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首页> 外文期刊>Pharmacogenetics and genomics >Impact of the CYP2C19*17 polymorphism on the clinical outcome of clopidogrel therapy in Asian patients undergoing percutaneous coronary intervention
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Impact of the CYP2C19*17 polymorphism on the clinical outcome of clopidogrel therapy in Asian patients undergoing percutaneous coronary intervention

机译:CYP2C19 * 17基因多态性对经皮冠状动脉介入治疗的亚洲患者氯吡格雷治疗的临床结局的影响

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The impact of the CYP2C19*17 polymorphism on the clinical outcome in Asians undergoing percutaneous coronary intervention (PCI) is unknown. We sought to assess the long-term impact of CYP2C19*17 on the risk for adverse clinical events in 2188 Korean patients taking clopidogrel after PCI. The prevalence of the CYP2C19*17 allele [*wt/*17: 2.4% (n=53), *17/*17: 0%] was very low. The 2-year cumulative event rates for bleeding [*wt/*17 vs. *wt/*wt: 2 vs. 2.3%; adjusted hazard ratio (HR), 1.23; 95% confidence interval (CI), 0.16-9.45], stent thrombosis (2 vs. 1.1%; HR, 3.98; 95% CI, 0.49-31.6) or composite of any death, and myocardial infarction or stroke (5.4 vs. 7.1%; HR, 1.37; 95% CI, 0.32-5.73) did not differ on the basis of the presence of CYP2C19*17. In conclusion, in our study population of Asian patients, the CYP2C19*17 polymorphism was not associated with adverse clinical outcomes after PCI because of its low prevalence, the rarity of homozygotes, and the relatively low rate of adverse clinical events.
机译:CYP2C19 * 17基因多态性对接受经皮冠状动脉介入治疗(PCI)的亚洲人临床结局的影响尚不清楚。我们试图评估CYP2C19 * 17对2188例接受PCI后服用氯吡格雷的韩国患者不良临床事件风险的长期影响。 CYP2C19 * 17等位基因[* wt / * 17:2.4%(n = 53),* 17 / * 17:0%]的患病率非常低。 2年累积出血事件发生率[* wt / * 17对* wt / * wt:2对2.3%;调整后的危险比(HR)为1.23; 95%置信区间(CI)为0.16-9.45],支架内血栓形成(2比1.1%; HR为3.98; 95%CI为0.49-31.6)或任何死亡的复合物,以及心肌梗塞或中风(5.4比7.1) %; HR,1.37; 95%CI,0.32-5.73)基于CYP2C19 * 17的存在没有差异。综上所述,在我们的亚洲患者研究人群中,CYP2C19 * 17基因多态性与PCI后的不良临床预后无关,因为其患病率低,纯合子稀有且不良临床事件发生率相对较低。

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