新型甘精胰岛素300u /mL夜间血糖控制

N. Yu
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引用次数: 1

摘要

甘精胰岛素300 U/mL (Gla-300)是新一代基础胰岛素产品,已被证明比甘精胰岛素100 U/mL (Gla-100)具有更稳定的药代动力学和药效学特性。为了评估Gla-300在减少夜间血糖水平波动和夜间低血糖方面的实际益处,10名使用Gla-100进行胰岛素治疗的台湾患者改用Gla-300,并在夜间应用连续血糖监测(CGM)来监测夜间血糖变异性参数的变化。测量用于评估夜间和夜间血糖变异性的血糖变异性参数包括平均夜间6小时(00:00-6:00 AM)血糖水平、标准偏差(SD)和平均夜间血糖水平和平均葡萄糖偏移(MAGE)的方差系数(CV)。在这项研究中,Gla-300表现出与Gla-100相当的降糖功效,并有进一步降低夜间低血糖风险的潜力。总体而言,在Gla-300治疗期间测量的夜间血糖变异性参数在数值上小于Gla-100治疗期间测量的参数,尽管没有达到统计学意义。在夜间血糖管理方面,在Gla-300治疗阶段,夜间平均夜间血糖水平的SD和CV值比Gla-100治疗阶段在夜间开始时血糖水平读数正常的个体有统计学意义上的降低。总之,本研究是台湾首个评估台湾糖尿病患者从Gla-100胰岛素治疗转为Gla-300胰岛素治疗,通过CGM降低夜间血糖变异性的实际临床益处的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Nocturnal Glycemic Control with New Insulin Glargine 300 U/mL
Insulin glargine 300 U/mL (Gla-300) is a new generation basal insulin product that has been demonstrated to have more stable pharmacokinetic and pharmacodynamic characteristics than insulin glargine 100 U/mL (Gla-100). To evaluate the real-world benefits of Gla-300 in reducing nocturnal fluctuations in blood glucose levels and nocturnal hypoglycemia, 10 Taiwanese patients using Gla-100 for insulin therapy were switched to Gla-300 and continuous glucose monitoring (CGM) was applied at nighttime to monitor changes to nocturnal glycemic variability parameters. Glycemic variability parameters measured to assess between- and within-night glycemic variability included mean 6-hour nocturnal (00:00–6:00 AM) glucose levels, standard deviation (SD), and coefficient of variance (CV) of mean nocturnal glucose levels and mean glucose excursion (MAGE). In this study, Gla-300 demonstrated comparable glycemic efficacy to Gla-100 and the potential to further reduce nocturnal hypoglycemia risk. Overall, nocturnal glycemic variability parameters measured during the Gla-300 treatment period were numerically smaller than those measured during the Gla-100 treatment phase although statistical significance was not reached. In terms of within-night glucose management, SD and CV values of mean nocturnal glucose levels were found to be statistically lower during the Gla-300 treatment phase than the Gla-100 treatment phase on nights individuals displayed normal blood glucose level readings at the beginning of the night. In summary, this study represents the first of its kind from Taiwan to evaluate the real-world clinical benefits of switching Taiwanese diabetes patients from Gla-100 to Gla-300 insulin therapy in reducing nighttime glucose variability by means of CGM.
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