Exploiting horizontal pleiotropy to search for causal pathways within a Mendelian randomization framework

被引:62
|
作者
Cho, Yoonsu [1 ]
Haycock, Philip C. [1 ]
Sanderson, Eleanor [1 ]
Gaunt, Tom R. [1 ]
Zheng, Jie [1 ]
Morris, Andrew P. [2 ,3 ]
Smith, George Davey [1 ]
Hemani, Gibran [1 ]
机构
[1] Univ Bristol, Bristol Med Sch, MRC Integrat Epidemiol Unit, Populat Hlth Sci, Bristol BS8 2BN, Avon, England
[2] Univ Liverpool, Dept Biostat, Liverpool L69 3GL, Merseyside, England
[3] Univ Manchester, Div Musculoskeletal & Dermatol Sci, Manchester M13 9NT, Lancs, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
CORONARY-HEART-DISEASE; GENETIC-VARIANTS; RISK; SCHIZOPHRENIA; INSTRUMENTS; OBESITY; BIAS; EDUCATION; TESTS;
D O I
10.1038/s41467-020-14452-4
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In Mendelian randomization (MR) analysis, variants that exert horizontal pleiotropy are typically treated as a nuisance. However, they could be valuable in identifying alternative pathways to the traits under investigation. Here, we develop MR-TRYX, a framework that exploits horizontal pleiotropy to discover putative risk factors for disease. We begin by detecting outliers in a single exposure-outcome MR analysis, hypothesising they are due to horizontal pleiotropy. We search across hundreds of complete GWAS summary datasets to systematically identify other (candidate) traits that associate with the outliers. We develop a multi-trait pleiotropy model of the heterogeneity in the exposure-outcome analysis due to pathways through candidate traits. Through detailed investigation of several causal relationships, many pleiotropic pathways are uncovered with already established causal effects, validating the approach, but also alternative putative causal pathways. Adjustment for pleiotropic pathways reduces the heterogeneity across the analyses.
引用
收藏
页数:13
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