探索一种协同方法:双 GLP-1 激动剂联合 Degludec 基础胰岛素用于 1 型糖尿病早期治疗及其对白蛋白-胰岛素生成细胞表达的影响"。

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
A. Ahmed, M. Akl
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引用次数: 0

摘要

本手稿探讨了与使用双 GLP-1 激动剂和德格鲁德基础胰岛素作为早期 1 型糖尿病潜在治疗方法有关的各个方面。背景部分强调了 1 型糖尿病中β细胞的破坏,以及 GLP-1 激动剂作为控制肥胖和 2 型糖尿病的一种有前途的选择的出现。作者讨论了一项关于 GLP-1 激动剂 semaglutide 对新诊断出的 1 型糖尿病患者疗效的回顾性分析。结果显示,患者餐前和基础胰岛素用量减少,C 肽水平升高,血糖控制得到改善。然而,该研究具有回顾性,且缺乏对照组,因此需要进行更大规模的前瞻性试验。解释部分强调了 GLP-1 激动剂在保护残留β细胞、刺激细胞增殖和将肝细胞重编程为胰岛素分泌细胞方面的潜力。此外,用白蛋白配体修饰 GLP-1 激动剂有望延长其半衰期并增强其抗糖尿病效果。展望部分对协同方法进行了全面概述,考虑了degludec的药代动力学特性、成人肝组织的可塑性以及改良GLP-1衍生物的益处。结论强调了进一步研究的必要性,以探索这种方法在 1 型糖尿病治疗中的全部潜力。所提出的方法为治疗 1 型糖尿病提供了一条前景广阔的途径,它整合了自身免疫假说、GLP-1 的增殖效应以及使用白蛋白配体的修饰作用。将这些因素结合起来,我们就能努力恢复β细胞的质量和功能,最终改善1型糖尿病患者的生活。该手稿计划于2024年进行临床试验,注册名为 "Amr Ahmed, Maher M. Akl, Semaglutide GLP1激动剂与Degludec基础胰岛素在早期1型糖尿病中的基础胰岛素",ClinicalTrials.gov识别码为NCT06057077。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exploring a Synergistic Approach: Dual GLP-1 Agonist Combined with Degludec Basal Insulin for Early Type 1 Diabetes Treatment and its Impact on Albumin-Insulin Producing Cells Expression."
This manuscript explores various aspects related to the use of dual GLP-1 agonist with degludec basal insulin as a potential treatment approach for early type 1 diabetes. The background section highlights the destruction of beta cells in type 1 diabetes and the emergence of GLP-1 agonists as a promising option for managing obesity and type 2 diabetes. The authors discuss a retrospective analysis of the efficacy of semaglutide, a GLP-1 agonist, in patients with newly diagnosed type 1 diabetes. The results show the elimination of prandial and basal insulin, increased C-peptide levels, and improved glycemic control. However, the study's retrospective nature and lack of a control group emphasize the need for larger prospective trials. The interpretation section highlights the potential of GLP-1 agonists in protecting residual beta cells, stimulating cell proliferation, and reprogramming liver cells into insulin-producing cells. Moreover, modifying GLP-1 agonists with albumin ligands shows promise in extending their half-life and enhancing their anti-diabetic effects. The perspective section provides a comprehensive overview of the synergistic approach, considering the pharmacokinetic properties of degludec, the plasticity of adult human hepatic tissue, and the benefits of modified GLP-1 derivatives. The conclusion emphasizes the need for further research to explore the full potential of this approach in type 1 diabetes treatment. The proposed approach offers a promising avenue for the treatment of type 1 diabetes, integrating the autoimmune hypothesis, the proliferative effects of GLP-1, and modifications using albumin ligands. By combining these elements, we can strive towards restoring beta cell mass and function, ultimately improving the lives of individuals living with type 1 diabetes. The manuscript is planned to undergo clinical trials in 2024, registered as 'Amr Ahmed, Maher M. Akl, Semaglutide GLP1 Agonists with Degludec Basal-bolus Insulin in Early Type 1 Diabetes to Basal-bolus' with ClinicalTrials.gov Identifier NCT06057077.
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来源期刊
Advanced pharmaceutical bulletin
Advanced pharmaceutical bulletin PHARMACOLOGY & PHARMACY-
CiteScore
6.80
自引率
2.80%
发文量
51
审稿时长
12 weeks
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