Assessment of Neurocognitive Functions in 7-Year-Old Children at Familial High Risk for Schizophrenia or Bipolar Disorder: The Danish High Risk and Resilience Study VIA 7.

Détails

ID Serval
serval:BIB_CBC859B8E134
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Assessment of Neurocognitive Functions in 7-Year-Old Children at Familial High Risk for Schizophrenia or Bipolar Disorder: The Danish High Risk and Resilience Study VIA 7.
Périodique
JAMA psychiatry
Auteur⸱e⸱s
Hemager N., Plessen K.J., Thorup A., Christiani C., Ellersgaard D., Spang K.S., Burton B.K., Gregersen M., Søndergaard A., Greve A.N., Gantriis D.L., Poulsen G., Seidman L.J., Mors O., Nordentoft M., Jepsen JRM
ISSN
2168-6238 (Electronic)
ISSN-L
2168-622X
Statut éditorial
Publié
Date de publication
01/08/2018
Peer-reviewed
Oui
Volume
75
Numéro
8
Pages
844-852
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
Children at familial high risk of schizophrenia spectrum disorders (FHR-SZ) or bipolar disorder (FHR-BP) exhibit neurocognitive impairments. Large studies of neurocognition in young children at familial high risk at the same age are important to differentiate the pathophysiology and developmental trajectory of these 2 groups.
To characterize neurocognitive functions in 7-year-old children with FHR-SZ or FHR-BP and a control population.
This multisite population-based cohort study collected data from January 1, 2013, to January 31, 2016, in the first wave of the Danish High Risk and Resilience Study VIA 7 at 2 university hospital research sites in Copenhagen and Aarhus using Danish registries. Participants (n = 514) included 197 children with FHR-SZ, 118 with FHR-BP, and 199 controls matched with the FHR-SZ group for age, sex, and municipality. Assessors were blinded to risk status.
Parents with schizophrenia, bipolar disorder, or neither diagnosis.
Neurocognitive functions were measured across 23 tests. Four neurocognitive domains were derived by principal component analysis, including processing speed and working memory, verbal functions, executive and visuospatial functions, and declarative memory and attention.
A total of 514 children aged 7 years were included in the analysis (46.3% girls), consisting of 197 children with FHR-SZ (46.2% girls), 118 with FHR-BP (46.6% girls), and 199 controls (46.2% girls). Children with FHR-SZ were significantly impaired compared with controls on processing speed and working memory (Cohen d = 0.50; P < .001), executive and visuospatial functions (Cohen d = 0.28; P = .03), and declarative memory and attention (Cohen d = 0.29; P = .02). Compared with children with FHR-BP, children with FHR-SZ performed significantly poorer in processing speed and working memory (Cohen d = 0.40; P = .002), executive and visuospatial functions (Cohen d = 0.35; P = .008), and declarative memory and attention (Cohen d = 0.31; P = .03). Children with FHR-BP and controls did not differ.
Children with FHR-SZ had widespread neurocognitive impairments, supporting the hypothesis of neurocognitive functions as endophenotypes of schizophrenia. The absence of neurocognitive deficits in children with FHR-BP suggests distinct neurodevelopmental manifestations in these familial high-risk groups at this age. Early detection of children with FHR-SZ and cognitive impairments is warranted to investigate associations of neurocognition with transition to psychosis, add to the knowledge of their developmental pathophysiology, and inform early intervention programs.
Mots-clé
Bipolar Disorder/diagnosis, Bipolar Disorder/epidemiology, Bipolar Disorder/genetics, Bipolar Disorder/psychology, Child, Denmark/epidemiology, Early Diagnosis, Early Medical Intervention/methods, Endophenotypes, Executive Function, Female, Humans, Male, Medical History Taking/statistics & numerical data, Mental Competency/psychology, Mental Status and Dementia Tests, Neurocognitive Disorders/diagnosis, Neurocognitive Disorders/etiology, Neuropsychological Tests, Registries, Schizophrenia/diagnosis, Schizophrenia/epidemiology, Schizophrenia/genetics, Schizophrenic Psychology
Pubmed
Web of science
Création de la notice
28/06/2018 8:47
Dernière modification de la notice
04/10/2019 5:08
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