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Does CYP2C19 polymorphisms affect neurological deterioration in stroke/TIA patients?

机译:CYP2C19多态性是否会影响中风/ TIA患者的神经系统恶化?

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BACKGROUND:The association between cytochrome P450 2C19 (CYP2C19) polymorphisms and neurological deterioration in stroke or transient ischemic attack (TIA) patients is not completely understood. Hence, we performed a systematic review and meta-analysis of prospective cohort studies to quantify this association.METHODS:PubMed, Cochrane Library, Excerpta Medica Database, China National Knowledge Infrastructure and WanFang databases were searched for studies published up to April 2019. Prospective cohort studies that reported an association between CYP2C19 polymorphisms and neurological deterioration in stroke/TIA patients were included. Data on risk ratio (RR) and 95% confidence intervals (CI) were extracted and pooled by the authors. Preferred Reporting Items for Systematic reviews and Meta-Analyses guidelines were followed.RESULTS:Twelve eligible studies were included. Twelve studies reported CYP2C19?2, ?3 loss-of-function alleles and 5 studies reported CYP2C19?17 gain-of-function allele. Compared to non-carriers, carriers of CYP2C19?2, ?3 loss-of-function alleles had a significantly higher risk of neurological deterioration (RR, 1.63; 95%CI, 1.32-2.02). Conversely, carriers of CYP2C19?17 gain-of-function allele had a significantly lower risk of neurological deterioration (RR, 0.520; 95%CI, 0.393-0.689) compared to non-carriers.CONCLUSIONS:This meta-analysis demonstrated that the carriers of CYP2C19?2, ?3 loss-of-function alleles have an increased risk of neurological deterioration compared to non-carriers in stroke or TIA patients. Additionally, CYP2C19?17 gain-of-function allele can reduce the risk of neurological deterioration.Copyright ? 2021 the Author(s). Published by Wolters Kluwer Health, Inc.
机译:背景:细胞色素P450 2C19(CYP2C19)多态性与中风或短暂性缺血性发作(TIA)患者的关联并未完全理解。因此,我们对未来队列研究进行了系统审查和荟萃分析,以量化本协会。方法:PubMed,Cochrane图书馆,Excerpta Medica数据库,中国国家知识基础设施和万方数据库被搜查于2019年4月出版的研究。潜在队列包括报告CYP2C19多态性和中风/ TIA患者神经劣化之间的关联的研究。提取作者的风险比(RR)和95%置信区间(CI)的数据。首选用于系统评价和META分析的报告项目进行了准则。结果:包括12项合格的研究。 12种研究报告了CYP2C19?2,?3次丧失功能等位基因和5项研究报告了CYP2C19?17个功能性等位基因。与非载体相比,CYP2C19α2的载体2,α3丧失的损失等位基因具有显着提高神经劣化风险(RR,1.63; 95%CI,1.32-2.02)。相反,CYP2C19的载体17次获得功能性等位基因的神经劣化风险显着降低(RR,0.520; 95%CI,0.393-0.689)的风险。结论:该元分析表明载体CYP2C19?2,?3次丧失功能等位基因与中风或TIA患者的非载体相比具有增加的神经劣化风险。此外,CYP2C19吗?17功能增益等位基因可以降低神经系统恶化的风险。 2021提交人。由Wolters Kluwer Health,Inc。出版

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