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The role of cognitive control in the positive symptoms of psychosis

BACKGROUND: Positive symptoms of psychosis (e.g., hallucinations) often limit everyday functioning and can persist despite adequate antipsychotic treatment. We investigated whether poor cognitive control is a mechanism underlying these symptoms. METHODS: 97 patients with early psychosis (30 with hig...

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Autores principales: Horne, Charlotte M., Sahni, Angad, Pang, Sze W., Vanes, Lucy D., Szentgyorgyi, Timea, Averbeck, Bruno, Moran, Rosalyn J., Shergill, Sukhwinder S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059151/
https://www.ncbi.nlm.nih.gov/pubmed/35468567
http://dx.doi.org/10.1016/j.nicl.2022.103004
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author Horne, Charlotte M.
Sahni, Angad
Pang, Sze W.
Vanes, Lucy D.
Szentgyorgyi, Timea
Averbeck, Bruno
Moran, Rosalyn J.
Shergill, Sukhwinder S.
author_facet Horne, Charlotte M.
Sahni, Angad
Pang, Sze W.
Vanes, Lucy D.
Szentgyorgyi, Timea
Averbeck, Bruno
Moran, Rosalyn J.
Shergill, Sukhwinder S.
author_sort Horne, Charlotte M.
collection PubMed
description BACKGROUND: Positive symptoms of psychosis (e.g., hallucinations) often limit everyday functioning and can persist despite adequate antipsychotic treatment. We investigated whether poor cognitive control is a mechanism underlying these symptoms. METHODS: 97 patients with early psychosis (30 with high positive symptoms (HS) and 67 with low positive symptoms (LS)) and 40 healthy controls (HC) underwent fMRI whilst performing a reward learning task with two conditions; low cognitive demand (choosing between neutral faces) and high cognitive demand (choosing between angry and happy faces – shown to induce an emotional bias). Decision and feedback phases were examined. RESULTS: Both patient groups showed suboptimal learning behaviour compared to HC and altered activity within a core reward network including occipital/lingual gyrus (decision), rostral Anterior Cingulate Cortex, left pre-central gyrus and Supplementary Motor Cortex (feedback). In the low cognitive demand condition, HS group showed significantly reduced activity in Supplementary Motor Area (SMA)/pre-SMA during the decision phase whilst activity was increased in LS group compared to HC. Recruitment of this region suggests a top-down compensatory mechanism important for control of positive symptoms. With additional cognitive demand (emotional vs. neutral contrast), HS patients showed further alterations within a subcortical network (increased left amygdala activity during decisions and reduced left pallidum and thalamus activity during feedback) compared to LS patients. CONCLUSIONS: The findings suggest a core reward system deficit may be present in both patient groups, but persistent positive symptoms are associated with a specific dysfunction within a network needed to integrate social-emotional information with reward feedback.
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spelling pubmed-90591512022-05-03 The role of cognitive control in the positive symptoms of psychosis Horne, Charlotte M. Sahni, Angad Pang, Sze W. Vanes, Lucy D. Szentgyorgyi, Timea Averbeck, Bruno Moran, Rosalyn J. Shergill, Sukhwinder S. Neuroimage Clin Regular Article BACKGROUND: Positive symptoms of psychosis (e.g., hallucinations) often limit everyday functioning and can persist despite adequate antipsychotic treatment. We investigated whether poor cognitive control is a mechanism underlying these symptoms. METHODS: 97 patients with early psychosis (30 with high positive symptoms (HS) and 67 with low positive symptoms (LS)) and 40 healthy controls (HC) underwent fMRI whilst performing a reward learning task with two conditions; low cognitive demand (choosing between neutral faces) and high cognitive demand (choosing between angry and happy faces – shown to induce an emotional bias). Decision and feedback phases were examined. RESULTS: Both patient groups showed suboptimal learning behaviour compared to HC and altered activity within a core reward network including occipital/lingual gyrus (decision), rostral Anterior Cingulate Cortex, left pre-central gyrus and Supplementary Motor Cortex (feedback). In the low cognitive demand condition, HS group showed significantly reduced activity in Supplementary Motor Area (SMA)/pre-SMA during the decision phase whilst activity was increased in LS group compared to HC. Recruitment of this region suggests a top-down compensatory mechanism important for control of positive symptoms. With additional cognitive demand (emotional vs. neutral contrast), HS patients showed further alterations within a subcortical network (increased left amygdala activity during decisions and reduced left pallidum and thalamus activity during feedback) compared to LS patients. CONCLUSIONS: The findings suggest a core reward system deficit may be present in both patient groups, but persistent positive symptoms are associated with a specific dysfunction within a network needed to integrate social-emotional information with reward feedback. Elsevier 2022-04-06 /pmc/articles/PMC9059151/ /pubmed/35468567 http://dx.doi.org/10.1016/j.nicl.2022.103004 Text en © 2022 Published by Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Horne, Charlotte M.
Sahni, Angad
Pang, Sze W.
Vanes, Lucy D.
Szentgyorgyi, Timea
Averbeck, Bruno
Moran, Rosalyn J.
Shergill, Sukhwinder S.
The role of cognitive control in the positive symptoms of psychosis
title The role of cognitive control in the positive symptoms of psychosis
title_full The role of cognitive control in the positive symptoms of psychosis
title_fullStr The role of cognitive control in the positive symptoms of psychosis
title_full_unstemmed The role of cognitive control in the positive symptoms of psychosis
title_short The role of cognitive control in the positive symptoms of psychosis
title_sort role of cognitive control in the positive symptoms of psychosis
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9059151/
https://www.ncbi.nlm.nih.gov/pubmed/35468567
http://dx.doi.org/10.1016/j.nicl.2022.103004
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