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- Title
Effect of High-Dose vs Standard-Dose Wintertime Vitamin D Supplementation on Viral Upper Respiratory Tract Infections in Young Healthy Children.
- Authors
Aglipay, Mary; Birken, Catherine S.; Parkin, Patricia C.; Loeb, Mark B.; Thorpe, Kevin; Yang Chen; Laupacis, Andreas; Mamdani, Muhammad; Macarthur, Colin; Hoch, Jeffrey S.; Mazzulli, Tony; Maguire, Jonathon L.; Chen, Yang; TARGet Kids! Collaboration
- Abstract
<bold>Importance: </bold>Epidemiological studies support a link between low 25-hydroxyvitamin D levels and a higher risk of viral upper respiratory tract infections. However, whether winter supplementation of vitamin D reduces the risk among children is unknown.<bold>Objective: </bold>To determine whether high-dose vs standard-dose vitamin D supplementation reduces the incidence of wintertime upper respiratory tract infections in young children.<bold>Design, Setting, and Participants: </bold>A randomized clinical trial was conducted during the winter months between September 13, 2011, and June 30, 2015, among children aged 1 through 5 years enrolled in TARGet Kids!, a multisite primary care practice-based research network in Toronto, Ontario, Canada.<bold>Interventions: </bold>Three hundred forty-nine participants were randomized to receive 2000 IU/d of vitamin D oral supplementation (high-dose group) vs 354 participants who were randomized to receive 400 IU/d (standard-dose group) for a minimum of 4 months between September and May.<bold>Main Outcome Measures: </bold>The primary outcome was the number of laboratory-confirmed viral upper respiratory tract infections based on parent-collected nasal swabs over the winter months. Secondary outcomes included the number of influenza infections, noninfluenza infections, parent-reported upper respiratory tract illnesses, time to first upper respiratory tract infection, and serum 25-hydroxyvitamin D levels at study termination.<bold>Results: </bold>Among 703 participants who were randomized (mean age, 2.7 years, 57.7% boys), 699 (99.4%) completed the trial. The mean number of laboratory-confirmed upper respiratory tract infections per child was 1.05 (95% CI, 0.91-1.19) for the high-dose group and 1.03 (95% CI, 0.90-1.16) for the standard-dose group, for a between-group difference of 0.02 (95% CI, -0.17 to 0.21) per child. There was no statistically significant difference in number of laboratory-confirmed infections between groups (incidence rate ratio [RR], 0.97; 95% CI, 0.80-1.16). There was also no significant difference in the median time to the first laboratory-confirmed infection: 3.95 months (95% CI, 3.02-5.95 months) for the high-dose group vs 3.29 months (95% CI, 2.66-4.14 months) for the standard-dose group, or number of parent-reported upper respiratory tract illnesses between groups (625 for high-dose vs 600 for standard-dose groups, incidence RR, 1.01; 95% CI, 0.88-1.16). At study termination, serum 25-hydroxyvitamin D levels were 48.7 ng/mL (95% CI, 46.9-50.5 ng/mL) in the high-dose group and 36.8 ng/mL (95% CI, 35.4-38.2 ng/mL) in the standard-dose group.<bold>Conclusions and Relevance: </bold>Among healthy children aged 1 to 5 years, daily administration of 2000 IU compared with 400 IU of vitamin D supplementation did not reduce overall wintertime upper respiratory tract infections. These findings do not support the routine use of high-dose vitamin D supplementation in children for the prevention of viral upper respiratory tract infections.<bold>Trial Registration: </bold>clinicaltrials.gov Identifier: NCT01419262.
- Subjects
THERAPEUTIC use of vitamin D; RESPIRATORY infections in children; DRUG dosage; JUVENILE diseases; INFLUENZA prevention; WINTER; PREVENTION; COMMON cold prevention; VIRAL disease prevention; INFLUENZA epidemiology; COMPARATIVE studies; DIETARY supplements; DOSE-effect relationship in pharmacology; RESEARCH methodology; MEDICAL cooperation; NOSE; ORAL drug administration; RESEARCH; RESPIRATORY infections; VITAMIN D; VITAMINS; EVALUATION research; RANDOMIZED controlled trials; DISEASE incidence
- Publication
JAMA: Journal of the American Medical Association, 2017, Vol 318, Issue 3, p245
- ISSN
0098-7484
- Publication type
journal article
- DOI
10.1001/jama.2017.8708