Genetic Variation in PEAR1 Is Associated With Platelet Aggregation and Cardiovascular Outcomes

Author:

Lewis Joshua P.1,Ryan Kathleen1,O’Connell Jeffrey R.1,Horenstein Richard B.1,Damcott Coleen M.1,Gibson Quince1,Pollin Toni I.1,Mitchell Braxton D.1,Beitelshees Amber L.1,Pakzy Ruth1,Tanner Keith1,Parsa Afshin1,Tantry Udaya S.1,Bliden Kevin P.1,Post Wendy S.1,Faraday Nauder1,Herzog William1,Gong Yan1,Pepine Carl J.1,Johnson Julie A.1,Gurbel Paul A.1,Shuldiner Alan R.1

Affiliation:

1. From the Division of Endocrinology, Diabetes, and Nutrition (J.P.L., K.R., J.R.O’C., R.B.H., C.M.D., Q.G., T.I.P., B.D.M., A.L.B., R.P., K.T., A.R.S.) and Division of Nephrology (A.P.), University of Maryland School of Medicine, Baltimore; Sinai Center for Thrombosis Research, Sinai Hospital of Baltimore, Baltimore, MD (U.S.T., K.P.B., W.H., P.A.G.); Division of Cardiology, Department of Medicine (W.S.P., W.H.) and Department of Anesthesiology and Critical Care Medicine (N.F.), Johns Hopkins...

Abstract

Background— Aspirin or dual antiplatelet therapy with aspirin and clopidogrel is a standard therapy for patients who are at increased risk for cardiovascular events. However, the genetic determinants of variable response to aspirin (alone and in combination with clopidogrel) are not known. Methods and Results— We measured ex vivo platelet aggregation before and after dual antiplatelet therapy in individuals (n=565) from the Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study and conducted a genome-wide association study of drug response. Significant findings were extended by examining genotype and cardiovascular outcomes in 2 independent aspirin-treated cohorts: 227 percutaneous coronary intervention patients and 1000 patients of the International Verapamil SR/Trandolapril Study (INVEST) Genetic Substudy (INVEST-GENES). Results from the genome-wide association study revealed a strong association between single-nucleotide polymorphisms on chromosome 1q23 and post–dual antiplatelet therapyplatelet aggregation. Further genotyping revealed rs12041331 in the platelet endothelial aggregation receptor-1 ( PEAR1 ) gene to be most strongly associated with dual antiplatelet therapy response ( P =7.66×10 −9 ). In white and black patients undergoing percutaneous coronary intervention, A-allele carriers of rs12041331 were more likely to experience a cardiovascular event or death compared with GG homozygotes (hazard ratio, 2.62; 95% confidence interval, 0.96–7.10; P =0.059; and hazard ratio, 3.97; 95% confidence interval, 1.10–14.31; P =0.035, respectively). In aspirin-treated INVEST-GENES patients, rs12041331 A-allele carriers had significantly increased risk of myocardial infarction compared with GG homozygotes (odds ratio, 2.03; 95% confidence interval, 1.01–4.09; P =0.048). Conclusion— Common genetic variation in PEAR1 may be a determinant of platelet response and cardiovascular events in patients on aspirin alone or in combination with clopidogrel. Clinical Trial Registration— URL: http://www.clinicaltrials.gov . Unique identifiers: NCT00799396 and NCT00370045

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Cardiology and Cardiovascular Medicine,Genetics

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3