Tóth László Imre, Harsányi Adrienn, Csiha Sára, Molnár Ágnes, Lőrincz Hajnalka, Nagy Attila Csaba, Paragh György, Harangi Mariann, Sztanek Ferenc
Division of Metabolism, Department of Internal Medicine, Faculty of Medicine, University of Debrecen, H-4032 Debrecen, Hungary.
Doctoral School of Health Sciences, University of Debrecen, H-4032 Debrecen, Hungary.
Int J Mol Sci. 2025 Jun 20;26(13):5951. doi: 10.3390/ijms26135951.
Recent studies have demonstrated the efficacy of glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in enhancing glycemic control, regulating body weight, and modulating lipid metabolism. However, their effects on lipoprotein subfractions have not been clarified. The objective of this 52-week, single-center, randomized trial was to compare the effects of subcutaneous semaglutide administered once weekly and oral sitagliptin administered once daily on anthropometric measurements and lipoprotein subfractions measured by Lipoprint gelelectrophoresis in patients with type 2 diabetes mellitus (T2DM). A total of 34 obese individuals with T2DM were enrolled in the study and randomly assigned to receive semaglutide ( = 18) or sitagliptin ( = 16). Thirty-one age- and body weight-matched non-diabetic obese individuals served as controls. Semaglutide treatment resulted in significant reductions in body mass index (BMI), waist circumference, and Hb, along with improvements in lipid parameters, including reductions in LDL cholesterol and non-HDL cholesterol levels, and redistribution of LDL and HDL subfractions toward a less atherogenic profile. Conversely, sitagliptin elicited modest glycemic improvements without substantial alterations in lipid composition. Multivariate regression analysis demonstrated that fluctuations in lipoprotein subfractions were not influenced by changes in BMI or HbA1c. These results support the pleiotropic metabolic benefits of semaglutide and its potential role in managing the cardiometabolic risk of T2DM.
近期研究已证实胰高血糖素样肽-1受体激动剂和二肽基肽酶-4抑制剂在改善血糖控制、调节体重和调节脂质代谢方面的疗效。然而,它们对脂蛋白亚组分的影响尚未明确。这项为期52周的单中心随机试验的目的是比较每周皮下注射一次司美格鲁肽和每日口服一次西格列汀对2型糖尿病(T2DM)患者人体测量指标和通过Lipoprint凝胶电泳测量的脂蛋白亚组分的影响。共有34名肥胖的T2DM患者参与该研究,并随机分配接受司美格鲁肽(n = 18)或西格列汀(n = 16)治疗。31名年龄和体重匹配的非糖尿病肥胖个体作为对照。司美格鲁肽治疗导致体重指数(BMI)、腰围和糖化血红蛋白(HbA1c)显著降低,同时脂质参数得到改善,包括低密度脂蛋白胆固醇(LDL-C)和非高密度脂蛋白胆固醇(non-HDL-C)水平降低,以及LDL和HDL亚组分重新分布为致动脉粥样硬化性更低的模式。相反,西格列汀仅适度改善血糖,脂质成分无实质性改变。多变量回归分析表明,脂蛋白亚组分的波动不受BMI或糖化血红蛋白(HbA1c)变化的影响。这些结果支持了司美格鲁肽多方面的代谢益处及其在管理T2DM心血管代谢风险中的潜在作用。