Clinical research of insulin glargine U300 in type 1 diabetes mellitus patients with frequent hypoglycaemia: real-world experience.

Savaş Volkan Kişioğlu, Ahmet Suat Demir, Damla Tufekci, Yasemin Emur Gunay, Hulya Coskun, Ozge Ucuncu, Irfan Nuhoglu, Mustafa Kocak, Serdar Karakullukcu, Halil Onder Ersoz
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Abstract

Introduction: We aimed to see whether insulin glargine U300 can provide better blood glucose control while reducing hypoglycaemia in a more homogeneous population compared to previous studies.

Material and methods: The retrospective study included type 1 diabetes mellitus (T1DM) patients with frequent hypoglycaemia. For evaluation of fasting blood glucose, haemoglobin glycated (HbA1c) and weight at 6 months and 12 months (final), observation windows of 120-240 days (4-8 months) and 240-480 days (9-16 months) after insulin glargine U300 initiation, respectively, were permitted. Mean follow-up time was 12 months. Hypoglycaemia was defined as blood glucose level < 70 mg/dl, either symptomatic or asymptomatic, measured in hospital or at home.

Results: Forty-four patients were included in the study, and 35 patients completed the study - 20 (57.1%) females and 15 (42.9%) males, with a mean age of 24.1 ±6.6 years. Mean body mass index was 24.4 ±7.4 kg/m2. A significant decrease was not found between baseline and HbA1c values at 6 months (p = 0.199), but a significant decrease was found in the final period (between 9-16 months) (p = 0.025). Hypoglycaemic events occurred in all patients (100%) before using insulin glargine U300, while the incidence of hypoglycaemic events gradually decreased to 74.3%, 68.6%, and 68.6% between months 1-3, 3-6, and 6-9, respectively. Of the 26 patients who declared their level of satisfaction, 23 (88.5%) were satisfied, 2 (7.7%) indicated that there was no significant difference, and 1 (3.8%) patient was unsatisfied.

Conclusions: Over 9-16 months of follow-up, insulin glargine U300 led to a significant reduction not only of HbA1c levels but also of the frequency of hypoglycaemia, and also yielded high satisfaction rates.

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甘精胰岛素U300治疗1型糖尿病多发低血糖的临床研究
与以往的研究相比,我们的目的是观察甘精胰岛素U300是否能在更均匀的人群中提供更好的血糖控制,同时降低低血糖。材料与方法:回顾性研究纳入1型糖尿病(T1DM)多发低血糖患者。为了评估6个月和12个月(最终)的空腹血糖、糖化血红蛋白(HbA1c)和体重,甘精胰岛素U300开始使用后的观察窗口分别为120-240天(4-8个月)和240-480天(9-16个月)。平均随访时间为12个月。低血糖被定义为血糖水平< 70 mg/dl,有症状或无症状,在医院或家中测量。结果:44例患者纳入研究,35例患者完成研究,其中女性20例(57.1%),男性15例(42.9%),平均年龄24.1±6.6岁。平均体重指数为24.4±7.4 kg/m2。基线和HbA1c值在6个月时没有显著下降(p = 0.199),但在最后一个阶段(9-16个月)有显著下降(p = 0.025)。使用甘精胰岛素U300前,所有患者(100%)均发生过低血糖事件,在1-3月、3-6月、6-9月期间,低血糖事件的发生率分别逐渐下降至74.3%、68.6%、68.6%。26例患者中,满意23例(88.5%),无显著性差异2例(7.7%),不满意1例(3.8%)。结论:在9-16个月的随访中,甘精胰岛素U300不仅显著降低了患者的HbA1c水平,而且降低了低血糖的发生频率,且患者满意度较高。
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