Abstract

BackgroundThe cytochrome P450 (CYP450) 2C19 681 genotypes affect the antiplatelet activity of clopidogrel. We investigated the correlation of CYP 2C19 681G > A mutation with clopidogrel resistance (CR). Additionally, we studied the effect of CR on clinical prognosis of patients with acute coronary syndrome (ACS).MethodsOne hundred ten ACS patients undergoing percutaneous coronary intervention, who were followed-up for 1 year, were included in the study. The patients were co-administered aspirin 100 mg/d and clopidogrel 75mg/d following a loading dose of 300 mg. CR was assessed on the basis of polymorphism observed in the CYP2C19 subgroup.ResultsPatients in GG genotype group exhibited greater inhibition of platelet aggregation than patients in GA and AA genotype groups (16.2 ± 10.1%; 10.2 ± 9.9%; 8.0 ± 5.9%, respectively, p < 0.01). CYP2C19 681GG genotype group was associated with lower CR than CYP2C19 681A allele (GA + AA) group (9/59 vs. (12+5)/51; p = 0.009). Over a follow-up of 12 months, the incidence of recurrent angina, acute myocardial infarction, and intra-stent thrombosis in CYP2C19 681 GG carriers was significantly lower than that in CYP2C19 681A allele (GA + AA) group (2/59 vs. 8/51, 1/59 vs. 6/51, 0 vs. 4/51, respectively, p < 0.05).ConclusionCYP 2C19*2 is associated with reduced clopidogrel antiplatelet activity and might be an important marker for poor prognosis of ACS.

Highlights

  • Clopidogrel, which irreversibly inhibits the adenosine diphosphate (ADP) platelet receptor P2Y12, has been widely used in preventing thromboembolic events in patients with acute coronary syndrome (ACS)

  • We investigated the correlation of CYP 2C19 681G > A mutation with clopidogrel resistance (CR)

  • We studied the effect of CR on clinical prognosis of patients with acute coronary syndrome (ACS)

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Summary

Introduction

Clopidogrel, which irreversibly inhibits the adenosine diphosphate (ADP) platelet receptor P2Y12, has been widely used in preventing thromboembolic events in patients with acute coronary syndrome (ACS). Various studies have demonstrated that the rate of clopidogrel resistance (CR) ranges 4.2–27.8% [1,2]. The findings from another study [5] were not in line with the current investigation, and did not show any influence of the CYP2C19 genotype on the antiplatelet effect after loading with 600 mg clopidogrel in patients with coronary artery disease. Bhatt et al [6] demonstrated no relationship between CYP2C19 genotype and ischemic events with clinically evident cardiovascular disease or multiple risk factors in patients treated with clopidogrel. The cytochrome P450 (CYP450) 2C19 681 genotypes affect the antiplatelet activity of clopidogrel. We investigated the correlation of CYP 2C19 681G > A mutation with clopidogrel resistance (CR). We studied the effect of CR on clinical prognosis of patients with acute coronary syndrome (ACS)

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