A Bayesian approach to Mendelian randomization using summary statistics in the univariable and multivariable settings with correlated pleiotropy

孟德尔随机化 因果推理 多效性 全基因组关联研究 推论 工具变量 贝叶斯概率 统计 遗传关联 计算机科学 因果关系(物理学) I类和II类错误 贝叶斯定理 多元统计 计量经济学 遗传变异 人工智能 生物 数学 遗传学 单核苷酸多态性 基因型 表型 物理 基因 量子力学
作者
Andrew J. Grant,Stephen Burgess
出处
期刊:American Journal of Human Genetics [Elsevier BV]
卷期号:111 (1): 165-180
标识
DOI:10.1016/j.ajhg.2023.12.002
摘要

Mendelian randomization uses genetic variants as instrumental variables to make causal inferences on the effect of an exposure on an outcome. Due to the recent abundance of high-powered genome-wide association studies, many putative causal exposures of interest have large numbers of independent genetic variants with which they associate, each representing a potential instrument for use in a Mendelian randomization analysis. Such polygenic analyses increase the power of the study design to detect causal effects; however, they also increase the potential for bias due to instrument invalidity. Recent attention has been given to dealing with bias caused by correlated pleiotropy, which results from violation of the “instrument strength independent of direct effect” assumption. Although methods have been proposed that can account for this bias, a number of restrictive conditions remain in many commonly used techniques. In this paper, we propose a Bayesian framework for Mendelian randomization that provides valid causal inference under very general settings. We propose the methods MR-Horse and MVMR-Horse, which can be performed without access to individual-level data, using only summary statistics of the type commonly published by genome-wide association studies, and can account for both correlated and uncorrelated pleiotropy. In simulation studies, we show that the approach retains type I error rates below nominal levels even in high-pleiotropy scenarios. We demonstrate the proposed approaches in applied examples in both univariable and multivariable settings, some with very weak instruments.

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