Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

There are striking sex differences in the prevalence and symptomology of Major Depressive Disorder. Here, we conduct the largest sex-stratified genome wide association and genotype-by-sex interaction meta-analyses of Major Depressive Disorder to date (Females: 130,471 cases, 159,521 controls. Males: 64,805 cases, 132,185 controls). We identify 16 and eight independent genome-wide significant variants in females and males, respectively, including one novel variant on the X chromosome. Major Depressive Disorder in females and males shows substantial genetic overlap with a large proportion of variants displaying similar effect sizes across sexes. However, we also provide evidence for a higher burden of genetic risk in females which could be due to female-specific variants. Additionally, sex-specific pleiotropic effects may contribute to the higher prevalence of metabolic symptoms in females with Major Depressive Disorder. These findings underscore the importance of considering sex-specific genetic architectures in the study of health conditions, including Major Depressive Disorder, paving the way for more targeted treatment strategies.

Original publication

DOI

10.1038/s41467-025-63236-1

Type

Journal article

Journal

Nature communications

Publication Date

08/2025

Volume

16

Addresses

Brain and Mental Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia. Jodi.Thomas@qimrb.edu.au.

Keywords

BIONIC consortium, GLAD Study, Humans, Genetic Predisposition to Disease, Depressive Disorder, Major, Sex Factors, Genotype, Polymorphism, Single Nucleotide, Female, Male, Genome-Wide Association Study