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Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis
BACKGROUND: Clinical High Risk (CHS) for psychosis is a state in which positive symptoms are predominant but do not reach a level of severity that fulfils the criteria for a psychotic episode. The aim of this study has been to investigate whether cognition in subjects with newly detected CHR affects...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340303/ https://www.ncbi.nlm.nih.gov/pubmed/34381698 http://dx.doi.org/10.1016/j.scog.2021.100210 |
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author | Aase, Ingvild Langeveld, Johannes Hendrik Johannessen, Jan Olav Joa, Inge Dalen, Ingvild ten Velden Hegelstad, Wenche |
author_facet | Aase, Ingvild Langeveld, Johannes Hendrik Johannessen, Jan Olav Joa, Inge Dalen, Ingvild ten Velden Hegelstad, Wenche |
author_sort | Aase, Ingvild |
collection | PubMed |
description | BACKGROUND: Clinical High Risk (CHS) for psychosis is a state in which positive symptoms are predominant but do not reach a level of severity that fulfils the criteria for a psychotic episode. The aim of this study has been to investigate whether cognition in subjects with newly detected CHR affects the longitudinal development of positive symptoms. METHODS: Fifty-three CHR individuals fulfilling the criteria for attenuated positive syndrome in the Structural Interview for Prodromal Syndromes (SIPS) were included. At inclusion, all participants completed a neurocognitive battery consisting of tests measuring attention, verbal memory, verbal fluency, executive functions and general intelligence. Cognitive domain z-scores were defined by contrasting with observed scores of a group of matched healthy controls (n = 40). Associations between cognitive performance at inclusion and longitudinal measures of positive symptoms were assessed by using generalised linear models including non-linear effects of time. All regression models were adjusted for age and gender. RESULTS: Overall, SIPS positive symptoms declined over the time period, with a steeper decline during the first six months. Deficits in executive functions were assossiated witn a higher load of positive symptoms at baseline (p=0.006), but also to a faster improvement (p=0.030), wheras those with poor verbal fluency improved more slowly (p=0.018). CONCLUSION: To our knowledge, this is the first study that follows CHR subjects by means of frequent clinical interviews over a sustained period of time. The study provides evidence of an association between executive functions, including verbal fluency, with the evolvement of positive symptoms. |
format | Online Article Text |
id | pubmed-8340303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-83403032021-08-10 Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis Aase, Ingvild Langeveld, Johannes Hendrik Johannessen, Jan Olav Joa, Inge Dalen, Ingvild ten Velden Hegelstad, Wenche Schizophr Res Cogn Research Paper BACKGROUND: Clinical High Risk (CHS) for psychosis is a state in which positive symptoms are predominant but do not reach a level of severity that fulfils the criteria for a psychotic episode. The aim of this study has been to investigate whether cognition in subjects with newly detected CHR affects the longitudinal development of positive symptoms. METHODS: Fifty-three CHR individuals fulfilling the criteria for attenuated positive syndrome in the Structural Interview for Prodromal Syndromes (SIPS) were included. At inclusion, all participants completed a neurocognitive battery consisting of tests measuring attention, verbal memory, verbal fluency, executive functions and general intelligence. Cognitive domain z-scores were defined by contrasting with observed scores of a group of matched healthy controls (n = 40). Associations between cognitive performance at inclusion and longitudinal measures of positive symptoms were assessed by using generalised linear models including non-linear effects of time. All regression models were adjusted for age and gender. RESULTS: Overall, SIPS positive symptoms declined over the time period, with a steeper decline during the first six months. Deficits in executive functions were assossiated witn a higher load of positive symptoms at baseline (p=0.006), but also to a faster improvement (p=0.030), wheras those with poor verbal fluency improved more slowly (p=0.018). CONCLUSION: To our knowledge, this is the first study that follows CHR subjects by means of frequent clinical interviews over a sustained period of time. The study provides evidence of an association between executive functions, including verbal fluency, with the evolvement of positive symptoms. Elsevier 2021-07-28 /pmc/articles/PMC8340303/ /pubmed/34381698 http://dx.doi.org/10.1016/j.scog.2021.100210 Text en © 2021 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 Hendrik Johannessen, Jan Olav Joa, Inge Dalen, Ingvild ten Velden Hegelstad, Wenche Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
title | Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
title_full | Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
title_fullStr | Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
title_full_unstemmed | Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
title_short | Cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
title_sort | cognitive predictors of longitudinal positive symptom course in clinical high risk for psychosis |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8340303/ https://www.ncbi.nlm.nih.gov/pubmed/34381698 http://dx.doi.org/10.1016/j.scog.2021.100210 |
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