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ABSTRACT: Context
Clopidogrel therapy improves cardiovascular outcomes in patients with acute coronary syndromes and following percutaneous coronary intervention by inhibiting adenosine diphosphate (ADP)-dependent platelet activation. However, nonresponsiveness is widely recognized and is related to recurrent ischemic events.Objective
To identify gene variants that influence clopidogrel response.Design, setting, and participants
In the Pharmacogenomics of Antiplatelet Intervention (PAPI) Study (2006-2008), we administered clopidogrel for 7 days to 429 healthy Amish persons and measured response by ex vivo platelet aggregometry. A genome-wide association study was performed followed by genotyping the loss-of-function cytochrome P450 (CYP) 2C19*2 variant (rs4244285). Findings i
SUBMITTER: Shuldiner AR
PROVIDER: S-EPMC3641569 | biostudies-literature | 2009 Aug
REPOSITORIES: biostudies-literature