Pharmacogenomic considerations for antiplatelet agents: the era of precision medicine in stroke prevention and neurointerventional practice

被引:4
|
作者
Bonney, Phillip A. [1 ]
Yim, Benjamin [1 ]
Brinjikji, Waleed [2 ,3 ]
Walcott, Brian P. [1 ]
机构
[1] Univ Southern Calif, Dept Neurol Surg, Los Angeles, CA 90033 USA
[2] Mayo Clin, Dept Neurosurg, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Radiol, Rochester, MN 55905 USA
来源
关键词
PERCUTANEOUS CORONARY INTERVENTION; CLOPIDOGREL PLATELET REACTIVITY; ASPIRIN RESISTANCE; CYP2C19; GENOTYPE; GENETIC-VARIANTS; CARDIOVASCULAR OUTCOMES; MYOCARDIAL-INFARCTION; CLINICAL EVENTS; INCREASED RISK; DOUBLE-BLIND;
D O I
10.1101/mcs.a003731
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Antiplatelet drugs are widely utilized in the setting of primary stroke prevention, secondary stroke prevention, and neuroendovascular device-related stroke prevention. These medications are effective in general, although significant variability in drug activity exists between patients. Although this variation may be related in part to a multitude of factors, a growing body of evidence suggests that individual genotypes are a main contributor. The PharmGKB database was mined to prioritize genetic variants with potential clinical relevance for response to aspirin, clopidogrel, prasugrel, and ticagrelor. Although variants were reported for all drugs, the highest level of evidence was found in cytochrome P450 (CYP450) genotype variation related to clopidogrel response. Individual genetic influences have an impact on the pharmacodynamics of antiplatelet agents. Current clinical practice for stroke prevention is primarily empiric or guided by functional assays; however, there now exists a third potential pathway to base treatment decisions: genotype-guided treatment.
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页数:13
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