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糖尿病性骨质疏松症的研究进展:综述

Research progress of diabetic osteoporosis: a comprehensive review.

作者信息

Ma Xun, Zhang Xiaoqian

机构信息

School of Clinical Medicine, Shandong Second Medical University, Weifang, China.

Department of Endocrinology and Metabology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Shandong Institute of Nephrology, Jinan, China.

出版信息

Front Endocrinol (Lausanne). 2025 Sep 2;16:1595228. doi: 10.3389/fendo.2025.1595228. eCollection 2025.

Abstract

Diabetic osteoporosis (DOP) is a complex metabolic bone disorder characterized by impaired bone quality and increased fracture risk in patients with diabetes mellitus. The interplay between hyperglycemia, insulin resistance, and bone metabolism underscores the need for integrated therapeutic strategies that address both glycemic control and bone health. This review systematically examines the molecular mechanisms of glucose-lowering and bone-protective agents, highlighting their dual roles in managing DOP. We discuss the pathophysiological pathways underlying DOP, including insulin/IGF-1 deficiency, advanced glycation end products (AGEs) accumulation, oxidative stress, and vascular damage. Furthermore, we explore the mechanisms of action of antidiabetic drugs (e.g., metformin, GLP - 1 receptor agonists, SGLT2 inhibitors) and anti-osteoporotic agents (e.g., bisphosphonates, teriparatide, strontium ranelate), emphasizing their potential synergies and risks. Finally, we outline future directions for developing novel therapeutics and optimizing combination therapies to achieve dual metabolic and skeletal benefits in DOP patients.

摘要

糖尿病性骨质疏松症(DOP)是一种复杂的代谢性骨病,其特征是糖尿病患者的骨质量受损和骨折风险增加。高血糖、胰岛素抵抗和骨代谢之间的相互作用突出了需要综合治疗策略来解决血糖控制和骨骼健康问题。本综述系统地研究了降糖和骨保护药物的分子机制,强调了它们在管理DOP中的双重作用。我们讨论了DOP潜在的病理生理途径,包括胰岛素/胰岛素样生长因子-1缺乏、晚期糖基化终产物(AGEs)积累、氧化应激和血管损伤。此外,我们探讨了抗糖尿病药物(如二甲双胍、胰高血糖素样肽-1受体激动剂、钠-葡萄糖协同转运蛋白2抑制剂)和抗骨质疏松药物(如双膦酸盐、特立帕肽、雷奈酸锶)的作用机制,强调它们潜在的协同作用和风险。最后,我们概述了开发新型疗法和优化联合疗法以在DOP患者中实现代谢和骨骼双重益处的未来方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e634/12436113/fe457c57c575/fendo-16-1595228-g001.jpg

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