Department of Biostatistics, Bloomberg School of Public Health, Johns Hopkins University, 615 N Wolfe St, Baltimore, MD 21205, United States.
Department of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, 423 Guardian Drive, Philadelphia, PA 19104-6021, United States.
Biostatistics. 2024 Oct 1;25(4):1015-1033. doi: 10.1093/biostatistics/kxae006.
Mendelian randomization (MR) analysis is increasingly popular for testing the causal effect of exposures on disease outcomes using data from genome-wide association studies. In some settings, the underlying exposure, such as systematic inflammation, may not be directly observable, but measurements can be available on multiple biomarkers or other types of traits that are co-regulated by the exposure. We propose a method for MR analysis on latent exposures (MRLE), which tests the significance for, and the direction of, the effect of a latent exposure by leveraging information from multiple related traits. The method is developed by constructing a set of estimating functions based on the second-order moments of GWAS summary association statistics for the observable traits, under a structural equation model where genetic variants are assumed to have indirect effects through the latent exposure and potentially direct effects on the traits. Simulation studies show that MRLE has well-controlled type I error rates and enhanced power compared to single-trait MR tests under various types of pleiotropy. Applications of MRLE using genetic association statistics across five inflammatory biomarkers (CRP, IL-6, IL-8, TNF-α, and MCP-1) provide evidence for potential causal effects of inflammation on increasing the risk of coronary artery disease, colorectal cancer, and rheumatoid arthritis, while standard MR analysis for individual biomarkers fails to detect consistent evidence for such effects.
孟德尔随机化(MR)分析越来越受欢迎,可用于使用全基因组关联研究的数据来测试暴露对疾病结局的因果效应。在某些情况下,潜在暴露(如系统性炎症)可能无法直接观察到,但可以在多个生物标志物或其他受暴露共同调节的性状上获得测量值。我们提出了一种针对潜在暴露的 MR 分析方法(MRLE),该方法通过利用多个相关性状的信息,检验潜在暴露的效应的显著性和方向。该方法通过构建一组基于可观察性状的 GWAS 汇总关联统计量的二阶矩的估计函数来开发,其中假设遗传变异通过潜在暴露具有间接效应,并且可能对性状具有直接效应。模拟研究表明,与单性状 MR 检验相比,MRLE 在各种类型的多效性下具有良好控制的Ⅰ型错误率和增强的功效。使用跨五个炎症生物标志物(CRP、IL-6、IL-8、TNF-α 和 MCP-1)的遗传关联统计数据应用 MRLE 提供了炎症可能导致冠心病、结直肠癌和类风湿关节炎风险增加的潜在因果效应的证据,而针对单个生物标志物的标准 MR 分析未能检测到此类效应的一致证据。