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.author | Prachason T. | |
| dc.contributor.author | Arias-Magnasco A. | |
| dc.contributor.author | Lin B.D. | |
| dc.contributor.author | van Os J. | |
| dc.contributor.author | Rutten B.P.F. | |
| dc.contributor.author | Pries L.K. | |
| dc.contributor.author | Guloksuz S. | |
| dc.contributor.correspondence | Prachason T. | |
| dc.contributor.other | Mahidol University | |
| dc.date.accessioned | 2026-02-06T18:09:05Z | |
| dc.date.available | 2026-02-06T18:09:05Z | |
| dc.date.issued | 2026-02-01 | |
| dc.description.abstract | Purpose: 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.citation | Archives of Women S Mental Health Vol.29 No.1 (2026) | |
| dc.identifier.doi | 10.1007/s00737-025-01644-4 | |
| dc.identifier.eissn | 14351102 | |
| dc.identifier.issn | 14341816 | |
| dc.identifier.pmid | 41493491 | |
| dc.identifier.scopus | 2-s2.0-105026822109 | |
| dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/123456789/114353 | |
| dc.rights.holder | SCOPUS | |
| dc.subject | Medicine | |
| dc.title | 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.type | Article | |
| mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105026822109&origin=inward | |
| oaire.citation.issue | 1 | |
| oaire.citation.title | Archives of Women S Mental Health | |
| oaire.citation.volume | 29 | |
| oairecerif.author.affiliation | The University of British Columbia | |
| oairecerif.author.affiliation | King's College London | |
| oairecerif.author.affiliation | Yale School of Medicine | |
| oairecerif.author.affiliation | University Medical Center Utrecht | |
| oairecerif.author.affiliation | Maastricht Universitair Medisch Centrum+ | |
| oairecerif.author.affiliation | University of British Columbia, Faculty of Medicine | |
| oairecerif.author.affiliation | Medizinische Fakultät | |
| oairecerif.author.affiliation | University of Northern British Columbia | |
| oairecerif.author.affiliation | Faculty of Medicine Ramathibodi Hospital, Mahidol University |
