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Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions

Age of onset in multiple sclerosis (MS) exerts an influence on the course of disease. This study examined whether global and regional brain volumes differed between “younger” and “older” onset MS subjects who were matched for short disease duration, mean 1.9 years and burden as measured by the MS Se...

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Autores principales: Bishop, Courtney A, Newbould, Rexford D, Lee, Jean SZ, Honeyfield, Lesley, Quest, Rebecca, Colasanti, Alessandro, Ali, Rehiana, Mattoscio, Miriam, Cortese, Antonio, Nicholas, Richard, Matthews, Paul M., Muraro, Paolo A, Waldman, Adam D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121150/
https://www.ncbi.nlm.nih.gov/pubmed/27896065
http://dx.doi.org/10.1016/j.nicl.2016.11.005
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author Bishop, Courtney A
Newbould, Rexford D
Lee, Jean SZ
Honeyfield, Lesley
Quest, Rebecca
Colasanti, Alessandro
Ali, Rehiana
Mattoscio, Miriam
Cortese, Antonio
Nicholas, Richard
Matthews, Paul M.
Muraro, Paolo A
Waldman, Adam D
author_facet Bishop, Courtney A
Newbould, Rexford D
Lee, Jean SZ
Honeyfield, Lesley
Quest, Rebecca
Colasanti, Alessandro
Ali, Rehiana
Mattoscio, Miriam
Cortese, Antonio
Nicholas, Richard
Matthews, Paul M.
Muraro, Paolo A
Waldman, Adam D
author_sort Bishop, Courtney A
collection PubMed
description Age of onset in multiple sclerosis (MS) exerts an influence on the course of disease. This study examined whether global and regional brain volumes differed between “younger” and “older” onset MS subjects who were matched for short disease duration, mean 1.9 years and burden as measured by the MS Severity Score and relapses. 21 younger-onset MS subjects (age 30.4 ± 3.2 years) were compared with 17 older-onset (age 48.7 ± 3.3 years) as well as age-matched controls (n = 31, 31.9 ± 3.5 years and n = 21, 47.3 ± 4.0 years). All subjects underwent 3D volumetric T1 and T2-FLAIR imaging. White matter (WM) and grey matter (GM) lesions were outlined manually. Lesions were filled prior to tissue and structural segmentation to reduce classification errors. Volume loss versus control was predominantly in the subcortical GM, at > 13% loss. Younger and older-onset MS subjects had similar, strong excess loss in the putamen, thalamus, and nucleus accumbens. No excess loss was detected in the amygdala or pallidum. The hippocampus and caudate showed significant excess loss in the younger group (p < 0.001) and a strong trend in the older-onset group. These results provide a potential imaging correlate of published neuropsychological studies that reported the association of younger age at disease onset with impaired cognitive performance, including decreased working memory.
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spelling pubmed-51211502016-11-28 Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions Bishop, Courtney A Newbould, Rexford D Lee, Jean SZ Honeyfield, Lesley Quest, Rebecca Colasanti, Alessandro Ali, Rehiana Mattoscio, Miriam Cortese, Antonio Nicholas, Richard Matthews, Paul M. Muraro, Paolo A Waldman, Adam D Neuroimage Clin Regular Article Age of onset in multiple sclerosis (MS) exerts an influence on the course of disease. This study examined whether global and regional brain volumes differed between “younger” and “older” onset MS subjects who were matched for short disease duration, mean 1.9 years and burden as measured by the MS Severity Score and relapses. 21 younger-onset MS subjects (age 30.4 ± 3.2 years) were compared with 17 older-onset (age 48.7 ± 3.3 years) as well as age-matched controls (n = 31, 31.9 ± 3.5 years and n = 21, 47.3 ± 4.0 years). All subjects underwent 3D volumetric T1 and T2-FLAIR imaging. White matter (WM) and grey matter (GM) lesions were outlined manually. Lesions were filled prior to tissue and structural segmentation to reduce classification errors. Volume loss versus control was predominantly in the subcortical GM, at > 13% loss. Younger and older-onset MS subjects had similar, strong excess loss in the putamen, thalamus, and nucleus accumbens. No excess loss was detected in the amygdala or pallidum. The hippocampus and caudate showed significant excess loss in the younger group (p < 0.001) and a strong trend in the older-onset group. These results provide a potential imaging correlate of published neuropsychological studies that reported the association of younger age at disease onset with impaired cognitive performance, including decreased working memory. Elsevier 2016-11-09 /pmc/articles/PMC5121150/ /pubmed/27896065 http://dx.doi.org/10.1016/j.nicl.2016.11.005 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Regular Article
Bishop, Courtney A
Newbould, Rexford D
Lee, Jean SZ
Honeyfield, Lesley
Quest, Rebecca
Colasanti, Alessandro
Ali, Rehiana
Mattoscio, Miriam
Cortese, Antonio
Nicholas, Richard
Matthews, Paul M.
Muraro, Paolo A
Waldman, Adam D
Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
title Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
title_full Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
title_fullStr Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
title_full_unstemmed Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
title_short Analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
title_sort analysis of ageing-associated grey matter volume in patients with multiple sclerosis shows excess atrophy in subcortical regions
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5121150/
https://www.ncbi.nlm.nih.gov/pubmed/27896065
http://dx.doi.org/10.1016/j.nicl.2016.11.005
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