Weekly Vitamin D Supplementation to Prevent Acute Respiratory Infections in Young Children at Different Latitudes: A Randomized Controlled Trial.
Reyes. María Loreto ML; Vizcaya. Cecilia C; Le Roy. Catalina C; Loureiro. Carolina C; Brinkmann. Karin K; Arancibia. Mónica M; Campos. Laura L; Iturriaga. Carolina C; Pérez-Mateluna. Guillermo G; Rojas-McKenzie. Maite M; Domínguez. Gonzalo G; Camargo. Carlos A CA; Borzutzky. Arturo A
Key Findings
- Weekly vitamin D (5600 IU or 11 200 IU) increased serum 25‑hydroxyvitamin D in a dose‑dependent way.
- No difference in the number of acute respiratory infections between vitamin D and placebo groups.
- LL‑37/cathelicidin levels did not change with vitamin D supplementation.
Practical Outcomes
- Vitamin D supplementation can be used to correct low vitamin D in young children, but don’t expect it to prevent colds or boost LL‑37. For biohackers, the data suggest that higher weekly doses are safe but don’t provide extra infection protection, so focus on other immunity strategies.
Summary
Giving preschool kids a weekly vitamin D pill (about 800 or 1600 IU per day) safely raised their blood vitamin D levels, but it didn’t cut down the number of colds or flu they got, and it didn’t change the body’s LL‑37 antimicrobial peptide levels.
Abstract
To evaluate the effectiveness of weekly vitamin D supplementation in reducing the number of acute respiratory infections (ARI) in preschool children. Randomized, double-blind, placebo-controlled trial in 303 children aged 1.5-3.5 years from 2014 to 2105 in 3 Chilean cities at different latitudes: Santiago (33°S, n = 101), Talcahuano (37°S, n = 103), and Punta Arenas (53°S, n = 99). Participants were allocated (1:1:1) to receive placebo, cholecalciferol (vitamin D3 (VD3)) 5600 IU/week (low-dose), or 11 200 IU/week (high-dose) for 6 months. Primary outcome was parent-reported number of ARI; secondary outcomes included number of ARI hospitalizations, change of serum 25-hydroxyvitamin D (25(OH)D) and LL-37/cathelicidin levels, and adverse events. The mean age of participants was 26 ± 6 months; 45% were female. Baseline 25(OH)D was 24.9 ± 6.1 ng/ml, with 23% having 25(OH)D <20 ng/ml. No significant baseline clinical or laboratory differences were observed among groups. Overall, 64% (n = 194) completed study participation, without baseline differences between subjects lost to follow-up vs those completing participation or differences in completion rates across groups. After 6 months, a dose-dependent increase in serum 25(OH)D was observed from the VD3 intervention (P < .001), with a higher proportion of subjects ending the trial with 25(OH)D <20 ng/ml in the placebo group (30.8%) vs the low-dose (7.4%) and high-dose groups (5.1%). However, no group differences were observed in number of ARI (P = .85), ARI hospitalizations (P = .20), LL-37/cathelicidin change (P = .30), or adverse events (P = .41). While weekly VD3 supplementation, in doses equivalent to 800 IU and 1600 IU daily, was associated with improved 25(OH)D levels in preschoolers, we did not find a reduced number of ARI in this sample.
Study Information
pubmed
2024
2024-08-22T00:00:00.000Z
10.1016/j.jpeds.2024.114249
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