氯吡格雷
前药
GCLC公司
药理学
药物代谢
血小板
基因
药品
医学
生物
遗传学
内科学
阿司匹林
下调和上调
作者
Abdullah Alkattan,Ahmed Alkhalifah,Eman Alsalameen,Fatimah Alghanim,Nashwa Radwan
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2022-01-01
卷期号:23 (1): 61-79
标识
DOI:10.2217/pgs-2021-0092
摘要
Clopidogrel is an antiplatelet drug commonly used to prevent coagulation. This review aimed to investigate the effect of polymorphisms of G6PD, GCLC, GCLM, GSS, GST, GSR, HK and GLRX genes on clopidogrel during phase II metabolism through exploring previous studies. The results revealed that low glutathione plasma levels caused by several alleles related to these genes could affect the bioactivation process of the clopidogrel prodrug, making it unable to inhibit platelet aggregation perfectly and thus leading to severe consequences in patients with a high risk of blood coagulation. However, the study recommends platelet reactivity tests to predict clopidogrel efficacy rather than studying gene mutations, as most of these mutations are rare and other nongenetic factors could affect the drug's efficacy.
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