Universitäts-Herzzentrum Freiburg-Bad Krozingen, Klinik für Kardiologie und Angiologie II, Bad Krozingen, Germany.
Clin Pharmacol Ther. 2012 Oct;92(4):476-85. doi: 10.1038/clpt.2012.133. Epub 2012 Sep 5.
Dual antiplatelet therapy with aspirin and clopidogrel is the accepted standard for prevention of ischemic complications after percutaneous coronary intervention and has been shown to reduce cardiovascular events in patients with acute coronary syndromes (ACSs). There is substantial interindividual variability in antiplatelet response to clopidogrel. Various clinical studies have demonstrated that patients with high on-clopidogrel platelet reactivity incur an increased risk for ischemic events. In recent years, several clinical and demographic variables as well as multiple genetic factors contributing to the variability in antiplatelet response to clopidogrel have been identified. We discuss strategies based on platelet function testing or genotyping for improvement of antiplatelet effects of clopidogrel and thereby clinical outcome.
双联抗血小板治疗(阿司匹林+氯吡格雷)是经皮冠状动脉介入治疗后预防缺血性并发症的标准治疗方法,已被证实可降低急性冠状动脉综合征(ACS)患者的心血管事件风险。氯吡格雷的抗血小板反应存在很大的个体间差异。多项临床研究表明,氯吡格雷高血小板反应性患者发生缺血事件的风险增加。近年来,已确定了多种与氯吡格雷抗血小板反应变异性相关的临床和人口统计学变量以及多种遗传因素。我们讨论了基于血小板功能检测或基因分型的策略,以改善氯吡格雷的抗血小板作用,从而改善临床结局。