Ahmed Amr, Monir Akl Maher
The public health department, MSc degree in gynecology and obstetrics, Riyadh First Health Cluster, Ministry of Health, Saudia Arabia.
Department of Chemistry, Faculty of Science, Mansoura University, 35516, Mansoura, Egypt.
Adv Pharm Bull. 2024 Jul;14(2):262-265. doi: 10.34172/apb.2024.040. Epub 2024 Mar 18.
This manuscript explores the potential of dual glucagon-like peptide 1 (GLP-1) agonists combined with degludec basal insulin as a treatment approach for early type 1 diabetes. The study aims to evaluate the efficacy and mechanistic impact of semaglutide, a GLP-1 agonist, on newly diagnosed type 1 diabetes patients.
A retrospective analysis was conducted to assess the effects of semaglutide on individuals with early type 1 diabetes. The analysis focused on the elimination of prandial and basal insulin, changes in C-peptide levels, and overall glycemic control. The study also examined the potential for GLP-1 agonists to protect residual beta cells, stimulate cell proliferation, and reprogram liver cells into insulin-producing cells. Additionally, the modification of GLP-1 agonists with albumin ligands to extend their half-life and enhance their anti-diabetic effects was investigated.
The findings demonstrate the elimination of both prandial and basal insulin requirements, an increase in C-peptide levels, and improved glycemic control among the patients. Despite the positive outcomes, the study's retrospective nature and absence of a control group highlight the necessity for larger, prospective trials.
GLP-1 agonists show considerable potential in the management of type 1 diabetes by protecting residual beta cells, promoting cell proliferation, and reprogramming hepatic cells. The integration of modified GLP-1 agonists with albumin ligands could further enhance these effects. The manuscript underscores the need for continued research to fully explore this therapeutic approach. The proposed treatment strategy, which combines the autoimmune hypothesis, the proliferative effects of GLP-1, and albumin ligand modifications, aims to restore beta cell mass and function, thereby improving the quality of life for individuals with type 1 diabetes. Clinical trials are planned for 2024 under the registration ‹Amr Ahmed, Maher M. Akl, Semaglutide GLP1 Agonists with Degludec Basal-bolus Insulin in Early Type 1 Diabetes to Basalbolus› (ClinicalTrials.gov Identifier NCT06057077).
本手稿探讨双胰高血糖素样肽1(GLP-1)激动剂与德谷胰岛素基础胰岛素联合作为1型糖尿病早期治疗方法的潜力。该研究旨在评估GLP-1激动剂司美格鲁肽对新诊断的1型糖尿病患者的疗效和机制影响。
进行回顾性分析以评估司美格鲁肽对1型糖尿病早期个体的影响。分析重点在于消除餐时和基础胰岛素、C肽水平变化以及总体血糖控制。该研究还考察了GLP-1激动剂保护残余β细胞、刺激细胞增殖以及将肝细胞重编程为胰岛素产生细胞的潜力。此外,研究了用白蛋白配体修饰GLP-1激动剂以延长其半衰期并增强其抗糖尿病作用。
研究结果表明患者的餐时和基础胰岛素需求均被消除,C肽水平升高,血糖控制得到改善。尽管有这些积极结果,但该研究的回顾性性质以及缺乏对照组凸显了进行更大规模前瞻性试验的必要性。
GLP-1激动剂在1型糖尿病管理中显示出巨大潜力,可通过保护残余β细胞、促进细胞增殖以及重编程肝细胞来实现。将修饰后的GLP-1激动剂与白蛋白配体整合可进一步增强这些效果。本手稿强调需要继续开展研究以充分探索这种治疗方法。所提出的治疗策略结合了自身免疫假说、GLP-1的增殖作用以及白蛋白配体修饰,旨在恢复β细胞质量和功能,从而改善1型糖尿病患者的生活质量。计划于2024年进行临床试验,登记名称为《司美格鲁肽GLP-1激动剂与德谷基础-餐时胰岛素用于1型糖尿病早期的基础-餐时治疗》(ClinicalTrials.gov标识符NCT06057077)。