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Comparison Between Clopidogrel and Prasugrel Associated With CYP2C19 Genotypes in Patients Receiving Percutaneous Coronary Intervention in a Japanese Population

机译:在日本人群中接受经皮冠状动脉介入的患者CYP2C19基因型的氯吡格雷和普拉塞尔的比较

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Background: The association between cytochrome P450 (CYP) 2C19 genotypes and adverse events in patients treated with clopidogrel or prasugrel after percutaneous coronary intervention (PCI) in the Japanese population is unclear. Methods?and?Results: This study consisted of 1,580 patients whose CYP2C19 genotypes were assessed at Shiga University of Medical Science Hospital, and 193 clopidogrel-treated and 217 prasugrel-treated patients who were followed more than 1 year after receiving PCI were analyzed. Among 1,580 patients, the prevalence of normal, intermediate, and poor metabolizers was 32%, 49%, and 17%, respectively. Overall incidence of the primary outcome, defined as a composite of cardiovascular death, myocardial infarction, definite stent thrombosis, ischemic stroke, or major bleeding was not significantly different between the clopidogrel and prasugrel groups (adjusted hazard ratio [HR] 1.98, 95% confidence interval [CI] 0.85–4.61, P=0.12). Among patients with the CYP2C19 loss-of-function (LOF) allele, however, the incidence of the primary outcome was significantly higher in the clopidogrel group (adjusted HR 3.19, 95% CI 1.10–9.24, P=0.03), whereas no difference was observed among patients without the CYP2C19 LOF allele (adjusted HR 0.67, 95% CI 0.14–3.26, P=0.62). Conclusions: Among patients with the CYP2C19 LOF allele, the use of clopidogrel was significantly associated with increased adverse events. Thus, further investigation is needed to establish the practical use of CYP2C19 genotyping.
机译:背景:日本人口经皮冠状动脉干预(PCI)在经皮冠状动脉介入(PCI)后,细胞色素P450(CYP)2C19基因型和不良事件的关联尚不清楚。方法?结果:该研究由1,580名患者组成,在滋贺医学院大学评估了1,580名患者,并分析了接受PCI后1年以上的氯吡格雷治疗和217名普拉布雷治疗的患者。在1,580名患者中,正常,中间体和差的代谢剂患病率分别为32%,49%和17%。主要结果的总发生率,定义为心血管死亡,心肌梗死,明确支架血栓形成,缺血性卒中或重大出血之间的综合性(调整后危险比[HR] 1.98,95%信心)没有显着差异间隔[CI] 0.85-4.61,P = 0.12)。然而,在CYP2C19的患者中,氯吡格雷基团的初级结果的发生率显着高(调节的HR 3.19,95%CI 1.10-9.24,P = 0.03),而没有差异在没有CYP2C19 LOF等位基因(调节的HR 0.67,95%CI 0.14-3.26,P = 0.62)的患者之间观察到。结论:CYP2C19 LOF等位基因患者,氯吡格雷的使用与增加的不良事件显着相关。因此,需要进一步调查来建立CYP2C19基因分型的实际使用。

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