PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment

Abstract Mendelian Randomisation (MR) estimates causal effects between risk factors and complex outcomes using genetic instruments. Pleiotropy, heritable confounders, and heterogeneous causal effects violate MR assumptions and can lead to biases. To alleviate these, we propose an approach employing...

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Main Authors: Liza Darrous, Gibran Hemani, George Davey Smith, Zoltán Kutalik
Format: Article
Language:English
Published: Nature Portfolio 2024-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-024-45655-8
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author Liza Darrous
Gibran Hemani
George Davey Smith
Zoltán Kutalik
author_facet Liza Darrous
Gibran Hemani
George Davey Smith
Zoltán Kutalik
author_sort Liza Darrous
collection DOAJ
description Abstract Mendelian Randomisation (MR) estimates causal effects between risk factors and complex outcomes using genetic instruments. Pleiotropy, heritable confounders, and heterogeneous causal effects violate MR assumptions and can lead to biases. To alleviate these, we propose an approach employing a Phenome-Wide association Clustering of the MR instruments (PWC-MR) and apply this method to revisit the surprisingly large apparent causal effect of body mass index (BMI) on educational attainment (EDU): $$\widehat{\alpha }$$ α ̂ = −0.19 [−0.22, −0.16]. First, we cluster 324 BMI-associated genetic instruments based on their association with 407 traits in the UK Biobank, which yields six distinct groups. Subsequent cluster-specific MR reveals heterogeneous causal effect estimates on EDU. A cluster enriched for socio-economic indicators yields the largest BMI-on-EDU causal effect estimate ( $$\widehat{\alpha }$$ α ̂ = −0.49 [−0.56, −0.42]) whereas a cluster enriched for body-mass specific traits provides a more likely estimate ( $$\widehat{\alpha }$$ α ̂ = −0.09 [−0.13, −0.05]). Follow-up analyses confirms these findings: within-sibling MR ( $$\widehat{\alpha }$$ α ̂ = −0.05 [−0.09, −0.01]); MR for childhood BMI on EDU ( $$\widehat{\alpha }$$ α ̂ = −0.03 [−0.06, −0.002]); step-wise multivariable MR ( $$\widehat{\alpha }$$ α ̂ = −0.05 [−0.07, −0.02]) where socio-economic indicators are jointly modelled. Here we show how the in-depth examination of the BMI-EDU causal relationship demonstrates the utility of our PWC-MR approach in revealing distinct pleiotropic pathways and confounder mechanisms.
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spelling doaj.art-91a46371bd0d42ca909c5a6040c3c8642024-03-05T19:38:25ZengNature PortfolioNature Communications2041-17232024-02-0115111110.1038/s41467-024-45655-8PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainmentLiza Darrous0Gibran Hemani1George Davey Smith2Zoltán Kutalik3University Center for Primary Care and Public HealthMedical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of BristolMedical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of BristolUniversity Center for Primary Care and Public HealthAbstract Mendelian Randomisation (MR) estimates causal effects between risk factors and complex outcomes using genetic instruments. Pleiotropy, heritable confounders, and heterogeneous causal effects violate MR assumptions and can lead to biases. To alleviate these, we propose an approach employing a Phenome-Wide association Clustering of the MR instruments (PWC-MR) and apply this method to revisit the surprisingly large apparent causal effect of body mass index (BMI) on educational attainment (EDU): $$\widehat{\alpha }$$ α ̂ = −0.19 [−0.22, −0.16]. First, we cluster 324 BMI-associated genetic instruments based on their association with 407 traits in the UK Biobank, which yields six distinct groups. Subsequent cluster-specific MR reveals heterogeneous causal effect estimates on EDU. A cluster enriched for socio-economic indicators yields the largest BMI-on-EDU causal effect estimate ( $$\widehat{\alpha }$$ α ̂ = −0.49 [−0.56, −0.42]) whereas a cluster enriched for body-mass specific traits provides a more likely estimate ( $$\widehat{\alpha }$$ α ̂ = −0.09 [−0.13, −0.05]). Follow-up analyses confirms these findings: within-sibling MR ( $$\widehat{\alpha }$$ α ̂ = −0.05 [−0.09, −0.01]); MR for childhood BMI on EDU ( $$\widehat{\alpha }$$ α ̂ = −0.03 [−0.06, −0.002]); step-wise multivariable MR ( $$\widehat{\alpha }$$ α ̂ = −0.05 [−0.07, −0.02]) where socio-economic indicators are jointly modelled. Here we show how the in-depth examination of the BMI-EDU causal relationship demonstrates the utility of our PWC-MR approach in revealing distinct pleiotropic pathways and confounder mechanisms.https://doi.org/10.1038/s41467-024-45655-8
spellingShingle Liza Darrous
Gibran Hemani
George Davey Smith
Zoltán Kutalik
PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
Nature Communications
title PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
title_full PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
title_fullStr PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
title_full_unstemmed PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
title_short PheWAS-based clustering of Mendelian Randomisation instruments reveals distinct mechanism-specific causal effects between obesity and educational attainment
title_sort phewas based clustering of mendelian randomisation instruments reveals distinct mechanism specific causal effects between obesity and educational attainment
url https://doi.org/10.1038/s41467-024-45655-8
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