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二甲双胍对糖耐量异常非酒精性脂肪性肝病患者IL-6、TNF-α的影响 被引量:4

Effect of metformin on the level of serum interleukin-6 and tumor necrosis factor-α of impaired glucose tolerance patients with non-alcoholic fatty liver disease
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摘要 目的观察二甲双胍对糖耐量异常非酒精性脂肪性肝病(nonalcoholic fatty liver disease,NAFLD)患者IL-6、TNF-α的影响。方法将160例糖耐量异常NAFLD患者随机分为观察组(n=90)和对照组(n=70)。在严格控制饮食和运动的基础上,观察组加用二甲双胍1500mg/d,对照组加用多烯磷脂酰胆碱胶囊456 mg/d,均治疗24周。结果治疗24周后,与对照组比较,观察疗组患者BMI、ALT、FPG、insulin、HOMA-IR、hs-CRP、TNF-α和IL-6水平均显著降低(P<0.05);两组间AST水平差异无统计学意义(P>0.05)。结论二甲双胍能改善糖耐量异常NAFLD患者糖代谢指标和胰岛素抵抗,降低肝酶和炎症细胞因子水平。 Objective To evaluate the efficacy of metformin on the level of interleukin-6 and tumor necrosis factor-or of impaired glucose tolerance patients with non-alcoholic fatty liver disease. Method 160 impaired glucose tolerance patients with non-alcoholic fatty liver disease were firstly divided into an experimental group (n = 90) and a control group( n = 70). On the basis of strict diet control and physical exercise, the experimental group was given mefformin 1500mg per day for a period of 24 weeks. The control group was treated with polyene phosphatidylcholine capsules 456mg per day also for a period of 24 weeks. Results After 24 weeks of treatment, the level of body mass index(BMl), anine aminotrans- ferase (ALT), fasting blood glucose (FPG), insulin, homeostasis model assessment-insulin resistance (HOMA IR) of the experimental group decreased more significantly than those of the control group( P 〈 0.05 ). The difference between the two groups in the level of aspartate transaminase (AST) was not statistically significant ( P 〉 0. 05 ). Conclusion The metformin treatment could improve the glucose metabolism indexes and insulin resistance of impaired glucose tolerance patients with non-alcoholic fatty liver disease, reduce liver enzyme and inflammatory eytokines, improve liver function, and lessen the degree of inflammation in liver.
出处 《健康研究》 CAS 2015年第6期643-645,共3页 Health Research
关键词 脂肪肝 非酒精性 二甲双胍 白介素-6 肿瘤坏死因子-α fatty liver non-alcoholic metformin interleukin-6 tumor necrosis factor-ct
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