METHODS: Pregnant women (n = 1300) were randomized into 5 groups: placebo, or vitamin D 4200 IU/week, 16 800 IU/week, or 28 000 IU/week from second trimester to delivery and placebo until 6 months postpartum; or 28 000 IU/week prenatally and until 6 months postpartum. Infants underwent biochemical rickets screening from 6 to 12 months of age (n = 790). Relative risks (RR) and 95% confidence intervals (95% CI) of biochemical rickets were estimated for each group versus placebo.
RESULTS: Overall, 39/790 (4.9%) infants had biochemical rickets. Prevalence was highest in the placebo group (7.8%), and the risk was significantly lower among infants whose mothers received combined prenatal and postpartum vitamin D at 28 000 IU/week (1.3%; RR, 0.16; 95% CI, 0.03-0.72). Risks among infants whose mothers received only prenatal supplementation (4200 IU, 16 800 IU, 28 000 IU weekly) were not significantly different from placebo: 3.8% (RR, 0.48; 95% CI, 0.19-1.22), 5.8% (RR, 0.74; 95% CI, 0.33-1.69), and 5.7% (RR, 0.73; 95% CI, 0.32-1.65), respectively.
CONCLUSIONS: Maternal vitamin D supplementation (28 000 IU/week) during the third trimester of pregnancy until 6 months postpartum reduced the risk of infantile biochemical rickets. Further research is needed to define optimal postpartum supplementation dosing during lactation.
■孕妇(n=1300)被随机分为5组:安慰剂,或维生素D4200IU/周,16800IU/周,或28000IU/周,从孕中期到分娩和安慰剂,直到产后6个月;或28000IU/周,直到产后6个月。6至12个月大的婴儿接受了生化病筛查(n=790)。与安慰剂相比,估计每组生化病的相对风险(RR)和95%置信区间(95%CI)。
■总的来说,39/790(4.9%)婴儿有生化性病。安慰剂组患病率最高(7.8%),母亲在28000IU/周时接受产前和产后联合维生素D的婴儿的风险显着降低(1.3%;RR,0.16;95%CI,0.03-0.72)。母亲仅接受产前补充的婴儿的风险(4200IU,16800IU,每周28000IU)与安慰剂没有显着差异:3.8%(RR,0.48;95%CI,0.19-1.22),5.8%(RR,0.74;95%CI,0.33-1.69),和5.7%(RR,0.73;95%CI,0.32-1.65),分别。
■在妊娠晚期至产后6个月期间,母亲补充维生素D(28000IU/周)可降低婴儿生化病的风险。需要进一步的研究来确定泌乳期间的最佳产后补充剂量。