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Published on: December 9, 2015
Vitamin D supplementation and systemic inflammation in relapsing-remitting multiple sclerosis
Egil Røsjø1,2, Linn H Steffensen3,4, Lone Jørgensen5,6
1Department of Neurology, Akershus University Hospital, Lørenskog, Norway. egil.rorvik.rosjo@ahus.no.
High-dose vitamin D3 supplementation increased vitamin D levels in relapsing-remitting multiple sclerosis (RRMS) patients but did not reduce systemic inflammation markers. Immunomodulatory treatments showed anti-inflammatory effects, independent of vitamin D.
Area of Science:
- Neurology
- Immunology
- Endocrinology
Background:
- Observational studies suggest vitamin D may reduce inflammation in relapsing-remitting multiple sclerosis (RRMS).
- Randomized controlled trials (RCTs) have not yet confirmed these anti-inflammatory effects.
- High-dose vitamin D supplementation is being explored for its potential therapeutic benefits in RRMS.
Purpose of the Study:
- To investigate the anti-inflammatory effects of high-dose oral vitamin D3 in RRMS patients.
- To examine the impact of vitamin D3 supplementation on eleven systemic inflammation markers.
- To assess potential interactions between vitamin D3 and immunomodulatory therapies in RRMS.
Main Methods:
- A double-blinded, randomized, placebo-controlled trial (NCT00785473) involving 68 RRMS patients.
- Supplementation with 20,000 IU/week of vitamin D3 or placebo for 96 weeks.
- Measurement of serum inflammation markers and 25-hydroxyvitamin D (25(OH)D) at baseline and week 96.
Main Results:
- Vitamin D3 supplementation significantly increased serum 25(OH)D levels (56 to 123 nmol/L).
- No significant differences in inflammation markers were observed between the vitamin D3 and placebo groups.
- Patients on immunomodulatory therapy exhibited higher levels of specific inflammatory markers (IL-1RA, CXCL16) but no synergistic effect with vitamin D3.
Conclusions:
- High-dose oral vitamin D3 effectively increases serum 25(OH)D levels in RRMS patients.
- Vitamin D3 supplementation did not significantly alter systemic inflammation markers in this study.
- Immunomodulatory treatments were associated with an anti-inflammatory phenotype, independent of vitamin D status.
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