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Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model

With the increasing availability of large-scale GWAS summary data on various traits, Mendelian randomization (MR) has become commonly used to infer causality between a pair of traits, an exposure and an outcome. It depends on using genetic variants, typically SNPs, as instrumental variables (IVs). T...

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Autores principales: Lin, Zhaotong, Deng, Yangqing, Pan, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639093/
https://www.ncbi.nlm.nih.gov/pubmed/34793444
http://dx.doi.org/10.1371/journal.pgen.1009922
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author Lin, Zhaotong
Deng, Yangqing
Pan, Wei
author_facet Lin, Zhaotong
Deng, Yangqing
Pan, Wei
author_sort Lin, Zhaotong
collection PubMed
description With the increasing availability of large-scale GWAS summary data on various traits, Mendelian randomization (MR) has become commonly used to infer causality between a pair of traits, an exposure and an outcome. It depends on using genetic variants, typically SNPs, as instrumental variables (IVs). The inverse-variance weighted (IVW) method (with a fixed-effect meta-analysis model) is most powerful when all IVs are valid; however, when horizontal pleiotropy is present, it may lead to biased inference. On the other hand, Egger regression is one of the most widely used methods robust to (uncorrelated) pleiotropy, but it suffers from loss of power. We propose a two-component mixture of regressions to combine and thus take advantage of both IVW and Egger regression; it is often both more efficient (i.e. higher powered) and more robust to pleiotropy (i.e. controlling type I error) than either IVW or Egger regression alone by accounting for both valid and invalid IVs respectively. We propose a model averaging approach and a novel data perturbation scheme to account for uncertainties in model/IV selection, leading to more robust statistical inference for finite samples. Through extensive simulations and applications to the GWAS summary data of 48 risk factor-disease pairs and 63 genetically uncorrelated trait pairs, we showcase that our proposed methods could often control type I error better while achieving much higher power than IVW and Egger regression (and sometimes than several other new/popular MR methods). We expect that our proposed methods will be a useful addition to the toolbox of Mendelian randomization for causal inference.
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spelling pubmed-86390932021-12-03 Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model Lin, Zhaotong Deng, Yangqing Pan, Wei PLoS Genet Research Article With the increasing availability of large-scale GWAS summary data on various traits, Mendelian randomization (MR) has become commonly used to infer causality between a pair of traits, an exposure and an outcome. It depends on using genetic variants, typically SNPs, as instrumental variables (IVs). The inverse-variance weighted (IVW) method (with a fixed-effect meta-analysis model) is most powerful when all IVs are valid; however, when horizontal pleiotropy is present, it may lead to biased inference. On the other hand, Egger regression is one of the most widely used methods robust to (uncorrelated) pleiotropy, but it suffers from loss of power. We propose a two-component mixture of regressions to combine and thus take advantage of both IVW and Egger regression; it is often both more efficient (i.e. higher powered) and more robust to pleiotropy (i.e. controlling type I error) than either IVW or Egger regression alone by accounting for both valid and invalid IVs respectively. We propose a model averaging approach and a novel data perturbation scheme to account for uncertainties in model/IV selection, leading to more robust statistical inference for finite samples. Through extensive simulations and applications to the GWAS summary data of 48 risk factor-disease pairs and 63 genetically uncorrelated trait pairs, we showcase that our proposed methods could often control type I error better while achieving much higher power than IVW and Egger regression (and sometimes than several other new/popular MR methods). We expect that our proposed methods will be a useful addition to the toolbox of Mendelian randomization for causal inference. Public Library of Science 2021-11-18 /pmc/articles/PMC8639093/ /pubmed/34793444 http://dx.doi.org/10.1371/journal.pgen.1009922 Text en © 2021 Lin et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lin, Zhaotong
Deng, Yangqing
Pan, Wei
Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
title Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
title_full Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
title_fullStr Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
title_full_unstemmed Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
title_short Combining the strengths of inverse-variance weighting and Egger regression in Mendelian randomization using a mixture of regressions model
title_sort combining the strengths of inverse-variance weighting and egger regression in mendelian randomization using a mixture of regressions model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8639093/
https://www.ncbi.nlm.nih.gov/pubmed/34793444
http://dx.doi.org/10.1371/journal.pgen.1009922
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