Abstract

Background: High serum levels of 25-hydroxyvitamin D (25(OH)D) have been found among patients with a favorable disease course in relapsing-remitting MS (RRMS), indicating that this may limit clinical deterioration. Clinical deterioration in RRMS correlates with increasing serum levels of neurofilament light chain (NfL).Objectives: To examine the association between physiological variations in serum 25(OH)D and NfL levels in RRMS patients before and during disease modifying therapy (DMT).Material and Methods: Serum 25(OH)D and NfL concentrations were measured in 85 newly diagnosed RRMS patients enrolled in a 24-month randomized double-blinded placebo-controlled trial of ω-3 fatty acid supplementation without vitamin D. Patients were without DMT until interferon β-1a (IFN-β) initiation at study month 6. Longitudinal serum measurements and brain magnetic resonance imaging (MRI) were obtained. Associations between 25(OH)D and NfL levels were analyzed with linear regression models for the whole study period and the periods before and during IFN-β treatment. Analyses with adjustment for inflammatory MRI disease activity were also performed.Results: No significant associations were found between variations in 25(OH)D and NfL levels during the whole study period (p = 0.95), or the periods without (p = 0.78) or with (p = 0.33) IFN-β therapy. Patients with inflammatory MRI disease activity had significantly higher serum NfL levels than patients without inflammatory MRI disease activity [mean (SD) difference 12.6 (2.0) pg/mL, p < 0.01]. Adjustment for this did not change the relationship between 25(OH)D and NfL concentrations.Conclusion: Natural variations in serum 25(OH)D values do not seem to be associated with alterations in serum NfL concentrations in RRMS patients.

Highlights

  • Central nervous tissue degeneration promotes disease progression in multiple sclerosis (MS), and neurofilament light chain (NfL) is a validated surrogate biomarker for this process in patients with relapsing-remitting MS (RRMS) (1)

  • Natural variations in serum 25(OH)D values do not seem to be associated with alterations in serum NfL concentrations in RRMS patients

  • We have previously reported results from a two-year observational study of 85 RRMS patients with rather high disease activity showing an inverse association between naturally increasing 25(OH)D levels and inflammatory magnetic resonance imaging (MRI) disease activity before introduction of interferon beta-1a (IFN-β) treatment (6), while NfL levels were positively correlated with inflammatory MRI disease activity and inversely with interferon β-1a (IFN-β) initiation (5)

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Summary

Introduction

Central nervous tissue degeneration promotes disease progression in multiple sclerosis (MS), and neurofilament light chain (NfL) is a validated surrogate biomarker for this process in patients with relapsing-remitting MS (RRMS) (1). High serum concentrations of NfL have been associated with inflammatory disease activity and development of atrophy on brain magnetic resonance imaging (MRI) and clinical disability (3). Increasing serum levels of 25(OH)D have been associated with decreased clinical and inflammatory MRI disease activity in observational studies in RRMS (6, 7). High serum levels of 25-hydroxyvitamin D (25(OH)D) have been found among patients with a favorable disease course in relapsing-remitting MS (RRMS), indicating that this may limit clinical deterioration. Clinical deterioration in RRMS correlates with increasing serum levels of neurofilament light chain (NfL)

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