Pharmacogenomics of Anti-platelet and Anti-coagulation Therapy

被引:0
作者
Adam S. Fisch
Christina G. Perry
Sarah H. Stephens
Richard B. Horenstein
Alan R. Shuldiner
机构
[1] University of Maryland School of Medicine,Division of Endocrinology, Diabetes and Nutrition, Department of Medicine, and the Program in Personalized and Genomic Medicine
[2] University of Maryland School of Medicine,undefined
[3] University of Maryland School of Medicine,undefined
[4] University of Maryland School of Medicine,undefined
[5] University of Maryland School of Medicine,undefined
[6] University of Maryland School of Medicine,undefined
来源
Current Cardiology Reports | 2013年 / 15卷
关键词
Pharmacogenomics; Personalized medicine; Anti-platelet therapy; Clopidogrel; Plavix; Warfarin; Coumadin; CYP2C19; CYP2C9; VKORC1; Platelet function; Cardiovascular disease; Thrombosis; Coronary artery disease; Percutaneous coronary intervention; Anti-coagulation;
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摘要
Arterial thrombosis is a major component of vascular disease, especially myocardial infarction (MI) and stroke. Current anti-thrombotic therapies such as warfarin and clopidogrel are effective in inhibiting cardiovascular events; however, there is great inter-individual variability in response to these medications. In recent years, it has been recognized that genetic factors play a significant role in drug response, and, subsequently, common variants in genes responsible for metabolism and drug action have been identified. These discoveries along with new diagnostic targets and therapeutic strategies hold promise for more effective individualized anti-coagulation and anti-platelet therapy.
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