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The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis
OBJECTIVE: To examine the association between baseline alterations in grey matter volume (GMV) and clinical and functional outcomes in people at clinical high risk (CHR) for psychosis. METHODS: 265 CHR individuals and 92 healthy controls were recruited as part of a prospective multi-center study. Af...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309497/ https://www.ncbi.nlm.nih.gov/pubmed/35903803 http://dx.doi.org/10.1093/schizbullopen/sgac040 |
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author | Tognin, Stefania Richter, Anja Kempton, Matthew J Modinos, Gemma Antoniades, Mathilde Azis, Matilda Allen, Paul Bossong, Matthijs G Perez, Jesus Pantelis, Christos Nelson, Barnaby Amminger, Paul Riecher-Rössler, Anita Barrantes-Vidal, Neus Krebs, Marie-Odile Glenthøj, Birte Ruhrmann, Stephan Sachs, Gabriele Rutten, Bart P F de Haan, Lieuwe van der Gaag, Mark Valmaggia, Lucia R McGuire, Philip |
author_facet | Tognin, Stefania Richter, Anja Kempton, Matthew J Modinos, Gemma Antoniades, Mathilde Azis, Matilda Allen, Paul Bossong, Matthijs G Perez, Jesus Pantelis, Christos Nelson, Barnaby Amminger, Paul Riecher-Rössler, Anita Barrantes-Vidal, Neus Krebs, Marie-Odile Glenthøj, Birte Ruhrmann, Stephan Sachs, Gabriele Rutten, Bart P F de Haan, Lieuwe van der Gaag, Mark Valmaggia, Lucia R McGuire, Philip |
author_sort | Tognin, Stefania |
collection | PubMed |
description | OBJECTIVE: To examine the association between baseline alterations in grey matter volume (GMV) and clinical and functional outcomes in people at clinical high risk (CHR) for psychosis. METHODS: 265 CHR individuals and 92 healthy controls were recruited as part of a prospective multi-center study. After a baseline assessment using magnetic resonance imaging (MRI), participants were followed for at least two years to determine clinical and functional outcomes, including transition to psychosis (according to the Comprehensive Assessment of an At Risk Mental State, CAARMS), level of functioning (according to the Global Assessment of Functioning), and symptomatic remission (according to the CAARMS). GMV was measured in selected cortical and subcortical regions of interest (ROI) based on previous studies (ie orbitofrontal gyrus, cingulate gyrus, gyrus rectus, inferior temporal gyrus, parahippocampal gyrus, striatum, and hippocampus). Using voxel-based morphometry, we analysed the relationship between GMV and clinical and functional outcomes. RESULTS: Within the CHR sample, a poor functional outcome (GAF < 65) was associated with relatively lower GMV in the right striatum at baseline (P < .047 after Family Wise Error correction). There were no significant associations between baseline GMV and either subsequent remission or transition to psychosis. CONCLUSIONS: In CHR individuals, lower striatal GMV was associated with a poor level of overall functioning at follow-up. This finding was not related to effects of antipsychotic or antidepressant medication. The failure to replicate previous associations between GMV and later psychosis onset, despite studying a relatively large sample, is consistent with the findings of recent large-scale multi-center studies. |
format | Online Article Text |
id | pubmed-9309497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-93094972022-07-26 The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis Tognin, Stefania Richter, Anja Kempton, Matthew J Modinos, Gemma Antoniades, Mathilde Azis, Matilda Allen, Paul Bossong, Matthijs G Perez, Jesus Pantelis, Christos Nelson, Barnaby Amminger, Paul Riecher-Rössler, Anita Barrantes-Vidal, Neus Krebs, Marie-Odile Glenthøj, Birte Ruhrmann, Stephan Sachs, Gabriele Rutten, Bart P F de Haan, Lieuwe van der Gaag, Mark Valmaggia, Lucia R McGuire, Philip Schizophr Bull Open Regular Article OBJECTIVE: To examine the association between baseline alterations in grey matter volume (GMV) and clinical and functional outcomes in people at clinical high risk (CHR) for psychosis. METHODS: 265 CHR individuals and 92 healthy controls were recruited as part of a prospective multi-center study. After a baseline assessment using magnetic resonance imaging (MRI), participants were followed for at least two years to determine clinical and functional outcomes, including transition to psychosis (according to the Comprehensive Assessment of an At Risk Mental State, CAARMS), level of functioning (according to the Global Assessment of Functioning), and symptomatic remission (according to the CAARMS). GMV was measured in selected cortical and subcortical regions of interest (ROI) based on previous studies (ie orbitofrontal gyrus, cingulate gyrus, gyrus rectus, inferior temporal gyrus, parahippocampal gyrus, striatum, and hippocampus). Using voxel-based morphometry, we analysed the relationship between GMV and clinical and functional outcomes. RESULTS: Within the CHR sample, a poor functional outcome (GAF < 65) was associated with relatively lower GMV in the right striatum at baseline (P < .047 after Family Wise Error correction). There were no significant associations between baseline GMV and either subsequent remission or transition to psychosis. CONCLUSIONS: In CHR individuals, lower striatal GMV was associated with a poor level of overall functioning at follow-up. This finding was not related to effects of antipsychotic or antidepressant medication. The failure to replicate previous associations between GMV and later psychosis onset, despite studying a relatively large sample, is consistent with the findings of recent large-scale multi-center studies. Oxford University Press 2022-06-20 /pmc/articles/PMC9309497/ /pubmed/35903803 http://dx.doi.org/10.1093/schizbullopen/sgac040 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the University of Maryland's school of medicine, Maryland Psychiatric Research Center. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Regular Article Tognin, Stefania Richter, Anja Kempton, Matthew J Modinos, Gemma Antoniades, Mathilde Azis, Matilda Allen, Paul Bossong, Matthijs G Perez, Jesus Pantelis, Christos Nelson, Barnaby Amminger, Paul Riecher-Rössler, Anita Barrantes-Vidal, Neus Krebs, Marie-Odile Glenthøj, Birte Ruhrmann, Stephan Sachs, Gabriele Rutten, Bart P F de Haan, Lieuwe van der Gaag, Mark Valmaggia, Lucia R McGuire, Philip The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis |
title | The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis |
title_full | The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis |
title_fullStr | The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis |
title_full_unstemmed | The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis |
title_short | The Relationship Between Grey Matter Volume and Clinical and Functional Outcomes in People at Clinical High Risk for Psychosis |
title_sort | relationship between grey matter volume and clinical and functional outcomes in people at clinical high risk for psychosis |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9309497/ https://www.ncbi.nlm.nih.gov/pubmed/35903803 http://dx.doi.org/10.1093/schizbullopen/sgac040 |
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