James Stein

Dr. James Stein

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2008 in Journal of the American Society of Echocardiography
Verified
Journal Article
Closed access
JSJames Stein
James Stein
CKClaudia E Korcarz
Claudia E Korcarz
RHR. Todd Hurst
R. Todd Hurst
ELEva Lonn
Eva Lonn
CKChristopher B. Kendall
Christopher B. Kendall
WPWendy S. Post
Wendy S. Post

29 November 2011 in Circulation
Verified
Journal Article
Closed access
SSSidney C. Smith
Sidney C. Smith
Emelia J. BenjaminEmelia J. Benjamin
Emelia J. Benjamin
RBRobert O. Bonow
Robert O. Bonow
LBLynne T. Braun
Lynne T. Braun
MCMark A. Creager
Mark A. Creager
KTKathryn A. Taubert
Kathryn A. Taubert

1 November 2011 in JACC
Verified
Journal Article
Closed access
SSSidney C. Smith
Sidney C. Smith
Emelia J. BenjaminEmelia J. Benjamin
Emelia J. Benjamin
RBRobert O. Bonow
Robert O. Bonow
LBLynne T. Braun
Lynne T. Braun
MCMark A. Creager
Mark A. Creager
KTKathryn A. Taubert
Kathryn A. Taubert

1 August 2016 in The Lancet
Verified
Journal Article
Closed access
JKJoel Kaufman
Joel Kaufman
SASara D Adar
Sara D Adar
RBR Graham Barr
R Graham Barr
MBMatthew Budoff
Matthew Budoff
GBGregory L Burke
Gregory L Burke
KWKarol E Watson
Karol E Watson

1 September 2003 in Clinical Infectious Diseases
Verified
Journal Article
Open access
PDF file
MDMichael P. Dubé
Michael P. Dubé
JSJames Stein
James Stein
JAJudith A. Aberg
Judith A. Aberg
CFCarl J. Fichtenbaum
Carl J. Fichtenbaum
JGJohn G. Gerber
John G. Gerber
ASAdult AIDS Clinical Trials Group Cardiovascular Subcommittee
Adult AIDS Clinical Trials Group Cardiovascular Subcommittee
Dyslipidemia is a common problem affecting HIV-infected patients receiving antiretroviral therapy. Since publication of preliminary guidelines in 2000 [1], nume

7 September 1999 in Circulation
Verified
Journal Article
Closed access
PDF file
JSJames Stein
James Stein
JKJon G. Keevil
Jon G. Keevil
DWDonald A. Wiebe
Donald A. Wiebe
SASusan Aeschlimann
Susan Aeschlimann
JFJohn D. Folts
John D. Folts
Background —In vitro, the flavonoid components of red wine and purple grape juice are powerful antioxidants that induce endothelium-dependent vasodilation of vascular rings derived from rat aortas and human coronary arteries. Although improved endothelial function and inhibition of LDL oxidation may be potential mechanisms by which red wine and flavonoids reduce cardiovascular risk, the in vivo effects of grape products on endothelial function and LDL oxidation have not been investigated. This study assessed the effects of ingesting purple grape juice on endothelial function and LDL susceptibility to oxidation in patients with coronary artery disease (CAD). Methods and Results —Fifteen adults with angiographically documented CAD ingested 7.7±1.2 mL · kg −1 · d −1 of purple grape juice for 14 days. Flow-mediated vasodilation (FMD) was measured using high-resolution brachial artery ultrasonography. Susceptibility of LDL particles to oxidation was determined from the rate of conjugated diene formation after exposure to copper chloride. At baseline, FMD was impaired (2.2±2.9%). After ingestion of grape juice, FMD increased to 6.4±4.7% ( P =0.003). In a linear regression model that included age, artery diameter, lipid values, and use of lipid-lowering and antioxidant therapies, the effect of grape juice on FMD remained significant (mean change 4.2±4.4%, P <0.001). After ingestion of grape juice, lag time increased by 34.5% ( P =0.015). Conclusions —Short-term ingestion of purple grape juice improves FMD and reduces LDL susceptibility to oxidation in CAD patients. Improved endothelium-dependent vasodilation and prevention of LDL oxidation are potential mechanisms by which flavonoids in purple grape products may prevent cardiovascular events, independent of alcohol content.