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Higher adiposity and mental health: causal inference using Mendelian randomization.

Authors :
Casanova F
O'Loughlin J
Martin S
Beaumont RN
Wood AR
Watkins ER
Freathy RM
Hagenaars SP
Frayling TM
Yaghootkar H
Tyrrell J
Source :
Human molecular genetics [Hum Mol Genet] 2021 Nov 30; Vol. 30 (24), pp. 2371-2382.
Publication Year :
2021

Abstract

Higher adiposity is an established risk factor for psychiatric diseases including depression and anxiety. The associations between adiposity and depression may be explained by the metabolic consequences and/or by the psychosocial impact of higher adiposity. We performed one- and two- sample Mendelian randomization (MR) in up to 145 668 European participants from the UK Biobank to test for a causal effect of higher adiposity on 10 well-validated mental health and well-being outcomes derived using the Mental Health Questionnaire (MHQ). We used three sets of adiposity genetic instruments: (a) a set of 72 BMI genetic variants, (b) a set of 36 favourable adiposity variants and (c) a set of 38 unfavourable adiposity variants. We additionally tested causal relationships (1) in men and women separately, (2) in a subset of individuals not taking antidepressants and (3) in non-linear MR models. Two-sample MR provided evidence that a genetically determined one standard deviation (1-SD) higher BMI (4.6 kg/m2) was associated with higher odds of current depression [OR: 1.50, 95%CI: 1.15, 1.95] and lower well-being [ß: -0.15, 95%CI: -0.26, -0.04]. Findings were similar when using the metabolically favourable and unfavourable adiposity variants, with higher adiposity associated with higher odds of depression and lower well-being scores. Our study provides further evidence that higher BMI causes higher odds of depression and lowers well-being. Using genetics to separate out metabolic and psychosocial effects, our study suggests that in the absence of adverse metabolic effects higher adiposity remains causal to depression and lowers well-being.<br /> (© The Author(s) 2021. Published by Oxford University Press.)

Details

Language :
English
ISSN :
1460-2083
Volume :
30
Issue :
24
Database :
MEDLINE
Journal :
Human molecular genetics
Publication Type :
Academic Journal
Accession number :
34270736
Full Text :
https://doi.org/10.1093/hmg/ddab204