INTRODUCTIONAlthough there is no consensus on optimum levels of serum vitamin D levels, vitamin D deficiency is defined as a 25-hydroxy vitamin D level of less than 20 ng per millilitre (50 nmol per litre). [1][2][3][4] No specific definition exists for preterm infants. With the use of such definitions, it has been estimated that 1 billion people worldwide have vitamin D deficiency or insufficiency. [5][6][7] High prevalence of physiologically significant hypovitaminosis D among pregnant women and their term newborns have been reported in India. 8 The active metabolite of vitamin D, 1,25-dihydroxyvitamin D3 (1,25(OH)2D3), exerts its bio-logical actions by binding to a nuclear receptor, the vitamin D receptor (VDR) and these are present in almost every organ system in the body. It is speculated that there is a physiologic role for vitamin D and its metabolites in general health. 9,12,13 The awareness of a role for vitamin D in the regulation of immune responses was triggered by the discovery of VDRs in almost all immune cells of the innate and adaptive immune system. 10 Moreover, immune signals can regulate expression levels of the VDR and the enzymes involved in vitamin D metabolism.
11The VDRs and vitamin D metabolizing enzymes have also been identified in both the vasculature and the heart ABSTRACT Background: The association of serum vitamin D levels to clinical outcome in VLBW infants has not been studied. Our objective was to measure the cord blood levels, and the dose response for two doses of vitamin D in preterm infants and correlate the relationship of vitamin D levels to the clinical outcome. Methods: We prospectively obtained cord blood levels in 80 preterm infants under 34 weeks gestation (mean gestation age 29±2 weeks and BW: 1210±350 gms). Infants were supplemented with 400 IU or 800-1000 IU vitamin D daily. Serun vitamin D levels were obtained at 2 -3 weeks after supplementation and levels were correlated to clinical outcome. Results: The mean cord blood vitamin D level was 12±8.5 ng/ml. Babies who developed sepsis and compared to those who did not develop these morbidities, ROP had vitamin D levels: 13.5±6 (ng/ml) versus 30.5±10 (ng/ml) (p < 0.01) and 15.7±11 (ng/ml) versus 34±18 (ng/ml) (p <0.03) respectively. Supplementation with 400 IU vitamin D resulted in levels of 17±8.6 (ng/ml) and infants given 800-1000 IU vitamin D had levels 46±17(ng/ml) (p <0.001). Conclusions: These data suggest that cord blood vitamin D levels are low in preterm infants and 800-1000 IU vitamin D supplementation is advisable to achieve levels >30 ng/ml. Infants with low levels of vitamin D have higher incidence of sepsis, and ROP.