Department of Cardiology, Patras University Hospital, Rion 26500, Patras, Greece.
Curr Pharm Des. 2013;19(13):2489-95. doi: 10.2174/1381612811319130017.
CYP2C19 is one of the principal enzymes involved in the metabolism of clopidogrel. The genes encoding CYP enzymes are polymorphic, with common alleles conferring reduced function. A loss-of-function allele, CYP2C19*2, is associated with an increased risk of major adverse cardiovascular events, particularly stent thrombosis, in patients with acute coronary syndromes who are receiving clopidogrel, especially among those undergoing percutaneous coronary intervention. Newer, more potent P2Y12 inhibitors like prasugrel and ticagrelor have been introduced recently in the daily clinical practice with better cardiovascular outcome in these patients. The purpose of this review article is to provide information regarding the clinical use of CYP2C19 genotyping in patients requiring antiplatelet therapy.
CYP2C19 是参与氯吡格雷代谢的主要酶之一。编码 CYP 酶的基因具有多态性,常见等位基因导致功能降低。一种失活等位基因 CYP2C19*2 与接受氯吡格雷治疗的急性冠脉综合征患者发生主要不良心血管事件(尤其是支架血栓形成)的风险增加相关,尤其是在接受经皮冠状动脉介入治疗的患者中。最近,在日常临床实践中引入了新型、更强效的 P2Y12 抑制剂,如普拉格雷和替格瑞洛,这些药物可改善此类患者的心血管结局。本文综述的目的是提供有关需要抗血小板治疗的患者 CYP2C19 基因分型的临床应用信息。