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在伴有高心血管风险的 2 型糖尿病患者中,用速效胰岛素和 GLP-1 激动剂进行餐时治疗 26 周的随机比较中葡萄糖变异性。

Glucose Variability in a 26-Week Randomized Comparison of Mealtime Treatment With Rapid-Acting Insulin Versus GLP-1 Agonist in Participants With Type 2 Diabetes at High Cardiovascular Risk.

出版信息

Diabetes Care. 2016 Jun;39(6):973-81. doi: 10.2337/dc15-2782. Epub 2016 Apr 19.

Abstract

OBJECTIVE

A1C is associated with diabetes complications but does not reflect glycemic variability (GV), which may worsen outcomes by inducing inflammation, oxidative stress, and cardiac arrhythmias. We tested whether a glucagon-like peptide 1 agonist-based regimen can reduce GV and cardiometabolic risk markers while maintaining similar A1C levels in people with insulin-requiring type 2 diabetes and high cardiovascular risk.

RESEARCH DESIGN AND METHODS

After run-in on metformin and basal-bolus insulin (BBI), 102 participants continued metformin and basal insulin and were randomized to exenatide dosing before the two largest meals (glucacon-like peptide-1 receptor agonist and insulin [GLIPULIN group]) or continuation of rapid-acting insulin analogs (BBI group). Indices of GV by continuous glucose monitoring (CGM), hypoglycemia, weight, risk markers, and cardiac arrhythmias were assessed. The primary end point was change in glucose coefficients of variation (CV) by CGM from baseline to 26 weeks.

RESULTS

At randomization, the median A1C was 7.3% (57 mmol/mol) for GLIPULIN and 7.4% (56.3 mmol/mol) for BBI, and glucose CVs were 30.3 for BBI and 31.9 for GLIPULIN. At 26 weeks, A1C levels were similar (7.1% [54 mmol/mol] vs. 7.2% [55 mmol/mol]), whereas mean CV improved with GLIPULIN (-2.4 vs. 0.4, P = 0.047). Other GV indices followed similar nonsignificant patterns of improvement with GLIPULIN. There were no differences in hypoglycemic events during CGM or arrhythmias during electrocardiographic monitoring. On-trial changes in body weight (-4.8 kg vs. +0.7 kg, P < 0.001), alanine aminotransferase (P = 0.0002), and serum amyloid A (P = 0.023) favored GLIPULIN.

CONCLUSIONS

GLIPULIN reduced GV, weight, and some cardiometabolic risk markers while maintaining equivalent A1C levels versus BBI and might improve clinical outcomes in a larger trial.

摘要

目的

A1C 与糖尿病并发症相关,但不能反映血糖变异性(GV),GV 可能通过诱导炎症、氧化应激和心律失常使结果恶化。我们检测了胰高血糖素样肽 1 激动剂治疗方案是否可以在有胰岛素需求的 2 型糖尿病和高心血管风险患者中降低 GV 和心血管代谢风险标志物,同时保持类似的 A1C 水平。

研究设计和方法

在二甲双胍和基础-餐时胰岛素(BBI)的导入期后,102 名参与者继续服用二甲双胍和基础胰岛素,并随机分为在两餐中最大的餐前给予 exenatide 剂量(胰高血糖素样肽-1 受体激动剂和胰岛素[GLIPULIN 组])或继续使用速效胰岛素类似物(BBI 组)。通过连续血糖监测(CGM)评估 GV 指数、低血糖、体重、风险标志物和心律失常。主要终点是 CGM 从基线到 26 周时的葡萄糖变异系数(CV)变化。

结果

随机分组时,GLIPULIN 组的 A1C 中位数为 7.3%(57mmol/mol),BBI 组为 7.4%(56.3mmol/mol),血糖 CV 为 BBI 组 30.3,GLIPULIN 组 31.9。26 周时,A1C 水平相似(7.1%[54mmol/mol]与 7.2%[55mmol/mol]),而 GLIPULIN 组的平均 CV 改善(-2.4 与 0.4,P=0.047)。其他 GV 指数也有类似的非显著改善趋势。在 CGM 期间,低血糖事件或心电图监测期间的心律失常无差异。试验期间,体重(-4.8kg 与 +0.7kg,P<0.001)、丙氨酸氨基转移酶(P=0.0002)和血清淀粉样蛋白 A(P=0.023)变化有利于 GLIPULIN。

结论

GLIPULIN 降低了 GV、体重和一些心血管代谢风险标志物,同时保持了与 BBI 相当的 A1C 水平,并且在更大的试验中可能改善临床结局。

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