Two years' effect of dimethyl fumarate on focal and diffuse gray matter pathology in multiple sclerosis.


Journal

Multiple sclerosis (Houndmills, Basingstoke, England)
ISSN: 1477-0970
Titre abrégé: Mult Scler
Pays: England
ID NLM: 9509185

Informations de publication

Date de publication:
Nov 2022
Historique:
pubmed: 30 6 2022
medline: 19 10 2022
entrez: 29 6 2022
Statut: ppublish

Résumé

Data on the effect of dimethyl fumarate (DMF) on focal and diffuse gray matter (GM) damage, a relevant pathological substrate of multiple sclerosis (MS)-related disability are lacking. To evaluate the DMF effect on cortical lesions (CLs) accumulation and global and regional GM atrophy in subjects with relapsing-remitting MS. A total of 148 patients (mean age 38.1 ± 9.7 years) treated with DMF ended a 2-year longitudinal study. All underwent regular Expanded Disability Status Scale (EDSS assessment), and at least two 3T-magnetic resonance imaging (MRI) at 3 and 24 months after DMF initiation. CLs and changes in global and regional atrophy of several brain regions were compared with 47 untreated age and sex-matched patients. DMF-treated patients showed lower CLs accumulation (median 0[0-3] vs 2[0-7], Beyond the well-known effect on disease activity, these results provide evidence of the effect of DMF through reduced progression of focal and diffuse GM damage.

Sections du résumé

BACKGROUND
Data on the effect of dimethyl fumarate (DMF) on focal and diffuse gray matter (GM) damage, a relevant pathological substrate of multiple sclerosis (MS)-related disability are lacking.
OBJECTIVE
To evaluate the DMF effect on cortical lesions (CLs) accumulation and global and regional GM atrophy in subjects with relapsing-remitting MS.
METHODS
A total of 148 patients (mean age 38.1 ± 9.7 years) treated with DMF ended a 2-year longitudinal study. All underwent regular Expanded Disability Status Scale (EDSS assessment), and at least two 3T-magnetic resonance imaging (MRI) at 3 and 24 months after DMF initiation. CLs and changes in global and regional atrophy of several brain regions were compared with 47 untreated age and sex-matched patients.
RESULTS
DMF-treated patients showed lower CLs accumulation (median 0[0-3] vs 2[0-7],
CONCLUSIONS
Beyond the well-known effect on disease activity, these results provide evidence of the effect of DMF through reduced progression of focal and diffuse GM damage.

Identifiants

pubmed: 35765211
doi: 10.1177/13524585221104014
doi:

Substances chimiques

Dimethyl Fumarate FO2303MNI2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2090-2098

Auteurs

Damiano Marastoni (D)

Regional Multiple Sclerosis Center, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Francesco Crescenzo (F)

Neurology Unit, "Mater Salutis" Hospital, AULSS 9, Verona, Italy.

Anna I Pisani (AI)

Regional Multiple Sclerosis Center, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Carmela Zuco (C)

Neurology Unit, "Carlo Poma" Hospital, ASST Mantua, Mantua, Italy.

Gianmarco Schiavi (G)

Regional Multiple Sclerosis Center, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Giulia Benedetti (G)

Regional Multiple Sclerosis Center, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Giuseppe K Ricciardi (GK)

Neuroradiology & Radiology Units, Department of Diagnostic and Pathology, Integrated University Hospital of Verona, Verona, Italy.

Stefania Montemezzi (S)

Neuroradiology & Radiology Units, Department of Diagnostic and Pathology, Integrated University Hospital of Verona, Verona, Italy.

Francesca B Pizzini (FB)

Radiology Unit, Department of Diagnostic and Public Health, University of Verona, Verona, Italy.

Agnese Tamanti (A)

Regional Multiple Sclerosis Center, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

Massimiliano Calabrese (M)

Regional Multiple Sclerosis Center, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, Verona, Italy.

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Classifications MeSH