使用2型钠-葡萄糖共转运蛋白抑制剂纠正2型糖尿病患者的代谢紊乱

A. V. Zhigareva, A. Ametov, H. H. Sharafetdinov, E. Pashkova
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At baseline and in 6 months, all patients underwent laboratory and instrumental examination methods, which included an assessment of carbohydrate metabolism (fasting glycemia (FG), postprandial glycemia (PPG), HbA1c); lipid profile (cholesterol levels, high and low density lipoproteins, triglycerides); content of adipocytokines- adiponectin (ADN), leptin (L). Visceral fat area (AVF) was assessed using a bioimpedance analyzer and magnetic resonance imaging (MRI) at the L4 level. Results. In 6 months, both groups showed significant positive dynamics of FG, PPG and HbA1c. In main group, HbA1c decreased by 2.7 ± 0.3% (p < 0.01), in control group by 0.2 ± 0.1% (p < 0.01). The FG and PPG levels in main group decreased by 4.5 ± 0.4 mmol/L (p < 0.01 ) and 5.8 ± 0.5 mmol/L (p < 0.01), respectively, in control group by 1.3 ± 0.2 mmol/L (p < 0.01) and 1.7 ± 0.4 mmol/L (p < 0.01). 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摘要

目的:综合(临床、实验室、仪器)评价2型钠-葡萄糖共转运蛋白抑制剂治疗2型糖尿病患者代谢紊乱的临床疗效。设计:随机比较研究。材料和方法。一项为期26周的研究纳入了130例存在内脏性肥胖的患者(56.3±2.1岁),这些患者在二甲双胍单药治疗2g /天后糖化血红蛋白(HbA1c)未达到目标参数。主要组(68人)接受卡格列净300 mg/天,联合二甲双胍2 g/天;对照组(62人)继续接受二甲双胍2 g/天的单药治疗。在基线和6个月后,所有患者都接受了实验室和仪器检查方法,其中包括评估碳水化合物代谢(空腹血糖(FG),餐后血糖(PPG), HbA1c);脂质谱(胆固醇水平、高、低密度脂蛋白、甘油三酯);脂肪细胞因子-脂联素(ADN)和瘦素(L)的含量。采用生物阻抗分析仪和磁共振成像(MRI)在L4水平评估内脏脂肪面积(AVF)。结果。6个月后,两组FG、PPG、HbA1c均呈显著阳性。治疗组HbA1c降低2.7±0.3% (p < 0.01),对照组降低0.2±0.1% (p < 0.01)。主组FG和PPG水平分别降低了4.5±0.4 mmol/L (p < 0.01)和5.8±0.5 mmol/L (p < 0.01),对照组分别降低了1.3±0.2 mmol/L (p < 0.01)和1.7±0.4 mmol/L (p < 0.01)。主组ADN水平升高102.8±4.8 mcg/ml (p < 0.01),对照组升高8.2±2.1 mcg/ml (p < 0.01)。主组L降低10.3±0.9 ng/ml (p < 0.01),对照组降低4.1±0.7 ng/ml (p < 0.01)。MRI显示,主组VFA减少18.6±2.3 cm2 (p < 0.01),对照组VFA减少4.7±2.4 cm2 (p < 0.01)。生物阻抗分析显示,主组AVF面积减少26.7±3.2 cm2 (p < 0.01),对照组AVF面积减少4.7±2.5 cm2 (p < 0.01)。结论。卡格列净和二甲双胍联合治疗,可以在碳水化合物代谢纠正、内脏脂肪储备减少和代谢健康主要指标正常化水平方面取得很高的临床疗效。关键词:2型糖尿病,瘦素,脂联素,卡格列净
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Correction of Metabolic Disorders in Patients with Type 2 Diabetes Mellitus Using a Type 2 Sodium-Glucose Cotransporter Inhibitor
Aim: Comprehensive (clinical, laboratory, instrumental) assessment of the clinical efficacy of metabolic disorders correction in patients with type 2 diabetes mellitus using a type 2 sodium-glucose cotransporter inhibitor. Design: Randomized comparative study. Materials and methods. A 26-week study included 130 patients with the presence of visceral obesity (56.3 ± 2.1 years) who did not reach the target parameters of glycated hemoglobin (HbA1c) on metformin monotherapy 2 g/day. The main group (68 people) received canagliflozin 300 mg/day, in combination with metformin 2 g/day; the control group (62 people) continued to receive monotherapy with metformin 2 g/day. At baseline and in 6 months, all patients underwent laboratory and instrumental examination methods, which included an assessment of carbohydrate metabolism (fasting glycemia (FG), postprandial glycemia (PPG), HbA1c); lipid profile (cholesterol levels, high and low density lipoproteins, triglycerides); content of adipocytokines- adiponectin (ADN), leptin (L). Visceral fat area (AVF) was assessed using a bioimpedance analyzer and magnetic resonance imaging (MRI) at the L4 level. Results. In 6 months, both groups showed significant positive dynamics of FG, PPG and HbA1c. In main group, HbA1c decreased by 2.7 ± 0.3% (p < 0.01), in control group by 0.2 ± 0.1% (p < 0.01). The FG and PPG levels in main group decreased by 4.5 ± 0.4 mmol/L (p < 0.01 ) and 5.8 ± 0.5 mmol/L (p < 0.01), respectively, in control group by 1.3 ± 0.2 mmol/L (p < 0.01) and 1.7 ± 0.4 mmol/L (p < 0.01). The level ADN in main group increased by 102.8 ± 4.8 mcg/ml (p < 0.01), in control group by 8.2 ± 2.1 mcg/ml (p < 0.01). L in main group decreased by 10.3 ± 0.9 ng/ml (p < 0.01), in control group by 4.1 ± 0.7 ng/ml (p < 0.01). In main group, there was a decrease in the VFA of by 18.6 ± 2.3 cm2 (p < 0.01) according to MRI, in control group by 4.7 ± 2.4 cm2 (p < 0.01). According to bioimpedance analysis, there was a decrease in the area of AVF by 26.7 ± 3.2 cm2 (p < 0.01) in the main group, and by 4.7 ± 2.5 cm2 (p < 0.01) in the control group. Conclusion. Combination therapy with canagliflozin and metformin makes it possible to achieve high clinical efficacy of carbohydrate metabolism correction in combination with a decrease in visceral fat depot and normalization levels of the main markers of metabolic health. Keywords: type 2 diabetes mellitus, leptin, adiponectin, canagliflozin.
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