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BMAL1 Genetic Variation in Metabolic and Mental Health

Published online by Cambridge University Press:  01 August 2024

Hamza H Daudali*
Affiliation:
Behavioural Epidemiology and Genetics, School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom
Breda Cullen
Affiliation:
Behavioural Epidemiology and Genetics, School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom
Nicholas Graham
Affiliation:
Behavioural Epidemiology and Genetics, School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom
Joey Ward
Affiliation:
Behavioural Epidemiology and Genetics, School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom
Rona Strawbridge
Affiliation:
Behavioural Epidemiology and Genetics, School of Health and Wellbeing, University of Glasgow, Glasgow, United Kingdom Cardiovascular Medicine Unit, Department of Medicine, Karolinska Institute, Stockholm, Sweden Health Data Research UK, Glasgow, United Kingdom
*
*Presenting author.
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Abstract

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Aims

Epidemiological studies have previously shown a link between cardiometabolic disease and severe mental illness. The extent and mechanisms behind this link are poorly understood currently but links to impairments in the stress response and cortisol regulation have been thought to play a significant role. BMAL1 is a circadian rhythm regulation gene found on chromosome 11 which has been associated with a variety of pro-inflammatory states as well as conditions such as depression, schizophrenia, type 2 diabetes mellitus and myocardial infarction. Our study aimed to investigate the genetic structure of the BMAL1 gene locus and its associations with both cardiometabolic and psychiatric traits and conditions.

Methods

We used genetic data from the UK Biobank which recruited ~500,000 participants. Of these we used a population of ~430,000 self-reported white British participants and data from a variety of questionnaires and investigations looking at severe mental illness and cardiometabolic traits. We performed association analyses using Plink 1.07 with Bonferroni correction being performed for multiple testing using a number of genetic variants. Our threshold for significance was defined as a p-value < 5.35 × 10−5. Conditional analysis was then performed to identify if there were multiple independent signals for each phenotype.

Results

BMAL1 variants were associated with BMI, diastolic, systolic blood pressure, waist-hip ratio and neuroticism score, and risk of anhedonia, major depressive disorder and risk-taking behaviour. Multiple significant independent signals were identified for BMI and waist-hip ratio. Linkage disequilibrium (LD) analysis showed significant coinheritance of specific traits which could suggest a role for BMAL1 and the encoded protein as a link between cardiometabolic and mental health traits.

Conclusion

This is the first study that systematically investigated associations between the BMAL1 locus across a variety of different mental and cardiometabolic phenotypes in a population-level cohort. Our study has shown that there is a link between the BMAL1 locus and both cardiometabolic and mental health phenotypes. Further research is required to investigate the exact biological mechanism by which BMAL1 connects severe mental illness and cardiometabolic disease.

Type
1 Research
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
Copyright © The Author(s), 2024. Published by Cambridge University Press on behalf of Royal College of Psychiatrists

Footnotes

Abstracts were reviewed by the RCPsych Academic Faculty rather than by the standard BJPsych Open peer review process and should not be quoted as peer-reviewed by BJPsych Open in any subsequent publication.

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