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Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial

BACKGROUND: Randomized controlled trials (RCT) of vitamin D supplementation to reduce fracture risk in children are lacking. METHODS: We conducted a Phase 3 RCT of weekly oral supplementation with 14,000 IU vitamin D(3) for 3 years in Mongolian schoolchildren aged 6-13 years. Serum 25-hydroxyvitamin...

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Autores principales: Ganmaa, Davaasambuu, Khudyakov, Polyna, Buyanjargal, Uyanga, Tserenkhuu, Enkhtsetseg, Erdenenbaatar, Sumiya, Achtai, Chuluun-Erdene, Yansan, Narankhuu, Delgererekh, Baigal, Ankhbat, Munkhzaya, Tsendjav, Enkhjargal, Ochirbat, Batbayar, Jargalsaikhan, Badamtsetseg, Davaasambuu, Enkhmaa, Martineau, Adrian R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246036/
https://www.ncbi.nlm.nih.gov/pubmed/37292864
http://dx.doi.org/10.1101/2023.05.18.23290181
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author Ganmaa, Davaasambuu
Khudyakov, Polyna
Buyanjargal, Uyanga
Tserenkhuu, Enkhtsetseg
Erdenenbaatar, Sumiya
Achtai, Chuluun-Erdene
Yansan, Narankhuu
Delgererekh, Baigal
Ankhbat, Munkhzaya
Tsendjav, Enkhjargal
Ochirbat, Batbayar
Jargalsaikhan, Badamtsetseg
Davaasambuu, Enkhmaa
Martineau, Adrian R
author_facet Ganmaa, Davaasambuu
Khudyakov, Polyna
Buyanjargal, Uyanga
Tserenkhuu, Enkhtsetseg
Erdenenbaatar, Sumiya
Achtai, Chuluun-Erdene
Yansan, Narankhuu
Delgererekh, Baigal
Ankhbat, Munkhzaya
Tsendjav, Enkhjargal
Ochirbat, Batbayar
Jargalsaikhan, Badamtsetseg
Davaasambuu, Enkhmaa
Martineau, Adrian R
author_sort Ganmaa, Davaasambuu
collection PubMed
description BACKGROUND: Randomized controlled trials (RCT) of vitamin D supplementation to reduce fracture risk in children are lacking. METHODS: We conducted a Phase 3 RCT of weekly oral supplementation with 14,000 IU vitamin D(3) for 3 years in Mongolian schoolchildren aged 6-13 years. Serum 25-hydroxyvitamin D (25[OH]D) concentrations and the proportion of participants reporting ≥1 fracture were secondary outcomes for the main trial. Radial bone mineral density (BMD) was assessed in a nested sub-study, with serum concentrations of parathyroid hormone (PTH) and bone-specific alkaline phosphatase (BALP) determined in a subset of participants. FINDINGS: 8851 children were enrolled in the main trial, of whom 1465 also participated in the sub-study. Vitamin D deficiency was prevalent at baseline (25[OH]D <20 ng/mL in 90.1%). The intervention elevated 25(OH)D concentrations (adjusted inter-arm mean difference [aMD] 20.3 ng/mL, 95% CI 19.9 to 20.6) and suppressed PTH concentrations (aMD −13.6 pmol/L, 95% CI −23.5 to −3.7), but it did not influence fracture risk (adjusted risk ratio 1.10, 95% CI 0.93 to 1.29, P=0.27) or radial BMD z-score (aMD −0.06, 95% CI −0.18 to 0.07, P=0.36). Vitamin D suppressed serum BALP concentrations more among participants with baseline 25(OH)D concentrations <10 vs. ≥10 ng/mL (P(interaction)=0.04). However, effects of the intervention on fracture risk and radial BMD were not modified by baseline vitamin D status (P(interaction)≥0.67). INTERPRETATION: Weekly oral vitamin D supplementation elevated serum 25(OH)D concentrations and suppressed PTH concentrations in vitamin D-deficient schoolchildren in Mongolia. However, this was not associated with reduced fracture risk or increased radial BMD. FUNDING: National Institutes of Health
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spelling pubmed-102460362023-06-08 Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial Ganmaa, Davaasambuu Khudyakov, Polyna Buyanjargal, Uyanga Tserenkhuu, Enkhtsetseg Erdenenbaatar, Sumiya Achtai, Chuluun-Erdene Yansan, Narankhuu Delgererekh, Baigal Ankhbat, Munkhzaya Tsendjav, Enkhjargal Ochirbat, Batbayar Jargalsaikhan, Badamtsetseg Davaasambuu, Enkhmaa Martineau, Adrian R medRxiv Article BACKGROUND: Randomized controlled trials (RCT) of vitamin D supplementation to reduce fracture risk in children are lacking. METHODS: We conducted a Phase 3 RCT of weekly oral supplementation with 14,000 IU vitamin D(3) for 3 years in Mongolian schoolchildren aged 6-13 years. Serum 25-hydroxyvitamin D (25[OH]D) concentrations and the proportion of participants reporting ≥1 fracture were secondary outcomes for the main trial. Radial bone mineral density (BMD) was assessed in a nested sub-study, with serum concentrations of parathyroid hormone (PTH) and bone-specific alkaline phosphatase (BALP) determined in a subset of participants. FINDINGS: 8851 children were enrolled in the main trial, of whom 1465 also participated in the sub-study. Vitamin D deficiency was prevalent at baseline (25[OH]D <20 ng/mL in 90.1%). The intervention elevated 25(OH)D concentrations (adjusted inter-arm mean difference [aMD] 20.3 ng/mL, 95% CI 19.9 to 20.6) and suppressed PTH concentrations (aMD −13.6 pmol/L, 95% CI −23.5 to −3.7), but it did not influence fracture risk (adjusted risk ratio 1.10, 95% CI 0.93 to 1.29, P=0.27) or radial BMD z-score (aMD −0.06, 95% CI −0.18 to 0.07, P=0.36). Vitamin D suppressed serum BALP concentrations more among participants with baseline 25(OH)D concentrations <10 vs. ≥10 ng/mL (P(interaction)=0.04). However, effects of the intervention on fracture risk and radial BMD were not modified by baseline vitamin D status (P(interaction)≥0.67). INTERPRETATION: Weekly oral vitamin D supplementation elevated serum 25(OH)D concentrations and suppressed PTH concentrations in vitamin D-deficient schoolchildren in Mongolia. However, this was not associated with reduced fracture risk or increased radial BMD. FUNDING: National Institutes of Health Cold Spring Harbor Laboratory 2023-05-19 /pmc/articles/PMC10246036/ /pubmed/37292864 http://dx.doi.org/10.1101/2023.05.18.23290181 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Ganmaa, Davaasambuu
Khudyakov, Polyna
Buyanjargal, Uyanga
Tserenkhuu, Enkhtsetseg
Erdenenbaatar, Sumiya
Achtai, Chuluun-Erdene
Yansan, Narankhuu
Delgererekh, Baigal
Ankhbat, Munkhzaya
Tsendjav, Enkhjargal
Ochirbat, Batbayar
Jargalsaikhan, Badamtsetseg
Davaasambuu, Enkhmaa
Martineau, Adrian R
Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
title Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
title_full Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
title_fullStr Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
title_full_unstemmed Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
title_short Influence of vitamin D supplementation on fracture risk, bone mineral density and bone biochemistry in Mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
title_sort influence of vitamin d supplementation on fracture risk, bone mineral density and bone biochemistry in mongolian schoolchildren: multicenter double-blind randomized placebo-controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10246036/
https://www.ncbi.nlm.nih.gov/pubmed/37292864
http://dx.doi.org/10.1101/2023.05.18.23290181
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