Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
42839001
TITLE
Association between polygenic liability to depression and lifetime depression in at-risk adolescents.
ABSTRACT
Internalising symptoms including depression, anxiety and somatic symptoms in adolescence are common. They can be transient, but they can also persist and progress to major depressive disorder (MDD) Polygenic risk scores for major depression (MD-PGS) may help identify which symptomatic adolescents are at greatest risk of later disorder. In a mega-analysis of two longitudinal population-based cohorts from Brisbane, Australia, we investigated whether polygenic liability to depression improves risk stratification among adolescents with elevated internalising symptoms. Internalising symptoms were assessed at age 14, lifetime MDD was assessed in young adulthood using the Composite International Diagnostic Interview, and MD-PGS were generated using summary statistics from the latest Psychiatric Genomics Consortium major depression genome-wide association study, excluding Australian cohorts. Analyses focused on comparisons between individuals in the top decile of risk and those in the remaining 90% of each cohort. A total of 302 cases with lifetime MDD and 1693 controls were included. Compared with adolescents outside the highest decile of internalising symptoms, those in the top decile at age 14 had a more than two-fold increased odds of lifetime MDD (OR = 2.56, 95% CI 1.92-3.49, p = 5.4 × 10 ). Individuals in the top decile of MD-PGS also showed increased odds of lifetime MDD compared with the remaining 90% (OR = 3.45, 95% CI 2.53-4.71, p = 4.4 × 10 ¹⁵). Adolescents who were simultaneously in the top decile of both internalising symptoms and MD-PGS had an approximately eight-fold increased odds of lifetime MDD compared with individuals outside the top decile for both risk factors (OR = 8.58, 95% CI 4.04-18.26, p = 1.2 × 10 ⁵). These findings indicate that polygenic risk scores for depression may have particular clinical utility for stratifying risk among adolescents already presenting with elevated internalising symptoms, identifying a subgroup at very high risk for later major depressive disorder.
© 2026. The Author(s).
DATE PUBLISHED
2026 Oct 06
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2025/05/23
accepted 2026/09/16
revised 2026/07/22
medline 2026/10/07 05:31
pubmed 2026/10/07 05:31
entrez 2026/10/06 23:43
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Byrne EM Byrne Enda M EM Child Health Research Centre, The University of Queensland, Brisbane, Australia. enda.byrne@uq.edu.au.
Gillespie NA Gillespie Nathan A NA Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond, VA, USA.
Najman JM Najman Jake M JM School of Public Health, The University of Queensland, Brisbane, Australia.
Henders AK Henders Anjali K AK Institute for Molecular Bioscience, The University of Queensland, Brisbane, Australia.
Mitchell BL Mitchell Brittany L BL QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Dwyer D Dwyer Dominic D Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.
Hartmann S Hartmann Simon S Adelaide Medical School, Discipline of Psychiatry, The University of Adelaide, Adelaide, Australia.
Cavve BS Cavve Blake S BS Telethon Kids Institute, The University of Western Australia, Perth, Australia.
Amminger GP Amminger G Paul GP Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.
Clark S Clark Scott S Adelaide Medical School, Discipline of Psychiatry, The University of Adelaide, Adelaide, Australia.
Gao C Gao Caroline C Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.
Lin A Lin Ashleigh A Telethon Kids Institute, The University of Western Australia, Perth, Australia.
Schmaal L Schmaal Lianne L Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.
Thompson A Thompson Andrew A Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.
Wood SJ Wood Stephen J SJ Centre for Human Brain Health, University of Birmingham, Birmingham, UK.
Wigman JTW Wigman J T W JTW Department of Psychiatry, Interdisciplinary Center for Psychopathology and Emotion Regulation, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Yung AR Yung Alison R AR Institute for Mental and Physical Health and Clinical Translation (IMPACT), Deakin University, Melbourne, Australia.
Medland SE Medland Sarah E SE QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Crouse JJ Crouse Jacob J JJ Youth Mental and Technology Health Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia.
Scott J Scott Jan J Universite de Paris, Paris, France.
Scott JG Scott James G JG Child and Youth Mental Health Service, Children's Health Queensland Hospital and Health Service, Brisbane, Australia.
Williams GM Williams Gail M GM School of Public Health, The University of Queensland, Brisbane, Australia.
Nelson B Nelson Barnaby B Centre for Youth Mental Health, The University of Melbourne, Melbourne, Australia.
Martin NG Martin Nicholas G NG QIMR Berghofer Medical Research Institute, Brisbane, Australia.
Hickie IB Hickie Ian B IB Youth Mental and Technology Health Team, Brain & Mind Centre, The University of Sydney, Camperdown, Australia.
Wray NR Wray Naomi R NR Queensland Brain Institute, The University of Queensland, Brisbane, Australia.
Middeldorp CM Middeldorp Christel M CM Levvel, Academic Centre for Child and Adolescent Psychiatry, Amsterdam, The Netherlands.
INVESTIGATORS
JOURNAL
VOLUME:
ISSUE:
TITLE: Molecular psychiatry
ISOABBREVIATION: Mol Psychiatry
YEAR: 2026
MONTH: Oct
DAY: 06
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Internet
ISSN: 1476-5578
ISSNTYPE: Electronic
MEDLINE JOURNAL
MEDLINETA: Mol Psychiatry
COUNTRY: England
ISSNLINKING: 1359-4184
NLMUNIQUEID: 9607835
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
COMMENTS AND CORRECTIONS
GRANTS
GRANTID AGENCY COUNTRY
1198304 Department of Health | National Health and Medical Research Council (NHMRC)
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