CYP2C19型
氯吡格雷
前药
医学
药效学
药理学
药物遗传学
药代动力学
活性代谢物
药品
精密医学
养生
内科学
阿司匹林
生物
基因型
遗传学
病理
基因
细胞色素P450
新陈代谢
作者
Sasidharan Pillai V Aswathy,Kotha Rohith Chandra,P Jyothikrishna,Kanniappan Parthasarathy Arun
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2022-02-01
卷期号:23 (3): 195-206
被引量:4
标识
DOI:10.2217/pgs-2020-0198
摘要
Clopidogrel is a prodrug chiefly metabolized by the hepatic isoenzyme CYP2C19 to its active metabolite that inhibits the platelet aggregation. It has been proven in many populations that the genetic polymorphism of CYP2C19 has influence on the pharmacokinetic and or pharmacodynamics of this drug and resulting in high inter-individual variability in the treatment outcomes. As CYP2C19 genetic polymorphism is highly prevalent among the Asian population, the influence of the same on the pharmacokinetics and; thereby, the pharmacodynamics of clopidogrel needs more attention. Using the pharmacogenetic information for drug therapy could help overcome these issues and to optimize the dosage regimen of clopidogrel, this review advocates the precision medicine approach for reducing the clopidogrel resistance and adverse cardiovascular events.
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