阿卡波糖联合二甲双胍对2型糖尿病患者炎性因子及细胞免疫功能的影响

The effects of acarbose combined with metformin on inflammatory factors and cellular immune function in patients with type 2 diabetes mellitus

  • 摘要: 目的 探讨阿卡波糖联合二甲双胍对2型糖尿病患者的临床疗效及作用机制。 方法 将114例2型糖尿病患者随机分为联合治疗组(n=58)、二甲双胍组(n=56)。二甲双胍组给予二甲双胍治疗,联合治疗组给予阿卡波糖联合二甲双胍治疗。治疗3个月后,比较2组血清炎性因子、T淋巴细胞亚群、血糖控制、不良反应发生率。 结果 联合治疗组血清白细胞介素-6(IL-6)、C-反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)水平低于二甲双胍组(P<0.05), CD3+、CD4+、CD4+/CD8+高于二甲双胍组, CD8+低于二甲双胍组,差异有统计学意义(P<0.05)。联合治疗组空腹血糖(FPG)、空腹胰岛素(FINS)、糖化血红蛋白(HbA1c)、胰岛素抵抗指数(HOMA-IR)低于二甲双胍组,差异有统计学意义(P<0.05)。2组不良反应发生率比较,差异无统计学意义(P>0.05)。 结论 阿卡波糖联合二甲双胍可抑制2型糖尿病患者的炎症反应,并调节其细胞免疫功功能和血糖水平。

     

    Abstract: Objective To explore the clinical effect of acarbose combined with metformin for patients with type 2 diabetes mellitus and its mechanism of action. Methods A total of 114 patients with type 2 diabetes were randomly divided into combined treatment group(n=58)and metformin group(n=56). The metformin group was treated with metformin, while the combined treatment group was given acarbose combined with metformin. After 3 months of treatment, serum inflammatory factors, T lymphocyte subsets, blood glucose control and incidence of adverse reactions were compared between the two groups. Results The levels of serum interleukin-6(IL-6), C-reactive protein(CRP)and tumor necrosis factor-α(TNF-α)in the combined treatment group were significantly lower than those in the metformin group(P<0.05), CD3+, CD4+, CD4+/CD8+ in the combined treatment group were significantly higher than those in the metformin group, and CD8+ was significantly lower than that in the metformin group(P<0.05). Fasting blood gluscose(FPG), fasting insulin(FINS), Hemoglobin A1c(HbA1c)and homeostasis model assessment of insulin resistance(HOMA-IR)in the combined treatment group were significantly lower than those in the metformin group(P<0.05). There was no significant difference in the incidence of adverse reactions between the two groups(P>0.05). Conclusion Acarbose combined with metformin can inhibit the inflammatory response of patients with type 2 diabetes mellitus, and regulate their cellular immune function and blood glucose level.

     

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