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Effect of large doses of parenteral vitamin D on glycaemic control and calcium/phosphate metabolism in patients with stable type 2 diabetes mellitus: a randomised, placebo-controlled, prospective pilot study.

机译:大剂量肠胃外维生素D对稳定的2型糖尿病患者血糖控制和钙/磷酸盐代谢的影响:一项随机,安慰剂对照,前瞻性研究。

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摘要

OBJECTIVEududVitamin D (D₃) status is reported to correlate negatively with insulin production and insulin sensitivity in patients with type 2 diabetes mellitus (T2DM). However, few placebo-controlled intervention data are available. We aimed to assess the effect of large doses of parenteral D3 on glycosylated haemoglobin (HbA(₁c)) and estimates of insulin action (homeostasis model assessment insulin resistance: HOMA-IR) in patients with stable T2DM.ududMATERIALS AND METHODSududWe performed a prospective, randomised, double-blind, placebo-controlled pilot study at a single university care setting in Switzerland. Fifty-five patients of both genders with T2DM of more than 10 years were enrolled and randomised to either 300,000 IU D₃ or placebo, intramuscularly. The primary endpoint was the intergroup difference in HbA(₁c) levels. Secondary endpoints were: changes in insulin sensitivity, albuminuria, calcium/phosphate metabolism, activity of the renin-aldosterone axis and changes in 24-hour ambulatory blood pressure values.ududRESULTSududAfter 6 months of D₃ supply, there was a significant intergroup difference in the change in HbA(₁c) levels (relative change [mean ± standard deviation] +2.9% ± 1.5% in the D₃ group vs +6.9% ± 2.1% the in placebo group, p = 0.041) as HOMA-IR decreased by 12.8% ± 5.6% in the D₃ group and increased by 10% ± 5.4% in the placebo group (intergroup difference, p = 0.032). Twenty-four-hour urinary albumin excretion decreased in the D₃ group from 200 ± 41 to 126 ± 39, p = 0.021). There was no significant intergroup difference for the other secondary endpoints.ududCONCLUSIONSududD₃ improved insulin sensitivity (based on HOMA-IR) and affected the course of HbA(₁c) positively compared with placebo in patients with T2DM.
机译:目的 ud ud维生素D(D₃)状态与2型糖尿病(T2DM)患者的胰岛素产生和胰岛素敏感性呈负相关。但是,几乎没有安慰剂控制的干预数据。我们旨在评估大剂量肠胃外D3对糖化血红蛋白(HbA(₁c))的影响,并评估稳定T2DM患者的胰岛素作用(稳态模型评估胰岛素抵抗:HOMA-IR)。 ud ud材料和方法 ud ud我们在瑞士的一家大学护理机构中进行了一项前瞻性,随机,双盲,安慰剂对照的前瞻性研究。研究入选了25名年龄在10年以上的T2DM男女患者,并经肌内随机分入300,000 IUD₃或安慰剂。主要终点是HbA(₁c)水平的组间差异。次要终点是:胰岛素敏感性,蛋白尿,钙/磷酸盐代谢,肾素-醛固酮轴活性和24小时动态血压值的变化。 ud udRESULTS ud ud供应D months 6个月后,组间HbA(₁c)水平变化的显着差异(相对变化[平均值±标准差]D₃组为+ 2.9%±1.5%,而安慰剂组为+ 6.9%±2.1%,p = 0.041)作为HOMA在D₃组中-IR下降了12.8%±5.6%,而在安慰剂组中上升了10%±5.4%(组间差异,p = 0.032)。 D₃组二十四小时尿白蛋白排泄从200±41降低至126±39,p = 0.021)。 T2DM患者与安慰剂组相比,其他次要终点之间没有显着的组间差异。 ud ud结论, ud udD₃与安慰剂相比,改善了胰岛素敏感性(基于HOMA-IR),对HbA(₁c)的进程产生了积极影响。

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