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首页> 外文期刊>Systematic Reviews >Genetic polymorphisms of organic cation transporters 1 (OCT1) and responses to metformin therapy in individuals with type 2 diabetes mellitus: a systematic review protocol
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Genetic polymorphisms of organic cation transporters 1 (OCT1) and responses to metformin therapy in individuals with type 2 diabetes mellitus: a systematic review protocol

机译:2型糖尿病患者中有机阳离子转运蛋白1(OCT1)的遗传多态性和对二甲双胍治疗的反应:系统综述

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Metformin is one of the most commonly used drugs for type 2 diabetes mellitus (T2DM). Despite its efficacy and safety, metformin is frequently associated with highly variable glycemic responses, which is hypothesized to be the result of genetic variations in its transport by organic cation transporters (OCTs). This systematic review aims to highlight and summarize the overall effects of OCT1 polymorphisms on therapeutic responses to metformin and to evaluate their potential role in terms of interethnic differences with metformin responses. We will systematically review observational studies reporting on the genetic association between OCT1 polymorphisms and metformin responses in T2DM patients. A comprehensive search strategy formulated with the help of a librarian will be used to search MEDLINE via PubMed, Embase, and CINAHL for relevant studies published between January 1990 and July 2017. Two review authors will independently screen titles and abstracts in duplicate, extract data, and assess the risk of bias with discrepancies resolved by discussion or arbitration of a third review author. Mined data will be grouped according to OCT1 polymorphisms, and their effects on therapeutic responses to metformin will be narratively synthesized. If sufficient numbers of homogeneous studies are scored, meta-analyses will be performed to obtain pooled effect estimates. Funnel plots analysis and Egger’s test will be used to assess publication bias. This study will be reported according to the Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) guidelines. This review will summarize the genetic effects of OCT1 polymorphisms associated with variabilities in glycemic responses to metformin. The findings of this study could help to develop genetic tests that could predict a person’s response to metformin treatment and create personalized drugs with greater efficacy and safety. Registration number: PROSPERO, CRD42017079978.
机译:二甲双胍是2型糖尿病(T2DM)最常用的药物之一。尽管二甲双胍具有疗效和安全性,但它经常与高度可变的血糖反应相关联,据推测这是有机阳离子转运蛋白(OCT)转运其遗传变异的结果。本系统综述旨在强调和总结OCT1多态性对二甲双胍治疗反应的总体影响,并评估其在族群间差异与二甲双胍反应方面的潜在作用。我们将系统地回顾性观察研究,以观察T2DM患者OCT1多态性与二甲双胍反应之间的遗传相关性。在馆员的帮助下制定的综合搜索策略将用于通过PubMed,Embase和CINAHL搜索MEDLINE,以查找1990年1月至2017年7月之间发表的相关研究。两名评论作者将独立筛查标题和摘要,重复进行两次,提取数据,并通过第三位评论作者的讨论或仲裁解决存在偏差的偏见风险。挖掘的数据将根据OCT1多态性进行分组,并且将对它们对二甲双胍治疗反应的影响进行叙述性合成。如果对足够数量的同类研究进行了评分,将进行荟萃分析以获得合并的效应估计值。漏斗图分析和Egger检验将用于评估发布偏差。该研究将根据系统评价和荟萃分析的首选报告项目(PRISMA)指南进行报告。这篇综述将总结OCT1基因多态性与二甲双胍血糖反应变异性相关的遗传效应。这项研究的结果可能有助于开展基因测试,从而预测人对二甲双胍治疗的反应,并开发出具有更高疗效和安全性的个性化药物。注册号:PROSPERO,CRD42017079978。

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