Stress precedes negative symptom exacerbations in clinical high risk and early psychosis: A time-lagged experience sampling study.


Journal

Schizophrenia research
ISSN: 1573-2509
Titre abrégé: Schizophr Res
Pays: Netherlands
ID NLM: 8804207

Informations de publication

Date de publication:
08 2019
Historique:
received: 18 09 2018
revised: 15 03 2019
accepted: 17 06 2019
pubmed: 30 6 2019
medline: 15 9 2020
entrez: 29 6 2019
Statut: ppublish

Résumé

The experience sampling method (ESM) has revealed associations between fluctuations in stress and positive symptoms in psychosis. It is unknown, however, how negative symptoms including anhedonia respond to stress. Stress is divided according to its source: event-related stress stemming from negative events, and activity-related stress stemming from engaging in tasks beyond one's skill or control. Anhedonia is divided into consummatory and anticipatory anhedonia, reflecting a lack of pleasure in current and expected activities. This study uses ESM to determine whether each form of anhedonia increases in response to stress. Antipsychotic-naïve individuals with first episode psychosis (n = 39), clinical high-risk states for psychosis (n = 44), and healthy controls (n = 34) responded to daily prompts on a palmtop computer for up to ten days by indicating levels of stress and anhedonia. Time-lagged multilevel modelling was employed to explore increases in anhedonia following increases in stress while controlling for prior levels of anhedonia. Mean levels of anhedonia were also compared across groups. Only activity-related stress produced increases in anhedonia. This effect did not vary between groups. Clinical groups showed greater overall levels of anhedonia than healthy controls, but did not differ from each other. Anhedonia responds only to activity-related stressors, suggesting that this form of stress has a specific causal role in anhedonia. The results also provide further evidence for global increases in anhedonia in antipsychotic-naïve psychosis spectrum individuals.

Identifiants

pubmed: 31248749
pii: S0920-9964(19)30236-1
doi: 10.1016/j.schres.2019.06.015
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

52-58

Subventions

Organisme : CIHR
Pays : Canada

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

Auteurs

Cory Gerritsen (C)

Centre for Addiction and Mental Health, 250 College St, Toronto, Ontario M5T 1R8, Canada; University of Toronto, 27 King's College Circle, Toronto, Ontario M5S 1A1, Canada. Electronic address: cory.gerritsen@camh.ca.

R Michael Bagby (RM)

Centre for Addiction and Mental Health, 250 College St, Toronto, Ontario M5T 1R8, Canada; University of Toronto, 27 King's College Circle, Toronto, Ontario M5S 1A1, Canada. Electronic address: rmichael.bagby@utoronto.ca.

Marcos Sanches (M)

Centre for Addiction and Mental Health, 250 College St, Toronto, Ontario M5T 1R8, Canada. Electronic address: marcos.sanches@camh.ca.

Michael Kiang (M)

Centre for Addiction and Mental Health, 250 College St, Toronto, Ontario M5T 1R8, Canada; University of Toronto, 27 King's College Circle, Toronto, Ontario M5S 1A1, Canada. Electronic address: michael.kiang@camh.ca.

Margaret Maheandiran (M)

Centre for Addiction and Mental Health, 250 College St, Toronto, Ontario M5T 1R8, Canada. Electronic address: margaret.maheandiran@camh.ca.

Ivana Prce (I)

Sunnybrook Research Institute, 2075 Bayview Ave, Toronto, Ontario M4N 3M5, Canada. Electronic address: ivana.prce@sunnybrook.ca.

Romina Mizrahi (R)

Centre for Addiction and Mental Health, 250 College St, Toronto, Ontario M5T 1R8, Canada; University of Toronto, 27 King's College Circle, Toronto, Ontario M5S 1A1, Canada. Electronic address: romina.mizrahi@camhpet.ca.

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