept Vet Affairs, Birmingham, AL USA.
[Ferrario, Carlos M.] Wake Forest Univ Hlth Sci, Dept Internal Med, Dept Nephrol, Med Ctr Blvd, Winston Salem, NC 27157 USA.
[Ferrario, Carlos M.] Wake Forest Univ Hlth Sci, Dept Physiol Pharmacol, Med Ctr Blvd, Winston Salem, NC 27157 USA.
RP Ferrario, CM (reprint author), Wake Forest Univ Hlth Sci, Dept Gen Surg, Med Ctr Blvd, Winston Salem, NC 27157 USA.; Ferrario, CM (reprint author), Wake Forest Univ Hlth Sci, Dept Internal Med, Dept Nephrol, Med Ctr Blvd, Winston Salem, NC 27157 USA.; Ferrario, CM (reprint author), Wake Forest Univ Hlth Sci, Dept Physiol Pharmacol, Med Ctr Blvd, Winston Salem, NC 27157 USA.
EM cferrari@wakehealth.edu
NR 121
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Z9 0
U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1522-6417
EI 1534-3111
J9 CURR HYPERTENS REP
JI Curr. Hypertens. Rep.
PD FEB
PY 2017
VL 19
IS 2
AR 16
DI 10.1007/s11906-017-0708-3
PG 11
WC Peripheral Vascular Disease
SC Cardiovascular System & Cardiology
GA EP3CK
UT WOS:000397259900003
PM 28233239
ER
PT J
AU McFarlane, AC
Lawrence-Wood, E
Van Hooff, M
Malhi, GS
Yehuda, R
AF McFarlane, Alexander Cowell
Lawrence-Wood, Eleanor
Van Hooff, Miranda
Malhi, Gin S.
Yehuda, Rachel
TI The Need to Take a Staging Approach to the Biological Mechanisms of PTSD
and its Treatment
SO CURRENT PSYCHIATRY REPORTS
LA English
DT Review
DE PTSD; Staging; Subsyndromal; Neurobiology; Inflammation; Medical
comorbidity; Duration of illness; Longitudinal course; Delayed onset;
Treatment
ID POSTTRAUMATIC-STRESS-DISORDER; PROSPECTIVE COHORT; POLICE OFFICERS;
MENTAL-HEALTH; AFGHANISTAN VETERANS; MILITARY DEPLOYMENT; TRAUMATIC
STRESSORS; ARMED-FORCES; SYMPTOMS; RISK
AB Despite the substantial body of neurobiological research, no specific drug target has been developed to treat PTSD and there are substantial limitations with the available interventions. We propose that advances are likely to depend on the development of better classification of the heterogeneity of PTSD using a staging approach of disease. A primary rationale for staging is to highlight the probability that distinct therapeutic approaches need to be utilised according to the degree of biological progression of the disorder. Prospective studies, particularly of military populations, provide substantial evidence about the emerging biological abnormalities that precede the full-blown disorder. These need to be targeted with tailored interventions to prevent disease progression. Equally, the neurobiology of chronic unremitting PTSD needs to be differentiated from the acute disorder which emerges across a spectrum of severity, and this range of presentations correspondingly needs to be addressed with differing therapeutic strategies. The staging approach also needs to take account of the range of somatic pathological outcomes that are being identified as a consequence of traumatic stress exposure. PTSD should be conceptualised as a systemic disorder underpinned a range of biological dysregulation, including metabolic and altered immune function, reflected in the increased rates of cardiovascular and autoimmune disease. The effectiveness of novel treatments needs to be judged across their effectiveness in addressing the spectrum of trauma-related pathology.
C1 [McFarlane, Alexander Cowell; Lawrence-Wood, Eleanor; Van Hooff, Miranda] Univ Adelaide, Ctr Traumat Stress Studies, Level 2,122 Frome St, Adelaide, SA 5000, Australia.
[Malhi, Gin S.] Univ Sydney, Sydney Med Sch, Dept Psychiat, Edward Ford Bldg A27,Fisher Rd, Sydney, NSW 2006, Australia.
[Yehuda, Rachel] Mt Sinai Sch Med, Traumat Stress Studies Div, James J Peters VA Med Ctr, 130 West Kingsbridge Rd, Bronx, NY USA.
RP McFarlane, AC (reprint author), Univ Adelaide, Ctr Traumat Stress Studies, Level 2,122 Frome St, Adelaide, SA 5000, Australia.
EM alexander.mcfarlane@adelaide.edu.au
FU National Health Medical and Research Council of Australia [568970]
FX This research was funded by program grant number 568970 of the National
Health Medical and Research Council of Australia.
NR 80
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Z9 0
U1 2
U2 2
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1523-3812
EI 1535-1645
J9 CURR PSYCHIAT REP
JI Curr. Psychiatry Rep.
PD FEB
PY 2017
VL 19
IS 2
AR 10
DI 10.1007/s11920-017-0761-2
PG 9
WC Psychiatry
SC Psychiatry
GA EO7UP
UT WOS:000396895900003
PM 28168596
ER
PT J
AU Shamsi, MM
Chekachak, S
Soudi, S
Quinn, LS
Ranjbar, K
Chenari, J
Yazdi, MH
Mandavi, M
AF Shamsi, M. Molanouri
Chekachak, S.
Soudi, S.
Quinn, L. S.
Ranjbar, K.
Chenari, J.
Yazdi, M. H.
Mandavi, M.
TI Combined effect of aerobic interval training and selenium nanoparticles
on expression of IL-15 and IL-10/TNF-a ratio in skeletal muscle of 4T1
breast cancer mice with cachexia
SO CYTOKINE
LA English
DT Article
DE 4T1 breast cancer; Cachexia; Interleukin-15; Inflammation; Aerobic
interval training
ID TUMOR-BEARING RATS; RESISTANCE EXERCISE; ANTIOXIDANT SUPPLEMENTATION;
MOLECULAR-MECHANISMS; PHYSICAL-ACTIVITY; OXIDATIVE STRESS;
ADIPOSE-TISSUE; CELL-GROWTH; TNF-ALPHA; INTERLEUKIN-15
AB Cancer cachexia is characterized by inflammation, loss of skeletal muscle and adipose tissue mass, and functional impairment. Oxidative stress and inflammation are believed to regulate pathways controlling skeletal muscle wasting. The aim of this study was to determine the effects of aerobic interval training and the purported antioxidant treatment, selenium nanoparticle supplementation, on expression of IL-15 and inflammatory cytokines in 4T1 breast cancer-bearing mice with cachexia. Selenium nanopar-ticle supplementation accelerated cachexia symptoms in tumor-bearing mice, while exercise training prevented muscle wasting in tumor-bearing mice. Also, aerobic interval training enhanced the anti-inflammatory indices IL-10/TNF-alpha ratio and IL-15 expression in skeletal muscle in tumor-bearing mice. However, combining exercise training and antioxidant supplementation prevented cachexia and muscle wasting and additionally decreased tumor volume in 4T1 breast cancer mice. These finding suggested that combining exercise training and antioxidant supplementation could be a strategy for managing tumor volume and preventing cachexia in breast cancer. (C) 2016 Elsevier Ltd. All rights reserved.
C1 [Shamsi, M. Molanouri; Chekachak, S.; Ranjbar, K.] Tarbiat Modares Univ, Fac Humanities, Phys Educ & Sport Sci Dept, POB 14117-13116, Tehran, Iran.
[Soudi, S.] Tarbiat Modares Univ, Fac Med Sci, Dept Immunol, POB 14117-13116, Tehran, Iran.
[Quinn, L. S.] Univ Washington, VA Puget Sound Hlth Care Syst, Res Serv, Seattle, WA 98108 USA.
[Quinn, L. S.] Univ Washington, Div Gerontol & Geriatr Med, Dept Med, Seattle, WA 98108 USA.
[Chenari, J.] Univ Tehran Med Sci, Neurosci Inst, Brain & Spinal Cord Injury Res Ctr, Tehran, Iran.
[Yazdi, M. H.] Univ Tehran Med Sci, Sch Pharm, Dept Pharmaceut Biotechnol, Tehran, Iran.
[Yazdi, M. H.] Univ Tehran Med Sci, Sch Pharm, Biotechnol Res Ctr, Tehran, Iran.
[Mandavi, M.] Pasteur Inst Iran, Dept Immunol, 69 Pasteur Ave, Tehran, Iran.
RP Shamsi, MM (reprint author), Tarbiat Modares Univ, Fac Humanities, Phys Educ & Sport Sci Dept, POB 14117-13116, Tehran, Iran.; Soudi, S (reprint author), Tarbiat Modares Univ, Fac Med Sci, Dept Immunol, POB 14117-13116, Tehran, Iran.
EM molanouri@modares.ac.ir; soodabeh.chekachak@modares.ac.ir;
Soudi@modares.ac.ir; quinnL@uw.edu; kia.ranjbar@modares.ac.ir;
chenari.jamal@gmail.com; mohammadhossein61@gmail.com;
mandavivac@gmail.com
OI Soudi, Sara/0000-0002-8978-3958; Yazdi, Mohammad
Hossein/0000-0001-8567-8555
FU Research Center of Tarbiat Modarres University (TMU), Tehran, Iran
FX This work was supported by the Research Center of Tarbiat Modarres
University (TMU), Tehran, Iran. We wish to thank Professor Yaghob
Fathoallahy for his kind help and sincere cooperation.
NR 73
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U1 5
U2 5
PU ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
PI LONDON
PA 24-28 OVAL RD, LONDON NW1 7DX, ENGLAND
SN 1043-4666
EI 1096-0023
J9 CYTOKINE
JI Cytokine
PD FEB
PY 2017
VL 90
BP 100
EP 108
DI 10.1016/j.cyto.2016.11.005
PG 9
WC Biochemistry & Molecular Biology; Cell Biology; Immunology
SC Biochemistry & Molecular Biology; Cell Biology; Immunology
GA EL1QM
UT WOS:000394396100015
ER
PT J
AU Andrews, JS
Trupin, L
Hough, CL
Daikh, DI
Yelin, EH
Katz, PP
AF Andrews, James S.
Trupin, Laura
Hough, Catherine L.
Daikh, David I.
Yelin, Edward H.
Katz, Patricia P.
TI Serum biomarkers of inflammation and muscle strength among women with
systemic lupus erythematosus
SO CYTOKINE
LA English
DT Article
DE Systemic lupus erythematosus; Inflammation; Cytokines; Outcomes research
ID ACTIVITY QUESTIONNAIRE; PHYSICAL FUNCTION; VALIDITY; DISEASE
AB Objectives: Muscle strength is an important determinant of physical function in women with systemic lupus erythematosus (SLE). Serum biomarkers of inflammation, including interleukin-6 (IL-6) and C Reactive Protein (CRP), are associated with differences in muscle strength among individuals without rheumatologic disease. We examined whether serum levels of IL-6 and CRP are associated with upper and lower extremity muscle strength among adult women with SLE.
Methods: One hundred thirty-six women with SLE participated in this cross-sectional study. High- sensitivity CRP was analyzed by nephelometry. IL-6 serum levels were analyzed by high sensitivity enzyme-linked immunosorbent assay. Upper and lower extremity muscle strength were assessed by grip strength and peak torque of knee extension and flexion, respectively. Regression analyses modeled asso-ciations of CRP and IL-6 with upper and lower extremity muscle strength controlling for age, SLE dura-tion, physical activity, prednisone use, BMI, plaquenil use, and pain.
Results: Higher serum levels of IL-6 and CRP were associated with significantly weaker upper and lower extremity muscle strength even when controlling for covariates.
Conclusions: Increased serum IL-6 and CRP are associated with clinically significant differences in upper and lower extremity muscle strength and may be useful in identifying those at risk for weakness and decreased physical function. (C) 2016 Elsevier Ltd. All rights reserved.
C1 [Andrews, James S.; Hough, Catherine L.] Univ Washington, Dept Med, Seattle, WA USA.
[Trupin, Laura; Daikh, David I.; Yelin, Edward H.; Katz, Patricia P.] Univ Calif San Francisco, Dept Med, San Francisco, CA USA.
[Daikh, David I.] San Francisco VA Med Ctr, Dept Med, San Francisco, CA USA.
RP Andrews, JS (reprint author), Univ Washington, Div Rheumatol, Box 356420,959 NE Pacific St, Seattle, WA 98195 USA.
EM jsa1@uw.edu
FU NIH/NIAMS grant [P60 AR053308]; NIH/NCRR UCSF-CTSI Grant [UL1 RR024131];
Rosalind Russell/Ephraim Engleman Rheumatology Research Center for
Arthritis
FX This research was supported by NIH/NIAMS grant P60 AR053308 and by
NIH/NCRR UCSF-CTSI Grant Number UL1 RR024131, and by the Rosalind
Russell/Ephraim Engleman Rheumatology Research Center for Arthritis.
NR 15
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U1 0
U2 0
PU ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
PI LONDON
PA 24-28 OVAL RD, LONDON NW1 7DX, ENGLAND
SN 1043-4666
EI 1096-0023
J9 CYTOKINE
JI Cytokine
PD FEB
PY 2017
VL 90
BP 109
EP 112
DI 10.1016/j.cyto.2016.11.003
PG 4
WC Biochemistry & Molecular Biology; Cell Biology; Immunology
SC Biochemistry & Molecular Biology; Cell Biology; Immunology
GA EL1QM
UT WOS:000394396100016
PM 27863333
ER
PT J
AU Wyte-Lake, T
Claver, M
Der-Martirosian, C
Davis, D
Dobalian, A
AF Wyte-Lake, Tamar
Claver, Maria
Der-Martirosian, Claudia
Davis, Darlene
Dobalian, Aram
TI Developing a Home-Based Primary Care Disaster Preparedness Toolkit
SO DISASTER MEDICINE AND PUBLIC HEALTH PREPAREDNESS
LA English
DT Article
DE community health planning; disaster planning; emergency preparedness;
home health agencies; standard of care; veterans health
ID ADULTS
AB Objective: Health agencies working with the homebound play a vital role in bolstering a community's resiliency by improving the preparedness of this vulnerable population. Nevertheless, this role is one for which agencies lack training and resources, which leaves many homebound at heightened risk. This study examined the utility of an evidence-based Disaster Preparedness Toolkit in Veterans Health Administration (VHA) Home-Based Primary Care (HBPC) programs.
Methods: We conducted an online survey of all VHA HBPC program managers (N = 77/146; 53% response rate).
Results: Respondents with fewer years with the HBPC program rated the toolkit as being more helpful (P<0.05). Of those who implemented their program's disaster protocol most frequently, two-thirds strongly agreed that the toolkit was relevant. Conversely, of those who implemented their disaster protocols very infrequently or never, 23% strongly agreed that the topics covered in the toolkit were relevant to their work (P<0.05).
Conclusion: This toolkit helps support programs as they fulfill their preparedness requirements, especially practitioners who are new to their position in HBPC. Programs that implement disaster protocols infrequently may require additional efforts to increase understanding of the toolkit's utility. Engaging all members of the team with their diverse clinical expertise could strengthen a patient's personal preparedness plan.
C1 [Wyte-Lake, Tamar; Claver, Maria; Der-Martirosian, Claudia; Dobalian, Aram] Vet Hlth Adm, Vet Emergency Management Evaluat Ctr, 16111 Plummer St,MS 152, Los Angeles, CA 91343 USA.
[Davis, Darlene] US Dept Vet Affairs, Natl Off, Home Based Primary Care, Tampa, FL USA.
RP Wyte-Lake, T (reprint author), Vet Hlth Adm, Vet Emergency Management Evaluat Ctr, 16111 Plummer St,MS 152, Los Angeles, CA 91343 USA.
EM tamar.wyte@va.gov
NR 22
TC 0
Z9 0
U1 1
U2 1
PU CAMBRIDGE UNIV PRESS
PI NEW YORK
PA 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA
SN 1935-7893
EI 1938-744X
J9 DISASTER MED PUBLIC
JI Dis. Med. Public Health Prep.
PD FEB
PY 2017
VL 11
IS 1
BP 56
EP 63
DI 10.1017/dmp.2016.145
PG 8
WC Public, Environmental & Occupational Health
SC Public, Environmental & Occupational Health
GA EM6TB
UT WOS:000395444000012
PM 27839522
ER
PT J
AU Phillips, HR
Smith, DA
AF Phillips, Hayden R., III
Smith, David A.
TI A patient with a curious case of cyclical vomiting
SO JAAPA-JOURNAL OF THE AMERICAN ACADEMY OF PHYSICIAN ASSISTANTS
LA English
DT Article
DE cannabis; hyperemesis syndrome; cyclical vomiting; abdominal pain;
cannabis adverse reactions; excessive bathing
ID CANNABINOID HYPEREMESIS
AB Cannabis-related ED visits are on the rise due to wider legalization and availability of marijuana, and habitual daily use is increasingly common. Cannabis abuse has long been associated with various short-term and longterm adverse reactions. One such reaction is cannabinoid hyperemesis syndrome: cyclical vomiting, nausea, and abdominal pain that only resolves with a warm bath or shower. Healthcare providers must understand the signs and symptoms of cannabinoid hyperemesis syndrome so the problem can be recognized early and patients avoid unnecessary testing.
C1 [Phillips, Hayden R., III] Sacred Heart Hosp, ED, Allentown, PA 18104 USA.
[Smith, David A.] Salus Univ, PA Program, Elkins Pk, PA USA.
[Smith, David A.] Philadelphia VA Med Ctr, Surg ICU, Philadelphia, PA USA.
[Smith, David A.] Mercy Suburban Hosp East Norriton, ED, Norristown, PA USA.
RP Phillips, HR (reprint author), Sacred Heart Hosp, ED, Allentown, PA 18104 USA.
NR 7
TC 0
Z9 0
U1 0
U2 0
PU LIPPINCOTT WILLIAMS & WILKINS
PI PHILADELPHIA
PA TWO COMMERCE SQ, 2001 MARKET ST, PHILADELPHIA, PA 19103 USA
SN 1547-1896
EI 0893-7400
J9 JAAPA-J AM ACAD PHYS
JI JAAPA-J. Am. Acad. Physician Assist.
PD FEB
PY 2017
VL 30
IS 2
DI 10.1097/01.JAA.0000511789.29560.74
PG 3
WC Medicine, General & Internal
SC General & Internal Medicine
GA EP3KQ
UT WOS:000397281600003
ER
PT J
AU Scott, AR
Alore, EA
Naik, AD
Berger, DH
Suliburk, JW
AF Scott, Aaron R.
Alore, Elizabeth A.
Naik, Aanand D.
Berger, David H.
Suliburk, James W.
TI Mixed-Methods Analysis of Factors Impacting Use of a Postoperative
mHealth App
SO JMIR MHEALTH AND UHEALTH
LA English
DT Article
DE mHealth; colorectal surgery; smartphone apps
ID PROMOTE PHYSICAL-ACTIVITY; COLORECTAL SURGERY; HOSPITAL READMISSION;
ENHANCED RECOVERY; MOBILE APPS; PROGRAM; COMPLICATIONS; INTERVENTIONS;
QUALITY; PATIENT
AB Background: Limited communication and care coordination following discharge from hospitals may contribute to surgical complications. Smartphone apps offer a novel mechanism for communication and care coordination. However, factors which may affect patient app use in a postoperative, at-home setting are poorly understood.
Objective: The objectives of this study were to (1) gauge interest in smartphone app use among patients after colorectal surgery and (2) better understand factors affecting patient app use in a postoperative, at-home setting.
Methods: A prospective feasibility study was performed at a hospital that principally serves low socioeconomic status patients. After colorectal surgery, patients were enrolled and given a smartphone app, which uses previously validated content to provide symptom-based recommendations. Patients were instructed to use the app daily for 14 days after discharge. Demographics and usability data were collected at enrollment. Usability was measured with the System Usability Scale (SUS). At follow-up, the SUS was repeated and patients underwent a structured interview covering ease of use, willingness to use, and utility of use. Two members of the research team independently reviewed the field notes from follow-up interviews and extracted the most consistent themes. Chart and app log reviews identified clinical endpoints.
Results: We screened 115 patients, enrolled 20 patients (17.4%), and completed follow-up interviews with 17 patients (85%). Reasons for nonenrollment included: failure to meet inclusion criteria (47/115, 40.9%), declined to participate (26/115, 22.6%), and other reasons (22/115, 19.1%). There was no difference in patient ratings between usability at first-use and after extended use, with SUS scores greater than the 95th percentile at both time points. Despite high usability ratings, 6/20 (30%) of patients never used the app at home after hospital discharge and 2/20 (10%) only used the app once. Interviews revealed three themes related to app use: (1) patient-related barriers could prevent use even though the app had high usability scores; (2) patients viewed the app as a second opinion, rather than a primary source of information; and (3) many patients viewed the app as an external burden.
Conclusions: Use patterns in this study, and response rates after prompts to contact the operative team, suggest that apps need to be highly engaging to be adopted by patients. The growing penetration of smartphones and the proliferation of app-based interventions are unlikely to improve care coordination and communication, unless apps address the barriers and patient perceptions identified in this study. This study shows that high usability alone is not sufficient to motivate patients to use smartphone apps in the postoperative period.
C1 [Scott, Aaron R.; Alore, Elizabeth A.; Berger, David H.; Suliburk, James W.] Baylor Coll Med, Michael E DeBakey Dept Surg, One Baylor Plaza,BCM 390, Houston, TX 77030 USA.
[Naik, Aanand D.; Berger, David H.] Hlth Serv Res & Dev Ctr Innovat, Michael E DeBakey Vet Affairs Med Ctr, Ctr Innovat Qual Effectiveness & Safety, Houston, TX USA.
[Naik, Aanand D.] Baylor Coll Med, Alkek Dept Med, Houston, TX 77030 USA.
[Suliburk, James W.] Ben Taub Gen Hosp, Dept Surg, Houston, TX 77030 USA.
RP Suliburk, JW (reprint author), Baylor Coll Med, Michael E DeBakey Dept Surg, One Baylor Plaza,BCM 390, Houston, TX 77030 USA.
EM suliburk@bcm.edu
FU Cancer Prevention and Research Institute of Texas [RP140102]; Gordon and
Betty Moore Foundation Early-Career Investigator [4603]; VA Health
Services Research and Development Center of Innovation grant [CIN
13-413]; Seamless Mobile Health, Inc.
FX Dr Scott holds a trainee grant from the Cancer Prevention and Research
Institute of Texas (RP140102). Dr Suliburk holds a Gordon and Betty
Moore Foundation Early-Career Investigator Award (#4603). Dr Naik
receives support from a VA Health Services Research and Development
Center of Innovation grant (CIN 13-413). This study was sponsored by
Seamless Mobile Health, Inc. Sponsorship was limited to access to app,
patient compensation, and the cost of a mobile hot-spot used to allow
patients to download the app. The authors retained full editorial rights
and have no other commercial interest with the sponsor. The Department
of Veterans Health was not a performance site for this study and was not
involved with any research activities associated with the commercial
sponsor.
NR 43
TC 0
Z9 0
U1 0
U2 0
PU JMIR PUBLICATIONS, INC
PI TORONTO
PA 59 WINNERS CIRCLE, TORONTO, ON M4L 3Y7, CANADA
SN 2291-5222
J9 JMIR MHEALTH UHEALTH
JI JMIR mHealth uHealth
PD FEB
PY 2017
VL 5
IS 2
AR e11
DI 10.2196/mhealth.6728
PG 13
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA EN2JY
UT WOS:000395837000003
PM 28179215
ER
PT J
AU Smiley, SL
Elmasry, H
Hooper, MW
Niaura, RS
Hamilton, AB
Milburn, NG
AF Smiley, Sabrina L.
Elmasry, Hoda
Hooper, Monica Webb
Niaura, Raymond S.
Hamilton, Alison B.
Milburn, Norweeta G.
TI Feasibility of Ecological Momentary Assessment of Daily Sexting and
Substance Use Among Young Adult African American Gay and Bisexual Men: A
Pilot Study
SO JMIR RESEARCH PROTOCOLS
LA English
DT Article
DE ecological momentary assessment; mobile phone; text messaging; sexting;
marijuana; alcohol; young adult; gay and bisexual; African American
ID MARIJUANA USE; SEX; ADOLESCENTS; STUDENTS; BEHAVIOR; RISK
AB Background: Recent evidence suggests that sexualized text communication ("sexting") is associated with substance use and sexual risk behaviors among young adults, yet little is known about this relationship among young adult African American gay and bisexual men, a population disproportionately impacted by HIV in the United States. Rapid advances in mobile phone technology indicate a clear need for research using mobile health (mHealth) methods such as ecological momentary assessment (EMA) to serve as a viable counterpart to retrospective evaluation methods by using real-time data collection to assess sexting and substance use among this population.
Objective: The objective of this pilot study was to (1) describe the EMA study design and protocol, (2) characterize the study population, and (3) assess the feasibility of a random prompt text message-based thrice-daily EMA over 14 days, as a means of prospectively studying sexting, marijuana, and alcohol use among a sample of young adult African American gay and bisexual men ages 21 to 25.
Methods: Participants were recruited through flyers and snowball sampling during spring and summer 2015 at a community-based HIV/AIDS prevention, care, and support organization in Washington, DC. Eligible participants were enrolled in a one-time in-person study visit that consisted of informed written consent to participate in the study, a self-administered survey, a semi-structured interview, and enrollment and training in EMA data collection. Commencing the day after the study visit, a random prompt survey was texted to participants on their personal mobile phones 3 times a day over a 14-day data collection period assessing mood, texts sent, texts received, sexts sent, sexts received, marijuana want, marijuana use, and alcohol use.
Results: EMA feasibility was tested with 25 self-identified African American gay (n=16) and bisexual (n=9) men (mean age of 23.48 years, SD 1.5). Each random prompt survey had 8 questions with responses including yes/no and Likert scale options. There were 104 total days of EMA observation, and the retention rate was 72% (18 out of 25 participants). Participants responded to the random prompt surveys with a 57.3% compliance rate providing a total of 544 completed surveys out of 949 surveys. The overall mean response time to complete a survey was 6.1 minutes. There were significant positive associations between EMA texts sent and received questions (rho 0.84, P <.001) as well as sexts sent and received queries (rho 0.72, P <.001).
Conclusions: The use of an EMA protocol has the potential to be a very useful research tool for understanding episodic behaviors such as sexting and substance use in this relatively understudied and underserved population, and has implications for practice. Additional research is needed on how to maximize survey compliance.
C1 [Smiley, Sabrina L.; Elmasry, Hoda; Niaura, Raymond S.] Truth Initiat, Schroeder Inst Tobacco Res & Policy Studies, 900 G St NW,Fourth Floor, Washington, DC 20001 USA.
[Hooper, Monica Webb] Case Western Reserve Univ, Sch Med, Case Comprehens Canc Ctr, Cleveland, OH USA.
[Niaura, Raymond S.] Johns Hopkins Univ, Johns Hopkins Bloomberg Sch Publ Hlth, Dept Hlth Behav & Soc, Baltimore, MD USA.
[Niaura, Raymond S.] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Washington, DC 20007 USA.
[Hamilton, Alison B.; Milburn, Norweeta G.] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Semel Inst Neurosci & Human Behav, Los Angeles, CA 90024 USA.
[Hamilton, Alison B.] Vet Adm Greater Los Angeles Healthcare Syst, Vet Adm Ctr Study Healthcare Innovat Implementat, Los Angeles, CA USA.
RP Smiley, SL (reprint author), Truth Initiat, Schroeder Inst Tobacco Res & Policy Studies, 900 G St NW,Fourth Floor, Washington, DC 20001 USA.
EM ssmiley@truthinitiative.org
FU National Institute on Drug Abuse [R25DA035692, 5R25DA035692]
FX At the time of the study, Sabrina L Smiley was a Scholar with the
HIV/AIDS, Substance Abuse, and Trauma Training Program at the University
of California Los Angeles supported through an award from the National
Institute on Drug Abuse (R25DA035692). The research reported in this
publication was supported by the National Institute on Drug Abuse under
grant number 5R25DA035692. The content is solely the responsibility of
the authors and does not necessarily represent the official views of the
National Institutes of Health.
NR 23
TC 0
Z9 0
U1 1
U2 1
PU JMIR PUBLICATIONS, INC
PI TORONTO
PA 59 WINNERS CIRCLE, TORONTO, ON M4L 3Y7, CANADA
SN 1929-0748
J9 JMIR RES PROTOC
JI JMIR RES. Protoc.
PD FEB
PY 2017
VL 6
IS 2
AR e9
DI 10.2196/resprot.6520
PG 11
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA EN2KH
UT WOS:000395837900014
PM 28153816
ER
PT J
AU Chandra, A
Lin, T
Young, T
Tong, W
Ma, XY
Tseng, WJ
Kramer, I
Kneissel, M
Levine, MA
Zhang, YJ
Cengel, K
Liu, XS
Qin, L
AF Chandra, Abhishek
Lin, Tiao
Young, Tiffany
Tong, Wei
Ma, Xiaoyuan
Tseng, Wei-Ju
Kramer, Ina
Kneissel, Michaela
Levine, Michael A.
Zhang, Yejia
Cengel, Keith
Liu, X. Sherry
Qin, Ling
TI Suppression of Sclerostin Alleviates Radiation-Induced Bone Loss by
Protecting Bone-Forming Cells and Their Progenitors Through Distinct
Mechanisms
SO JOURNAL OF BONE AND MINERAL RESEARCH
LA English
DT Article
DE RADIOTHERAPY; SCL-AB; OSTEOBLASTS; MESENCHYMAL PROGENITORS; DNA REPAIR
ID MESENCHYMAL STEM-CELLS; TRABECULAR BONE; POSTMENOPAUSAL WOMEN;
IRRADIATION ALTERS; MINERAL DENSITY; MURINE MODEL; IN-VIVO; ANTIBODY;
MICE; RADIOTHERAPY
AB Focal radiotherapy is frequently associated with skeletal damage within the radiation field. Our previous in vitro study showed that activation of Wnt/beta-catenin pathway can overcome radiation-induced DNA damage and apoptosis of osteoblastic cells. Neutralization of circulating sclerostin with a monoclonal antibody (Scl-Ab) is an innovative approach for treating osteoporosis by enhancing Wnt/beta-catenin signaling in bone. Together with the fact that focal radiation increases sclerostin amount in bone, we sought to determine whether weekly treatment with Scl-Ab would prevent focal radiotherapy-induced osteoporosis in mice. MicroCT and histomorphometric analyses demonstrated that Scl-Ab blocked trabecular bone structural deterioration after radiation by partially preserving osteoblast number and activity. Consistently, trabecular bone in sclerostin null mice was resistant to radiation via the same mechanism. Scl-Ab accelerated DNA repair in osteoblasts after radiation by reducing the number of gamma-H2AX foci, a DNA double-strand break marker, and increasing the amount of Ku70, a DNA repair protein, thus protecting osteoblasts from radiation-induced apoptosis. In osteocytes, apart from using similar DNA repair mechanism to rescue osteocyte apoptosis, Scl-Ab restored the osteocyte canaliculi structure that was otherwise damaged by radiation. Using a lineage tracing approach that labels all mesenchymal lineage cells in the endosteal bone marrow, we demonstrated that radiation damage to mesenchymal progenitors mainly involves shifting their fate to adipocytes and arresting their proliferation ability but not inducing apoptosis, which are different mechanisms from radiation damage to mature bone forming cells. Scl-Ab treatment partially blocked the lineage shift but had no effect on the loss of proliferation potential. Taken together, our studies provide proof-of-principle evidence for a novel use of Scl-Ab as a therapeutic treatment for radiation-induced osteoporosis and establish molecular and cellular mechanisms that support such treatment. (C) 2016 American Society for Bone and Mineral Research.
C1 [Chandra, Abhishek; Lin, Tiao; Young, Tiffany; Tong, Wei; Ma, Xiaoyuan; Tseng, Wei-Ju; Zhang, Yejia; Liu, X. Sherry; Qin, Ling] Univ Penn, Perelman Sch Med, Dept Orthopaed Surg, 424 Stemmler Hall,36th St & Hamilton Walk, Philadelphia, PA 19104 USA.
[Lin, Tiao] Sun Yat Sen Univ, Musculoskeletal Oncol Ctr, Affiliated Hosp 1, Guangzhou, Guangdong, Peoples R China.
[Tong, Wei] Huazhong Univ Sci & Technol, Dept Orthopaed Surg, Union Hosp, Tongji Med Coll, Wuhan, Hubei, Peoples R China.
[Kramer, Ina; Kneissel, Michaela] Novartis Inst BioMed Res, Musculoskeletal Dis Area, Basel, Switzerland.
[Levine, Michael A.] Univ Penn, Dept Pediat, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Levine, Michael A.] Childrens Hosp Philadelphia, Div Endocrinol & Diabet, Philadelphia, PA 19104 USA.
[Levine, Michael A.] Childrens Hosp Philadelphia, Ctr Bone Hlth, Philadelphia, PA 19104 USA.
[Zhang, Yejia] Univ Penn, Philadelphia Vet Affairs Med Ctr, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Zhang, Yejia] Univ Penn, Dept Phys Med & Rehabil, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Cengel, Keith] Univ Penn, Dept Radiat Oncol, Perelman Sch Med, Philadelphia, PA 19104 USA.
RP Qin, L (reprint author), Univ Penn, Perelman Sch Med, Dept Orthopaed Surg, 424 Stemmler Hall,36th St & Hamilton Walk, Philadelphia, PA 19104 USA.
EM qinling@mail.med.upenn.edu
RI Liu, Xiaowei/H-1664-2017
OI Liu, Xiaowei/0000-0001-7247-2232
FU NIH [NIH/NIAMS R01AR066098, R01DK095803, K01AR066743, P30AR050950];
NICHD [1K08HD049598]
FX We thank Dr Henry Kronenberg from Harvard Medical School and Dr Robert
Gagel and Dr Huifang Liu from the MD Anderson Cancer Center for their
kind suggestions and advice on this project. We thank Dr Eileen Shore
for providing qRT-PCR primers for DKK1, PPAR gamma, and aP2 genes. This
study was supported by NIH grants NIH/NIAMS R01AR066098, R01DK095803 (to
LQ), K01AR066743 (to XSL), P30AR050950 (to Penn Center for
Musculoskeletal Disorders), and NICHD 1K08HD049598 (to YZ). The authors
gratefully thank Martin Heyworth, MD, for critically editing the
manuscript.
NR 54
TC 1
Z9 1
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0884-0431
EI 1523-4681
J9 J BONE MINER RES
JI J. Bone Miner. Res.
PD FEB
PY 2017
VL 32
IS 2
BP 360
EP 372
DI 10.1002/jbmr.2996
PG 13
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EO8JL
UT WOS:000396935300018
PM 27635523
ER
PT J
AU Kittiskulnam, P
Carrero, JJ
Chertow, GM
Kaysen, GA
Delgado, C
Johansen, KL
AF Kittiskulnam, Piyawan
Carrero, Juan J.
Chertow, Glenn M.
Kaysen, George A.
Delgado, Cynthia
Johansen, Kirsten L.
TI Sarcopenia among patients receiving hemodialysis: weighing the evidence
SO JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE
LA English
DT Article
DE Low muscle mass; Sarcopenia; Handgrip strength; Gait speed; Hemodialysis
ID CLINICALLY RELEVANT WEAKNESS; SKELETAL-MUSCLE MASS; BIOIMPEDANCE
SPECTROSCOPY; ALTERNATIVE DEFINITIONS; FUNCTIONAL IMPAIRMENT;
PHYSICAL-DISABILITY; OLDER WOMEN; LEAN MASS; PREVALENCE; CUTPOINTS
AB BackgroundThere is no consensus on how best to define low muscle mass in patients with end-stage renal disease. Use of muscle mass normalized to height-squared has been suggested by geriatric societies but may underestimate sarcopenia, particularly in the setting of excess adiposity. We compared four definitions of low muscle mass in a prevalent hemodialysis cohort.
MethodsACTIVE/ADIPOSE enrolled prevalent patients receiving hemodialysis from the San Francisco and Atlanta areas from June 2009 to August 2011. Whole-body muscle mass was estimated using bioelectrical impedance spectroscopy, performed before a midweek dialysis session (n=645; age 56.714.5years, 41% women). We defined low muscle mass as muscle mass of 2SD or more below sex-specific bioelectrical impedance spectroscopy-derived means for young adults (18-49years) from National Health and Nutrition Examination Survey and indexed to height(2), body weight (percentage), body surface area (BSA) by the DuBois formula, or Quetelet's body mass index (BMI). We compared prevalence of low muscle mass among the four methods and assessed their correlation with strength and physical performance.
ResultsThe prevalence of low muscle mass ranged from 8 to 32%. Muscle mass indexed to height(2) classified the smallest percentage of patients as having low muscle mass, particularly among women, whereas indexing by BSA classified the largest percentage. Low muscle mass/height(2) was present almost exclusively among normal or underweight patients, whereas indexing to body weight and BMI classified more overweight and obese patients as having low muscle mass. Handgrip strength was lower among those with low muscle mass by all methods except height(2). Handgrip strength was directly and modestly correlated with muscle mass normalized by percentage of body weight, BSA, and BMI (=0.43, 0.56, and, 0.64, respectively) and less so with muscle/height(2) (=0.31, P<0.001). The difference in grip strength among patients with low vs. normal muscle mass was largest according to muscle/BMI (-6.84kg, 95% CI -8.66 to -5.02, P<0.001). There were significant direct correlations of gait speed with muscle mass indexed to percentage of body weight, BSA, and BMI but not with muscle mass indexed to height(2).
ConclusionsSkeletal muscle mass normalized to height(2) may underestimate the prevalence of low muscle mass, particularly among overweight and obese patients on hemodialysis. Valid detection of sarcopenia among obese patients receiving hemodialysis requires adjustment for body size.
C1 [Kittiskulnam, Piyawan; Delgado, Cynthia; Johansen, Kirsten L.] Univ Calif San Francisco, Div Nephrol, San Francisco, CA 94143 USA.
[Kittiskulnam, Piyawan; Delgado, Cynthia; Johansen, Kirsten L.] San Francisco VA Med Ctr, San Francisco, CA USA.
[Kittiskulnam, Piyawan] Chulalongkorn Univ, Div Nephrol, Dept Med, Bangkok, Thailand.
[Kittiskulnam, Piyawan] King Chulalongkorn Mem Hosp, Thai Red Cross Soc, Bangkok, Thailand.
[Carrero, Juan J.] Karolinska Inst, Div Renal Med, Ctr Mol Med, Stockholm, Sweden.
[Chertow, Glenn M.] Stanford Univ, Dept Med, Div Nephrol, Sch Med, Stanford, CA 94305 USA.
[Kaysen, George A.] Univ Calif Davis, Div Nephrol, Sacramento, CA 95616 USA.
[Kaysen, George A.] Univ Calif Davis, Dept Biochem & Mol Med, Sacramento, CA 95616 USA.
RP Johansen, KL (reprint author), 111 J San Francisco VA Med Ctr, Nephrol Sect, 4150 Clement St, San Francisco, CA 94121 USA.
EM kirsten.johansen@ucsf.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
[N01-DK-7-0005, KD-7-5004, K24DK085153]; Department of Veterans Affairs,
Clinical Science Research and Development Program [1IK2CX000527-01A2];
International Society of Nephrology; Stockholm County Council; Swedish
Research Council
FX This work was supported through contracts N01-DK-7-0005 and KD-7-5004
from the National Institute of Diabetes and Digestive and Kidney
Diseases (NIDDK). Dr. Johansen's effort was also supported by
K24DK085153 from the NIDDK. Dr. Delgado's work is supported by the
Department of Veterans Affairs, Clinical Science Research and
Development Program under Career Development Award 1IK2CX000527-01A2.
Her contribution is the result of work supported with the resources and
the use of facilities at the San Francisco VA Medical Center. This work
has been made possible in part by an International Society of Nephrology
funded Fellowship to Dr. Kittiskulnam. Dr. Carrero-Roig acknowledges
grant support from Stockholm County Council and the Swedish Research
Council.
NR 39
TC 0
Z9 0
U1 5
U2 5
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2190-5991
EI 2190-6009
J9 J CACHEXIA SARCOPENI
JI J. Caxhexia Sarcopenia Muscle
PD FEB
PY 2017
VL 8
IS 1
BP 57
EP 68
DI 10.1002/jcsm.12130
PG 12
WC Medicine, General & Internal
SC General & Internal Medicine
GA EM0FJ
UT WOS:000394993900007
PM 27897415
ER
PT J
AU McClatchey, PM
Wu, F
Olfert, IM
Ellis, CG
Goldman, D
Reusch, JEB
Frisbee, JC
AF McClatchey, P. Mason
Wu, Fan
Olfert, I. Mark
Ellis, Christopher G.
Goldman, Daniel
Reusch, Jane E. B.
Frisbee, Jefferson C.
TI Impaired Tissue Oxygenation in Metabolic Syndrome Requires Increased
Microvascular Perfusion Heterogeneity
SO JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH
LA English
DT Article
DE Microcirculation; Oxygenation; Rodent models of obesity; Blood flow
control; Simulation
ID OBESE ZUCKER RATS; SKELETAL-MUSCLE; EXERCISE CAPACITY; BLOOD-FLOW;
DYSFUNCTION; RESISTANCE; MORTALITY; MODELS; SYSTEM; MEN
AB Metabolic syndrome (MS) in obese Zucker rats (OZR) is associated with impaired skeletal muscle performance and blunted hyperemia. Studies suggest that reduced O-2 diffusion capacity is required to explain compromised muscle performance and that heterogeneous microvascular perfusion distribution is critical. We modeled tissue oxygenation during muscle contraction in control and OZR skeletal muscle using physiologically realistic relationships. Using a network model of Krogh cylinders with increasing perfusion asymmetry and increased plasma skimming, we predict increased perfusion heterogeneity and decreased muscle oxygenation in OZR, with partial recovery following therapy. Notably, increasing O-2 delivery had less impact on VO2 than equivalent decreases in O-2 delivery, providing a mechanism for previous empirical work associating perfusion heterogeneity and impaired O-2 extraction. We demonstrate that increased skeletal muscle perfusion asymmetry is a defining characteristic of MS and must be considered to effectively model and understand blood-tissue O-2 exchange in this model of human disease.
C1 [McClatchey, P. Mason] Univ Colorado Anschutz Med Campus, Div Endocrinol, Aurora, CO USA.
[McClatchey, P. Mason; Reusch, Jane E. B.] Univ Colorado Anschutz Med Campus, Dept Bioengn, Aurora, CO USA.
[McClatchey, P. Mason] Denver Vet Affairs Med Ctr, Dept Med, Denver, CO USA.
[Wu, Fan; Reusch, Jane E. B.] Novartis Inst BioMed Res, Drug Metab & Pharmacokinet, E Hanover, NJ USA.
[Olfert, I. Mark] West Virginia Univ, Div Exercise Physiol, Hlth Sci Ctr, Morgantown, WV 26506 USA.
[Ellis, Christopher G.; Goldman, Daniel; Frisbee, Jefferson C.] Univ Western Ontario, Dept Med Biophys, Schulich Sch Med & Dent, Med Sci Bldg,M407,1151 Richmond St North, London, ON N6A 5C1, Canada.
RP Frisbee, JC (reprint author), Univ Western Ontario, Dept Med Biophys, Schulich Sch Med & Dent, Med Sci Bldg,M407,1151 Richmond St North, London, ON N6A 5C1, Canada.
EM jfrisbee@uwo.ca
FU American Heart Association [IRG 14330015, EIA 0740129N]; National
Institutes of Health [RR 2865AR, R01 DK64668]; VA Merit Review
[BX002046]; CU SOM Center for Women's Health Research, Bioengineering
[5T32HL072738]
FX This work was supported by the American Heart Association (IRG 14330015,
EIA 0740129N) and the National Institutes of Health (RR 2865AR; R01
DK64668), VA Merit Review BX002046 (JEBR), CU SOM Center for Women's
Health Research, Bioengineering T32 (5T32HL072738).
NR 34
TC 0
Z9 0
U1 0
U2 0
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1937-5387
EI 1937-5395
J9 J CARDIOVASC TRANSL
JI J. Cardiovasc. Transl. Res.
PD FEB
PY 2017
VL 10
IS 1
BP 69
EP 81
DI 10.1007/s12265-017-9732-6
PG 13
WC Cardiac & Cardiovascular Systems; Medicine, Research & Experimental
SC Cardiovascular System & Cardiology; Research & Experimental Medicine
GA EM0MP
UT WOS:000395012700008
ER
PT J
AU Goldstein, KM
Callegari, LS
AF Goldstein, Karen M.
Callegari, Lisa S.
TI Should a history of assisted reproductive technology be another
consideration when assessing cardiovascular risk?
SO JOURNAL OF CLINICAL HYPERTENSION
LA English
DT Editorial Material
ID HYPERTENSIVE DISORDERS; PRECONCEPTION CARE; PREGNANCY; RECOMMENDATIONS;
MORTALITY; DISEASE; STATE
C1 [Goldstein, Karen M.] Durham Vet Affairs Med Ctr, Ctr Hlth Serv Res Primary Care, Durham, NC 27705 USA.
[Goldstein, Karen M.] Duke Univ, Med Ctr, Dept Med, Div Gen Internal Med, Durham, NC 27710 USA.
[Callegari, Lisa S.] VA Puget Sound Hlth Care Syst, Dept Vet Affairs, Hlth Serv Res & Dev, Seattle, WA USA.
[Callegari, Lisa S.] Univ Washington, Dept Obstet & Gynecol, Seattle, WA 98195 USA.
[Callegari, Lisa S.] Univ Washington, Dept Hlth Serv, Seattle, WA 98195 USA.
RP Goldstein, KM (reprint author), Durham Vet Affairs Med Ctr, Ctr Hlth Serv Res Primary Care, Durham, NC 27705 USA.
EM karen.goldstein@va.gov
NR 16
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1524-6175
EI 1751-7176
J9 J CLIN HYPERTENS
JI J. Clin. Hypertens.
PD FEB
PY 2017
VL 19
IS 2
BP 170
EP 172
DI 10.1111/jch.12937
PG 3
WC Peripheral Vascular Disease
SC Cardiovascular System & Cardiology
GA EL3GP
UT WOS:000394507900010
PM 28194918
ER
PT J
AU Perez, CM
Munoz, F
Andriankaja, OM
Ritchie, CS
Martinez, S
Vergara, J
Vivaldi, J
Lopez, L
Campos, M
Joshipura, KJ
AF Perez, Cynthia M.
Munoz, Francisco
Andriankaja, Oelisoa M.
Ritchie, Christine S.
Martinez, Sasha
Vergara, Jose
Vivaldi, Jose
Lopez, Lydia
Campos, Maribel
Joshipura, Kaumudi J.
TI Cross-sectional associations of impaired glucose metabolism measures
with bleeding on probing and periodontitis
SO JOURNAL OF CLINICAL PERIODONTOLOGY
LA English
DT Article
DE bleeding on probing; impaired fasting glucose; impaired glucose
tolerance; impaired glycated haemoglobin; insulin resistance;
periodontitis; pre-diabetes
ID NUTRITION EXAMINATION SURVEY; CONTINUOUS NATIONAL-HEALTH; BETA-CELL
FUNCTION; INSULIN-RESISTANCE; DIABETES-MELLITUS; FASTING GLUCOSE;
ORAL-HEALTH; DISEASE; ADULTS; INFLAMMATION
AB Aim: This study assessed the associations of pre-diabetes and insulin resistance with bleeding on probing (BOP) and periodontitis among adults.
Materials and methods: We included 1191 Hispanic adults aged 40-65 years, free of diabetes, enrolled in San Juan Overweight Adults Longitudinal Study. Pre-diabetes was defined as impaired fasting glucose (IFG), impaired glucose tolerance (IGT), or impaired glycated haemoglobin. Impaired one-hour plasma glucose (1hPG) was defined as levels >155 mg/dl. Insulin resistance was defined using the study population-specific 75th percentile (HOMA-IR >= 3.13). High BOP was defined as percentage of teeth with bleeding >= 30%. Periodontitis was defined according to the CDC/AAP definition.
Results: After multivariable adjustment for age, gender, education, smoking status, alcohol consumption, physical activity, obesity, HDL-C, and plaque index, pre-diabetes with and without 1hPG, IFG, impaired 1hPG, IGT, and HOMA-IR were significantly associated with high BOP; pre-diabetes, IFG, and impaired 1hPG were significantly associated with severe periodontitis. Most of these associations remained significant when the analyses were restricted to non-smokers.
Conclusions: This study suggests associations between pre-diabetes and insulin resistance with BOP and periodontitis. Given the high prevalence of impaired glucose metabolism and periodontitis, the assessment of the temporal sequence of these associations is of utmost importance.
C1 [Perez, Cynthia M.] Univ Puerto Rico, Dept Biostat & Epidemiol, Grad Sch Publ Hlth, Med Sci Campus,POB 365067, San Juan, PR 00936 USA.
[Munoz, Francisco; Andriankaja, Oelisoa M.; Martinez, Sasha; Campos, Maribel; Joshipura, Kaumudi J.] Univ Puerto Rico, Ctr Clin Res & Hlth Promot, Sch Dent Med, Med Sci Campus, San Juan, PR 00936 USA.
[Ritchie, Christine S.] San Francisco VA Med Ctr, Ctr Res Aging Jewish Home San Francisco, San Francisco, CA USA.
[Vergara, Jose; Vivaldi, Jose] Univ Puerto Rico, Sch Dent Med, Med Sci Campus, San Juan, PR 00936 USA.
[Joshipura, Kaumudi J.] Harvard Univ, Dept Epidemiol, Harvard TH Chan Sch Publ Hlth, Cambridge, MA 02138 USA.
RP Perez, CM (reprint author), Univ Puerto Rico, Dept Biostat & Epidemiol, Grad Sch Publ Hlth, Med Sci Campus,POB 365067, San Juan, PR 00936 USA.
EM cynthia.perez1@upr.edu
OI Joshipura, Kaumudi/0000-0003-1964-7579
FU NIDCR NIH HHS [R01 DE020111, K23 DE025313]; NIMHD NIH HHS [U54 MD007587]
NR 40
TC 0
Z9 0
U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0303-6979
EI 1600-051X
J9 J CLIN PERIODONTOL
JI J. Clin. Periodontol.
PD FEB
PY 2017
VL 44
IS 2
BP 142
EP 149
DI 10.1111/jcpe.12662
PG 8
WC Dentistry, Oral Surgery & Medicine
SC Dentistry, Oral Surgery & Medicine
GA EM8ML
UT WOS:000395565400003
PM 27978601
ER
PT J
AU McGinn, MM
Hoerster, KD
Stryczek, KC
Malte, CA
Jakupcak, M
AF McGinn, Meghan M.
Hoerster, Katherine D.
Stryczek, Krysttel C.
Malte, Carol A.
Jakupcak, Matthew
TI Relationship Satisfaction, PTSD Symptom Severity, and Mental Healthcare
Utilization Among OEF/OIF Veterans
SO JOURNAL OF FAMILY PSYCHOLOGY
LA English
DT Article
DE mental health care utilization; PTSD; relationship satisfaction
ID AFGHANISTAN VETERANS; COUPLE THERAPY; IRAQ; BARRIERS; SERVICES; STRESS;
MODEL
AB Despite the availability of evidence-based PTSD treatments at most facilities within the VA Healthcare System, most Iraq and Afghanistan veterans returning from deployments with posttraumatic stress symptoms do not receive an adequate dose of mental health treatment, prompting the need to identify potential barriers to or facilitators of mental health care utilization. Previous research demonstrated self-reported mental health care utilization in the prior year varies as a function of PTSD symptom severity, and the interaction of PTSD symptom severity and romantic relationship satisfaction (Meis et al., 2010). We extended these findings by objectively measuring the degree of utilization over a 1-year period (i. e., number of sessions attended) in a sample of 130 Iraq and Afghanistan veterans who presented to primary care/deployment health and completed an initial mental health evaluation. Results indicated main and interactive effects of PTSD symptom severity and relationship satisfaction, such that greater PTSD symptom severity was associated with greater utilization at average to high relationship satisfaction (p < .05), but not low relationship satisfaction. Implications for future research and couple/family based interventions for veterans with PTSD are discussed.
C1 [McGinn, Meghan M.; Hoerster, Katherine D.; Stryczek, Krysttel C.; Malte, Carol A.; Jakupcak, Matthew] VA Puget Sound Healthcare Syst, 1660 South Columbian Way, Seattle, WA 98108 USA.
[McGinn, Meghan M.; Hoerster, Katherine D.; Jakupcak, Matthew] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
RP McGinn, MM (reprint author), VA Puget Sound Healthcare Syst, 1660 South Columbian Way, Seattle, WA 98108 USA.
EM meghan.mcginn@va.gov
FU Department of Veterans Affairs Office of Academic Affiliations, Advanced
Fellowship Program in Mental Illness Research and Treatment; VA Puget
Sound Healthcare System, Seattle, Washington; University of Washington
School of Medicine, Department of Psychiatry & Behavioral Sciences,
Seattle, Washington
FX This material is the result of work supported by resources from the
Department of Veterans Affairs Office of Academic Affiliations, Advanced
Fellowship Program in Mental Illness Research and Treatment, the VA
Puget Sound Healthcare System, Seattle, Washington, and the University
of Washington School of Medicine, Department of Psychiatry & Behavioral
Sciences, Seattle, Washington. The views expressed in this article are
those of the authors and do not necessarily reflect the position or
policy of the Department of Veterans Affairs or the United States
Government. Some of the ideas and data from an earlier version of this
article were presented at the 2013 American Psychological Association's
Annual Convention in Honolulu, HI.
NR 22
TC 0
Z9 0
U1 0
U2 0
PU AMER PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST NE, WASHINGTON, DC 20002-4242 USA
SN 0893-3200
EI 1939-1293
J9 J FAM PSYCHOL
JI J. Fam. Psychol.
PD FEB
PY 2017
VL 31
IS 1
BP 111
EP 116
DI 10.1037/fam0000224
PG 6
WC Psychology, Clinical; Family Studies
SC Psychology; Family Studies
GA EN1QW
UT WOS:000395785900014
PM 27668933
ER
PT J
AU Wheldon, CW
Kolar, SK
Hernandez, ND
Daley, EM
AF Wheldon, Christopher W.
Kolar, Stephanie K.
Hernandez, Natalie D.
Daley, Ellen M.
TI Factorial Invariance and Convergent Validity of the Group-Based Medical
Mistrust Scale across Gender and Ethnoracial Identity
SO JOURNAL OF HEALTH CARE FOR THE POOR AND UNDERSERVED
LA English
DT Article
DE Medical mistrust; psychometrics; minorities; measurement
ID HEALTH-CARE; PERCEIVED DISADVANTAGES; AFRICAN-AMERICAN; FIT INDEXES;
SATISFACTION; TRUST
AB The objective of this study was to assess the factorial invariance and convergent validity of the Group-Based Medical Mistrust Scale (GBMMS) across gender (male and female) and ethnoracial identity (Latino and Black). Minority students (N = 686) attending a southeastern university were surveyed in the fall of 2011. Psychometric analysis of the GBMMS was performed. A three-factor solution fit the data after the omission of two problematic items. This revised version of the GBMMS exhibited sufficient configural, metric, and scalar invariance. Convergence of the GBMMS with conceptually related measures provided further evidence of validity; however, there was variation across ethnoracial identity. The GBMMS has viable psychometric properties across gender and ethnoracial identity in Black and Latino populations.
C1 [Wheldon, Christopher W.] NCI, Div Canc Control & Populat Sci, Room 3E-212,9609 Med Ctr Dr, Bethesda, MD 20892 USA.
[Kolar, Stephanie K.] US Dept Vet Affairs, Washington, DC USA.
[Hernandez, Natalie D.] Univ S Florida, Dept Community Hlth & Prevent Med, Tampa, FL USA.
[Daley, Ellen M.] Univ S Florida, Dept Community & Family Hlth, Tampa, FL USA.
RP Wheldon, CW (reprint author), NCI, Div Canc Control & Populat Sci, Room 3E-212,9609 Med Ctr Dr, Bethesda, MD 20892 USA.
EM christopher.wheldon@nih.gov
NR 19
TC 0
Z9 0
U1 0
U2 0
PU JOHNS HOPKINS UNIV PRESS
PI BALTIMORE
PA JOURNALS PUBLISHING DIVISION, 2715 NORTH CHARLES ST, BALTIMORE, MD
21218-4363 USA
SN 1049-2089
EI 1548-6869
J9 J HEALTH CARE POOR U
JI J. Health Care Poor Underserved
PD FEB
PY 2017
VL 28
IS 1
BP 88
EP 99
PG 12
WC Health Policy & Services; Public, Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EL6JU
UT WOS:000394729200012
PM 28238990
ER
PT J
AU Makaroun, LK
Bowman, C
Duan, K
Handley, N
Wheeler, DJ
Pierluissi, E
Chen, AH
AF Makaroun, Lena K.
Bowman, Chelsea
Duan, Kevin
Handley, Nathan
Wheeler, Daniel J.
Pierluissi, Edgar
Chen, Alice Hm
TI Specialty Care Access in the Safety Net-the Role of Public Hospitals and
Health Systems
SO JOURNAL OF HEALTH CARE FOR THE POOR AND UNDERSERVED
LA English
DT Article
DE Specialty care; access to care; safety net; health care reform
ID ELECTRONIC REFERRALS; PROVIDERS; GASTROENTEROLOGY; CENTERS
AB Access to specialty care in the United States safety net, already strained, is facing increasing pressure with an influx of patients following the passage of the Affordable Care Act (ACA). We surveyed 18 public hospitals and health systems across the country to describe the current state of specialty care delivery in safety-net systems. We elicited information regarding challenges, provider models, metrics of access and productivity, and strategies for improving access. Based on our findings, we propose a framework for assessing and improving specialty care access with a focus on population health planning.
C1 [Makaroun, Lena K.] Univ Washington, Dept Med, Div Geriatr, Seattle, WA 98195 USA.
[Makaroun, Lena K.] VA Puget Sound Healthcare Syst, Seattle, WA USA.
[Bowman, Chelsea] Palo Alto Med Fdn, Palo Alto, CA USA.
[Duan, Kevin; Pierluissi, Edgar] Univ Calif San Francisco, Dept Med, Div Hosp Med, San Francisco, CA 94143 USA.
[Handley, Nathan] Univ Penn, Dept Med, Div Hematol Oncol, Philadelphia, PA 19104 USA.
[Wheeler, Daniel J.] Univ Minnesota, Dept Med, Minneapolis, MN 55455 USA.
[Pierluissi, Edgar] Univ Calif San Francisco, Dept Med, Div Geriatr, San Francisco, CA 94143 USA.
[Chen, Alice Hm] Univ Calif San Francisco, Dept Med, Div Gen Internal Med, San Francisco, CA 94143 USA.
RP Makaroun, LK (reprint author), Univ Washington, Dept Med, Div Geriatr, VA Puget Sound Healthcare Syst, 1660 South Columbia Way,S-152, Seattle, WA 98108 USA.
EM makaroun@uw.edu
NR 33
TC 0
Z9 0
U1 1
U2 1
PU JOHNS HOPKINS UNIV PRESS
PI BALTIMORE
PA JOURNALS PUBLISHING DIVISION, 2715 NORTH CHARLES ST, BALTIMORE, MD
21218-4363 USA
SN 1049-2089
EI 1548-6869
J9 J HEALTH CARE POOR U
JI J. Health Care Poor Underserved
PD FEB
PY 2017
VL 28
IS 1
BP 566
EP 581
PG 16
WC Health Policy & Services; Public, Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EL6JU
UT WOS:000394729200041
PM 28239019
ER
PT J
AU Lee, MH
Appleton, KM
El-Shewy, HM
Sorci-Thomas, MG
Thomas, MJ
Lopes-Virella, MF
Luttrell, LM
Hammad, SM
Klein, RL
AF Lee, Mi-Hye
Appleton, Kathryn M.
El-Shewy, Hesham M.
Sorci-Thomas, Mary G.
Thomas, Michael J.
Lopes-Virella, Maria F.
Luttrell, Louis M.
Hammad, Samar M.
Klein, Richard L.
TI S1P in HDL promotes interaction between SR-BI and S1PR1 and activates
S1PR1-mediated biological functions: calcium flux and S1PR1
internalization
SO JOURNAL OF LIPID RESEARCH
LA English
DT Article
DE high density lipoprotein; sphingosine 1-phosphate; protein-fragment
complementation assay; scavenger receptor BI; S1P receptors
ID HIGH-DENSITY-LIPOPROTEIN; RECEPTOR CLASS-B; APOLIPOPROTEIN-A-I;
ENDOTHELIAL-CELL MIGRATION; NITRIC-OXIDE SYNTHASE; SCAVENGER RECEPTOR;
SPHINGOSINE 1-PHOSPHATE; PLASMA-MEMBRANE; MASS-SPECTROMETRY;
PROTEIN-KINASE
AB HDL normally transports about 50-70% of plasma sphingosine 1-phosphate (S1P), and the S1P in HDL reportedly mediates several HDL-associated biological effects and signaling pathways. The HDL receptor, SR-BI, as well as the cell surface receptors for S1P (S1PRs) may be involved partially and/or completely in these HDL-induced processes. Here we investigate the nature of the HDL-stimulated interaction between the HDL receptor, SR-BI, and S1PR1 using a protein-fragment complementation assay and confocal microscopy. In both primary rat aortic vascular smooth muscle cells and HEK293 cells, the S1P content in HDL particles increased intracellular calcium concentration, which was mediated by S1PR1. Mechanistic studies performed in HEK293 cells showed that incubation of cells with HDL led to an increase in the physical interaction between the SR-BI and S1PR1 receptors that mainly occurred on the plasma membrane. Model recombinant HDL (rHDL) particles formed in vitro with S1P incorporated into the particle initiated the internalization of S1PR1, whereas rHDL without supplemented S1P did not, suggesting that S1P transported in HDL can selectively activate S1PR1. In conclusion, these data suggest that S1P in HDL stimulates the transient interaction between SR-BI and S1PRs that can activate S1PRs and induce an elevation in intracellular calcium concentration.
C1 [Lee, Mi-Hye; El-Shewy, Hesham M.; Lopes-Virella, Maria F.; Luttrell, Louis M.; Klein, Richard L.] Med Univ South Carolina, Div Endocrinol Metab & Med Genet, Dept Med, Coll Pharm, Charleston, SC 29425 USA.
[Appleton, Kathryn M.; Luttrell, Louis M.] Med Univ South Carolina, Dept Pharmaceut & Biomed Sci, Coll Pharm, Charleston, SC USA.
[Hammad, Samar M.] Med Univ South Carolina, Dept Regenerat Med & Cell Biol, Charleston, SC USA.
[Sorci-Thomas, Mary G.] Med Coll Wisconsin, Dept Med, Div Endocrinol Metab & Clin Nutr, Milwaukee, WI 53226 USA.
[Thomas, Michael J.] Med Coll Wisconsin, Dept Pharmacol & Toxicol, Milwaukee, WI 53226 USA.
[Lopes-Virella, Maria F.; Luttrell, Louis M.; Klein, Richard L.] Ralph H Johnson Dept Vet Affairs Med Ctr, Res Serv, Charleston, SC 29401 USA.
RP Klein, RL (reprint author), Med Univ South Carolina, Div Endocrinol Metab & Med Genet, Dept Med, Coll Pharm, Charleston, SC 29425 USA.; Klein, RL (reprint author), Ralph H Johnson Dept Vet Affairs Med Ctr, Res Serv, Charleston, SC 29401 USA.
EM kleinrl@musc.edu
FU Department of Veterans Affairs Merit Review Program; National Institutes
of Health/National Heart, Lung, and Blood Institute [HL079274, HL127649,
HL112276]; National Institutes of Health [RR027777]; National Cancer
Institute Center Grant [5P30CA12197]
FX This work was supported by the Department of Veterans Affairs Merit
Review Program (M.L.V. and R.L.K.) and by National Institutes of
Health/National Heart, Lung, and Blood Institute Grants HL079274
(S.M.H.), HL127649, and HL112276 (M.S.T.). The FLIPRTETRA
facility was supported by National Institutes of Health Grant RR027777
(L.M.L.). The mass spectroscopy analyses were performed in the Mass
Spectrometer Facility of the Comprehensive Cancer Center of Wake Forest
School of Medicine supported in part by National Cancer Institute Center
Grant 5P30CA12197. The contents of this manuscript do not represent the
views of the Department of Veterans Affairs or the United States
Government. The content is solely the responsibility of the authors and
does not necessarily represent the official views of the National
Institutes of Health.
NR 57
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Z9 0
U1 2
U2 2
PU AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
PI BETHESDA
PA 9650 ROCKVILLE PIKE, BETHESDA, MD 20814-3996 USA
SN 0022-2275
EI 1539-7262
J9 J LIPID RES
JI J. Lipid Res.
PD FEB
PY 2017
VL 58
IS 2
BP 325
EP 338
DI 10.1194/jlr.M070706
PG 14
WC Biochemistry & Molecular Biology
SC Biochemistry & Molecular Biology
GA EM1WW
UT WOS:000395108900003
PM 27881715
ER
PT J
AU Neuss, M
Rocque, G
Zuckerman, D
Chiang, A
Katta, S
Wollins, D
Kamin, D
Edge, S
AF Neuss, Michael
Rocque, Gabrielle
Zuckerman, Dan
Chiang, Anne
Katta, Sweatha
Wollins, Dana
Kamin, Deborah
Edge, Stephen
TI Establishing a Core Set of Performance Measures to Improve Value in
Cancer Care: ASCO Consensus Conference Recommendation Report
SO JOURNAL OF ONCOLOGY PRACTICE
LA English
DT Editorial Material
ID UNITED-STATES
C1 Vanderbilt Ingram Canc Ctr, Nashville, TN USA.
Univ Alabama Birmingham, Birmingham, AL USA.
Birmingham Vet Affairs Med Ctr, Birmingham, AL USA.
St Lukes Mt States Tumor Inst, Boise, ID USA.
Amer Soc Clin Oncol, Alexandria, VA USA.
Roswell Pk Canc Inst, Buffalo, NY USA.
RP Neuss, M (reprint author), Michael Neuss, 2220 Pierce Ave, Nashville, MD USA.; Rocque, G (reprint author), 2318 Mill Rd,Suite 800, Alexandria, VA 22314 USA.
EM michael.n.neuss@vanderbilt.edu; cancerpolicy@asco.org
FU PackHealth; Medscape; Carevive Systems; Genentech; OncoMed; Millennium;
Onyx; Boehringer Ingelheim; Eli Lilly; Bristol Myers Squibb; Medivation
FX PackHealth, Medscape, Carevive Systems, Genentech; OncoMed, Millennium,
Onyx, Boehringer Ingelheim, Eli Lilly, Bristol Myers Squibb, Medivation
NR 7
TC 1
Z9 1
U1 0
U2 0
PU AMER SOC CLINICAL ONCOLOGY
PI ALEXANDRIA
PA 2318 MILL ROAD, STE 800, ALEXANDRIA, VA 22314 USA
SN 1554-7477
EI 1935-469X
J9 J ONCOL PRACT
JI J. Oncol. Pract.
PD FEB 1
PY 2017
VL 13
IS 2
BP 135
EP +
DI 10.1200/JOP.2016.017954
PG 10
WC Health Care Sciences & Services
SC Health Care Sciences & Services
GA EP3LD
UT WOS:000397282900022
ER
PT J
AU Kudsk, KA
Munoz-del-Rio, A
Busch, RA
Kight, CE
Schoeller, DA
AF Kudsk, Kenneth A.
Munoz-del-Rio, Alejandro
Busch, Rebecca A.
Kight, Cassandra E.
Schoeller, Dale A.
TI Stratification of Fat-Free Mass Index Percentiles for Body Composition
Based on National Health and Nutrition Examination Survey III
Bioelectric Impedance Data
SO JOURNAL OF PARENTERAL AND ENTERAL NUTRITION
LA English
DT Article
DE nutrition assessment; nutrition; outcomes research; quality; nutrition
support practice; adult; life cycle
ID LENGTH-OF-STAY; HOSPITAL ADMISSION; POSTOPERATIVE COMPLICATIONS;
NHANES-III; MALNUTRITION; OUTCOMES; CANCER; RISK; SURGERY; IMPACT
AB Background: Loss of protein mass and lower fat-free mass index (FFMI) are associated with longer length of stay, postsurgical complications, and other poor outcomes in hospitalized patients. Normative data for FFMI of U.S. populations do not exist. This work aims to create a stratified FFMI percentile table for the U.S. population using the large bioelectric impedance analysis data obtained from National Health and Nutrition Examination Surveys (NHANES). Methods: Fat-free mass (FFM) was calculated from the NHANES III bioelectric impedance analysis and anthropometric data for males and females ages 12 to >90 years for 3 race/ethnicities (non-Hispanic white, non-Hispanic black, and Mexican American). FFM was normalized by subject height to create an FFMI distribution table for the U.S. population. Selected percentiles were obtained by age, sex, and race/ethnicity. Data were collapsed by race/ethnicity before and after removing obese and underweight participants to create an FFMI decile table for males and females 12 years and older for the healthy-weight U.S. population. Results: FFMI increased during adolescent growth but stabilized in the early 20s. The FFMI deciles were similar by race/ethnicity, with age group remaining relatively stable between ages 25 and 80 years. The FFMI deciles for males and females were significantly different. Conclusions: After eliminating the obese and extremely thin, FFMI percentiles remain stable during adult years allowing creation of age- and race/ethnicity-independent decile tables for males and females. These tables allow stratification of individuals for nutrition intervention trials to depict changing nutrition status during medical, surgical, and nutrition interventions.
C1 [Kudsk, Kenneth A.] William S Middleton Mem Vet Adm Med Ctr, Vet Adm Surg Serv, Madison, WI USA.
[Kudsk, Kenneth A.; Munoz-del-Rio, Alejandro; Busch, Rebecca A.] Univ Wisconsin, Dept Surg, Sch Med & Publ Hlth, Madison, WI USA.
[Munoz-del-Rio, Alejandro] Univ Wisconsin, Dept Radiol, Madison, WI 53706 USA.
[Munoz-del-Rio, Alejandro] Univ Wisconsin, Dept Med Phys, 1530 Med Sci Ctr, Madison, WI 53706 USA.
[Kight, Cassandra E.] Univ Wisconsin Hosp & Clin, Clin Nutr Serv, Madison, WI 53792 USA.
[Schoeller, Dale A.] Univ Wisconsin, Dept Nutr Sci, 1415 Linden Dr, Madison, WI 53706 USA.
RP Kudsk, KA (reprint author), William S Middleton Mem Vet Adm Med Ctr, Clin Sci Ctr G5 341, 600 Highland Ave, Madison, WI 53792 USA.
EM kudsk@surgery.wisc.edu
FU National Institutes of Health Surgical Oncology Research Training
Program [T32CA090217]
FX The project described was supported in part by the National Institutes
of Health Surgical Oncology Research Training Program (grant number
T32CA090217; to R.A.B.). This material is the result of work supported
with the resources and use of facilities at the William S. Middleton
Memorial Veterans Hospital, Madison, Wisconsin. The contents of this
article do not represent the views of the Department of Veterans Affairs
or the U.S. government.
NR 35
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Z9 1
U1 1
U2 1
PU SAGE PUBLICATIONS INC
PI THOUSAND OAKS
PA 2455 TELLER RD, THOUSAND OAKS, CA 91320 USA
SN 0148-6071
EI 1941-2444
J9 JPEN-PARENTER ENTER
JI J. Parenter. Enter. Nutr.
PD FEB
PY 2017
VL 41
IS 2
BP 249
EP 257
DI 10.1177/0148607115592672
PG 9
WC Nutrition & Dietetics
SC Nutrition & Dietetics
GA EL8UW
UT WOS:000394896800013
PM 26092851
ER
PT J
AU Ellinger, RL
Jakien, KM
Gallun, FJ
AF Ellinger, Rachel L.
Jakien, Kasey M.
Gallun, Frederick J.
TI The role of interaural differences on speech intelligibility in complex
multi- talker environments
SO JOURNAL OF THE ACOUSTICAL SOCIETY OF AMERICA
LA English
DT Article
ID MASKING-LEVEL DIFFERENCES; CANCELLATION THEORY; TIME DIFFERENCES;
EQUALIZATION; INTENSITY; RELEASE; PHASE
AB Interaural differences in time (ITDs) and interaural differences in level (ILDs) contribute to a listener's ability to achieve spatial release from masking (SRM), and help to improve speech intelligibility in noisy environments. In this study, the extent to which ITDs and ILDs contribute to SRM and the relationships with aging and hearing loss were examined. SRM was greatest when stimuli were presented with consistent ITD and ILD, relative to ITD or ILD alone, all of which produced greater SRM than when ITD and ILD cues were in conflict with each other. This pattern was independent of age and hearing loss.
C1 [Ellinger, Rachel L.; Jakien, Kasey M.; Gallun, Frederick J.] US Dept Vet Affairs, Natl Ctr Rehabilitat Auditory Res, VA Portland Hlth Care Syst, 3710 Southwest US Vet Hosp Rd,P5 NCRAR, Portland, OR 97239 USA.
[Ellinger, Rachel L.] Northwestern Univ, Commun Sci & Disorders Dept, 2240 Campus Dr, Evanston, IL 60208 USA.
[Jakien, Kasey M.; Gallun, Frederick J.] Oregon Hlth & Sci Univ, Dept Otolaryngol Head & Neck Surg, 3181 SW Sam Jackson Pk Rd, Portland, OR 97239 USA.
RP Gallun, FJ (reprint author), US Dept Vet Affairs, Natl Ctr Rehabilitat Auditory Res, VA Portland Hlth Care Syst, 3710 Southwest US Vet Hosp Rd,P5 NCRAR, Portland, OR 97239 USA.
EM RachelEllinger@gmail.com; Kasey.Jakien@va.gov; Frederick.Gallun@va.gov
FU National Institutes of Health/National Institute on Deafness and Other
Communication Disorders (NIH/NIDCD) [R01 DC011828]; Department of
Veterans Affairs Rehabilitation Research & Development Service; Reed
College Department of Psychology
FX Thank you to all of the participants who volunteered their time to be
involved in this experiment. Thank you to Sean Kampel, Meghan Stansell,
and Nirmal Srinivasan for help with data collection, Kathryn Oleson for
help with data analysis, and Enriqueta CansecoGonzalez for advisement
while working on this experiment and the thesis document. This work was
supported by National Institutes of Health/National Institute on
Deafness and Other Communication Disorders (NIH/NIDCD; R01 DC011828),
Department of Veterans Affairs Rehabilitation Research & Development
Service (VA RR&D), and Reed College Department of Psychology. The
contents of this article are the private views of the authors and should
not be assumed to represent the views of the Department of Veterans
Affairs or the United States Government.
NR 16
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U1 0
U2 0
PU ACOUSTICAL SOC AMER AMER INST PHYSICS
PI MELVILLE
PA STE 1 NO 1, 2 HUNTINGTON QUADRANGLE, MELVILLE, NY 11747-4502 USA
SN 0001-4966
EI 1520-8524
J9 J ACOUST SOC AM
JI J. Acoust. Soc. Am.
PD FEB
PY 2017
VL 141
IS 2
BP EL170
EP EL176
DI 10.1121/1.4976113
PG 7
WC Acoustics; Audiology & Speech-Language Pathology
SC Acoustics; Audiology & Speech-Language Pathology
GA EM4VD
UT WOS:000395310100015
PM 28253635
ER
PT J
AU Folmer, RL
Vachhani, J
McMillan, GP
Watson, C
Kidd, GR
Feeney, MP
AF Folmer, Robert L.
Vachhani, Jay
McMillan, Garnett P.
Watson, Charles
Kidd, Gary R.
Feeney, M. Patrick
TI Validation of a Computer-Administered Version of the Digits-in-Noise
Test for Hearing Screening in the United States
SO JOURNAL OF THE AMERICAN ACADEMY OF AUDIOLOGY
LA English
DT Article
DE assessment; computer -administered; digits-in-noise; hearing screening;
hearing test
ID QUALITY-OF-LIFE; OLDER-ADULTS; COGNITIVE DYSFUNCTION; HANDICAP
INVENTORY; TELEPHONE; IMPAIRMENT; MILD; INTELLIGIBILITY; DEMENTIA;
PEOPLE
AB Background: The sooner people receive treatment for hearing loss (HL), the quicker they are able to recognize speech and to master hearing aid technology. Unfortunately, a majority of people with HL wait until their impairments have progressed from moderate to severe levels before seeking auditory rehabilitation. To increase the number of individuals with HL who pursue and receive auditory rehabilitation, it is necessary to improve methods for identifying and informing these people via widely accessible hearing screening procedures. Screening for HL is the first in a chain of events that must take place to increase the number of patients who enter the hearing health-care system. New methods for hearing screening should be readily accessible through a common medium (e.g., telephone or computer) and should be relatively easy and quick for people to self-administer.
Purpose: The purpose of this study was to assess a digits-in-noise (DIN) hearing screening test that was delivered via personal computer.
Research Design: Participants completed the Hearing Handicap Inventory for Adults (HHIA) questionnaire, audiometric testing in a sound booth, and computerized DIN testing. During the DIN test, sequences of three spoken digits were presented in noise via headphones at varying signal-to-noise ratios (SNRs). Participants entered each three-digit sequence they heard using an on-screen keypad.
Study Sample: Forty adults (16 females, 24 males) participated in the study, of whom 20 had normal hearing and 20 had HL (pure-tone average [PTA] thresholds for 0.5, 1, 2, and 4 kHz >25 dB HL).
Data Collection and Analysis: DIN SNR and PTA data were analyzed and compared for each ear tested. Receiver operating characteristic curves based on these data were plotted. A measure of overall accuracy of a screening test is the area under the receiver operating characteristic curve (AUC). This measures the average true positive rate across false positives at varying DIN SNR cutoffs. Larger values of the AUC indicate, on average, more accurate screening tests. HHIA responses were analyzed and compared to PTA and DIN SNR results using Pearson correlation statistics.
Results: HHIA scores were positively correlated with audiometric PTA and DIN SNR results (p < 0.001 for all correlations). For an HL criterion of one or more frequencies from 0.25 to 8 kHz >25 dB HL, the AUC for the DIN test was 0.95. When a criterion of hearling level was set at one or more frequencies from 0.25 to 8 kHz >20 dB HL, the AUC for the DIN test was 0.96.
Conclusions: The computer version of the DIN test demonstrated excellent sensitivity and specificity for our sample of 40 participants. AUC results (>= 0.95) suggest that this DIN test administered via computer should be very useful for adult hearing screening.
C1 [Folmer, Robert L.; Vachhani, Jay; McMillan, Garnett P.; Feeney, M. Patrick] Portland VA Med Ctr, Natl Ctr Rehabil Auditory Res, Portland, OR 97239 USA.
[Folmer, Robert L.; Feeney, M. Patrick] Oregon Hlth & Sci Univ, Dept Otolaryngol, Portland, OR 97201 USA.
[McMillan, Garnett P.] Oregon Hlth & Sci Univ, Dept Prevent Med, Portland, OR 97201 USA.
[Watson, Charles] Commun Disorders Technol Inc, Bloomington, IN USA.
[Kidd, Gary R.] Indiana Univ, Bloomington, IN USA.
RP Folmer, RL (reprint author), Portland VA Med Ctr, Natl Ctr Rehabil Auditory Res, Portland, OR 97239 USA.
EM robert.folmer@va.gov
FU NIH/NIDCD [R21 DC011769 01]; VA National Center for Rehabilitative
Auditory Research - VA RR&D Center of Excellence at Portland VA Medical
Center [C9230C]
FX This research was supported by grant R21 DC011769 01 from NIH/NIDCD.
Additional support was provided by the VA National Center for
Rehabilitative Auditory Research (funded by VA RR&D Center of Excellence
grant C9230C) at Portland VA Medical Center.
NR 39
TC 0
Z9 0
U1 1
U2 1
PU AMER ACAD AUDIOLOGY
PI RESTON
PA 11730 PLAZA DR, STE 300, RESTON, VA 20190 USA
SN 1050-0545
EI 2157-3107
J9 J AM ACAD AUDIOL
JI J. Am. Acad. Audiol.
PD FEB
PY 2017
VL 28
IS 2
BP 161
EP 169
DI 10.3766/jaaa.16038
PG 9
WC Audiology & Speech-Language Pathology; Otorhinolaryngology
SC Audiology & Speech-Language Pathology; Otorhinolaryngology
GA EL2VL
UT WOS:000394478500007
PM 28240983
ER
PT J
AU Liu, JB
Huffman, KM
Palis, BE
Shulman, LN
Winchester, DP
Ko, CY
Hall, BL
AF Liu, Jason B.
Huffman, Kristopher M.
Palis, Bryan E.
Shulman, Lawrence N.
Winchester, David P.
Ko, Clifford Y.
Hall, Bruce L.
TI Reliability of the American College of Surgeons Commission on Cancer's
Quality of Care Measures for Hospital and Surgeon Profiling
SO JOURNAL OF THE AMERICAN COLLEGE OF SURGEONS
LA English
DT Article
ID LYMPH-NODES; MIX ADJUSTMENT; COLON-CANCER; LUNG-CANCER; DATA-BASE;
PATIENT; RETRIEVAL; RESECTION; NUMBER; RISK
AB BACKGROUND: Efforts to improve healthcare quality involve profiling hospitals and providers. Whether cancer-specific measures can be used reliably for profiling purposes has not been reported.
STUDY DESIGN: Hospitals and surgeons were profiled with 3 measures assessing the adequacy of lymphadenectomy for colon (ie at least 12 regional lymph nodes [12RLN] are removed and pathologically examined for resected colon cancer), gastric (ie at least 15 regional lymph nodes [G15RLN] are removed and pathologically examined for resected gastric cancer), and non-small cell lung (ie at least 10 regional lymph nodes [10RLN] are removed and pathologically examined for American Joint Committee on Cancer stage IA, IB, IIA, and IIB resected non-small cell lung cancer) cancers using hierarchical models. National Cancer Data Base cases spanning 2010 to 2013 were included if they met measure eligibility. Reliability estimates for hospital and surgeon performance across cumulative years of data (2013, 2012 to 2013, 2011 to 2013, and 2010 to 2013) were calculated with and without risk adjustment. Surgeon caseload minimums were projected to achieve reliabilities of 0.40 and 0.70.
RESULTS: Reliability estimates tended to increase with longer periods of data collection but at different rates, depending on measure, level of aggregation, and performance outlier status. Profiling hospitals using 12RLN with 2 years of data yielded a median reliability of 0.72 (interquartile range [IQR] 0.55 to 0.83); however, 4 years of data yielded a median reliability of only 0.31 (IQR 0.14 to 0.54) for surgeons. The G15RLN performance was poor overall; 10RLN had high reliability at both hospital (0.74; IQR 0.50 to 0.86) and surgeon (0.61; IQR 0.34 to 0.80) levels using 1 year of data, but the literature questions this measure's validity. Few surgeons could achieve appropriate levels of reliability regardless of increased data collection duration.
CONCLUSIONS: Profiling hospitals based on measures such as these can achieve acceptable reliability in reasonable timeframes, but does not always. Either lower levels of reliability should be accepted to profile surgeons with these measures or longer timeframes should be used. (J Am Coll Surg 2017; 224: 180e190. (C) 2016 by the American College of Surgeons. Published by Elsevier Inc. All rights reserved.)
C1 [Liu, Jason B.; Huffman, Kristopher M.; Palis, Bryan E.; Winchester, David P.; Ko, Clifford Y.; Hall, Bruce L.] Amer Coll Surg, Div Res & Optimal Patient Care, Chicago, IL USA.
[Liu, Jason B.] Univ Chicago Hosp, Dept Surg, Chicago, IL 60637 USA.
[Shulman, Lawrence N.] Univ Penn, Dept Med, Abramson Canc Ctr, Philadelphia, PA 19104 USA.
[Ko, Clifford Y.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, Los Angeles, CA 90095 USA.
[Ko, Clifford Y.] VA Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
[Hall, Bruce L.] Washington Univ, Dept Surg, St Louis, MO USA.
[Hall, Bruce L.] Washington Univ, Ctr Hlth Policy, St Louis, MO USA.
[Hall, Bruce L.] Washington Univ, Olin Business Sch, St Louis, MO USA.
[Hall, Bruce L.] St Louis Vet Affairs Med Ctr, St Louis, MO USA.
[Hall, Bruce L.] BJC Healthcare, St Louis, MO USA.
RP Liu, JB (reprint author), Amer Coll Surg, 633 N St Clair,22nd Floor, Chicago, IL 60611 USA.
EM jliu@facs.org
FU Department of Surgery, University of Chicago Hospitals; American College
of Surgeons Clinical Scholar in Residence Program
FX Dr Liu is supported by a research fellowship from the Department of
Surgery, University of Chicago Hospitals and the American College of
Surgeons Clinical Scholar in Residence Program.
NR 44
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1072-7515
EI 1879-1190
J9 J AM COLL SURGEONS
JI J. Am. Coll. Surg.
PD FEB
PY 2017
VL 224
IS 2
BP 180
EP 190E8
DI 10.1016/j.jamcollsurg.2016.10.053
PG 19
WC Surgery
SC Surgery
GA EO9PC
UT WOS:000397019600013
PM 27979711
ER
PT J
AU de Mazieres, CL
Morley, JE
Levy, C
Agenes, F
Barbagallo, M
Cesari, M
Barreto, PD
Donini, LM
Fitten, J
Franco, A
Izquierdo, M
Kane, RA
Martin, FC
Onder, G
Ouslander, J
Pitkala, K
Saliba, D
Sinclair, A
Manas, LR
Vellas, B
Rolland, Y
AF de Mazieres, Clarisse Laffon
Morley, John E.
Levy, Cari
Agenes, Fabien
Barbagallo, Mario
Cesari, Matteo
Barreto, Philipe De Souto
Donini, Lorenzo Maria
Fitten, Jaime
Franco, Alain
Izquierdo, Mikel
Kane, Rosalie A.
Martin, Finbarr C.
Onder, Graziano
Ouslander, Joseph
Pitkala, Kaisu
Saliba, Debra
Sinclair, Alan
Rodriguez Manas, Leocadio
Vellas, Bruno
Rolland, Yves
TI Prevention of Functional Decline by Reframing the Role of Nursing Homes?
SO JOURNAL OF THE AMERICAN MEDICAL DIRECTORS ASSOCIATION
LA English
DT Article
DE Nursing home; prevention; functional decline; frailty
ID EMERGENCY-DEPARTMENT VISITS; RANDOMIZED CONTROLLED-TRIAL; OLDER-ADULTS;
HIP FRACTURE; GERIATRIC ASSESSMENT; STIMULATION THERAPY; PHYSICAL
RESTRAINTS; ELDERLY-PATIENTS; RESIDENTS; INTERVENTIONS
AB Institutionalization is generally a consequence of functional decline driven by physical limitations, cognitive impairments, and/or loss of social supports. At this stage, intervention to reverse functional losses is often too late. To be more effective, geriatric medicine must evolve to intervene at an earlier stage of the disability process. Could nursing homes (NHs) transform from settings in which many residents dwell to settings in which the NH residents and those living in neighboring communities benefit from staff expertise to enhance quality of life and maintain or slow functional decline? A task force of clinical researchers met in Toulouse on December 2, 2015, to address some of these challenges: how to prevent or slow functional decline and disabilities for NH residents and how NHs may promote the prevention of functional decline in community-dwelling frail elderly. The present article reports the main results of the Task Force discussions to generate a new paradigm. (C) 2016 AMDA - The Society for Post-Acute and Long-Term Care Medicine. Published by Elsevier Inc. All rights reserved.
C1 [de Mazieres, Clarisse Laffon; Cesari, Matteo; Barreto, Philipe De Souto; Vellas, Bruno; Rolland, Yves] CHU Toulouse, Toulouse Univ Hosp, Dept Geriatr Med, Gerontopole, Toulouse, France.
[de Mazieres, Clarisse Laffon; Cesari, Matteo; Barreto, Philipe De Souto; Vellas, Bruno; Rolland, Yves] INSERM, UMR 1027, Toulouse, France.
[Morley, John E.] St Louis Univ, Sch Med, Div Geriatr Med, St Louis, MO 63104 USA.
[Morley, John E.] St Louis Univ, Sch Med, Div Endocrinol, St Louis, MO USA.
[Levy, Cari] Denver VA Med Ctr, Denver Seattle Ctr Innovat, Denver, CO USA.
[Levy, Cari] Univ Colorado, Sch Med, Div Hlth Care Policy & Res, Aurora, CO USA.
[Agenes, Fabien] Embassy France US, Off Sci & Technol, French Consulate Los Angeles, Los Angeles, CA USA.
[Barbagallo, Mario] Univ Palermo, Geriatr Unit, Palermo, Italy.
[Donini, Lorenzo Maria] Sapienza Univ Rome, Rome, Italy.
[Fitten, Jaime] Univ Calif Los Angeles, David Geffen Sch Med, Psychiat & Behav Sci, Los Angeles, CA 90095 USA.
[Fitten, Jaime] Greater Los Angeles VA, Geriatr Psychiat, Sepulveda Campus, Los Angeles, CA USA.
[Martin, Finbarr C.] Univ Nice Sophia Antipolis, Nice, France.
[Izquierdo, Mikel] Univ Publ Navarra, Dept Hlth Sci, Pamplona, Spain.
[Kane, Rosalie A.] Univ Minnesota, Sch Publ Hlth, Ctr Aging, Div Hlth Policy & Management, Minneapolis, MN USA.
[Martin, Finbarr C.] Kings Coll London, London, England.
[Onder, Graziano] Univ Cattolica Sacro Cuore, Ctr Med Invecchiamento, Dept Geriatr, Rome, Italy.
[Ouslander, Joseph] Florida Atlantic Univ, Charles E Schmidt Coll Med, Boca Raton, FL 33431 USA.
[Ouslander, Joseph] Florida Atlantic Univ, Christine E Lynn Coll Nursing, Boca Raton, FL 33431 USA.
[Pitkala, Kaisu] Univ Helsinki, Helsinki Univ Hosp, Unit Primary Hlth Care, Dept Gen Practice & Primary Hlth Care, Helsinki, Finland.
[Saliba, Debra] Univ Calif Los Angeles, UCLA JH Borun Ctr Gerontol Res, Los Angeles, CA USA.
[Saliba, Debra] Los Angeles Vet Adm, Geriatr Res Educ & Clin Ctr, Los Angeles, CA USA.
[Sinclair, Alan] Fdn Diabet Res Older People, Medici Med Practice, Diabet Frail, Luton, Beds, England.
[Rodriguez Manas, Leocadio] Univ Europea Madrid, Hosp Univ Getafe, Dept Geriatr, Getafe, Spain.
[Rodriguez Manas, Leocadio] Univ Europea Madrid, Sch Hlth Sci, Getafe, Spain.
RP de Mazieres, CL (reprint author), Toulouse Univ Hosp, Dept Geriatr Med, Gerontopole, 224 Ave Casselardit,TSA 40031, F-31059 Toulouse 9, France.
EM laffondemazieres.c@chu-toulouse.fr
FU Office for Science and Technology of the Consulate General of France in
Los Angeles, USA
FX This work was supported by an educational grant from the Office for
Science and Technology of the Consulate General of France in Los
Angeles, USA.
NR 54
TC 1
Z9 1
U1 2
U2 2
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1525-8610
EI 1538-9375
J9 J AM MED DIR ASSOC
JI J. Am. Med. Dir. Assoc.
PD FEB 1
PY 2017
VL 18
IS 2
BP 105
EP 110
DI 10.1016/j.jamda.2016.11.019
PG 6
WC Geriatrics & Gerontology
SC Geriatrics & Gerontology
GA EP3TB
UT WOS:000397303500005
ER
PT J
AU Kohli, P
Naik, AN
Harruff, EE
Nguyen, SA
Schlosser, RJ
Soler, ZM
AF Kohli, Preeti
Naik, Akash N.
Harruff, E. Emily
Nguyen, Shaun A.
Schlosser, Rodney J.
Soler, Zachary M.
TI The Prevalence of Olfactory Dysfunction in Chronic Rhinosinusitis
SO LARYNGOSCOPE
LA English
DT Review
DE Olfaction; smell; chronic rhinosinusitis; sinusitis; prevalence
ID ENDOSCOPIC SINUS SURGERY; QUALITY-OF-LIFE; COMPUTED-TOMOGRAPHY FINDINGS;
CLINICAL-PRACTICE GUIDELINE; SMELL IDENTIFICATION TEST;
PLACEBO-CONTROLLED TRIAL; NASAL POLYPOSIS; DOUBLE-BLIND; DISEASE
SEVERITY; ALLERGIC RHINITIS
AB Objectives: Many studies have reported that olfactory dysfunction frequently occurs in chronic rhinosinusitis (CRS) populations; however, the prevalence and degree of olfactory loss has not been systematically studied. The aims of this study were to use combined data to report the prevalence of olfactory dysfunction and to calculate weighted averages of olfactory test scores in CRS patients.
Data Sources: A search was conducted in PubMed and Scopus, following the methods of Preferred Reporting Items for Systematic Review and Meta-Analysis guidelines.
Review Methods: Studies reporting the prevalence of olfactory dysfunction using objective measures or olfactory test scores using validated scales were included.
Results: A total of 47 articles were included in a systematic review and 35 in the pooled data analysis. The prevalence of olfactory dysfunction in chronic rhinosinusitis was found to be 30.0% using the Brief Smell Identification Test, 67.0% using the 40-item Smell Identification Test, and 78.2% using the total Sniffin' Sticks score. Weighted averages 6 standard deviation of olfactory test scores were 25.96 +/- 7.11 using the 40-item Smell Identification Test, 8.60 +/- 2.81 using the Brief Smell Identification Test, 21.96 +/- 8.88 using total Sniffin' Sticks score, 5.65 +/- 1.51 using Sniffin' Sticks-Threshold, 9.21 +/- 4.63 using Sniffin' Sticks-Discrimination, 9.47 +/- 3.92 using Sniffin' Sticks-Identification, and 8.90 +/- 5.14 using the Questionnaire for Olfactory Disorders-Negative Statements.
Conclusions: In CRS populations, a significant percentage of patients experience olfactory dysfunction, and mean olfactory scores are within the dysosmic range.
C1 [Kohli, Preeti; Naik, Akash N.; Harruff, E. Emily; Nguyen, Shaun A.; Schlosser, Rodney J.; Soler, Zachary M.] Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, 135 Rutledge Ave,MSC 550, Charleston, SC 29425 USA.
[Schlosser, Rodney J.] Ralph H Johnson VA Med Ctr, Dept Surg, Charleston, SC USA.
RP Kohli, P (reprint author), Med Univ South Carolina, Dept Otolaryngol Head & Neck Surg, 135 Rutledge Ave,MSC 550, Charleston, SC 29425 USA.
EM pkohli89@gmail.com
FU National Institute on Deafness and Other Communication Disorders,
National Institutes of Health, Bethesda, Maryland, U.S.A [R03
DC013651-01]; Entellus; Intersect; Optinose; IntersectENT
FX This work was supported by grants from the National Institute on
Deafness and Other Communication Disorders, one of the National
Institutes of Health, Bethesda, Maryland, U.S.A. (R03 DC013651-01; PI:
Z.M.S.).; Z.M.S. is supported by grants from Entellus, Intersect, and
Optinose, which are not affiliated with this study. Z.M.S. is a
consultant for Olympus, which is not affiliated with this study. R.J.S.
is supported by grants from OptiNose, Entellus, and IntersectENT, none
of which are associated with this study. R.J.S. is a consultant for
Olympus and Meda, which are not affiliated with this study. S.A.N. is a
consultant for Roche Products Limited (United Kingdom) and CSL Behring,
which are not affiliated with this study.
NR 74
TC 0
Z9 0
U1 2
U2 2
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0023-852X
EI 1531-4995
J9 LARYNGOSCOPE
JI Laryngoscope
PD FEB
PY 2017
VL 127
IS 2
BP 309
EP 320
DI 10.1002/lary.26316
PG 12
WC Medicine, Research & Experimental; Otorhinolaryngology
SC Research & Experimental Medicine; Otorhinolaryngology
GA EL9TI
UT WOS:000394962600013
PM 27873345
ER
PT J
AU Byne, W
AF Byne, William
TI Sustaining Progress Toward LGBT Health Equity: A Time for Vigilance,
Advocacy, and Scientific Inquiry
SO LGBT HEALTH
LA English
DT Editorial Material
DE barriers to care; clinical research; gender identity; health
disparities; public policy and advocacy; sexual orientation
C1 [Byne, William] Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.
[Byne, William] James J Peters VA Med Ctr, Dept Psychiat, Bronx, NY 10468 USA.
RP Byne, W (reprint author), Icahn Sch Med Mt Sinai, Dept Psychiat, New York, NY 10029 USA.; Byne, W (reprint author), James J Peters VA Med Ctr, Dept Psychiat, Bronx, NY 10468 USA.
EM william.byne@mssm.edu
NR 18
TC 0
Z9 0
U1 1
U2 1
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 2325-8292
EI 2325-8306
J9 LGBT HEALTH
JI LGBT Health
PD FEB
PY 2017
VL 4
IS 1
BP 1
EP 3
DI 10.1089/lgbt.2016.0211
PG 3
WC Public, Environmental & Occupational Health
SC Public, Environmental & Occupational Health
GA EL3GC
UT WOS:000394506600001
PM 28051348
ER
PT J
AU Roberts, SE
Thibaudeau, S
Burrell, JC
Zager, EL
Cullen, DK
Levin, LS
AF Roberts, S. E.
Thibaudeau, S.
Burrell, J. C.
Zager, E. L.
Cullen, D. K.
Levin, L. S.
TI To reverse or not to reverse? A systematic review of autograft polarity
on functional outcomes following peripheral nerve repair surgery
SO MICROSURGERY
LA English
DT Review
ID REGENERATING MOTOR AXONS; REINNERVATION; GUIDANCE; MUSCLES; GRAFTS
AB Background: The literature describing the best clinical practice for proximal- distal autograft orientation, otherwise known as nerve graft polarity, is inconsistent. With existing disparities in the peripheral nerve literature, the clinical question remains whether reversing nerve autograft polarity bears an advantage for nerve regeneration.
Methods: A comprehensive review of the literature using Embase and PubMed databases (1940June 2015) was performed to retrieve all original articles on the effects of nerve autograft polarity on nerve regeneration and functional recovery following primary repair of peripheral nerve defects.
Results: The initial database search yielded 318 titles. Duplicate exclusion, title review and full text review yielded six articles which directly compared nerve autograft polarity. Histological, morphometric, electrophysiological, and behavioral outcomes were reviewed. All retained articles were animal studies, of which none demonstrated significant differences in outcomes between the normal and reversed polarity groups. A reversed graft may ensure that regenerating nerve fibers are not lost at branching points, however this may not translate into improved function.
Conclusion: There is insufficient data to suggest that nerve autograft polarity has an impact on nerve regeneration and functional outcomes.
C1 [Roberts, S. E.; Burrell, J. C.; Zager, E. L.; Cullen, D. K.] Univ Pennsylvania, Perelman Sch Med, Dept Neurosurgery, Philadelphia, PA USA.
[Roberts, S. E.; Burrell, J. C.; Cullen, D. K.] Vet Affairs Med Ctr, Philadelphia, PA USA.
[Thibaudeau, S.; Levin, L. S.] Hosp Univ Pennsylvania, Div Plast Surg & Dept Orthoped Surg, Philadelphia, PA USA.
RP Thibaudeau, S (reprint author), 3737 Market St Suite 600, Philadelphia, PA 19104 USA.
EM sthiba@gmail.com
NR 31
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0738-1085
EI 1098-2752
J9 MICROSURG
JI Microsurgery
PD FEB
PY 2017
VL 37
IS 2
BP 169
EP 174
DI 10.1002/micr.30133
PG 6
WC Surgery
SC Surgery
GA EP4ED
UT WOS:000397332600013
PM 27935644
ER
PT J
AU Rosen, LE
Ananthanarayanan, V
Gallan, A
Tjota, MY
Attanoos, R
Alchami, FS
Brcic, L
Butnor, K
Hiroshima, K
Klampatsa, A
Litzky, L
Marchevsky, AM
Medeiros, F
Montero-Fernandez, MA
Moore, DA
Nabeshima, K
Pavlisko, EN
Sharma, A
Sheaff, M
Walts, AE
Galateau, F
Le Stang, N
Krausz, T
Husain, AN
AF Rosen, Lauren E.
Ananthanarayanan, Vijayalakshmi
Gallan, Alexander
Tjota, Melissa Yuwono
Attanoos, Richard
Alchami, Fouad S.
Brcic, Luka
Butnor, Kelly
Hiroshima, Kenzo
Klampatsa, Astero
Litzky, Leslie
Marchevsky, Alberto M.
Medeiros, Filomena
Montero-Fernandez, M. Angeles
Moore, David A.
Nabeshima, Kazuki
Pavlisko, Elizabeth N.
Sharma, Anupama
Sheaff, Michael
Walts, Ann E.
Galateau, Francoise
Le Stang, Nolwenn
Krausz, Thomas
Husain, Aliya N.
TI Nuclear Grade, Necrosis and Solid Growth Pattern Predict Survival in
Epithelioid Malignant Mesothelioma: An International, Multi
Institutional Study
SO MODERN PATHOLOGY
LA English
DT Meeting Abstract
CT 106th Annual Meeting of the
United-States-and-Canadian-Academy-of-Pathology (USCAP)
CY MAR 04-10, 2017
CL San Antonio, TX
SP US & Canadian Acad Pathol
C1 Univ Chicago, Chicago, IL 60637 USA.
Loyola, Maywood, IL USA.
Univ Wales Coll Cardiff, Cardiff, S Glam, Wales.
Med Univ Graz, Graz, Austria.
Univ Vermont, Burlington, VT USA.
Tokyo Womens Med Ctr, Kawadacho, Japan.
Univ Penn, Philadelphia, PA 19104 USA.
Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA.
Basildon & Thurrock Univ Hosp, Basildon, England.
Royal Brompton & Harefield Hosp, London, England.
Univ Leicester, Leicester, Leics, England.
Fukuoka Univ, Fukuoka, Japan.
Duke Univ, Durham, NH USA.
Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
Barts Hlth NHS Trust, London, England.
Ctr Leon Berard, Lyon, France.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 0893-3952
EI 1530-0285
J9 MODERN PATHOL
JI Mod. Pathol.
PD FEB
PY 2017
VL 30
SU 2
MA 1980
BP 492A
EP 492A
PG 1
WC Pathology
SC Pathology
GA EL2RO
UT WOS:000394467302551
ER
PT J
AU Raskind, WH
Friedman, JR
Roze, E
Meneret, A
Chen, DH
Bird, TD
AF Raskind, Wendy H.
Friedman, Jennifer R.
Roze, Emmanuel
Meneret, Aurelie
Chen, Dong-Hui
Bird, Thomas D.
TI ADCY5-related dyskinesia: Comments on characteristic manifestations and
variant-associated severity
SO MOVEMENT DISORDERS
LA English
DT Letter
ID FAMILIAL DYSKINESIA; FACIAL MYOKYMIA
C1 [Raskind, Wendy H.] Univ Washington, Dept Med Med Genet, Seattle, WA 98195 USA.
[Raskind, Wendy H.] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Raskind, Wendy H.; Bird, Thomas D.] US Dept Vet Affairs, Geriatr Res Educ & Clin Ctr, Seattle, WA 98174 USA.
[Friedman, Jennifer R.] Univ Calif San Diego, Dept Neurosci & Pediat, San Diego, CA 92103 USA.
[Friedman, Jennifer R.] Rady Childrens Hosp, San Diego, CA USA.
[Roze, Emmanuel; Meneret, Aurelie] UPMC Univ Paris 06, Sorbonne Univ, Inst Cerveau & Moelle Epiniere, Inserm,CNRS,UMR 7225,UMR S 1127,U1127, Paris, France.
[Roze, Emmanuel; Meneret, Aurelie] Hop La Pitie Salpetriere, AP HP, Dept Neurol, Paris, France.
[Chen, Dong-Hui; Bird, Thomas D.] Univ Washington, Dept Neurol, Seattle, WA 98195 USA.
RP Raskind, WH (reprint author), Univ Washington, Dept Med Med Genet, Seattle, WA 98195 USA.; Raskind, WH (reprint author), Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.; Raskind, WH (reprint author), US Dept Vet Affairs, Geriatr Res Educ & Clin Ctr, Seattle, WA 98174 USA.
EM wendyrun@uw.edu
FU National Institute of Neurological Diseases and Stroke [R01 NS069719];
Department of Veterans Affairs; Athena Diagnostics; CNRS; INSERM
(COSSEC),; AP-HP (DRC-PHRC); MerzPharma; Orkyn; Aguettant; IP sante;
Ultragenix; UCB pharma; Teva; Sanofi-Genzyme; Dystonia Coalition;
Dystonia Medical Research Foundation; Movement Disorders Society; JNLF
(Journees de Neurologie en Langue Francaise)
FX Dr. Raskind is funded by the National Institute of Neurological Diseases
and Stroke (R01 NS069719) and the Department of Veterans Affairs. She
receives licensing fees from Athena Diagnostics for Patent 7655401
"Mutations in PKCc are the cause for spinocerebellar ataxia." Dr.
Friedman reports family financial interest in biotechnology. Dr. Roze
received research support from CNRS, INSERM (COSSEC), AP-HP (DRC-PHRC),
MerzPharma, Orkyn, Aguettant, IP sante, Ultragenix, UCB pharma; served
on scientific advisory boards for Orkyn, Ultragenix, and Merz-Pharma;
received speech honoraria from Orkyn, Aguettant, Merz-Pharma, and
Ultragenix; and received travel funding from Teva, Sanofi-Genzyme, the
Dystonia Coalition, the Dystonia Medical Research Foundation, and the
Movement Disorders Society. Dr. Meneret received a grant from JNLF
(Journees de Neurologie en Langue Francaise). Dr. Chen receives
licensing fees from Athena Diagnostics for Patent 7655401 "Mutations in
PKCc are the cause for spinocerebellar ataxia." Dr. Bird receives
licensing fees from Athena Diagnostics for Patent 7655401 "Mutations in
PKCc are the cause for spinocerebellar ataxia." He is funded by the
Department of Veterans Affairs.
NR 5
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0885-3185
EI 1531-8257
J9 MOVEMENT DISORD
JI Mov. Disord.
PD FEB
PY 2017
VL 32
IS 2
BP 305
EP 306
DI 10.1002/mds.26888
PG 2
WC Clinical Neurology
SC Neurosciences & Neurology
GA EM9QJ
UT WOS:000395645900026
PM 27933653
ER
PT J
AU Cummings, DE
Schauer, PR
AF Cummings, David E.
Schauer, Philip R.
TI Endoscopic Gastric Plication for Obesity: Where Might It Fit in the
Scheme of Things?
SO OBESITY
LA English
DT Editorial Material
ID SURGERY; WEIGHT
C1 [Cummings, David E.] Univ Washington, Seattle, WA 98195 USA.
[Cummings, David E.] VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Schauer, Philip R.] Cleveland Clin Fdn, 9500 Euclid Ave, Cleveland, OH 44195 USA.
RP Cummings, DE (reprint author), Univ Washington, Seattle, WA 98195 USA.; Cummings, DE (reprint author), VA Puget Sound Hlth Care Syst, Seattle, WA USA.
EM davidec@u.washington.edu
FU Johnson Johnson; Ethicon; Medtronic; The Medicines Company; Pacira
Pharmaceuticals
FX Dr. Cummings reports research funding from Johnson & Johnson, and he is
on the Scientific Advisory Board of Metavention. Dr. Schauer reports
grants and consulting fees from Ethicon, grants from Medtronic,
consulting fees from The Medicines Company, and grants from Pacira
Pharmaceuticals, as well as stock in SE Healthcare Quality Consulting
and SurgiQuest.
NR 7
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1930-7381
EI 1930-739X
J9 OBESITY
JI Obesity
PD FEB
PY 2017
VL 25
IS 2
BP 284
EP 285
DI 10.1002/oby.21766
PG 2
WC Endocrinology & Metabolism; Nutrition & Dietetics
SC Endocrinology & Metabolism; Nutrition & Dietetics
GA EL9WF
UT WOS:000394970100006
PM 28124503
ER
PT J
AU Xiao, L
Lv, N
Rosas, LG
Au, D
Ma, J
AF Xiao, Lan
Lv, Nan
Rosas, Lisa G.
Au, David
Ma, Jun
TI Validation of Clinic Weights from Electronic Health Records Against
Standardized Weight Measurements in Weight Loss Trials
SO OBESITY
LA English
DT Article
ID RANDOMIZED CONTROLLED-TRIAL; PRIMARY-CARE; LIFE-STYLE; UNITED-STATES;
OBESITY; INTERVENTION; VALIDITY; ADULTS
AB Objective: To validate clinic weights in electronic health records against researcher-measured weights for outcome assessment in weight loss trials.
Methods: Clinic and researcher-measured weights from a published trial ( BE WELL) were compared using Lin's concordance correlation coefficient, Bland and Altman's limits of agreement, and polynomial regression model. Changes in clinic and researcher-measured weights in BE WELL and another trial, ELITE, were analyzed using growth curve modeling.
Results: Among BE WELL ( n = 330) and E-LITE ( n = 241) participants, 96% and 90% had clinic weights ( mean [ SD] of 5.8 [ 6.1] and 3.7 [ 3.9] records) over 12 and 15 months of follow-up, respectively. The concordance correlation coefficient was 0.99, and limits of agreement plots showed no pattern between or within treatment groups, suggesting overall good agreement between researcher-measured and nearest-in-time clinic weights up to 3 months. The 95% confidence intervals for predicted percent differences fell within 63% for clinic weights within 3 months of the researcher-measured weights. Furthermore, the growth curve slopes for clinic and researcher-measured weights by treatment group did not differ significantly, suggesting similar inferences about treatment effects over time, in both trials.
Conclusions: Compared with researcher-measured weights, close-in-time clinic weights showed high agreement and inference validity. Clinic weights could be a valid pragmatic outcome measure in weight loss studies.
C1 [Xiao, Lan; Lv, Nan; Rosas, Lisa G.; Ma, Jun] Palo Alto Med Fdn, Res Inst, Palo Alto, CA 94301 USA.
[Rosas, Lisa G.] Stanford Univ, Dept Med, Sch Med, Stanford, CA 94305 USA.
[Au, David] Univ Washington, Div Pulm & Crit Care Med, VA Puget Sound Hlth Care Syst, HSR&D, Seattle, WA 98195 USA.
[Ma, Jun] Univ Illinois, Dept Hlth Policy & Adm, Sch Publ Hlth, Chicago, IL 60607 USA.
[Ma, Jun] Univ Illinois, Div Acad Internal Med & Geriatr, Dept Med, Coll Med, Chicago, IL 60607 USA.
RP Ma, J (reprint author), Palo Alto Med Fdn, Res Inst, Palo Alto, CA 94301 USA.; Ma, J (reprint author), Univ Illinois, Dept Hlth Policy & Adm, Sch Publ Hlth, Chicago, IL 60607 USA.; Ma, J (reprint author), Univ Illinois, Div Acad Internal Med & Geriatr, Dept Med, Coll Med, Chicago, IL 60607 USA.
EM maj2015@uic.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases;
American Heart Association [0830362N]; National Heart, Lung, and Blood
Institute [R01HL094466]; Palo Alto Medical Foundation Research Institute
FX The E-LITE study was supported by grant R34DK080878 from the National
Institute of Diabetes and Digestive and Kidney Diseases and a Scientist
Development Grant award (0830362N) from the American Heart Association,
and the BE WELL study was supported by grant R01HL094466 from the
National Heart, Lung, and Blood Institute. This study was also supported
by internal funding from the Palo Alto Medical Foundation Research
Institute.
NR 21
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1930-7381
EI 1930-739X
J9 OBESITY
JI Obesity
PD FEB
PY 2017
VL 25
IS 2
BP 363
EP 369
DI 10.1002/oby.21737
PG 7
WC Endocrinology & Metabolism; Nutrition & Dietetics
SC Endocrinology & Metabolism; Nutrition & Dietetics
GA EL9WF
UT WOS:000394970100019
PM 28059466
ER
PT J
AU Marathe, CS
Rayner, CK
Lange, K
Bound, M
Wishart, J
Jones, KL
Kahn, SE
Horowitz, M
AF Marathe, Chinmay S.
Rayner, Christopher K.
Lange, Kylie
Bound, Michelle
Wishart, Judith
Jones, Karen L.
Kahn, Steven E.
Horowitz, Michael
TI Relationships of the early insulin secretory response and oral
disposition index with gastric emptying in subjects with normal glucose
tolerance
SO PHYSIOLOGICAL REPORTS
LA English
DT Article
DE Gastric emptying; insulin secretory response; oral disposition index;
oral glucose tolerance test
ID DEPENDENT DIABETES-MELLITUS; GLUCAGON-LIKE PEPTIDE-1; INHIBITORY
POLYPEPTIDE; POSTPRANDIAL GLYCEMIA; INCRETIN RESPONSES; CARBOHYDRATE
MEAL; DUODENAL GLUCOSE; HEALTHY-SUBJECTS; HORMONES; EXTRACTION
AB The oral disposition index, the product of the early insulin secretory response during an oral glucose tolerance test and insulin sensitivity, is used widely for both the prediction of, and evaluation of the response to interventions, in type 2 diabetes. Gastric emptying, which determines small intestinal exposure of nutrients, modulates postprandial glycemia. The aim of this study was to determine whether the insulin secretory response and the disposition index (DI) related to gastric emptying in subjects with normal glucose tolerance. Thirty-nine subjects consumed a 350 mL drink containing 75 g glucose labeled with Tc-99m-sulfur colloid. Gastric emptying (by scintigraphy), blood glucose (G) and plasma insulin (I) were measured between t = 0-120 min. The rate of gastric emptying was derived from the time taken for 50% emptying (T-50) and expressed as kcal/min. The early insulin secretory response was estimated by the ratio of the change in insulin (Delta I0-30) to that of glucose at 30 min (Delta G(0-30)) represented as Delta I0-30/Delta G(0-30). Insulin sensitivity was estimated as 1/fasting insulin and the DI was then calculated as Delta I0-30/Delta G(0-30) x 1/fasting insulin. There was a direct relationship between Delta G(0-30) and gastric emptying (r = 0.47, P = 0.003). While there was no association of either Delta I0-30 (r = -0.16, P = 0.34) or fasting insulin (r = 0.21, P = 0.20), there were inverse relationships between the early insulin secretory response (r = -0.45, P = 0.004) and the DI (r = -0.33, P = 0.041), with gastric emptying. We conclude that gastric emptying is associated with both insulin secretion and the disposition index in subjects with normal glucose tolerance, such that when gastric emptying is relatively more rapid, both the early insulin secretory response and the disposition index are less. These findings should be interpreted as "hypothesis generating" and provide the rationale for longitudinal studies to examine the impact of baseline rate of gastric emptying on the prospective risk of type 2 diabetes.
C1 [Marathe, Chinmay S.; Rayner, Christopher K.; Lange, Kylie; Bound, Michelle; Wishart, Judith; Jones, Karen L.; Horowitz, Michael] Univ Adelaide, Royal Adelaide Hosp, Discipline Med, Adelaide, SA, Australia.
[Marathe, Chinmay S.; Rayner, Christopher K.; Lange, Kylie; Bound, Michelle; Wishart, Judith; Jones, Karen L.; Horowitz, Michael] Univ Adelaide, Ctr Res Excellence Translating Nutr Sci Good Hlth, Adelaide, SA, Australia.
[Kahn, Steven E.] VA Puget Sound Hlth Care Syst, Div Metab Endocrinol & Nutr, Seattle, WA USA.
[Kahn, Steven E.] Univ Washington, Seattle, WA 98195 USA.
RP Marathe, CS (reprint author), Univ Adelaide, Royal Adelaide Hosp, Ctr Res Excellence CRE Translating Nutr Sci Good, Adelaide, SA 5005, Australia.
EM chinmaymarathe@gmail.com
OI Jones, Karen/0000-0002-1155-5816
FU National Health and Medical Research Council, Australia
FX This study was funded by a grant from the National Health and Medical
Research Council, Australia.
NR 29
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 2051-817X
J9 PHYSIOL REP
JI PHYSIOL. REP.
PD FEB
PY 2017
VL 5
IS 4
AR e13122
DI 10.14814/phy2.13122
PG 6
WC Physiology
SC Physiology
GA EP5PN
UT WOS:000397431000013
ER
PT J
AU Der-Martirosian, C
Radcliff, TA
Gable, AR
Riopelle, D
Hagigi, FA
Brewster, P
Dobalian, A
AF Der-Martirosian, Claudia
Radcliff, Tiffany A.
Gable, Alicia R.
Riopelle, Deborah
Hagigi, Farhad A.
Brewster, Pete
Dobalian, Aram
TI Assessing Hospital Disaster Readiness Over Time at the US Department of
Veterans Affairs
SO PREHOSPITAL AND DISASTER MEDICINE
LA English
DT Article
DE assessment; capabilities; disaster readiness; emergency management;
hospital preparedness
ID EMERGENCY MANAGEMENT; SURGE CAPACITY; PREPAREDNESS
AB Introduction: There have been numerous initiatives by government and private organizations to help hospitals become better prepared for major disasters and public health emergencies. This study reports on efforts by the US Department of Veterans Affairs (VA), Veterans Health Administration, Office of Emergency Management's (OEM) Comprehensive Emergency Management Program (CEMP) to assess the readiness of VA Medical Centers (VAMCs) across the nation.
Hypothesis/Problem: This study conducts descriptive analyses of preparedness assessments of VAMCs and examines change in hospital readiness over time.
Methods: To assess change, quantitative analyses of data from two phases of preparedness assessments (Phase I: 2008-2010; Phase II: 2011-2013) at 137 VAMCs were conducted using 61 unique capabilities assessed during the two phases. The initial five-point Likert-like scale used to rate each capability was collapsed into a dichotomous variable: "not-developed = 0" versus "developed = 1." To describe changes in preparedness over time, four new categories were created from the Phase I and Phase II dichotomous variables: (1) rated developed in both phases; (2) rated not-developed in Phase I but rated developed in Phase II; (3) rated not-developed in both phases; and (4) rated developed in Phase I but rated not-developed in Phase II.
Results: From a total of 61 unique emergency preparedness capabilities, 33 items achieved the desired outcome - they were rated either "developed in both phases" or "became developed" in Phase II for at least 80% of VAMCs. For 14 items, 70%-80% of VAMCs achieved the desired outcome. The remaining 14 items were identified as "low-performing" capabilities, defined as less than 70% of VAMCs achieved the desired outcome.
Conclusion: Measuring emergency management capabilities is a necessary first step to improving those capabilities. Furthermore, assessing hospital readiness over time and creating robust hospital readiness assessment tools can help hospitals make informed decisions regarding allocation of resources to ensure patient safety, provide timely access to high-quality patient care, and identify best practices in emergency management during and after disasters. Moreover, with some minor modifications, this comprehensive, all-hazardsbased, hospital preparedness assessment tool could be adapted for use beyond the VA.
C1 [Der-Martirosian, Claudia] 16111 Plummer St MS 152, North Hills, CA 91343 USA.
[Der-Martirosian, Claudia; Radcliff, Tiffany A.; Gable, Alicia R.; Hagigi, Farhad A.; Dobalian, Aram] US Dept Vet Affairs, Vet Emergency Management Evaluat Ctr, North Hills, CA USA.
[Radcliff, Tiffany A.] Texas A&M Univ, Sch Publ Hlth, Dept Hlth Policy Management, College Stn, TX USA.
[Riopelle, Deborah] VA Greater Angeles Healthcare Syst, VA Hlth Serv Res & Dev Ctr Study Healthcare Innov, North Hills, CA USA.
[Hagigi, Farhad A.] Univ Calif Angeles, Sch Med, Dept Family Med, Los Angeles, CA USA.
[Hagigi, Farhad A.] Univ Calif Angeles, Anderson Sch Management, Los Angeles, CA USA.
[Brewster, Pete] Dept Vet Affairs, Vet Hlth Adm, Off Emergency Management, Martinsburg, WV USA.
[Dobalian, Aram] Univ Calif Angeles, Fielding Sch Publ Hlth, Dept Hlth Policy & Management, Los Angeles, CA USA.
[Dobalian, Aram] Univ Calif Angeles, Sch Nursing, Los Angeles, CA USA.
RP Der-Martirosian, C (reprint author), 16111 Plummer St MS 152, North Hills, CA 91343 USA.
EM Claudia.Der-Martirosian@va.gov
FU Department of Veterans Affairs (VA), Veterans Health Administration,
Office of Patient Care Services (PCS; Washington DC, USA)
FX This material is based upon work supported by the Department of Veterans
Affairs (VA), Veterans Health Administration, Office of Patient Care
Services (PCS; Washington DC, USA). The views expressed in this article
are those of the authors and do not necessarily reflect the position or
policy of the VA or the US government.
NR 32
TC 0
Z9 0
U1 0
U2 0
PU CAMBRIDGE UNIV PRESS
PI NEW YORK
PA 32 AVENUE OF THE AMERICAS, NEW YORK, NY 10013-2473 USA
SN 1049-023X
EI 1945-1938
J9 PREHOSPITAL DISASTER
JI Prehospital Disaster Med.
PD FEB
PY 2017
VL 32
IS 1
BP 46
EP 57
DI 10.1017/S1049023X16001266
PG 12
WC Emergency Medicine
SC Emergency Medicine
GA EL5LY
UT WOS:000394663800007
PM 27964767
ER
PT J
AU Geller, J
Ranby, K
Maikovich-Fong, A
Simoneau, T
Kilbourn, K
Avram, D
AF Geller, Jessica
Ranby, Krista
Maikovich-Fong, Andrea
Simoneau, Teri
Kilbourn, Kristin
Avram, David
TI Perceived social support effectiveness: A dyadic predictor of
psychosocial distress in patients undergoing autologous hematopoietic
stem cell transplant (HSCT)
SO PSYCHO-ONCOLOGY
LA English
DT Meeting Abstract
C1 [Geller, Jessica; Simoneau, Teri] Denver Vet Affairs Med Ctr, Denver, CO USA.
[Ranby, Krista; Kilbourn, Kristin; Avram, David] Univ Colorado, Denver, CO 80202 USA.
[Maikovich-Fong, Andrea] Colorado Blood Canc Inst Presbyterian, Denver, CO USA.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1057-9249
EI 1099-1611
J9 PSYCHO-ONCOLOGY
JI Psycho-Oncol.
PD FEB
PY 2017
VL 26
SU 1
SI SI
MA F2
BP 78
EP 79
PG 2
WC Oncology; Psychology; Psychology, Multidisciplinary; Social Sciences,
Biomedical
SC Oncology; Psychology; Biomedical Social Sciences
GA EL9UX
UT WOS:000394966700177
ER
PT J
AU Schmidt, EM
Krahn, DD
McGuire, MH
Tavakoli, S
Wright, DM
Solares, HE
Lemke, S
Trafton, J
AF Schmidt, Eric M.
Krahn, Dean D.
McGuire, Marsden H.
Tavakoli, Sara
Wright, David M.
Solares, Hugo E.
Lemke, Sonne
Trafton, Jodie
TI Using Organizational and Clinical Performance Data to Increase the Value
of Mental Health Care
SO PSYCHOLOGICAL SERVICES
LA English
DT Article
DE mental health services; veterans; quality improvement; quality
indicators; program evaluation; organization and administration
ID QUALITY-OF-CARE; INFORMATION-TECHNOLOGY; ACCOUNTABLE CARE; SERVICES;
IMPLEMENTATION; IMPROVEMENT; CONTINUITY; INSURANCE; SCIENCE; SYSTEM
AB U.S. health systems, policy makers, and patients increasingly demand high-value care that improves health outcomes at lower cost. This study describes the initial design and analysis of the Mental Health Management System (MHMS), a performance data and quality improvement tool used by the Veterans Health Administration (VHA) to increase the value of its mental health care. The MHMS evaluates access to and quality of mental health care, organizational structure and efficiency, implementation of innovative treatment options, and, in collaboration with management, resource needs for delivering care. Performance on 31 measures was calculated for all U.S. VHA facilities (N = 139). Pearson correlations revealed that better access to care was significantly associated with fewer mental health provider staffing vacancies (r = -.24) and higher staff-topatient ratios for psychiatrists (r =.19) and other outpatient mental health providers (r =.27). Higher staff-to-patient ratios were significantly associated with higher performance on a number of patient and provider satisfaction measures (range of r =.18-.51) and continuity of care measures (range of r =.26-.43). Relationships observed between organizational and clinical performance measures suggest that the MHMS is a robust informatics and quality improvement tool that can serve as a model for health systems planning to adopt a value perspective. Future research should expand the MHMS framework to measure patient and health systems costs and psychosocial outcomes, as well as evaluate whether quality improvement solutions implemented as a result of using organizational information leads to higher-value mental health care.
C1 [Schmidt, Eric M.; Tavakoli, Sara; Wright, David M.; Solares, Hugo E.; Lemke, Sonne; Trafton, Jodie] Vet Affairs Palo Alto Hlth Care Syst, Menlo Pk, CA USA.
[Krahn, Dean D.] William S Middleton Mem Vet Adm Med Ctr, Madison, WI USA.
[McGuire, Marsden H.] Vet Affairs Cent Off, Washington, DC USA.
[McGuire, Marsden H.] Johns Hopkins Univ, Baltimore, MD USA.
[Schmidt, Eric M.; Trafton, Jodie] Stanford Univ, Stanford, CA USA.
[McGuire, Marsden H.] Univ Maryland, College Pk, MD USA.
[Tavakoli, Sara; Wright, David M.; Solares, Hugo E.; Lemke, Sonne; Trafton, Jodie] VA Off Mental Hlth Operat, Washington, DC USA.
RP Trafton, J (reprint author), Vet Affairs Palo Alto Hlth Care Syst, Menlo Pk, CA USA.
EM jodie.trafton@va.gov
FU Department of Veterans Affairs (VA) Office of Academic Affiliations
Advanced Fellowship in Health Services Research and Development (HSRD);
VA HSRD Service
FX Dr. Eric M. Schmidt was supported by the Department of Veterans Affairs
(VA) Office of Academic Affiliations Advanced Fellowship in Health
Services Research and Development (HSR&D) and the VA HSR&D Service.
NR 43
TC 0
Z9 0
U1 1
U2 1
PU AMER PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST NE, WASHINGTON, DC 20002-4242 USA
SN 1541-1559
EI 1939-148X
J9 PSYCHOL SERV
JI Psychol. Serv.
PD FEB
PY 2017
VL 14
IS 1
BP 13
EP 22
DI 10.1037/ser0000098
PG 10
WC Psychology, Clinical
SC Psychology
GA EM0QJ
UT WOS:000395022500002
PM 28134553
ER
PT J
AU Dopp, AR
Hanson, RF
Saunders, BE
Dismuke, CE
Moreland, AD
AF Dopp, Alex R.
Hanson, Rochelle F.
Saunders, Benjamin E.
Dismuke, Clara E.
Moreland, Angela D.
TI Community-Based Implementation of Trauma-Focused Interventions for
Youth: Economic Impact of the Learning Collaborative Model
SO PSYCHOLOGICAL SERVICES
LA English
DT Article
DE cost-effectiveness; implementation; trauma-focused cognitive-behavioral
therapy; training; community services
ID COST-EFFECTIVENESS; CHILD MALTREATMENT; ADOLESCENTS; DISORDERS;
DISSEMINATION; CLINICIAN
AB This study investigated the economics of the learning collaborative (LC) model in the implementation of Trauma-Focused Cognitive-Behavioral Therapy (TF-CBT), an evidence-based intervention for traumatic stress in youth. We evaluated the cost-effectiveness of the LC model based on data from 13 LCs completed in the southeastern United States. Specifically, we calculated cost-effectiveness ratios (CERs) for 2 key service outcomes: (a) clinician TF-CBT competence, based on pre-and post-LC self-ratings (n = 574); and (b) trauma-related mental health symptoms (i.e.,traumatic stress and depression), selfand caregiver-reported, for youth who received TF-CBT (n = 1,410). CERs represented the cost of achieving 1 standard unit of change on a measure (i.e., d = 1.0). The results indicated that (a) costs of $18,679 per clinician were associated with each unit increase in TF-CBT competency and (b) costs from $5,318 to $6,548 per youth were associated with each unit decrease in mental health symptoms. Thus, although the impact of LC participation on clinician competence did not produce a favorable CER, subsequent reductions in youth psychopathology demonstrated high cost-effectiveness. Clinicians and administrators in community provider agencies should consider these findings in their decisions about implementation of evidence-based interventions for youth with traumatic stress disorders.
C1 [Dopp, Alex R.; Hanson, Rochelle F.; Saunders, Benjamin E.; Moreland, Angela D.] Med Univ South Carolina, Columbia, SC USA.
[Dismuke, Clara E.] Med Univ South Carolina, Charleston, SC 29425 USA.
[Dismuke, Clara E.] Ralph H Johnson Vet Affairs Med Ctr, Charleston, SC USA.
RP Dopp, AR (reprint author), Univ Arkansas, Dept Psychol Sci, 216 Mem Hall, Fayetteville, AR 72701 USA.
EM dopp@uark.edu
FU National Institute of Mental Health [5 R34 MH104470]; Substance Abuse
and Mental Health Services Administration [5 U79 SM061269]; Duke
Endowment [1582-SP]
FX This research was supported by grants from the National Institute of
Mental Health (5 R34 MH104470), Substance Abuse and Mental Health
Services Administration (5 U79 SM061269), and the Duke Endowment
(1582-SP). We sincerely thank the many families who participated in this
project as well as the therapists and other community professionals, too
numerous to mention individually, who participated in the learning
collaboratives. Finally, we extend special thanks to Faraday Davies,
Sara delMas, and Emily Fanguy for their assistance with data collection
and management.
NR 41
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U1 2
U2 2
PU AMER PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST NE, WASHINGTON, DC 20002-4242 USA
SN 1541-1559
EI 1939-148X
J9 PSYCHOL SERV
JI Psychol. Serv.
PD FEB
PY 2017
VL 14
IS 1
BP 57
EP 65
DI 10.1037/ser0000131
PG 9
WC Psychology, Clinical
SC Psychology
GA EM0QJ
UT WOS:000395022500006
PM 28134556
ER
PT J
AU Moore, JT
AF Moore, Jon T.
TI Multicultural and Idiosyncratic Considerations for Measuring the
Relationship Between Religious and Secular Forms of Spirituality With
Positive Global Mental Health
SO PSYCHOLOGY OF RELIGION AND SPIRITUALITY
LA English
DT Article
DE secular; multicultural; spiritual values; belief in God; mental health
ID WELL-BEING QUESTIONNAIRE; VALIDATION; PSYCHOLOGY; SCALE; LIFE;
INVOLVEMENT; FITNESS
AB The current study espouses an alternative methodology using an ideologically diverse sample of 4,667 respondents who reported their spirituality levels (i.e., the extent one lives in accordance with one's self-defined spiritual values) and their mental health levels. The sample predominately included agnostic, atheist, Buddhist, Christian, Jewish, and spiritual nonreligious participants. Multigroup analyses within structural equation models revealed that spirituality held a large relationship strength with mental health for both religious and secular forms of spirituality, even with multiple configurations determining the constituents of the secular group. An exploratory analysis demonstrated that when spirituality, demographic factors, social support, and spiritual coping usage were all examined as predictors of mental health, religious and secular forms of spirituality were the only variables that maintained a large predictive strength. The results indicated that living in accordance with one's spiritual values, even when defined in a variety of ways, is characteristic of greater mental health.
C1 [Moore, Jon T.] Vet Affairs Puget Sound Hlth Care Syst, Amer Lake Div, 9600 Vet Dr A-116, Tacoma, WA 98493 USA.
[Moore, Jon T.] Univ Oregon, Dept Psychol, Eugene, OR 97403 USA.
RP Moore, JT (reprint author), Vet Affairs Puget Sound Hlth Care Syst, Amer Lake Div, 9600 Vet Dr A-116, Tacoma, WA 98493 USA.
EM jonmoorephd@gmail.com
NR 72
TC 0
Z9 0
U1 3
U2 3
PU EDUCATIONAL PUBLISHING FOUNDATION-AMERICAN PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST, NE, WASHINGTON, DC 20002-4242 USA
SN 1941-1022
EI 1943-1562
J9 PSYCHOL RELIG SPIRIT
JI Psychol. Relig. Spiritual.
PD FEB
PY 2017
VL 9
IS 1
BP 21
EP 33
DI 10.1037/rel0000083
PG 13
WC Psychology, Multidisciplinary; Religion
SC Psychology; Religion
GA EM8JJ
UT WOS:000395557100003
ER
PT J
AU Melzer, AC
Ghassemieh, BJ
Gillespie, SE
Lindenauer, PK
McBurnie, MA
Mularski, RA
Naureckas, ET
Vollmer, WM
Au, DH
AF Melzer, Anne C.
Ghassemieh, Bijan J.
Gillespie, Suzanne E.
Lindenauer, Peter K.
McBurnie, Mary Ann
Mularski, Richard A.
Naureckas, Edward T.
Vollmer, William M.
Au, David H.
TI Patient characteristics associated with poor inhaler technique among a
cohort of patients with COPD
SO RESPIRATORY MEDICINE
LA English
DT Article
DE Chronic obstructive pulmonary disease (COPD); Inhaled therapy;
Technique; Adherence
ID OBSTRUCTIVE PULMONARY-DISEASE; METERED-DOSE INHALER; INCORRECT
INHALATION TECHNIQUE; HEALTH LITERACY; ASTHMA; MANAGEMENT; ADHERENCE;
EDUCATION
AB Background: Inhaled therapies are the cornerstone of pharmacologic management for COPD. Each device requires a unique series of steps to be most effective, making appropriate instruction in inhaler technique a key part of the management of COPD.
Objectives: Examine characteristics of patients and devices associated with poor technique among patients with COPD.
Methods: Cross-sectional study of subjects with COPD using at least one of: metered dose inhaler, Advair Diskus, Spiriva Handihaler, identified from the COPD Outcomes-based Network for Clinical Effectiveness and Research Translation (CONCERT) registry. Technique was assessed face-to-face using manufacturer provided dummy inhalers, with standardized checklists for each device. We used logistic regression to model associations with poor inhaler technique, defined as an error in >= 20% of the steps, as a function of patient characteristics, with educational attainment the primary predictor.
Results: 688 individuals meet eligibility criteria, 65.5% had poor technique for at least one device. In adjusted analyses, Black race was associated with poor technique (OR 3.25, 95%CI 1.86-5.67) while greater than high school education was associated with decreased odds of poor technique (OR 0.35, 95% CI 0.17-0.70 for trade school/some college, OR 0.25, 95%Cl 0.11-0.61 for college or more, p <= 0.001 for test of linear trend). The percentage of errors varied between devices, with subjects making proportionally the most errors for MDIs.
Conclusions: Poor inhaler technique is common among individuals with COPD, varies between devices, and is associated with race and educational attainment. Tailored educational interventions to teach inhaler technique should be part of the process of initiating and monitoring inhaled therapies. Published by Elsevier Ltd.
C1 [Melzer, Anne C.; Ghassemieh, Bijan J.; Au, David H.] Univ Washington, Div Pulm & Crit Care, Seattle, WA 98195 USA.
[Melzer, Anne C.; Au, David H.] VA Puget Sound, Ctr Innovat Vet Ctr & Value Driven Care, Seattle, WA USA.
[Gillespie, Suzanne E.; McBurnie, Mary Ann; Mularski, Richard A.; Vollmer, William M.] Kaiser Permanente Northwest, Ctr Hlth Res, Portland, OR USA.
[Lindenauer, Peter K.] Baystate Med Ctr, Dept Med, Springfield, MA 01199 USA.
[Naureckas, Edward T.] Univ Chicago, Dept Med, Chicago, IL 60637 USA.
[Melzer, Anne C.] VA Puget Sound Hlth Care Syst, 1660 S Columbian Way,Mailstop S-152, Seattle, WA 98108 USA.
RP Melzer, AC (reprint author), Univ Washington, Div Pulm & Crit Care, Seattle, WA 98195 USA.; Melzer, AC (reprint author), VA Puget Sound, Ctr Innovat Vet Ctr & Value Driven Care, Seattle, WA USA.; Melzer, AC (reprint author), VA Puget Sound Hlth Care Syst, 1660 S Columbian Way,Mailstop S-152, Seattle, WA 98108 USA.; Melzer, AC (reprint author), 1 Vet Dr, Minneapolis, MN 55417 USA.
EM acmelzer@uw.edu
FU National Heart, Lung, and Blood Institute [HL101618]
FX This material is based upon work supported by the Department of Veterans
Affairs, Health Services Research and Development (HSR&D), who provided
access to data, office space, and programming and data management. The
views expressed in this article are those of the authors and do not
necessarily reflect the position or policy of the Department of Veterans
Affairs. We would like to acknowledge the other member sites of the
CONCERT Consortium, without whom this project could not have been
completed. Dr. Au has personally reviewed the data, understands the
statistical methods employed for efficacy analysis, and confirms an
understanding of this analysis, that the methods are clearly described
and that they are a fair way to report the results. Dr. Melzer was
supported by an institutional F-32 (HL007287) through the University of
Washington Department of Pulmonary and Critical Care. Additional support
was received through the VA Health Services Research and Development
(HSR&D). Support for this project was also provided by the National
Heart, Lung, and Blood Institute (HL101618) for the CONCERT group. The
views presented are that of the researchers and do not necessary reflect
those of the Department of Veterans Affairs.
NR 39
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Z9 0
U1 1
U2 1
PU W B SAUNDERS CO LTD
PI LONDON
PA 32 JAMESTOWN RD, LONDON NW1 7BY, ENGLAND
SN 0954-6111
EI 1532-3064
J9 RESP MED
JI Respir. Med.
PD FEB
PY 2017
VL 123
BP 124
EP 130
DI 10.1016/j.rmed.2016.12.011
PG 7
WC Cardiac & Cardiovascular Systems; Respiratory System
SC Cardiovascular System & Cardiology; Respiratory System
GA EL1QY
UT WOS:000394397300018
PM 28137488
ER
PT J
AU Madden, EB
Robinson, RM
Kendall, DL
AF Madden, Elizabeth Brookshire
Robinson, Reva M.
Kendall, Diane L.
TI Phonological Treatment Approaches for Spoken Word Production in Aphasia
SO SEMINARS IN SPEECH AND LANGUAGE
LA English
DT Review
DE Aphasia; anomia; phonology; treatment; phonomotor
ID PHONOMOTOR TREATMENT; COMPONENTS-ANALYSIS; NAMING IMPAIRMENTS; LEXICAL
ACCESS; THERAPY; RETRIEVAL; ANOMIA; ALEXIA; REHABILITATION; PROGRAM
AB This article provides an overview of phonological treatment approaches for anomia in individuals with aphasia. The role of phonology in language processing, as well as the impact of phonological impairment on communication is initially discussed. Then, traditional phonologically based treatment approaches, including phonological, orthographic, indirect, guided, and mixed cueing methods, are described. Collectively, these cueing treatment approaches aim to facilitate word retrieval by stimulating residual phonological abilities. An alternative treatment approach, phonomotor treatment, is also examined. Phonomotor treatment aims to rebuild sublexical, phonological sequence knowledge and phonological awareness as a means to strengthen lexical processing and whole-word naming. This treatment is supported by a parallel-distributed processing model of phonology and therefore promotes multimodal training of individual phonemes and phoneme sequences in an effort to enhance the neural connectivity supporting underlying phonological processing mechanisms. The article concludes with suggestions for clinical application and implementation.
C1 [Madden, Elizabeth Brookshire] Florida State Univ, Sch Commun Sci & Disorders, Tallahassee, FL 32306 USA.
[Robinson, Reva M.] Univ Washington, Dept Speech & Hearing Sci, Seattle, WA 98195 USA.
[Kendall, Diane L.] Univ Washington, Dept Speech & Hearing Sci, VA Puget Sound Healthcare Syst, Seattle, WA 98195 USA.
[Kendall, Diane L.] Univ Pretoria, Dept Speech Language Pathol & Audiol, Pretoria, South Africa.
RP Madden, EB (reprint author), 201 West Bloxham St, Tallahassee, FL 32306 USA.
EM ebmadden@fsu.edu
FU United States Department of Veterans Affairs [RRD3-15-12W,
1I01RX001145-01A1]
FX The authors would like to acknowledge the United States Department of
Veterans Affairs for providing tremendous funding for aphasia research,
especially for the two grants (#RRD3-15-12W and #1I01RX001145-01A1) that
supported this work.
NR 46
TC 0
Z9 0
U1 7
U2 7
PU THIEME MEDICAL PUBL INC
PI NEW YORK
PA 333 SEVENTH AVE, NEW YORK, NY 10001 USA
SN 0734-0478
EI 1098-9056
J9 SEMIN SPEECH LANG
JI Semin. Speech Lang.
PD FEB
PY 2017
VL 38
IS 1
BP 62
EP 74
DI 10.1055/s-0036-1597258
PG 13
WC Audiology & Speech-Language Pathology; Linguistics; Rehabilitation
SC Audiology & Speech-Language Pathology; Linguistics; Rehabilitation
GA EM6CC
UT WOS:000395399400008
PM 28201838
ER
PT J
AU Pfeiffer, PN
Valenstein, M
Ganoczy, D
Henry, J
Dobscha, SK
Piette, JD
AF Pfeiffer, Paul N.
Valenstein, Marcia
Ganoczy, Dara
Henry, Jennifer
Dobscha, Steven K.
Piette, John D.
TI Pilot study of enhanced social support with automated telephone
monitoring after psychiatric hospitalization for depression
SO SOCIAL PSYCHIATRY AND PSYCHIATRIC EPIDEMIOLOGY
LA English
DT Article
DE Depression; Discharge; Inpatient; Peer support; Family; Mobile;
Monitoring
ID PEER SUPPORT; PSYCHOMETRIC PROPERTIES; RANDOMIZED-TRIAL; CARE; SUICIDE;
SCALE; INTERVENTION; PREFERENCES; PATIENT; CRISIS
AB Following discharge, patients hospitalized for depression are at high risk for poor retention in outpatient care and adverse outcomes.
Pilot tests a post-hospital monitoring and enhanced support program for depression.
48 patients at a Veterans Affairs Medical Center discharged following a depression-related inpatient stay received weekly visits or phone calls for 6 months from their choice of either a family member/friend (n = 19) or a certified peer support specialist (n = 29). Participants also completed weekly automated telephone monitoring calls assessing depressive symptoms and antidepressant medication adherence.
Over 90% of participants were more satisfied with their care due to the service. The mean change from baseline to 6 months in depression symptoms was -7.9 (p < 0.05) according to the Patient Health Questionnaire and -11.2 (p < 0.05) according to the Beck Depression Inventory-II for those supported by a family member/friend, whereas those supported by a peer specialist had mean changes of -3.5 (p < 0.05) and -1.7 (p > 0.10), respectively.
Increased contact with a chosen support person coupled with automated telephone monitoring after psychiatric hospitalization is an acceptable service for patients with depression. Those who received the service, and particularly those supported by a family member/friend, experienced reductions in symptoms of depression.
C1 [Pfeiffer, Paul N.; Valenstein, Marcia; Piette, John D.] Univ Michigan, Sch Med, Ann Arbor, MI 48109 USA.
[Pfeiffer, Paul N.; Valenstein, Marcia; Ganoczy, Dara; Henry, Jennifer; Piette, John D.] VA Ann Arbor Healthcare Syst, VA Ctr Clin Management Res, Ann Arbor, MI 48105 USA.
[Dobscha, Steven K.] Portland VA Med Ctr, VA Ctr Vet Involvement Care, Portland, MI USA.
[Dobscha, Steven K.] Oregon Hlth & Sci Univ, Portland, OR 97201 USA.
[Piette, John D.] Univ Michigan, Sch Publ Hlth, Ann Arbor, MI 48109 USA.
RP Pfeiffer, PN (reprint author), Univ Michigan, Sch Med, Ann Arbor, MI 48109 USA.; Pfeiffer, PN (reprint author), VA Ann Arbor Healthcare Syst, VA Ctr Clin Management Res, Ann Arbor, MI 48105 USA.
EM ppfeiffe@umich.edu
NR 30
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U1 0
U2 0
PU SPRINGER HEIDELBERG
PI HEIDELBERG
PA TIERGARTENSTRASSE 17, D-69121 HEIDELBERG, GERMANY
SN 0933-7954
EI 1433-9285
J9 SOC PSYCH PSYCH EPID
JI Soc. Psychiatry Psychiatr. Epidemiol.
PD FEB
PY 2017
VL 52
IS 2
BP 183
EP 191
DI 10.1007/s00127-016-1288-2
PG 9
WC Psychiatry
SC Psychiatry
GA EM3EL
UT WOS:000395197200010
PM 27783130
ER
PT J
AU Barnes, SM
Bahraini, NH
Forster, JE
Stearns-Yoder, KA
Hostetter, TA
Smith, G
Nagamoto, HT
Nock, MK
AF Barnes, Sean M.
Bahraini, Nazanin H.
Forster, Jeri E.
Stearns-Yoder, Kelly A.
Hostetter, Trisha A.
Smith, Geoffrey
Nagamoto, Herbert T.
Nock, Matthew K.
TI Moving Beyond Self-Report: Implicit Associations about Death/Life
Prospectively Predict Suicidal Behavior among Veterans
SO SUICIDE AND LIFE-THREATENING BEHAVIOR
LA English
DT Article
ID RISK-ASSESSMENT; INJURIOUS THOUGHTS; IDEATION; ADOLESCENTS; DEPRESSION;
COGNITION; MIND
AB Reliance on self-report limits clinicians' ability to accurately predict suicidal behavior. In this study the predictive validity of an objective measure, the death/suicide Implicit Association Test (d/sIAT), was tested among psychiatrically hospitalized veterans. Following acute stabilization, 176 participants completed the d/sIAT and traditional suicide risk assessments. Participants had similar d/sIAT scores regardless of whether they had recently attempted suicide. However, d/sIAT scores significantly predicted suicide attempts during the 6-month follow-up above and beyond other known risk factors for suicidal behavior (OR=1.89; 95% CI: 1.15-3.12; based on 1SD increase). The d/sIAT may augment the accuracy of suicide risk assessment.
C1 [Barnes, Sean M.; Bahraini, Nazanin H.; Forster, Jeri E.; Stearns-Yoder, Kelly A.; Hostetter, Trisha A.; Smith, Geoffrey; Nagamoto, Herbert T.] Rocky Mt Mental Illness Res Educ & Clin Ctr, Denver, CO USA.
[Barnes, Sean M.; Bahraini, Nazanin H.; Nagamoto, Herbert T.] Univ Colorado, Sch Med, Dept Psychiat, Anschutz Med Campus, Aurora, CO USA.
[Bahraini, Nazanin H.; Forster, Jeri E.] Univ Colorado, Sch Med, Dept Phys Med & Rehabil, Anschutz Med Campus, Aurora, CO USA.
[Forster, Jeri E.] Univ Colorado, Sch Med, Dept Biostat & Informat, Anschutz Med Campus, Aurora, CO USA.
[Nock, Matthew K.] Harvard Univ, Dept Psychol, 33 Kirkland St, Cambridge, MA 02138 USA.
RP Barnes, SM (reprint author), Denver VA Med Ctr, Rocky Mt MIRECC, 1055 Clermont St, Denver, CO 80220 USA.
EM Sean.Barnes2@va.gov
FU Military Suicide Research Consortium, through the Office of the
Assistant Secretary of Defense for Health Affairs; Rocky Mountain Mental
Illness, Research, Education, and Clinical Center; U.S. Government.
Denver VA Medical Center [W81XWH-10-2-0178]
FX This research was funded by the Military Suicide Research Consortium,
through the Office of the Assistant Secretary of Defense for Health
Affairs, and by the Rocky Mountain Mental Illness, Research, Education,
and Clinical Center. Opinions, interpretations, conclusions, and
recommendations are those of the authors and are not necessarily
endorsed by the Military Suicide Research Consortium, Department of
Defense, Department of Veterans Affairs, or the U.S. Government. Denver
VA Medical Center Grant Number: W81XWH-10-2-0178.
NR 23
TC 0
Z9 0
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0363-0234
EI 1943-278X
J9 SUICIDE LIFE-THREAT
JI Suicide Life-Threat. Behav.
PD FEB
PY 2017
VL 47
IS 1
BP 67
EP 77
DI 10.1111/sltb.12265
PG 11
WC Psychiatry; Psychology, Multidisciplinary
SC Psychiatry; Psychology
GA EL9QI
UT WOS:000394954700007
PM 27387836
ER
PT J
AU Ashong, CN
Raheem, SA
Hunter, AS
Mindru, C
Barshes, NR
AF Ashong, Chester N.
Raheem, Shazia A.
Hunter, Andrew S.
Mindru, Cezarina
Barshes, Neal R.
TI Methicillin-Resistant Staphylococcus aureus in Foot Osteomyelitis
SO SURGICAL INFECTIONS
LA English
DT Article
DE diabetes; MRSA; MSSA; osteomyelitis; staphylococcal infections
ID INFECTIONS; DIAGNOSIS; PATHOGENS; BONE
AB Background: Conflicting studies exist regarding the impact of methicillin-resistant Staphylococcus aureus (MRSA) on increased time to wound healing, future need for surgical procedures, and likelihood of treatment failure in patients with diabetic foot osteomyelitis. The purpose of this study is to determine the overall significance of MRSA in predicting treatment failure in bone infections of the foot and to determine an appropriate pre-operative and empiric post-operative antibiotic regimen.
Patients and Methods: Patients presenting with an initial episode of "probable" or "definite" foot osteomyelitis were included for review and analysis if the following criteria were met: (1) Osteomyelitis occurred in the foot (i.e., distal to the malleoli of the ankle); episodes occurring above the ankle were excluded. (2) Patients received either no antibiotics or only oral antibiotics for long-term treatment; episodes managed with long-term parenteral antibiotics were excluded. (3) The infection was managed initially with medical therapy or conservative surgical therapy; episodes managed with major (above-ankle) amputation as the initial treatment were excluded. The primary objective of this study was to assess whether episodes of foot osteomyelitis associated with MRSA resulted in treatment failure more frequently than not.
Results: Of 178 episodes included in the study, 50 (28.1%) episodes had treatment failure. Median time-to-treatment failure was 60 days (range 7-598 days). In 28.1% (9/32 episodes) in which treatment failure occurred and 39.0% (41/105) episodes in which no treatment failure occurred, MRSA was present. The presence of MRSA was not significantly associated with treatment failure (p = 0.99).
Conclusions: The presence of MRSA in bone culture and whether antibiotic use had anti-MRSA activity was not associated with increased treatment failure of diabetic foot osteomyelitis in our institution. Empiric antibiotic coverage of MRSA may not be necessary for many patients presenting with foot osteomyelitis.
C1 [Ashong, Chester N.; Raheem, Shazia A.; Hunter, Andrew S.] Michael E DeBakey VA Med Ctr, Dept Pharm, Houston, TX USA.
[Mindru, Cezarina] Michael E DeBakey VA Med Ctr, Dept Infect Dis, Houston, TX USA.
[Barshes, Neal R.] Baylor Coll Med, Michael E DeBakey Vet Affairs Med Ctr, Michael E DeBakey Dept Surg, Div Vasc & Endovasc Surg, 2002 Holcombe Blvd,OCL 112, Houston, TX 77030 USA.
RP Barshes, NR (reprint author), Baylor Coll Med, Michael E DeBakey Vet Affairs Med Ctr, Michael E DeBakey Dept Surg, Div Vasc & Endovasc Surg, 2002 Holcombe Blvd,OCL 112, Houston, TX 77030 USA.
EM nbarshes@bcm.tmc.edu
FU Michael E. DeBakey Veterans Affairs Medical Center
FX We would like to acknowledge research support from the Michael E.
DeBakey Veterans Affairs Medical Center. Dr. Barshes has received
$25,000 from the Michael E. DeBakey Veterans Affairs Medical Center, a
federal institution, for the study of foot osteomyelitis.
NR 18
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Z9 0
U1 0
U2 0
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1096-2964
EI 1557-8674
J9 SURG INFECT
JI Surg. Infect.
PD FEB-MAR
PY 2017
VL 18
IS 2
BP 143
EP 148
DI 10.1089/sur.2016.165
PG 6
WC Infectious Diseases; Surgery
SC Infectious Diseases; Surgery
GA EL3DU
UT WOS:000394500600010
PM 27898266
ER
PT J
AU Zhou, J
Chong, SY
Lim, A
Singh, BK
Sinha, RA
Salmon, AB
Yen, PM
AF Zhou, Jin
Chong, Shu Yun
Lim, Andrea
Singh, Brijesh K.
Sinha, Rohit A.
Salmon, Adam B.
Yen, Paul M.
TI Changes in macroautophagy, chaperone-mediated autophagy, and
mitochondrial metabolism in murine skeletal and cardiac muscle during
aging
SO AGING-US
LA English
DT Article
DE aging; muscle; heart; autophagy; chaperone-mediated autophagy (CMA);
fatty acid oxidation; ceramide
ID INSULIN-RESISTANCE; DISEASE; HUMANS; DYSFUNCTION; STRESS; OBESE;
STIMULATION; INHIBITION; LIPIDATION; SIGNATURE
AB Aging causes a general decline in cellular metabolic activity, and function in different tissues and whole body homeostasis. However, the understanding about the metabolomic and autophagy changes in skeletal muscle and heart during aging is still limited. We thus examined markers for macroautophagy, chaperone-mediated autophagy (CMA), mitochondrial quality control, as well as cellular metabolites in skeletal and cardiac muscle from young (5 months old) and aged (27 months old) mice. We found decreased autophagic degradation of p62 and increased ubiquitinated proteins in both tissues from aged mice, suggesting a decline in macroautophagy during aging. In skeletal muscle from aged mice, there also was a decline in LC3B-I conjugation to phosphatidylethanolamine (PE) possibly due to decreased protein levels of ATG3 and ATG12-ATG5. The CMA markers, LAMP-2A and Hsc70, and mitochondrial turnover markers, Drp1, PINK1 and PGC1 alpha also were decreased. Metabolomics analysis showed impaired a-oxidation in heart of aged mice, whereas increased branched-chain amino acids (BCAAs) and ceramide levels were found in skeletal muscle of aged mice that in turn, may contribute to insulin resistance in muscle. Taken together, our studies showed similar declines in macroautophagy but distinct effects on CMA, mitochondrial turnover, and metabolic dysfunction in muscle vs. heart during aging.
C1 [Zhou, Jin; Lim, Andrea; Singh, Brijesh K.; Sinha, Rohit A.; Yen, Paul M.] Duke NUS Med Sch Singapore, Program Cardiovas & Metab Disorders, Singapore 169857, Singapore.
[Chong, Shu Yun] Nanyang Technol Univ, Dept Biomed Sci, Singapore 637551, Singapore.
[Salmon, Adam B.] Univ Texas Hlth Sci Ctr San Antonio, Barshop Inst Longev & Aging Studies, Dept Mol Med, San Antonio, TX 78245 USA.
[Salmon, Adam B.] South Texas Vet Hlth Care Syst, Geriatr Res Educ & Clin Ctr, San Antonio, TX 78229 USA.
[Yen, Paul M.] Duke Univ, Med Ctr, Duke Mol Physiol Inst, Dept Med & Pharmacol, Durham, NC 27710 USA.
[Yen, Paul M.] Duke Univ, Med Ctr, Dept Canc Biol, Durham, NC 27710 USA.
RP Yen, PM (reprint author), Duke NUS Med Sch Singapore, Program Cardiovas & Metab Disorders, Singapore 169857, Singapore.; Yen, PM (reprint author), Duke Univ, Med Ctr, Duke Mol Physiol Inst, Dept Med & Pharmacol, Durham, NC 27710 USA.; Yen, PM (reprint author), Duke Univ, Med Ctr, Dept Canc Biol, Durham, NC 27710 USA.
EM paul.yen@duke-nus.edu.sg
FU Duke-NUS Medical School Faculty Funds; Singapore National Medical
Research Council grant [NMRC/CSA/0054/2013, NMRC/CIRG/1340/2012];
National Institute of Health [R01 AG050797]; American Heart Association
[15BGIA23220016]; Geriatric Research, Education and Clinical Center of
the South Texas Veterans Health Care System
FX This work was supported by Duke-NUS Medical School Faculty Funds (to
PMY), Singapore National Medical Research Council grant
NMRC/CSA/0054/2013 (to PMY), NMRC/CIRG/1340/2012 (to PMY), National
Institute of Health R01 AG050797 (to ABS), the American Heart
Association 15BGIA23220016 (to ABS) and the Geriatric Research,
Education and Clinical Center of the South Texas Veterans Health Care
System (to ABS).
NR 45
TC 0
Z9 0
U1 3
U2 3
PU IMPACT JOURNALS LLC
PI ORCHARD PARK
PA 6666 E QUAKER ST, STE 1, ORCHARD PARK, NY 14127 USA
SN 1945-4589
J9 AGING-US
JI Aging-US
PD FEB
PY 2017
VL 9
IS 2
BP 583
EP 599
DI 10.18632/aging.101181
PG 17
WC Cell Biology
SC Cell Biology
GA EO7TH
UT WOS:000396892500022
PM 28238968
ER
PT J
AU Yarns, BC
Glass, OM
AF Yarns, Brandon C.
Glass, Oliver M.
TI Why Trainees Should Consider a Career in Geriatric Psychiatry:
Reflections From Two AAGP Trainee Board Members
SO AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY
LA English
DT Editorial Material
C1 [Yarns, Brandon C.] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Gen Internal Med, 10940 Wilshire Blvd,Suite 710, Los Angeles, CA 90024 USA.
[Yarns, Brandon C.] VA Greater Los Angeles Healthcare Syst, Dept Psychiat, Los Angeles, CA USA.
[Glass, Oliver M.] East Carolina Univ, Dept Psychiat & Behav Med, Greenville, NC USA.
RP Yarns, BC (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Gen Internal Med, 10940 Wilshire Blvd,Suite 710, Los Angeles, CA 90024 USA.
EM byarns@mednet.ucla.edu
FU VA Office of Academic Affiliations through the VA National Clinician
Scholars Program [TPH 65-005]
FX Dr. Yarns was supported by the VA Office of Academic Affiliations
through the VA National Clinician Scholars Program, funding ID #TPH
65-005.
NR 7
TC 0
Z9 0
U1 0
U2 0
PU ELSEVIER SCIENCE INC
PI NEW YORK
PA 360 PARK AVE SOUTH, NEW YORK, NY 10010-1710 USA
SN 1064-7481
EI 1545-7214
J9 AM J GERIAT PSYCHIAT
JI Am. J. Geriatr. Psychiatr.
PD FEB
PY 2017
VL 25
IS 2
BP 204
EP 206
DI 10.1016/j.jagp.2016.11.016
PG 3
WC Geriatrics & Gerontology; Gerontology; Psychiatry
SC Geriatrics & Gerontology; Psychiatry
GA EP1FF
UT WOS:000397130100014
PM 28040428
ER
PT J
AU Gonzalez, DA
Soble, JR
Marceaux, JC
McCoy, KJM
AF Gonzalez, David Andres
Soble, Jason R.
Marceaux, Janice C.
McCoy, Karin J. M.
TI An Evaluation of the Texas Functional Living Scale's Latent Structure
and Subscales
SO ARCHIVES OF CLINICAL NEUROPSYCHOLOGY
LA English
DT Article
DE Everyday functioning; Test construction; Assessment
AB Objective: Performance-based functional assessment is a critical component of neuropsychological practice. The Texas Functional Living Scale (TFLS) has promise given its brevity, nationally representative norms, and co-norming with Wechsler scales. However, its subscale structure has not been evaluated. The purpose of this study was to evaluate the TFLS in a mixed clinical sample (n = 197).
Method: Reliability and convergent and discriminant validity coefficients were calculated with neurocognitive testing and collateral reports and factor analysis was performed.
Results: The Money and Calculation subscale had the best psychometric properties of the subscales. The evidence did not support solitary interpretation of the Time subscale. A three-factor latent structure emerged representing memory and semantic retrieval, performance and visual scanning, and financial calculation.
Conclusions: This study added psychometric support for interpretation of the TFLS total score and some of its subscales. Study limitations included sample characteristics (e.g., gender ratio) and low power for collateral report analyses.
C1 [Gonzalez, David Andres; Soble, Jason R.; Marceaux, Janice C.; McCoy, Karin J. M.] South Texas Vet Hlth Care Syst, Psychol Serv 116B, San Antonio, TX USA.
[Gonzalez, David Andres] Univ Texas Hlth Sci Ctr San Antonio, Dept Neurol, 8300 Floyd Curl Dr MC 7883, San Antonio, TX 78229 USA.
RP Gonzalez, DA (reprint author), Univ Texas Hlth Sci Ctr San Antonio, Dept Neurol, 8300 Floyd Curl Dr MC 7883, San Antonio, TX 78229 USA.
EM gonzalezD15@uthscsa.edu
NR 21
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0887-6177
EI 1873-5843
J9 ARCH CLIN NEUROPSYCH
JI Arch. Clin. Neuropsychol.
PD FEB
PY 2017
VL 32
IS 1
BP 104
EP 109
DI 10.1093/arclin/acw082
PG 6
WC Psychology, Clinical; Psychology
SC Psychology
GA EO9KJ
UT WOS:000397007300013
PM 28122769
ER
PT J
AU Renfroe, JB
Turner, TH
Hinson, VK
AF Renfroe, Jenna B.
Turner, Travis H.
Hinson, Vanessa K.
TI Assessing Visuospatial Skills in Parkinson's: Comparison of
Neuropsychological Assessment Battery Visual Discrimination to the
Judgment of Line Orientation
SO ARCHIVES OF CLINICAL NEUROPSYCHOLOGY
LA English
DT Article
DE Parkinson's disease; Assessment
ID MILD COGNITIVE IMPAIRMENT; SOCIETY TASK-FORCE; ALZHEIMERS-DISEASE;
BENTON JUDGMENT; LEWY BODIES; SHORT FORMS; DEMENTIA; CRITERIA
AB Objective: Judgment of Line Orientation (JOLO) test is widely used in assessing visuospatial deficits in Parkinson's disease (PD). The neuropsychological assessment battery (NAB) offers the Visual Discrimination test, with age and education correction, parallel forms, and co-normed standardization sample for comparisons within and between domains. However, NAB Visual Discrimination has not been validated in PD, and may not measure the same construct as JOLO.
Method: A heterogeneous sample of 47 PD patients completed the JOLO and NAB Visual Discrimination within a broader neuropsychological evaluation. Pearson correlations assessed relationships between JOLO and NAB Visual Discrimination performances.
Results: Raw and demographically corrected scores from JOLO and Visual Discrimination were only weakly correlated. NAB Visual Discrimination subtest was moderately correlated with overall cognitive functioning, whereas the JOLO was not.
Conclusions: Despite apparent virtues, results do not support NAB Visual Discrimination as an alternative to JOLO in assessing visuospatial functioning in PD.
C1 [Renfroe, Jenna B.; Turner, Travis H.; Hinson, Vanessa K.] Med Univ South Carolina, Dept Neurol, 208 B Rutledge Ave,MSC 108, Charleston, SC 29425 USA.
[Hinson, Vanessa K.] Ralph H Johnson VAMC, Neurol Serv, Charleston, SC USA.
RP Renfroe, JB (reprint author), Med Univ South Carolina, Dept Neurol, 208 B Rutledge Ave,MSC 108, Charleston, SC 29425 USA.
EM jennarenfroephd@gmail.com
FU Michael J. Fox Foundation
FX This work was supported by the Michael J. Fox Foundation.
NR 21
TC 0
Z9 0
U1 0
U2 0
PU OXFORD UNIV PRESS
PI OXFORD
PA GREAT CLARENDON ST, OXFORD OX2 6DP, ENGLAND
SN 0887-6177
EI 1873-5843
J9 ARCH CLIN NEUROPSYCH
JI Arch. Clin. Neuropsychol.
PD FEB
PY 2017
VL 32
IS 1
BP 123
EP 127
DI 10.1093/arclin/acw102
PG 5
WC Psychology, Clinical; Psychology
SC Psychology
GA EO9KJ
UT WOS:000397007300016
PM 28122771
ER
PT J
AU Hassan, RI
Gaffo, AL
AF Hassan, Romina I.
Gaffo, Angelo L.
TI Rituximab in ANCA-Associated Vasculitis
SO CURRENT RHEUMATOLOGY REPORTS
LA English
DT Article
DE Rituximab. Vasculitis; ANCA; Granulomatosis with polyangiitis (GPA);
Microscopic polyangiitis (MPA); Eosinophilicgranulomatosiswith
polyangiitis (EGPA)
ID ANTIBODY-ASSOCIATED VASCULITIS; WEGENERS-GRANULOMATOSIS;
RANDOMIZED-TRIAL; RENAL VASCULITIS; PLASMA-EXCHANGE; CYCLOPHOSPHAMIDE;
INDUCTION; REMISSION; THERAPY; MAINTENANCE
AB Purpose of Review The purpose of this review is to describe the efficacy and safety of rituximab (RTX) as a remission induction and maintenance therapy in ANCA-associated vasculitis (AAV).
Recent Findings A PubMed search was carried out to track down articles published between February 2006 and February 2016. Randomized controlled trials (RCTs) that encompassed patients with AAV were included. The American College of Rheumatology (ACR) and the European League against Rheumatism (EULAR) 2014-2015 online abstracts were also reviewed whether they were RTCs or not. Ten PubMed RCTs were analyzed along with eight ACR and four EULAR abstracts. RTX was not inferior to cyclophosphamide (CYC) for remission induction in AAV; it was superior to CYC in patients with relapsing disease and superior for remission maintenance in comparison with azathioprine (AZA).
Summary Rituximab is a therapeutic option to induce and maintain remission in patients with AAV.
C1 [Hassan, Romina I.] JM Ramos Mejia Hosp, Div Rheumatol, 609 Gen Urquiza St, RA-1221 Buenos Aires, DF, Argentina.
[Gaffo, Angelo L.] Birmingham VA Med Ctr, 700 19th St S, Birmingham, AL 35233 USA.
[Gaffo, Angelo L.] Univ Alabama Birmingham, Div Rheumatol & Clin Immunol, 1825 Univ Blvd,SHEL 306, Birmingham, AL 35294 USA.
RP Hassan, RI (reprint author), JM Ramos Mejia Hosp, Div Rheumatol, 609 Gen Urquiza St, RA-1221 Buenos Aires, DF, Argentina.
EM rominahassan@gmail.com
NR 35
TC 1
Z9 1
U1 1
U2 1
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1523-3774
EI 1534-6307
J9 CURR RHEUMATOL REP
JI Curr. Rheumatol. Rep.
PD FEB
PY 2017
VL 19
IS 2
AR 6
DI 10.1007/s11926-017-0632-1
PG 8
WC Rheumatology
SC Rheumatology
GA EP0XM
UT WOS:000397110000004
PM 28155022
ER
PT J
AU Hogan, MF
Liu, AW
Peters, MJ
Willard, JR
Rabbani, Z
Bartholomew, EC
Ottley, A
Hull, RL
AF Hogan, Meghan F.
Liu, Amy W.
Peters, Michael J.
Willard, Joshua R.
Rabbani, Zaheen
Bartholomew, Erik C.
Ottley, Adam
Hull, Rebecca L.
TI Markers of Islet Endothelial Dysfunction Occur in Male B6.BKS(D)-
Lepr(db)/J Mice and May Contribute to Reduced Insulin Release
SO ENDOCRINOLOGY
LA English
DT Article
ID GLYCATION END-PRODUCTS; PANCREATIC BETA-CELL; DIABETES-MELLITUS;
OXIDATIVE STRESS; BLOOD-VESSELS; DB/DB MICE; IN-VITRO; EXPRESSION;
MOUSE; RATS
AB Islet endothelial cells produce paracrine factors that support beta-cell function and growth. Endothelial dysfunction underlies diabetic microvascular complications; thus, we hypothesized that in diabetes, islet endothelial cells become dysfunctional, which may contribute to beta-cell secretory dysfunction. Islets/islet endothelial cells were isolated from diabetic B6.BKS(D)-Lepr(db)/J male (db/db) mice, treated with or without the glucose-lowering agent phlorizin, or from C57BL/6J mice fed a high-fat diet for 18 weeks and appropriate controls. Messenger RNA(mRNA) and/or the protein levels of the cell adhesion molecule E-selectin (Sele), proinflammatory cytokine interleukin-6 (II6), vasoconstrictor endothelin-1 (Edn1), and endothelial nitric oxide synthase (Nos3; Nos3) were evaluated, alongwith advanced glycation end product immunoreactivity. Furthermore, an islet endothelial cell line(MS-1) was exposed to diabetic factors (glucose, palmitate, insulin, and tumor necrosis factor-a) for six days. Conditioned media were collected from these cells, incubated with isolated islets, and glucose-stimulated insulin secretion and insulin content were assessed. Islet endothelial cells from db/db mice exhibited increased Sele, II6, and Edn1 mRNA levels, decreased Nos3 protein, and accumulation of advanced glycation end products. Phlorizin treatment significantly increased Nos3 protein levels but did not alter expression of the other markers. High-fat feeding in C57BL/6J mice resulted in increased islet Sele, II6, andEdn1 but no change in Nos3. Exposure of islets to conditionedmedia from MS-1 cells cultured in diabetic conditions resulted in a 50% decrease in glucose-stimulated insulin secretion and 30% decrease in insulin content. These findings demonstrate that, in diabetes, islet endothelial cells show evidence of a dysfunctional phenotype, which may contribute to loss of beta-cell function.
C1 [Hogan, Meghan F.; Liu, Amy W.; Peters, Michael J.; Willard, Joshua R.; Rabbani, Zaheen; Hull, Rebecca L.] Vet Affairs Puget Sound Hlth Care Syst, Div Metab Endocrinol & Nutr, Seattle, WA 98108 USA.
[Hogan, Meghan F.; Liu, Amy W.; Rabbani, Zaheen; Bartholomew, Erik C.; Ottley, Adam; Hull, Rebecca L.] Univ Washington, Dept Med, Seattle, WA 98195 USA.
RP Hull, RL (reprint author), Vet Affairs Puget Sound Hlth Care Syst 151, 1660 South Columbian Way, Seattle, WA 98108 USA.
EM rhull@uw.edu
FU Department of Veterans Affairs, Veterans Affairs Puget Sound Health Care
System; National Institutes of Health (University of Washington Diabetes
Research Center) [R01DK088082, P30DK017047]; University of Washington
Royalty Research; HHMI Medical Research Fellows Program; National
Institute of Diabetes and Digestive Kidney Diseases Medical Research
Program in Diabetes [T32 DK007247]; University of Washington Medical
Student Research Training Program; [T32HL007028]; [F32DK109584]
FX This work was supported by the Department of Veterans Affairs, Veterans
Affairs Puget Sound Health Care System (Seattle, WA), National
Institutes of Health grants R01DK088082 (R.L.H.) and P30 DK017047
(University of Washington Diabetes Research Center), and a University of
Washington Royalty Research Fund Award. A.W.L. was supported by the HHMI
Medical Research Fellows Program and the National Institute of Diabetes
and Digestive and Kidney Diseases Medical Research Program in Diabetes
through grant T32 DK007247. M.F.H. was supported by grants T32 HL007028
and F32 DK109584. Z.R., A.O., and E.C.B. were supported by the
University of Washington Medical Student Research Training Program and
the National Institute of Diabetes and Digestive and Kidney Diseases
Medical Research Program in Diabetes through T32 DK007247.
NR 41
TC 1
Z9 1
U1 0
U2 0
PU ENDOCRINE SOC
PI WASHINGTON
PA 2055 L ST NW, SUITE 600, WASHINGTON, DC 20036 USA
SN 0013-7227
EI 1945-7170
J9 ENDOCRINOLOGY
JI Endocrinology
PD FEB
PY 2017
VL 158
IS 2
BP 293
EP 303
DI 10.1210/en.2016-1393
PG 11
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EP0UH
UT WOS:000397101700012
PM 27870582
ER
PT J
AU Khodyakov, D
Stockdale, SE
Smith, N
Booth, M
Altman, L
Rubenstein, LV
AF Khodyakov, Dmitry
Stockdale, Susan E.
Smith, Nina
Booth, Marika
Altman, Lisa
Rubenstein, Lisa V.
TI Patient engagement in the process of planning and designing outpatient
care improvements at the Veterans Administration Health-care System:
findings from an online expert panel
SO HEALTH EXPECTATIONS
LA English
DT Article
DE ExpertLens; modified Delphi; online expert panel; patient engagement;
quality improvement; VA
ID QUALITY-IMPROVEMENT; PUBLIC INVOLVEMENT; DECISION-MAKING; SERVICES;
PARTICIPATION; STRATEGIES; FRAMEWORK; CANCER
AB Context There is a strong interest in the Veterans Administration (VA) Health-care System in promoting patient engagement to improve patient care.
Methods We solicited expert opinion using an online expert panel system with a modified Delphi structure called ExpertLens (TM). Experts reviewed, rated and discussed eight scenarios, representing four patient engagement roles in designing and improving VA outpatient care (consultant, implementation advisor, equal stakeholder and lead stakeholder) and two VA levels (local and regional). Rating criteria included desirability, feasibility, patient ability, physician/ staff acceptance and impact on patient-centredness and care quality. Data were analysed using the RAND/UCLA Appropriateness Method for determining consensus.
Findings Experts rated consulting with patients at the local level as the most desirable and feasible patient engagement approach. Engagement at the local level was considered more desirable than engagement at the regional level. Being an equal stakeholder at the local level received the highest ratings on the patient-centredness and health-care quality criteria.
Conclusions Our findings illustrate expert opinion about different approaches to patient engagement and highlight the benefits and challenges posed by each. Although experts rated local consultations with patients on an as-needed basis as most desirable and feasible, they rated being an equal stakeholder at the local level as having the highest potential impact on patient-centredness and care quality.
C1 [Khodyakov, Dmitry; Booth, Marika; Rubenstein, Lisa V.] RAND Corp, 1776 Main St, Santa Monica, CA 90401 USA.
[Stockdale, Susan E.; Rubenstein, Lisa V.] VA Greater Los Angeles Healthcare Syst 152, Ctr Study Healthcare Innovat Implementat & Policy, Med & Publ Hlth, VISN Vet Assessment & Improvement PACT Demonstrat, Los Angeles, CA USA.
[Smith, Nina] VA Greater Los Angeles Healthcare Syst 152, Ctr Implementat Practice & Res Support CIPRS, Los Angeles, CA USA.
[Rubenstein, Lisa V.] VA Greater Los Angeles Healthcare Syst 152, Ctr Implementat Practice & Res Support CIPRS, Med & Publ Hlth, Los Angeles, CA USA.
[Altman, Lisa] VA Greater Los Angeles Healthcare Syst GLA, Off Healthcare Transformat & Innovat, Healthcare Transformat, Los Angeles, CA USA.
[Stockdale, Susan E.] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90024 USA.
[Altman, Lisa] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
RP Khodyakov, D (reprint author), RAND Corp, 1776 Main St, Santa Monica, CA 90401 USA.
EM Dmitry_Khodyakov@rand.org
FU VA Office of Patient-Centered Care and Cultural Transformation; VA
Quality Enhancement and Research Initiative's (QUERI's) Center for
Implementation Practice and Research Support (CIPRS) [TRA 08-379]
FX This study is co-funded by the VA Office of Patient-Centered Care and
Cultural Transformation and the VA Quality Enhancement and Research
Initiative's (QUERI's) Center for Implementation Practice and Research
Support (CIPRS) grant number TRA 08-379.
NR 48
TC 1
Z9 1
U1 1
U2 1
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 1369-6513
EI 1369-7625
J9 HEALTH EXPECT
JI Health Expect.
PD FEB
PY 2017
VL 20
IS 1
BP 130
EP 145
DI 10.1111/hex.12444
PG 16
WC Health Care Sciences & Services; Health Policy & Services; Public,
Environmental & Occupational Health
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health
GA EP0PK
UT WOS:000397089000013
PM 26914249
ER
PT J
AU Su, F
Green, PK
Berry, K
Ioannou, GN
AF Su, Feng
Green, Pamela K.
Berry, Kristin
Ioannou, George N.
TI The Association Between Race/Ethnicity and the Effectiveness of Direct
Antiviral Agents for Hepatitis C Virus Infection
SO HEPATOLOGY
LA English
DT Article
ID GENOTYPE 1 INFECTION; SUSTAINED VIROLOGICAL RESPONSE; SIMEPREVIR PLUS
SOFOSBUVIR; HEPATOCELLULAR-CARCINOMA; CHRONIC HCV; PEGINTERFERON
ALPHA-2A; TREATMENT-NAIVE; BLACK PATIENTS; LIVER-DISEASE; US VETERANS
AB Black race and Hispanic ethnicity were associated with lower rates of sustained virologic response (SVR) to interferonbased treatments for chronic hepatitis C virus infection, whereas Asian race was associated with higher SVR rates compared to white patients. We aimed to describe the association between race/ ethnicity and effectiveness of new direct-acting antiviral regimens in the Veterans Affairs health care system nationally. We identified 21,095 hepatitis C virus-infected patients (11,029 [52%] white, 6,171 [29%] black, 1,187 [6%] Hispanic, 348 [2%] Asian/ Pacific Islander/ American Indian/ Alaska Native, and 2,360 [11%] declined/ missing race or ethnicity) who initiated antiviral treatment with regimens containing sofosbuvir, simeprevir + sofosbuvir, ledipasvir/ sofosbuvir, or paritaprevir/ ombitasvir/ ritonavir/ dasabuvir during the 18-month period from January 1, 2014, to June 30, 2015. Overall SVR rates were 89.8% (95% confidence interval [CI] 89.2-90.4) in white, 89.8% (95% CI 89.0-90.6) in black, 86.0% (95% CI 83.7-88.0) in Hispanic, and 90.7% (95% CI 87.0-93.5) in Asian/ Pacific Islander/ American Indian/ Alaska Native patients. However, after adjustment for baseline characteristics, black (adjusted odds ratio 5 0.77, P < 0.001) and Hispanic (adjusted odds ratio = 0.76, P = 0.007) patients were less likely to achieve SVR than white patients, a difference that was not explained by early treatment discontinuations. Among genotype 1-infected patients treated with ledipasvir/ sofosbuvir monotherapy, black patients had significantly lower SVR than white patients when treated for 8 weeks but not when treated for 12 weeks.
Conclusion: Direct-acting antivirals produce high SVR rates in white, black, Hispanic, and Asian/ Pacific Islander/ American Indian/ Alaska Native patients; but after adjusting for baseline characteristics, black race and Hispanic ethnicity remain independent predictors of treatment failure. Short 8-week ledipasvir/ sofosbuvir monotherapy regimens should perhaps be avoided in black patients with genotype 1 hepatitis C virus.
C1 [Ioannou, George N.] Vet Affairs Puget Sound Hlth Care Syst, Div Gastroenterol, S-111Gastro,1660 S Columbian Way, Seattle, WA 98108 USA.
RP Ioannou, GN (reprint author), Vet Affairs Puget Sound Hlth Care Syst, Div Gastroenterol, S-111Gastro,1660 S Columbian Way, Seattle, WA 98108 USA.
EM georgei@medicine.washington.edu
FU Clinical Science Research and Development, Office of Research and
Development, US Department of Veterans Affairs [I01CX000320,
I01CX001156]
FX Supported by Clinical Science Research and Development, Office of
Research and Development, US Department of Veterans Affairs (Merit
Review grants I01CX000320 and I01CX001156, to G. N. I.).
NR 48
TC 1
Z9 1
U1 0
U2 0
PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0270-9139
EI 1527-3350
J9 HEPATOLOGY
JI Hepatology
PD FEB
PY 2017
VL 65
IS 2
BP 426
EP 438
DI 10.1002/hep.28901
PG 13
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EP3RZ
UT WOS:000397300700007
PM 27775854
ER
PT J
AU Stelmack, JA
Tang, XC
Wei, Y
Wilcox, DT
Morand, T
Brahm, K
Sayers, S
Massof, RW
AF Stelmack, Joan A.
Tang, X. Charlene
Wei, Yongliang
Wilcox, Denise Thomas
Morand, Timothy
Brahm, Karen
Sayers, Scott
Massof, Robert W.
CA LOVIT II Study Grp
TI Outcomes of the Veterans Affairs Low Vision Intervention Trial II (LOVIT
II)
SO JAMA OPHTHALMOLOGY
LA English
DT Article
ID VISUAL FUNCTIONING QUESTIONNAIRE; OF-THE-LITERATURE; MACULAR
DEGENERATION; IMPAIRED VISION; REHABILITATION; HEALTH; DEPRESSION;
PEOPLE; PARTICIPATION; IMPAIRMENTS
C1 [Stelmack, Joan A.; Sayers, Scott] Edward Hines Jr Vet Affairs Hosp, Blind Rehabil Ctr, Mail Stop 124,5000 S Fifth Ave, Hines, IL 60141 USA.
[Stelmack, Joan A.; Sayers, Scott] Univ Illinois, Sch Med, Dept Ophthalmol & Visual Sci, Chicago, IL USA.
[Stelmack, Joan A.] Illinois Coll Optometry, Chicago, IL USA.
[Tang, X. Charlene; Wei, Yongliang] Edward Hines Jr Vet Affairs Hosp, Vet Affairs Cooperat Studies Program, Coordinating Ctr, Hines, IL USA.
[Wilcox, Denise Thomas] Philadelphia Vet Affairs Med Ctr, Surg Serv, Philadelphia, PA USA.
[Morand, Timothy] Dayton Vet Affairs Med Ctr, Rehabil Med Serv, Dayton, OH USA.
[Brahm, Karen] William S Middleton Mem Vet Adm Med Ctr, Surg Serv, Madison, WI USA.
[Massof, Robert W.] Johns Hopkins Univ, Sch Med, Wilmer Eye Inst, Baltimore, MD 21205 USA.
RP Stelmack, JA (reprint author), Edward Hines Jr Vet Affairs Hosp, Blind Rehabil Ctr, Mail Stop 124,5000 S Fifth Ave, Hines, IL 60141 USA.
EM joan.stelmack@va.gov
FU Department of Veterans Affairs (VA) Rehabilitation Research and
Development [C6958R]; Department of Veterans Affairs Prosthetics Service
FX Funding for this research was provided by Department of Veterans Affairs
(VA) Rehabilitation Research and Development grant C6958R. Funding for
the low-vision devices prescribed and dispensed to veteran participants
was provided by the Department of Veterans Affairs Prosthetics Service.
NR 47
TC 0
Z9 0
U1 1
U2 1
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6165
EI 2168-6173
J9 JAMA OPHTHALMOL
JI JAMA Ophthalmol.
PD FEB 1
PY 2017
VL 135
IS 2
BP 96
EP 104
DI 10.1001/jamaophthalmol.2016.4742
PG 9
WC Ophthalmology
SC Ophthalmology
GA EM9PE
UT WOS:000395642800009
ER
PT J
AU Dawes, AJ
Dawes, DM
Maggard-Gibbons, M
AF Dawes, Aaron J.
Dawes, Danielle M.
Maggard-Gibbons, Melinda
TI Corrected vs Uncorrected Obesity in Childbearing Women-What Really
Drives Fetal Risks
SO JAMA SURGERY
LA English
DT Editorial Material
C1 [Dawes, Aaron J.; Maggard-Gibbons, Melinda] Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, 757 Westwood Plaza,Room B711, Los Angeles, CA 90095 USA.
[Dawes, Danielle M.] Magella Med Grp Inc, Maternal Fetal Med Practice, Long Beach, CA USA.
[Maggard-Gibbons, Melinda] Vet Affairs Greater Los Angeles Healthcare Syst, Los Angeles, CA USA.
RP Dawes, AJ (reprint author), Univ Calif Los Angeles, David Geffen Sch Med, Dept Surg, 757 Westwood Plaza,Room B711, Los Angeles, CA 90095 USA.
EM adawes@mednet.ucla.edu
NR 5
TC 0
Z9 0
U1 0
U2 0
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6254
EI 2168-6262
J9 JAMA SURG
JI JAMA Surg.
PD FEB
PY 2017
VL 152
IS 2
BP 135
EP 135
DI 10.1001/jamasurg.2016.3597
PG 1
WC Surgery
SC Surgery
GA EM9HZ
UT WOS:000395623800007
PM 27760247
ER
PT J
AU Hall, DE
Arya, S
Schmid, KK
Blaser, C
Carlson, MA
Bailey, TL
Purviance, G
Bockman, T
Lynch, TG
Johanning, J
AF Hall, Daniel E.
Arya, Shipra
Schmid, Kendra K.
Blaser, Casey
Carlson, Mark A.
Bailey, Travis L.
Purviance, Georgia
Bockman, Tammy
Lynch, Thomas G.
Johanning, Jason
TI Development and Initial Validation of the Risk Analysis Index for
Measuring Frailty in Surgical Populations
SO JAMA SURGERY
LA English
DT Article
ID MORTALITY; MORBIDITY; SURGERY; SPECIALTIES; DISABILITY; PREDICTOR;
OUTCOMES; HEALTH; CARE
AB IMPORTANCE Growing consensus suggests that frailty-associated risks should inform shared surgical decision making. However, it is not clear how best to screen for frailty in preoperative surgical populations.
OBJECTIVE To develop and validate the Risk Analysis Index (RAI), a 14-item instrument used to measure surgical frailty. It can be calculated prospectively (RAI-C), using a clinical questionnaire, or retrospectively (RAI-A), using variables from the surgical quality improvement databases (Veterans Affairs or American College of Surgeons National Surgical Quality Improvement Projects).
DESIGN, SETTING, AND PARTICIPANTS Single-site, prospective cohort from July 2011 to September 2015 at the Veterans Affairs Nebraska-Western Iowa Heath Care System, a Level 1b Veterans Affairs Medical Center. The study included all patients presenting to the medical center for elective surgery.
EXPOSURES We assessed the RAI-C for all patients scheduled for surgery, linking these scores to administrative and quality improvement data to calculate the RAI-A and the modified Frailty Index.
MAIN OUTCOMES AND MEASURES Receiver operator characteristics and C statistics for each measure predicting postoperative mortality and morbidity.
RESULTS Of the participants, the mean (SD) age was 60.7 (13.9) years and 249 participants (3.6%) were women. We assessed the RAI-C 10 698 times, from which we linked 6856 unique patients to mortality data. The C statistic predicting 180-day mortality for the RAI-C was 0.772. Of these 6856 unique patients, we linked 2785 to local Veterans Affairs Surgeons National Surgical Quality Improvement Projects data and calculated the C statistic for both the RAI-A (0.823) and RAI-C (0.824), along with the correlation between the 2 scores (r = 0.478; P < .001). Of these 2785 patients, there were sufficient data to calculate the modified Frailty Index for 1021, in which the C statistics were 0.865 (RAI-A), 0.797 (RAI-C), and 0.811 (modified Frailty Index). The correlation between the RAI-A and RAI-C was 0.547, and the correlations of the modified Frailty Index to the RAI-A and RAI-C were 0.301 and 0.269, respectively (all P < .001). A cutoff of RAI-C of at least 21 classified 18.3% patients as "frail" with a sensitivity of 0.50 and specificity of 0.82, whereas the RAI-A was less sensitive (0.25) and more specific (0.97), classifying only 3.7% as "frail."
CONCLUSIONS AND RELEVANCE The RAI-C and RAI-A represent effective tools for measuring frailty in surgical populations with predictive ability on par with other frailty tools. Moderate correlation between the measures suggests convergent validity. The RAI-C offers the advantage of prospective, preoperative assessment that is proved feasible for large-scale screening in clinical practice. However, further efforts should be directed at determining the optimal components of preoperative frailty assessment.
C1 [Hall, Daniel E.] Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
[Hall, Daniel E.] Univ Pittsburgh, Pittsburgh, PA USA.
[Arya, Shipra] Atlanta Vet Affairs Med Ctr, Atlanta, GA USA.
[Arya, Shipra] Emory Univ, Atlanta, GA 30322 USA.
[Schmid, Kendra K.; Blaser, Casey; Carlson, Mark A.; Johanning, Jason] Univ Nebraska Med Ctr, Omaha, NE USA.
[Carlson, Mark A.; Bailey, Travis L.; Purviance, Georgia; Bockman, Tammy; Johanning, Jason] Vet Affairs Nebraska Western Iowa Hlth Care Syst, Omaha, NE USA.
[Bailey, Travis L.] Univ Utah, Sch Med, Salt Lake City, UT USA.
[Lynch, Thomas G.] Vet Affairs Cent Off, Washington, DC USA.
RP Hall, DE (reprint author), UPMC Presbyterian, 200 Lothrop St,Ste 1264, Pittsburgh, PA 15213 USA.
EM hallde@upmc.edu
FU US Department of Veterans Affairs, Veterans Health Administration,
Office of Research and Development, Health Services Research and
Development [CDA 08-281]
FX This research was supported by the US Department of Veterans Affairs,
Veterans Health Administration, Office of Research and Development,
Health Services Research and Development (CDA 08-281; Dr Hall).
NR 24
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U2 1
PU AMER MEDICAL ASSOC
PI CHICAGO
PA 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA
SN 2168-6254
EI 2168-6262
J9 JAMA SURG
JI JAMA Surg.
PD FEB
PY 2017
VL 152
IS 2
BP 175
EP 182
DI 10.1001/jamasurg.2016.4202
PG 8
WC Surgery
SC Surgery
GA EM9HZ
UT WOS:000395623800017
PM 27893030
ER
PT J
AU McFarland, EJ
Powell, TM
Onyango-Makumbi, C
Zhang, WM
Melander, K
Naluyima, P
Okurut, S
Eller, MA
Fowler, MG
Janoff, EN
AF McFarland, Elizabeth J.
Powell, Tina M.
Onyango-Makumbi, Carolyne
Zhang, Weiming
Melander, Kelsey
Naluyima, Prossy
Okurut, Samuel
Eller, Michael A.
Fowler, Mary Glenn
Janoff, Edward N.
TI Ontogeny of CD4(+) T Lymphocytes With Phenotypic Susceptibility to HIV-1
During Exclusive and Nonexclusive Breastfeeding in HIV-1-Exposed Ugandan
Infants
SO JOURNAL OF INFECTIOUS DISEASES
LA English
DT Article
DE HIV-1; breastfeeding; postnatal transmission; CD4+T lymphocytes;
lymphocyte activation; T cell homing; CCR5; alpha 4 beta 7.
ID ACUTE CYTOMEGALOVIRUS-INFECTION; UNINFECTED CHILDREN BORN; INTEGRIN
ALPHA(4)BETA(7); IMMUNODEFICIENCY-VIRUS; TRANSMISSION; CELLS; MOTHER;
EXPRESSION; MUCOSAL; GUT
AB Background. Among infants exposed to human immunodeficiency virus (HIV) type 1, mixed breastfeeding is associated with higher postnatal HIV-1 transmission than exclusive breastfeeding, but the mechanisms of this differential risk are uncertain.
Methods. HIV-1-exposed Ugandan infants were prospectively assessed during the first year of life for feeding practices and T-cell maturation, intestinal homing (beta 7(hi)), activation, and HIV-1 coreceptor (CCR5) expression in peripheral blood. Infants receiving only breast milk and those with introduction of other foods before 6 months were categorized as exclusive and nonexclusive, respectively.
Results. Among CD4(+) and CD8(+) T cells, the expression of memory, activation, and CCR5 markers increased rapidly from birth to week 2, peaking at week 6, whereas cells expressing the intestinal homing marker increased steadily in the central memory ( CM) and effector memory T cells over 48 weeks. At 24 weeks, when feeding practices had diverged, nonexclusively breastfed infants showed increased frequencies and absolute counts of beta 7(hi) CM CD4+ and CD8+ T cells, including the HIV-1-targeted cells with CD4(+)beta 7(hi)/CCR5(+) coexpression, as well as increased activation.
Conclusions. The T-cell phenotype associated with susceptibility to HIV-1 infection (CCR5(+), gut-homing, CM CD4+ T cells) was preferentially expressed in nonexclusively breastfed infants, a group of infants at increased risk for HIV-1 acquisition.
C1 [McFarland, Elizabeth J.; Powell, Tina M.] Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Dept Pediat, Aurora, CO USA.
[Melander, Kelsey; Janoff, Edward N.] Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Dept Med, Aurora, CO USA.
[Zhang, Weiming] Univ Colorado Anschutz Med Campus, Colorado Sch Publ Hlth, Dept Biostat & Informat, Aurora, CO USA.
[McFarland, Elizabeth J.; Janoff, Edward N.] Univ Colorado Anschutz Med Campus, Mucosal & Vaccine Res Program Colorado Infect Dis, Aurora, CO USA.
[Janoff, Edward N.] Denver Vet Affairs Med Ctr, Denver, CO USA.
[Eller, Michael A.] Walter Reed Army Inst Res, US Mil HIV Res Program, Silver Spring, MD USA.
[Eller, Michael A.] Henry M Jackson Fdn Adv Mil Med, Bethesda, MD USA.
[Fowler, Mary Glenn] Johns Hopkins Univ, Sch Med, Baltimore, MD USA.
[Onyango-Makumbi, Carolyne; Fowler, Mary Glenn] Makerere Univ, Johns Hopkins Univ Res Collaborat, Kampala, Uganda.
[Naluyima, Prossy; Okurut, Samuel] Makerere Univ Walter Reed Project, Kampala, Uganda.
RP McFarland, EJ (reprint author), Univ Colorado, Childrens Hosp Colorado, Div Pediat Infect Dis, Anschutz Med Campus,13123 E 16th Ave, Aurora, CO 80045 USA.
EM betsy.mcfarland@ucdenver.edu
NR 49
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U2 0
PU OXFORD UNIV PRESS INC
PI CARY
PA JOURNALS DEPT, 2001 EVANS RD, CARY, NC 27513 USA
SN 0022-1899
EI 1537-6613
J9 J INFECT DIS
JI J. Infect. Dis.
PD FEB 1
PY 2017
VL 215
IS 3
BP 368
EP 377
DI 10.1093/infdis/jiw553
PG 10
WC Immunology; Infectious Diseases; Microbiology
SC Immunology; Infectious Diseases; Microbiology
GA EP2HT
UT WOS:000397204700006
PM 27932619
ER
PT J
AU Pardeshi, NN
Qi, W
Dahl, K
Caplan, L
Carpenter, JF
AF Pardeshi, Neha N.
Qi, Wei
Dahl, Kevin
Caplan, Liron
Carpenter, John F.
TI Microparticles and Nanoparticles Delivered in Intravenous Saline and in
an Intravenous Solution of a Therapeutic Antibody Product
SO JOURNAL OF PHARMACEUTICAL SCIENCES
LA English
DT Article
DE protein aggregation; microparticles; nanoparticles; IgG antibody;
protein delivery; adsorption; particle size
ID POLYVINYL-CHLORIDE BAGS; MONOCLONAL-ANTIBODY; PROTEIN AGGREGATION;
GROWTH-HORMONE; FACTOR-VIII; PARTICLES; STABILITY; INFUSION; MICE;
IMMUNOGENICITY
AB Intravenous ( IV) infusion is used for administration of a large proportion of biologic therapeutics, including most monoclonal antibody products. In this study, we determined the subvisible particle levels in IV solutions and after the solutions were processed with an IV administration setup that mimicked the typical clinical method of administration. IV saline in bags manufactured by both Hospira and Baxter contained 1600-8000 microparticles/mL and 4-73 x 10(6) nanoparticles/mL in solution. When IV immunoglobulin was diluted into the IV saline, 3700-23,000 microparticles/mL and 18-240 x 10(6) nanoparticles/mL were detected. During processing of the solution through the IV system, in-line filters removed most microparticles. However, there were still 1-21 x 10(6) nanoparticles/mL in IV saline and 7-83 x 10(6) nanoparticles/mL in IV immunoglobulin diluted in saline. Finally, in samples processed through in-line filters, we found relatively large microparticles ( 20-60 mm) that were composed of protein or polycarbonate. These particles resulted from shedding of polycarbonate and sloughing off of protein films downstream from the filter membrane. Overall, the results document that even with in-line filters in place, high levels of subvisible particles are delivered to patients and there is a need for improved, more effective filters and IV solutions with lower particle levels. (C) 2017 American Pharmacists Association (R). Published by Elsevier Inc. All rights reserved.
C1 [Pardeshi, Neha N.; Carpenter, John F.] Univ Colorado, Sch Pharm, Dept Pharmaceut Sci, Anschutz Med Campus, Aurora, CO 80045 USA.
[Qi, Wei; Dahl, Kevin] Malvern Instruments, Columbia, MD 21046 USA.
[Caplan, Liron] Univ Colorado, Denver Vet Affairs Hosp, Rheumatol Sect, Aurora, CO 80045 USA.
[Caplan, Liron] Univ Colorado, Sch Med, Aurora, CO 80045 USA.
RP Carpenter, JF (reprint author), Univ Colorado, Sch Pharm, Dept Pharmaceut Sci, Anschutz Med Campus, Aurora, CO 80045 USA.
EM john.carpenter@ucdenver.edu
FU NIH [5RO1 EB006006]
FX The authors would like to thank Beth Moran, RN, and Mary Cousins, RN,
for expert advice about the clinical practices for preparation and IV
infusion of therapeutic proteins and for their help in replicating the
IV infusion system in the laboratory. We gratefully acknowledge support
from NIH Grant 5RO1 EB006006.
NR 30
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PU WILEY
PI HOBOKEN
PA 111 RIVER ST, HOBOKEN 07030-5774, NJ USA
SN 0022-3549
EI 1520-6017
J9 J PHARM SCI-US
JI J. Pharm. Sci.
PD FEB
PY 2017
VL 106
IS 2
BP 511
EP 520
DI 10.1016/j.xphs.2016.09.028
PG 10
WC Chemistry, Medicinal; Chemistry, Multidisciplinary; Pharmacology &
Pharmacy
SC Pharmacology & Pharmacy; Chemistry
GA EP3KE
UT WOS:000397280400008
PM 27832839
ER
PT J
AU Murillo, R
Lambiase, MJ
Rockette-Wagner, BJ
Kriska, AM
Halbach, JP
Thurston, RC
AF Murillo, Rosenda
Lambiase, Maya J.
Rockette-Wagner, Bonny J.
Kriska, Andrea M.
Halbach, Jeffrey P.
Thurston, Rebecca C.
TI Racial/Ethnic Differences in the Associations Between Physical Activity
and Sleep Duration: A Population-Based Study
SO JOURNAL OF PHYSICAL ACTIVITY & HEALTH
LA English
DT Article
DE health disparities; exercise; epidemiology
ID HEALTH DISPARITIES; MIDLIFE WOMEN; LEISURE-TIME; WORK; METAANALYSIS;
EXERCISE
AB Background: This study examined associations between physical activity (recreational, nonrecreational) and sleep duration among a nationally representative diverse sample of U.S. adults. Methods: We used cross-sectional data from 9,205 National Health and Nutrition Examination Survey 2007 to 2012 participants aged 20 to 65 years who identified as White, Black, or Hispanic. Activity (ie, recreation, occupation, and transportation activity) was categorized into quartiles. Sleep duration was categorized as short (56 hours/night) or normal (>6 to 59 hours/night). Logistic regression was used to estimate associations of activity with sleep duration. Results: Recommended levels of recreation activity and moderate levels of transportation activity were associated with normal sleep duration [Odds Ratio (OR): = 1.33, 95% Confidence Interval (CI) = 1.08, 1.65; OR = 1.28, 95% CI = 1.02, 1.62, respectively]. High occupation physical activity was associated with shorter sleep duration (OR = 0.59, 95% CI = 0:49, 0.71). Differences were observed by race/ethnicity in associations of recreation and occupation activity with sleep duration. Conclusions: White individuals who engaged in some recreation activity, relative to being inactive, had more favorable sleep duration; whereas, high levels of occupation activity were associated with worse sleep duration among White and Black individuals. Physical activity was not associated with sleep duration among Hispanics.
C1 [Murillo, Rosenda] Univ Houston, Dept Psychol Hlth & Learning Sci, Houston, TX 77004 USA.
[Lambiase, Maya J.] VA Pittsburgh Healthcare Syst, Dept Vet Affairs, Pittsburgh, PA USA.
[Rockette-Wagner, Bonny J.; Kriska, Andrea M.] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA 15260 USA.
[Halbach, Jeffrey P.] US Dept Vet Affairs, Hlth Serv Res & Dev, Washington, DC USA.
[Thurston, Rebecca C.] Univ Pittsburgh, Dept Psychiat, Pittsburgh, PA USA.
RP Murillo, R (reprint author), Univ Houston, Dept Psychol Hlth & Learning Sci, Houston, TX 77004 USA.
EM rmurillo3@uh.edu
FU Department of Veterans Affairs Advanced Fellowship in Women's Health, VA
Pittsburgh Healthcare System
FX This work was supported by resources and funding from the Department of
Veterans Affairs Advanced Fellowship in Women's Health, VA Pittsburgh
Healthcare System. The contents do not represent the views of the
Department of Veterans Affairs, Department of Defense, or the United
States Government.
NR 36
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U2 2
PU HUMAN KINETICS PUBL INC
PI CHAMPAIGN
PA 1607 N MARKET ST, PO BOX 5076, CHAMPAIGN, IL 61820-2200 USA
SN 1543-3080
EI 1543-5474
J9 J PHYS ACT HEALTH
JI J. Phys. Act. Health
PD FEB
PY 2017
VL 14
IS 2
BP 138
EP 144
DI 10.1123/jpah.2015-0638
PG 7
WC Public, Environmental & Occupational Health
SC Public, Environmental & Occupational Health
GA EO8UB
UT WOS:000396964900009
PM 27918684
ER
PT J
AU Roshanravan, B
Patel, KV
Fried, LF
Robinson-Cohen, C
de Boer, IH
Harris, T
Murphy, RA
Satterfield, S
Goodpaster, BH
Shlipak, M
Newman, AB
Kestenbaum, B
AF Roshanravan, Baback
Patel, Kushang V.
Fried, Linda F.
Robinson-Cohen, Cassianne
de Boer, Ian H.
Harris, Tamara
Murphy, Rachel A.
Satterfield, Suzanne
Goodpaster, Bret H.
Shlipak, Michael
Newman, Anne B.
Kestenbaum, Bryan
CA Hlth ABC Study
TI Association of Muscle Endurance, Fatigability, and Strength With
Functional Limitation and Mortality in the Health Aging and Body
Composition Study
SO JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL
SCIENCES
LA English
DT Article
DE Mobility; Muscle; Fatigue; Strength; Sarcopenia
ID CHRONIC KIDNEY-DISEASE; OLDER-ADULTS; WALKING SPEED; MOBILITY
DISABILITY; CYSTATIN C; GAIT SPEED; FRAILTY; PREVALENCE; CREATININE;
INCHIANTI
AB Background: Mobility limitation is highly prevalent among older adults and is central to the loss of functional independence. Dynamic isokinetic muscle fatigue testing may reveal increased vulnerability to disability and mortality beyond strength testing.
Methods: We studied community-dwelling older adults enrolled in the Health Aging and Body Composition study (age range: 71-82) free of mobility disability and who underwent isokinetic muscle fatigue testing in 1999-2000 (n = 1,963). Isokinetic quadriceps work and fatigue index was determined over 30 repetitions and compared with isometric quadriceps maximum torque. Work was normalized to leg lean mass accounting for gender-specific differences (specific work). The primary outcome was incident persistent severe lower extremity limitation (PSLL), defined as two consecutive reports of either having a lot of difficulty or being unable to walk 1/4 mile or climb 10 steps without resting. The secondary outcome was all-cause mortality.
Results: There were 608 (31%) occurrences of incident PSLL and 488 (25%) deaths during median follow-up of 9.3 years. After adjustment, lower isokinetic work was associated with significantly greater risks of PSLL and mortality across the full measured range. Hazard ratios per standard deviation lower specific isokinetic work were 1.22 (95% CI 1.12, 1.33) for PSLL and 1.21 (95% CI 1.13, 1.30) for mortality, respectively. Lower isometric strength was associated with PSLL, but not mortality. Fatigue index was not associated with PSLL or mortality.
Conclusions: Muscle endurance, estimated by isokinetic work, is an indicator of muscle health associated with mobility limitation and mortality providing important insight beyond strength testing.
C1 [Roshanravan, Baback; Robinson-Cohen, Cassianne; de Boer, Ian H.; Kestenbaum, Bryan] Univ Washington, Dept Med, Div Nephrol, Kidney Res Inst, 325 9th Ave,Room 3NJ350,Box 359606, Seattle, WA 98104 USA.
[Patel, Kushang V.] Univ Washington, Dept Anesthesiol & Pain Med, Seattle, WA 98195 USA.
[Fried, Linda F.] Univ Pittsburgh, Sch Med, Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA 15260 USA.
[Harris, Tamara] NIA, Lab Epidemiol & Populat Sci, Bethesda, MD 20892 USA.
[Murphy, Rachel A.] Univ British Columbia, Sch Populat & Publ Hlth, Vancouver, BC, Canada.
[Satterfield, Suzanne] Univ Tennessee, Ctr Hlth Sci, Dept Prevent Med, Memphis, TN 38163 USA.
[Goodpaster, Bret H.] Florida Hosp, Orlando, FL USA.
[Goodpaster, Bret H.] Sanford Burnham Presbys Translat Res Inst Metab &, Orlando, FL USA.
[Shlipak, Michael] San Francisco VA Med Ctr, Gen Internal Med Sect, San Francisco, CA USA.
[Newman, Anne B.] Univ Pittsburgh, Sch Med, Dept Epidemiol, Pittsburgh, PA 15260 USA.
RP Roshanravan, B (reprint author), Univ Washington, Dept Med, Div Nephrol, Kidney Res Inst, 325 9th Ave,Room 3NJ350,Box 359606, Seattle, WA 98104 USA.
EM broshanr@uw.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases
[K23-DK099442]; National Institute on Aging (NIA) [N01-AG-6-2101,
N01-AG-6-2103, N01-AG-6-2106]; NIA [R01-AG028050]; NINR [R01-NR012459];
NIH, National Institute on Aging; Northwest Kidney Centers
FX This research was supported by the National Institute of Diabetes and
Digestive and Kidney Diseases (K23-DK099442 to B.R.); National Institute
on Aging (NIA) Contracts N01-AG-6-2101, N01-AG-6-2103, and
N01-AG-6-2106; NIA grant R01-AG028050; and NINR grant R01-NR012459. This
research was supported in part by the Intramural Research Program of the
NIH, National Institute on Aging. This work was also supported by an
unrestricted fund from the Northwest Kidney Centers (B.R.).
NR 30
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PU OXFORD UNIV PRESS INC
PI CARY
PA JOURNALS DEPT, 2001 EVANS RD, CARY, NC 27513 USA
SN 1079-5006
EI 1758-535X
J9 J GERONTOL A-BIOL
JI J. Gerontol. Ser. A-Biol. Sci. Med. Sci.
PD FEB
PY 2017
VL 72
IS 2
BP 284
EP 291
DI 10.1093/gerona/glw210
PG 8
WC Geriatrics & Gerontology; Gerontology
SC Geriatrics & Gerontology
GA EP2EC
UT WOS:000397194800019
PM 27907890
ER
PT J
AU Sigel, K
Wisnivesky, J
Crothers, K
Gordon, K
Brown, ST
Rimland, D
Rodriguez-Barradas, MC
Gibert, C
Goetz, MB
Bedimo, R
Park, LS
Dubrow, R
AF Sigel, Keith
Wisnivesky, Juan
Crothers, Kristina
Gordon, Kirsha
Brown, Sheldon T.
Rimland, David
Rodriguez-Barradas, Maria C.
Gibert, Cynthia
Goetz, Matthew Bidwell
Bedimo, Roger
Park, Lesley S.
Dubrow, Robert
TI Immunological and infectious risk factors for lung cancer in US veterans
with HIV: a longitudinal cohort study
SO LANCET HIV
LA English
DT Article
ID CIGARETTE-SMOKING; UNITED-STATES; ANTIRETROVIRAL THERAPY; CD4/CD8 RATIO;
AIDS; INDIVIDUALS; IMMUNODEFICIENCY; DISEASE; PEOPLE; PROGRESSION
AB Background HIV infection is independently associated with risk of lung cancer, but few data exist for the relation between longitudinal measurements of immune function and lung-cancer risk in people living with HIV.
Methods We followed up participants with HIV from the Veterans Aging Cohort Study for a minimum of 3 years between Jan 1, 1998, and Dec 31, 2012, and used cancer registry data to identify incident cases of lung cancer. The index date for each patient was the later of the date HIV care began or Jan 1, 1998. We excluded patients with less than 3 years' follow-up, prevalent diagnoses of lung cancer, or incomplete laboratory data. We used Cox regression models to investigate the relation between different time-updated lagged and cumulative exposures (CD4 cell count, CD8 cell count, CD4/CD8 ratio, HIV RNA, and bacterial pneumonia) and risk of lung cancer. Models were adjusted for age, race or ethnicity, smoking, hepatitis C virus infection, alcohol use disorders, drug use disorders, and history of chronic obstructive pulmonary disease and occupational lung disease.
Findings We identified 277 cases of incident lung cancer in 21 666 participants with HIV. In separate models for each time-updated 12 month lagged, 24 month simple moving average cumulative exposure, increased risk of lung cancer was associated with low CD4 cell count (p trend= 0.001), low CD4/CD8 ratio (p trend= 0.0001), high HIV RNA concentration (p=0.004), and more cumulative bacterial pneumonia episodes (12 month lag only; p trend= 0.0004). In a mutually adjusted model including these factors, CD4/CD8 ratio and cumulative bacterial pneumonia episodes remained significant (p trends 0.003 and 0.004, respectively).
Interpretation In our large HIV cohort in the antiretroviral therapy era, we found evidence that dysfunctional immune activation and chronic inflammation contribute to the development of lung cancer in the setting of HIV infection. These findings could be used to target lung-cancer prevention measures to high-risk groups.
C1 [Sigel, Keith; Wisnivesky, Juan; Brown, Sheldon T.] Icahn Sch Med Mt Sinai, Dept Med, 17 East 102nd St, New York, NY 10029 USA.
[Crothers, Kristina] Univ Washington, Sch Med, Dept Med, Seattle, WA 98195 USA.
[Gordon, Kirsha] VA Connecticut Healthcare Syst, Dept Med, New Haven, CT USA.
[Gordon, Kirsha] Yale Sch Med & Publ Hlth, New Haven, CT USA.
[Brown, Sheldon T.] James J Peters VA Med Ctr, Infect Dis Sect, Bronx, NY USA.
[Rimland, David] Atlanta VA Med Ctr, Infect Dis Sect, Decatur, GA USA.
[Rimland, David] Emory Univ, Sch Med, Decatur, GA 30033 USA.
[Rodriguez-Barradas, Maria C.] Michael E DeBakey VA Med Ctr, Infect Dis Sect, Houston, TX USA.
[Rodriguez-Barradas, Maria C.] Baylor Coll Med, Houston, TX 77030 USA.
[Gibert, Cynthia] George Washington Univ, Sch Med, Dept Med, Washington, DC USA.
[Gibert, Cynthia] Washington DC Vet Affairs Med Ctr, Washington, DC USA.
[Goetz, Matthew Bidwell] VA Los Greater Angeles Healthcare Syst, Dept Med, Los Angeles, CA USA.
[Goetz, Matthew Bidwell] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
[Bedimo, Roger] VA North Texas Hlth Care Syst, Div Infect Dis, Dallas, TX USA.
[Park, Lesley S.] Stanford Univ, Sch Med, Ctr Populat Hlth Sci, Palo Alto, CA 94304 USA.
[Dubrow, Robert] Yale Sch Publ Hlth, Dept Chron Dis Epidemiol, New Haven, CT USA.
RP Sigel, K (reprint author), Icahn Sch Med Mt Sinai, Dept Med, 17 East 102nd St, New York, NY 10029 USA.
EM keith.sigel@mssm.edu
OI Sigel, Keith/0000-0002-4051-4861
FU US National Institutes of Health
FX US National Institutes of Health.
NR 30
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U1 1
U2 1
PU ELSEVIER INC
PI SAN DIEGO
PA 525 B STREET, STE 1900, SAN DIEGO, CA 92101-4495 USA
SN 2352-3018
J9 LANCET HIV
JI Lancet HIV
PD FEB
PY 2017
VL 4
IS 2
BP E67
EP E73
DI 10.1016/S2352-3018(16)30215-6
PG 7
WC Immunology; Infectious Diseases
SC Immunology; Infectious Diseases
GA EP3EV
UT WOS:000397266500008
PM 27916584
ER
PT J
AU Ray, SK
Samantaray, S
Banik, NL
AF Ray, Swapan K.
Samantaray, Supriti
Banik, Naren L.
TI Future directions for using estrogen receptor agonists in the treatment
of acute and chronic spinal cord injury (vol 11, pg 1418, 2016)
SO NEURAL REGENERATION RESEARCH
LA English
DT Correction
C1 [Ray, Swapan K.] Univ South Carolina, Dept Pathol Microbiol & Immunol, Sch Med, Columbia, SC 29208 USA.
[Samantaray, Supriti] Med Univ South Carolina, Dept Neurosci, Columbia, SC USA.
[Banik, Naren L.] Med Univ South Carolina, Dept Neurol & Neurosurg, Charleston, SC USA.
[Banik, Naren L.] Ralph H Johnson Vet Adm Med Ctr, Charleston, SC USA.
RP Ray, SK (reprint author), Univ South Carolina, Dept Pathol Microbiol & Immunol, Sch Med, Columbia, SC 29208 USA.
EM swapan.ray@uscmed.sc.edu
NR 1
TC 0
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U1 0
U2 0
PU MEDKNOW PUBLICATIONS & MEDIA PVT LTD
PI MUMBAI
PA B-9, KANARA BUSINESS CENTRE, OFF LINK RD, GHAKTOPAR-E, MUMBAI, 400075,
INDIA
SN 1673-5374
EI 1876-7958
J9 NEURAL REGEN RES
JI Neural Regen. Res.
PD FEB
PY 2017
VL 12
IS 2
BP 266
EP 266
DI 10.4103/1673-5374.200818
PG 1
WC Cell Biology; Neurosciences
SC Cell Biology; Neurosciences & Neurology
GA EO9QN
UT WOS:000397023300021
PM 28400809
ER
PT J
AU Zhang, PP
Bookstaver, ML
Jewell, CM
AF Zhang, Peipei
Bookstaver, Michelle L.
Jewell, Christopher M.
TI Engineering Cell Surfaces with Polyelectrolyte Materials for
Translational Applications
SO POLYMERS
LA English
DT Review
DE polyelectrolyte; multilayer; cell modification; sensing and signaling;
drug delivery; vaccine and immunotherapy; surface protein; tissue
engineering; regenerative medicine
ID LYMPH-NODE MICROENVIRONMENT; STEM-CELLS; GENE-THERAPY; DRUG-DELIVERY;
LIVING CELLS; BIOMEDICAL APPLICATIONS; ISLET TRANSPLANTATION; MEDIATED
DELIVERY; INDIVIDUAL CELLS; CLINICAL-TRIALS
AB Engineering cell surfaces with natural or synthetic materials is a unique and powerful strategy for biomedical applications. Cells exhibit more sophisticated migration, control, and functional capabilities compared to nanoparticles, scaffolds, viruses, and other engineered materials or agents commonly used in the biomedical field. Over the past decade, modification of cell surfaces with natural or synthetic materials has been studied to exploit this complexity for both fundamental and translational goals. In this review we present the existing biomedical technologies for engineering cell surfaces with one important class of materials, polyelectrolytes. We begin by introducing the challenges facing the cell surface engineering field. We then discuss the features of polyelectrolytes and how these properties can be harnessed to solve challenges in cell therapy, tissue engineering, cell-based drug delivery, sensing and tracking, and immune modulation. Throughout the review, we highlight opportunities to drive the field forward by bridging new knowledge of polyelectrolytes with existing translational challenges.
C1 [Zhang, Peipei; Bookstaver, Michelle L.; Jewell, Christopher M.] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA.
[Jewell, Christopher M.] Univ Maryland, Sch Med, Dept Microbiol & Immunol, Baltimore, MD 21201 USA.
[Jewell, Christopher M.] Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA.
[Jewell, Christopher M.] US Dept Vet Affairs, Baltimore, MA 21201 USA.
RP Jewell, CM (reprint author), Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA.; Jewell, CM (reprint author), Univ Maryland, Sch Med, Dept Microbiol & Immunol, Baltimore, MD 21201 USA.; Jewell, CM (reprint author), Marlene & Stewart Greenebaum Canc Ctr, Baltimore, MD 21201 USA.; Jewell, CM (reprint author), US Dept Vet Affairs, Baltimore, MA 21201 USA.
EM pzhang14@umd.edu; mlbooks@umd.edu; cmjewell@umd.edu
OI Jewell, Christopher/0000-0002-6668-6928
FU NSF CAREER Award [1351688]; Damon Runyon Foundation [DRR3415]; Young
Investigator of the Alliance for Cancer Gene Therapy [15051543];
Melanoma Research Alliance [348963]
FX This work was supported in part by NSF CAREER Award # 1351688.
Christopher M. Jewell is a Damon Runyon-Rachleff Innovator supported by
the Damon Runyon Foundation (# DRR3415), and a Young Investigator of the
Alliance for Cancer Gene Therapy (# 15051543) and the Melanoma Research
Alliance (# 348963).
NR 115
TC 0
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U1 2
U2 2
PU MDPI AG
PI BASEL
PA ST ALBAN-ANLAGE 66, CH-4052 BASEL, SWITZERLAND
SN 2073-4360
J9 POLYMERS-BASEL
JI Polymers
PD FEB
PY 2017
VL 9
IS 2
AR 40
DI 10.3390/polym9020040
PG 21
WC Polymer Science
SC Polymer Science
GA EP2RL
UT WOS:000397230800010
ER
PT J
AU Nelson, K
Taylor, L
Silverman, J
Kiefer, M
Hebert, P
Lessler, D
Krieger, J
AF Nelson, Karin
Taylor, Leslie
Silverman, Julie
Kiefer, Meghan
Hebert, Paul
Lessler, Dan
Krieger, James
TI Randomized Controlled Trial of a Community Health Worker Self-Management
Support Intervention Among Low-Income Adults With Diabetes, Seattle,
Washington, 2010-2014
SO PREVENTING CHRONIC DISEASE
LA English
DT Article
ID BASE-LINE CHARACTERISTICS; GLYCEMIC CONTROL; CARE; ADHERENCE; VALIDITY;
PEOPLE; COMPLICATIONS; AMERICAN; DESIGN; IMPACT
AB Introduction
Community health workers (CHWs) can improve diabetes outcomes; however, questions remain about translating research findings into practical low-intensity models for safety-net providers. We tested the effectiveness of a home-based low-intensity CHW intervention for improving health outcomes among low-income adults with diabetes.
Methods
Low-income patients with glycated hemoglobin A 1c (HbA 1c) of 8.0% or higher in the 12 months before enrollment from 3 safetynet providers were randomized to a 12-month CHW-delivered diabetes self-management intervention or usual care. CHWs were based at a local health department. The primary outcome was change in HbA 1c from baseline enrollment to 12 months; secondary outcomes included blood pressure and lipid levels, quality of life, and health care use.
Results
The change in HbA 1c in the intervention group (n = 145) (unadjusted mean of 9.09% to 8.58%, change of -0.51) compared with the control group (n = 142) (9.04% to 8.71%, change of -0.33) was not significant (P =.54). In an analysis of participants with poor glycemic control (HbA 1c > 10%), the intervention group had a 1.23-point greater decrease in HbA 1c compared with controls (P =.046). For the entire study population, we found a decrease in reported physician visits (P <.001) and no improvement in healthrelated quality of life (P =.07) in the intervention group compared with the control group.
Conclusion
A low-intensity CHW-delivered intervention to support diabetes self-management did not significantly improve HbA 1c relative to usual care. Among the subgroup of participants with poor glycemic control (HbA 1c > 10% at baseline), the intervention was effective.
C1 [Nelson, Karin; Taylor, Leslie; Silverman, Julie; Kiefer, Meghan; Hebert, Paul] VA Hlth Serv Res & Dev, Seattle Denver Ctr Innovat Veteran Ctr & Value Dr, Seattle, WA USA.
[Nelson, Karin; Silverman, Julie; Kiefer, Meghan] VA Puget Sound Hlth Care Syst, Gen Internal Med Serv, Seattle, WA USA.
[Nelson, Karin; Silverman, Julie; Kiefer, Meghan; Hebert, Paul; Lessler, Dan; Krieger, James] Univ Washington, Sch Med, Seattle, WA USA.
[Nelson, Karin; Krieger, James] Univ Washington, Sch Publ Hlth, Seattle, WA 98195 USA.
[Krieger, James] Publ Hlth Seattle & King Cty, Seattle, WA USA.
RP Nelson, K (reprint author), VA Puget Sound Hlth Care Syst, Hlth Serv Res & Dev, 1660 S Columbian Way, Seattle, WA 98108 USA.
EM Karin.Nelson@va.gov
FU National Institutes of Health, National Institute for Diabetes and
Digestive and Kidney Diseases [5R18DK088072]; Veterans Health
Administration (VHA) Diabetes Quality Enhancement Research Initiative
FX This study was supported by the National Institutes of Health, National
Institute for Diabetes and Digestive and Kidney Diseases grant
5R18DK088072 (K. Nelson and J. Krieger, co-principal investigators).
Supplemental funding was provided by the Veterans Health Administration
(VHA) Diabetes Quality Enhancement Research Initiative. The views
expressed in this article are those of the authors and do not
necessarily reflect the views of the US Department of Veterans Affairs.
The authors have no financial conflicts of interest to report.
NR 29
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PU CENTERS DISEASE CONTROL
PI ATLANTA
PA 1600 CLIFTON RD, ATLANTA, GA 30333 USA
SN 1545-1151
J9 PREV CHRONIC DIS
JI Prev. Chronic Dis.
PD FEB
PY 2017
VL 14
AR 160344
DI 10.5888/pcd14.160344
PG 9
WC Public, Environmental & Occupational Health
SC Public, Environmental & Occupational Health
GA EP1KW
UT WOS:000397144800006
ER
PT J
AU Rosen, CS
Azevedo, KJ
Tiet, QQ
Greene, CJ
Wood, AE
Calhoun, P
Bowe, T
Capehart, BP
Crawford, EF
Greenbaum, MA
Harris, AHS
Hertzberg, M
Lindley, SE
Smith, BN
Schnurr, PP
AF Rosen, Craig S.
Azevedo, Kathryn J.
Tiet, Quyen Q.
Greene, Carolyn J.
Wood, Amanda E.
Calhoun, Patrick
Bowe, Thomas
Capehart, Bruce P.
Crawford, Eric F.
Greenbaum, Mark A.
Harris, Alex H. S.
Hertzberg, Michael
Lindley, Steven E.
Smith, Brandy N.
Schnurr, Paula P.
TI An RCT of Effects of Telephone Care Management on Treatment Adherence
and Clinical Outcomes Among Veterans With PTSD
SO PSYCHIATRIC SERVICES
LA English
DT Article
ID POSTTRAUMATIC-STRESS-DISORDER; MENTAL-HEALTH TREATMENT; COGNITIVE
PROCESSING THERAPY; RANDOMIZED CONTROLLED-TRIAL; ADDICTION SEVERITY
INDEX; AFGHANISTAN VETERANS; MEDICATION ADHERENCE; TREATMENT ENGAGEMENT;
PROLONGED EXPOSURE; TREATMENT-SEEKING
AB Objective: This study assessed whether adding telephone care management to usual outpatient mental health care improved treatment attendance, medication compliance, and clinical outcomes of veterans with posttraumatic stress disorder (PTSD).
Methods: In a multisite randomized controlled trial, 358 veterans were assigned to either usual outpatient mental health treatment (N=165) or usual care plus twice-a-month telephone care management (TCM) and support in the first three months of treatment (N=193). Treatment utilization and medication refills were determined from U.S. Department of Veterans Affairs administrative data. PTSD, depression, quality of life, aggressive behavior, and substance use were assessed with self-report questionnaires at intake, four months, and 12 months.
Results: Telephone care managers reached 95% of TCM participants (N=182), completing an average 5.1 of 6.0 planned telephone calls. During the three-month intervention period, TCM participants completed 43% more mental health visits (M +/- SD=5.9 +/- 6.8) than did those in usual care (4.1 +/- 4.2) ( incident rate ratio=1.36, x(2)=6.56, df=1, p<.01).Treatment visits in the nine-month follow-up period and medication refills did not differ by condition. Only 9% of participants were scheduled to receive evidence-based psychotherapy. Slopes of improvement in PTSD, depression, alcohol misuse, drug problems, aggressive behavior, and quality of life did not differ by condition or treatment attendance.
Conclusions: TCM improved PTSD patients' treatment attendance but not their outcomes. TCM can enhance treatment engagement, but outcomes depend on the effectiveness of the treatments that patients receive.
C1 [Rosen, Craig S.] Vet Affairs VA Palo Alto Hlth Care Syst, Natl Ctr PTSD Disseminat & Training Div, Menlo Pk, CA 94025 USA.
[Rosen, Craig S.; Tiet, Quyen Q.; Lindley, Steven E.] Stanford Univ, Sch Med, Dept Psychiat & Behav Sci, Stanford, CA 94305 USA.
[Lindley, Steven E.] VA Palo Alto Hlth Care Syst, Menlo Pk, CA USA.
[Azevedo, Kathryn J.; Bowe, Thomas; Harris, Alex H. S.] VA Palo Alto Hlth Care Syst, Ctr Innovat Implementat, Hlth Serv Res & Dev Serv, Menlo Pk, CA USA.
[Harris, Alex H. S.] Stanford Univ, Sch Med, Dept Surg, Stanford, CA 94305 USA.
[Greene, Carolyn J.] VA Off Mental Hlth Serv, Menlo Pk, CA USA.
[Wood, Amanda E.] VA Puget Sound Hlth Care Syst, Mental Hlth Serv Amer Lake Div, Tacoma, WA USA.
[Calhoun, Patrick] VA Midatlantic Mental Illness Res Educ & Clin Ctr, Durham, NC USA.
[Capehart, Bruce P.; Hertzberg, Michael] Durham VA Med Ctr, Dept Psychiat, Durham, NC USA.
[Calhoun, Patrick; Capehart, Bruce P.; Hertzberg, Michael] Duke Univ, Sch Med, Dept Psychiat & Behav Sci, Durham, NC 27706 USA.
[Crawford, Eric F.] Midatlantic Reg MIRECC, Clin Core, Durham, NC USA.
[Crawford, Eric F.] Sheridan VA Med Ctr, Sheridan, WY USA.
[Greenbaum, Mark A.] VA Sierra Pacific MIRECC, Menlo Pk, CA USA.
[Schnurr, Paula P.] White River Junct VA Med Ctr, Natl Ctr PTSD Execut Div, White River Jct, VT USA.
[Schnurr, Paula P.] Dartmouth Coll, Geisel Sch Med, Hanover, NH 03755 USA.
RP Rosen, CS (reprint author), Vet Affairs VA Palo Alto Hlth Care Syst, Natl Ctr PTSD Disseminat & Training Div, Menlo Pk, CA 94025 USA.
EM craig.rosen@va.gov
FU Congressionally Directed Medical Research Program [W81XWH-08-2-0096]
FX Dr. Rosen, Dr. Azevedo, Dr. Tiet, and Ms. Smith are with the National
Center for PTSD Dissemination and Training Division, Veterans Affairs
(VA) Palo Alto Health Care System, Menlo Park, California (e-mail:
craig.rosen@va.gov). Dr. Rosen and Dr. Tiet are also with the Department
of Psychiatry and Behavioral Sciences, Stanford University School of
Medicine, Stanford, California, where Dr. Lindley is affiliated. Dr.
Lindley is also with the VA Palo Alto Health Care System, Menlo Park.
Dr. Azevedo is also with the Center for Innovation to Implementation,
Health Services Research and Development Service, VA Palo Alto Health
Care System, Menlo Park, where Dr. Bowe and Dr. Harris are affiliated.
Dr. Harris is also with the Department of Surgery, Stanford University
School of Medicine, Stanford. Dr. Greene is with the VA Office of Mental
Health Services, Menlo Park. Dr. Wood is with Mental Health Services
American Lake Division, VA Puget Sound Health Care System, Tacoma,
Washington. Dr. Calhoun is with the VA Mid-Atlantic Mental Illness
Research, Education and Clinical Center (MIRECC). Dr. Capehart and Dr.
Hertzberg are with the Department of Psychiatry, Durham VA Medical
Center, Durham, North Carolina. Dr. Calhoun, Dr. Capehart, and Dr.
Hertzberg are also with the Department of Psychiatry and Behavioral
Sciences, Duke University School of Medicine, Durham. Dr. Crawford,
formerly with the Clinical Core, Mid-Atlantic Region MIRECC, Durham, is
now with the Sheridan VA Medical Center, Sheridan, Wyoming. Mr.
Greenbaum is with the VA Sierra-Pacific MIRECC, Menlo Park. Dr. Schnurr
is with the National Center for PTSD Executive Division, White River
Junction VA Medical Center, White River Junction, Vermont, and the
Geisel School of Medicine, Dartmouth College, Hanover, New Hampshire.
This study is registered on Clinicaltrials.gov as NCT02655991. This
research was supported by the Congressionally Directed Medical Research
Program, grant W81XWH-08-2-0096 awarded to Dr. Rosen. The authors thank
the veterans who participated in this research; the VA staff members who
supported this study; study coordinator Emerald Adler; and Kathy Blau,
Julia Hernandez, Nate Hawkins, Niall Kavanagh, Caitlin McLean, and Olga
Rosito, who provided compassionate telephone support to the veterans in
this trial. The opinions expressed are those of the authors and do not
represent the position of the U.S. Department of Veterans Affairs.
NR 58
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PU AMER PSYCHIATRIC PUBLISHING, INC
PI ARLINGTON
PA 1000 WILSON BOULEVARD, STE 1825, ARLINGTON, VA 22209-3901 USA
SN 1075-2730
EI 1557-9700
J9 PSYCHIAT SERV
JI Psychiatr. Serv.
PD FEB 1
PY 2017
VL 68
IS 2
BP 151
EP 158
DI 10.1176/appi.ps.201600069
PG 8
WC Health Policy & Services; Public, Environmental & Occupational Health;
Psychiatry
SC Health Care Sciences & Services; Public, Environmental & Occupational
Health; Psychiatry
GA EP0PZ
UT WOS:000397090500010
PM 27745535
ER
PT J
AU Wilson, SM
Krenek, M
Dennis, PA
Yard, SS
Browne, KC
Simpson, TL
AF Wilson, Sarah M.
Krenek, Marketa
Dennis, Paul A.
Yard, Samantha S.
Browne, Kendall C.
Simpson, Tracy L.
TI Daily Associations Between PTSD, Drinking, and Self-Appraised
Alcohol-Related Problems
SO PSYCHOLOGY OF ADDICTIVE BEHAVIORS
LA English
DT Article
DE alcohol use disorder (AUD); posttraumatic stress disorder (PTSD);
psychiatric comorbidities; longitudinal; interactive voice recognition
(IVR)
ID POSTTRAUMATIC-STRESS-DISORDER; NATIONAL EPIDEMIOLOGIC SURVEY;
CONFIRMATORY FACTOR-ANALYSIS; TIMELINE FOLLOW BACK; ALL-CAUSE MORTALITY;
SUBSTANCE USE; BETWEEN-PERSON; CONDITIONS-III; LIFETIME PTSD;
WITHIN-PERSON
AB Alcohol dependence (AD) and posttraumatic stress disorder (PTSD) are highly comorbid, yet limited research has focused on PTSD and daily drinking as they relate to self-appraised alcohol-related problems. In treatment contexts, patients' appraisals of alcohol-related problems have implications for assessment, intervention strategies, and prognosis. This study investigated the moderating effect of within-person (daily symptoms) and between-person (overall severity) differences in PTSD on the association between daily drinking and same-day alcohol-related problems. Participants with comorbid AD and PTSD (N = 86) completed 1 week of Interactive Voice Recognition data collection, and logistic and gamma-adjusted multilevel models were used to estimate odds and magnitude of self-appraised alcohol-related problems. Results revealed that both within-person and between-person PTSD moderated the association between number of drinks and severity of self-appraised problems. As within-person and between-person PTSD symptoms increased, there was a weaker association between number of drinks consumed and perceived alcohol-related problems. Contrasts further revealed that on nondrinking and light-drinking days, PTSD (both daily symptoms and overall severity) was positively associated with ratings of alcohol-related problems. However, PTSD was not associated with alcohol-related problems on heavier drinking days. In conclusion, more severe PTSD is associated with a less directly contingent relationship between drinking quantity and perceived alcohol-related problems. These findings suggest the importance of further investigations of this moderating effect as well as clinical treatment of comorbid AD and severe PTSD with functional analysis of drinking.
C1 [Wilson, Sarah M.] Midatlantic Mental Illness Res Educ & Clin Ctr MI, 508 Fulton St, Durham, NC 27705 USA.
[Wilson, Sarah M.; Dennis, Paul A.] Durham VA Hlth Care Syst, Durham, NC USA.
[Krenek, Marketa; Browne, Kendall C.] VA Puget Sound Hlth Care Syst, VISN MIRECC 20, Seattle, WA USA.
[Dennis, Paul A.] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC USA.
[Yard, Samantha S.] VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Browne, Kendall C.; Simpson, Tracy L.] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA 98195 USA.
[Simpson, Tracy L.] VA Puget Sound Hlth Care Syst, CESATE, Seattle, WA USA.
RP Wilson, SM (reprint author), Midatlantic Mental Illness Res Educ & Clin Ctr MI, 508 Fulton St, Durham, NC 27705 USA.
EM sarah.wilson@duke.edu
FU NIH/NIAAA [R21AA17130-01]; U.S. Department of Veterans Affairs Office of
Academic Affiliations, Advanced Fellowship Program in Mental Illness
Research and Treatment
FX This study was supported in part by a grant from NIH/NIAAA award
(R21AA17130-01; PI: TLS) and by resources from the Center of Excellence
in Substance Abuse Treatment and Education (CESATE; TLS), the VISN 20
and VISN 6 Mental Illness Research, Education, and Clinical Centers
(MIRECC), the U.S. Department of Veterans Affairs Office of Academic
Affiliations, Advanced Fellowship Program in Mental Illness Research and
Treatment (SMW, MK, SSY, and KCB), and the VA Puget Sound Health Care
System, Seattle, WA.
NR 50
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PU EDUCATIONAL PUBLISHING FOUNDATION-AMERICAN PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST, NE, WASHINGTON, DC 20002-4242 USA
SN 0893-164X
EI 1939-1501
J9 PSYCHOL ADDICT BEHAV
JI Psychol. Addict. Behav.
PD FEB
PY 2017
VL 31
IS 1
BP 27
EP 35
DI 10.1037/adb0000238
PG 9
WC Substance Abuse; Psychology, Multidisciplinary
SC Substance Abuse; Psychology
GA EN1SZ
UT WOS:000395791600003
PM 28068120
ER
PT J
AU Fernandez, AC
Yurasek, AM
Merrill, JE
Miller, MB
Zamboanga, BL
Carey, KB
Borsari, B
AF Fernandez, Anne C.
Yurasek, Ali M.
Merrill, Jennifer E.
Miller, Mary Beth
Zamboanga, Byron L.
Carey, Kate B.
Borsari, Brian
TI Do Brief Motivational Interventions Reduce Drinking Game Frequency in
Mandated Students? An Analysis of Data From Two Randomized Controlled
Trials
SO PSYCHOLOGY OF ADDICTIVE BEHAVIORS
LA English
DT Article
DE drinking games; brief intervention; motivational interviewing; college;
alcohol
ID COLLEGE-STUDENTS; ALCOHOL INTERVENTIONS; AUSTRALIAN UNIVERSITY; STEPPED
CARE; PARTICIPATION; CONSUMPTION; DRINKERS; DETERMINANTS; METAANALYSIS;
EFFICACY
AB College students frequently engage in drinking games (DGs) and experience a variety of consequences as a result. It is currently unknown whether brief motivational interventions (BMIs) that provide feedback on DG participation can reduce this high risk behavior. This study examined outcome data from 2 randomized clinical trials to examine whether BMIs facilitate change in DG frequency and how these changes may occur. Mandated college students (Trial 1, N = 198, 46% female; Trial 2, N = 412; 32% female) were randomized to BMI or comparison control conditions. Hierarchical linear modeling (HLM) was used to compare the BMI and comparison groups to determine whether the BMI reduced DG participation over time. Percent change talk (PCT) during the discussion of DG during the session was examined as a predictor of change in DG frequency, and gender was examined as a moderator of treatment effects. Controlling for regular drinking frequency, participants who received a BMI did not significantly reduce their DG frequency relative to the comparison group in either sample, and the BMI was equally ineffective at reducing DG behavior for men and women. DG-related PCT during the BMI was associated with lower DG frequency at the second follow-up in both trials. In Trial 1, PCT during the BMI was associated with less steep increases in DG frequency across the course of all follow-ups. Effects of PCT on DG behavior were not moderated by gender. Findings did not support hypothesized reductions in DG participation following a BMI. Future research should explore whether targeted DG-specific interventions could reduce DG participation and the role of in-session client language in facilitating such change.
C1 [Fernandez, Anne C.] Univ Michigan, Dept Psychiat, North Campus Res Complex,2800 Plymouth Rd, Ann Arbor, MI 48109 USA.
[Yurasek, Ali M.] Univ Florida, Coll Hlth & Human Performance, Dept Hlth Educ & Behav, Gainesville, FL 32611 USA.
[Merrill, Jennifer E.; Miller, Mary Beth; Carey, Kate B.] Brown Univ, Ctr Alcohol & Addict Studies, Sch Publ Hlth, Providence, RI 02912 USA.
[Zamboanga, Byron L.] Smith Coll, Dept Psychol, Northampton, MA 01063 USA.
[Borsari, Brian] San Francisco VA Med Ctr, San Francisco, CA USA.
[Borsari, Brian] Univ Calif San Francisco, Dept Psychiat, San Francisco, CA 94143 USA.
RP Fernandez, AC (reprint author), Univ Michigan, Dept Psychiat, North Campus Res Complex,2800 Plymouth Rd, Ann Arbor, MI 48109 USA.
EM acfernan@med.umich.edu
FU National Institute on Alcohol Abuse and Alcoholism [R01-AA015518, R01
AA017427, T32 AA007459]; VISN1 Career Development Award [V1CDA2012-18];
[R01 AA012518]
FX This work was supported by National Institute on Alcohol Abuse and
Alcoholism Grants R01-AA015518, R01 AA017427, and VISN1 Career
Development Award V1CDA2012-18 to Brian Borsari and Grant R01 AA012518
to Kate B. Carey. The contributions of Anne C. Fernandez, Ali M. Yurasek
and Mary Beth Miller were supported by Grant T32 AA007459 from the
National Institute on Alcohol Abuse and Alcoholism.
NR 50
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U2 1
PU EDUCATIONAL PUBLISHING FOUNDATION-AMERICAN PSYCHOLOGICAL ASSOC
PI WASHINGTON
PA 750 FIRST ST, NE, WASHINGTON, DC 20002-4242 USA
SN 0893-164X
EI 1939-1501
J9 PSYCHOL ADDICT BEHAV
JI Psychol. Addict. Behav.
PD FEB
PY 2017
VL 31
IS 1
BP 36
EP 45
DI 10.1037/adb0000239
PG 10
WC Substance Abuse; Psychology, Multidisciplinary
SC Substance Abuse; Psychology
GA EN1SZ
UT WOS:000395791600004
PM 27936818
ER
PT J
AU Uraki, R
Hwang, J
Jurado, KA
Householder, S
Yockey, LJ
Hastings, AK
Homer, RJ
Iwasaki, A
Fikrig, E
AF Uraki, Ryuta
Hwang, Jesse
Jurado, Kellie Ann
Householder, Sarah
Yockey, Laura J.
Hastings, Andrew K.
Homer, Robert J.
Iwasaki, Akiko
Fikrig, Erol
TI Zika virus causes testicular atrophy
SO SCIENCE ADVANCES
LA English
DT Article
ID HUMAN LEYDIG-CELLS; SEXUAL TRANSMISSION; NEURAL PROGENITORS; MICE;
INFECTION; BRAIN; ORGANOIDS; EXPOSURE; LEADS; PERSISTENCE
AB Zika virus (ZIKV) is an emerging mosquito-borne flavivirus that has recently been found to cause fetal infection and neonatal abnormalities, including microcephaly and neurological dysfunction. ZIKV persists in the semen months after the acute viremic phase in humans. To further understand the consequences of ZIKV persistence in males, we infected Ifnar1(-/-) mice via subcutaneous injection of a pathogenic but nonlethal ZIKV strain. ZIKV replication persists within the testes even after clearance from the blood, with interstitial, testosterone-producing Leydig cells supporting virus replication. We found high levels of viral RNA and antigen within the epididymal lumen, where sperm is stored, and within surrounding epithelial cells. Unexpectedly, at 21 days post-infection, the testes of the ZIKV-infected mice were significantly smaller compared to those of mock-infected mice, indicating progressive testicular atrophy. ZIKV infection caused a reduction in serum testosterone, suggesting that male fertility can be affected. Our findings have important implications for nonvector-borne vertical transmission, as well as long-term potential reproductive deficiencies, in ZIKV-infected males.
C1 [Uraki, Ryuta; Hwang, Jesse; Householder, Sarah; Hastings, Andrew K.; Fikrig, Erol] Yale Univ, Sch Med, Dept Internal Med, Sect Infect Dis, 333 Cedar St, New Haven, CT 06520 USA.
[Jurado, Kellie Ann; Yockey, Laura J.; Iwasaki, Akiko] Yale Univ, Sch Med, Dept Immunobiol, 333 Cedar St, New Haven, CT 06520 USA.
[Homer, Robert J.] Yale Univ, Sch Med, Dept Pathol, 333 Cedar St, New Haven, CT 06520 USA.
[Homer, Robert J.] US Dept Vet Affairs, Affairs Connecticut Healthcare Syst Pathol & Lab, West Haven, CT 06516 USA.
[Iwasaki, Akiko; Fikrig, Erol] Howard Hughes Med Inst, Chevy Chase, MD 20815 USA.
RP Fikrig, E (reprint author), Yale Univ, Sch Med, Dept Internal Med, Sect Infect Dis, 333 Cedar St, New Haven, CT 06520 USA.; Fikrig, E (reprint author), Howard Hughes Med Inst, Chevy Chase, MD 20815 USA.
EM erol.fikrig@yale.edu
FU NIH [5T32 AI007019-40, 4T32HL007974-15, T32 GM007205]
FX This work was supported by NIH grants 5T32 AI007019-40 (to K.A.J.),
4T32HL007974-15 (to J.H.), and T32 GM007205 (to L.J.Y.).
NR 43
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U1 1
U2 1
PU AMER ASSOC ADVANCEMENT SCIENCE
PI WASHINGTON
PA 1200 NEW YORK AVE, NW, WASHINGTON, DC 20005 USA
SN 2375-2548
J9 SCI ADV
JI Sci. Adv.
PD FEB
PY 2017
VL 3
IS 2
AR e1602899
DI 10.1126/sciadv.1602899
PG 6
WC Multidisciplinary Sciences
SC Science & Technology - Other Topics
GA EO9WT
UT WOS:000397039500038
ER
PT J
AU Sonnenberg, A
AF Sonnenberg, Amnon
TI A Bias Toward Action in Gastrointestinal Bleeding
SO AMERICAN JOURNAL OF GASTROENTEROLOGY
LA English
DT Letter
C1 [Sonnenberg, Amnon] Oregon Hlth & Sci Univ, Portland VA Med Ctr, P3-GI,3710 SW US Vet Hosp Rd, Portland, OR 97239 USA.
[Sonnenberg, Amnon] Oregon Hlth & Sci Univ, Div Gastroenterol Hepatol, P3-GI,3710 SW US Vet Hosp Rd, Portland, OR 97239 USA.
RP Sonnenberg, A (reprint author), Oregon Hlth & Sci Univ, Portland VA Med Ctr, P3-GI,3710 SW US Vet Hosp Rd, Portland, OR 97239 USA.; Sonnenberg, A (reprint author), Oregon Hlth & Sci Univ, Div Gastroenterol Hepatol, P3-GI,3710 SW US Vet Hosp Rd, Portland, OR 97239 USA.
EM sonnenbe@ohsu.edu
NR 0
TC 0
Z9 0
U1 0
U2 0
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 0002-9270
EI 1572-0241
J9 AM J GASTROENTEROL
JI Am. J. Gastroenterol.
PD FEB
PY 2017
VL 112
IS 2
BP 395
EP 396
DI 10.1038/ajg.2016.558
PG 2
WC Gastroenterology & Hepatology
SC Gastroenterology & Hepatology
GA EK7VP
UT WOS:000394133600042
PM 28154390
ER
PT J
AU Alday, PH
Bruzual, I
Nilsen, A
Pou, S
Winter, R
Ben Mamoun, C
Riscoe, MK
Doggett, JS
AF Alday, P. Holland
Bruzual, Igor
Nilsen, Aaron
Pou, Sovitj
Winter, Rolf
Ben Mamoun, Choukri
Riscoe, Michael K.
Doggett, J. Stone
TI Genetic Evidence for Cytochrome b Q(i) Site Inhibition by
4(1H)-Quinolone-3-Diarylethers and Antimycin in Toxoplasma gondii
SO ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
LA English
DT Article
DE Toxoplasma gondii; apicomplexan parasites; cytochrome b; cytochrome
bc(1); drug targets; experimental therapeutics; mechanisms of action;
mitochondria; parasitology; preclinical drug studies
ID ENDOCHIN-LIKE QUINOLONE; BC(1) COMPLEX; PLASMODIUM-FALCIPARUM; QUINONE
REDUCTION; CRYSTAL-STRUCTURE; BOUND SUBSTRATE; ATOVAQUONE; ENCEPHALITIS;
BABESIOSIS
AB Toxoplasma gondii is an apicomplexan parasite that causes fatal and debilitating brain and eye disease. Endochinlike quinolones (ELQs) are preclinical compounds that are efficacious against apicomplexan-caused diseases, including toxoplasmosis, malaria, and babesiosis. Of the ELQs, ELQ-316 has demonstrated the greatest efficacy against acute and chronic experimental toxoplasmosis. Although genetic analyses in other organisms have highlighted the importance of the cytochrome bc(1) complex Q(i) site for ELQ sensitivity, the mechanism of action of ELQs against T. gondii and the specific mechanism of ELQ-316 remain unknown. Here, we describe the selection and genetic characterization of T. gondii clones resistant to ELQ-316. A T. gondii strain selected under ELQ-316 drug pressure was found to possess a Thr222-Pro amino acid substitution that confers 49-fold resistance to ELQ-316 and 19-fold resistance to antimycin, a well-characterized Q(i) site inhibitor. These findings provide further evidence for ELQ Q(i) site inhibition in T. gondii and greater insight into the interactions of Q(i) site inhibitors with the apicomplexan cytochrome bc(1) complex.
C1 [Alday, P. Holland; Doggett, J. Stone] Oregon Hlth & Sci Univ, Div Infect Dis, Portland, OR 97201 USA.
[Bruzual, Igor; Nilsen, Aaron; Pou, Sovitj; Winter, Rolf; Riscoe, Michael K.; Doggett, J. Stone] Portland VA Med Ctr, Dept Res & Dev, Portland, OR USA.
[Ben Mamoun, Choukri] Yale Sch Med, Infect Dis Sect, Dept Internal Med, New Haven, CT USA.
RP Doggett, JS (reprint author), Oregon Hlth & Sci Univ, Div Infect Dis, Portland, OR 97201 USA.; Doggett, JS (reprint author), Portland VA Med Ctr, Dept Res & Dev, Portland, OR USA.
EM doggettj@ohsu.edu
FU U.S. Department of Veterans Affairs Biomedical Laboratory Research and
Development [BX002440]; NIH [R01 AI100569]; Peer Reviewed Medical
Research Program Project [PR130649]; U.S. Department of Veterans Affairs
[BX003312]
FX This work was supported by Career Development Award BX002440 to J. Stone
Doggett from the U.S. Department of Veterans Affairs Biomedical
Laboratory Research and Development. We also acknowledge support for
Michael K. Riscoe from NIH R01 AI100569, Peer Reviewed Medical Research
Program Project PR130649, and VA Merit Review Funds from the U.S.
Department of Veterans Affairs BX003312.
NR 29
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Z9 0
U1 0
U2 0
PU AMER SOC MICROBIOLOGY
PI WASHINGTON
PA 1752 N ST NW, WASHINGTON, DC 20036-2904 USA
SN 0066-4804
EI 1098-6596
J9 ANTIMICROB AGENTS CH
JI Antimicrob. Agents Chemother.
PD FEB
PY 2017
VL 61
IS 2
AR e01866-16
DI 10.1128/AAC.01866-16
PG 8
WC Microbiology; Pharmacology & Pharmacy
SC Microbiology; Pharmacology & Pharmacy
GA EK7JQ
UT WOS:000394102500042
ER
PT J
AU Han, JH
Gordon, K
Womack, JA
Gibert, CL
Leaf, DA
Rimland, D
Rodriguez-Barradas, MC
Bisson, GP
AF Han, Jennifer H.
Gordon, Kirsha
Womack, Julie A.
Gibert, Cynthia L.
Leaf, David A.
Rimland, David
Rodriguez-Barradas, Maria C.
Bisson, Gregory P.
TI Comparative Effectiveness of Diabetic Oral Medications Among
HIV-Infected and HIV-Uninfected Veterans
SO DIABETES CARE
LA English
DT Article
ID HUMAN-IMMUNODEFICIENCY-VIRUS; CORONARY-HEART-DISEASE; NUCLEOSIDE ANALOG;
CLINICAL-TRIALS; DATA-COLLECTION; TOTAL BILIRUBIN; ADVERSE EVENTS;
ASSOCIATION; MELLITUS; THERAPY
AB OBJECTIVE Type 2 diabetes is increasingly common in HIV-infected individuals. The objective of this study was to compare the glycemic effectiveness of oral diabetic medications among patients with and without HIV infection.
RESEARCH DESIGN AND METHODS A longitudinal cohort study was conducted among HIV-infected and uninfected veterans with type 2 diabetes initiating diabetic medications between 1999 and 2010. Generalized estimating equations were used to compare changes in hemoglobin A(1c) (HbA(1c)) through the year after medication initiation, adjusting for baseline HbA1c level and clinical covariates. A subanalysis using propensity scores was conducted to account for confounding by indication.
RESULTS A total of 2,454 HIV-infected patients and 8,892 HIV-uninfected patients initiated diabetic medications during the study period. The most commonly prescribed medication was metformin (n = 5,647, 50%), followed by a sulfonylurea (n = 5,554, 49%) and a thiazolidinedione (n = 145, 1%). After adjustment for potential confounders, there was no significant difference in the change in HbA(1c) level among the three groups of new users. HIV infection was not significantly associated with glycemic response (P = 0.24). Black and Hispanic patients had a poorer response to therapy compared with white patients, with a relative increase in HbA1c level of 0.16% (95% CI 0.08, 0.24) [1.7 mmol/mol (0.9, 2.6)] (P < 0.001) and 0.25% (0.11, 0.39) [2.7 mmol/mol (1.2, 4.3)] (P = 0.001), respectively.
CONCLUSIONS We found that glycemic response was independent of the initial class of diabetic medication prescribed among HIV-uninfected and HIV-infected adults with type 2 diabetes. The mechanisms leading to poorer response among black and Hispanic patients, who make up a substantial proportion of those with HIV infection and type 2 diabetes, require further investigation.
C1 [Han, Jennifer H.; Bisson, Gregory P.] Univ Penn, Dept Med, Perelman Sch Med, Div Infect Dis, Philadelphia, PA 19104 USA.
[Han, Jennifer H.; Bisson, Gregory P.] Univ Penn, Dept Biostat & Epidemiol, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Han, Jennifer H.; Bisson, Gregory P.] Univ Penn, Ctr Clin Epidemiol & Biostat, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Gordon, Kirsha; Womack, Julie A.] West Haven VA Med Ctr, Dept Internal Med, West Haven, CT USA.
[Womack, Julie A.] Yale Univ, Yale Sch Nursing, New Haven, CT USA.
[Gibert, Cynthia L.] George Washington Univ, Sch Med & Hlth Sci, Sect Infect Dis, Washington, DC 20052 USA.
[Gibert, Cynthia L.] Washington DC VA Med Ctr, Dept Med, Washington, DC USA.
[Leaf, David A.] Univ Calif Los Angeles, David Geffen Sch Med, Div Infect Dis, Los Angeles, CA 90095 USA.
[Leaf, David A.] VA Greater Los Angeles Healthcare Syst, Dept Med, Los Angeles, CA USA.
[Rimland, David] Emory Univ, Sch Med, Div Infect Dis, Atlanta, GA USA.
[Rimland, David] Atlanta VA Med Ctr, Div Infect Dis, Atlanta, GA USA.
[Rodriguez-Barradas, Maria C.] Michael E DeBakey VA Med Ctr, Infect Dis Sect, Houston, TX USA.
[Rodriguez-Barradas, Maria C.] Baylor Coll Med, Dept Med, Houston, TX 77030 USA.
RP Han, JH (reprint author), Univ Penn, Dept Med, Perelman Sch Med, Div Infect Dis, Philadelphia, PA 19104 USA.; Han, JH (reprint author), Univ Penn, Dept Biostat & Epidemiol, Perelman Sch Med, Philadelphia, PA 19104 USA.; Han, JH (reprint author), Univ Penn, Ctr Clin Epidemiol & Biostat, Perelman Sch Med, Philadelphia, PA 19104 USA.
EM jennifer.han@uphs.upenn.edu
FU Veterans Aging Cohort Study; National Institute on Alcohol Abuse and
Alcoholism [U10-AA-13566]
FX This study was supported by the Veterans Aging Cohort Study and by
National Institute on Alcohol Abuse and Alcoholism grant U10-AA-13566.
NR 37
TC 0
Z9 0
U1 0
U2 0
PU AMER DIABETES ASSOC
PI ALEXANDRIA
PA 1701 N BEAUREGARD ST, ALEXANDRIA, VA 22311-1717 USA
SN 0149-5992
EI 1935-5548
J9 DIABETES CARE
JI Diabetes Care
PD FEB
PY 2017
VL 40
IS 2
BP 218
EP 225
DI 10.2337/dc16-0718
PG 8
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EL2ZL
UT WOS:000394489300020
PM 27634393
ER
PT J
AU Cefalu, WT
Buse, JB
Tuomilehto, J
Fleming, GA
Ferrannini, E
Gerstein, HC
Bennett, PH
Ramachandran, A
Raz, I
Rosenstock, J
Kahn, SE
AF Cefalu, William T.
Buse, John B.
Tuomilehto, Jaakko
Fleming, G. Alexander
Ferrannini, Ele
Gerstein, Hertzel C.
Bennett, Peter H.
Ramachandran, Ambady
Raz, Itamar
Rosenstock, Julio
Kahn, Steven E.
TI Update and Next Steps for Real-World Translation of Interventions for
Type 2 Diabetes Prevention: Reflections From a Diabetes Care Editors'
Expert Forum. Diabetes Care 2016; 39: 1186-1201
SO DIABETES CARE
LA English
DT Editorial Material
C1 [Cefalu, William T.] Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA.
[Buse, John B.] Univ N Carolina, Sch Med, Chapel Hill, NC USA.
[Tuomilehto, Jaakko] Natl Inst Hlth & Welf, Chron Dis Prevent Unit, Helsinki, Finland.
[Tuomilehto, Jaakko] Dasman Diabet Inst, Dasman, Kuwait.
[Tuomilehto, Jaakko] King Abdulaziz Univ, Saudi Diabet Res Grp, Jeddah, Saudi Arabia.
[Tuomilehto, Jaakko] Danube Univ Krems, Ctr Vasc Prevent, Krems, Austria.
[Fleming, G. Alexander] Kinexum, Harpers Ferry, WV USA.
[Ferrannini, Ele] CNR, Inst Clin Physiol, Pisa, Italy.
[Gerstein, Hertzel C.] McMaster Univ, Hamilton, ON, Canada.
[Gerstein, Hertzel C.] Hamilton Hlth Sci, Hamilton, ON, Canada.
[Bennett, Peter H.] NIH, Phoenix, AZ USA.
[Ramachandran, Ambady] India Diabet Res Fdn, Madras, Tamil Nadu, India.
[Ramachandran, Ambady] Dr A Ramachandrans Diabet Hosp, Madras, Tamil Nadu, India.
[Raz, Itamar] Hadassah Hebrew Univ Hosp, Dept Internal Med, Diabet Unit, Jerusalem, Israel.
[Rosenstock, Julio] Med City, Dallas Diabet Res Ctr, Dallas, TX 75390 USA.
[Rosenstock, Julio] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA.
[Kahn, Steven E.] VA Puget Sound Hlth Care Syst, Seattle, WA USA.
[Kahn, Steven E.] Univ Washington, Seattle, WA 98195 USA.
RP Cefalu, WT (reprint author), Louisiana State Univ, Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA.
EM william.cefalu@pbrc.edu
FU National Institutes of Health (NIH) [1U54-GM-104940, P50-AT-002776]
FX W.T.C. is supported in part by National Institutes of Health (NIH) grant
1U54-GM-104940, which funds the Louisiana Clinical and Translational
Science Center, and NIH grant P50-AT-002776.
NR 6
TC 0
Z9 0
U1 1
U2 1
PU AMER DIABETES ASSOC
PI ALEXANDRIA
PA 1701 N BEAUREGARD ST, ALEXANDRIA, VA 22311-1717 USA
SN 0149-5992
EI 1935-5548
J9 DIABETES CARE
JI Diabetes Care
PD FEB
PY 2017
VL 40
IS 2
BP E23
EP E24
DI 10.2337/dci16-0036
PG 2
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EL2ZL
UT WOS:000394489300009
PM 28108540
ER
PT J
AU Garvey, WT
AF Garvey, W. Timothy
TI Update and Next Steps for Real-World Translation of Interventions for
Type 2 Diabetes Prevention: Reflections From a Diabetes Care Editors'
Expert Forum. Diabetes Care 2016; 39: 1186-1201
SO DIABETES CARE
LA English
DT Editorial Material
ID METABOLIC SYNDROME; OBESITY
C1 [Garvey, W. Timothy] Univ Alabama Birmingham, Dept Nutr Sci, Birmingham, AL 35294 USA.
[Garvey, W. Timothy] Birmingham VA Med Ctr, Birmingham, AL 35233 USA.
RP Garvey, WT (reprint author), Univ Alabama Birmingham, Dept Nutr Sci, Birmingham, AL 35294 USA.; Garvey, WT (reprint author), Birmingham VA Med Ctr, Birmingham, AL 35233 USA.
EM garveyt@uab.edu
FU National Institute of Diabetes and Digestive and Kidney Diseases
[DK-038765]; National Institute of Diabetes and Digestive and Kidney
Diseases (UAB Diabetes Research Center) [P30 DK079626]; U.S. Department
of Veterans Affairs (Merit Review program)
FX W.T.G. acknowledges support from grants awarded by the National
Institute of Diabetes and Digestive and Kidney Diseases (DK-038765 and
UAB Diabetes Research Center [P30 DK079626]) and the U.S. Department of
Veterans Affairs (Merit Review program).
NR 6
TC 1
Z9 1
U1 1
U2 1
PU AMER DIABETES ASSOC
PI ALEXANDRIA
PA 1701 N BEAUREGARD ST, ALEXANDRIA, VA 22311-1717 USA
SN 0149-5992
EI 1935-5548
J9 DIABETES CARE
JI Diabetes Care
PD FEB
PY 2017
VL 40
IS 2
BP E21
EP E22
DI 10.2337/dci16-0022
PG 2
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EL2ZL
UT WOS:000394489300008
PM 28108539
ER
PT J
AU Hammad, H
Kaltenbach, T
Soetikno, R
AF Hammad, Hazem
Kaltenbach, Tonya
Soetikno, Roy
TI Surveillance for dysplasia in inflammatory bowel disease: it is time to
move forward
SO ENDOSCOPY
LA English
DT Editorial Material
ID DEPRESSED COLORECTAL NEOPLASMS; STANDING ULCERATIVE-COLITIS; NONPOLYPOID
FLAT; COLONOSCOPY; MANAGEMENT; ENDOSCOPY; CONSENSUS; BIOPSIES
C1 [Hammad, Hazem] Univ Colorado, Div Gastroenterol & Hepatol, Anschutz Med Campus, Aurora, CO USA.
[Kaltenbach, Tonya] Univ Calif San Francisco, Dept Med, Div Gastroenterol, San Francisco Vet Affairs Med Ctr, San Francisco, CA USA.
[Soetikno, Roy] Grad Sch Business, Stanford, CA 94305 USA.
RP Soetikno, R (reprint author), Grad Sch Business, Stanford, CA 94305 USA.
EM soetikno@earthlink.net
NR 16
TC 0
Z9 0
U1 0
U2 0
PU GEORG THIEME VERLAG KG
PI STUTTGART
PA RUDIGERSTR 14, D-70469 STUTTGART, GERMANY
SN 0013-726X
EI 1438-8812
J9 ENDOSCOPY
JI Endoscopy
PD FEB
PY 2017
VL 49
IS 2
BP 110
EP 112
DI 10.1055/s-0043-100097
PG 3
WC Gastroenterology & Hepatology; Surgery
SC Gastroenterology & Hepatology; Surgery
GA EK9PX
UT WOS:000394257500003
PM 28147393
ER
PT J
AU Nin, N
Muriel, A
Penuelas, O
Brochard, L
Lorente, JA
Ferguson, ND
Raymondos, K
R-Os, F
Violi, DA
Thille, AW
Gonzalez, M
Villagomez, AJ
Hurtado, J
Davies, AR
Du, B
Maggiore, SM
Soto, L
D'Empaire, G
Matamis, D
Abroug, F
Moreno, RP
Soares, MA
Arabi, Y
Sandi, F
Jibaja, M
Amin, P
Koh, Y
Kuiper, MA
Bulow, HH
Zeggwagh, AA
Anzueto, A
Sznajder, JI
Esteban, A
AF Nin, Nicolas
Muriel, Alfonso
Penuelas, Oscar
Brochard, Laurent
Angel Lorente, Jose
Ferguson, Niall D.
Raymondos, Konstantinos
R-Os, Fernando
Violi, Damian A.
Thille, Arnaud W.
Gonzalez, Marco
Villagomez, Asisclo J.
Hurtado, Javier
Davies, Andrew R.
Du, Bin
Maggiore, Salvatore M.
Soto, Luis
D'Empaire, Gabriel
Matamis, Dimitrios
Abroug, Fekri
Moreno, Rui P.
Soares, Marco Antonio
Arabi, Yaseen
Sandi, Freddy
Jibaja, Manuel
Amin, Pravin
Koh, Younsuck
Kuiper, Michael A.
Bulow, Hans-Henrik
Zeggwagh, Amine Ali
Anzueto, Antonio
Sznajder, Jacob I.
Esteban, Andres
CA VENTILA Grp
TI Severe hypercapnia and outcome of mechanically ventilated patients with
moderate or severe acute respiratory distress syndrome
SO INTENSIVE CARE MEDICINE
LA English
DT Article
DE Mechanical ventilation; Acute respiratory distress syndrome;
Hypercapnia; ICU mortality
ID ACUTE LUNG INJURY; END-EXPIRATORY PRESSURE; PERMISSIVE HYPERCAPNIA;
PROTECTIVE-VENTILATION; CARBON-DIOXIDE; PULMONARY-EDEMA; TIDAL VOLUME;
MORTALITY; ACIDOSIS; DYSFUNCTION
AB Purpose: To analyze the relationship between hypercapnia developing within the first 48 h after the start of mechanical ventilation and outcome in patients with acute respiratory distress syndrome (ARDS).
Patients and methods: We performed a secondary analysis of three prospective non-interventional cohort studies focusing on ARDS patients from 927 intensive care units (ICUs) in 40 countries. These patients received mechanical ventilation for more than 12 h during 1-month periods in 1998, 2004, and 2010. We used multivariable logistic regression and a propensity score analysis to examine the association between hypercapnia and ICU mortality.
Main outcomes: We included 1899 patients with ARDS in this study. The relationship between maximum PaCO2 in the first 48 h and mortality suggests higher mortality at or above PaCO2 of >= 50 mmHg. Patients with severe hypercapnia (PaCO2 >= 50 mmHg) had higher complication rates, more organ failures, and worse outcomes. After adjusting for age, SAPS II score, respiratory rate, positive end-expiratory pressure, PaO2/FiO(2) ratio, driving pressure, pressure/volume limitation strategy (PLS), corrected minute ventilation, and presence of acidosis, severe hypercapnia was associated with increased risk of ICU mortality [odds ratio (OR) 1.93, 95% confidence interval (CI) 1.32 to 2.81; p = 0.001]. In patients with severe hypercapnia matched for all other variables, ventilation with PLS was associated with higher ICU mortality (OR 1.58, CI 95% 1.04-2.41; p = 0.032).
Conclusions: Severe hypercapnia appears to be independently associated with higher ICU mortality in patients with ARDS.
Trial registration: Clinicaltrials.gov identifier, NCT01093482.
C1 [Nin, Nicolas] Hosp Torrejon, Madrid, Spain.
[Muriel, Alfonso] Hosp Ramon & Cajal, Dept Clin Biostat, IRICYS, Madrid, Spain.
[Muriel, Alfonso] CIBERESP, Madrid, Spain.
[Penuelas, Oscar; Angel Lorente, Jose; Esteban, Andres] CIBER Enfermedades Resp, Madrid, Spain.
[Brochard, Laurent] St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr, Toronto, ON, Canada.
[Brochard, Laurent; Ferguson, Niall D.] Univ Toronto, Interdept Div Crit Care Med, Toronto, ON, Canada.
[Ferguson, Niall D.] Univ Toronto, Dept Med, Toronto, ON, Canada.
[Ferguson, Niall D.] Univ Toronto, Dept Physiol, Toronto, ON, Canada.
[Raymondos, Konstantinos] Hannover Med Sch, Hannover, Germany.
[R-Os, Fernando] Hosp Nacl Alejandro Posadas, Buenos Aires, DF, Argentina.
[Violi, Damian A.] Hosp HIGA Guemes, Haedo, Argentina.
[Thille, Arnaud W.] Univ Hosp Poitiers, Poitiers, France.
[Gonzalez, Marco] Clin Medellin, Medellin, Colombia.
[Gonzalez, Marco] Univ Pontificia Bolivariana, Medellin, Colombia.
[Villagomez, Asisclo J.] Hosp Reg 1 Octubre, Mexico City, DF, Mexico.
[Hurtado, Javier] Hosp Espanol, Montevideo, Uruguay.
[Davies, Andrew R.] Alfred Hosp, Melbourne, Vic, Australia.
[Davies, Andrew R.] Monash Univ, Melbourne, Vic, Australia.
[Du, Bin] Beijing Union Med Coll Hosp, Beijing, Peoples R China.
[Maggiore, Salvatore M.] Univ Cattolica Sacro Cuore, Policlin Agostino Gemelli, Rome, Italy.
[Soto, Luis] Inst Nacl Torax Santiago, Santiago, Chile.
[D'Empaire, Gabriel] Hosp Clin Caracas, Caracas, Venezuela.
[Matamis, Dimitrios] Papageorgiou Hosp, Thessaloniki, Greece.
[Abroug, Fekri] Hosp Fattouma Bourguina, Monastir, Tunisia.
[Moreno, Rui P.] Ctr Hosp Lisboa Cent, EPE, UCINC, Hosp Sao Jose, Lisbon, Portugal.
[Soares, Marco Antonio] Hosp Univ Sao Jose, Belo Horizonte, MG, Brazil.
[Arabi, Yaseen] King Saud Bin Abdulaziz Univ Hlth Sci, Riyadh, Saudi Arabia.
[Sandi, Freddy] Hosp Obrero 1, La Paz, Bolivia.
[Jibaja, Manuel] Hosp Eugenio Espejo, Quito, Ecuador.
[Amin, Pravin] Bombay Hosp Inst Med Sci, Bombay, Maharashtra, India.
[Koh, Younsuck] Univ Ulsan, Asan Med Ctr, Seoul, South Korea.
[Kuiper, Michael A.] Med Ctr Leeuwarden MCL, Leeuwarden, Netherlands.
[Bulow, Hans-Henrik] Univ Copenhagen, Holbaek Hosp, Copenhagen, Region Zealand, Denmark.
[Zeggwagh, Amine Ali] Hosp Ibn Sina, Rabat, Morocco.
[Anzueto, Antonio] South Texas Vet Hlth Care Syst, San Antonio, TX USA.
[Anzueto, Antonio] Univ Texas Hlth Sci Ctr San Antonio, San Antonio, TX 78229 USA.
[Sznajder, Jacob I.] Northwestern Univ, Dept Med, Feinberg Sch Med, Chicago, IL 60611 USA.
[Esteban, Andres] Hosp Univ Getafe, Carretera Toledo,Km 12,500, Madrid 28905, Spain.
RP Esteban, A (reprint author), Hosp Univ Getafe, Carretera Toledo,Km 12,500, Madrid 28905, Spain.
EM aesteban@ucigetafe.com
OI Muriel, Alfonso /0000-0002-4805-4011
FU CIBER Enfermedades Respiratorias (CIBERES); CIBER en Epidemiologia y
Salud Publica (CIBERESP); Instituto de Salud Carlos III, Madrid, Spain;
Instituto Ramon y Cajal de Investigacion Sanitaria (IRYCIS), Madrid,
Spain; Canadian Institutes of Health Research New Investigator Award
(Ottawa, Canada); [HL-048129]; [HL-071643]; [HL-085534]
FX Funding for this study was provided by CIBER Enfermedades Respiratorias
(CIBERES), CIBER en Epidemiologia y Salud Publica (CIBERESP), Instituto
de Salud Carlos III, Madrid, Spain and the Instituto Ramon y Cajal de
Investigacion Sanitaria (IRYCIS), Madrid, Spain. Dr. Ferguson was
supported by a Canadian Institutes of Health Research New Investigator
Award (Ottawa, Canada). Dr. Sznajder is funded by HL-048129, HL-071643
and HL-085534.
NR 40
TC 1
Z9 1
U1 1
U2 1
PU SPRINGER
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0342-4642
EI 1432-1238
J9 INTENS CARE MED
JI Intensive Care Med.
PD FEB
PY 2017
VL 43
IS 2
BP 200
EP 208
DI 10.1007/s00134-016-4611-1
PG 9
WC Critical Care Medicine
SC General & Internal Medicine
GA EL0OE
UT WOS:000394320900005
PM 28108768
ER
PT J
AU Haibach, JP
Haibach, MA
Hall, KS
Masheb, RM
Little, MA
Shepardson, RL
Dobmeyer, AC
Funderburk, JS
Hunter, CL
Dundon, M
Hausmann, LRM
Trynosky, SK
Goodrich, DE
Kilbourne, AM
Knight, SJ
Talcott, GW
Goldstein, MG
AF Haibach, Jeffrey P.
Haibach, Michael Ann
Hall, Katherine S.
Masheb, Robin M.
Little, Melissa A.
Shepardson, Robyn L.
Dobmeyer, Anne C.
Funderburk, Jennifer S.
Hunter, Christopher L.
Dundon, Margaret
Hausmann, Leslie R. M.
Trynosky, Stephen K.
Goodrich, David E.
Kilbourne, Amy M.
Knight, Sara J.
Talcott, Gerald W.
Goldstein, Michael G.
TI Military and veteran health behavior research and practice: challenges
and opportunities
SO JOURNAL OF BEHAVIORAL MEDICINE
LA English
DT Article
DE Military; Veteran; Servicemember; Health behavior; Health promotion;
Healthcare; Behavioral health
ID POSTTRAUMATIC-STRESS-DISORDER; RANDOMIZED CONTROLLED-TRIAL;
SUBSTANCE-USE DISORDERS; DEPARTMENT-OF-DEFENSE; ACTIVE-DUTY MILITARY; US
AIR-FORCE; WEIGHT MANAGEMENT PROGRAM; ALCOHOL-RELATED OUTCOMES;
BODY-MASS INDEX; PRIMARY-CARE
AB There are 2.1 million current military servicemembers and 21 million living veterans in the United States. Although they were healthier upon entering military service compared to the general U.S. population, in the longer term veterans tend to be of equivalent or worse health than civilians. One primary explanation for the veterans' health disparity is poorer health behaviors during or after military service, especially areas of physical activity, nutrition, tobacco, and alcohol. In response, the Department of Defense and Department of Veterans Affairs continue to develop, evaluate, and improve health promotion programs and healthcare services for military and veteran health behavior in an integrated approach. Future research and practice is needed to better understand and promote positive health behavior during key transition periods in the military and veteran life course. Also paramount is implementation and evaluation of existing interventions, programs, and policies across the population using an integrated and person centered approach.
C1 [Haibach, Jeffrey P.; Kilbourne, Amy M.] US Dept Vet Affairs, Hlth Serv Res & Dev Serv, 810 Vermont Ave NW 10P9H, Washington, DC 20420 USA.
[Haibach, Michael Ann] US Air Force, Wright Patterson AFB, OH USA.
[Hall, Katherine S.] Durham VA Med Ctr, Durham, NC USA.
[Hall, Katherine S.] Duke Univ, Dept Med, Durham, NC USA.
[Masheb, Robin M.] VA Connecticut Healthcare Syst, West Haven, CT USA.
[Masheb, Robin M.] Yale Sch Med, New Haven, CT USA.
[Little, Melissa A.; Talcott, Gerald W.] Univ Tennessee, Ctr Hlth Sci, Ctr Populat Sci, Memphis, TN 38163 USA.
[Shepardson, Robyn L.; Funderburk, Jennifer S.] Syracuse VA Med Ctr, VA Ctr Integrated Healthcare, Syracuse, NY USA.
[Shepardson, Robyn L.; Funderburk, Jennifer S.] Syracuse Univ, Dept Psychol, Syracuse, NY USA.
[Dobmeyer, Anne C.] Deployment Hlth Clin Ctr, Def Ctr Excellence Psychol Hlth, Bethesda, MD USA.
[Dobmeyer, Anne C.] Deployment Hlth Clin Ctr, Def Ctr Traumat Brain Injury, Bethesda, MD USA.
[Funderburk, Jennifer S.] Univ Rochester, Dept Psychiat, Rochester, NY USA.
[Hunter, Christopher L.] Def Hlth Agcy, Patient Ctr Med Home Branch, Clin Support Div, Washington, DC USA.
[Dundon, Margaret; Goldstein, Michael G.] US Dept Vet Affairs, Natl Ctr Hlth Promot & Dis Prevent, Durham, NC USA.
[Hausmann, Leslie R. M.] VA Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA USA.
[Hausmann, Leslie R. M.] Univ Pittsburgh, Sch Med, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15213 USA.
[Trynosky, Stephen K.] US Dept Vet Affairs, Off Acad Affiliat, Washington, DC USA.
[Trynosky, Stephen K.] US Army Reserve, Med Serv Corps, Washington, DC USA.
[Goodrich, David E.] VA Ann Arbor Healthcare Syst, Ctr Clin Management Res, Ann Arbor, MI USA.
[Kilbourne, Amy M.] Univ Michigan, Sch Med, Dept Psychiat, Ann Arbor, MI USA.
[Knight, Sara J.] Birmingham VA Med Ctr, Birmingham, AL USA.
[Knight, Sara J.] Univ Alabama Birmingham, Div Prevent Med, Birmingham, AL USA.
RP Haibach, JP (reprint author), US Dept Vet Affairs, Hlth Serv Res & Dev Serv, 810 Vermont Ave NW 10P9H, Washington, DC 20420 USA.
EM Jeffrey.Haibach@va.gov; Michael.Glotfelter.1@us.af.mil;
Katherine.Hall@duke.edu; Robin.Masheb@yale.edu; Mlittl18@uthsc.edu;
Robyn.Shepardson@va.gov; Anne.C.Dobmeyer.mil@mail.mil;
Jennifer.Funderburk@va.gov; Christopher.L.Hunter16.mil@mail.mil;
Margaret.Dundon@va.gov; Leslie.Hausmann@va.gov; Steve.Trynosky@va.gov;
David.Goodrich2@va.gov; Amy.Kilbourne@va.gov; Sara.Knight@va.gov;
Wtalcott@uthsc.edu; Michael.Goldstein2@va.gov
NR 168
TC 1
Z9 1
U1 4
U2 4
PU SPRINGER/PLENUM PUBLISHERS
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0160-7715
EI 1573-3521
J9 J BEHAV MED
JI J. Behav. Med.
PD FEB
PY 2017
VL 40
IS 1
BP 175
EP 193
DI 10.1007/s10865-016-9794-y
PG 19
WC Psychology, Clinical
SC Psychology
GA EL0WK
UT WOS:000394342300013
PM 27678001
ER
PT J
AU Haibach, JP
Haibach, MA
Hall, KS
Masheb, RM
Little, MA
Shepardson, RL
Dobmeyer, AC
Funderburk, JS
Hunter, CL
Dundon, M
Hausmann, LRM
Trynosky, SK
Goodrich, DE
Kilbourne, AM
Knight, SJ
Talcott, GW
Goldstein, M
AF Haibach, Jeffrey P.
Haibach, Michael Ann
Hall, Katherine S.
Masheb, Robin M.
Little, Melissa A.
Shepardson, Robyn L.
Dobmeyer, Anne C.
Funderburk, Jennifer S.
Hunter, Christopher L.
Dundon, Margaret
Hausmann, Leslie R. M.
Trynosky, Stephen K.
Goodrich, David E.
Kilbourne, Amy M.
Knight, Sara J.
Talcott, Gerald W.
Goldstein, Michael
TI Military and veteran health behavior research and practice: challenges
and opportunities (vol 40, pg 175, 2017)
SO JOURNAL OF BEHAVIORAL MEDICINE
LA English
DT Correction
C1 [Haibach, Jeffrey P.; Kilbourne, Amy M.] US Dept Vet Affairs, Hlth Serv Res & Dev Serv, 810 Vermont Ave NW 10P9H, Washington, DC 20420 USA.
[Haibach, Michael Ann] US Air Force, Wright Patterson AFB, OH USA.
[Hall, Katherine S.] Durham VA Med Ctr, Durham, NC USA.
[Hall, Katherine S.] Duke Univ, Dept Med, Durham, NC USA.
[Masheb, Robin M.] VA Connecticut Healthcare Syst, West Haven, CT USA.
[Masheb, Robin M.] Yale Sch Med, New Haven, CT USA.
[Little, Melissa A.; Talcott, Gerald W.] Univ Tennessee, Ctr Hlth Sci, Ctr Populat Sci, Memphis, TN 38163 USA.
[Shepardson, Robyn L.; Funderburk, Jennifer S.] Syracuse VA Med Ctr, VA Ctr Integrated Healthcare, Syracuse, NY USA.
[Shepardson, Robyn L.; Funderburk, Jennifer S.] Syracuse Univ, Dept Psychol, Syracuse, NY USA.
[Dobmeyer, Anne C.] Deployment Hlth Clin Ctr, Def Ctr Excellence Psychol Hlth, Bethesda, MD USA.
[Dobmeyer, Anne C.] Deployment Hlth Clin Ctr, Def Ctr Traumat Brain Injury, Bethesda, MD USA.
[Funderburk, Jennifer S.] Univ Rochester, Dept Psychiat, Rochester, NY USA.
[Hunter, Christopher L.] Def Hlth Agcy, Patient Ctr Med Home Branch, Clin Support Div, Washington, DC USA.
[Dundon, Margaret; Goldstein, Michael] US Dept Vet Affairs, Natl Ctr Hlth Promot & Dis Prevent, Durham, NC USA.
[Hausmann, Leslie R. M.] VA Pittsburgh Healthcare Syst, Ctr Hlth Equity Res & Promot, Pittsburgh, PA USA.
[Hausmann, Leslie R. M.] Univ Pittsburgh, Sch Med, Dept Med, Div Gen Internal Med, Pittsburgh, PA 15213 USA.
[Trynosky, Stephen K.] US Dept Vet Affairs, Off Acad Affiliat, Washington, DC USA.
[Trynosky, Stephen K.] US Army Reserve, Med Serv Corps, Washington, DC USA.
[Goodrich, David E.] VA Ann Arbor Healthcare Syst, Ctr Clin Management Res, Ann Arbor, MI USA.
[Kilbourne, Amy M.] Univ Michigan, Sch Med, Dept Psychiat, Ann Arbor, MI USA.
[Knight, Sara J.] Birmingham VA Med Ctr, Birmingham, AL USA.
[Knight, Sara J.] Univ Alabama Birmingham, Div Prevent Med, Birmingham, AL USA.
RP Haibach, JP (reprint author), US Dept Vet Affairs, Hlth Serv Res & Dev Serv, 810 Vermont Ave NW 10P9H, Washington, DC 20420 USA.
EM Jeffrey.Haibach@va.gov; Michael.Glotfelter.1@us.af.mil;
Katherine.Hall@duke.edu; Robin.Masheb@yale.edu; Mlittl18@uthsc.edu;
Robyn.Shepardson@va.gov; Anne.C.Dobmeyer.mil@mail.mil;
Jennifer.Funderburk@va.gov; Christopher.L.Hunter16.mil@mail.mil;
Margaret.Dundon@va.gov; Leslie.Hausmann@va.gov; Steve.Trynosky@va.gov;
David.Goodrich2@va.gov; Amy.Kilbourne@va.gov; Sara.Knight@va.gov;
Wtalcott@uthsc.edu; Michael.Goldstein2@va.gov
NR 1
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PU SPRINGER/PLENUM PUBLISHERS
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 0160-7715
EI 1573-3521
J9 J BEHAV MED
JI J. Behav. Med.
PD FEB
PY 2017
VL 40
IS 1
BP 227
EP 228
DI 10.1007/s10865-016-9801-3
PG 2
WC Psychology, Clinical
SC Psychology
GA EL0WK
UT WOS:000394342300017
PM 27757768
ER
PT J
AU Rosen, LE
Ananthanarayanan, V
Gallan, A
Tjota, MY
Attanoos, R
Alchami, FS
Brcic, L
Butnor, K
Hiroshima, K
Klampatsa, A
Litzky, L
Marchevsky, AM
Medeiros, F
Montero-Fernandez, MA
Moore, DA
Nabeshima, K
Pavlisko, EN
Sharma, A
Sheaf, M
Walls, AE
Galateau, F
Le Stang, N
Krausz, T
Husain, AN
AF Rosen, Lauren E.
Ananthanarayanan, Vijayalakshmi
Gallan, Alexander
Tjota, Melissa Yuwono
Attanoos, Richard
Alchami, Fouad S.
Brcic, Luka
Butnor, Kelly
Hiroshima, Kenzo
Klampatsa, Astero
Litzky, Leslie
Marchevsky, Alberto M.
Medeiros, Filomena
Montero-Fernandez, M. Angeles
Moore, David A.
Nabeshima, Kazuki
Pavlisko, Elizabeth N.
Sharma, Anupama
Sheaf, Michael
Walls, Ann E.
Galateau, Francoise
Le Stang, Nolwenn
Krausz, Thomas
Husain, Aliya N.
TI Nuclear Grade, Necrosis and Solid Growth Pattern Predict Survival in
Epithelioid Malignant Mesothelioma: An International, Multi
Institutional Study
SO LABORATORY INVESTIGATION
LA English
DT Meeting Abstract
CT 106th Annual Meeting of the
United-States-and-Canadian-Academy-of-Pathology (USCAP)
CY MAR 04-10, 2017
CL San Antonio, TX
SP US & Canadian Acad Pathol
C1 Univ Chicago, Chicago, IL 60637 USA.
Loyola, Maywood, IL USA.
Univ Wales Coll Cardiff, Cardiff, S Glam, Wales.
Med Univ Graz, Graz, Austria.
Univ Vermont, Burlington, VT USA.
Tokyo Womens Med Ctr, Kawadacho, Japan.
Univ Penn, Philadelphia, PA 19104 USA.
Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA.
Basildon & Thurrock Univ Hosp, Basildon, England.
Royal Brompton & Harefield Hosp, London, England.
Univ Leicester, Leicester, Leics, England.
Fukuoka Univ, Fukuoka, Japan.
Duke Univ, Durham, NH USA.
Vet Affairs Pittsburgh Healthcare Syst, Pittsburgh, PA USA.
Barts Hlth NHS Trust, London, England.
Ctr Leon Berard, Lyon, France.
NR 0
TC 0
Z9 0
U1 0
U2 0
PU NATURE PUBLISHING GROUP
PI NEW YORK
PA 75 VARICK ST, 9TH FLR, NEW YORK, NY 10013-1917 USA
SN 0023-6837
EI 1530-0307
J9 LAB INVEST
JI Lab. Invest.
PD FEB
PY 2017
VL 97
SU 1
MA 1980
BP 492A
EP 492A
PG 1
WC Medicine, Research & Experimental; Pathology
SC Research & Experimental Medicine; Pathology
GA EK1YT
UT WOS:000393724402461
ER
PT J
AU Katon, J
Cypel, Y
Raza, M
Zephyrin, L
Reiber, G
Yano, EM
Barth, S
Schneiderman, A
AF Katon, Jodie
Cypel, Yasmin
Raza, Mubashra
Zephyrin, Laurie
Reiber, Gayle
Yano, Elizabeth M.
Barth, Shannon
Schneiderman, Aaron
TI Deployment and Adverse Pregnancy Outcomes: Primary Findings and
Methodological Considerations
SO MATERNAL AND CHILD HEALTH JOURNAL
LA English
DT Article
DE Deployment; Preterm birth; Low birth weight; Women Veterans; OEF/OIF
ID GULF-WAR VETERANS; POSTTRAUMATIC-STRESS-DISORDER; LOW-BIRTH-WEIGHT;
PRETERM BIRTH; UNITED-STATES; VIETNAM VETERANS; GESTATIONAL-AGE;
MATERNAL RECALL; WOMEN VETERANS; RISK
AB Objective To characterize the pregnancy outcomes of women Operation Enduring Freedom/Operation Iraqi Freedom (OEF/OIF) Veterans including prevalence of preterm delivery, low birth weight, and macrosomia, and to highlight methodological limitations that can impact findings. Methods A retrospective cohort study was conducted starting in 2014 analyzing data from the 2009 to 2011 National Health Study for a New Generation of US Veterans, which sampled Veterans deployed and not deployed to OIF/OEF. All pregnancies resulting in a live birth were included, and categorized as occurring among non-deployers, before deployment, during deployment, or after deployment. Outcomes included preterm birth, low birth weight, and macrosomia. The association of deployment with selected outcomes was estimated using separate general estimating equations to account for lack of outcome independence among women contributing multiple pregnancies. Adjustment variables included maternal age at outcome, and race/ethnicity. Results There were 2276 live births (191 preterm births, 153 low birth weight infants, and 272 macrosomic infants). Compared with pregnancies before deployment, pregnancies among non-deployers and those after deployment appeared to have greater risk of preterm birth [non-deployers: odds ratio (OR) = 2.16, 95 % confidence interval (CI) 1.25, 3.72; after deployment: OR = 1.90, 95 % CI 0.90, 4.02]. A similar pattern was observed for low birth weight. No association of deployment with macrosomia was detected. Discussion Compared with non-deployers, those who eventually deploy appear to have better pregnancy outcomes prior to deployment, but this advantage is no longer apparent after deployment. Non-deployers may not be an appropriate reference group to study the putative health impacts of deployment on pregnancy outcomes.
C1 [Katon, Jodie; Zephyrin, Laurie] US Dept Vet Affairs VA, Off Patient Care Serv, Womens Hlth Serv, Washington, DC 20420 USA.
[Katon, Jodie; Reiber, Gayle] VA Puget Sound Hlth Care Syst, Sch Med, Ctr Innovat Vet Ctr & Value Driven Care, VA Hlth Serv Res & Dev HSR&D, 1660 South Columbia Way S-152, Seattle, WA 98108 USA.
[Katon, Jodie; Reiber, Gayle] Univ Washington, Dept Hlth Serv, Sch Publ Hlth, Seattle, WA 98195 USA.
[Cypel, Yasmin; Raza, Mubashra; Barth, Shannon; Schneiderman, Aaron] VA Off Publ Hlth, Post Deployment Hlth Strateg Healthcare Grp, Washington, DC USA.
[Reiber, Gayle] Univ Washington, Dept Epidemiol, Sch Publ Hlth, Seattle, WA 98195 USA.
[Zephyrin, Laurie] New York Harbor VA Healthcare Syst, New York, NY USA.
[Yano, Elizabeth M.] VA Greater Los Angeles Healthcare Syst, VA HSR&D Ctr Study Healthcare Innovat Implementat, Los Angeles, CA USA.
[Yano, Elizabeth M.] Univ Calif Los Angeles, Jonathan & Karin Fielding Sch Publ Hlth, Dept Hlth Policy & Management, Los Angeles, CA USA.
RP Katon, J (reprint author), US Dept Vet Affairs VA, Off Patient Care Serv, Womens Hlth Serv, Washington, DC 20420 USA.; Katon, J (reprint author), VA Puget Sound Hlth Care Syst, Sch Med, Ctr Innovat Vet Ctr & Value Driven Care, VA Hlth Serv Res & Dev HSR&D, 1660 South Columbia Way S-152, Seattle, WA 98108 USA.; Katon, J (reprint author), Univ Washington, Dept Hlth Serv, Sch Publ Hlth, Seattle, WA 98195 USA.
EM jodie.katon@va.gov
FU US Department of Veterans Affairs (VA), Office of Public Health; Office
of Academic Affiliations' Associated Health Postdoctoral Fellowship [TTP
61-026]; VA Office of Patient Care, Women's Health Services; VA Puget
Sound Center of Innovation in Patient-Centered and Value-Driven Care; VA
HSR&D Senior Research Career Scientist awards [RCS-98-353, RCS-05-195]
FX This study was funded by the US Department of Veterans Affairs (VA),
Office of Public Health. Dr. Katon was supported by an Office of
Academic Affiliations' Associated Health Postdoctoral Fellowship (#TTP
61-026), by the VA Office of Patient Care, Women's Health Services, and
by the VA Puget Sound Center of Innovation in Patient-Centered and
Value-Driven Care. Drs. Reiber (#RCS-98-353) and Yano (#RCS-05-195) are
supported by VA HSR&D Senior Research Career Scientist awards. The views
expressed within are solely those of the authors, and do not necessarily
reflect the position or policy of the Department of Veterans Affairs or
the United States government. The authors would like to acknowledge
Katherine Hoggatt, PhD and Kristen Gray, PhD for providing a critical
review of the manuscript.
NR 40
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U2 0
PU SPRINGER/PLENUM PUBLISHERS
PI NEW YORK
PA 233 SPRING ST, NEW YORK, NY 10013 USA
SN 1092-7875
EI 1573-6628
J9 MATERN CHILD HLTH J
JI Matern. Child Health J.
PD FEB
PY 2017
VL 21
IS 2
BP 376
EP 386
DI 10.1007/s10995-016-2122-x
PG 11
WC Public, Environmental & Occupational Health
SC Public, Environmental & Occupational Health
GA EK9VQ
UT WOS:000394272400019
PM 27449782
ER
PT J
AU Jensen, KP
Smith, AH
Herman, AI
Farrer, LA
Kranzler, HR
Sofuoglu, M
Gelernter, J
AF Jensen, K. P.
Smith, A. H.
Herman, A. I.
Farrer, L. A.
Kranzler, H. R.
Sofuoglu, M.
Gelernter, J.
TI A protocadherin gene cluster regulatory variant is associated with
nicotine withdrawal and the urge to smoke
SO MOLECULAR PSYCHIATRY
LA English
DT Article
ID GENOME-WIDE ASSOCIATION; STATE FUNCTIONAL CONNECTIVITY; INTRAVENOUS
NICOTINE; QUIT SMOKING; ACETYLCHOLINE-RECEPTOR; ANXIETY SENSITIVITY;
EUROPEAN-AMERICANS; DISTRESS TOLERANCE; PREFRONTAL CORTEX;
NUCLEUS-ACCUMBENS
AB Nicotine withdrawal symptoms contribute to relapse in smokers, thereby prolonging the harm caused by smoking. To investigate the molecular basis for this phenomenon, we conducted a genome-wide association study of DSM-IV nicotine withdrawal in a sample of African American (AA) and European American (EA) smokers. A combined AA and EA meta-analysis (n = 8021) identified three highly correlated single nucleotide polymorphisms (SNPs) in the protocadherin (PCDH)-alpha, -beta and -gamma gene cluster on chromosome 5 that were associated with nicotine withdrawal (P<5x10(-8)). We then studied one of the SNPs, rs31746, in an independent sample of smokers who participated in an intravenous nicotine infusion study that followed overnight smoking abstinence. After nicotine infusion, abstinent smokers with the withdrawal risk allele experienced greater alleviation of their urges to smoke, as assessed by the Brief Questionnaire on Smoking Urges (BQSU). Prior work has shown that the PCDH-alpha, -beta and -gamma genes are expressed in neurons in a highly organized manner. We found that rs31746 mapped to a long-range neuron-specific enhancer element shown previously to regulate PCDH-alpha, -beta and -gamma gene expression. Using Braincloud mRNA expression data, we identified a robust and specific association between rs31746 and PCDH-beta 8 mRNA expression in frontal cortex tissue (P<1x10(-5)). We conclude that PCDH-alpha, -beta and -gamma gene cluster regulatory variation influences the severity of nicotine withdrawal. Further studies on the PCDH-alpha, -beta and -gamma genes and their role in nicotine withdrawal may inform the development of novel smoking cessation treatments and reduce the harm caused by tobacco smoking.
C1 [Jensen, K. P.; Smith, A. H.; Herman, A. I.; Sofuoglu, M.; Gelernter, J.] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT USA.
[Jensen, K. P.; Smith, A. H.; Herman, A. I.; Sofuoglu, M.; Gelernter, J.] VA Connecticut Healthcare Syst, 950 Campbell Ave, West Haven, CT 06516 USA.
[Smith, A. H.] Yale Univ, Sch Med, Interdept Neurosci Program, New Haven, CT USA.
[Smith, A. H.] Yale Univ, Sch Med, Med Scientist Training Program, New Haven, CT USA.
[Farrer, L. A.] Boston Univ, Sch Med & Publ Hlth, Dept Med Biomed Genet, Boston, MA 02215 USA.
[Farrer, L. A.] Boston Univ, Dept Neurol, Sch Med & Publ Hlth, Boston, MA 02215 USA.
[Farrer, L. A.] Boston Univ, Dept Ophthalmol, Sch Med & Publ Hlth, Boston, MA 02215 USA.
[Farrer, L. A.] Boston Univ, Dept Epidemiol, Sch Med & Publ Hlth, Boston, MA 02215 USA.
[Farrer, L. A.] Boston Univ, Dept Biostat, Sch Med & Publ Hlth, Boston, MA 02215 USA.
[Kranzler, H. R.] Univ Penn, Dept Psychiat, Perelman Sch Med, Philadelphia, PA 19104 USA.
[Kranzler, H. R.] Philadelphia VA Med Ctr, MIRECC VISN4, Philadelphia, PA 19104 USA.
[Gelernter, J.] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT USA.
[Gelernter, J.] Yale Univ, Sch Med, Dept Genet, New Haven, CT USA.
RP Gelernter, J (reprint author), VA Connecticut Healthcare Syst, 950 Campbell Ave, West Haven, CT 06516 USA.; Gelernter, J (reprint author), Yale Univ, Dept Psychiat, Sch Med, 950 Campbell Ave, West Haven, CT 06516 USA.
EM joel.gelernter@yale.edu
FU Veterans Administration (VA) Mental Illness Research, Education and
Clinical Center (MIRECC); VA VISN1 Career Development Award; NIH [R03
DA027474, R01 AA017535, R01 DA030976, R01 DA12690, MSTP 5T32GM007205-38,
CTSA 8UL1TR000142 TL1, F30 DA037665]; Army STARRS; Department of the
Army; US Department of Health and Human Services, National Institutes of
Health, National Institute of Mental Health (NIH/NIMH) [U01MH087981];
NIH/NCRR [1 S10 RR19895-01]; NIH Genes, Environment and Health
Initiative (GEI) [U01 HG004422, U01HG004438]; Gene Environment
Association Studies (GENEVA) under GEI; National Institute on Alcohol
Abuse and Alcoholism; National Institute on Drug Abuse; NIH contract
'High throughput genotyping for studying the genetic contributions to
human disease' [HHSN268200782096C]
FX This research was supported by the Veterans Administration (VA) Mental
Illness Research, Education and Clinical Center (MIRECC) and a VA VISN1
Career Development Award; NIH grants R03 DA027474, R01 AA017535, R01
DA030976, R01 DA12690, MSTP 5T32GM007205-38, CTSA 8UL1TR000142 TL1, F30
DA037665; and Army STARRS, which is sponsored by the Department of the
Army and funded under cooperative agreement number U01MH087981 with the
US Department of Health and Human Services, National Institutes of
Health, National Institute of Mental Health (NIH/NIMH). The Yale
Biomedical Supercomputer, funded by NIH/NCRR (1 S10 RR19895-01), was
used for some analyses. The publically available datasets used for the
analyses described in this manuscript were obtained from dbGaP
(accession number phs000092.v1.p and phs000417.v2.p1). Funding support
for the Study of Addiction: Genetics and Environment (SAGE) was provided
through the NIH Genes, Environment and Health Initiative (GEI) (U01
HG004422). SAGE is one of the genome-wide association studies funded as
part of the Gene Environment Association Studies (GENEVA) under GEI.
Assistance with phenotype harmonization and genotype cleaning and with
general study coordination was provided by the GENEVA Coordinating
Center (U01 HG004446). Assistance with data cleaning was provided by the
National Center for Biotechnology Information. Support for collection of
datasets and samples was provided by the Collaborative Study on the
Genetics of Alcoholism (COGA; U10 AA008401), the Collaborative Genetic
Study of Nicotine Dependence (COGEND; P01 CA089392) and the Family Study
of Cocaine Dependence (FSCD; R01 DA013423). Funding for genotyping,
which was performed at the Johns Hopkins University Center for Inherited
Disease Research, was provided by the NIH GEI (U01HG004438), the
National Institute on Alcohol Abuse and Alcoholism, the National
Institute on Drug Abuse and the NIH contract 'High throughput genotyping
for studying the genetic contributions to human disease'
(HHSN268200782096C).
NR 80
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U1 1
U2 1
PU NATURE PUBLISHING GROUP
PI LONDON
PA MACMILLAN BUILDING, 4 CRINAN ST, LONDON N1 9XW, ENGLAND
SN 1359-4184
EI 1476-5578
J9 MOL PSYCHIATR
JI Mol. Psychiatr.
PD FEB
PY 2017
VL 22
IS 2
BP 242
EP 249
DI 10.1038/mp.2016.43
PG 8
WC Biochemistry & Molecular Biology; Neurosciences; Psychiatry
SC Biochemistry & Molecular Biology; Neurosciences & Neurology; Psychiatry
GA EK7JR
UT WOS:000394102600013
PM 27067016
ER
PT J
AU Hixon, AM
Yu, GX
Leser, JS
Yagi, S
Clarke, P
Chiu, CY
Tyler, KL
AF Hixon, Alison M.
Yu, Guixia
Leser, J. Smith
Yagi, Shigeo
Clarke, Penny
Chiu, Charles Y.
Tyler, Kenneth L.
TI A mouse model of paralytic myelitis caused by enterovirus D68
SO PLOS PATHOGENS
LA English
DT Article
ID ACUTE FLACCID MYELITIS; UNKNOWN ETIOLOGY; IDENTIFICATION; INFECTION;
CHILDREN; FEATURES; SEROTYPE; ILLNESS
AB In 2014, the United States experienced an epidemic of acute flaccid myelitis (AFM) cases in children coincident with a nationwide outbreak of enterovirus D68 (EV-D68) respiratory disease. Up to half of the 2014 AFM patients had EV-D68 RNA detected by RT-PCR in their respiratory secretions, although EV-D68 was only detected in cerebrospinal fluid (CSF) from one 2014 AFM patient. Given previously described molecular and epidemiologic associations between EV-D68 and AFM, we sought to develop an animal model by screening seven EV-D68 strains for the ability to induce neurological disease in neonatal mice. We found that four EV-D68 strains from the 2014 outbreak (out of five tested) produced a paralytic disease in mice resembling human AFM. The remaining 2014 strain, as well as 1962 prototype EV-D68 strains Fermon and Rhyne, did not produce, or rarely produced, paralysis in mice. In-depth examination of the paralysis caused by a representative 2014 strain, MO/14-18947, revealed infectious virus, virion particles, and viral genome in the spinal cords of paralyzed mice. Paralysis was elicited in mice following intramuscular, intracerebral, intraperitoneal, and intranasal infection, in descending frequency, and was associated with infection and loss of motor neurons in the anterior horns of spinal cord segments corresponding to paralyzed limbs. Virus isolated from spinal cords of infected mice transmitted disease when injected into naive mice, fulfilling Koch's postulates in this model. Finally, we found that EV-D68 immune sera, but not normal mouse sera, protected mice from development of paralysis and death when administered prior to viral challenge. These studies establish an experimental model to study EV-D68-induced myelitis and to better understand disease pathogenesis and develop potential therapies.
C1 [Hixon, Alison M.] Univ Colorado, Sch Med, Med Sci Training Program, Boulder, CO 80309 USA.
[Hixon, Alison M.] Univ Colorado, Sch Med, Aurora, CO 80309 USA.
[Yu, Guixia; Chiu, Charles Y.] Univ Calif San Francisco, Dept Lab Med & Med, Div Infect Dis, San Francisco, CA USA.
[Yu, Guixia; Chiu, Charles Y.] Univ Calif San Francisco, UCSF Abbott Viral Diagnost & Discovery Ctr, San Francisco, CA 94143 USA.
[Leser, J. Smith; Clarke, Penny; Tyler, Kenneth L.] Univ Colorado, Sch Med, Dept Neurol, Aurora, CO 80309 USA.
[Yagi, Shigeo] Calif Dept Publ Hlth, Richmond, CA USA.
[Tyler, Kenneth L.] Denver VA Med Ctr, Denver, CO USA.
[Tyler, Kenneth L.] Univ Colorado, Sch Med, Dept Immunol & Microbiol, Boulder, CO 80309 USA.
[Tyler, Kenneth L.] Univ Colorado, Sch Med, Dept Med, Boulder, CO 80309 USA.
RP Tyler, KL (reprint author), Univ Colorado, Sch Med, Dept Neurol, Aurora, CO 80309 USA.; Tyler, KL (reprint author), Denver VA Med Ctr, Denver, CO USA.; Tyler, KL (reprint author), Univ Colorado, Sch Med, Dept Immunol & Microbiol, Boulder, CO 80309 USA.; Tyler, KL (reprint author), Univ Colorado, Sch Med, Dept Med, Boulder, CO 80309 USA.
EM ken.tyler@ucdenver.edu
OI Chiu, Charles/0000-0003-2915-2094
FU United States National Institutes of Health [RO1-NS076512, R33-AI101064,
R01-HL105704]; United States Department of Veterans Affairs
[101BX000963]; University of California San Francisco (UCSF)-Abbott
Pathogen Discovery Award
FX We would like to acknowledge support by grants (to KLT) from the United
States National Institutes of Health (https://www.nih.gov/)
(RO1-NS076512, R33-AI101064) and United States Department of Veterans
Affairs (http://www.va.gov/) merit grant support (101BX000963). This
study was also supported in part by grants (to CYC) from the United
States National Institutes of Health (R01-HL105704) and a University of
California San Francisco (UCSF)-Abbott Pathogen Discovery Award. The
funders had no role in study design, data collection and analysis,
decision to publish, or preparation of the manuscript.
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PU PUBLIC LIBRARY SCIENCE
PI SAN FRANCISCO
PA 1160 BATTERY STREET, STE 100, SAN FRANCISCO, CA 94111 USA
SN 1553-7366
EI 1553-7374
J9 PLOS PATHOG
JI PLoS Pathog.
PD FEB
PY 2017
VL 13
IS 2
AR e1006199
DI 10.1371/journal.ppat.1006199
PG 19
WC Microbiology; Parasitology; Virology
SC Microbiology; Parasitology; Virology
GA EN1BH
UT WOS:000395744700023
ER
PT J
AU Ma, RS
Morshed, SA
Latif, R
Davies, TF
AF Ma, Risheng
Morshed, Syed A.
Latif, Rauf
Davies, Terry F.
TI TAZ Induction Directs Differentiation of Thyroid Follicular Cells from
Human Embryonic Stem Cells
SO THYROID
LA English
DT Article
DE thyroid follicular cells; human embryonic stem cells; NK2 homeobox 1
(NKX2-1); Paired box gene 8 (PAX8); transcriptional co-activator with
PDZ-binding motif (TAZ); ethacridine
ID SYNERGISTICALLY ACTIVATE; TRANSCRIPTION FACTOR-1; COACTIVATOR; PAX8;
ENDODERM; MORPHOGENESIS; ENHANCER; PROTEIN; TTF-1; GLAND
AB Objective: The differentiation program for human thyroid follicular cells (TFCs) relies on the interplay between sequence-specific transcription factors and transcriptional co-regulators. Transcriptional co-activator with PDZbinding motif (TAZ) is a co-activator that regulates several transcription factors, including PAX8 and NKX2-1, which play a central role in thyroid-specific gene transcription. TAZ and PAX8/ NKX2-1 are co-expressed in the nuclei of thyroid cells, and TAZ interacts directly with both PAX8 and NKX2-1, leading to their enhanced transcriptional activity on the thyroglobulin (TG) promoter and additional genes.
Methods: The use of a small molecule, ethacridine, recently identified as a TAZ activator, in the differentiation of thyroid cells from human embryonic stem (hES) cells was studied. First, endodermal cells were derived from hES cells using Activin A, followed by induction of differentiation into thyroid cells directed by ethacridine and thyrotropin (TSH).
Results: The expression of TAZ was increased in the Activin A-derived endodermal cells by ethacridine in a dose-dependent manner and followed by increases in PAX8 and NKX2-1 when assessed by both quantitative polymerase chain reaction and immunostaining. Following further differentiation with the combination of ethacridine and TSH, the thyroid-specific genes TG, TPO, TSHR, and NIS were all induced in the differentiated hES cells. When these cells were cultured with extracellular matrix-coated dishes, thyroid follicle formation and abundant TG protein expression were observed. Furthermore, such hES cell-derived thyroid follicles showed a marked TSH-induced and dose-dependent increase in radioiodine uptake and protein-bound iodine accumulation.
Conclusion: These data show that fully functional human thyroid cells can be derived from hES cells using ethacridine, a TAZ activator, which induces thyroid-specific gene expression and promotes thyroid cell differentiation from the hES cells. These studies again demonstrate the importance of transcriptional regulation in thyroid cell development. This approach also yields functional human thyrocytes, without any gene transfection or complex culture conditions, by directly manipulating the transcriptional machinery without interfering with intermediate signaling events.
C1 Mt Sinai Beth Israel Med Ctr, Icahn Sch Med Mt Sinai, Dept Med, Thyroid Res Unit, New York, NY USA.
James J Peters VA Med Ctr, New York, NY USA.
RP Ma, RS (reprint author), Icahn Sch Med Mt Sinai, 1 Gustave L Levy Pl BOX 1055, New York, NY 10029 USA.
EM risheng.ma@mssm.edu
FU National Institutes of Health [DK069713]; David Owen Segal Endowment; VA
Merit Review Program
FX Supported in part by DK069713 from the National Institutes of Health,
the David Owen Segal Endowment, and the VA Merit Review Program (to
T.F.D.).
NR 27
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U1 0
U2 0
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1050-7256
EI 1557-9077
J9 THYROID
JI Thyroid
PD FEB
PY 2017
VL 27
IS 2
BP 292
EP 299
DI 10.1089/thy.2016.0264
PG 8
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EK6RK
UT WOS:000394051600019
PM 27829313
ER
PT J
AU Seger, CD
He, XM
Braverman, LE
Yeh, MW
Bernet, VJ
Singh, RJ
Rhee, CM
Leung, AM
AF Seger, Christian D.
He, Xuemei
Braverman, Lewis E.
Yeh, Michael W.
Bernet, Victor J.
Singh, Ravinder J.
Rhee, Connie M.
Leung, Angela M.
TI Negligible Thyroid Hormone Content Present in Nonprescription U. S.
Weight Loss Products
SO THYROID
LA English
DT Letter
C1 [Yeh, Michael W.] Sect Endocrine Surg, Los Angeles, CA USA.
[Leung, Angela M.] Div Endocrinol, Los Angeles, CA USA.
[Seger, Christian D.; Yeh, Michael W.] Univ Calif Los Angeles, David Geffen Sch Med, Los Angeles, CA 90095 USA.
[He, Xuemei; Braverman, Lewis E.] Boston Univ, Sch Med, Sect Endocrinol Diabet & Nutr, Boston, MA 02118 USA.
[Bernet, Victor J.] Mayo Clin Florida, Div Endocrinol, Jacksonville, FL USA.
[Singh, Ravinder J.] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN USA.
[Rhee, Connie M.] Univ Calif Irvine, Div Nephrol & Hypertens, Irvine, CA USA.
[Leung, Angela M.] VA Greater Los Angeles Healthcare Syst, Div Endocrinol, 111D,11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
RP Leung, AM (reprint author), VA Greater Los Angeles Healthcare Syst, Div Endocrinol, 111D,11301 Wilshire Blvd, Los Angeles, CA 90073 USA.
EM amleung@mednet.ucla.edu
FU NIH [K23HD068552]
FX Supported by NIH K23HD068552 (A.M.L.).
NR 3
TC 0
Z9 0
U1 0
U2 0
PU MARY ANN LIEBERT, INC
PI NEW ROCHELLE
PA 140 HUGUENOT STREET, 3RD FL, NEW ROCHELLE, NY 10801 USA
SN 1050-7256
EI 1557-9077
J9 THYROID
JI Thyroid
PD FEB
PY 2017
VL 27
IS 2
BP 300
EP 301
DI 10.1089/thy.2016.0534
PG 2
WC Endocrinology & Metabolism
SC Endocrinology & Metabolism
GA EK6RK
UT WOS:000394051600020
PM 27897088
ER
EF