Pharmacokinetics of Oral Vitamin D in Children with Obesity and Asthma

Abstract

Background and objective: Vitamin D insufficiency is common in several pediatric diseases including obesity and asthma. Little data exist describing the pharmacokinetics of oral vitamin D in children or the optimal dosing to achieve therapeutic 25(OH)D targets. Describe the pharmacokinetics of oral Vitamin D in children with asthma.

Methods: This was a multi-center, randomized, open-label, oral supplementation study to describe the pharmacokinetics of vitamin D in children aged 6-17 years who have asthma and were overweight/obese. Participants had a serum 25(OH)D concentration between 10 and < 30 ng/mL at baseline. In Part 1 of the study, we assessed four 16-week dosing regimens for their ability to achieve 25(OH)D concentrations ≥ 40 ng/mL. Using serial serum 25(OH)D sampling over 28 weeks, we created a population pharmacokinetic model and performed dosing simulations to achieve 25(OH)D concentrations ≥ 40 ng/mL. In Part 2, the optimal regimen chosen from Part 1 was compared (2:1) to a standard-of-care control dose (600 international units [IU] daily) over 16 weeks. A final population pharmacokinetic model using both parts was developed to perform dosing simulations and determine important co-variates in the pharmacokinetics of vitamin D.

Results: Based on empiric and simulation data, the daily dose of 8000 IU and a loading dose of 50,000 IU were chosen; this regimen raised 25(OH)D concentrations above 40 ng/mL in the majority of participants while avoiding concentrations > 100 ng/mL. A 50,000-IU loading dose led to faster achievement of 25(OH)D therapeutic concentrations (≥ 40 ng/mL). The estimated median (5th-95th percentiles) apparent clearance of vitamin D from the final population pharmacokinetic model was 0.181 (0.155-0.206) L/h. The body mass index z-score was a significant covariate on apparent clearance and was associated with a significantly decreased median half-life in 25(OH)D (body mass index z-score 1.00-1.99: 97.7 days, body mass index z-score 2.00-2.99: 65.9 days, body mass index z-score ≥ 3.00: 39.1 days, p < 0.001).

Conclusions: Obesity impacts vitamin D clearance and the half-life, but serum concentrations > 40 ng/mL can be reached in most children using a loading dose of 50,000 IU followed by a daily dose of 8000 IU.

Clinical trial registration: ClinicalTrials.gov identifier number NCT03686150.

Fig. 1

25(OH)D concentration versus time in each Part 1 dosing cohort. Gray shading on the x-axis denotes the treatment period. IU international units, LD loading dose

Fig. 2

Simulated 25(OH)D concentration–time profiles of 25(OH)D after 52 weeks. Simulations assumed treatment for 16 weeks. Gray boxes show post-treatment samples. LD loading dose

Fig. 3

Simulated 25(OH)D concentrations with 52 weeks of treatment. A Simulation assumed a 50,000-international unit (IU) loading dose plus 10,000 IU daily. B Simulation assumed a 50,000-IU loading dose plus 8000 IU daily

Fig. 4

25(OH)D concentration versus time by dosing cohort in Part 2. Gray shading on the x-axis denotes the treatment period. IU international unit, LD loading dose