Personalizing Antiplatelet Therapy With Clopidogrel

被引:12
|
作者
Trenk, D. [1 ]
Zolk, O. [2 ]
Fromm, M. F. [2 ]
Neumann, F-J [1 ]
Hochholzer, W. [1 ]
机构
[1] Univ Herzzentrum Freiburg Bad Krozingen, Klin Kardiol & Angiol 2, Bad Krozingen, Germany
[2] Univ Erlangen Nurnberg, Inst Expt & Clin Pharmacol & Toxicol, D-91054 Erlangen, Germany
关键词
PERCUTANEOUS CORONARY INTERVENTION; OF-FUNCTION POLYMORPHISM; PLATELET REACTIVITY; CYP2C19; GENOTYPE; RESPONSE VARIABILITY; CLINICAL-OUTCOMES; GENETIC-VARIANTS; CARDIOVASCULAR EVENTS; MAJOR DETERMINANT; DOSE CLOPIDOGREL;
D O I
10.1038/clpt.2012.133
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:476 / 485
页数:10
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