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首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >Biological effect of increased maintenance dose of clopidogrel in cardiovascular outpatients and influence of the cytochrome P450 2C19*2 allele on clopidogrel responsiveness.
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Biological effect of increased maintenance dose of clopidogrel in cardiovascular outpatients and influence of the cytochrome P450 2C19*2 allele on clopidogrel responsiveness.

机译:心血管门诊患者增加氯吡格雷维持剂量的生物学效应以及细胞色素P450 2C19 * 2等位基因对氯吡格雷反应性的影响。

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INTRODUCTION: The first aim of this study is to evaluate the biological effect of doubling the maintenance dose of clopidogrel in pre-defined clopidogrel "low responders", compared to the biological effect of the standard dose in "responders". The second aim is to test the influence of the CYP 2C19*2 allele on clopidogrel responsiveness. MATERIALS AND METHODS: The platelet reactivity index (PRI), based on the phosphorylation status of the vasodilatator phosphoprotein, was determined in 81 consecutive cardiovascular outpatients who had been taking clopidogrel 75 mg/day for at least 15 days (visit 1). Patients with PRI>or=50% ("low responders") were then given clopidogrel 150 mg/day. All the patients were again evaluated 15 days later (visit 2) and were genotyped for the CYP 2C19*2 allele. RESULTS: At visit 1, PRI values ranged from 12.6% to 80.4%. In "low responders" (n=45), the mean PRI fell from 62.0+/-6.7% to 49.4+/-11.3% (P<0.001) after 15 days of clopidogrel 150 mg/day, while no significant change was observed in the other patients ("responders"), who remained on the standard dose (mean PRI: 37.7+/-10.4% and 39.9+/-10.8%, P=0.22, in visit 1 and 2, respectively). The CYP 2C19*2 allele was not associated with clopidogrel responsiveness. CONCLUSIONS: Increasing the maintenance dose of clopidogrel from 75 to 150 mg/day for 15 days in "low responders" is associated with a relative 20%-increase in its biological effect, independently of the CYP2C19 genotype, but without reaching the levels observed in "responders". The CYP 2C19*2 allele is not associated with clopidogrel responsiveness in our population of cardiovascular outpatients.
机译:引言:这项研究的第一个目的是评估将标准剂量的氯吡格雷“低反应者”中的氯吡格雷维持剂量加倍的生物学效应,而不是“反应者”中标准剂量的生物效应。第二个目的是测试CYP 2C19 * 2等位基因对氯吡格雷反应性的影响。材料与方法:基于血管扩张剂磷蛋白的磷酸化状态,在81位连续每天服用氯吡格雷75 mg /天至少15天的心血管门诊患者中确定了血小板反应性指数(PRI)(访问1)。然后将PRI≥50%(“低反应者”)的患者给予氯吡格雷150 mg /天。 15天后再次评估所有患者(第2次访问),并对CYP 2C19 * 2等位基因进行基因分型。结果:在第1次访问时,PRI值的范围为12.6%至80.4%。在氯吡格雷150 mg /天的15天后,“低反应者”(n = 45)的平均PRI从62.0 +/- 6.7%降至49.4 +/- 11.3%(P <0.001),但未观察到显着变化在其他患者(“应答者”)中,他们仍保持标准剂量(平均PRI:分别在第1次和第2次访视中分别为37.7 +/- 10.4%和39.9 +/- 10.8%,P = 0.22)。 CYP 2C19 * 2等位基因与氯吡格雷反应性无关。结论:将“低应答者”中氯吡格雷的维持剂量从75毫克/天增加为15天/天,与CYP2C19基因型无关,其生物学作用相对增加20%,但未达到在CYP2C19基因型中观察到的水平。 “响应者”。在我们的心血管门诊患者中,CYP 2C19 * 2等位基因与氯吡格雷反应性无关。

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