基因决定的血小板反应性的临床影响。

Clinical impact of genetically determined platelet reactivity.

机构信息

Département de Cardiologie, Centre Hospitalo-Universitaire Nord, Chemin des Bourrely, Marseille, France.

出版信息

J Cardiovasc Transl Res. 2013 Jun;6(3):398-403. doi: 10.1007/s12265-012-9421-4. Epub 2012 Nov 13.

Abstract

Dual antiplatelet therapy with aspirin and clopidogrel dramatically reduced the rate of major adverse cardiac events following percutaneous coronary intervention. Clopidogrel is a prodrug which requires a two-step hepatic biotransformation thanks to the cytochrome P450 (CYP450) enzyme system. Genetic polymorphism of CYP450 system (e.g., CYP2C19*2) responsible for altered clopidogrel metabolism is a major cause of high on-treatment platelet reactivity (HTPR), which translates into thrombotic events in stented patients. Studies demonstrated that HTPR could be overcome in poor metabolizers thanks to increased loading doses or maintenance doses of clopidogrel or with the use of more potent antiplatelet agents such as prasugrel. Other genetic polymorphisms have also been correlated with HTPR: ABCB1, ATP2B2, and TIAM2. Large-scale randomized trials with clinical endpoints remain necessary to determine the optimal antiplatelet therapy in patients carrying genetic polymorphism associated with HTPR and thrombotic events.

摘要

双重抗血小板治疗,即阿司匹林联合氯吡格雷,可显著降低经皮冠状动脉介入治疗后主要不良心脏事件的发生率。氯吡格雷是一种前体药物,需要细胞色素 P450(CYP450)酶系统的两步肝生物转化。CYP450 系统(如 CYP2C19*2)的遗传多态性负责改变氯吡格雷的代谢,是导致治疗中血小板高反应性(HTPR)的主要原因,这会导致支架置入患者发生血栓事件。研究表明,在代谢不良者中,可以通过增加氯吡格雷的负荷剂量或维持剂量,或使用更强效的抗血小板药物如普拉格雷来克服 HTPR。其他遗传多态性也与 HTPR 相关:ABCB1、ATP2B2 和 TIAM2。仍需要进行大规模随机临床试验,以确定与 HTPR 和血栓事件相关的遗传多态性患者的最佳抗血小板治疗方案。

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