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Glucagon-like peptide-1 receptor agonists as a possible intervention to delay the onset of type 1 diabetes:A new horizon 被引量:1
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作者 Mahmoud Nassar Ajay Chaudhuri +1 位作者 Husam Ghanim paresh dandona 《World Journal of Diabetes》 SCIE 2024年第2期133-136,共4页
Type 1 diabetes(T1D)is a chronic autoimmune condition that destroys insulinproducing beta cells in the pancreas,leading to insulin deficiency and hyperglycemia.The management of T1D primarily focuses on exogenous insu... Type 1 diabetes(T1D)is a chronic autoimmune condition that destroys insulinproducing beta cells in the pancreas,leading to insulin deficiency and hyperglycemia.The management of T1D primarily focuses on exogenous insulin replacement to control blood glucose levels.However,this approach does not address the underlying autoimmune process or prevent the progressive loss of beta cells.Recent research has explored the potential of glucagon-like peptide-1 receptor agonists(GLP-1RAs)as a novel intervention to modify the disease course and delay the onset of T1D.GLP-1RAs are medications initially developed for treating type 2 diabetes.They exert their effects by enhancing glucose-dependent insulin secretion,suppressing glucagon secretion,and slowing gastric emptying.Emerging evidence suggests that GLP-1RAs may also benefit the treatment of newly diagnosed patients with T1D.This article aims to highlight the potential of GLP-1RAs as an intervention to delay the onset of T1D,possibly through their potential immunomodulatory and anti-inflammatory effects and preservation of beta-cells.This article aims to explore the potential of shifting the paradigm of T1D management from reactive insulin replacement to proactive disease modification,which should open new avenues for preventing and treating T1D,improving the quality of life and long-term outcomes for individuals at risk of T1D. 展开更多
关键词 Type 1 diabetes Semaglutide Glucagon-like peptide-1 receptor agonists Insulin therapy Autoimmune response Blood glucose monitoring Β-cell preservation Early screening Teplizumab Randomized controlled trials
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炎症、动脉粥样硬化与胰岛素 被引量:6
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作者 paresh dandona 《国外医学(内分泌学分册)》 2005年第3期192-193,共2页
动脉粥样硬化是一个炎症反应的过程。内皮损伤后,产生黏附因子,吸附大量的单核细胞,激活核因子(NF)κB,并导致一系列超氧化自由基的产生,促进趋化因子等炎症因子产生,从而引起一系列继发反应。胰岛素具有扩张血管、抗血小板聚集、抗炎... 动脉粥样硬化是一个炎症反应的过程。内皮损伤后,产生黏附因子,吸附大量的单核细胞,激活核因子(NF)κB,并导致一系列超氧化自由基的产生,促进趋化因子等炎症因子产生,从而引起一系列继发反应。胰岛素具有扩张血管、抗血小板聚集、抗炎、抗动脉粥样硬化及保护心脏的作用。总之,胰岛素具有抑制炎症反应的重要作用,从而可以防止动脉粥样硬化的发生、发展。 展开更多
关键词 胰岛素 抗动脉粥样硬化 超氧化自由基 抗血小板聚集 抑制炎症反应 内皮损伤 黏附因子 单核细胞 炎症因子 趋化因子 继发反应 扩张血管 核因子
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