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首页> 外文期刊>Calcified tissue international. >The effect of high-dose vitamin D supplementation on calciotropic hormones and bone mineral density in obese subjects with low levels of circulating 25-hydroxyvitamin D: Results from a randomized controlled study
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The effect of high-dose vitamin D supplementation on calciotropic hormones and bone mineral density in obese subjects with low levels of circulating 25-hydroxyvitamin D: Results from a randomized controlled study

机译:大剂量维生素D补充对循环水平低的25-羟基维生素D的肥胖受试者钙合激素和骨矿物质密度的影响:一项随机对照研究的结果

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摘要

Low levels of 25-hydroxyvitamin D (25OHD) are associated with increased bone turnover and risk of fractures. Plasma 25OHD is inversely related to body mass index, and vitamin D deficiency is common in obesity. We aimed to determine whether vitamin D supplementation affects bone turnover and bone mineral density (BMD) in obese subjects. Fifty-two healthy obese men and women aged 18-50 years with plasma 25OHD levels below 50 nmol/L were randomized to 7,000 IU of cholecalciferol daily or placebo for 26 weeks. We measured plasma levels of 25OHD, parathyroid hormone (PTH), and markers of bone turnover, as well as BMD at the hip, spine, forearm, and whole body. Compared with placebo, treatment with cholecalciferol increased mean plasma 25OHD from 35 to 110 nmol/L (p < 0.00001) and significantly decreased PTH (p < 0.05). BMD increased significantly at the forearm by 1.6 ± 0.7 % (p = 0.03). The bone resorption marker C-terminal telopetide of type 1 collagen (CTX) decreased borderline significantly in the cholecalciferol group compared with the placebo group (p = 0.07). Changes in plasma 25OHD correlated inversely with changes in plasma levels of bone-specific alkaline phosphatase (r = -0.38, p = 0.01) and CTX (r = -0.33, p = 0.03). Changes in CTX correlated inversely with changes in spine BMD (r = -0.45, p = 0.04). Increasing circulating 25OHD levels by cholecalciferol treatment is of importance to bone health in young obese subjects as increased levels of 25OHD are associated with a decrease in both PTH and bone turnover and with an increase in BMD at the forearm.
机译:低水平的25-羟基维生素D(25OHD)与增加的骨转换和骨折风险相关。血浆25OHD与体重指数成反比,而维生素D缺乏症在肥胖症中很常见。我们旨在确定补充维生素D是否会影响肥胖受试者的骨转换和骨矿物质密度(BMD)。 52名年龄在18-50岁,血浆25OHD水平低于50 nmol / L的健康肥胖男性和女性被随机分配至每天7,000 IU胆钙化固醇或安慰剂治疗26周。我们测量了血浆中25OHD,甲状旁腺激素(PTH)的水平以及骨转换的标志,以及髋部,脊柱,前臂和全身的BMD。与安慰剂相比,胆钙化固醇可使平均血浆25OHD从35 nmD / L增加到110 nmol / L(p <0.00001),并显着降低PTH(p <0.05)。前臂的BMD显着增加1.6±0.7%(p = 0.03)。与安慰剂组相比,胆钙化固醇组的1型胶原(CTX)骨吸收标志物C端四肽明显降低了边界线(p = 0.07)。血浆25OHD的变化与骨特异性碱性磷酸酶(r = -0.38,p = 0.01)和CTX(r = -0.33,p = 0.03)的血浆水平变化呈负相关。 CTX的变化与脊柱BMD的变化呈负相关(r = -0.45,p = 0.04)。通过胆钙化固醇治疗增加循环中的25OHD水平对于年轻肥胖受试者的骨骼健康至关重要,因为25OHD水平的升高与PTH和骨转换的减少以及前臂BMD的增加有关。

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