Motor-related circuit dysfunction in MSA-P: Usefulness of combined whole-brain imaging analysis.
Identifieur interne : 002522 ( Ncbi/Curation ); précédent : 002521; suivant : 002523Motor-related circuit dysfunction in MSA-P: Usefulness of combined whole-brain imaging analysis.
Auteurs : Mélissa Tir [France] ; Christine Delmaire ; Vianney Le Thuc ; Alain Duhamel ; Alain Destée [France] ; Jean-Pierre Pruvo ; Luc Defebvre [France]Source :
- Movement disorders : official journal of the Movement Disorder Society [ 1531-8257 ] ; 2009.
English descriptors
- KwdEn :
- Aged, Analysis of Variance, Anisotropy, Brain (pathology), Brain Mapping, Cephalometry, Diffusion Magnetic Resonance Imaging, Female, Functional Laterality, Humans, Image Processing, Computer-Assisted, Male, Middle Aged, Multiple System Atrophy (pathology), Neural Pathways (pathology), Parkinson Disease (pathology), Statistics, Nonparametric.
- MESH :
- pathology : Brain, Multiple System Atrophy, Neural Pathways, Parkinson Disease.
- Aged, Analysis of Variance, Anisotropy, Brain Mapping, Cephalometry, Diffusion Magnetic Resonance Imaging, Female, Functional Laterality, Humans, Image Processing, Computer-Assisted, Male, Middle Aged, Statistics, Nonparametric.
Abstract
The aim of this study was to evaluate in vivo changes in the brain's macro- and microstructure (notably in the motor system) in the parkinsonian variant of multiple system atrophy (MSA-P) and in Parkinson's disease (PD) and to characterize the cerebral anatomical differences between the two conditions. We used a combination of voxel-based morphometry (VBM) and whole-brain, voxel-based diffusion tensor imaging analysis (VB-DTI). Forty-seven right-handed subjects (14 MSA-P patients, 19 PD patients, and 14 controls) were evaluated using VBM and VB-DTI in an analysis of covariance (ANCOVA) with a significance threshold set to P < 0.005. In MSA-P patients, VBM analysis revealed a lower density of grey matter (GM) in a motor-related circuit (especially in the left primary motor cortex, PMC), relative to PD patients, and in the left supplementary motor area (SMA), relative to controls). Diffusion tensor imaging analysis revealed lower fractional anisotropy (FA) values in the left PMC and the right cerebellum in MSA-P patients, compared with controls. Using a volumetric diffusion technique, our study revealed selective tissue degeneration in motor circuits, regardless of the volume loss detected in VBM and in agreement with pathology reports and clinical motor characteristics. Our findings suggest that MSA-P is characterized by both macro- and microstructural changes in the sensorimotor circuit.
DOI: 10.1002/mds.22463
PubMed: 19194988
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first="Vianney" last="Le Thuc">Vianney Le Thuc</name></author><author><name sortKey="Duhamel, Alain" sort="Duhamel, Alain" uniqKey="Duhamel A" first="Alain" last="Duhamel">Alain Duhamel</name></author><author><name sortKey="Destee, Alain" sort="Destee, Alain" uniqKey="Destee A" first="Alain" last="Destée">Alain Destée</name><affiliation><country>France</country><placeName><settlement type="city">Lille</settlement><region type="region" nuts="2">Nord-Pas-de-Calais</region></placeName><orgName type="university" n="3">Université Lille 2</orgName><orgName type="institution" wicri:auto="newGroup">Université Lille Nord de France</orgName></affiliation></author><author><name sortKey="Pruvo, Jean Pierre" sort="Pruvo, Jean Pierre" uniqKey="Pruvo J" first="Jean-Pierre" last="Pruvo">Jean-Pierre Pruvo</name></author><author><name sortKey="Defebvre, Luc" sort="Defebvre, Luc" uniqKey="Defebvre L" first="Luc" last="Defebvre">Luc Defebvre</name><affiliation><country>France</country><placeName><settlement type="city">Lille</settlement><region type="region" nuts="2">Nord-Pas-de-Calais</region></placeName><orgName type="university" n="3">Université Lille 2</orgName><orgName type="institution" wicri:auto="newGroup">Université Lille Nord de France</orgName></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2009">2009</date><idno type="doi">10.1002/mds.22463</idno><idno type="RBID">pubmed:19194988</idno><idno type="pmid">19194988</idno><idno type="wicri:Area/PubMed/Corpus">001E42</idno><idno type="wicri:Area/PubMed/Curation">001E42</idno><idno type="wicri:Area/PubMed/Checkpoint">001D10</idno><idno type="wicri:Area/Ncbi/Merge">002522</idno><idno type="wicri:Area/Ncbi/Curation">002522</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Motor-related circuit dysfunction in MSA-P: Usefulness of combined whole-brain imaging analysis.</title><author><name sortKey="Tir, Melissa" sort="Tir, Melissa" uniqKey="Tir M" first="Mélissa" last="Tir">Mélissa Tir</name><affiliation wicri:level="1"><nlm:affiliation>Department of Neurology, Roger Salengro Hospital, Lille University Medical Centre, Lille Cedex, France. tirmelissa@yahoo.fr</nlm:affiliation><country xml:lang="fr">France</country><wicri:regionArea>Department of Neurology, Roger Salengro Hospital, Lille University Medical Centre, Lille Cedex</wicri:regionArea><wicri:noRegion>Lille Cedex</wicri:noRegion><wicri:noRegion>Lille Cedex</wicri:noRegion></affiliation></author><author><name sortKey="Delmaire, Christine" sort="Delmaire, Christine" uniqKey="Delmaire C" first="Christine" last="Delmaire">Christine Delmaire</name></author><author><name sortKey="Le Thuc, Vianney" sort="Le Thuc, Vianney" uniqKey="Le Thuc V" first="Vianney" last="Le Thuc">Vianney Le Thuc</name></author><author><name sortKey="Duhamel, Alain" sort="Duhamel, Alain" uniqKey="Duhamel A" first="Alain" last="Duhamel">Alain Duhamel</name></author><author><name sortKey="Destee, Alain" sort="Destee, Alain" uniqKey="Destee A" first="Alain" last="Destée">Alain Destée</name><affiliation><country>France</country><placeName><settlement type="city">Lille</settlement><region type="region" nuts="2">Nord-Pas-de-Calais</region></placeName><orgName type="university" n="3">Université Lille 2</orgName><orgName type="institution" wicri:auto="newGroup">Université Lille Nord de France</orgName></affiliation></author><author><name sortKey="Pruvo, Jean Pierre" sort="Pruvo, Jean Pierre" uniqKey="Pruvo J" first="Jean-Pierre" last="Pruvo">Jean-Pierre Pruvo</name></author><author><name sortKey="Defebvre, Luc" sort="Defebvre, Luc" uniqKey="Defebvre L" first="Luc" last="Defebvre">Luc Defebvre</name><affiliation><country>France</country><placeName><settlement type="city">Lille</settlement><region type="region" nuts="2">Nord-Pas-de-Calais</region></placeName><orgName type="university" n="3">Université Lille 2</orgName><orgName type="institution" wicri:auto="newGroup">Université Lille Nord de France</orgName></affiliation></author></analytic><series><title level="j">Movement disorders : official journal of the Movement Disorder Society</title><idno type="eISSN">1531-8257</idno><imprint><date when="2009" type="published">2009</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aged</term><term>Analysis of Variance</term><term>Anisotropy</term><term>Brain (pathology)</term><term>Brain Mapping</term><term>Cephalometry</term><term>Diffusion Magnetic Resonance Imaging</term><term>Female</term><term>Functional Laterality</term><term>Humans</term><term>Image Processing, Computer-Assisted</term><term>Male</term><term>Middle Aged</term><term>Multiple System Atrophy (pathology)</term><term>Neural Pathways (pathology)</term><term>Parkinson Disease (pathology)</term><term>Statistics, Nonparametric</term></keywords><keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Brain</term><term>Multiple System Atrophy</term><term>Neural Pathways</term><term>Parkinson Disease</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Aged</term><term>Analysis of Variance</term><term>Anisotropy</term><term>Brain Mapping</term><term>Cephalometry</term><term>Diffusion Magnetic Resonance Imaging</term><term>Female</term><term>Functional Laterality</term><term>Humans</term><term>Image Processing, Computer-Assisted</term><term>Male</term><term>Middle Aged</term><term>Statistics, Nonparametric</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The aim of this study was to evaluate in vivo changes in the brain's macro- and microstructure (notably in the motor system) in the parkinsonian variant of multiple system atrophy (MSA-P) and in Parkinson's disease (PD) and to characterize the cerebral anatomical differences between the two conditions. We used a combination of voxel-based morphometry (VBM) and whole-brain, voxel-based diffusion tensor imaging analysis (VB-DTI). Forty-seven right-handed subjects (14 MSA-P patients, 19 PD patients, and 14 controls) were evaluated using VBM and VB-DTI in an analysis of covariance (ANCOVA) with a significance threshold set to P < 0.005. In MSA-P patients, VBM analysis revealed a lower density of grey matter (GM) in a motor-related circuit (especially in the left primary motor cortex, PMC), relative to PD patients, and in the left supplementary motor area (SMA), relative to controls). Diffusion tensor imaging analysis revealed lower fractional anisotropy (FA) values in the left PMC and the right cerebellum in MSA-P patients, compared with controls. Using a volumetric diffusion technique, our study revealed selective tissue degeneration in motor circuits, regardless of the volume loss detected in VBM and in agreement with pathology reports and clinical motor characteristics. Our findings suggest that MSA-P is characterized by both macro- and microstructural changes in the sensorimotor circuit.</div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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