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Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis

INTRODUCTION: Clinical high risk for psychosis (CHR) is associated with mild cognitive impairments. Symptoms are clustered into positive, negative and disorganization symptoms. The association between specific symptom dimensions and cognitive functions remains unclear. The aim of this study was to i...

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Autores principales: Aase, Ingvild, Langeveld, Johannes H., Joa, Inge, Johannessen, Jan Olav, Dalen, Ingvild, ten Velden Hegelstad, Wenche
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168614/
https://www.ncbi.nlm.nih.gov/pubmed/35677653
http://dx.doi.org/10.1016/j.scog.2022.100260
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author Aase, Ingvild
Langeveld, Johannes H.
Joa, Inge
Johannessen, Jan Olav
Dalen, Ingvild
ten Velden Hegelstad, Wenche
author_facet Aase, Ingvild
Langeveld, Johannes H.
Joa, Inge
Johannessen, Jan Olav
Dalen, Ingvild
ten Velden Hegelstad, Wenche
author_sort Aase, Ingvild
collection PubMed
description INTRODUCTION: Clinical high risk for psychosis (CHR) is associated with mild cognitive impairments. Symptoms are clustered into positive, negative and disorganization symptoms. The association between specific symptom dimensions and cognitive functions remains unclear. The aim of this study was to investigate the associations between cognitive functions and positive, negative, and disorganization symptoms. METHOD: 53 CHR subjects fulfilling criteria for attenuated psychotic syndrome in the Structural Interview for Prodromal Syndromes (SIPS) were assessed for cognitive function. Five cognitive domain z-scores were defined by contrasting with observed scores of a group of healthy controls (n = 40). Principal Components Analyses were performed to construct general cognitive composite scores; one using all subtests and one using the cognitive domains. Associations between cognitive functions and symptoms are presented as Spearman's rank correlations and partial Spearman's rank correlations adjusted for age and gender. RESULTS: Positive symptoms were negatively associated with executive functions and verbal memory, and disorganization symptoms with poorer verbal fluency. Negative symptoms were associated with better executive functioning. There were no significant associations between the general cognitive composites and any of the symptom domains, except for a trend for positive symptoms. CONCLUSION: In line with previous research, data indicated associations between positive symptoms and poorer executive functioning. Negative symptoms may not be related to executive functions in CHR the same way as in psychosis. Our results could indicate that attenuated positive symptoms are more related to cognitive deficits in CHR than positive symptoms in schizophrenia and FEP.
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spelling pubmed-91686142022-06-07 Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis Aase, Ingvild Langeveld, Johannes H. Joa, Inge Johannessen, Jan Olav Dalen, Ingvild ten Velden Hegelstad, Wenche Schizophr Res Cogn Research Paper INTRODUCTION: Clinical high risk for psychosis (CHR) is associated with mild cognitive impairments. Symptoms are clustered into positive, negative and disorganization symptoms. The association between specific symptom dimensions and cognitive functions remains unclear. The aim of this study was to investigate the associations between cognitive functions and positive, negative, and disorganization symptoms. METHOD: 53 CHR subjects fulfilling criteria for attenuated psychotic syndrome in the Structural Interview for Prodromal Syndromes (SIPS) were assessed for cognitive function. Five cognitive domain z-scores were defined by contrasting with observed scores of a group of healthy controls (n = 40). Principal Components Analyses were performed to construct general cognitive composite scores; one using all subtests and one using the cognitive domains. Associations between cognitive functions and symptoms are presented as Spearman's rank correlations and partial Spearman's rank correlations adjusted for age and gender. RESULTS: Positive symptoms were negatively associated with executive functions and verbal memory, and disorganization symptoms with poorer verbal fluency. Negative symptoms were associated with better executive functioning. There were no significant associations between the general cognitive composites and any of the symptom domains, except for a trend for positive symptoms. CONCLUSION: In line with previous research, data indicated associations between positive symptoms and poorer executive functioning. Negative symptoms may not be related to executive functions in CHR the same way as in psychosis. Our results could indicate that attenuated positive symptoms are more related to cognitive deficits in CHR than positive symptoms in schizophrenia and FEP. Elsevier 2022-06-02 /pmc/articles/PMC9168614/ /pubmed/35677653 http://dx.doi.org/10.1016/j.scog.2022.100260 Text en © 2022 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Paper
Aase, Ingvild
Langeveld, Johannes H.
Joa, Inge
Johannessen, Jan Olav
Dalen, Ingvild
ten Velden Hegelstad, Wenche
Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
title Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
title_full Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
title_fullStr Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
title_full_unstemmed Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
title_short Associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
title_sort associations between symptom and neurocognitive dimensions in clinical high risk for psychosis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9168614/
https://www.ncbi.nlm.nih.gov/pubmed/35677653
http://dx.doi.org/10.1016/j.scog.2022.100260
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