Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/130248
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Type: Journal article
Title: Adrenergic-pathway gene variants influence beta-blockerrelated outcomes after acute coronary syndrome in a race-specific manner
Author: Cresci, S.
Dorn, G.W.
Jones, P.G.
Beitelshees, A.L.
Li, A.Y.
Lenzini, P.A.
Province, M.A.
Spertus, J.A.
Lanfear, D.E.
Citation: Journal of the American College of Cardiology, 2012; 60(10):898-907
Publisher: Elsevier
Issue Date: 2012
ISSN: 0735-1097
1558-3597
Statement of
Responsibility: 
Sharon Cresci, Gerald W. Dorn, Philip G. Jones, Amber L. Beitelshees, Allie Y. Li ... John Spertus ... et al.
Abstract: Overcoming racial differences in acute coronary syndrome (ACS) outcomes is a strategic goal for U.S. health care. Genetic polymorphisms in the adrenergic pathway seem to explain some outcome differences by race in other cardiovascular diseases treated with β-adrenergic receptor blockade (BB). Whether these genetic variants are associated with survival among ACS patients treated with BB, and if this differs by race, is unknown.β-adrenergic receptor blockade after ACS is a measure of quality care, but the effectiveness across racial groups is less clear.A prospective cohort of 2,673 ACS patients (2,072 Caucasian; 601 African-American) discharged on BB from 22 U.S. hospitals were followed for 2 years. Subjects were genotyped for polymorphisms in ADRB1, ADRB2, ADRA2C, and GRK5. We used proportional hazards regression to model the effect of genotype on mortality, stratified by race and adjusted for baseline factors.The overall 2-year mortality rate was 7.5% for Caucasians and 16.7% for African Americans. The prognosis associated with different genotypes in these BB-treated patients differed by race. In Caucasians, ADRA2C 322-325 deletion carriers had significantly lower mortality as compared with homozygous individuals lacking the deletion (hazard ratio: 0.46; confidence interval [CI]: 0.21 to 0.99; p = 0.047; race × genotype interaction p = 0.053). In African Americans, the ADRB2 16R allele was associated with significantly increased mortality (hazard ratio for RG vs. GG: 2.10; CI: 1.14 to 3.86; RR vs. GG: 2.65; CI: 1.38 to 5.08; p = 0.013; race × genotype interaction p = 0.096).Adrenergic pathway polymorphisms are associated with mortality in ACS patients receiving BB in a race-specific manner. Understanding the mechanism by which different genes impact post-ACS mortality differently in Caucasians and African Americans might illuminate opportunities to improve BB therapy in these groups.
Keywords: Beta-blocker therapy; pharmacogenetics; racial disparities
Rights: © 2012 by the American College of Cardiology Foundation
RMID: 0030104500
DOI: 10.1016/j.jacc.2012.02.051
Appears in Collections:Medicine publications

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