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Multimodal MRI Response to Fingolimod in Multiple Sclerosis: A Nonrandomized, Single Arm, Observational Study
Evanthia Bernitsas1, Hannah Kopinsky1, Samuel Lichtman-Mikol1
1Department of Neurology, Wayne State University School of Medicine, Detroit, MI.
Summary
Fingolimod may promote neurorepair in multiple sclerosis (MS) patients by improving white matter integrity in lesions and normal-appearing white matter (NAWM) over two years, as shown by advanced MRI metrics.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Fingolimod shows benefits in conventional MRI but its neuroprotective capacity remains unclear.
- Investigating fingolimod's effects on both lesion and normal-appearing white matter (NAWM) is crucial for understanding its full impact.
Purpose of the Study:
- To assess changes in conventional and advanced MRI measures in lesions and NAWM over two years in patients with multiple sclerosis treated with fingolimod.
- To evaluate potential neuroreparative effects of fingolimod.
Main Methods:
- Fifty relapsing-remitting multiple sclerosis patients and 27 controls underwent 3T MRI scans at baseline, 1 year, and 2 years.
- Advanced MRI metrics including magnetization transfer ratio (MTR), fractional anisotropy (FA), and median diffusivity (MD) were calculated for lesions and NAWM.
- Longitudinal changes were analyzed using repeated measures ANOVA with Bonferroni correction.
Main Results:
- Conventional MRI measures showed no significant changes.
- Significant improvements were observed in lesion magnetization transfer ratio (MTR) and fractional anisotropy (FA), along with changes in lesion median diffusivity (MD).
- Normal-appearing white matter (NAWM) fractional anisotropy (FA) showed significant improvement over two years, while NAWM-MD also changed significantly within the first year.
Conclusions:
- Fingolimod treatment may exert a neuroreparative effect on both MS lesions and NAWM.
- Further large-scale, randomized studies are necessary to confirm these promising findings on fingolimod's neuroprotective potential.
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