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Cognitive functioning in a group of adolescents at risk for psychosis

Cognitive deficits are a core feature of schizophrenia, and impairments are present in groups at-risk for psychosis. Most at-risk studies include young adults and not younger age-groups, such as adolescents. Participants are usually help-seeking individuals, even though risk factors may also be pres...

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Autores principales: Mohn-Haugen, Caroline Ranem, Mohn, Christine, Larøi, Frank, Teigset, Charlotte M., Øie, Merete Glenne, Rund, Bjørn Rishovd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753978/
https://www.ncbi.nlm.nih.gov/pubmed/36532169
http://dx.doi.org/10.3389/fpsyt.2022.1075222
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author Mohn-Haugen, Caroline Ranem
Mohn, Christine
Larøi, Frank
Teigset, Charlotte M.
Øie, Merete Glenne
Rund, Bjørn Rishovd
author_facet Mohn-Haugen, Caroline Ranem
Mohn, Christine
Larøi, Frank
Teigset, Charlotte M.
Øie, Merete Glenne
Rund, Bjørn Rishovd
author_sort Mohn-Haugen, Caroline Ranem
collection PubMed
description Cognitive deficits are a core feature of schizophrenia, and impairments are present in groups at-risk for psychosis. Most at-risk studies include young adults and not younger age-groups, such as adolescents. Participants are usually help-seeking individuals, even though risk factors may also be present in non-help seeking adolescents. We aim to explore cognitive functions in a group of non-help-seeking 15-year-old adolescents at risk for psychosis compared to age- and gender matched controls, including particular focus on specific cognitive domains. Hundred participants (mean age = 15.3) were invited after completing the 14-year-old survey distributed by the Norwegian Mother-, Father- and Child Study. At-risk adolescents were selected based on high scores on 19 items assessing both psychotic experiences and anomalous self-experiences. Matched controls were selected from the same sample. Cognitive functioning was assessed using the MATRICS Consensus Cognitive Battery and IQ using Wechsler’s Abbreviated Test of Intelligence. We found that the adolescents at-risk for psychosis had significantly poorer scores than controls on the composite score of the MCCB. IQ scores were also significantly lower in the at-risk group. The results highlight general cognitive deficits as central in a group of non-help-seeking adolescents at-risk for psychosis. Results indicate that the development of cognitive impairments starts early in life in at-risk groups. It is still unclear whether specific cognitive domains, such as verbal learning, are related to psychotic symptoms or may be specifically vulnerable to symptoms of depression and anxiety.
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spelling pubmed-97539782022-12-16 Cognitive functioning in a group of adolescents at risk for psychosis Mohn-Haugen, Caroline Ranem Mohn, Christine Larøi, Frank Teigset, Charlotte M. Øie, Merete Glenne Rund, Bjørn Rishovd Front Psychiatry Psychiatry Cognitive deficits are a core feature of schizophrenia, and impairments are present in groups at-risk for psychosis. Most at-risk studies include young adults and not younger age-groups, such as adolescents. Participants are usually help-seeking individuals, even though risk factors may also be present in non-help seeking adolescents. We aim to explore cognitive functions in a group of non-help-seeking 15-year-old adolescents at risk for psychosis compared to age- and gender matched controls, including particular focus on specific cognitive domains. Hundred participants (mean age = 15.3) were invited after completing the 14-year-old survey distributed by the Norwegian Mother-, Father- and Child Study. At-risk adolescents were selected based on high scores on 19 items assessing both psychotic experiences and anomalous self-experiences. Matched controls were selected from the same sample. Cognitive functioning was assessed using the MATRICS Consensus Cognitive Battery and IQ using Wechsler’s Abbreviated Test of Intelligence. We found that the adolescents at-risk for psychosis had significantly poorer scores than controls on the composite score of the MCCB. IQ scores were also significantly lower in the at-risk group. The results highlight general cognitive deficits as central in a group of non-help-seeking adolescents at-risk for psychosis. Results indicate that the development of cognitive impairments starts early in life in at-risk groups. It is still unclear whether specific cognitive domains, such as verbal learning, are related to psychotic symptoms or may be specifically vulnerable to symptoms of depression and anxiety. Frontiers Media S.A. 2022-12-01 /pmc/articles/PMC9753978/ /pubmed/36532169 http://dx.doi.org/10.3389/fpsyt.2022.1075222 Text en Copyright © 2022 Mohn-Haugen, Mohn, Larøi, Teigset, Øie and Rund. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Mohn-Haugen, Caroline Ranem
Mohn, Christine
Larøi, Frank
Teigset, Charlotte M.
Øie, Merete Glenne
Rund, Bjørn Rishovd
Cognitive functioning in a group of adolescents at risk for psychosis
title Cognitive functioning in a group of adolescents at risk for psychosis
title_full Cognitive functioning in a group of adolescents at risk for psychosis
title_fullStr Cognitive functioning in a group of adolescents at risk for psychosis
title_full_unstemmed Cognitive functioning in a group of adolescents at risk for psychosis
title_short Cognitive functioning in a group of adolescents at risk for psychosis
title_sort cognitive functioning in a group of adolescents at risk for psychosis
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753978/
https://www.ncbi.nlm.nih.gov/pubmed/36532169
http://dx.doi.org/10.3389/fpsyt.2022.1075222
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