Tromsø Endocrine Research Group, The University of Tromsø - The Arctic University of Norway, Tromsø, NorwayDivision of Internal Medicine, University Hospital of North Norway, Tromsø, Norway
Tromsø Endocrine Research Group, The University of Tromsø - The Arctic University of Norway, Tromsø, NorwayDivision of Rehabilitation Services, University Hospital of North Norway, Tromsø, Norway.
Diabetes Care. 2014 Aug;37(8):2123-31. doi: 10.2337/dc14-0218. Epub 2014 Jun 19.
In observational studies, low serum 25-hydroxyvitamin D [25(OH)D] concentrations have been associated with insulin resistance and other risk factors for cardiovascular disease.
We present 1-year data from an ongoing 5-year trial in 511 individuals with impaired fasting glucose (IFG) and/or impaired glucose tolerance (IGT) randomly assigned to 20,000 IU/week vitamin D3 or placebo. An oral glucose tolerance test was performed at baseline and after 1 year.
Mean baseline serum 25(OH)D was 59.9 nmol/L and 61.1 nmol/L in the vitamin D and placebo groups, respectively, and increased by 45.8 nmol/L and 3.4 nmol/L, respectively. With adjustment for baseline concentrations, no differences in measures of glucose metabolism, insulin secretion or sensitivity, blood pressure, or hs-CRP were found after 1 year. There was a slight, but significant decrease in total and LDL cholesterol in the vitamin D group compared with the placebo group, but as there was also a decrease in HDL cholesterol, the change in the total/HDL cholesterol ratio did not differ significantly. Only analyzing subjects with 25(OH)D <50 nmol/L did not change the results.
This study shows that vitamin D supplementation does not improve glycemic indices, blood pressure, or lipid status in subjects with IFG and/or IGT.
在观察性研究中,血清 25-羟维生素 D [25(OH)D] 浓度较低与胰岛素抵抗和心血管疾病的其他危险因素有关。
我们呈现了一项正在进行的为期 5 年的临床试验中的 511 名空腹血糖受损(IFG)和/或糖耐量受损(IGT)个体的 1 年数据,这些个体被随机分配到每天补充 20,000IU 维生素 D3 或安慰剂。在基线和 1 年后进行口服葡萄糖耐量试验。
维生素 D 组和安慰剂组的平均基线血清 25(OH)D 分别为 59.9 和 61.1 nmol/L,分别增加了 45.8 和 3.4 nmol/L。在调整基线浓度后,1 年后血糖代谢、胰岛素分泌或敏感性、血压或 hs-CRP 等指标均无差异。与安慰剂组相比,维生素 D 组的总胆固醇和 LDL 胆固醇略有但显著降低,但由于 HDL 胆固醇也降低,总胆固醇/HDL 胆固醇比值的变化无显著差异。仅分析 25(OH)D <50 nmol/L 的受试者并没有改变结果。
本研究表明,维生素 D 补充剂不能改善 IFG 和/或 IGT 患者的血糖指数、血压或血脂状况。