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Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions

BACKGROUND: Mendelian randomization (MR) has developed into an established method for strengthening causal inference and estimating causal effects, largely due to the proliferation of genome-wide association studies. However, genetic instruments remain controversial, as horizontal pleiotropic effect...

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Autores principales: Spiller, Wes, Slichter, David, Bowden, Jack, Davey Smith, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659360/
https://www.ncbi.nlm.nih.gov/pubmed/30462199
http://dx.doi.org/10.1093/ije/dyy204
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author Spiller, Wes
Slichter, David
Bowden, Jack
Davey Smith, George
author_facet Spiller, Wes
Slichter, David
Bowden, Jack
Davey Smith, George
author_sort Spiller, Wes
collection PubMed
description BACKGROUND: Mendelian randomization (MR) has developed into an established method for strengthening causal inference and estimating causal effects, largely due to the proliferation of genome-wide association studies. However, genetic instruments remain controversial, as horizontal pleiotropic effects can introduce bias into causal estimates. Recent work has highlighted the potential of gene–environment interactions in detecting and correcting for pleiotropic bias in MR analyses. METHODS: We introduce MR using Gene-by-Environment interactions (MRGxE) as a framework capable of identifying and correcting for pleiotropic bias. If an instrument–covariate interaction induces variation in the association between a genetic instrument and exposure, it is possible to identify and correct for pleiotropic effects. The interpretation of MRGxE is similar to conventional summary MR approaches, with a particular advantage of MRGxE being the ability to assess the validity of an individual instrument. RESULTS: We investigate the effect of adiposity, measured using body mass index (BMI), upon systolic blood pressure (SBP) using data from the UK Biobank and a single weighted allelic score informed by data from the GIANT consortium. We find MRGxE produces findings in agreement with two-sample summary MR approaches. Further, we perform simulations highlighting the utility of the approach even when the MRGxE assumptions are violated. CONCLUSIONS: By utilizing instrument–covariate interactions in MR analyses implemented within a linear-regression framework, it is possible to identify and correct for horizontal pleiotropic bias, provided the average magnitude of pleiotropy is constant across interaction-covariate subgroups.
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spelling pubmed-66593602019-08-02 Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions Spiller, Wes Slichter, David Bowden, Jack Davey Smith, George Int J Epidemiol Mendelian Randomization BACKGROUND: Mendelian randomization (MR) has developed into an established method for strengthening causal inference and estimating causal effects, largely due to the proliferation of genome-wide association studies. However, genetic instruments remain controversial, as horizontal pleiotropic effects can introduce bias into causal estimates. Recent work has highlighted the potential of gene–environment interactions in detecting and correcting for pleiotropic bias in MR analyses. METHODS: We introduce MR using Gene-by-Environment interactions (MRGxE) as a framework capable of identifying and correcting for pleiotropic bias. If an instrument–covariate interaction induces variation in the association between a genetic instrument and exposure, it is possible to identify and correct for pleiotropic effects. The interpretation of MRGxE is similar to conventional summary MR approaches, with a particular advantage of MRGxE being the ability to assess the validity of an individual instrument. RESULTS: We investigate the effect of adiposity, measured using body mass index (BMI), upon systolic blood pressure (SBP) using data from the UK Biobank and a single weighted allelic score informed by data from the GIANT consortium. We find MRGxE produces findings in agreement with two-sample summary MR approaches. Further, we perform simulations highlighting the utility of the approach even when the MRGxE assumptions are violated. CONCLUSIONS: By utilizing instrument–covariate interactions in MR analyses implemented within a linear-regression framework, it is possible to identify and correct for horizontal pleiotropic bias, provided the average magnitude of pleiotropy is constant across interaction-covariate subgroups. Oxford University Press 2019-06 2018-11-20 /pmc/articles/PMC6659360/ /pubmed/30462199 http://dx.doi.org/10.1093/ije/dyy204 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mendelian Randomization
Spiller, Wes
Slichter, David
Bowden, Jack
Davey Smith, George
Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions
title Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions
title_full Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions
title_fullStr Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions
title_full_unstemmed Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions
title_short Detecting and correcting for bias in Mendelian randomization analyses using Gene-by-Environment interactions
title_sort detecting and correcting for bias in mendelian randomization analyses using gene-by-environment interactions
topic Mendelian Randomization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659360/
https://www.ncbi.nlm.nih.gov/pubmed/30462199
http://dx.doi.org/10.1093/ije/dyy204
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