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Effect of Vitamin D Supplementation on Recurrent Wheezing in Black Infants Who Were Born Preterm: The D-Wheeze
Anna Maria Hibbs1,2, Kristie Ross1,2, Leigh Ann Kerns1,2
1Case Western Reserve University, Cleveland, Ohio.
Insights
Sustained vitamin D supplementation reduced recurrent wheezing in preterm Black infants. This finding suggests vitamin D plays a role in infant respiratory health.
Area of Science:
- Pediatrics
- Neonatology
- Nutritional Science
Background:
- Black infants born preterm have high rates of recurrent wheezing.
- Vitamin D may influence wheezing via pulmonary and immune system modulation.
Purpose of the Study:
- To evaluate two vitamin D dosing strategies for preventing recurrent wheezing in preterm Black infants.
Main Methods:
- A randomized clinical trial involved 300 preterm Black infants.
- Infants received either sustained vitamin D supplementation (400 IU/d) or diet-limited supplementation until 6 months corrected age.
Main Results:
- Recurrent wheezing occurred in 31.1% of the sustained supplementation group vs. 41.8% in the diet-limited group.
- Sustained supplementation showed a relative risk of 0.66 (95% CI, 0.47 to 0.94) for recurrent wheezing.
- Adverse events like upper and lower respiratory infections were similar between groups.
Conclusions:
- Sustained vitamin D supplementation reduced the risk of recurrent wheezing in preterm Black infants.
- Further research is needed to understand vitamin D's mechanisms and long-term effects on wheezing in this population.
Importance:
Black infants born preterm face high rates of recurrent wheezing throughout infancy. Vitamin D supplementation has the potential to positively or negatively affect wheezing through modulation of the pulmonary and immune systems.
Objective:
To assess the effectiveness of 2 vitamin D dosing strategies in preventing recurrent wheezing.
Design, Setting, And Participants:
A randomized clinical trial enrolled 300 black infants born at 28 to 36 weeks' gestation between January 2013 and January 2016 at 4 sites in the United States, and followed them up through March 2017. Randomization was stratified by site and maternal milk exposure.
Interventions:
Patients were enrolled prior to discharge from the neonatal intensive care unit or newborn nursery and received open-label multivitamin until they were consuming 200 IU/d of cholecalciferol from formula or fortifier added to human milk, after which they received either 400 IU/d of cholecalciferol until 6 months of age adjusted for prematurity (sustained supplementation) or placebo (diet-limited supplementation). One-hundred fifty three infants were randomized to the sustained group, and 147 were randomized to the diet-limited group.
Main Outcomes And Measures:
Recurrent wheezing by 12 months' adjusted age was the primary outcome.
Results:
Among 300 patients who were randomized (mean gestational age, 33 weeks; median birth weight, 1.9 kg), 277 (92.3%) completed the trial. Recurrent wheezing was experienced by 31.1% of infants in the sustained supplementation group and 41.8% of infants in the diet-limited supplementation group (difference, -10.7% [95% CI, -27.4% to -2.9%]; relative risk, 0.66 [95% CI, 0.47 to 0.94]). Upper and lower respiratory tract infections were among the most commonly reported adverse events. Upper respiratory infections were experienced by 84 of 153 infants (54.9%) in the sustained group and 83 of 147 infants (56.5%) in the diet-limited group (difference, -1.6% [95% CI, -17.1% to 7.0%]). Lower respiratory infections were experienced by 33 of 153 infants (21.6%) in the sustained group and 37 of 147 infants (25.2%) in the diet-limited group (difference, -3.6% [95% CI, -16.4% to 4.4%]).
Conclusions And Relevance:
Among black infants born preterm, sustained supplementation with vitamin D, compared with diet-limited supplementation, resulted in a reduced risk of recurrent wheezing by 12 months' adjusted age. Future research is needed to better understand the mechanisms and longer-term effects of vitamin D supplementation on wheezing in children born preterm.
Trial Registration:
ClinicalTrials.gov Identifier: NCT01601847.
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