Childhood Trauma May Increase Risk of Psychosis and Mood Disorder in Genetically High-risk Children and Adolescents by Enhancing the Accumulation of Risk Indicators.

bipolar disorder child abuse cumulative major depressive disorder maltreatment offspring risk studies schizophrenia vulnerable

Journal

Schizophrenia bulletin open
ISSN: 2632-7899
Titre abrégé: Schizophr Bull Open
Pays: United States
ID NLM: 101770329

Informations de publication

Date de publication:
Jan 2022
Historique:
medline: 8 2 2022
pubmed: 8 2 2022
entrez: 15 8 2024
Statut: epublish

Résumé

Genetically high-risk children carry indicators of brain dysfunctions that adult patients with schizophrenia or bipolar disorder display. The accumulation of risk indicators would have a higher predictive value of a later transition to psychosis or mood disorder than each individual risk indicator. Since more than 50% of adult patients report having been exposed to childhood trauma, we investigated whether exposure to trauma during childhood was associated with the early accumulation of risk indicators in youths at genetic risk. We first inspected the characteristics of childhood trauma in 200 young offspring (51% male) born to a parent affected by DSM-IV schizophrenia, bipolar disorder, or major depressive disorder. A subsample of 109 offspring (51% male) had measurements on four risk indicators: cognitive impairments, psychotic-like experiences, nonpsychotic nonmood childhood DSM diagnoses, poor global functioning. Trauma was assessed from direct interviews and reviews of lifetime medical and school records of offspring. Trauma was present in 86 of the 200 offspring (43%). The relative risk of accumulating risk indicators in offspring exposed to trauma was 3.33 (95% CI 1.50, 7.36), but more pronounced in males (RR = 4.64, 95% CI 1.71, 12.6) than females (RR = 2.01, 95% CI 0.54, 7.58). Childhood trauma would be related to the accumulation of developmental precursors of major psychiatric disorders and more so in young boys at high genetic risk. Our findings may provide leads for interventions targeting the early mechanisms underlying the established relation between childhood trauma and adult psychiatric disorders.

Sections du résumé

Background UNASSIGNED
Genetically high-risk children carry indicators of brain dysfunctions that adult patients with schizophrenia or bipolar disorder display. The accumulation of risk indicators would have a higher predictive value of a later transition to psychosis or mood disorder than each individual risk indicator. Since more than 50% of adult patients report having been exposed to childhood trauma, we investigated whether exposure to trauma during childhood was associated with the early accumulation of risk indicators in youths at genetic risk.
Methods UNASSIGNED
We first inspected the characteristics of childhood trauma in 200 young offspring (51% male) born to a parent affected by DSM-IV schizophrenia, bipolar disorder, or major depressive disorder. A subsample of 109 offspring (51% male) had measurements on four risk indicators: cognitive impairments, psychotic-like experiences, nonpsychotic nonmood childhood DSM diagnoses, poor global functioning. Trauma was assessed from direct interviews and reviews of lifetime medical and school records of offspring.
Results UNASSIGNED
Trauma was present in 86 of the 200 offspring (43%). The relative risk of accumulating risk indicators in offspring exposed to trauma was 3.33 (95% CI 1.50, 7.36), but more pronounced in males (RR = 4.64, 95% CI 1.71, 12.6) than females (RR = 2.01, 95% CI 0.54, 7.58).
Conclusion UNASSIGNED
Childhood trauma would be related to the accumulation of developmental precursors of major psychiatric disorders and more so in young boys at high genetic risk. Our findings may provide leads for interventions targeting the early mechanisms underlying the established relation between childhood trauma and adult psychiatric disorders.

Identifiants

pubmed: 39144791
doi: 10.1093/schizbullopen/sgac017
pii: sgac017
pmc: PMC11206050
doi:

Types de publication

Journal Article

Langues

eng

Pagination

sgac017

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the University of Maryland's school of medicine, Maryland Psychiatric Research Center.

Auteurs

Nicolas Berthelot (N)

Department of Nursing Sciences, Université du Québec à Trois-Rivières, Trois-Rivières, QC, Canada.
CERVO Brain Research Center, Centre intégré de santé et de services sociaux de la Capitale-Nationale, Quebec City, QC, Canada.
Centre d'études interdisciplinaires sur le développement de l'enfant et la famille, Trois-Rivières, QC, Canada.
Interdisciplinary Research Center on Intimate Relationship Problems and Sexual Abuse, Montreal, QC, Canada.

Julia Garon-Bissonnette (J)

CERVO Brain Research Center, Centre intégré de santé et de services sociaux de la Capitale-Nationale, Quebec City, QC, Canada.
Centre d'études interdisciplinaires sur le développement de l'enfant et la famille, Trois-Rivières, QC, Canada.
Interdisciplinary Research Center on Intimate Relationship Problems and Sexual Abuse, Montreal, QC, Canada.
Department of Psychology, Université du Québec à Trois-Rivières, Trois-Rivières, QC, Canada.

Valérie Jomphe (V)

CERVO Brain Research Center, Centre intégré de santé et de services sociaux de la Capitale-Nationale, Quebec City, QC, Canada.

Hélène Doucet-Beaupré (H)

CERVO Brain Research Center, Centre intégré de santé et de services sociaux de la Capitale-Nationale, Quebec City, QC, Canada.
Department of Psychiatry and Neurosciences, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.

Alexandre Bureau (A)

CERVO Brain Research Center, Centre intégré de santé et de services sociaux de la Capitale-Nationale, Quebec City, QC, Canada.
Department of Psychiatry and Neurosciences, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.

Michel Maziade (M)

CERVO Brain Research Center, Centre intégré de santé et de services sociaux de la Capitale-Nationale, Quebec City, QC, Canada.
Department of Psychiatry and Neurosciences, Faculty of Medicine, Université Laval, Quebec City, QC, Canada.

Classifications MeSH