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Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity

OBJECTIVES: Low ultraviolet‐B (UVB) radiation causes hypovitaminosis D, which is a known risk factor for multiple sclerosis (MS) and associated with MS disease activity. Our objective is to test whether vitamin D supplementation is most effective in lowering disease activity during the period of the...

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Detalles Bibliográficos
Autores principales: Miclea, Andrei, Miclea, Marius, Pistor, Maximilian, Hoepner, Andreas, Chan, Andrew, Hoepner, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561321/
https://www.ncbi.nlm.nih.gov/pubmed/28828221
http://dx.doi.org/10.1002/brb3.761
Descripción
Sumario:OBJECTIVES: Low ultraviolet‐B (UVB) radiation causes hypovitaminosis D, which is a known risk factor for multiple sclerosis (MS) and associated with MS disease activity. Our objective is to test whether vitamin D supplementation is most effective in lowering disease activity during the period of the year with low UVB radiation and consequently low serum 25‐hydroxyvitamin D(3) (25(OH)D(3)) concentration. METHODS: Retrospective analysis of medical records from our outpatient department identified 40 MS patients with available data of at least 6 months before and during oral vitamin D supplementation. Serum 25(OH)D(3) concentration was analyzed using immunoassay. UVB radiation data were provided by the local government. Annualized and quarterly relapse rates before and during vitamin D supplementation served as outcome parameters. RESULTS: During vitamin D supplementation (18,950 international units/week (mean, SD 3,397)), serum 25(OH)D(3) concentration increased by 51 nmol/L and the UVB‐related seasonal variability in 25(OH)D(3) levels ceased (rho = −0.13, p > .05). Furthermore, the annualized relapse rate decreased by approximately 50%. This was almost solely driven by the prominent reduction in the quarterly relapse rate in late winter/early spring, when 25(OH)D(3) levels of nonsupplemented patients were the lowest. CONCLUSIONS: Our study demonstrated the modulation of seasonal MS disease activity through vitamin D supplementation. Given the prominent reduction in the quarterly relapse rate in late winter/early spring, our data indicate a beneficial effect of supplementing MS patients with vitamin D, especially during this period of the year.