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Does Vitamin D-Binding Protein Predict Response to Vitamin D Supplementation in Term and Preterm Newborns? A
Burcu Cebeci1, Mehmet Emin Arvas2, Dilek Kurnaz1
1Department of Neonatology, Haseki Training and Research Hospital, University of Health Sciences, 34265 Istanbul, Türkiye.
Insights
Neonatal vitamin D supplementation with 800 IU/day for 8 weeks effectively increased 25-hydroxyvitamin D levels in infants. Baseline vitamin D-binding protein did not predict supplementation response, indicating it offers no additional clinical value.
Area of Science:
- Neonatal nutrition and metabolism
- Endocrinology and vitamin D research
- Pediatric supplementation efficacy
Background:
- Vitamin D-binding protein (DBP) is crucial for transporting 25-hydroxyvitamin D [25(OH)D] in circulation.
- Neonates synthesize their own DBP, but its role in predicting vitamin D supplementation response is not well understood.
- Clarifying DBP's predictive value is essential for optimizing neonatal vitamin D therapy.
Purpose of the Study:
- To determine if neonatal vitamin D-binding protein (DBP) levels at birth predict the response to vitamin D supplementation.
- To assess the predictive value of baseline DBP beyond baseline 25-hydroxyvitamin D [25(OH)D] levels.
- To evaluate the efficacy of 800 IU/day oral cholecalciferol supplementation in neonates.
Main Methods:
- A prospective cohort study involving 101 neonates was conducted.
- Fifty-nine neonates with 25(OH)D < 20 ng/mL received 800 IU/day cholecalciferol for 8 weeks.
- Serum 25(OH)D and DBP levels were measured at baseline and 8 weeks; multivariable regression analyzed predictors of change in 25(OH)D.
Main Results:
- Supplementation significantly increased 25(OH)D levels (median Δ = 17.7 ng/mL), with 93.2% achieving sufficiency.
- Gestational age (β = -0.440, p = 0.001) and baseline 25(OH)D (β = -0.314, p = 0.015) independently predicted greater increases in 25(OH)D.
- Baseline DBP levels did not significantly predict the change in 25(OH)D (β = 0.072, p = 0.551).
Conclusions:
- Baseline DBP levels do not independently predict neonatal vitamin D supplementation response.
- Lower gestational age and lower baseline 25(OH)D are associated with greater vitamin D increases post-supplementation.
- Routine DBP measurement is not clinically valuable for guiding neonatal vitamin D supplementation; 800 IU/day is effective.
Abstract:
Background: Vitamin D-binding protein (DBP) is the principal carrier of circulating 25-hydroxyvitamin D [25(OH)D] and is independently synthesized by the neonate. Whether neonatal DBP at birth adds predictive value beyond baseline 25(OH)D for supplementation response remains unclear. Methods: This single-center prospective cohort study enrolled 101 neonates. Neonates with 25(OH)D < 20 ng/mL (supplementation-response cohort; n = 59: 29 preterm, 30 term) received 800 IU/day oral cholecalciferol for 8 weeks; neonates with 25(OH)D ≥ 20 ng/mL served as baseline reference controls (n = 42). Serum 25(OH)D and DBP were measured at baseline and week 8 in the supplementation-response cohort. Results: Median baseline 25(OH)D was 8.6 [6.7-12.0] ng/mL and median baseline DBP was 4.9 [3.7-8.1] µg/mL. After supplementation, 25(OH)D increased significantly (median Δ = 17.7 ng/mL; p < 0.001), with 55/59 (93.2%) achieving sufficiency. In multivariable regression, gestational age was the strongest independent predictor of Δ25(OH)D (β = -0.440, p = 0.001), followed by baseline 25(OH)D (β = -0.314, p = 0.015); baseline DBP was not significant (β = 0.072, p = 0.551). Conclusions: Baseline DBP did not independently predict supplementation response. Lower gestational age and lower baseline 25(OH)D were associated with greater increases in 25(OH)D after supplementation, whereas baseline DBP provided no additional predictive value. Supplementation with 800 IU/day for 8 weeks was effective across gestational-age categories. Routine DBP measurement does not appear to provide additional clinical value for guiding neonatal vitamin D supplementation.
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