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在保加利亚常规临床实践中,甘精胰岛素300 U/mL用于NPH或预混胰岛素治疗血糖控制不佳的2型糖尿病患者的真实世界有效性和安全性:ToUPGRADE研究

Real-World Effectiveness and Safety of Insulin Glargine 300 U/mL in Patients with T2D Uncontrolled on NPH or Premixed Insulins as Part of Routine Clinical Practice in Bulgaria: ToUPGRADE Study.

作者信息

Kamenov Zdravko, Pehlivanova Veselina, Kuneva Tsvetodara, Kirilov Kiril, Bobeva Roza, Stoykova Julija, Mihalevska Svetla

机构信息

University Hospital "Aleksandrovska", Medical University of Sofia, Sofia, Bulgaria.

Sanofi, Sofia, Bulgaria.

出版信息

Diabetes Ther. 2021 Mar;12(3):913-930. doi: 10.1007/s13300-021-01022-0. Epub 2021 Feb 19.

Abstract

INTRODUCTION

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.

METHODS

This was a 24-week prospective, observational study performed in 40 inpatient and outpatient sites across the country.

RESULTS

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).

CONCLUSIONS

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.

摘要

引言

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。

方法

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。

结果

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)。

结论

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6d9/7947095/c2d3e875561f/13300_2021_1022_Fig1_HTML.jpg

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