MedPath

Wheezing in Black Preterm Infants: Impact of Vitamin D Supplementation Strategy

Phase 4
Completed
Conditions
Allergy
Wheezing
Interventions
Registration Number
NCT01601847
Lead Sponsor
Case Western Reserve University
Brief Summary

The goal of this study is to identify a vitamin D supplementation strategy that best promotes the lung, immune, and overall health of black infants born preterm (28-36 weeks gestational age). This is a high risk population that seems to have unique vitamin D needs, and inappropriate supplementation may promote wheezing or allergy. The results of this study will help form nutritional recommendations for the approximately 100,000 black infants born at 30-36 weeks gestational age in the U.S. every year.

Detailed Description

Black infants face the highest rates of prematurity in the U.S. (18%), have high rates of prematurity-associated wheezing illnesses, and tend to have lower vitamin D levels. The goal of this \[comparative effectiveness\] study is to identify a vit. D supplementation strategy that minimizes recurrent wheezing in infancy. Long recognized as important for bone health, a growing body of evidence suggests that vit. D may play a role in the regulation and development of many organ systems. The D pathway regulates lung inflammation and impacts morphogenesis, structure, and cell growth and survival in bronchial smooth muscle. Vit. D exposure has the potential to skew cytokine expression from a Th1 (less allergic) to a Th2 (more allergic) phenotype. Due to their developmental immaturity, preterm infants may be particularly vulnerable to any positive or negative effects of vit. D supplementation on the lung, airway, and immune system. Our preliminary data, supported by the literature, suggests that overly aggressive vit. D supplementation may inadvertently increase wheezing in infancy in black, but not white, preterm infants; however, vit. D deficiency could theoretically also increase wheezing via vulnerability to respiratory pathogens. The proposed study is a randomized clinical trial comparing the effect of two different enteral vitamin D supplementation strategies on recurrent wheezing in infancy in 300 black infants born preterm at 28 0/7-36 6/7 wks gestational age, a population for whom neither vit. D requirements nor optimal vit. D serum levels have been established. The investigators will test two strategies: (I) sustained supplementation until 6 mo. of age adjusted for prematurity, and (II) cessation of supplementation when a minimum dietary intake of 200 IU/day is reached. The specific aims are to characterize the effect of each strategy on (aim 1) recurrent wheezing and (aim 2) allergic sensitization and atopy. The investigators will (aim 3) explore the relationship between vit. D serum levels and recurrent wheezing. The investigators hypothesize that strategy II will be more effective in promoting pulmonary health by minimizing recurrent wheezing, allergic sensitization, and overall healthcare utilization, and will be sufficient to prevent clinical vit. D deficiency. The investigators also hypothesize that optimal vit. D serum levels will be lower than the norms for other populations.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SustainedCholecalciferolInfants will remain on 400 IU/day of cholecalciferol until 6 months of age adjusted for prematurity, regardless of dietary intake
Diet-LimitedCholecalciferolInfants will receive placebo once their dietary intake of vitamin D has exceeded 200 IU/day
Primary Outcome Measures
NameTimeMethod
Number of Infants With Recurrent Wheezingup to 12 months adjusted age

Recurrent wheezing was defined as more than 1 episode of wheezing reported during the study period. Separate episodes were defined as occurring at least 2 weeks apart.

Secondary Outcome Measures
NameTimeMethod
Number With Infants With Allergic Sensitization as Measured by the PhadiaTop Infant AssayMeasured at the 12 month adjusted age visit

Measured using the Phadiatop Infant IgE panel

Bone DensityMeasured at the 12 month adjusted age visit

Measured by bone speed of sound (ultrasound)

Trial Locations

Locations (5)

MetroHealth Medical Center

🇺🇸

Cleveland, Ohio, United States

Medical University of South Carolina

🇺🇸

Charleston, South Carolina, United States

University Hospitals

🇺🇸

Cleveland, Ohio, United States

Case Western Reserve University

🇺🇸

Cleveland, Ohio, United States

Montefiore Medical Center

🇺🇸

New York, New York, United States

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