Vitamin D Supplementation and Antibiotic Use in Older Australian Adults: An Analysis of Data From the D-Health Trial.


Journal

The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675

Informations de publication

Date de publication:
21 09 2022
Historique:
received: 12 04 2022
accepted: 30 06 2022
pubmed: 4 7 2022
medline: 24 9 2022
entrez: 3 7 2022
Statut: ppublish

Résumé

Vitamin D supplementation may reduce the risk or severity of infection, but this has been investigated in few large population-based trials. We analyzed data from the D-Health Trial, using prescription of antibiotics as a surrogate for infection. The D-Health Trial is a randomized, double-blind, placebo-controlled trial in which 21 315 Australians aged 60-84 years were randomized to 60 000 IU of supplementary vitamin D3 or placebo monthly for 5 years. For this analysis, the primary outcome was the number of antibiotic prescription episodes; secondary outcomes were total number of prescriptions, repeat prescription episodes, and antibiotics for urinary tract infection. We estimated incidence rate ratios (IRRs) using negative binomial regression, and odds ratios using logistic regression. Vitamin D supplementation slightly reduced the number of prescription episodes (IRR, 0.98; 95% confidence interval [CI], .95-1.01), total prescriptions (IRR, 0.97; 95% CI, .93-1.00), and repeat prescription episodes (IRR, 0.96; 95% CI, .93-1.00). There was stronger evidence of benefit in people predicted to have insufficient vitamin D at baseline (prescription episodes IRR, 0.93; 95% CI, .87-.99). Vitamin D may reduce the number of antibiotic prescriptions, particularly in people with low vitamin D status. This supports the hypothesis that vitamin D has a clinically relevant effect on the immune system. Australian New Zealand Clinical Trials Registry: ACTRN12613000743763. https://www.anzctr.org.au/.

Sections du résumé

BACKGROUND
Vitamin D supplementation may reduce the risk or severity of infection, but this has been investigated in few large population-based trials. We analyzed data from the D-Health Trial, using prescription of antibiotics as a surrogate for infection.
METHODS
The D-Health Trial is a randomized, double-blind, placebo-controlled trial in which 21 315 Australians aged 60-84 years were randomized to 60 000 IU of supplementary vitamin D3 or placebo monthly for 5 years. For this analysis, the primary outcome was the number of antibiotic prescription episodes; secondary outcomes were total number of prescriptions, repeat prescription episodes, and antibiotics for urinary tract infection. We estimated incidence rate ratios (IRRs) using negative binomial regression, and odds ratios using logistic regression.
RESULTS
Vitamin D supplementation slightly reduced the number of prescription episodes (IRR, 0.98; 95% confidence interval [CI], .95-1.01), total prescriptions (IRR, 0.97; 95% CI, .93-1.00), and repeat prescription episodes (IRR, 0.96; 95% CI, .93-1.00). There was stronger evidence of benefit in people predicted to have insufficient vitamin D at baseline (prescription episodes IRR, 0.93; 95% CI, .87-.99).
CONCLUSIONS
Vitamin D may reduce the number of antibiotic prescriptions, particularly in people with low vitamin D status. This supports the hypothesis that vitamin D has a clinically relevant effect on the immune system.
CLINICAL TRIALS REGISTRATION
Australian New Zealand Clinical Trials Registry: ACTRN12613000743763. https://www.anzctr.org.au/.

Identifiants

pubmed: 35780325
pii: 6628138
doi: 10.1093/infdis/jiac279
doi:

Substances chimiques

Anti-Bacterial Agents 0
Vitamins 0
Vitamin D 1406-16-2
Cholecalciferol 1C6V77QF41

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

949-957

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Déclaration de conflit d'intérêts

Potential conflicts of interest. R. E. N. has received funding from Viatris for an unrelated study of pancreatic cancer. P. M. W. has received funding from Astra Zeneca for an unrelated study of ovarian cancer. P. R. E. reports grants from Amgen, grants from Sanofi, and grants from Alexion. All other authors declare no potential conflicts of interests. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.

Auteurs

Hai Pham (H)

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

Mary Waterhouse (M)

Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Catherine Baxter (C)

Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Briony Duarte Romero (B)

Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Donald S A McLeod (DSA)

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

Bruce K Armstrong (BK)

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

Peter R Ebeling (PR)

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

Dallas R English (DR)

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

Gunter Hartel (G)

Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Michael G Kimlin (MG)

School of Biomedical Sciences, Queensland University of Technology, Brisbane, Australia.

Rachel L O'Connell (RL)

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

Jolieke C van der Pols (JC)

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

Alison J Venn (AJ)

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

Penelope M Webb (PM)

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

David C Whiteman (DC)

Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, Australia.

Rachel E Neale (RE)

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

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Classifications MeSH