Cargando…
DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime?
BACKGROUND: The extent and clinical relevance of grey matter (GM) pathology in multiple sclerosis (MS) are increasingly recognised. GM pathology may present as focal lesions, which can be visualised using double inversion recovery (DIR) MRI, or as diffuse pathology, which can manifest as atrophy. It...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853554/ https://www.ncbi.nlm.nih.gov/pubmed/25926483 http://dx.doi.org/10.1136/jnnp-2014-310142 |
_version_ | 1782430091450515456 |
---|---|
author | van de Pavert, Steven H P Muhlert, Nils Sethi, Varun Wheeler-Kingshott, Claudia A M Ridgway, Gerard R Geurts, Jeroen J G Ron, Maria Yousry, Tarek A Thompson, Alan J Miller, David H Chard, Declan T Ciccarelli, Olga |
author_facet | van de Pavert, Steven H P Muhlert, Nils Sethi, Varun Wheeler-Kingshott, Claudia A M Ridgway, Gerard R Geurts, Jeroen J G Ron, Maria Yousry, Tarek A Thompson, Alan J Miller, David H Chard, Declan T Ciccarelli, Olga |
author_sort | van de Pavert, Steven H P |
collection | PubMed |
description | BACKGROUND: The extent and clinical relevance of grey matter (GM) pathology in multiple sclerosis (MS) are increasingly recognised. GM pathology may present as focal lesions, which can be visualised using double inversion recovery (DIR) MRI, or as diffuse pathology, which can manifest as atrophy. It is, however, unclear whether the diffuse atrophy centres on focal lesions. This study aimed to determine if GM lesions and GM atrophy colocalise, and to assess their independent relationship with motor and cognitive deficits in MS. METHODS: Eighty people with MS and 30 healthy controls underwent brain volumetric T1-weighted and DIR MRI at 3 T, and had a comprehensive neurological and cognitive assessment. Probability mapping of GM lesions marked on the DIR scans and voxel- based morphometry (assessing GM atrophy) were carried out. The associations of GM lesion load and GM volume with clinical scores were tested. RESULTS: DIR-visible GM lesions were most commonly found in the right cerebellum and most apparent in patients with primary progressive MS. Deep GM structures appeared largely free from lesions, but showed considerable atrophy, particularly in the thalamus, caudate, pallidum and putamen, and this was most apparent in secondary progressive patients with MS. Very little co-localisation of GM atrophy and lesions was seen, and this was generally confined to the cerebellum and postcentral gyrus. In both regions, GM lesions and volume independently correlated with physical disability and cognitive performance. CONCLUSIONS: DIR-detectable GM lesions and GM atrophy do not significantly overlap in the brain but, when they do, they independently contribute to clinical disability. |
format | Online Article Text |
id | pubmed-4853554 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48535542016-05-06 DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? van de Pavert, Steven H P Muhlert, Nils Sethi, Varun Wheeler-Kingshott, Claudia A M Ridgway, Gerard R Geurts, Jeroen J G Ron, Maria Yousry, Tarek A Thompson, Alan J Miller, David H Chard, Declan T Ciccarelli, Olga J Neurol Neurosurg Psychiatry Multiple Sclerosis BACKGROUND: The extent and clinical relevance of grey matter (GM) pathology in multiple sclerosis (MS) are increasingly recognised. GM pathology may present as focal lesions, which can be visualised using double inversion recovery (DIR) MRI, or as diffuse pathology, which can manifest as atrophy. It is, however, unclear whether the diffuse atrophy centres on focal lesions. This study aimed to determine if GM lesions and GM atrophy colocalise, and to assess their independent relationship with motor and cognitive deficits in MS. METHODS: Eighty people with MS and 30 healthy controls underwent brain volumetric T1-weighted and DIR MRI at 3 T, and had a comprehensive neurological and cognitive assessment. Probability mapping of GM lesions marked on the DIR scans and voxel- based morphometry (assessing GM atrophy) were carried out. The associations of GM lesion load and GM volume with clinical scores were tested. RESULTS: DIR-visible GM lesions were most commonly found in the right cerebellum and most apparent in patients with primary progressive MS. Deep GM structures appeared largely free from lesions, but showed considerable atrophy, particularly in the thalamus, caudate, pallidum and putamen, and this was most apparent in secondary progressive patients with MS. Very little co-localisation of GM atrophy and lesions was seen, and this was generally confined to the cerebellum and postcentral gyrus. In both regions, GM lesions and volume independently correlated with physical disability and cognitive performance. CONCLUSIONS: DIR-detectable GM lesions and GM atrophy do not significantly overlap in the brain but, when they do, they independently contribute to clinical disability. BMJ Publishing Group 2016-05 2015-04-29 /pmc/articles/PMC4853554/ /pubmed/25926483 http://dx.doi.org/10.1136/jnnp-2014-310142 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Multiple Sclerosis van de Pavert, Steven H P Muhlert, Nils Sethi, Varun Wheeler-Kingshott, Claudia A M Ridgway, Gerard R Geurts, Jeroen J G Ron, Maria Yousry, Tarek A Thompson, Alan J Miller, David H Chard, Declan T Ciccarelli, Olga DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
title | DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
title_full | DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
title_fullStr | DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
title_full_unstemmed | DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
title_short | DIR-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
title_sort | dir-visible grey matter lesions and atrophy in multiple sclerosis: partners in crime? |
topic | Multiple Sclerosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4853554/ https://www.ncbi.nlm.nih.gov/pubmed/25926483 http://dx.doi.org/10.1136/jnnp-2014-310142 |
work_keys_str_mv | AT vandepavertstevenhp dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT muhlertnils dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT sethivarun dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT wheelerkingshottclaudiaam dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT ridgwaygerardr dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT geurtsjeroenjg dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT ronmaria dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT yousrytareka dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT thompsonalanj dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT millerdavidh dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT charddeclant dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime AT ciccarelliolga dirvisiblegreymatterlesionsandatrophyinmultiplesclerosispartnersincrime |