Chen Alissa S, Batsis John A
National Clinician Scholars Program, Yale School of Medicine, New Haven, CT.
Section of General Internal Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT.
Diabetes. 2025 Jul 11. doi: 10.2337/dbi25-0004.
Sarcopenic obesity, a subtype of obesity, is marked by reduced skeletal muscle mass and function, or sarcopenia, and poses a significant health challenge to older adults as it affects an estimated 28.3% of people aged >60 years. This subtype is unique to older adults as aging exacerbates sarcopenia and obesity due to changes in energy metabolism, hormones and inflammatory markers, and lifestyle factors. Traditional treatments for sarcopenic obesity have been focused on exercise and dietary modifications to reduce fat while maintaining muscle mass. Newer glucagon-like peptide 1 receptor agonists (GLP-1RA) and dual gastric inhibitory polypeptide/GLP-1 receptor agonists (GIP/GLP-1RAs), including liraglutide, semaglutide, and tirzepatide, have shown great promise to reduce weight, treat obesity-related complications, improve physical function, and improve quality of life, in younger clinical trial populations. However, the use of GLP-1RAs and GIP/GLP-1RAs has not been exhaustively evaluated in older adults with sarcopenic obesity. These medications come with the risk of loss of muscle mass and an increased rate of adverse events. Thus, clinicians should use them cautiously by weighing the potential benefits against their risks. Herein, we discuss a possible approach to using GLP-1RAs and GIP/GLP-1RAs in patients with sarcopenic obesity, including considerations for patient identification, monitoring, maintenance, and discontinuation. In this article we also discuss the emerging treatments that will be available, which may include activin type II receptor antibodies and selective androgen receptor agonists. We conclude by highlighting the advancement of geroscience as a promising field for individualizing treatments in the future.
Sarcopenic obesity, reduced muscle mass and strength coupled with obesity, poses significant health risks to older adults. Aging exacerbates sarcopenia and obesity due to metabolic, hormonal, inflammatory, and lifestyle changes. Traditional interventions emphasize exercise and diet to reduce fat mass while preserving muscle mass. Incretin therapies show promise in weight reduction and physical improvement in younger populations but are minimally studied in older adults. These medications can be used to treat several obesity-related complications, which older adults with sarcopenic obesity are prone to developing. These medications need to be used cautiously among older adults, considering potential muscle mass loss and adverse events.
肌少症性肥胖是肥胖的一种亚型,其特征是骨骼肌质量和功能下降,即肌少症,这对老年人构成了重大的健康挑战,因为据估计,60岁以上人群中有28.3%受其影响。这种亚型在老年人中较为独特,因为衰老会因能量代谢、激素和炎症标志物以及生活方式因素的变化而加剧肌少症和肥胖。肌少症性肥胖的传统治疗方法一直侧重于通过运动和饮食调整来减少脂肪,同时维持肌肉质量。新型胰高血糖素样肽1受体激动剂(GLP-1RA)和双重胃抑制多肽/GLP-1受体激动剂(GIP/GLP-1RA),包括利拉鲁肽、司美格鲁肽和替尔泊肽,在较年轻的临床试验人群中已显示出在减轻体重、治疗肥胖相关并发症、改善身体功能和提高生活质量方面具有巨大潜力。然而,GLP-1RA和GIP/GLP-1RA在患有肌少症性肥胖的老年人中的使用尚未得到详尽评估。这些药物存在肌肉质量流失和不良事件发生率增加的风险。因此,临床医生在使用时应谨慎权衡其潜在益处与风险。在此,我们讨论了在肌少症性肥胖患者中使用GLP-1RA和GIP/GLP-1RA的一种可能方法,包括患者识别、监测、维持和停药的注意事项。在本文中,我们还讨论了即将出现的治疗方法,可能包括激活素II型受体抗体和选择性雄激素受体激动剂。我们强调老年科学作为未来个性化治疗的一个有前景的领域所取得的进展作为结论。
肌少症性肥胖,即肌肉质量和力量下降并伴有肥胖,对老年人构成重大健康风险。由于代谢、激素、炎症和生活方式的改变,衰老会加剧肌少症和肥胖。传统干预措施强调运动和饮食,以减少脂肪量同时保留肌肉质量。肠促胰岛素疗法在较年轻人群的体重减轻和身体改善方面显示出前景,但在老年人中的研究较少。这些药物可用于治疗几种肥胖相关并发症,肌少症性肥胖的老年人容易出现这些并发症。考虑到潜在的肌肉质量流失和不良事件,这些药物在老年人中需要谨慎使用。