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

Liza Darrous (), Gibran Hemani, George Davey Smith and Zoltán Kutalik ()
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Liza Darrous: University Center for Primary Care and Public Health
Gibran Hemani: University of Bristol
George Davey Smith: University of Bristol
Zoltán Kutalik: University Center for Primary Care and Public Health

Nature Communications, 2024, vol. 15, issue 1, 1-11

Abstract: 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.

Date: 2024
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DOI: 10.1038/s41467-024-45655-8

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