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Exploring polygenic-environment and residual-environment interactions for depressive symptoms within the UK Biobank.

Authors :
Gillett AC
Jermy BS
Lee SH
Pain O
Howard DM
Hagenaars SP
Hanscombe KB
Coleman JRI
Lewis CM
Source :
Genetic epidemiology [Genet Epidemiol] 2022 Jul; Vol. 46 (5-6), pp. 219-233. Date of Electronic Publication: 2022 Apr 19.
Publication Year :
2022

Abstract

Substantial advances have been made in identifying genetic contributions to depression, but little is known about how the effect of genes can be modulated by the environment, creating a gene-environment interaction. Using multivariate reaction norm models (MRNMs) within the UK Biobank (Nā€‰=ā€‰61294-91644), we investigate whether the polygenic and residual variance components of depressive symptoms are modulated by 17 a priori selected covariate traits-12 environmental variables and 5 biomarkers. MRNMs, a mixed-effects modelling approach, provide unbiased polygenic-covariate interaction estimates for a quantitative trait by controlling for outcome-covariate correlations and residual-covariate interactions. A continuous depressive symptom variable was the outcome in 17 MRNMs-one for each covariate trait. Each MRNM had a fixed-effects model (fixed effects included the covariate trait, demographic variables, and principal components) and a random effects model (where polygenic-covariate and residual-covariate interactions are modelled). Of the 17 selected covariates, 11 significantly modulate deviations in depressive symptoms through the modelled interactions, but no single interaction explains a large proportion of phenotypic variation. Results are dominated by residual-covariate interactions, suggesting that covariate traits (including neuroticism, childhood trauma, and BMI) typically interact with unmodelled variables, rather than a genome-wide polygenic component, to influence depressive symptoms. Only average sleep duration has a polygenic-covariate interaction explaining a demonstrably nonzero proportion of the variability in depressive symptoms. This effect is small, accounting for only 1.22% (95% confidence interval: [0.54, 1.89]) of variation. The presence of an interaction highlights a specific focus for intervention, but the negative results here indicate a limited contribution from polygenic-environment interactions.<br /> (© 2022 The Authors. Genetic Epidemiology published by Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1098-2272
Volume :
46
Issue :
5-6
Database :
MEDLINE
Journal :
Genetic epidemiology
Publication Type :
Academic Journal
Accession number :
35438196
Full Text :
https://doi.org/10.1002/gepi.22449