长期补充维生素D对缺乏维生素D的2型糖尿病合并冠心病患者代谢状态的影响

A. Farrokhian, F. Raygan, F. Bahmani, H. Talari, Reza Esfandiari, Ahmad Esmaillzadeh, Z. Asemi
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引用次数: 53

摘要

背景:维生素D可能通过其对代谢谱和炎症和氧化应激生物标志物的有利影响而对糖尿病合并冠心病(CAD)患者有益。目的:本研究旨在研究补充维生素D 6个月对糖尿病合并冠心病患者代谢状况的影响。方法:这项随机、双盲、安慰剂对照的临床试验在60例40-85岁的冠心病维生素D缺乏症糖尿病患者中进行。受试者被随机分为两组,每2周服用50,000-IU维生素D补充剂(n = 30)或安慰剂(n = 30),持续6个月。在研究开始时和6个月干预后获得空腹血液样本,以量化血糖指标、脂质浓度以及炎症和氧化应激的生物标志物。结果:与安慰剂相比,补充维生素D可显著降低空腹血糖(-14.9±7.1 mg/dL与+19.3±7.1 mg/dL相比;P = 0.001),血清胰岛素(-2.7±1.1 μIU/mL比+1.8±1.1 μIU/mL;P = 0.006),体内平衡模型评估胰岛素抵抗(-0.7±0.3比+0.5±0.3;P = 0.01), β细胞功能(-9.1±4.2比+5.7±4.2;P = 0.01),血清维生素D(+6.8±0.9 ng/mL比+0.1±0.9 ng/mL显著升高;P < 0.001)和胰岛素敏感性定量检查指数(+0.008±0.004比-0.007±0.004;P = 0.01)。此外,血清高敏c反应蛋白(hs-CRP;-1.0±0.5 μg/mL与+0.6±0.5 μg/mL比较;P = 0.02),血浆一氧化氮(NO;+7.0±2.0 μmol/L比-4.6±2.0 μmol/L;P < 0.001),总还原性谷胱甘肽(GSH;+104±16.4 μmol/L与+24.8±16.4 μmol/L比较;P = 0.001),丙二醛浓度(-0.2±0.1 μmol/L与+0.2±0.1 μmol/L比较;P < 0.001),与安慰剂组这些指标的变化有显著差异。结论:总的来说,维生素D缺乏的糖尿病合并CAD患者补充6个月的维生素D对血糖控制和血清hs-CRP、NO、GSH和丙二醛浓度有有益的影响。本试验已在伊朗临床试验注册网站(www.irct.ir)注册,注册编号为IRCT201510315623N56。
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Long-Term Vitamin D Supplementation Affects Metabolic Status in Vitamin D-Deficient Type 2 Diabetic Patients with Coronary Artery Disease.
Background: Vitamin D might be beneficial in diabetic patients with coronary artery disease (CAD) through its favorable effects on metabolic profiles and biomarkers of inflammation and oxidative stress.Objective: This study was performed to examine the effects of 6 mo of vitamin D supplementation on metabolic status in diabetic patients with CAD.Methods: This randomized, double-blind, placebo-controlled clinical trial was conducted in 60 vitamin D-deficient diabetic patients with CAD aged 40-85 y. Subjects were randomly assigned into 2 groups to take either 50,000-IU vitamin D supplements (n = 30) or placebo (n = 30) every 2 wk for 6 mo. Fasting blood samples were obtained at the beginning of the study and after the 6-mo intervention to quantify glycemic indicators, lipid concentrations, and biomarkers of inflammation and oxidative stress.Results: Compared with placebo, vitamin D supplementation resulted in significant reductions in fasting plasma glucose (-14.9 ± 7.1 compared with +19.3 ± 7.1 mg/dL; P = 0.001), serum insulin (-2.7 ± 1.1 compared with +1.8 ± 1.1 μIU/mL; P = 0.006), homeostasis model assessment of insulin resistance (-0.7 ± 0.3 compared with +0.5 ± 0.3; P = 0.01), and β cell function (-9.1 ± 4.2 compared with +5.7 ± 4.2; P = 0.01) and a significant increase in serum vitamin D (+6.8 ± 0.9 compared with +0.1 ± 0.9 ng/mL; P < 0.001) and the Quantitative Insulin Sensitivity Check Index (+0.008 ± 0.004 compared with -0.007 ± 0.004; P = 0.01). In addition, changes in serum high-sensitivity C-reactive protein (hs-CRP; -1.0 ± 0.5 compared with +0.6 ± 0.5 μg/mL; P = 0.02), plasma nitric oxide (NO; +7.0 ± 2.0 compared with -4.6 ± 2.0 μmol/L; P < 0.001), total reduced glutathione (GSH; +104 ± 16.4 compared with +24.8 ± 16.4 μmol/L; P = 0.001), and malondialdehyde concentrations (-0.2 ± 0.1 compared with +0.2 ± 0.1 μmol/L; P < 0.001) in the supplemented group were significantly different from the changes in these indicators in the placebo group.Conclusions: Overall, 6 mo of vitamin D supplementation among vitamin D-deficient diabetic patients with CAD had beneficial effects on glycemic control and serum hs-CRP, NO, GSH, and malondialdehyde concentrations. This trial was registered on the Iranian website (www.irct.ir) for registration of clinical trials as IRCT201510315623N56.
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