实用肝脏病杂志 ›› 2019, Vol. 22 ›› Issue (1): 93-96.doi: 10.3969/j.issn.1672-5069.2019.01.025

• 肝硬化 • 上一篇    下一篇

恩替卡韦联合聚乙二醇干扰素或胸腺素治疗代偿期乙型肝炎肝硬化2年疗效随访*

曹艳平, 隋洪婷, 潘猛, 曲宝聚, 朴红心   

  1. 133000 吉林省延吉市 延边大学(曹艳平,隋洪婷,潘猛); 附属医院感染病科(曲宝聚,朴红心)
  • 收稿日期:2018-01-19 出版日期:2019-01-10 发布日期:2019-01-16
  • 通讯作者: 朴红心,E-mail:15526770394@163.com
  • 作者简介:曹艳平,女,硕士研究生。E-mail:569905136@qq.com
  • 基金资助:
    *国家科技重大专项973课题(编号:2017ZX10203202-003-006)

Efficacy of entecavir and peg-IFNα-2a or thymosin α1 combination in the treatment of patient with compensated hepatitis B liver cirrhosis

Cao Yanping, Sui Hongting, Pan Meng, et al.   

  1. Department of Infectious Diseases,Affiliated Hospital,Yanbian University,Yanji 133000,Jilin Province,China
  • Received:2018-01-19 Online:2019-01-10 Published:2019-01-16

摘要: 目的 探讨应用恩替卡韦联合聚乙二醇干扰素α-2a(PEG-IFNα-2a)或胸腺素治疗代偿期乙型肝炎肝硬化患者的效果。方法 在88例代偿期乙型肝炎肝硬化患者中,接受恩替卡韦治疗者38例,接受恩替卡韦联合PEG-IFNα-2a治疗者17例,联合胸腺素治疗者33例,随访2年。结果 恩替卡韦治疗组治疗前和治疗104 w末血清HBV DNA水平分别为(5.6±1.7) IU/ml和(1.0±0.7) IU/ml(P<0.05),联合PEG-IFNα-2a组分别为(5.8±1.3) IU/ml和(1.0±0.7) IU/ml(P<0.05),联合胸腺素组分别为(6.1±2.0) IU/ml和(1.0±0.9) IU/ml(P<0.05);恩替卡韦组治疗前和治疗104 w末血清ALB水平分别为(43.1±5.4) g/L和(46.9±4.9) g/L(P<0.05),联合胸腺素组分别为(43.0±4.0) g/L和(46.8±5.4) g/L(P<0.05);三组治疗前和治疗104 w末肝脏硬度值和INR无统计学差异(P>0.05)。结论 恩替卡韦能有效抑制HBV DNA复制,维持代偿期肝硬化患者的肝功能,本研究结果看不出联合用药有任何好处,需要进一步观察。

关键词: 肝硬化, 乙型肝炎, 恩替卡韦, 聚乙二醇干扰素, 胸腺素, 疗效

Abstract: Objective To evaluate the efficacy of entecavir and peg-IFNα-2a or thymosin α1 combination in the treatment of patient with compensated hepatitis B liver cirrhosis. Methods In this study,88 patients with compensated hepatitis B cirrhosis were selected,and 38 received entecavir, 17 received entecavir combined with PEG-IFNα-2a and 33 received entecavir and thymosin α1 combination for 104 weeks. Results Serum HBV DNA levels in the entecavir monotherapy group before treatment and at the end of 104 week were (5.6±1.7) IU/ml and (1.0±0.7) IU/ml,respectively (P<0.05),in PEG-IFNα-2a combination group were (5.8±1.3) IU/ml and (1.0±0.7) IU/ml,respectively(P<0.05) and in combined with thymosin group were (6.1±2.0) IU/ml and(1.0±0.9) IU/ml, respectively(P<0.05);serum albumin levels in the entecavir group before treatment and at the end of 104 week were (43.1±5.4) g/L and (46.9±4.9) g/L,respectively (P<0.05),and in combined thymosin group were (43.0±4.0) g/L and(46.8±5.4)g/L,respectively(P<0.05);there were no significant differences as respect to liver stiffness measures and INRs among the three groups (P>0.05). Conclusion Entecavir monotherapy could effectively inhibit the replication of HBV DNA, and improve liver function tests and we don’t find any advantages of combination with PEG-IFNα-2a or thymosin-α1 from the results of this study.

Key words: Liver cirrhosis, Hepatitis B, Entecavir, Peg-IFNα-2a, Thymosin-α1, Therapy