Asphyxia at birth affects brain structure in patients on the schizophrenia-bipolar disorder spectrum and healthy participants.


Journal

Psychological medicine
ISSN: 1469-8978
Titre abrégé: Psychol Med
Pays: England
ID NLM: 1254142

Informations de publication

Date de publication:
04 2022
Historique:
pubmed: 11 8 2020
medline: 22 12 2022
entrez: 11 8 2020
Statut: ppublish

Résumé

Uncertainty exists about what causes brain structure alterations associated with schizophrenia (SZ) and bipolar disorder (BD). Whether a history of asphyxia-related obstetric complication (ASP) - a common but harmful condition for neural tissue - contributes to variations in adult brain structure is unclear. We investigated ASP and its relationship to intracranial (ICV), global brain volumes and regional cortical and subcortical structures. A total of 311 patients on the SZ - BD spectrum and 218 healthy control (HC) participants underwent structural magnetic resonance imaging. They were evaluated for ASP using prospective information obtained from the Medical Birth Registry of Norway. In all groups, ASP was related to smaller ICV, total brain, white and gray matter volumes and total surface area, but not to cortical thickness. Smaller cortical surface areas were found across frontal, parietal, occipital, temporal and insular regions. Smaller hippocampal, amygdala, thalamus, caudate and putamen volumes were reported for all ASP subgroups. ASP effects did not survive ICV correction, except in the caudate, which remained significantly smaller in both patient ASP subgroups, but not in the HC. Since ASP was associated with smaller brain volumes in all groups, the genetic risk of developing a severe mental illness, alone, cannot easily explain the smaller ICV. Only the smaller caudate volumes of ASP patients specifically suggest that injury from ASP can be related to disease development. Our findings give support for the ICV as a marker of aberrant neurodevelopment and ASP in the etiology of brain development in BD and SZ.

Sections du résumé

BACKGROUND
Uncertainty exists about what causes brain structure alterations associated with schizophrenia (SZ) and bipolar disorder (BD). Whether a history of asphyxia-related obstetric complication (ASP) - a common but harmful condition for neural tissue - contributes to variations in adult brain structure is unclear. We investigated ASP and its relationship to intracranial (ICV), global brain volumes and regional cortical and subcortical structures.
METHODS
A total of 311 patients on the SZ - BD spectrum and 218 healthy control (HC) participants underwent structural magnetic resonance imaging. They were evaluated for ASP using prospective information obtained from the Medical Birth Registry of Norway.
RESULTS
In all groups, ASP was related to smaller ICV, total brain, white and gray matter volumes and total surface area, but not to cortical thickness. Smaller cortical surface areas were found across frontal, parietal, occipital, temporal and insular regions. Smaller hippocampal, amygdala, thalamus, caudate and putamen volumes were reported for all ASP subgroups. ASP effects did not survive ICV correction, except in the caudate, which remained significantly smaller in both patient ASP subgroups, but not in the HC.
CONCLUSIONS
Since ASP was associated with smaller brain volumes in all groups, the genetic risk of developing a severe mental illness, alone, cannot easily explain the smaller ICV. Only the smaller caudate volumes of ASP patients specifically suggest that injury from ASP can be related to disease development. Our findings give support for the ICV as a marker of aberrant neurodevelopment and ASP in the etiology of brain development in BD and SZ.

Identifiants

pubmed: 32772969
doi: 10.1017/S0033291720002779
pii: S0033291720002779
pmc: PMC9069351
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1050-1059

Auteurs

Laura Anne Wortinger (LA)

Department of Psychiatric Research, Diakonhjemmet Hospital, Oslo, Norway.
NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Kristine Engen (K)

Department of Psychiatric Research, Diakonhjemmet Hospital, Oslo, Norway.
NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Claudia Barth (C)

NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Ole A Andreassen (OA)

NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Division of Mental Health and Addiction, NORMENT, Oslo University Hospital, Oslo, Norway.

Kjetil Nordbø Jørgensen (K)

Department of Psychiatric Research, Diakonhjemmet Hospital, Oslo, Norway.
NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

Ingrid Agartz (I)

Department of Psychiatric Research, Diakonhjemmet Hospital, Oslo, Norway.
NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Clinical Neuroscience, Centre for Psychiatric Research, Karolinska Institute, Stockholm, Sweden.

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Classifications MeSH