High-Dose Vitamin D Intervention in Infants-Effects on Vitamin D Status, Calcium Homeostasis, and Bone Strength
High-Dose Vitamin D Intervention in Infants-Effects on Vitamin D Status, Calcium Homeostasis, and Bone Strength
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DOI:
10.1210/jc.2012-1575
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发表时间:
2012-11-01
影响因子:
5.8
通讯作者:
Makitie, Outi
中科院分区:
文献类型:
--
作者:
Holmlund-Suila, Elisa;Viljakainen, Heli;Makitie, Outi
Context: Guidelines in Finland recommend 10 mu g of vitamin D3 daily for all infants. Recent observations suggest that this may be insufficient to maintain optimal serum 25-hydroxyvitamin D (S-25-OHD).Objective: The aim of the study was to evaluate effects of various vitamin D doses and determine a dose ensuring S-25-OHD of at least 80 nmol/liter in infants without signs of vitamin D excess.Design: We conducted a randomized double-blind intervention study. Cord blood was obtained at birth for S-25-OHD; 113 infants were randomized to receive vitamin D3 10, 30, or 40 mu g/d from age 2 wk to 3 months.Setting: An investigator-initiated study was performed in a single maternity hospital in Helsinki, Finland.Main Outcome Measures: S-25-OHD, calcium homeostasis, and skeletal characteristics were evaluated with peripheral quantitative computed tomography at age 3 months.Results: Baseline S-25-OHD was similar in all three groups (median, 53 nmol/liter). At 3 months, the mean S-25-OHD values were 88, 124, and 153 nmol/liter, and the minimum values were 46, 57, and 86 nmol/liter in the groups receiving 10, 30, and 40 mu g (ANOVA; P < 0.001). No hypercalcemia occurred; plasma calcium, serum PTH, and urine calcium excretion was similar between the groups. Peripheral quantitative computed tomography showed a trend toward larger tibial total bone and cortical bone area with higher vitamin D doses.Conclusion: Vitamin D3 supplementation with up to 40 mu g/d from age 2 wk to 3 months was safe and caused no hypercalcemia or hypercalciuria. The 40-mu g dose maintained S-25-OHD above 80 nmol/liter in all infants. More extensive and longer intervention studies are necessary to assess long-term effects. (J Clin Endocrinol Metab 97: 4139-4147, 2012)