Migrant status, clinical symptoms and functional outcome in youth at clinical high risk for psychosis: findings from the NAPLS-3 study.


Journal

Social psychiatry and psychiatric epidemiology
ISSN: 1433-9285
Titre abrégé: Soc Psychiatry Psychiatr Epidemiol
Pays: Germany
ID NLM: 8804358

Informations de publication

Date de publication:
Apr 2023
Historique:
received: 25 11 2021
accepted: 28 10 2022
medline: 4 4 2023
pubmed: 9 11 2022
entrez: 8 11 2022
Statut: ppublish

Résumé

Migrant status is a known risk factor for psychosis, but the underlying causes of this vulnerability are poorly understood. Recently, studies have begun to explore whether migrant status predicts transition to psychosis in individuals at clinical high risk (CHR) for psychosis. Results, however, have been inconclusive. The present study assessed the impact of migrant status on clinical symptoms and functional outcome in individuals at CHR for psychosis who took part in the NAPLS-3 study. Participants' migrant status was classified as native-born, first-generation, or second-generation migrant. Clinical symptoms were assessed using the Structured Interview for Psychosis-Risk Syndromes (SIPS); functional outcome was measured using the Global Functioning Scales:Social and Role (GF:S; GF:R). Assessments were conducted at baseline, 12-months, 18-months, and 24-months follow-up. Generalized linear mixed models for repeated measures were used to examine changes over time and differences between groups. The overall sample included 710 individuals at CHR for psychosis (54.2% males; Age: M = 18.19; SD = 4.04). A mixed model analysis was conducted, and no significant differences between groups in symptoms or functioning were observed at any time point. Over time, significant improvement in symptoms and functioning was observed within each group. Transition rates did not differ across groups. We discuss potential factors that might explain the lack of group differences. Overall, migrants are a heterogeneous population. Discerning the impact of migration from that of neighborhood ethnic density, social disadvantage or socio-economic status of different ethnic groups could help better understand vulnerability and resilience to psychosis.

Identifiants

pubmed: 36348056
doi: 10.1007/s00127-022-02383-y
pii: 10.1007/s00127-022-02383-y
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

559-568

Subventions

Organisme : NIMH NIH HHS
ID : U01MH081984
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081928
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081944
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081902
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH082004
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081988
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH082022
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH076989
Pays : United States
Organisme : NIMH NIH HHS
ID : UO1MH081857
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081984
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081928
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081944
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081902
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081902
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH082004
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH081988
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH082022
Pays : United States
Organisme : NIMH NIH HHS
ID : U01MH076989
Pays : United States
Organisme : NIMH NIH HHS
ID : UO1MH081857
Pays : United States

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.

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Auteurs

Mariapaola Barbato (M)

Department of Psychology, College of Natural and Health Sciences, Zayed University, Dubai, UAE.

Lu Liu (L)

Department of Psychiatry, Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada.

Carrie E Bearden (CE)

Departments of Psychiatry and Biobehavioral Sciences and Psychology, Semel Institute for Neuroscience and Human Behavior, UCLA, Los Angeles, CA, USA.

Kristin S Cadenhead (KS)

Department of Psychiatry, UCSD, San Diego, CA, USA.

Barbara A Cornblatt (BA)

Department of Psychiatry, Zucker Hillside Hospital, Long Island, NY, USA.

Matcheri Keshavan (M)

Department of Psychiatry, Harvard Medical School at Beth Israel Deaconess Medical Center and Massachusetts General Hospital, Boston, MA, USA.

Daniel H Mathalon (DH)

Department of Psychiatry, UCSF, and SFVA Medical Center, San Francisco, CA, USA.

Thomas H McGlashan (TH)

Department of Psychiatry, Yale University, New Haven, CT, USA.

Diana O Perkins (DO)

Department of Psychiatry, University of North Carolina, Chapel Hill, NC, USA.

Larry J Seidman (LJ)

Department of Psychiatry, Harvard Medical School at Beth Israel Deaconess Medical Center and Massachusetts General Hospital, Boston, MA, USA.

William Stone (W)

Department of Psychiatry, Harvard Medical School at Beth Israel Deaconess Medical Center and Massachusetts General Hospital, Boston, MA, USA.

Ming T Tsuang (MT)

Department of Psychiatry, UCSD, San Diego, CA, USA.
Institute of Genomic Medicine, University of California, La Jolla, CA, USA.

Elaine F Walker (EF)

Departments of Psychology and Psychiatry, Emory University, Atlanta, GA, USA.

Scott W Woods (SW)

Department of Psychiatry, Yale University, New Haven, CT, USA.

Tyrone D Cannon (TD)

Department of Psychiatry, Yale University, New Haven, CT, USA.
Department of Psychology, Yale University, New Haven, CT, USA.

Jean Addington (J)

Department of Psychiatry, Hotchkiss Brain Institute, University of Calgary, Calgary, AB, Canada. jmadding@ucalgary.ca.
Mathison Centre for Mental Health Research & Education, University of Calgary, 3280 Hospital Drive NW, Calgary, AB, T2N 4Z6, Canada. jmadding@ucalgary.ca.

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