Graphical analysis for phenome-wide causal discovery in genotyped population-scale biobanks

David Amar, Nasa Sinnott-Armstrong, Euan A. Ashley, Manuel A. Rivas*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

Causal inference via Mendelian randomization requires making strong assumptions about horizontal pleiotropy, where genetic instruments are connected to the outcome not only through the exposure. Here, we present causal Graphical Analysis Using Genetics (cGAUGE), a pipeline that overcomes these limitations using instrument filters with provable properties. This is achievable by identifying conditional independencies while examining multiple traits. cGAUGE also uses ExSep (Exposure-based Separation), a novel test for the existence of causal pathways that does not require selecting instruments. In simulated data we illustrate how cGAUGE can reduce the empirical false discovery rate by up to 30%, while retaining the majority of true discoveries. On 96 complex traits from 337,198 subjects from the UK Biobank, our results cover expected causal links and many new ones that were previously suggested by correlation-based observational studies. Notably, we identify multiple risk factors for cardiovascular disease, including red blood cell distribution width.

Original languageEnglish
Article number350
JournalNature Communications
Volume12
Issue number1
DOIs
StatePublished - Dec 2021
Externally publishedYes

Funding

FundersFunder number
National Institute of Health center for Multi-and Trans-ethnic Mapping of Mendelian and Complex Diseases5U01 HG009080
National Institutes of Health
U.S. Department of Defense
National Human Genome Research InstituteR01HG010140
Stanford University

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