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A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis

Previous studies have shown a preferential loss of grey matter in fronto-temporal regions in patients with multiple sclerosis. Studies of correlates of disease severity are more controversial, because some studies have suggested an association between sensorimotor cortex atrophy and Expanded Disabil...

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Autores principales: Prinster, A, Quarantelli, M, Lanzillo, R, Orefice, G, Vacca, G, Carotenuto, B, Alfano, B, Brunetti, A, Morra, V Brescia, Salvatore, M
Formato: Texto
Lenguaje:English
Publicado: SAGE Publications 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841518/
https://www.ncbi.nlm.nih.gov/pubmed/20028706
http://dx.doi.org/10.1177/1352458509351896
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author Prinster, A
Quarantelli, M
Lanzillo, R
Orefice, G
Vacca, G
Carotenuto, B
Alfano, B
Brunetti, A
Morra, V Brescia
Salvatore, M
author_facet Prinster, A
Quarantelli, M
Lanzillo, R
Orefice, G
Vacca, G
Carotenuto, B
Alfano, B
Brunetti, A
Morra, V Brescia
Salvatore, M
author_sort Prinster, A
collection PubMed
description Previous studies have shown a preferential loss of grey matter in fronto-temporal regions in patients with multiple sclerosis. Studies of correlates of disease severity are more controversial, because some studies have suggested an association between sensorimotor cortex atrophy and Expanded Disability Status Scale score, while others did not find such a correlation. The objective of this study was to assess the correlation of regional loss of grey matter and white matter with indexes of clinical and radiological severity in relapsing–remitting multiple sclerosis, including the Expanded Disability Status Scale and lesion load. Correlations between Expanded Disability Status Scale, lesion load and disease duration were assessed in 128 patients with relapsing–remitting multiple sclerosis (Expanded Disability Status Scale range 1.0–6.0) using optimized voxel-based morphometry. Bilateral loss of grey matter in sensorimotor cortices was correlated with Expanded Disability Status Scale, and tissue loss also involved adjacent white matter, extending along pyramidal tracts to the brainstem. Increasing lesion load was correlated with loss of deep grey matter and white matter. No specific region of grey matter or white matter showed a significant correlation with disease duration. These findings support the hypothesis that motor neuron involvement plays a major role in the progression of physical disability. Lesion load accrual affects mainly highly interconnected subcortical structures, while disease duration has a less significant impact on brain atrophy, probably owing to the inter-subject heterogeneity of the clinical course of the disease.
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spelling pubmed-28415182010-03-31 A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis Prinster, A Quarantelli, M Lanzillo, R Orefice, G Vacca, G Carotenuto, B Alfano, B Brunetti, A Morra, V Brescia Salvatore, M Mult Scler Research Paper Previous studies have shown a preferential loss of grey matter in fronto-temporal regions in patients with multiple sclerosis. Studies of correlates of disease severity are more controversial, because some studies have suggested an association between sensorimotor cortex atrophy and Expanded Disability Status Scale score, while others did not find such a correlation. The objective of this study was to assess the correlation of regional loss of grey matter and white matter with indexes of clinical and radiological severity in relapsing–remitting multiple sclerosis, including the Expanded Disability Status Scale and lesion load. Correlations between Expanded Disability Status Scale, lesion load and disease duration were assessed in 128 patients with relapsing–remitting multiple sclerosis (Expanded Disability Status Scale range 1.0–6.0) using optimized voxel-based morphometry. Bilateral loss of grey matter in sensorimotor cortices was correlated with Expanded Disability Status Scale, and tissue loss also involved adjacent white matter, extending along pyramidal tracts to the brainstem. Increasing lesion load was correlated with loss of deep grey matter and white matter. No specific region of grey matter or white matter showed a significant correlation with disease duration. These findings support the hypothesis that motor neuron involvement plays a major role in the progression of physical disability. Lesion load accrual affects mainly highly interconnected subcortical structures, while disease duration has a less significant impact on brain atrophy, probably owing to the inter-subject heterogeneity of the clinical course of the disease. SAGE Publications 2010-03 /pmc/articles/PMC2841518/ /pubmed/20028706 http://dx.doi.org/10.1177/1352458509351896 Text en © The Author(s) 2010. Published by SAGE. All rights reserved. SAGE Publications http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Prinster, A
Quarantelli, M
Lanzillo, R
Orefice, G
Vacca, G
Carotenuto, B
Alfano, B
Brunetti, A
Morra, V Brescia
Salvatore, M
A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
title A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
title_full A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
title_fullStr A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
title_full_unstemmed A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
title_short A voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
title_sort voxel-based morphometry study of disease severity correlates in relapsing–remitting multiple sclerosis
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2841518/
https://www.ncbi.nlm.nih.gov/pubmed/20028706
http://dx.doi.org/10.1177/1352458509351896
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