Genetic architecture of brain age and its casual relations with brain and mental disorders

Author:

Wang Yunpeng1ORCID,Leonardsen Esten,Vidal-Pineiro Didac1ORCID,Roe James,Frei Oleksandr2,Shadrin Alexey,Iakunchykova Olena,De Lange Ann-Marie,Kaufmann Tobias3ORCID,Taschler Bernd4ORCID,Smith Stephen5ORCID,Wolfers Thomas,Andreassen Ole2ORCID,Westlye Lars T.1ORCID

Affiliation:

1. University of Oslo

2. Oslo University Hospital & Institute of Clinical Medicine, University of Oslo

3. University of Tübingen

4. University of Oxford

5. Wellcome Centre for Integrative Neuroimaging, FMRIB, Nuffield Department of Clinical Neurosciences, University of Oxford

Abstract

Abstract The difference between chronological age and the apparent age of the brain estimated from brain imaging data — the brain age gap (BAG) — is widely considered a general indicator of brain health. Converging evidence supports that BAG is sensitive to an array of genetic and non-genetic traits and diseases, yet few studies have examined the genetic architecture and its corresponding causal relationships with common brain disorders. Here, we estimate BAG using state-of-the-art neural networks trained on brain scans from 53,542 individuals (age range 3-95 years). A genome-wide association analysis across 28,104 individuals (40-84 years) from the UK Biobank revealed eight independent genomic regions significantly associated with BAG (p<5x10-8) implicating neurological, metabolic, and immunological pathways – among which seven are novel. No significant genetic correlations or causal relationships with BAG were found for Parkinson’s disease, major depressive disorder, or schizophrenia, but two-sample Mendelian randomization indicated a causal influence of AD (p=7.9x10-4) and bipolar disorder (p=1.35x10-2) on BAG. These results emphasize the polygenic architecture of brain age and provide insights into the causal relationship between selected neurological and neuropsychiatric disorders and BAG.

Publisher

Research Square Platform LLC

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