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Effect of vitamin D(3)-supplementation on bone markers (serum P1NP and CTX): A randomized, double blinded, placebo controlled trial among healthy immigrants living in Norway

OBJECTIVE: Vitamin D is essential for the maintenance of calcium homeostasis and bone mineralization; and low serum 25-hydroxyvitamin D (s-25-(OH)D) concentrations are associated with increased bone turnover. However, there is a lack of randomized controlled trials that have investigated the effect...

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Detalles Bibliográficos
Autores principales: Madar, Ahmed A., Knutsen, Kirsten V., Stene, Lars C., Brekke, Mette, Lagerløv, Per, Meyer, Haakon E., Macdonald, Helen M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5365165/
https://www.ncbi.nlm.nih.gov/pubmed/28377958
http://dx.doi.org/10.1016/j.bonr.2015.05.004
Descripción
Sumario:OBJECTIVE: Vitamin D is essential for the maintenance of calcium homeostasis and bone mineralization; and low serum 25-hydroxyvitamin D (s-25-(OH)D) concentrations are associated with increased bone turnover. However, there is a lack of randomized controlled trials that have investigated the effect of vitamin D treatment on bone turnover in immigrant populations. We aimed to investigate the effect of 16-week daily vitamin D(3) supplementation on bone formation marker serum procollagen type 1 amino-terminal propeptide (P1NP) and bone resorption marker C-terminal crosslinked telopeptide of type I collagen (CTX). DESIGN: Double-blind, randomized, placebo-controlled trial. SETTING: Immigrant community centers in Oslo, Norway. PARTICIPANTS: 251 healthy adults aged 18–50 years with a non-Western immigrant background were recruited. INTERVENTION: 16 weeks of daily oral supplementation with either 10 μg vitamin D(3), 25 μg vitamin D(3), or placebo. MAIN OUTCOME MEASURES: Difference in change during the 16-week intervention between the intervention groups combined (10 or 25 μg of vitamin D(3)/day) and placebo, in serum P1NP and serum CTX. RESULTS: A total of 214 (85%) participants completed the study. S-25-(OH)D increased from 29 nmol/L at baseline to 49 nmol/L in the intervention group with no significant change in the placebo group. However, there was no difference in change of serum P1NP (mean difference: − 1.2 μg/L (95% CI: − 5.4, 2.9, P = 0.6)) and serum CTX (mean difference: − 0.005 μg/L (95% CI: − 0.03, 0.02, P = 0.7)) between those receiving vitamin D(3) supplementation compared with placebo. The plasma PTH had decreased by a mean of − 1.97 pmol/L (95% CI: − 2.7, − 1.3, P < 0.0001) in the vitamin D(3) group compared to placebo. CONCLUSIONS: Supplementation with 10 or 25 μg oral vitamin D(3) during winter and spring for 16 weeks did not significantly affect serum P1NP and serum CTX, despite increasing s-25(OH)D and decreasing PTH in a healthy immigrant population with low baseline vitamin D status. Trial registration number: NCT01263288.