肝脏 ›› 2024, Vol. 29 ›› Issue (11): 1378-1381.

• 病毒性肝炎 • 上一篇    下一篇

聚乙二醇干扰素联合富马酸丙酚替诺福韦治疗慢性乙型肝炎的疗效

郑昌荣, 黄晓丽   

  1. 210031 江苏 南京医科大学第四附属医院消化内科
  • 收稿日期:2024-01-15 出版日期:2024-11-30 发布日期:2025-01-10
  • 基金资助:
    南京市中医药科技项目( ZYYB202219)

The therapeutic effect of polyethylene glycol interferon and propofol fumarate tenofovir in the treatment of chronic hepatitis B

ZHENG Chang-rong, HUANG Xiao-li   

  1. Department of Gastroenterology, the Fourth Affiliated Hospital of Nanjing Medical University, Jiangsu 210031, China
  • Received:2024-01-15 Online:2024-11-30 Published:2025-01-10

摘要: 目的 探讨聚乙二醇干扰素联合富马酸丙酚替诺福韦治疗慢性乙型肝炎患者的临床效果。方法 选取南京医科大学第四附属医院2021年1月至2022年12月治疗的慢性乙型肝炎患者131例,将其分为研究组66例和对照组65例。对照组采用基础治疗+富马酸丙酚替诺福韦,研究组在对照组基础上加用聚乙二醇干扰素,治疗48周后观察疗效。结果 治疗前,两组血清HBeAg、HBsAg、HBV DNA水平差异均无统计学意义(P>0.05)。治疗24周、48周后,两组血清HBeAg、HBsAg、HBV DNA均降低,研究组降低更显著(P<0.05);而HBV DNA转阴率差异无统计学意义(P>0.05);治疗48周后,研究组患者的HBeAg转阴率高于对照组(P<0.05);治疗前,两组血清ALT、AST、IL-17、IL-4、INF-α水平差异均无统计学意义(P>0.05);治疗48周后,两组血清ALT、AST、IL-17、IL-4水平均显著的降低(P<0.05),INF-α水平显著升高(P<0.05);研究组患者的血清ALT、AST、IL-17、IL-4水平较对照组降低更为显著(P<0.05),INF-α水平较对照组升高更为显著(P<0.05);治疗48周后研究组患者的总体疗效优于对照组,差异有统计学意义(P<0.05)。结论 聚乙二醇干扰素联合富马酸丙酚替诺福韦治疗慢性乙型肝炎有利于降低HBV标志物及炎症因子水平,可提高临床治疗效果。

关键词: 聚乙二醇干扰素, 富马酸丙酚替诺福韦, 慢性乙型肝炎, 抗病毒, 病毒载量

Abstract: Objective To explore the clinical efficacy of polyethylene glycol interferon combined with propofol tenofovir fumarate in the treatment of patients with chronic hepatitis B. Methods This study adopted a prospective research method and selected 131 patients with chronic hepatitis B admitted to our hospital from January 2021 to December 2022 for a single blind randomized trial. They were divided into a study group of 66 patients and a control group of 65 patients. The control group was treated with basic treatment and propofol tenofovir fumarate, while the study group added pegylated interferon to the treatment plan of the control group. The therapeutic effects were observed after 48 weeks of continuous treatment in both groups. Results Before treatment, there was no difference in serum levels of HBeAg, HBsAg, and HBV-DNA between the study group and the control group patients (P>0.05). After 24 and 48 weeks of treatment, the serum levels of HBeAg, HBsAg, and HBV-DNA in both groups decreased (P<0.05), with the study group showing a more significant decrease (P<0.05). There was no significant difference in the HBV-DNA conversion rate between the two groups of patients after 24 and 48 weeks of treatment (P>0.05). After 48 weeks of treatment, the HBeAg conversion rate in the study group was higher than that in the control group (P<0.05). Before treatment, two groups of serum levels of ALT, AST, IL-17, IL-4, and INF- α had no significant difference (P>0.05) and after 48 weeks of treatment, the serum levels of ALT, AST, IL-17, and IL-4 in both groups significantly decreased (P<0.05), and the serum level of INF- α was significantly increased (P<0.05). The serum levels of ALT, AST, IL-17, and IL-4 in the study group patients were significantly lower than those in the control group (P<0.05), and INF- α’s serum level increased more significantly when comparing to the control group (P<0.05). After 48 weeks of treatment, two groups’ clinical efficacy were evaluated. The overall efficacy of the study group was better than that of the control group, and the difference was statistically significant (P<0.05). Conclusion Polyethylene glycol interferon combined with propofol tenofovir fumarate in the treatment of chronic hepatitis B is conducive to reducing the levels of hepatitis B infection markers and inflammatory factors, which is generally conducive to improving the clinical treatment effect.

Key words: Polyethylene glycol interferon, Prophenofovir fumarate, Chronic hepatitis B, Antivirus, Virus load