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CYP2C19 genotype, clopidogrel metabolism, platelet function, and cardiovascular events: a systematic review and meta-analysis.

机译:CYP2C19基因型,氯吡格雷代谢,血小板功能和心血管事件:系统审查和荟萃分析。

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CONTEXT: The US Food and Drug Administration recently recommended that CYP2C19 genotyping be considered prior to prescribing clopidogrel, but the American Heart Association and American College of Cardiologists have argued evidence is insufficient to support CYP2C19 genotype testing. OBJECTIVE: To appraise evidence on the association of CYP2C19 genotype and clopidogrel response through systematic review and meta-analysis. DATA SOURCES: PubMed and EMBASE from their inception to October 2011. STUDY SELECTION: Studies that reported clopidogrel metabolism, platelet reactivity or clinically relevant outcomes (cardiovascular disease [CVD] events and bleeding), and information on CYP2C19 genotype were included. DATA EXTRACTION: We extracted information on study design, genotyping, and disease outcomes and investigated sources of bias. RESULTS: We retrieved 32 studies of 42,016 patients reporting 3545 CVD events, 579 stent thromboses, and 1413 bleeding events. Six studies were randomized trials ("effect-modification
机译:背景信息:美国食品和药物管理局最近建议在规定氯吡格雷之前考虑CYP2C19基因分型,但美国心脏协会和美国的心脏病学家曾认为证据不足以支持CYP2C19基因型测试。目的:通过系统审查和荟萃分析评估CYP2C19基因型和氯吡格雷响应协定的证据。数据来源:PUBMED和EMBASE从他们的成立到2011年10月。研究选择:报告氯吡格雷代谢,血小板反应性或临床相关结果(心血管疾病[CVD]事件和出血)的研究以及CYP2C19基因型的信息。数据提取:我们提取有关研究设计,基因分型和疾病结果以及调查偏倚来源的信息。结果:我们检索了32例研究了42,016名患者,报告了3545例CVD事件,579个支架血栓形成,1413名出血事件。六项研究是随机试验(“效果改性

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