Division of Aging, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.
Curr Protoc. 2021 Dec;1(12):e335. doi: 10.1002/cpz1.335.
Mendelian randomization is a framework that uses measured variation in genes for assessing and estimating the causal effect of an exposure on an outcome. Multivariable Mendelian randomization is an extension that can assess the causal effect of multiple exposures on an outcome, and can be advantageous when considering a set (>1) of potentially correlated candidate risk factors in evaluating the causal effect of each on a health outcome, accounting for measured pleiotropy. This can be seen, for example, in determining the causal effects of lipids and cholesterol on type 2 diabetes risk, where the correlated risk factors share genetic predictors. Similar to univariate Mendelian randomization, multivariable Mendelian randomization can be conducted using two-sample summary-level data where the gene-exposure and gene-outcome associations are derived from separate samples from the same underlying population. Here, we present a protocol for conducting a two-sample multivariable Mendelian randomization study using the 'MVMR' package in R and summary-level genetic data. We also provide a protocol for searching and obtaining instruments using available data sources in the 'MRInstruments' R package. Finally, we provide general guidelines and discuss the utility of performing a multivariable Mendelian randomization analysis for simultaneously assessing causality of multiple exposures. © 2021 Wiley Periodicals LLC. Basic Protocol: Performing a two-sample multivariable Mendelian randomization analysis using the 'MVMR' package in R and summarized genetic data Support Protocol 1: Installing the 'MVMR' R package Support Protocol 2: Obtaining instruments from the 'MRInstruments' R package.
孟德尔随机化是一种利用基因变异来评估和估计暴露对结局影响的因果效应的方法。多变量孟德尔随机化是一种扩展方法,可以评估多种暴露对结局的因果效应,并且在考虑一组(>1)潜在相关的候选风险因素来评估每个因素对健康结局的因果效应时是有利的,可以考虑到测量的多效性。例如,在确定脂质和胆固醇对 2 型糖尿病风险的因果效应时,可以看到这一点,其中相关的风险因素具有共同的遗传预测因子。与单变量孟德尔随机化类似,多变量孟德尔随机化可以使用两样本汇总水平数据进行,其中基因-暴露和基因-结局关联来自同一基础人群的两个独立样本。在这里,我们使用 R 中的 'MVMR' 包和汇总遗传数据,提出了一种进行两样本多变量孟德尔随机化研究的方案。我们还提供了一个使用 'MRInstruments' R 包中可用数据源搜索和获取工具的方案。最后,我们提供了一般指南,并讨论了同时评估多种暴露的因果关系进行多变量孟德尔随机化分析的效用。