Department of Endocrinology, Diabetes and Metabolic Disease, University Medical Centre Ljubljana, Zaloška cesta 7, 1000, Ljubljana, Slovenia.
Faculty of Medicine, University of Ljubljana, Vrazov trg 2, 1000, Ljubljana, Slovenia.
Adv Ther. 2022 Jun;39(6):2452-2467. doi: 10.1007/s12325-022-02153-x. Epub 2022 May 3.
The approval of once daily liraglutide, 3.0 mg, and once weekly semaglutide, 2.4 mg, for chronic weight management provides a novel effective strategy against obesity. The reliable models that might predict weight reducing potential at the individual level have not been identified yet. However, the coexistence of diabetes has been consistently related with less effective response than in people without this comorbidity. We aimed to review the efficacy of GLP-1 RAs approved for weight management in individuals with and without diabetes and discuss some potential mechanisms for consistently observed differences in efficacy between these two populations. The mean weight loss difference between GLP-1 RAs and placebo as add-on to lifestyle intervention in patients with diabetes was 4% to 6.2% compared to 6.1 to 17.4% in people without diabetes. Semaglutide compared to liraglutide resulted in greater weight loss. Some hypothetical explanations for the weaker anti-obesity response for both GLP-1 RAs in people with diabetes include the background medications that promote weight gain, the fear of hypoglycaemia inherently related to the treatment of diabetes, a decrease in glycosuria and subsequently less weight loss in diabetics, an altered microbiota in patients with obesity and diabetes and a genetic background that predispose to weight gain in patients with diabetes. Moreover, people with diabetes may have had obesity for longer and may be less adherent to exercise, which seems to potentiate the effects of GLP-1 RA. Emerging multimodal approaches combining peptides targeting receptors at different levels might therefore be of additional benefit particularly in patients with diabetes.
每日一次利拉鲁肽 3.0mg 和每周一次司美格鲁肽 2.4mg 的获批用于慢性体重管理为肥胖症提供了一种新的有效治疗策略。然而,尚未确定能够预测个体减重潜力的可靠模型。但是,与没有这种合并症的患者相比,合并糖尿病的患者的反应通常不太有效。我们旨在回顾已批准用于体重管理的 GLP-1RA 在合并和不合并糖尿病的个体中的疗效,并讨论这两种人群之间观察到的疗效差异的一些潜在机制。与不合并糖尿病的患者相比,GLP-1RA 联合生活方式干预治疗糖尿病患者的体重平均减轻差异为 4%至 6.2%,而不合并糖尿病的患者为 6.1%至 17.4%。与利拉鲁肽相比,司美格鲁肽导致的体重减轻更大。对于合并糖尿病的患者,GLP-1RA 的抗肥胖反应较弱的一些假设解释包括促增重的背景药物、与糖尿病治疗相关的低血糖固有恐惧、糖尿减少以及随后糖尿病患者体重减轻减少、肥胖和糖尿病患者的微生物群改变以及易患糖尿病患者体重增加的遗传背景。此外,糖尿病患者的肥胖可能持续时间更长,并且可能不太遵守运动,这似乎会增强 GLP-1RA 的作用。因此,联合针对不同水平受体的肽的新兴多模式方法可能特别有益于糖尿病患者。