Linking Microstructural Integrity and Motor Cortex Excitability in Multiple Sclerosis.
Adult
Diffusion Tensor Imaging
Disability Evaluation
Electromyography
Evoked Potentials, Motor
Female
Gray Matter
/ diagnostic imaging
Humans
Male
Middle Aged
Models, Neurological
Motor Cortex
/ diagnostic imaging
Multiple Sclerosis, Relapsing-Remitting
/ diagnostic imaging
Neurites
/ ultrastructure
Neuroimaging
Neuropsychological Tests
Psychomotor Performance
Transcranial Magnetic Stimulation
White Matter
/ diagnostic imaging
NODDI
excitability
motor threshold
multiple sclerosis
neurite orientation dispersion and density imaging
tract-based spatial statistics
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
27
07
2021
accepted:
23
09
2021
entrez:
29
10
2021
pubmed:
30
10
2021
medline:
28
12
2021
Statut:
epublish
Résumé
Motor skills are frequently impaired in multiple sclerosis (MS) patients following grey and white matter damage with cortical excitability abnormalities. We applied advanced diffusion imaging with 3T magnetic resonance tomography for neurite orientation dispersion and density imaging (NODDI), as well as diffusion tensor imaging (DTI) in 50 MS patients and 49 age-matched healthy controls to quantify microstructural integrity of the motor system. To assess excitability, we determined resting motor thresholds using non-invasive transcranial magnetic stimulation. As measures of cognitive-motor performance, we conducted neuropsychological assessments including the Nine-Hole Peg Test, Trail Making Test part A and B (TMT-A and TMT-B) and the Symbol Digit Modalities Test (SDMT). Patients were evaluated clinically including assessments with the Expanded Disability Status Scale. A hierarchical regression model revealed that lower neurite density index (NDI) in primary motor cortex, suggestive for axonal loss in the grey matter, predicted higher motor thresholds, i.e. reduced excitability in MS patients (
Identifiants
pubmed: 34712236
doi: 10.3389/fimmu.2021.748357
pmc: PMC8546169
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
748357Informations de copyright
Copyright © 2021 Radetz, Mladenova, Ciolac, Gonzalez-Escamilla, Fleischer, Ellwardt, Krämer, Bittner, Meuth, Muthuraman and Groppa.
Déclaration de conflit d'intérêts
JK received honoraria for lecturing from Biogen, Novartis, Merck Serono, Sanofi-Genzyme, Roche, Mylan and Teva, and financial research support from Sanofi Genzyme. SB has received honoraria and compensation for travel from Biogen Idec, Merck Serono, Novartis, Sanofi-Genzyme and Roche. SM has received honoraria for lecturing and travel expenses for attending meetings from Almirall, Amicus Therapeutics Germany, Bayer Health Care, Biogen, Celgene, Diamed, Genzyme, MedDay Pharmaceuticals, Merck Serono, Novartis, Novo Nordisk, ONO Pharma, Roche, Sanofi-Aventis, Chugai Pharma, QuintilesIMS, and Teva. His research is funded by the German Ministry for Education and Research (BMBF), Deutsche Forschungsgemeinschaft (DFG), Else Kröner Fresenius Foundation, German Academic Exchange Service, Hertie Foundation, Interdisciplinary Center for Clinical Studies (IZKF) Muenster, German Foundation Neurology, and by Almirall, Amicus Therapeutics Germany, Biogen, Diamed, Fresenius Medical Care, Genzyme, Merck Serono, Novartis, ONO Pharma, Roche, and Teva. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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