Resumen
Background: Cognitive impairment is a feature of severe mental illness (SMI; schizophrenia, bipolar disorder, major depressive disorder). Psychotic forms of SMI may be associated with greater cognitive impairment, but it is unclear if this differential impairment pre-dates illness onset or whether it reflects a consequence of the disorder. To establish if there is a developmental impairment related to familial risk of psychotic SMI, we investigated cognition in offspring of parents with psychotic and non-psychotic SMI. Method: Participants included 360 children and youth (mean age 11.10, SD 4.03, range 6–24), including 68 offspring of parents with psychotic SMI, 193 offspring of parents with non-psychotic SMI, and 99 offspring of control parents. The cognitive battery assessed a range of functions using standardized tests and executive function tasks from the Cambridge Automated Neuropsychological Test Battery. Results: Compared to controls, offspring of parents with psychotic SMI performed worse on overall cognition (β = −0.32; p < 0.001) and 6 of 15 cognitive domains, including verbal intelligence, verbal working memory, processing speed, verbal learning and memory, verbal fluency, and sustained attention. Offspring of parents with non-psychotic SMI performed worse than controls on 3 of the 15 domain specific cognitive tests, including verbal intelligence, visual memory and decision-making. Conclusions: Widespread mild-to-moderate cognitive impairments are present in young offspring at familial risk for transdiagnostic psychotic SMI. Offspring at familial risk for non-psychotic SMI showed fewer and more specific impairments in the domains of verbal intelligence, visual memory and decision-making.
Idioma original | English |
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Páginas (desde-hasta) | 306-312 |
Número de páginas | 7 |
Publicación | Journal of Psychiatric Research |
Volumen | 130 |
DOI | |
Estado | Published - nov. 2020 |
Nota bibliográfica
Funding Information:The work leading to this publication has been supported by funding from the Canada Research Chairs Program (award number 231397), the Canadian Institutes of Health Research (Grant reference numbers 124976, 142738 and 148394), the Brain & Behavior Research Foundation (NARSAD) Independent Investigator Grant 24684, Nova Scotia Health Research Foundation (grants 275319, 1716 and 353892), the Sutton Family Youth Mental Health Innovation Fund, and the Dalhousie Medical Research Foundation.
Funding Information:
The work leading to this publication has been supported by funding from the Canada Research Chairs Program (award number 231397 ), the Canadian Institutes of Health Research (Grant reference numbers 124976 , 142738 and 148394 ), the Brain & Behavior Research Foundation (NARSAD) Independent Investigator Grant 24684 , Nova Scotia Health Research Foundation (grants 275319 , 1716 and 353892 ), the Sutton Family Youth Mental Health Innovation Fund, and the Dalhousie Medical Research Foundation .
Publisher Copyright:
© 2020 Elsevier Ltd
ASJC Scopus Subject Areas
- Psychiatry and Mental health
- Biological Psychiatry
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't