Effect of dimethyl fumarate on gray and white matter pathology in subjects with relapsing multiple sclerosis: a

R Zivadinov1,2, J Hagemeier1, N Bergsland1

  • 1Department of Neurology, Buffalo Neuroimaging Analysis Center, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York, Buffalo, NY, USA.

Abstract

Insights

Dimethyl fumarate (DMF) may protect against white matter and gray matter damage in multiple sclerosis (MS). This study found DMF-treated MS patients showed less diffusivity changes over 24 months compared to healthy individuals.

Area of Science:

  • Neuroscience
  • Radiology
  • Pharmacology

Background:

  • Relapsing-remitting multiple sclerosis (MS) is an inflammatory and neurodegenerative disease.
  • Dimethyl fumarate (DMF) is an oral immunomodulator used to treat MS.
  • The precise impact of DMF on white matter and gray matter pathology in MS remains incompletely understood.

Purpose of the Study:

  • To longitudinally characterize the effects of DMF on normal-appearing white matter (NAWM) and thalamic pathology in patients with MS.
  • To compare diffusion tensor imaging (DTI) metrics in the thalamus and NAWM between MS patients treated with DMF and healthy controls over 24 months.

Main Methods:

  • An observational, longitudinal 24-month magnetic resonance imaging (MRI) study.
  • Inclusion of 75 patients with relapsing-remitting MS treated with DMF and 40 age- and sex-matched healthy controls.
  • Assessment of regional DTI metrics (mean diffusivity, axial diffusivity, radial diffusivity, fractional anisotropy) in the thalamus and NAWM using tract-based spatial statistics.

Main Results:

  • At baseline, MS patients exhibited significantly higher diffusivity and lower fractional anisotropy in the thalamus and NAWM compared to healthy individuals.
  • No significant changes in DTI metrics were observed within either group over the 24-month study period.
  • Healthy individuals demonstrated a significantly greater increase in diffusivity parameters in the thalamus and NAWM over 24 months compared to MS patients.

Conclusions:

  • The stability of DTI metrics in MS patients treated with DMF over 24 months suggests a potential neuroprotective effect of the drug.
  • These findings support the beneficial role of DMF in mitigating MS-related white matter and gray matter pathology.

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