Vitamin D Oral Replacement in Children With Obesity Related Asthma: VDORA1 Randomized Clinical Trial

Author:

O'Sullivan Brian1,Ounpraseuth Song2,James Laura2,Majure Marc3,Lang Jason4ORCID,Hu Zhuopei2,Simon Alan5,Bickel Scott6,Ely Brian7,Faricy L.E.8,Garza Maryam2ORCID,Greer Melody2ORCID,Hsia Daniel9,Jefferson Akilah2,Knight Lisa10,Lee Jeannette2,Liptzin Deborah11,Haktanir Abul Mehtap12ORCID,Perry Tamara T.2,Prior Fred2,SanGiovanni Christine13,Tam‐Williams Jade14ORCID,Wu Brian15,Snowden Jessica2ORCID,

Affiliation:

1. Geisel School of Medicine at Dartmouth Hanover New Hampshire USA

2. University of Arkansas for Medical Sciences Little Rock Arkansas USA

3. University of Mississippi Medical Center Jackson Mississippi USA

4. Duke University School of Medicine Durham North Carolina USA

5. National Institutes of Health Office of the Director Bethesda Maryland USA

6. Norton Children's and University of Louisville School of Medicine Louisville Kentucky USA

7. West Virginia University Morgantown West Virginia USA

8. University of Vermont Burlington Vermont USA

9. Pennington Biomedical Research Institute Baton Rouge Louisiana USA

10. University of South Carolina School of Medicine Columbia South Carolina USA

11. Community Medical Center Missoula Montana USA

12. Hasbro Children's Hospital and Warren Alpert Medical School of Brown University Providence Rhode Island USA

13. Medical University of South Carolina Charleston South Carolina USA

14. Children's Mercy Kansas City Missouri USA

15. Kapiolani Medical Center for Women and Children Honolulu Hawaii USA

Abstract

Children with asthma and obesity are more likely to have lower vitamin D levels, but the optimal replacement dose is unknown in this population. The objective of this study is identifying a vitamin D dose in children with obesity‐related asthma that safely achieves serum vitamin D levels of ≥ 40 ng/mL. This prospective multisite randomized controlled trial recruited children/adolescents with asthma and body mass index ≥ 85% for age/sex. Part 1 (dose finding), evaluated 4 oral vitamin D regimens for 16 weeks to identify a replacement dose that achieved serum vitamin D levels ≥ 40 ng/mL. Part 2 compared the replacement dose calculated from part 1 (50,000 IU loading dose with 8,000 IU daily) to standard of care (SOC) for 16 weeks to identify the proportion of children achieving target serum 25(OH)D level. Part 1 included 48 randomized participants. Part 2 included 64 participants. In Part 1, no SOC participants achieved target serum level, but 50–72.7% of participants in cohorts A‐C achieved the target serum level. In part 2, 78.6% of replacement dose participants achieved target serum level compared with none in the SOC arm. No related serious adverse events were reported. This trial confirmed a 50,000 IU loading dose plus 8,000 IU daily oral vitamin D as safe and effective in increasing serum 25(OH)D levels in children/adolescents with overweight/obesity to levels ≥ 40 ng/mL. Given the critical role of vitamin D in many conditions complicating childhood obesity, these data close a critical gap in our understanding of vitamin D dosing in children.

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

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