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Microstructural white matter changes are correlated with the stage of psychiatric illness

Microstructural white matter changes have been reported in the brains of patients across a range of psychiatric disorders. Evidence now demonstrates significant overlap in these regions in patients with affective and psychotic disorders, thus raising the possibility that these conditions share commo...

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Autores principales: Lagopoulos, J, Hermens, D F, Hatton, S N, Battisti, R A, Tobias-Webb, J, White, D, Naismith, S L, Scott, E M, Ryder, W J, Bennett, M R, Hickie, I B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641412/
https://www.ncbi.nlm.nih.gov/pubmed/23612047
http://dx.doi.org/10.1038/tp.2013.25
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author Lagopoulos, J
Hermens, D F
Hatton, S N
Battisti, R A
Tobias-Webb, J
White, D
Naismith, S L
Scott, E M
Ryder, W J
Bennett, M R
Hickie, I B
author_facet Lagopoulos, J
Hermens, D F
Hatton, S N
Battisti, R A
Tobias-Webb, J
White, D
Naismith, S L
Scott, E M
Ryder, W J
Bennett, M R
Hickie, I B
author_sort Lagopoulos, J
collection PubMed
description Microstructural white matter changes have been reported in the brains of patients across a range of psychiatric disorders. Evidence now demonstrates significant overlap in these regions in patients with affective and psychotic disorders, thus raising the possibility that these conditions share common neurobiological processes. If affective and psychotic disorders share these disruptions, it is unclear whether they occur early in the course or develop gradually with persistence or recurrence of illness. Utilisation of a clinical staging model, as an adjunct to traditional diagnostic practice, is a viable mechanism for measuring illness progression. It is particularly relevant in young people presenting early in their illness course. It also provides a suitable framework for determining the timing of emergent brain alterations, including disruptions of white matter tracts. Using diffusion tensor imaging, we investigated the integrity of white matter tracts in 74 patients with sub-syndromal psychiatric symptoms as well as in 69 patients diagnosed with established psychosis or affective disorder and contrasted these findings with those of 39 healthy controls. A significant disruption in white matter integrity was found in the left anterior corona radiata and in particular the anterior thalamic radiation for both the patients groups when separately contrasted with healthy controls. Our results suggest that patients with sub-syndromal symptoms exhibit discernable early white matter changes when compared with healthy control subjects and more significant disruptions are associated with clinical evidence of illness progression.
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spelling pubmed-36414122013-05-02 Microstructural white matter changes are correlated with the stage of psychiatric illness Lagopoulos, J Hermens, D F Hatton, S N Battisti, R A Tobias-Webb, J White, D Naismith, S L Scott, E M Ryder, W J Bennett, M R Hickie, I B Transl Psychiatry Original Article Microstructural white matter changes have been reported in the brains of patients across a range of psychiatric disorders. Evidence now demonstrates significant overlap in these regions in patients with affective and psychotic disorders, thus raising the possibility that these conditions share common neurobiological processes. If affective and psychotic disorders share these disruptions, it is unclear whether they occur early in the course or develop gradually with persistence or recurrence of illness. Utilisation of a clinical staging model, as an adjunct to traditional diagnostic practice, is a viable mechanism for measuring illness progression. It is particularly relevant in young people presenting early in their illness course. It also provides a suitable framework for determining the timing of emergent brain alterations, including disruptions of white matter tracts. Using diffusion tensor imaging, we investigated the integrity of white matter tracts in 74 patients with sub-syndromal psychiatric symptoms as well as in 69 patients diagnosed with established psychosis or affective disorder and contrasted these findings with those of 39 healthy controls. A significant disruption in white matter integrity was found in the left anterior corona radiata and in particular the anterior thalamic radiation for both the patients groups when separately contrasted with healthy controls. Our results suggest that patients with sub-syndromal symptoms exhibit discernable early white matter changes when compared with healthy control subjects and more significant disruptions are associated with clinical evidence of illness progression. Nature Publishing Group 2013-04 2013-04-23 /pmc/articles/PMC3641412/ /pubmed/23612047 http://dx.doi.org/10.1038/tp.2013.25 Text en Copyright © 2013 Macmillan Publishers Limited http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Original Article
Lagopoulos, J
Hermens, D F
Hatton, S N
Battisti, R A
Tobias-Webb, J
White, D
Naismith, S L
Scott, E M
Ryder, W J
Bennett, M R
Hickie, I B
Microstructural white matter changes are correlated with the stage of psychiatric illness
title Microstructural white matter changes are correlated with the stage of psychiatric illness
title_full Microstructural white matter changes are correlated with the stage of psychiatric illness
title_fullStr Microstructural white matter changes are correlated with the stage of psychiatric illness
title_full_unstemmed Microstructural white matter changes are correlated with the stage of psychiatric illness
title_short Microstructural white matter changes are correlated with the stage of psychiatric illness
title_sort microstructural white matter changes are correlated with the stage of psychiatric illness
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3641412/
https://www.ncbi.nlm.nih.gov/pubmed/23612047
http://dx.doi.org/10.1038/tp.2013.25
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