Association between family functioning and psychotic transition in ultra-high risk adolescents and young adults.

FAD-60 adolescent environment family functioning psychotic transition

Journal

Frontiers in psychiatry
ISSN: 1664-0640
Titre abrégé: Front Psychiatry
Pays: Switzerland
ID NLM: 101545006

Informations de publication

Date de publication:
2023
Historique:
received: 01 03 2023
accepted: 24 05 2023
medline: 7 7 2023
pubmed: 7 7 2023
entrez: 7 7 2023
Statut: epublish

Résumé

Psychotic transition (PT) is a crucial stage in schizophrenia. The Comprehensive Assessment of At-Risk Mental States (CAARMS) scale can be used to identify individuals at ultra-high risk (UHR) for psychosis and to evaluate their risk of PT. Many environmental and genetic factors have been identified as contributing to the development and decompensation of schizophrenia. This study aimed to determine if the quality of family functioning is associated with PT risk in UHR individuals aged between 11 and 25 years after 1 year of follow-up. From January to November 2017, 45 patients aged 12 to 25 consulting for psychiatric reasons were included. Twenty-six were classified as UHR of PT at the CAARMS. Family functioning was assessed by the Family Assessment Device-Global Functioning (FAD-GF). Thirty-seven of these patients (30% men, mean age 16 ± 2.5) were reassessed at 8-14 months of recruitment. Survival analysis was used to examine the impact of family functioning on PT risk. A total of 40% of UHR patients were classified as psychotic at reassessment. Survival analysis showed that better family functioning is a significant protective factor for PT in this population. This result suggests that the global family functioning has an impact at 1 year on the risk of PT in the population of adolescents and young adults who consult the hospital for psychiatric reasons. A family intervention may be effective in reducing PT risk in this population and should be considered as a potential therapeutic option.

Sections du résumé

Background UNASSIGNED
Psychotic transition (PT) is a crucial stage in schizophrenia. The Comprehensive Assessment of At-Risk Mental States (CAARMS) scale can be used to identify individuals at ultra-high risk (UHR) for psychosis and to evaluate their risk of PT. Many environmental and genetic factors have been identified as contributing to the development and decompensation of schizophrenia. This study aimed to determine if the quality of family functioning is associated with PT risk in UHR individuals aged between 11 and 25 years after 1 year of follow-up.
Methods UNASSIGNED
From January to November 2017, 45 patients aged 12 to 25 consulting for psychiatric reasons were included. Twenty-six were classified as UHR of PT at the CAARMS. Family functioning was assessed by the Family Assessment Device-Global Functioning (FAD-GF). Thirty-seven of these patients (30% men, mean age 16 ± 2.5) were reassessed at 8-14 months of recruitment. Survival analysis was used to examine the impact of family functioning on PT risk.
Results UNASSIGNED
A total of 40% of UHR patients were classified as psychotic at reassessment. Survival analysis showed that better family functioning is a significant protective factor for PT in this population.
Discussion UNASSIGNED
This result suggests that the global family functioning has an impact at 1 year on the risk of PT in the population of adolescents and young adults who consult the hospital for psychiatric reasons. A family intervention may be effective in reducing PT risk in this population and should be considered as a potential therapeutic option.

Identifiants

pubmed: 37415693
doi: 10.3389/fpsyt.2023.1177311
pmc: PMC10320389
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1177311

Informations de copyright

Copyright © 2023 Adrien, Liewig, Diot, Ferreri, Mouchabac, Dubertret and Bourgin.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Vladimir Adrien (V)

AP-HP, Department of Psychiatry, Saint-Antoine Hospital, Sorbonne Université, Paris, France.
Infrastructure for Clinical Research in Neuroscience (iCRIN), Paris Brain Institute, Sorbonne Université, INSERM, CNRS, Paris, France.

Justine Liewig (J)

Department of Child and Adolescent Psychiatry, Nord-Essonne Hospital, Bures-sur-Yvette, France.

Thomas Diot (T)

AP-HP, Department of Psychiatry, Saint-Antoine Hospital, Sorbonne Université, Paris, France.

Florian Ferreri (F)

AP-HP, Department of Psychiatry, Saint-Antoine Hospital, Sorbonne Université, Paris, France.
Infrastructure for Clinical Research in Neuroscience (iCRIN), Paris Brain Institute, Sorbonne Université, INSERM, CNRS, Paris, France.

Stephane Mouchabac (S)

AP-HP, Department of Psychiatry, Saint-Antoine Hospital, Sorbonne Université, Paris, France.
Infrastructure for Clinical Research in Neuroscience (iCRIN), Paris Brain Institute, Sorbonne Université, INSERM, CNRS, Paris, France.

Caroline Dubertret (C)

AP-HP, Department of Psychiatry, Louis Mourier Hospital, Université Paris Cité, Faculté de Médecine, Colombes, France.

Julie Bourgin (J)

Department of Child and Adolescent Psychiatry, Nord-Essonne Hospital, Bures-sur-Yvette, France.

Classifications MeSH