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High dose vitamin D supplementation does not affect biochemical bone markers in multiple sclerosis - a randomized
Trygve Holmøy1,2, Jonas Christoffer Lindstrøm3,4, Erik Fink Eriksen3,5
1Department of Neurology, Akershus University Hospital, Lørenskog, Norway. Trygve.holmoy@medisin.uio.no.
BMC Neurology
|April 6, 2017
Summary
High-dose vitamin D supplementation did not prevent bone loss in multiple sclerosis patients. While it improved vitamin D levels and lowered parathyroid hormone, bone metabolism markers showed no significant changes.
Area of Science:
- Neurology
- Endocrinology
- Bone Metabolism
Background:
- Multiple sclerosis (MS) patients face increased risks of osteoporosis and fractures.
- Poor vitamin D status is a risk factor for MS and may impact bone health.
- Vitamin D supplementation is often recommended for MS patients to manage progression and bone health.
Purpose of the Study:
- To evaluate the impact of high-dose weekly vitamin D3 supplementation on bone metabolism markers in individuals with relapsing-remitting MS.
- To assess the effect of vitamin D on bone formation and resorption in MS patients.
Main Methods:
- A randomized controlled trial involving 68 relapsing-remitting MS patients.
- Participants received either 20,000 IU of vitamin D3 weekly or a placebo for 96 weeks.
- Biochemical markers of bone metabolism, including PINP and CTX1, were measured.
Main Results:
- Vitamin D supplementation significantly increased serum 25-hydroxyvitamin D levels and decreased parathyroid hormone.
- No significant effect was observed on bone formation markers (PINP) or bone resorption markers (CTX1).
- Neither PINP nor CTX1 levels predicted bone loss over the 96-week study period.
Conclusions:
- Weekly high-dose vitamin D supplementation does not appear to prevent bone loss in MS patients.
- Findings align with previous studies showing no effect on bone mass density in the same patient cohort.
- Vitamin D supplementation may not be effective for preventing bone loss in MS patients unless they have a vitamin D deficiency.