Department of Endocrinology and Metabolism, First Hospital of Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Institute of Translational Medicine, First Hospital of Jilin University, Changchun, Jilin, 130021, People's Republic of China.
Drug Des Devel Ther. 2024 Sep 23;18:4257-4272. doi: 10.2147/DDDT.S476815. eCollection 2024.
Obesity represents a substantial risk factor for a multitude of metabolic disorders, which seriously threatens human life and health. As the global obesity epidemic intensifies, obesity-related nephropathy (ORN) has attracted great attention. ORN arises from both physical/mechanical and non-physical insults to the glomerular and tubular structures precipitated by obesity, culminating in structural impairments and functional aberrations within the kidneys. Physical injury factors include changes in renal hemodynamics, renal compression, and mechanical stretching of podocytes. Non-physical injury factors include overactivation of the RAAS system, insulin resistance, lipotoxicity, inflammation, and dysregulation of bile acid metabolism. Exploring molecules that target modulation of physical or nonphysical injury factors is a potential approach to ORN treatment. ORN is characterized clinically by microproteinuria and pathologically by glomerulomegaly, which is atypical and makes early diagnosis difficult. Investigating early diagnostic markers for ORN thus emerges as a critical direction for future research. Additionally, there is no specific drug for ORN in clinical treatment, which mainly focuses on weight reduction, mitigating proteinuria, and preserving renal function. In our review, we delineate a progressive therapeutic approach involving enhancements in lifestyle, pharmacotherapy, and bariatric surgery. Our emphasis underscores glucagon-like peptide-1 receptor agonists (GLP-1 RAs) as poised to emerge as pivotal therapeutic modalities for ORN in forthcoming clinical avenues.
肥胖是多种代谢紊乱的重要危险因素,严重威胁人类的生命和健康。随着全球肥胖症的加剧,肥胖相关性肾病(ORN)引起了极大关注。ORN 源于肥胖引起的肾小球和肾小管结构的物理/机械和非物理损伤,最终导致肾脏结构损伤和功能异常。物理损伤因素包括肾血流动力学改变、肾压迫和足细胞的机械拉伸。非物理损伤因素包括肾素-血管紧张素-醛固酮系统过度激活、胰岛素抵抗、脂毒性、炎症和胆汁酸代谢失调。探索针对物理或非物理损伤因素调节的分子是 ORN 治疗的一种潜在方法。ORN 的临床特征是微量蛋白尿,病理特征是肾小球肥大,其非典型性使得早期诊断变得困难。因此,寻找 ORN 的早期诊断标志物成为未来研究的一个关键方向。此外,临床治疗中没有针对 ORN 的特定药物,主要集中在减肥、减少蛋白尿和保护肾功能上。在我们的综述中,我们描述了一种渐进的治疗方法,包括改善生活方式、药物治疗和减肥手术。我们强调胰高血糖素样肽-1 受体激动剂(GLP-1 RAs)有望成为 ORN 未来临床治疗的重要治疗方式。