Pharmacogenomics of Anti-platelet and Anti-coagulation Therapy

被引:10
|
作者
Fisch, Adam S. [1 ,2 ,3 ]
Perry, Christina G. [3 ]
Stephens, Sarah H. [3 ]
Horenstein, Richard B. [3 ]
Shuldiner, Alan R. [3 ]
机构
[1] Univ Maryland, Sch Med, Dept Med, Div Endocrinol Diabet & Nutr, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Program Personalized & Genom Med, Baltimore, MD 21201 USA
[3] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
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; PERCUTANEOUS CORONARY INTERVENTION; CLOPIDOGREL PLATELET REACTIVITY; IMPLEMENTATION CONSORTIUM GUIDELINES; ADVERSE CLINICAL-OUTCOMES; GENETIC POLYMORPHISMS; CYP2C19; GENOTYPE; RESPONSE VARIABILITY; STENT THROMBOSIS; CARDIOVASCULAR OUTCOMES; ADENOSINE-DIPHOSPHATE;
D O I
10.1007/s11886-013-0381-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
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.
引用
收藏
页数:12
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