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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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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 |
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author | Miclea, Andrei Miclea, Marius Pistor, Maximilian Hoepner, Andreas Chan, Andrew Hoepner, Robert |
author_facet | Miclea, Andrei Miclea, Marius Pistor, Maximilian Hoepner, Andreas Chan, Andrew Hoepner, Robert |
author_sort | Miclea, Andrei |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5561321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-55613212017-08-21 Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity Miclea, Andrei Miclea, Marius Pistor, Maximilian Hoepner, Andreas Chan, Andrew Hoepner, Robert Brain Behav Original Research 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. John Wiley and Sons Inc. 2017-07-11 /pmc/articles/PMC5561321/ /pubmed/28828221 http://dx.doi.org/10.1002/brb3.761 Text en © 2017 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Miclea, Andrei Miclea, Marius Pistor, Maximilian Hoepner, Andreas Chan, Andrew Hoepner, Robert Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity |
title | Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity |
title_full | Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity |
title_fullStr | Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity |
title_full_unstemmed | Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity |
title_short | Vitamin D supplementation differentially affects seasonal multiple sclerosis disease activity |
title_sort | vitamin d supplementation differentially affects seasonal multiple sclerosis disease activity |
topic | Original Research |
url | 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 |
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