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

Yoonsu Cho, Philip C Haycock, Eleanor Sanderson, Tom R Gaunt, Jie Zheng, Andrew P Morris, George Davey Smith, Gibran Hemani

Research output: Contribution to journalArticlepeer-review

Abstract

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.

Original languageEnglish
Article number1010
Pages (from-to)1010
JournalNature Communications
Volume11
Issue number1
DOIs
Publication statusPublished - 21 Feb 2020

Keywords

  • Causality
  • Computer Simulation
  • Databases, Genetic
  • Disease/genetics
  • Genetic Pleiotropy
  • Genetic Variation
  • Genome-Wide Association Study
  • Humans
  • Mendelian Randomization Analysis
  • Models, Genetic
  • Phenotype
  • Polymorphism, Single Nucleotide
  • Risk Factors

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