Kamenov Zdravko, Pehlivanova Veselina, Kuneva Tsvetodara, Kirilov Kiril, Bobeva Roza, Stoykova Julija, Mihalevska Svetla
University Hospital "Aleksandrovska", Medical University of Sofia, Sofia, Bulgaria.
Sanofi, Sofia, Bulgaria.
Diabetes Ther. 2021 Mar;12(3):913-930. doi: 10.1007/s13300-021-01022-0. Epub 2021 Feb 19.
The aim of this study is to demonstrate the real-life effectiveness and safety of insulin glargine 300 U/mL (Gla-300) in patients with type 2 diabetes (T2D) previously uncontrolled on NPH ± prandial insulin or premixed insulins in routine clinical practice in Bulgaria.
This was a 24-week prospective, observational study performed in 40 inpatient and outpatient sites across the country.
A total of 286 patients were included in the study. The mean age (± SD) was 61.2 ± 10.0 years with duration of diabetes of 11.64 ± 7.5 years and body mass index (BMI) of 32.1 ± 5.7 kg/m. HbA1c before Gla-300 initiation was 9.8 ± 1.0%, and fasting plasma glucose (FPG) was 13.1 ± 3.4 mmol/L. HbA1c and FPG change from baseline to week 24 was - 1.86% (p < 0.001) and - 4.8 mmol/L (p < 0.001), respectively. The proportion of patients reaching their individualized HbA1c at week 24 was 39.1% (95% CI 33.3-45.1%), while the proportion of patients reaching their individualized HbA1c target without confirmed and/or severe hypoglycaemia was 34.8% (95% CI 29.2-40.7%). At study end, 19.0% (95% CI 14.6-24.1%) achieved HbA1c < 7%. Body weight decreased from 88.3 to 87.0 kg from baseline to week 24 with mean change of - 1.3 kg (p < 0.001). The incidence and event rates of anytime confirmed (≤ 3.9 mmol/L) and/or severe hypoglycaemia were low: 7.7% and 0.42 events per patient-year, respectively. The overall Insulin Treatment Satisfaction Questionnaire (ITSQ) score increased from 53.2 to 78.2 from baseline to week 24 and the difference of 25.1 ± 21.5 points was significant (p < 0.001).
In real-life settings, Gla-300 significantly improved glycaemic control and insulin treatment satisfaction in people with T2D who were inadequately controlled with NPH ± prandial insulin or premixed insulin analogues. Improvement of glycaemic control was associated with a very low risk of hypoglycaemia and with significant weight loss irrespective of the previous insulin regimen.
本研究旨在证明在保加利亚的常规临床实践中,甘精胰岛素300 U/mL(Gla-300)对之前使用NPH ± 餐时胰岛素或预混胰岛素血糖控制不佳的2型糖尿病(T2D)患者的实际疗效和安全性。
这是一项在全国40个住院和门诊地点进行的为期24周的前瞻性观察性研究。
共有286例患者纳入研究。平均年龄(±标准差)为61.2 ± 10.0岁,糖尿病病程为11.64 ± 7.5年,体重指数(BMI)为32.1 ± 5.7 kg/m²。开始使用Gla-300之前的糖化血红蛋白(HbA1c)为9.8 ± 1.0%,空腹血糖(FPG)为13.1 ± 3.4 mmol/L。从基线到第24周,HbA1c和FPG的变化分别为-1.86%(p < 0.001)和-4.8 mmol/L(p < 0.001)。在第24周达到个体化HbA1c目标的患者比例为39.1%(95%置信区间33.3 - 45.1%),而在无确诊和/或严重低血糖情况下达到个体化HbA1c目标的患者比例为34.8%(95%置信区间29.2 - 40.7%)。在研究结束时,19.0%(95%置信区间14.6 - 24.1%)的患者糖化血红蛋白<7%。体重从基线时的88.3 kg降至第24周的87.0 kg,平均变化为-1.3 kg(p < 0.001)。任何时间确诊(≤3.9 mmol/L)和/或严重低血糖的发生率和事件率较低:分别为7.7%和0.42事件/患者年。胰岛素治疗满意度问卷(ITSQ)总分从基线时的53.2分增加到第24周的78.2分,25.1 ± 21.5分的差异具有统计学意义(p < 0.001)。
在实际临床环境中,Gla-300显著改善了使用NPH ± 餐时胰岛素或预混胰岛素类似物血糖控制不佳的T2D患者的血糖控制和胰岛素治疗满意度。血糖控制的改善与低血糖风险极低以及显著体重减轻相关,且与之前的胰岛素治疗方案无关。