MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Population Health Sciences, University of Bristol, Bristol, UK.
Stat Med. 2021 Nov 10;40(25):5434-5452. doi: 10.1002/sim.9133. Epub 2021 Aug 2.
Multivariable Mendelian randomization (MVMR) is a form of instrumental variable analysis which estimates the direct effect of multiple exposures on an outcome using genetic variants as instruments. Mendelian randomization and MVMR are frequently conducted using two-sample summary data where the association of the genetic variants with the exposures and outcome are obtained from separate samples. If the genetic variants are only weakly associated with the exposures either individually or conditionally, given the other exposures in the model, then standard inverse variance weighting will yield biased estimates for the effect of each exposure. Here, we develop a two-sample conditional F-statistic to test whether the genetic variants strongly predict each exposure conditional on the other exposures included in a MVMR model. We show formally that this test is equivalent to the individual level data conditional F-statistic, indicating that conventional rule-of-thumb critical values of 10, can be used to test for weak instruments. We then demonstrate how reliable estimates of the causal effect of each exposure on the outcome can be obtained in the presence of weak instruments and pleiotropy, by repurposing a commonly used heterogeneity Q-statistic as an estimating equation. Furthermore, the minimized value of this Q-statistic yields an exact test for heterogeneity due to pleiotropy. We illustrate our methods with an application to estimate the causal effect of blood lipid fractions on age-related macular degeneration.
多变量孟德尔随机化(MVMR)是一种工具变量分析形式,它使用遗传变异作为工具来估计多个暴露因素对结果的直接影响。孟德尔随机化和 MVMR 通常使用两样本汇总数据进行,其中遗传变异与暴露和结局的关联是从单独的样本中获得的。如果遗传变异与暴露因素的关联较弱,无论是单独还是在模型中考虑其他暴露因素的情况下,那么标准的逆方差加权将导致对每个暴露因素的影响的估计值存在偏差。在这里,我们开发了一个两样本条件 F 统计量来检验遗传变异是否在 MVMR 模型中包含的其他暴露因素的条件下强烈预测每个暴露因素。我们正式证明了该检验等同于个体水平数据条件 F 统计量,表明可以使用传统的经验法则临界值 10 来检验弱工具。然后,我们通过重新利用常用的异质性 Q 统计量作为估计方程,展示了在存在弱工具和多效性的情况下如何获得每个暴露因素对结果的因果效应的可靠估计。此外,这个 Q 统计量的最小化值可用于检验由于多效性引起的异质性的精确检验。我们通过应用于估计血脂分数对年龄相关性黄斑变性的因果效应来说明我们的方法。