Vitamin D₃ supplementation and neurofilament light chain in multiple sclerosis

Low circulating vitamin D levels are associated with an increased risk of active MRI lesions and relapses in several cohorts with relapsing remitting multiple sclerosis (RRMS). Randomized controlled supplementation trials are, however, negative on their primary endpoints, while secondary MRI endpoints suggest anti-inflammatory effects. Circulating levels of neurofilament light chain (NfL) are a biomarker of disease activity in RRMS. We explored whether 48-week high-dose vitamin D₃ supplements were associated with lower circulating NfL levels.

Of N = 40 Dutch interferon beta-treated participants with RRMS of the SOLAR trial, plasma samples at baseline and 48-week follow-up were available. Of these participants, N = 24 were supplemented with 14 000 IU/d vitamin D₃ and N = 16 with placebo. Twenty-five hydroxyvitamin D₃ (25(OH)D₃ ) levels were measured with LC-MS/MS, and NfL levels were measured in duplicate with Simoa.

Serum 25(OH)D₃ levels at 48 weeks were increased in the vitamin D₃ when compared to placebo group (median level 281 [IQR 205-330] vs 72 [39-88] nmol/L; P < .01). NfL levels at 48 weeks did not differ between the treatment groups (median level 25.4 [IQR 19.6-32.2] vs 25.3 [17.9-30.1] pg/mL; P = .74). Higher week 48 NfL level showed a trend toward association with a higher risk of combined unique active lesions on the week 48 MRI scan (OR 2.39 [95% CI 0.93-6.12] for each 10 pg/mL increase; P = .07).

Supplementation of high-dose vitamin D₃ for 48 weeks was not associated with lower NfL levels. This study does not support an effect of vitamin D₃ on this biomarker of neuro-axonal injury.