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Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis

BACKGROUND: Impairments in the attribution of salience are thought to be fundamental to the development of psychotic symptoms and the onset of psychotic disorders. The aim of the present study was to explore longitudinal alterations in salience processing in ultra-high-risk subjects for psychosis. M...

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Autores principales: Schmidt, A., Antoniades, M., Allen, P., Egerton, A., Chaddock, C. A., Borgwardt, S., Fusar-Poli, P., Roiser, J. P., Howes, O., McGuire, P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216461/
https://www.ncbi.nlm.nih.gov/pubmed/27697078
http://dx.doi.org/10.1017/S0033291716002439
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author Schmidt, A.
Antoniades, M.
Allen, P.
Egerton, A.
Chaddock, C. A.
Borgwardt, S.
Fusar-Poli, P.
Roiser, J. P.
Howes, O.
McGuire, P.
author_facet Schmidt, A.
Antoniades, M.
Allen, P.
Egerton, A.
Chaddock, C. A.
Borgwardt, S.
Fusar-Poli, P.
Roiser, J. P.
Howes, O.
McGuire, P.
author_sort Schmidt, A.
collection PubMed
description BACKGROUND: Impairments in the attribution of salience are thought to be fundamental to the development of psychotic symptoms and the onset of psychotic disorders. The aim of the present study was to explore longitudinal alterations in salience processing in ultra-high-risk subjects for psychosis. METHOD: A total of 23 ultra-high-risk subjects and 13 healthy controls underwent functional magnetic resonance imaging at two time points (mean interval of 17 months) while performing the Salience Attribution Test to assess neural responses to task-relevant (adaptive salience) and task-irrelevant (aberrant salience) stimulus features. RESULTS: At presentation, high-risk subjects were less likely than controls to attribute salience to relevant features, and more likely to attribute salience to irrelevant stimulus features. These behavioural differences were no longer evident at follow-up. When attributing salience to relevant cue features, ultra-high-risk subjects showed less activation than controls in the ventral striatum at both baseline and follow-up. Within the high-risk sample, amelioration of abnormal beliefs over the follow-up period was correlated with an increase in right ventral striatum activation during the attribution of salience to relevant cue features. CONCLUSIONS: These findings confirm that salience processing is perturbed in ultra-high-risk subjects for psychosis, that this is linked to alterations in ventral striatum function, and that clinical outcomes are related to longitudinal changes in ventral striatum function during salience processing.
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spelling pubmed-52164612017-01-17 Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis Schmidt, A. Antoniades, M. Allen, P. Egerton, A. Chaddock, C. A. Borgwardt, S. Fusar-Poli, P. Roiser, J. P. Howes, O. McGuire, P. Psychol Med Original Articles BACKGROUND: Impairments in the attribution of salience are thought to be fundamental to the development of psychotic symptoms and the onset of psychotic disorders. The aim of the present study was to explore longitudinal alterations in salience processing in ultra-high-risk subjects for psychosis. METHOD: A total of 23 ultra-high-risk subjects and 13 healthy controls underwent functional magnetic resonance imaging at two time points (mean interval of 17 months) while performing the Salience Attribution Test to assess neural responses to task-relevant (adaptive salience) and task-irrelevant (aberrant salience) stimulus features. RESULTS: At presentation, high-risk subjects were less likely than controls to attribute salience to relevant features, and more likely to attribute salience to irrelevant stimulus features. These behavioural differences were no longer evident at follow-up. When attributing salience to relevant cue features, ultra-high-risk subjects showed less activation than controls in the ventral striatum at both baseline and follow-up. Within the high-risk sample, amelioration of abnormal beliefs over the follow-up period was correlated with an increase in right ventral striatum activation during the attribution of salience to relevant cue features. CONCLUSIONS: These findings confirm that salience processing is perturbed in ultra-high-risk subjects for psychosis, that this is linked to alterations in ventral striatum function, and that clinical outcomes are related to longitudinal changes in ventral striatum function during salience processing. Cambridge University Press 2017-01 2016-10-04 /pmc/articles/PMC5216461/ /pubmed/27697078 http://dx.doi.org/10.1017/S0033291716002439 Text en © Cambridge University Press 2016 http://creativecommons.org/licenses/by/4.0/ This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Schmidt, A.
Antoniades, M.
Allen, P.
Egerton, A.
Chaddock, C. A.
Borgwardt, S.
Fusar-Poli, P.
Roiser, J. P.
Howes, O.
McGuire, P.
Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
title Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
title_full Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
title_fullStr Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
title_full_unstemmed Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
title_short Longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
title_sort longitudinal alterations in motivational salience processing in ultra-high-risk subjects for psychosis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5216461/
https://www.ncbi.nlm.nih.gov/pubmed/27697078
http://dx.doi.org/10.1017/S0033291716002439
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