The effect of monthly vitamin D supplementation on fractures: a tertiary outcome from the population-based, double-blind, randomised, placebo-controlled D-Health trial.


Journal

The lancet. Diabetes & endocrinology
ISSN: 2213-8595
Titre abrégé: Lancet Diabetes Endocrinol
Pays: England
ID NLM: 101618821

Informations de publication

Date de publication:
05 2023
Historique:
received: 22 01 2023
revised: 27 02 2023
accepted: 27 02 2023
medline: 24 4 2023
pubmed: 4 4 2023
entrez: 3 4 2023
Statut: ppublish

Résumé

Low serum 25-hydroxy vitamin D concentration is associated with increased fracture risk. It is uncertain whether vitamin D supplementation reduces fractures, or whether intermittent doses are harmful. We aimed to investigate if supplementing adults living in Australia with monthly doses of 60 000 international units (IU) vitamin D We did a population-based, double-blind, randomised, placebo-controlled trial of oral vitamin D Between Feb 14, 2014, and June 17, 2015, we recruited 21 315 participants. For the current analysis, we included 20 326 participants (vitamin D 10 154 [50·0%]; placebo 10 172 [50·0%]). 9295 (45·7%) of 20 326 participants were women and the mean age was 69·3 years (SD 5·5). Over a median follow-up of 5·1 years (IQR 5·1-5·1), 568 (5·6%) participants in the vitamin D group and 603 (5·9%) in the placebo group had one or more fractures. There was no effect on fracture risk overall (HR 0·94 [95% CI 0·84-1·06]), and the interaction between randomisation group and time was not significant (p=0·14). However, the HR for total fractures appeared to decrease with increasing follow-up time. The overall HRs for non-vertebral, major osteoporotic, and hip fractures were 0·96 (95% CI 0·85-1·08), 1·00 (0·85-1·18), and 1·11 (0·86-1·45), respectively. These findings do not support concerns that bolus doses of vitamin D administered monthly increase fracture risk. Long-term supplementation might reduce the incidence of total fractures, but additional research is needed to clarify this effect. Australian National Health and Medical Research Council.

Sections du résumé

BACKGROUND
Low serum 25-hydroxy vitamin D concentration is associated with increased fracture risk. It is uncertain whether vitamin D supplementation reduces fractures, or whether intermittent doses are harmful. We aimed to investigate if supplementing adults living in Australia with monthly doses of 60 000 international units (IU) vitamin D
METHODS
We did a population-based, double-blind, randomised, placebo-controlled trial of oral vitamin D
FINDINGS
Between Feb 14, 2014, and June 17, 2015, we recruited 21 315 participants. For the current analysis, we included 20 326 participants (vitamin D 10 154 [50·0%]; placebo 10 172 [50·0%]). 9295 (45·7%) of 20 326 participants were women and the mean age was 69·3 years (SD 5·5). Over a median follow-up of 5·1 years (IQR 5·1-5·1), 568 (5·6%) participants in the vitamin D group and 603 (5·9%) in the placebo group had one or more fractures. There was no effect on fracture risk overall (HR 0·94 [95% CI 0·84-1·06]), and the interaction between randomisation group and time was not significant (p=0·14). However, the HR for total fractures appeared to decrease with increasing follow-up time. The overall HRs for non-vertebral, major osteoporotic, and hip fractures were 0·96 (95% CI 0·85-1·08), 1·00 (0·85-1·18), and 1·11 (0·86-1·45), respectively.
INTERPRETATION
These findings do not support concerns that bolus doses of vitamin D administered monthly increase fracture risk. Long-term supplementation might reduce the incidence of total fractures, but additional research is needed to clarify this effect.
FUNDING
Australian National Health and Medical Research Council.

Identifiants

pubmed: 37011645
pii: S2213-8587(23)00063-3
doi: 10.1016/S2213-8587(23)00063-3
pii:
doi:

Substances chimiques

Vitamin D 1406-16-2
Vitamins 0
Cholecalciferol 1C6V77QF41

Banques de données

ANZCTR
['ACTRN12613000743763']

Types de publication

Randomized Controlled Trial Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

324-332

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests PMW has funding from AstraZeneca for an unrelated study of ovarian cancer and funding from the National Health and Medical Research Council (NHMRC). PRE reports grants and speaker fees from Amgen, grants from Sanofi, grants from Alexion, and a grant from the NHMRC. PRE is past-president and a councilor (unpaid) of the American Society for Bone and Mineral Research, a board member (unpaid) of the International Osteoporosis Foundation, and chair of the board of directors (unpaid) of Health Bones Australia. REN has funding from Viatris for an unrelated study of pancreatic cancer, has received speaker fees and travels cost from Viatris to speak at the Australasian Gastrointestinal Trials Group annual meeting, and has grant payments from the NHMRC paid to QIMR Berghofer Medical Research Institute. REN is leader of one of the working groups of the Environmental Effects Assessment Panel (unpaid) of the UN Environment Program. DE reports funding from the NHMRC, paid to QIMR Berghofer Medical Research Institute. DCW reports funding from the NHMRC, paid to QIMR Berghofer Medical Research Institute, and speaker fees from Pierre Fabre Australia for the 2020 COSA Conference. DCW is also an unpaid director for a not-for-profit research institute (Sax Institute). MK is a board director of the Skin Cancer College Australasia, and a board director of Melanoma and Skin Cancer Trials Limited. All other authors declare no competing interests.

Auteurs

Mary Waterhouse (M)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Peter R Ebeling (PR)

Department of Medicine, School of Clinical Sciences, Monash University, Melbourne, VIC, Australia.

Donald S A McLeod (DSA)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia; Department of Endocrinology and Diabetes, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.

Dallas English (D)

Melbourne School of Population Health, University of Melbourne, Melbourne, VIC, Australia; Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, VIC, Australia.

Briony Duarte Romero (BD)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Catherine Baxter (C)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Bruce K Armstrong (BK)

School of Public Health, University of Sydney, Sydney, NSW, Australia; School of Global and Population Health, University of Western Australia, Perth, WA, Australia.

Gunter Hartel (G)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Michael Kimlin (M)

School of Biomedical Science, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.

Rachel L O'Connell (RL)

NHMRC Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia.

Jolieke C van der Pols (JC)

School of Exercise and Nutrition Sciences, Faculty of Health, Queensland University of Technology, Brisbane, QLD, Australia.

Alison J Venn (AJ)

Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.

Penelope M Webb (PM)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia; School of Public Health, University of Queensland, Brisbane, QLD, Australia.

David C Whiteman (DC)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.

Rachel E Neale (RE)

Population Health Program, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia; School of Public Health, University of Queensland, Brisbane, QLD, Australia. Electronic address: rachel.neale@qimrberghofer.edu.au.

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