{"title":"Conducting a Reproducible Mendelian Randomization Analysis Using the R Analytic Statistical Environment","authors":"Danielle Rasooly, Chirag J. Patel","doi":"10.1002/cphg.82","DOIUrl":null,"url":null,"abstract":"<p>Mendelian randomization (MR) is defined as the utilization of genetic variants as instrumental variables to assess the causal relationship between an exposure and an outcome. By leveraging genetic polymorphisms as proxy for an exposure, the causal effect of an exposure on an outcome can be assessed while addressing susceptibility to biases prone to conventional observational studies, including confounding and reverse causation, where the outcome causes the exposure. Analogous to a randomized controlled trial where patients are randomly assigned to subgroups based on different treatments, in an MR analysis, the random allocation of alleles during meiosis from parent to offspring assigns individuals to different subgroups based on genetic variants. Recent methods use summary statistics from genome-wide association studies to perform MR, bypassing the need for individual-level data. Here, we provide a straightforward protocol for using summary-level data to perform MR and provide guidance for utilizing available software. © 2019 by John Wiley & Sons, Inc.</p>","PeriodicalId":40007,"journal":{"name":"Current Protocols in Human Genetics","volume":"101 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cphg.82","citationCount":"34","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Human Genetics","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cphg.82","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 34
Abstract
Mendelian randomization (MR) is defined as the utilization of genetic variants as instrumental variables to assess the causal relationship between an exposure and an outcome. By leveraging genetic polymorphisms as proxy for an exposure, the causal effect of an exposure on an outcome can be assessed while addressing susceptibility to biases prone to conventional observational studies, including confounding and reverse causation, where the outcome causes the exposure. Analogous to a randomized controlled trial where patients are randomly assigned to subgroups based on different treatments, in an MR analysis, the random allocation of alleles during meiosis from parent to offspring assigns individuals to different subgroups based on genetic variants. Recent methods use summary statistics from genome-wide association studies to perform MR, bypassing the need for individual-level data. Here, we provide a straightforward protocol for using summary-level data to perform MR and provide guidance for utilizing available software. © 2019 by John Wiley & Sons, Inc.
利用R分析统计环境进行可重复的孟德尔随机化分析
孟德尔随机化(MR)被定义为利用遗传变异作为工具变量来评估暴露与结果之间的因果关系。通过利用遗传多态性作为暴露的代理,可以评估暴露对结果的因果关系,同时解决传统观察性研究中容易出现的偏见的易感性,包括混淆和反向因果关系,其中结果导致暴露。类似于随机对照试验,患者根据不同的治疗方法被随机分配到亚组,在MR分析中,减数分裂期间等位基因从亲本到后代的随机分配将个体根据遗传变异分配到不同的亚组。最近的方法使用来自全基因组关联研究的汇总统计数据来执行MR,绕过了对个人水平数据的需要。在这里,我们提供了一个使用摘要级数据执行MR的简单协议,并提供了使用可用软件的指导。©2019 by John Wiley &儿子,Inc。
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