A two-year study using cerebral gray matter volume to assess the response to fingolimod therapy in multiple sclerosis

Abstract Background Cerebral gray matter (GM) atrophy has clinical relevance in multiple sclerosis (MS). Fingolimod has known efficacy on clinical and conventional MRI findings in MS; the effect on GM is unknown. Objective To explore fingolimod's treatment effect on cerebral GM atrophy over two years in patients with relapsing forms of MS. Design/methods Patients starting fingolimod [n = 24, age (mean ± SD) 41.2 ± 11.6 years, Expanded Disability Status Scale (EDSS) score 1.1 ± 1.4; 58% women] were compared to untreated patients [n = 29, age 45.7 ± 8.4 years, EDSS 1.0 ± 1.2; 93% women]. Baseline, one and two year MRI was applied to an SPM12 pipeline to assess brain parenchymal fraction (BPF) and cortical GM fraction (cGMF). T2 lesion volume (T2LV) and gadolinium-enhancing lesions were assessed. Change was modeled using a mixed effects linear regression with a random intercept and fixed effects for time, group, and the time-by-group interaction. The group slope difference was assessed using the interaction term. Results Over two years, cGMF remained stable in the fingolimod group (p > 0.05), but decreased in the untreated group (p   0.05). T2LV increased over two years in the untreated group (p  Conclusion These results suggest a treatment effect of fingolimod on cerebral GM atrophy in the first two years. GM atrophy is more sensitive to such effects than whole brain atrophy. However, due to the non-randomized, retrospective design, heterogeneous between-group characteristics, and small sample size, these results require confirmation in future studies.