Department of Infectious Diseases, Second Affiliated Hospital, Harbin Medical UniversityNangang District, Harbin, China.
Int J Infect Dis. 2012 Jun;16(6):e436-41. doi: 10.1016/j.ijid.2012.02.004. Epub 2012 Apr 7.
Insulin resistance (IR) affects sustained virological response (SVR) in chronic hepatitis C (CHC). The aim of this study was to investigate the effect of adding metformin to peginterferon alfa-2a and ribavirin on the efficacy in patients with genotype 1 CHC and IR.
Ninety-eight patients with genotype 1 CHC and IR were randomized into the treatment group (n=49) and the control group (n=49). Patients in the control group received peginterferon alfa-2a and ribavirin, and patients in the treatment group received metformin in addition to peginterferon alfa-2a and ribavirin. The rate of virological response, changes in the homeostasis model assessment of insulin resistance (HOMA-IR) index, and the incidence of side effects were compared between the two groups. Factors influencing the SVR were studied by multivariate analysis.
The SVR rate of the treatment group was significantly higher than that of the control group (59.2%, 29/49 vs. 38.8%, 19/49; Chi-square=4.083, p=0.043). The HOMA-IR index of patients in the treatment group was lower than that of patients in the control group at weeks 12, 24, and 48 of the treatment period, and at week 24 of follow-up (3.00±0.65 vs. 3.50±0.72, 1.90±0.45 vs. 2.90±0.64, 1.75±0.40 vs. 2.74±0.48, and 1.60±0.35 vs. 2.60±0.55, respectively; t=3.610, 8.947, 11.091, and 10.738, respectively; p<0.01). Diarrhea was more often seen in the treatment group (28.6%, 14/49 vs. 10.2%, 5/49; Chi-square=5.288, p=0.021). In the multivariate logistic regression analysis, the independent factors associated with SVR were treatment method (p=0.009) and HOMA-IR <2 at week 24 (p=0.011).
A combination of metformin, peginterferon alfa-2a, and ribavirin improved insulin sensitivity and increased the SVR rate of patients with hepatitis C genotype 1 and IR, with a good safety profile.
胰岛素抵抗(IR)会影响慢性丙型肝炎(CHC)的持续病毒学应答(SVR)。本研究旨在探讨在基因 1 型 CHC 合并 IR 的患者中,加用二甲双胍对聚乙二醇干扰素 alfa-2a 和利巴韦林疗效的影响。
将 98 例基因 1 型 CHC 合并 IR 的患者随机分为治疗组(n=49)和对照组(n=49)。对照组接受聚乙二醇干扰素 alfa-2a 和利巴韦林治疗,治疗组在此基础上加用二甲双胍。比较两组患者的病毒学应答率、稳态模型评估的胰岛素抵抗指数(HOMA-IR)的变化以及不良反应的发生率。采用多因素分析研究影响 SVR 的因素。
治疗组的 SVR 率明显高于对照组(59.2%,29/49 比 38.8%,19/49;卡方=4.083,p=0.043)。治疗期间第 12、24、48 周及随访第 24 周,治疗组患者的 HOMA-IR 指数均低于对照组(3.00±0.65 比 3.50±0.72,1.90±0.45 比 2.90±0.64,1.75±0.40 比 2.74±0.48,1.60±0.35 比 2.60±0.55;t=3.610、8.947、11.091、10.738;p<0.01)。治疗组腹泻更常见(28.6%,14/49 比 10.2%,5/49;卡方=5.288,p=0.021)。多因素 logistic 回归分析显示,与 SVR 相关的独立因素为治疗方法(p=0.009)和第 24 周 HOMA-IR<2(p=0.011)。
二甲双胍联合聚乙二醇干扰素 alfa-2a 和利巴韦林可改善胰岛素敏感性,提高丙型肝炎基因 1 型合并 IR 患者的 SVR 率,且安全性良好。