Suppr超能文献

直接比较两种固定比例的胰高血糖素样肽受体激动剂和基础胰岛素在 2 型糖尿病患者的血糖和非血糖参数方面的差异。

Direct comparison two fixed-ratio combination glucagon-like peptide receptor agonist and basal insulin on glycemic and non glycemic parameters in type 2 diabetes.

机构信息

Faculty of Medicine, University of Banja Luka, Banja Luka, Bosnia and Herzegovina.

Department of Endocrinology, University Clinical Center of the Republic of Srpska, Banja Luka, Bosnia and Herzegovina.

出版信息

BMC Endocr Disord. 2023 Feb 1;23(1):28. doi: 10.1186/s12902-023-01282-w.

Abstract

BACKGROUND

Two types of fixed-ratio combinations of basal insulin and a glucagon-like peptide-1 receptor agonist (GLP-1RA) have been approved for use in type 2 diabetes. One is insulin degludec/liraglutide (iDergLira), and the other is insulin glargine/lixisenatide (iGlarLixi). Direct comparisons between these two combination is not available.

METHODS

The retrospective study included 186 patients with type 2 diabetes mellitus (DM) with inadequate glycemic control on metformin and basal insulin (degludec, glargine 100, glargine 300) who were switched to fixed-ratio combination GLP-1 RA and basal insulin. Patients were divided into two groups based on the basal insulin before study: group I (n = 86) treated with degludec were switched to iDegLira and patients group II (n = 99), treated with glargine were switched to iGlarLixi. The aim of this study was to directly compare the effects between two fixed - ratio combination on glycemic parameters and non glycemic parameters. Follow up was 6 months.

RESULTS

Mean HbA1c decreased similarly (- 1.2% vs.-1.1%). Higher percentage patients in iDegLira group had reached the HbA1c < 7% after 6 months (22% vs. 18.2%, p < 0.05). The mean change in fasting plasma glucose (FPG) was comparable for the two groups, while mean decrease postprandial plasma glucose (PPG) level were lower in iGlarLixi group (2 vs 1.8 mmol/l, p > 0.05). Change in body weight was significant in iDegLira group (1.8 kg vs. 0.7 kg, p < 0.001). At the end of the study patients showed decrease in total cholesterol (TC) and low-density lipoprotein (LDL) for 0.2 mmol/L in iDegLira, 0.1 mmol/l in iGlarLixi, triglycerides decreased 0.3 mmol/l in both groups, high-density lipoprotein(HDL) increased 0.1 mm/l in iGlarLixi.

CONCLUSION

Our results showed that more patients with iDegLira had HbA1c less than 7% and these combination had better effect on weight loss. There was no difference observed in FPG and PPG, lipid profile and rate of hypoglycemia.

摘要

背景

两种基础胰岛素与胰高血糖素样肽-1 受体激动剂(GLP-1RA)的固定比例组合已被批准用于 2 型糖尿病。一种是胰岛素德古鲁肽/利拉鲁肽(iDergLira),另一种是胰岛素甘精/利西那肽(iGlarLixi)。这两种组合之间没有直接比较。

方法

这项回顾性研究纳入了 186 例在二甲双胍和基础胰岛素(德古鲁肽、甘精胰岛素 100、甘精胰岛素 300)治疗下血糖控制不佳的 2 型糖尿病患者,他们改用了固定比例的 GLP-1RA 和基础胰岛素。根据研究前的基础胰岛素,患者分为两组:I 组(n=86)接受德古鲁肽治疗者换用 iDegLira,II 组(n=99)接受甘精胰岛素治疗者换用 iGlarLixi。本研究旨在直接比较两种固定比例组合在血糖参数和非血糖参数方面的效果。随访 6 个月。

结果

平均 HbA1c 降低相似(-1.2%比-1.1%)。6 个月后,iDegLira 组达到 HbA1c<7%的患者比例更高(22%比 18.2%,p<0.05)。两组空腹血糖(FPG)的平均变化相当,而 iGlarLixi 组餐后血糖(PPG)水平降低更明显(2 比 1.8mmol/l,p>0.05)。iDegLira 组体重变化显著(1.8kg 比 0.7kg,p<0.001)。研究结束时,患者总胆固醇(TC)和低密度脂蛋白(LDL)分别降低 0.2mmol/L,iGlarLixi 组降低 0.1mmol/l,两组甘油三酯均降低 0.3mmol/l,高密度脂蛋白(HDL)iGlarLixi 组增加 0.1mm/l。

结论

我们的结果表明,更多的 iDegLira 患者的 HbA1c 小于 7%,并且这种组合对体重减轻有更好的效果。FPG 和 PPG、血脂谱和低血糖发生率无差异。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验