Sex differences in the independent and combined effects of genomic and exposomic risks for schizophrenia on distressing psychotic experiences: insights from the ABCD study

dc.contributor.authorPrachason T.
dc.contributor.authorArias-Magnasco A.
dc.contributor.authorLin B.D.
dc.contributor.authorvan Os J.
dc.contributor.authorRutten B.P.F.
dc.contributor.authorPries L.K.
dc.contributor.authorGuloksuz S.
dc.contributor.correspondencePrachason T.
dc.contributor.otherMahidol University
dc.date.accessioned2026-02-06T18:09:05Z
dc.date.available2026-02-06T18:09:05Z
dc.date.issued2026-02-01
dc.description.abstractPurpose: To investigate sex-dependent effects of polygenic risk (PRS-SCZ) and exposome score (ES-SCZ) for schizophrenia, both independently and jointly, on distressing psychotic experiences (PEs) in early adolescents. Method: Baseline to 3-year follow-up data of the Adolescent Brain and Cognitive Development Study (ABCD) were used. PRS-SCZ and ES-SCZ were calculated to assess cumulative genetic and environmental (childhood adversity, cannabis use, hearing impairment, and winter births) risk for schizophrenia, respectively. The primary outcome was past-month distressing PEs at the 3-year follow-up. Secondary outcomes included distressing PEs across four yearly assessments: lifetime (≥ 1 wave), repeated (≥ 2 or ≥ 3 waves), and persisting (≥ 4 waves). Sex-stratified multilevel logistic regression models were used to test the independent and joint associations of binary modes (> 75th percentile) of PRS-SCZ (PRS-SCZ<inf>75</inf>) and ES-SCZ (ES-SCZ<inf>75</inf>) on the outcomes. As sensitivity analysis, the sex-stratified analyses were repeated on a randomly selected unrelated sample, and the coefficients of males and females were compared. Results: PRS-SCZ<inf>75</inf> was not associated with past-month distressing PEs in either sex but significantly associated with lifetime and repeated (≥ 2 waves) distressing PEs only in females. In both sexes, ES-SCZ<inf>75</inf> was significantly associated with all PE outcomes but did not additively interact with PRS-SCZ<inf>75</inf> in predicting them. Sensitivity analysis confirmed the findings and revealed a significant sex difference in the association between PRS-SCZ<inf>75</inf> and lifetime distressing PEs. Conclusion: The influence of genomic risk for schizophrenia on distressing PEs might be sex-dependent, whereas that of the exposomic risk was universal in early adolescence. Further studies in larger samples are needed.
dc.identifier.citationArchives of Women S Mental Health Vol.29 No.1 (2026)
dc.identifier.doi10.1007/s00737-025-01644-4
dc.identifier.eissn14351102
dc.identifier.issn14341816
dc.identifier.pmid41493491
dc.identifier.scopus2-s2.0-105026822109
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/114353
dc.rights.holderSCOPUS
dc.subjectMedicine
dc.titleSex differences in the independent and combined effects of genomic and exposomic risks for schizophrenia on distressing psychotic experiences: insights from the ABCD study
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105026822109&origin=inward
oaire.citation.issue1
oaire.citation.titleArchives of Women S Mental Health
oaire.citation.volume29
oairecerif.author.affiliationThe University of British Columbia
oairecerif.author.affiliationKing's College London
oairecerif.author.affiliationYale School of Medicine
oairecerif.author.affiliationUniversity Medical Center Utrecht
oairecerif.author.affiliationMaastricht Universitair Medisch Centrum+
oairecerif.author.affiliationUniversity of British Columbia, Faculty of Medicine
oairecerif.author.affiliationMedizinische Fakultät
oairecerif.author.affiliationUniversity of Northern British Columbia
oairecerif.author.affiliationFaculty of Medicine Ramathibodi Hospital, Mahidol University

Files

Collections