肝脏 ›› 2025, Vol. 30 ›› Issue (9): 1215-1218.

• 肝纤维化及肝硬化 • 上一篇    下一篇

恩替卡韦抗病毒治疗逆转慢性乙型肝炎肝纤维化和早期肝硬化的临床观察

李凌洁, 杨明, 吴伟平, 吴亚男, 黄永鹏   

  1. 637600 南充 仪陇县人民医院(李凌洁,吴伟平,吴亚男,黄永鹏);637000 南充 川北医学院附属医院(杨明)
  • 收稿日期:2025-01-17 出版日期:2025-09-30 发布日期:2025-11-05
  • 通讯作者: 杨明,Eamil:yangming1211@nsmc.edu.cn
  • 基金资助:
    四川省科技计划项目(2020YFS0301)

A clinical observation on the reversal of liver fibrosis and early cirrhosis in patients with chronic hepatitis B by entecavir antiviral therapy

LI Ling-jie1, YANG Ming2, WU Wei-ping1, WU Ya-nan1, HUANG Yong-peng1   

  1. 1. Yilong County People's Hospital, Nanchong 637600,China;
    2. Affiliated Hospital of North Sichuan Medical College, Nanchong 637000,China
  • Received:2025-01-17 Online:2025-09-30 Published:2025-11-05
  • Contact: YANG Ming,Eamil:yangming1211@nsmc.edu.cn

摘要: 目的 观察恩替卡韦抗病毒治疗在逆转慢性乙型肝炎肝纤维化和早期肝硬化的临床应用。方法 选取2020年2月至2022年2月慢性乙型肝炎患者80例,在满足川北医学院附属医院药学部用药规范的前提下分成观察组、对照组。观察组予以恩替卡韦治疗,对照组予以聚乙二醇干扰素α-2b注射液治疗。比较两组乙型肝炎病毒指标、肝功能指标、肝纤维化指标和临床疗效。结果 观察组HBV DNA定量、HBsAg和HBeAg水平分别为(4.2±0.1)IU/mL、(848.6±115.6)U/mL和(181.3±70.0)U/mL,均显著低于对照组[(4.6±0.2)IU/mL、(939.1±125.2)U/mL和(222.2±82.3)U/mL,均P<0.05];治疗3个月后,观察组ALT、AST、Alb、TBil分别为(48.2±10.1)U/L、(45.6±15.6)U/L、(43.2±4.1)g/L、(18.3±3.0)μmol /L,显著低于对照组[(55.6±10.2)U/L、(56.1±15.2)U/L、(41.1±3.2)g/L、(20.2±4.1)μmol /L,均P<0.05];治疗后观察组透明质酸、Ⅲ型前胶原、层黏连蛋白、Ⅳ型胶原为(84.22±28.1)、(38.2±5.6)、(36.2±5.1)、(69.6±6.6),均显著低于对照组[(115.1±40.2)、(41.1±5.2)、(40.1±6.2)、(76.1±8.2),均P<0.05]。结论 恩替卡韦抗病毒治疗在迅速恢复患者肝功能的同时,还可以进一步降低各项乙肝病毒指标以及肝纤维化指标,临床疗效确切。

关键词: 恩替卡韦, 逆转慢性乙型肝炎, 肝纤维化, 早期肝硬化

Abstract: Objective To observe the clinical application of entecavir antiviral therapy in reversing liver fibrosis and early cirrhosis in patients with chronic hepatitis B. Methods Eighty patients with chronic hepatitis B between February 2020 and February 2022 were selected in this study. They were divided into an observation group and a control group on the premise of meeting the drug use standard of the pharmacy department of the affiliated hospital of North Sichuan Medical College. Patients in the former group were given entecavir and those in the latter group were given pegylated interferon α-2b injection. The indexes of hepatitis B virus, liver function, liver fibrosis and clinical efficacy of the above groups were compared. Results In the observation group, the levels of deoxyribonucleic acid quantification of hepatitis B virus (HBV DNA), hepatitis B surface antigen (HBsAg), and hepatitis B virus e antigen (HBeAg) were (4.2 ± 0.1) IU/mL, (848.6 ± 115.6) U/mL, and (181.3 ± 70.0) U/mL respectively, all of which were significantly lower than those of [(4.6 ± 0.2) IU/mL, (939.1 ± 125.2) U/mL, and (222.2 ± 82.3) U/mL, P<0.05] in the control group. After 3 months of treatment, the levels of alanine aminotransferase (ALT), aspartate aminotransferase (AST), albumin (Alb), and total bilirubin (TBil) in the observation group were (48.2 ± 10.1) U/L, (45.6 ± 15.6) U/L, (43.2 ± 4.1) g/L, and (18.3 ± 3.0) μmol/L respectively, which were significantly lower than those of [(55.6 ± 10.2) U/L, (56.1 ± 15.2) U/L, (41.1 ± 3.2) g/L, and (20.2 ± 4.1) μmol/L, P<0.05] in the control group. After treatment, the levels of hyaluronic acid, type Ⅲ procollagen, laminin, and type Ⅳ collagen in the observation group were (84.22 ± 28.1), (38.2 ± 5.6), (36.2 ± 5.1), and (69.6 ± 6.6) respectively, all of which were significantly lower than those of [(115.1 ± 40.2), (41.1 ± 5.2), (40.1 ± 6.2), and (76.1 ± 8.2), P<0.05] in the control group. Conclusion Entecavir antiviral therapy can not only quickly restore liver function, but also further reduce the indicators of hepatitis B viral infection and liver fibrosis, with definite clinical effect.

Key words: Entecavir, Chronic hepatitis B, Liver fibrosis, Early cirrhosis, Reversal