• 中国核心期刊(遴选)数据库收录期刊
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中国药物评价 ›› 2025, Vol. 42 ›› Issue (4): 306-310.

• 药品评价 • 上一篇    下一篇

利拉鲁肽联合阿卡波糖和二甲双胍治疗T2DM的疗效及对糖脂代谢和胰岛功能的影响

罗政委   

  1. 商丘市第三人民医院急诊科, 河南 商丘 476000
  • 收稿日期:2025-05-27 修回日期:2025-07-11 接受日期:2025-10-10 出版日期:2025-08-28 发布日期:2025-10-11

Efficacy of Liraglutide Combined with Acarbose and Metformin in the Treatment of T2DM and Its Effects on Glycolipid Metabolism and Islet Function

 LUO Zhengwei   

  1. Emergency Department of the Third People′s Hospital of Shangqiu City, Henan Shangqiu 476000, China
  • Received:2025-05-27 Revised:2025-07-11 Accepted:2025-10-10 Online:2025-08-28 Published:2025-10-11

摘要: 目的:评估在阿卡波糖联合二甲双胍基础上加用利拉鲁肽对2型糖尿病(T2DM)患者糖脂代谢、胰岛功能及炎症与氧化应激的影响。方法:采用回顾性对照研究,选取2022年4月至2024年12月本院收治的92例T2DM患者(效应量d=0.8,α=0.05,β=0.2),分为对照组(阿卡波糖+二甲双胍,n=46)和试验组(联用利拉鲁肽,n=46)。比较两组治疗前后糖代谢指标(FPG、HbA1c)、血脂指标(TG、TC、LDL-C、HDL-C)、胰岛功能参数(HOMA-IR、ISI、HOMA-β)以及炎症(NLRP3)与氧化应激指标(MDA、GSH-PX、SOD)的变化,同时记录不良反应发生率。结果:试验组总有效率高于对照组(93.48% vs 78.26%,P<0.05)。治疗后,两组患者FPG、HbA1c、TG、TC、LDL-C均降低而HDL-C升高,且试验组改善更明显(P<0.05)。试验组胰岛功能改善更明显:HOMA-IR降低幅度更大,ISI及HOMA-β升高幅度更大(均P<0.05)。此外,试验组炎症指标(NLRP3)和氧化应激指标(MDA)降低幅度,以及抗氧化指标(GSH-PX、SOD)升高幅度均大于对照组(均P<0.05)。两组患者不良反应发生率比较,差异无统计学意义(P>0.05)。结论:在阿卡波糖和二甲双胍治疗基础上联合利拉鲁肽,能更有效改善T2DM患者的糖脂代谢,减轻胰岛素抵抗并增强胰岛β细胞功能,同时抑制炎症反应和氧化应激,且安全性良好。

关键词:  , 2型糖尿病(T2DM);利拉鲁肽;阿卡波糖;二甲双胍;胰岛功能;糖脂代谢

Abstract: Objective: To evaluate the effects of liraglutide combined with acarbose and metformin on glucose and lipid metabolism, islet function, inflammation, and oxidative stress in patients with type 2 diabetes mellitus (T2DM). Methods: A retrospective controlled analysis was conducted on 92 T2DM patients treated at our hospital from April 2022 to December 2024 (effect sized=0.8, α=0.05, β=0.2). The patients were divided into the control group (acarbose+metformin, n=46) and the experimental group (combined with liraglutide, n=46). Changes in glucose metabolism indicators(FPG, HbA1C), blood lipid parameter(TG, TC, LDL-C, HDL-C), islet function parameters(HOMA-IR、ISI、HOMA-β), and biomarkers related to inflammation(NLRP3) and oxidative stress(MDA, GSH-PX, SOD) were compared between the two groups before and after treatment. The incidence of adverse reactions was also recorded. Results: The total effective rate in the experimental group was higher than that in the control group (93.48% vs 78.26%, P<0.05). After treatment, levels of FPG, HbA1c, TG, TC, and LDL-C decreased and HDL-C increased in both groups of patipats, with greater improvements observed in the experimental group (P<0.05). The experimental group showed a significant advantage in improving islet function parameters: greater reduction in HOMA-IR and greater increases in ISI and HOMA-β compared to the control group (P<0.05). Meanwhile, the experimental group exhibited greater reductions in the inflammatory marker NLRP3 and the oxidative stress marker MDA, as well as greater increases in GSH-PX and SOD (P<0.05). There was no statistically significant difference in the incidence of adverse reactions between the two groups (P>0.05). Conclusion: Liraglutide combined with the acarbose and metformin can more effectively improve glucose and lipid metabolism in T2DM patients, reduce insulin resistance, and promote the recovery of islet β-cell function, while also suppressing inflammatory responses and oxidative damage, and with good safety.

Key words: Type 2 diabetes mellitus(T2DM), Liraglutide, Acarbose, Metformin, Islet function, Glucose and lipid metabolism

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