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评价艾塞那肽与甘精胰岛素对血管内皮功能和心血管风险标志物的影响。

Evaluation of exenatide versus insulin glargine for the impact on endothelial functions and cardiovascular risk markers.

机构信息

Department of Endocrinology and Metabolism, Kocaeli University Faculty of Medicine, Kocaeli, Turkey.

Department of Endocrinology and Metabolism, Kocaeli University Faculty of Medicine, Kocaeli, Turkey.

出版信息

Diabetes Res Clin Pract. 2014 Dec;106(3):567-75. doi: 10.1016/j.diabres.2014.09.046. Epub 2014 Oct 7.

DOI:10.1016/j.diabres.2014.09.046
PMID:25458329
Abstract

AIMS

To demonstrate the efficacy of exenatide versus insulin glargine on endothelial functions and cardiovascular risk markers.

METHODS

Thirty-four insulin and incretin-naive patients with type 2 diabetes mellitus (body mass index 25-45 kg/m(2)) who received metformin for at least two months were randomized to exenatide or insulin glargine treatment arms and followed-up for 26 weeks. Measurements of endothelial functions were done by ultrasonography, cardiovascular risk markers by serum enzyme-linked immunosorbent assay, and total body fat mass by bioimpedance.

RESULTS

Levels of high sensitivity-C-reactive protein and endothelin-1 decreased (27.5% and 18.75%, respectively) in the exenatide arm. However, in the insulin glargine arm, fibrinogen, monocyte chemoattractant protein-1, leptin and endothelin-1 levels (13.4, 30.2, 47.5, and 80%, respectively) increased. Post-treatment flow mediated dilatation and endothelium independent vascular responses were significantly higher in both arms (p=0.0001, p=0.0001). Positive correlation was observed between the changes in body weight and endothelium-independent vasodilatation, leptin, plasminogen activator inhibitor type 1 and endothelin-1 in both arms (r=0.376, r=0.507, r=0.490, r=0.362, respectively).

CONCLUSIONS

Insulin glargine improved endothelial functions, without leading to positive changes in cardiovascular risk markers. Exenatide treatment of 26 weeks resulted in reduced body weight and improvement in certain cardiovascular risk markers and endothelial functions.

摘要

目的

展示艾塞那肽对比甘精胰岛素对血管内皮功能和心血管风险标志物的疗效。

方法

34 例 2 型糖尿病(BMI 25-45kg/m²)且从未使用过胰岛素和肠降血糖素的患者,至少接受二甲双胍治疗 2 个月后,被随机分配到艾塞那肽或甘精胰岛素治疗组,随访 26 周。通过超声心动图测量血管内皮功能,用酶联免疫吸附法检测心血管风险标志物,用生物阻抗法检测全身脂肪量。

结果

艾塞那肽组的高敏 C 反应蛋白和内皮素-1 水平分别降低(分别为 27.5%和 18.75%)。然而,甘精胰岛素组的纤维蛋白原、单核细胞趋化蛋白-1、瘦素和内皮素-1 水平分别升高(分别为 13.4%、30.2%、47.5%和 80%)。治疗后,两组的血流介导的扩张和内皮非依赖性血管反应均显著升高(p=0.0001,p=0.0001)。在两组中,体重变化与内皮非依赖性血管扩张、瘦素、纤溶酶原激活物抑制剂-1 和内皮素-1 之间均呈正相关(r=0.376,r=0.507,r=0.490,r=0.362)。

结论

甘精胰岛素改善了血管内皮功能,但没有导致心血管风险标志物的正向变化。艾塞那肽治疗 26 周可降低体重,并改善某些心血管风险标志物和血管内皮功能。

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