Association between P2RY12 gene polymorphisms and adverse clinical events in coronary artery disease patients treated with clopidogrel: A systematic review and meta-analysis

Abstract Objective Investigate the association between P2Y12 Purinoceptor ( P2RY12 ) polymorphisms and adverse clinical events in coronary artery disease (CAD) patients treated with clopidogrel. Methods We performed a comprehensive database search, with a particular focus on P2RY12 polymorphisms and their effects on clopidogrel-treated CAD patients, in the PubMed, EMBASE, Cochrane Library, clinicaltrials.gov , Web of Science, and Chinese databases from their inceptions to April 8, 2017. The primary endpoints were composite ischemic events (including cardiovascular and cerebrovascular ischemic events), the secondary endpoints were independent cardiovascular events (mortality, non-fatal myocardial infarction, stent thrombosis, unstable angina, and target vessel revascularization) and the safety endpoints were bleeding events. Results Overall 10 studies and 10,810 clopidogrel-treated CAD patients were studied in the present work. Subjects of the common alleles of P2RY12 polymorphisms showed higher risk for composite ischemic events compared to non-carriers ( n  = 434 of 3268[13.3%] vs. n  = 646 of 6133[10.5%]; RR: 1.39, 95%CI: 1.14–1.69; p  = 0.001). These allele carriers also showed increased risk for stent thrombosis (RR: 2.67, 95%CI: 1.03–6.91; p  = 0.04), myocardial infarction (RR: 1.60, 95%CI: 1.06–2.42; p  = 0.03), and unstable angina (RR: 1.72, 95%CI: 1.37–2.16; p p  = 0.29; p  = 0.48, respectively). Conclusions P2RY12 gene polymorphisms might associate with higher risk of composite ischemic events, stent thrombosis, non-fatal myocardial infarction, unstable angina. While we found no significant effect on mortality, target vessel revascularization or bleeding.