Sun Liping, Yuan Yuhong, Li Yongmei, Rao Xiaopang
Department of Endocrinology, Chengyang People's Hospital in Qingdao, Qingdao, Shandong 266109, P.R. China.
Department of Pharmacy, Chengyang People's Hospital in Qingdao, Qingdao, Shandong 266109, P.R. China.
Exp Ther Med. 2023 Apr 13;25(6):249. doi: 10.3892/etm.2023.11948. eCollection 2023 Jun.
Glucagon-like peptide-1 receptor agonist liraglutide may have beneficial effects on atherosclerosis development in impaired glucose tolerance (IGT). To the best of our knowledge, however, little conclusive evidence from clinical trials has been presented. The present study aimed to investigate the effect of liraglutide on atherosclerosis progression in patients with IGT. The present study was a double-blind, randomized controlled clinical trial. A total of 39 of patients aged 20-75 years who were overweight or obese (BMI, 27-40 kg/m) and presented IGT were randomized to receive liraglutide (n=17) or lifestyle interventions (n=22) for 6 months. Serum glucose and insulin (INS) levels, lipid profile, inflammatory biomarkers and carotid intima-media thickness (CIMT) were assessed at the start and end of each treatment. Side effects were also recorded. Liraglutide treatment was found to significantly improve glycaemia, including glycosylated hemoglobin, fasting and postprandial glucose as well as INS levels (all P<0.001). Liraglutide also significantly decreased serum total cholesterol and low-density lipoprotein levels (all P<0.001). Furthermore, serum levels of inflammatory biomarkers, as well as CIMT, were decreased following liraglutide treatment compared with those in the lifestyle intervention group (all P<0.001). Kaplan-Meier analysis showed that the risk of vasculopathy in the liraglutide group was lower than that in the lifestyle intervention group (log-rank test; P=0.041). The monitoring of drug-associated side effects indicated that the dose of liraglutide (0.6 to 1.2 mg/QD via subcutaneous injection) was safe and well-tolerated. The present study suggested that liraglutide may slow atherosclerosis development and improve inflammatory status as well as intimal function in patients with IGT with few side effects. The trial was registered through the Chinese Clinical Trial Registry (ChiCTR; trial registration no. ChiCTR2200063693; retrospectively registered) on Sep 14, 2022.
胰高血糖素样肽-1受体激动剂利拉鲁肽可能对糖耐量受损(IGT)患者的动脉粥样硬化发展具有有益作用。然而,据我们所知,临床试验中几乎没有确凿证据。本研究旨在探讨利拉鲁肽对IGT患者动脉粥样硬化进展的影响。本研究为双盲、随机对照临床试验。共有39例年龄在20 - 75岁、超重或肥胖(BMI,27 - 40 kg/m)且患有IGT的患者被随机分为接受利拉鲁肽治疗组(n = 17)或生活方式干预组(n = 22),为期6个月。在每次治疗开始和结束时评估血糖和胰岛素(INS)水平、血脂谱、炎症生物标志物和颈动脉内膜中层厚度(CIMT)。同时记录副作用。结果发现,利拉鲁肽治疗可显著改善血糖,包括糖化血红蛋白、空腹和餐后血糖以及INS水平(均P < 0.001)。利拉鲁肽还显著降低血清总胆固醇和低密度脂蛋白水平(均P < 0.001)。此外,与生活方式干预组相比,利拉鲁肽治疗后炎症生物标志物水平以及CIMT均降低(均P < 0.001)。Kaplan-Meier分析显示,利拉鲁肽组血管病变风险低于生活方式干预组(对数秩检验;P = 0.041)。药物相关副作用监测表明,利拉鲁肽剂量(皮下注射0.6至1.2 mg/每日一次)安全且耐受性良好。本研究表明,利拉鲁肽可能减缓IGT患者的动脉粥样硬化发展,改善炎症状态以及内膜功能,且副作用较少。该试验于2022年9月14日通过中国临床试验注册中心(ChiCTR;试验注册号ChiCTR2200063693;回顾性注册)注册。