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靶向慢性肾脏病中的肌肉减少症:胰高血糖素样肽-1受体激动剂的新作用

Targeting Sarcopenia in CKD: The Emerging Role of GLP-1 Receptor Agonists.

作者信息

Llinares-Arvelo Vicente, Martínez-Alberto Carlos E, González-Luis Ainhoa, Macía-Heras Manuel, Siverio-Morales Orlando, Navarro-González Juan F, Donate-Correa Javier

机构信息

Escuela de Enfermería Nuestra Señora de Candelaria, Carretera General del Rosario, 145, 38010 Santa Cruz de Tenerife, Spain.

Doctoral and Graduate School, University of La Laguna, 38200 San Cristóbal de La Laguna, Spain.

出版信息

Int J Mol Sci. 2025 Aug 21;26(16):8096. doi: 10.3390/ijms26168096.

Abstract

Sarcopenia is a prevalent and disabling complication of chronic kidney disease (CKD), associated with frailty, diminished quality of life, and increased morbidity and mortality. Despite its clinical significance, no pharmacological treatments are currently approved to address muscle wasting in this population. Glucagon-like peptide-1 receptor agonists (GLP-1RAs), widely used in the management of type 2 diabetes and obesity, have shown potential to support muscle mass and function through pleiotropic mechanisms. These include anti-inflammatory and antioxidant actions, improvements in insulin sensitivity and energy metabolism, and mitochondrial support. Given the high burden of sarcopenia in CKD and the frequent overlap with metabolic and cardiovascular comorbidities, GLP-1RAs may offer a novel therapeutic approach. This review examines the biological plausibility and emerging evidence supporting the role of GLP-1RAs in preserving muscle health in CKD, highlighting the need for targeted clinical trials and mechanistic investigations to establish their efficacy in this high-risk group.

摘要

肌肉减少症是慢性肾脏病(CKD)常见且导致功能障碍的并发症,与身体虚弱、生活质量下降以及发病率和死亡率增加相关。尽管其具有临床重要性,但目前尚无获批用于解决该人群肌肉萎缩问题的药物治疗方法。胰高血糖素样肽-1受体激动剂(GLP-1RAs)广泛用于2型糖尿病和肥胖症的管理,已显示出通过多效机制支持肌肉质量和功能的潜力。这些机制包括抗炎和抗氧化作用、胰岛素敏感性和能量代谢的改善以及线粒体支持。鉴于CKD中肌肉减少症的高负担以及与代谢和心血管合并症的频繁重叠,GLP-1RAs可能提供一种新的治疗方法。本综述探讨了支持GLP-1RAs在维持CKD患者肌肉健康中作用的生物学合理性和新出现的证据,强调需要进行有针对性的临床试验和机制研究,以确定其在这一高危人群中的疗效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4011/12386527/34e3a02c84b1/ijms-26-08096-g001.jpg

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