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Published on: December 31, 2015
Trial of daily vitamin D supplementation in preterm infants
Chandra Kumar Natarajan1, M Jeeva Sankar, Ramesh Agarwal
1Divisions of Neonatology and.
Insights
Higher daily vitamin D3 supplementation (800 IU) significantly reduced vitamin D deficiency in preterm infants. While effective, this higher dose may rarely lead to vitamin D excess.
Area of Science:
- Neonatal nutrition and metabolism
- Pediatric endocrinology
- Public health and preventive medicine
Background:
- Preterm infants born between 28 to 34 weeks' gestation are at high risk for vitamin D deficiency (VDD).
- Optimal vitamin D supplementation strategies are crucial for preventing VDD and ensuring proper bone development in this vulnerable population.
Purpose of the Study:
- To compare the efficacy of 800 IU versus 400 IU of daily oral vitamin D3 in preventing VDD.
- To assess the impact of different vitamin D3 dosages on VDD prevalence at 40 weeks' postmenstrual age (PMA) and 3 months' corrected age (CA) in preterm infants.
Main Methods:
- A randomized double-blind trial involving 96 preterm infants (28-34 weeks' gestation) allocated to receive either 800 IU or 400 IU of vitamin D3 daily.
- Primary outcome: VDD (serum 25-hydroxyvitamin D <20 ng/mL) at 40 weeks' PMA.
- Secondary outcomes: VDD, bone mineral content, and bone mineral density at 3 months' CA.
Main Results:
- The 800 IU group showed a significantly lower prevalence of VDD at 40 weeks' PMA (38.1% vs. 66.7%) and 3 months' CA (12.5% vs. 35%) compared to the 400 IU group.
- No significant differences in bone mineral content or bone mineral density were observed between the two groups.
- One infant (2.4%) in the 800 IU group experienced vitamin D excess (serum levels 100-150 ng/mL).
Conclusions:
- Supplementation with 800 IU of vitamin D daily effectively reduces VDD in preterm infants at 40 weeks' PMA and 3 months' CA.
- The higher dose did not improve bone mineralization compared to the lower dose.
- A potential risk of vitamin D excess exists with the 800 IU daily dose in this population.
Objective:
To compare the effect of 800 vs 400 IU of daily oral vitamin D3 on the prevalence of vitamin D deficiency (VDD) at 40 weeks' postmenstrual age (PMA) in preterm infants of 28 to 34 weeks' gestation.
Methods:
In this randomized double-blind trial, we allocated eligible infants to receive either 800 or 400 IU of vitamin D3 per day (n = 48 in both groups). Primary outcome was VDD (serum 25-hydroxyvitamin D levels <20 ng/mL) at 40 weeks' PMA. Secondary outcomes were VDD, bone mineral content, and bone mineral density at 3 months' corrected age (CA).
Results:
Prevalence of VDD in the 800-IU group was significantly lower than in the 400-IU group at 40 weeks (38.1% vs. 66.7%; relative risk: 0.57; 95% confidence interval: 0.37-0.88) and at 3 months' CA (12.5% vs. 35%; relative risk: 0.36; 95% confidence interval: 0.14-0.90). One infant (2.4%) in the 800-IU group had vitamin D excess (100-150 ng/mL). Bone mineral content (mean ± SD: 79.6 ± 16.8 vs. 84.7 ± 20.7 g; P = .27) and bone mineral density (0.152 ± 0.019 vs. 0.158 ± 0.021 g/cm2; P = .26) were not different between the 2 groups.
Conclusions:
Daily supplementation with 800 IU of vitamin D reduces the prevalence of VDD at 40 weeks' PMA and at 3 months' CA in preterm infants without showing any improvement in bone mineralization. However, there is a possibility that this dose may occasionally result in vitamin D excess.
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