肠促胰岛素
肌萎缩
医学
内分泌学
内科学
瘦体质量
胰岛素抵抗
脂肪组织
骨骼肌
2型糖尿病
肥胖
激素
肌萎缩性肥胖
减肥
受体
糖尿病
生物信息学
肌动蛋白
2型糖尿病
代谢综合征
胰岛素
合成代谢
磷酸西他列汀
兴奋剂
临床试验
生物
动物研究
作者
Lampros Chrysavgis,Niki Gerasimoula Mourelatou,Maria Evangelia Koloutsou,Sofia Rozani,Εvangelos Cholongitas
标识
DOI:10.3390/ijms262412130
摘要
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) and newer incretin-based co-agonists have transformed obesity and type 2 diabetes (T2D) management, achieving unprecedented weight loss and cardiometabolic benefits. However, their effects on body composition, particularly lean and skeletal muscle mass, remain incompletely defined. In this current review, we examined the influence of GLP-1 RAs and incretin hormone agonists on lean tissue, integrating physiological, clinical, and mechanistic perspectives. We first outlined the physiology of incretin hormones, with emphasis on their metabolic roles and potential relevance to muscle health. We then discussed sarcopenia and sarcopenic obesity as conditions of rising clinical concern, given their overlap with obesity and metabolic disease. Evidence from preclinical studies and randomized clinical trials indicates that while GLP-1-based therapies predominantly reduce adipose tissue, including visceral and ectopic depots, but they also produce absolute reductions in lean mass, generally representing 20-30% of total weight loss. The extent to which these changes translate into impaired muscle function or increased vulnerability to frailty remains unclear. Preservation of lean and skeletal muscle mass is a critical yet underexplored aspect of incretin-based weight loss. Current studies are constrained by methodological heterogeneity, small sample sizes, and limited assessment of functional outcomes. Data on dual and triple agonists are emerging but remain limited. Future research should integrate standardized body-composition measures, mechanistic exploration, and adjunctive interventions such as resistance training or protein optimization.
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