文章摘要
王慧李建忠柳富会侯青顺郭宝营.干扰素-α治疗慢性乙型肝炎的疗效及其影响因素的研究[J].,2011,11(9):1741-1743
干扰素-α治疗慢性乙型肝炎的疗效及其影响因素的研究
Study of Therapeutic Efficiency and Efficient Factor of Interferonfor Chronic Hepatitis B
  
DOI:
中文关键词: 慢性肝炎,乙型  干扰素-α  治疗  影响因素
英文关键词: Chronic hepatitis B  Efficiency  Interferon-α  Influencing factors
基金项目:
作者单位
王慧李建忠柳富会侯青顺郭宝营 青岛大学医学院 
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中文摘要:
      目的:分析影响干扰素-α(IFN-α)治疗慢性乙型肝炎(CHB)疗效的因素。方法:选择2006 年到2009 年青岛市传染病医院 住院的CHB 患者46 例,应用IFN-α 治疗48 周,根据IFN-α 治疗的疗效将其分为应答组与无应答组,评价患者的宿主、病毒载 量及生化指标等因素对疗效的影响。结果:两组间的性别比例、年龄和病程无显著差异(P>0.05),应答组治疗前HBV-DNA 载 量低于无应答组,ALT 水平高于无应答组,HBeAg 阳性患者的应答率高于HBeAg 阴性患者,差异均具有统计学意义(P<0.05), 应答组在治疗12 周时HBV-DNA 载量下降>2log 的比例高于无应答组,差异具有统计学意义(P<0.05)。结论:治疗前HBV DNA 载量低、ALT 水平高和HBeAg 阳性以及治疗12 周时的HBV DNA 应答可以作为干扰素-α 治疗慢性乙型肝炎48 周时应 答的预测因素。
英文摘要:
      Objective: To investigate the influencing factors of the efficacy of interferon α (IFN-α) on patients with chronic hepatitis B (CHB). Methods: 46 cases of CHB patients were chosen in this study, who were treated with IFN-α for 48 weeks in Qingdao Hospital for Infectious Diseases from January 2006 to June 2009, which were divided into responding group and non-responding group according to the efficacy of IFN-α. The influence of host factors, viral loads and biochemical factors on the efficacy of IFN-α was detected. Results: The proportions of sex and the mean ages and courses of disease were similar in the two groups (P> 0.05). The pre-treatment HBV-DNA loads were lower and the ALT levels were higher in responding group than those in non-responding group (P <0.05), while the responding rate of the patients with HBeAg positive was higher than that with HBeAg negative (P <0.05). The rate of HBV-DNA load decreased more than that of 2 log at the 12 weeks of treatment was significantly higher in the responding group than that in the non-responding group (P <0.05). Conclusion: The lower HBV DNA load, higher ALT level and HBeAg positive before treatment and the response of HBV DNA at the week 12 of treatment may be the predicting factors of the response at week 48 of IFN-α treatment in the CHB patients.
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