Atrophy mainly affects the limbic system and the deep grey matter at the first stage of multiple sclerosis
BackgroundThe existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atro...
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Published in | Journal of neurology, neurosurgery and psychiatry Vol. 81; no. 6; pp. 690 - 695 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd
01.06.2010
BMJ Publishing Group BMJ Publishing Group LTD |
Subjects | |
Online Access | Get full text |
ISSN | 0022-3050 1468-330X 1468-330X |
DOI | 10.1136/jnnp.2009.188748 |
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Abstract | BackgroundThe existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients.MethodsSixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T1-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery.ResultsVBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (ρ=−0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy.ConclusionThe present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. |
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AbstractList | The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients. Sixty two patients with a clinically isolated syndrome (CIS) were examined on a 1.5T MR imager within six months after their first clinical events. A group of thirty seven matched healthy control subjects were also included in the study. An optimized Voxel Based Morphometric (VBM) method customised for MS was applied on volumetric T1-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery. VBM analysis (p<0.005, FWE corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei, and the bilateral cerebellum. EDSS was slightly correlated (rho=-0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy. The present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. Background The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients. Methods Sixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T1 -weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery. Results VBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (Ï=-0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy. Conclusion The present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. BackgroundThe existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients.MethodsSixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T1-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery.ResultsVBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (ρ=−0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy.ConclusionThe present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients.BACKGROUNDThe existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients.Sixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T(1)-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery.METHODSSixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T(1)-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery.VBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (rho=-0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy.RESULTSVBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (rho=-0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy.The present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system.CONCLUSIONThe present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. Background The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients. Methods Sixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T1-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery. Results VBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (ρ=−0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy. Conclusion The present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this study was therefore to establish whether regional GM atrophy is already present in the earliest stage of MS assessing regional GM atrophy in a large group of patients. Sixty-two patients with a clinically isolated syndrome (CIS) were examined on a 1.5 T MR imager within 6 months after their first clinical events. A group of 37 matched healthy control subjects were also included in the study. An optimised voxel-based morphometry (VBM) method customised for MS was applied on volumetric T(1)-weighted images. The functional status of patients was assessed using the Expanded Disability Status Scale (EDSS) and the Brief Repeatable Battery. VBM analysis (p<0.005, familywise error corrected) on patients versus control subjects showed the presence of significant focal GM atrophy in patients involving the bilateral insula, the bilateral orbitofrontal cortices, the bilateral internal and inferior temporal regions, the posterior cingulate cortex, the bilateral thalami, the bilateral caudate nuclei, the bilateral lenticular nuclei and the bilateral cerebellum. EDSS was slightly correlated (rho=-0.37 p=0.0027) with the atrophy of the right cerebellum. No correlations have been evidenced between the cognitive status of patients and the regional GM atrophy. The present study performed on a large group of CIS patients demonstrated that regional GM atrophy is present right after the first clinical event of multiple sclerosis and mainly affects the deep GM and the limbic system. |
Author | Rico, Audrey Malikova, Irina Cozzone, Patrick J Audoin, Bertrand Reuter, Françoise Ranjeva, Jean-Philippe Zaaraoui, Wafaa Confort-Gouny, Sylviane Pelletier, Jean |
Author_xml | – sequence: 1 givenname: Bertrand surname: Audoin fullname: Audoin, Bertrand email: bertrand.audoin@ap-hm.fr organization: Pôle de Neurosciences Cliniques, Centre Hospitalier Universitaire Timone, Marseille, France – sequence: 2 givenname: Wafaa surname: Zaaraoui fullname: Zaaraoui, Wafaa email: bertrand.audoin@ap-hm.fr organization: Centre de Résonance Magnétique Biologique et Médicale, UMR CNRS , Faculté de Médecine, Université de la Méditerranée, Marseille, France – sequence: 3 givenname: Françoise surname: Reuter fullname: Reuter, Françoise email: bertrand.audoin@ap-hm.fr organization: Pôle de Neurosciences Cliniques, Centre Hospitalier Universitaire Timone, Marseille, France – sequence: 4 givenname: Audrey surname: Rico fullname: Rico, Audrey email: bertrand.audoin@ap-hm.fr organization: Pôle de Neurosciences Cliniques, Centre Hospitalier Universitaire Timone, Marseille, France – sequence: 5 givenname: Irina surname: Malikova fullname: Malikova, Irina email: bertrand.audoin@ap-hm.fr organization: Pôle de Neurosciences Cliniques, Centre Hospitalier Universitaire Timone, Marseille, France – sequence: 6 givenname: Sylviane surname: Confort-Gouny fullname: Confort-Gouny, Sylviane email: bertrand.audoin@ap-hm.fr organization: Centre de Résonance Magnétique Biologique et Médicale, UMR CNRS , Faculté de Médecine, Université de la Méditerranée, Marseille, France – sequence: 7 givenname: Patrick J surname: Cozzone fullname: Cozzone, Patrick J email: bertrand.audoin@ap-hm.fr organization: Centre de Résonance Magnétique Biologique et Médicale, UMR CNRS , Faculté de Médecine, Université de la Méditerranée, Marseille, France – sequence: 8 givenname: Jean surname: Pelletier fullname: Pelletier, Jean email: bertrand.audoin@ap-hm.fr organization: Pôle de Neurosciences Cliniques, Centre Hospitalier Universitaire Timone, Marseille, France – sequence: 9 givenname: Jean-Philippe surname: Ranjeva fullname: Ranjeva, Jean-Philippe email: bertrand.audoin@ap-hm.fr organization: Centre de Résonance Magnétique Biologique et Médicale, UMR CNRS , Faculté de Médecine, Université de la Méditerranée, Marseille, France |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22842581$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/20392976$$D View this record in MEDLINE/PubMed https://hal.science/hal-00557410$$DView record in HAL |
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ContentType | Journal Article |
Copyright | 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. 2015 INIST-CNRS Copyright: 2010 (c) 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. Distributed under a Creative Commons Attribution 4.0 International License |
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DOI | 10.1136/jnnp.2009.188748 |
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Keywords | Atrophy Nervous system diseases Multiple sclerosis Grey matter Central nervous system disease Central nervous system Limbic system Encephalon Inflammatory disease MULTIPLE SCLEROSIS MRI |
Language | English |
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PublicationTitle | Journal of neurology, neurosurgery and psychiatry |
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References | Tao, Datta, He 2009; 282 Charil, Dagher, Lerch 2007; 34 Amato, Portaccio, Goretti 2007; 64 Bo, Geurts, van der Valk 2007; 64 Feuillet, Reuter, Audoin 2007; 13 Boringa, Lazeron, Reuling 2001; 7 Good, Johnsrude, Ashburner 2001; 14 Ceccarelli, Rocca, Pagani 2008; 42 McDonald, Compston, Edan 2001; 50 Audoin, Davies, Finisku 2006; 253 Chard, Miller 2009; 282 Khaleeli, Cercignani, Audoin 2007; 37 Sdika, Pelletier 2009; 30 Evangelou, Konz, Esiri 2001; 124 Dalton, Chard, Davies 2004; 127 Sicotte, Kern, Giesser 2008; 131 Ito 2008; 9 Henry, Shieh, Okuda 2008; 79 Sepulcre, Sastre-Garriga, Cercignani 2006; 63 Bakshi, Benedict, Bermel 2002; 59 Geurts, Barkhof 2008; 7 Kurtzke 1983; 33 Evangelou, Konz, Esiri 2000; 123 Geurts, Bo, Roosendaal 2007; 66 Pelvig, Pakkenberg, Stark 2008; 29 Audoin, Guye, Reuter 2007; 36 Sailer, Fischl, Salat 2003; 126 Achiron, Barak 2003; 74 Audoin, Ranjeva, Au Duong 2004; 20 Sanfilipo, Benedict, Weinstock-Guttman 2006; 66 Amato, Bartolozzi, Zipoli 2004; 63 Ramasamy, Benedict, Cox 2009; 282 Kutzelnigg, Lucchinetti, Stadelmann 2005; 128 Henry, Shieh, Amirbekian 2009; 282 Battaglini, Giorgio, Stromillo 2009; 282 Audoin, Fernando, Swanton 2006; 129 Ge, Jensen, Lu 2007; 28 |
References_xml | – volume: 127 start-page: 1101 year: 2004 article-title: Early development of multiple sclerosis is associated with progressive grey matter atrophy in patients presenting with clinically isolated syndromes publication-title: Brain – volume: 131 start-page: 1134 year: 2008 article-title: Regional hippocampal atrophy in multiple sclerosis publication-title: Brain – volume: 33 start-page: 1444 year: 1983 article-title: Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS) publication-title: Neurology – volume: 282 start-page: 47 year: 2009 article-title: Extent of cerebellum, subcortical and cortical atrophy in patients with MS: a case-control study publication-title: J Neurol Sci – volume: 37 start-page: 253 year: 2007 article-title: Localized grey matter damage in early primary progressive multiple sclerosis contributes to disability publication-title: Neuroimage – volume: 7 start-page: 263 year: 2001 article-title: The brief 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study of ageing in 465 normal adult human brains publication-title: Neuroimage – volume: 124 start-page: 1813 year: 2001 article-title: Size-selective neuronal changes in the anterior optic pathways suggest a differential susceptibility to injury in multiple sclerosis publication-title: Brain – volume: 64 start-page: 76 year: 2007 article-title: Lack of correlation between cortical demyelination and white matter pathologic changes in multiple sclerosis publication-title: Arch Neurol – volume: 66 start-page: 685 year: 2006 article-title: Gray and white matter brain atrophy and neuropsychological impairment in multiple sclerosis publication-title: Neurology – volume: 29 start-page: 1754 year: 2008 article-title: Neocortical glial cell numbers in human brains publication-title: Neurobiol Aging – volume: 20 start-page: 765 year: 2004 article-title: Voxel-based analysis of MTR images: a method to locate gray matter abnormalities in patients at the earliest stage of multiple sclerosis 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volume: 253 start-page: 1495 year: 2006 article-title: Localization of grey matter atrophy in early RRMS: a longitudinal study publication-title: J Neurol – volume: 129 start-page: 1031 year: 2006 article-title: Selective magnetization transfer ratio decrease in the visual cortex following optic neuritis publication-title: Brain – volume: 282 start-page: 5 year: 2009 article-title: Grey matter pathology in clinically early multiple sclerosis: evidence from magnetic resonance imaging publication-title: J Neurol Sci – volume: 282 start-page: 39 year: 2009 article-title: Deep gray matter atrophy in multiple sclerosis: a tensor based morphometry publication-title: J Neurol Sci – volume: 63 start-page: 89 year: 2004 article-title: Neocortical volume decrease in relapsing-remitting MS patients with mild cognitive impairment publication-title: Neurology |
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Snippet | BackgroundThe existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim... Background The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim... The existence of grey matter (GM) atrophy right after the first clinical event suggestive of multiple sclerosis (MS) remains controversial. The aim of this... |
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SubjectTerms | Adult Amygdala - pathology Anniversaries Atrophy Atrophy - pathology Biological and medical sciences Brain research Cerebral Cortex - pathology clinically isolated syndrome Cognitive ability Female Humans Magnetic Resonance Imaging Male Medical sciences Middle Aged MRI Multiple sclerosis Multiple Sclerosis - pathology Multiple sclerosis and variants. Guillain barré syndrome and other inflammatory polyneuropathies. Leukoencephalitis Nervous system Neurology Neuropsychology Severity of Illness Index Spinal cord voxel based morphometry Young Adult |
Title | Atrophy mainly affects the limbic system and the deep grey matter at the first stage of multiple sclerosis |
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