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[评估氯吡格雷的生物学疗效:基因型还是表型?]

[Evaluating the biological efficacy of clopidogrel: genotype or phenotype?].

作者信息

Fontana Pierre, Bonvini Robert F, Roffi Marco, Boehlen Françoise, Reber Guido, de Moerloose Philippe, Reny Jean-Luc

机构信息

Service d'angiologie et d'hémostase, HUG, Genève.

出版信息

Rev Med Suisse. 2010 Feb 10;6(235):302-5.

Abstract

Clopidogrel has a known biological variability that has been consistently associated with recurrence of coronary ischemic events in clinical studies. Among the tests that are currently available, quantification of the phosphorylation status of the vasodilator phosphoprotein (VASP assay) is probably the most specific assay to evaluate the inhibition of the P2Y12 receptor by clopidogrel. A genetic polymorphism of the cytochrome 2C19 has been associated with the biological efficacy of clopidogrel and is also associated with recurrent ischemic events. The VASP assay and the 2C19 genotyping are candidates for the identification of patients at risk; this is the focus of the present review.

摘要

氯吡格雷存在已知的生物学变异性,在临床研究中这种变异性一直与冠状动脉缺血事件的复发相关。在目前可用的检测方法中,血管舒张磷蛋白磷酸化状态的定量检测(VASP检测)可能是评估氯吡格雷对P2Y12受体抑制作用的最特异性检测方法。细胞色素2C19的基因多态性与氯吡格雷的生物学疗效相关,也与复发性缺血事件相关。VASP检测和2C19基因分型是识别高危患者的候选方法;这是本综述的重点。

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