Neural alterations of emotion processing in atypical trajectories of psychotic-like experiences.


Journal

Schizophrenia (Heidelberg, Germany)
ISSN: 2754-6993
Titre abrégé: Schizophrenia (Heidelb)
Pays: Germany
ID NLM: 9918367987006676

Informations de publication

Date de publication:
21 Apr 2022
Historique:
received: 05 08 2021
accepted: 30 03 2022
entrez: 19 7 2022
pubmed: 20 7 2022
medline: 20 7 2022
Statut: epublish

Résumé

The aim of this study was to investigate the neural bases of facial emotion processing before the onset of clinical psychotic symptoms in youth belonging to well-defined developmental trajectories of psychotic-like experiences (PLEs). A unique sample of 86 youths was recruited from a population-based sample of over 3800 adolescents who had been followed from 13 to 17 years of age. Three groups were identified based on validated developmental trajectories: a control trajectory with low and decreasing PLEs, and two atypical trajectories with moderate to elevated baseline PLEs that subsequently decreased or increased. All had functional magnetic resonance imaging data collected during a facial emotion processing task. Functional activation and connectivity data were analyzed for different contrasts. The increasing PLE trajectory displayed more positive psychotic symptoms while the decreasing trajectory exhibited more negative symptoms relative to the control group. During face processing, both atypical trajectories displayed decreased activations of the right inferior frontal gyrus (IFG), while the increasing trajectory displayed a negative signal in the precentral gyrus. The increasing PLE trajectory also displayed impaired connectivity between the amygdala, ventromedial prefrontal cortex, and cerebellum, and between the IFG, precuneus, and temporal regions, while the decreasing trajectory exhibited reduced connectivity between the amygdala and visual regions during emotion processing. Both atypical PLE trajectories displayed alterations in brain regions involved in attention salience. While the increasing trajectory with more positive symptoms exhibited dysconnectivity in areas that influence emotion salience and face perception, the decreasing trajectory with more negative symptoms had impairments in visual information integration areas. These group-specific features might account for the differential symptom expression.

Identifiants

pubmed: 35853901
doi: 10.1038/s41537-022-00250-y
pii: 10.1038/s41537-022-00250-y
pmc: PMC9261083
doi:

Types de publication

Journal Article

Langues

eng

Pagination

40

Subventions

Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN114887
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : SHI155406
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN148561
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : SHI155406
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN114887
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN148561
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN148561
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN114887
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : SHI155406
Organisme : Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada)
ID : FRN148561

Informations de copyright

© 2022. The Author(s).

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Auteurs

Roxane Assaf (R)

Centre de Recherche de l'Institut Universitaire en Santé Mentale De Montréal, Montreal, QC, Canada.
Department of Psychiatry and Addiction, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.

Julien Ouellet (J)

Department of Psychiatry and Addiction, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.
Centre de Recherche du Centre Hospitalier Universitaire Sainte-Justine, Montreal, QC, Canada.

Josiane Bourque (J)

Department of Psychiatry, Perelman Faculty of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

Emmanuel Stip (E)

Department of Psychiatry and Addiction, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.

Marco Leyton (M)

Department of Psychiatry, Faculty of Medicine, McGill University, Montreal, QC, Canada.

Patricia Conrod (P)

Department of Psychiatry and Addiction, Faculty of Medicine, University of Montreal, Montreal, QC, Canada.
Centre de Recherche du Centre Hospitalier Universitaire Sainte-Justine, Montreal, QC, Canada.

Stéphane Potvin (S)

Centre de Recherche de l'Institut Universitaire en Santé Mentale De Montréal, Montreal, QC, Canada. stephane.potvin@umontreal.ca.
Department of Psychiatry and Addiction, Faculty of Medicine, University of Montreal, Montreal, QC, Canada. stephane.potvin@umontreal.ca.

Classifications MeSH