首都医科大学学报 ›› 2010, Vol. 31 ›› Issue (5): 573-577.

• 慢性乙肝临床转归个体化治疗预测模型研究 • 上一篇    下一篇

核苷(酸)类似物治疗失代偿期乙肝肝硬化的随访研究

杨烨, 陈景寿, 欧晓娟, 贾继东, 尤红*

  

  1. 首都医科大学附属北京友谊医院肝病中心
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2010-10-21 发布日期:2010-10-21
  • 通讯作者: 尤红

Follow up Study of HBV-induced Decompensated Cirrhosis Treated with Nucleot(s)ide Analogues

YANG Ye, CHEN Jing-shou, OU Xiao-juan, JIA Ji-dong, YOU Hong*

  

  1. Liver Research Center, Beijing Friendship Hospital, Capital Medical University
  • Received:1900-01-01 Revised:1900-01-01 Online:2010-10-21 Published:2010-10-21
  • Contact: YOU Hong

摘要: 目的 观察中国上市的4种核苷(酸)类似物拉米夫定(lamivudine,LAM)、阿德福韦酯(adefovir,ADV)、恩替卡韦(entecavir,ETV)和替比夫定(telbivudine,LDT)治疗失代偿期乙肝肝硬化对病毒复制、肝功能以及病程进展的影响。方法 接受及未接受核苷(酸)类似物抗病毒治疗的失代偿期乙肝肝硬化患者52例,中位随访时间为11个月,在随访开始、第1年每3月1次、以后每6月1次,定期监测HBV DNA、肝功能、Child-Pugh评分、MELD评分等指标和安全性,对比用药前后各项指标变化。结果 共111例符合入组条件的乙肝肝硬化失代偿期患者,因各种原因排除59例,最终52例入选,其中治疗组40例,对照组12例。对照组中HBV DNA、血清丙氨酸氨基转移酶(alanine aminotransferase,ALT)、门冬氨酸氨基转移酶(aspartate aminotransferase,AST)、白蛋白(albumin,ALB)、总胆红素(total bilinobin,TBIL)、胆碱酯酶(cholinesterase,CHE)、国际标准化比值(international normalized ratio,INR)、ChildPugh评分、MELD评分在随访期间差异无统计学意义;在治疗组中,HBV DNA、ALT、ALB、CHE、INR、ChildPugh评分在核苷(酸)类似物治疗前后有显著改善(P<0.05),而AST、TBIL、MELD评分在治疗前后无明显变化。结论 失代偿期乙肝肝硬化患者应用核苷(酸)类似物治疗,可以抑制HBV DNA的复制,改善肝功能,稳定或逆转疾病进展,安全性较好。

关键词: 核苷(酸)类似物, 抗病毒治疗, 失代偿期肝硬化, 乙型肝炎病毒

Abstract:

Objective To observes the efficacy of the four nucleot(s)ide analogues including lamivudine, adefovir, entecavir and telbivudine in treatment of HBV-induced decompensated cirrhosis. Methods Patients with HBV-induced decompensated hepatitis B cirrhosis treated with and without nucleot(s)ide analogues(NAs) were followed up for a median of 11 months. HBV DNA, liver function, Child-Pugh-Turcotte scores, and MELD scores. Results A total of 52 patients were enrolled in this study after excluding 59 patients out of 111 patients with HBV-induced decompensated hepatitis B cirrhosis. Forty patients were assigned into the NAs group and 12 patients into the control group. In the control group, the HBV DNA, ALT, AST, ALB, TBIL, CHE, INR, Child-Pugh scores and MELD scores had no improvement between as compared with the baseline values and the end-of-follow up values. In the NAs group, the HBV DNA, ALT, ALB, CHE, INR, Child-Pugh scores had significant improvement(P<0.05) and AST, TBIL, MELD scores had no improvement(P>0.05). Conclusion Nucleot(s)ide analogues could suppress HBV replication, improve liver function,stabilize or even reverse the development of decompensated cirrhosis and be welltolerated. Further studies are needed to observe the longterm efficacy and the rate of liver cancer development.

Key words: nucleot(s)ide analogues, antiviral therapy, decompensated hepatic cirrhosis, hepatitis B virus

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