CYP2C19型
雷贝拉唑
幽门螺杆菌
荟萃分析
内科学
埃索美拉唑
基因型
科克伦图书馆
胃肠病学
质子抑制剂泵
基因多态性
医学
泮托拉唑
奥美拉唑
药理学
生物
遗传学
基因
作者
Juan Fu,Changfeng Sun,Hongyan He,Suvash Chandra Ojha,Han Shi,Cunliang Deng,Yunjian Sheng
出处
期刊:Pharmacogenomics
[Future Medicine]
日期:2021-08-01
卷期号:22 (13): 859-879
被引量:16
标识
DOI:10.2217/pgs-2020-0127
摘要
Premise: The effects of proton pump inhibitors (PPI) depend on metabolic enzyme CYP2C19 that has different activity due to gene polymorphism. The purpose of this meta-analysis is to determine the potential effects of CYP2C19 polymorphism on the efficiency of PPI-based treatment. Materials & methods: The PubMed, EMBASE, Cochrane Library, etc. were searched for relevant articles published in English or Chinese from inception to 31 May 2020. Finally, 26 randomized controlled trials and 15 cohort studies met the inclusion criteria and used for the meta-analysis via STATA version 15. Results: Poor metabolizer (PM) genotype Helicobacter pylori eradication rates were highest for Asian individuals receiving triple or quadruple first-line therapy based on PPIs (p < 0.05). CYP2C19 polymorphism could influence H. pylori eradication rate only in Mainland China and Japan (p < 0.05). Conclusion: PM genotype facilitates the elimination of H. pylori in Asian populations. Rabeprazole-, esomeprazole- and pantoprazole-based eradication program was less affected by the CYP2C19 polymorphism.
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