Cognitive heterogeneity in the offspring of patients with schizophrenia or bipolar disorder: a cluster analysis across family risk

dc.contributor.author
Valli, Isabel
dc.contributor.author
Serna Gómez, Elena de la
dc.contributor.author
Borràs, Roger
dc.contributor.author
Ilzarbe, Daniel
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Baeza, Inmaculada, 1970-
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Picouto, María Dolores
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Baltasar, Itziar
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Moreno, Dolores
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Bernardo Arroyo, Miquel
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Young, Allan H.
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Vieta i Pascual, Eduard, 1963-
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Sugranyes, Gisela
dc.contributor.author
Castro Fornieles, Josefina
dc.date.issued
2022-02-16T08:47:47Z
dc.date.issued
2022-03-01T06:10:23Z
dc.date.issued
2021-03-01
dc.date.issued
2022-02-16T08:47:48Z
dc.identifier
0165-0327
dc.identifier
https://hdl.handle.net/2445/183215
dc.identifier
705959
dc.identifier
9164867
dc.description.abstract
Background: Neurocognitive impairment is considered to lie on a continuum of severity across schizophrenia (SZ) and bipolar disorder (BP), possibly reflecting a gradient of neurodevelopmental load. Cluster analyses have identified different levels of impairment across the two disorders, from none to widespread and severe. We for the first time used this approach to examine cognitive function pooling together children and adolescents at familial risk of SZ or BP. Methods: 220 participants, 49 offspring of individuals with schizophrenia (SZO), 90 offspring of individuals with bipolar disorder (BPO) and 81 offspring of healthy control parents (HC), aged 6 to 17 years, underwent a comprehensive clinical and cognitive assessment. Cognitive measures were used to group SZO and BPO using K-means clustering. Cognitive performance within each of the clusters was compared to that of HC and clinical variables were compared between clusters. Results: We identified three cognitive subgroups: a moderate impairment group, a mild impairment group, and a cognitively intact group. Both SZO and BPO were represented in each of the clusters, yet not evenly, with a larger proportion of the SZO in the moderately impaired cluster, but also a subgroup of BPO showing moderate cognitive dysfunction. Limitations: Participants have yet to reach the age of onset for the examined disorders. Conclusions: The findings point to a range of neurodevelopmental loadings across youth at familial risk of both SZ and BP. They have therefore important implications for the stratification of cognitive functioning and the possibility to tailor interventions to individual levels of impairment.
dc.format
14 p.
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application/pdf
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier B.V.
dc.relation
Versió postprint del document publicat a: https://doi.org/10.1016/j.jad.2020.12.090
dc.relation
Journal of Affective Disorders, 2021, vol. 282, p. 752-765
dc.relation
https://doi.org/10.1016/j.jad.2020.12.090
dc.rights
cc-by-nc-nd (c) Elsevier B.V., 2021
dc.rights
https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Medicina)
dc.subject
Trastorn bipolar
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Esquizofrènia
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Trastorn bipolar en els infants
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Factors de risc en les malalties
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Manic-depressive illness in adolescence
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Schizophrenia
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Manic-depressive illness in children
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Risk factors in diseases
dc.title
Cognitive heterogeneity in the offspring of patients with schizophrenia or bipolar disorder: a cluster analysis across family risk
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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