Department of Internal Medicine, Minami Osaka Hospital, Osaka, Japan.
J Diabetes Investig. 2019 Mar;10(2):343-351. doi: 10.1111/jdi.12884. Epub 2018 Jul 28.
AIMS/INTRODUCTION: Compared with glargine 100 U/mL (Gla100), glargine 300 U/mL (Gla300) and degludec (Deg) - the ultralong-acting insulins - reportedly have more stable effects and reduce the risk of hypoglycemia. Currently, they are considered to be the most useful basal insulins. The present study aimed to compare the efficacy and safety of Gla300 and Deg on glycemic control using continuous glucose monitoring.
In this single-center, open-label, parallel-group, two-period, cross-over study, 30 patients with type 2 diabetes were randomized to once-daily Gla300 followed by Deg with the same units (n = 15) or vice versa (n = 15). The primary end-points of this study were the mean percentage of time within the target glucose range of 70-180 mg/dL as efficacy and hypoglycemia of <70 mg/dL as safety indicators, as measured using continuous glucose monitoring during each treatment period.
The mean percentage of time within the target glucose range was not different between Gla300 and Deg (77.8 ± 19.2 vs 76.9 ± 18.3%, P = 0.848). However, the mean percentage of time of hypoglycemia with Gla300 was significantly lower than that of Deg (1.3 ± 2.7 vs 5.5 ± 6.4%, P = 0.002). In the secondary safety end-points, the mean percentage of time of severe hypoglycemia (<54 mg/dL) or nocturnal hypoglycemia with Gla300 was also significantly lower than that of Deg.
The present study showed the comparable efficacy of Gla300 and Deg on glycemic control; however, the risk of hypoglycemia was markedly lower for Gla300 than for Deg.
目的/引言:与甘精胰岛素 100U/mL(Gla100)相比,甘精胰岛素 300U/mL(Gla300)和德谷胰岛素(Deg)——这些超长效胰岛素——据称具有更稳定的效果,并降低低血糖风险。目前,它们被认为是最有用的基础胰岛素。本研究旨在通过连续血糖监测比较 Gla300 和 Deg 对血糖控制的疗效和安全性。
在这项单中心、开放标签、平行组、两周期、交叉研究中,30 例 2 型糖尿病患者被随机分为每日一次 Gla300 治疗组,然后用相同剂量的 Deg 治疗(n=15)或反之(n=15)。本研究的主要终点是使用连续血糖监测评估的疗效指标(70-180mg/dL 目标血糖范围内的时间百分比)和安全性指标(<70mg/dL 的低血糖)。
Gla300 和 Deg 组的目标血糖范围内的时间百分比无差异(77.8±19.2%与 76.9±18.3%,P=0.848)。然而,Gla300 组的低血糖时间百分比明显低于 Deg 组(1.3±2.7%与 5.5±6.4%,P=0.002)。在次要安全性终点方面,Gla300 组严重低血糖(<54mg/dL)或夜间低血糖的时间百分比也明显低于 Deg 组。
本研究表明 Gla300 和 Deg 在血糖控制方面具有相当的疗效;然而,Gla300 的低血糖风险明显低于 Deg。