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

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 (N = 61294–916...

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Autores principales: Gillett, Alexandra C., Jermy, Bradley S., Lee, Sang Hong, Pain, Oliver, Howard, David M., Hagenaars, Saskia P., Hanscombe, Ken B., Coleman, Jonathan R. I., Lewis, Cathryn M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541465/
https://www.ncbi.nlm.nih.gov/pubmed/35438196
http://dx.doi.org/10.1002/gepi.22449
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author Gillett, Alexandra C.
Jermy, Bradley S.
Lee, Sang Hong
Pain, Oliver
Howard, David M.
Hagenaars, Saskia P.
Hanscombe, Ken B.
Coleman, Jonathan R. I.
Lewis, Cathryn M.
author_facet Gillett, Alexandra C.
Jermy, Bradley S.
Lee, Sang Hong
Pain, Oliver
Howard, David M.
Hagenaars, Saskia P.
Hanscombe, Ken B.
Coleman, Jonathan R. I.
Lewis, Cathryn M.
author_sort Gillett, Alexandra C.
collection PubMed
description 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 (N = 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.
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spelling pubmed-95414652022-10-14 Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank Gillett, Alexandra C. Jermy, Bradley S. Lee, Sang Hong Pain, Oliver Howard, David M. Hagenaars, Saskia P. Hanscombe, Ken B. Coleman, Jonathan R. I. Lewis, Cathryn M. Genet Epidemiol Research Articles 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 (N = 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. John Wiley and Sons Inc. 2022-04-19 2022 /pmc/articles/PMC9541465/ /pubmed/35438196 http://dx.doi.org/10.1002/gepi.22449 Text en © 2022 The Authors. Genetic Epidemiology published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Gillett, Alexandra C.
Jermy, Bradley S.
Lee, Sang Hong
Pain, Oliver
Howard, David M.
Hagenaars, Saskia P.
Hanscombe, Ken B.
Coleman, Jonathan R. I.
Lewis, Cathryn M.
Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank
title Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank
title_full Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank
title_fullStr Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank
title_full_unstemmed Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank
title_short Exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the UK Biobank
title_sort exploring polygenic‐environment and residual‐environment interactions for depressive symptoms within the uk biobank
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9541465/
https://www.ncbi.nlm.nih.gov/pubmed/35438196
http://dx.doi.org/10.1002/gepi.22449
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