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比较拉米夫定、阿德福韦酯、替比夫定和恩替卡韦治疗 HBeAg 阴性乙型肝炎中具有中等 HBV DNA 水平的核苷酸类似物初治患者的疗效。

Comparing Efficacy of Lamivudine, Adefovir Dipivoxil, Telbivudine, and Entecavir in Treating Nucleoside Analogues Naïve for HBeAg-Negative Hepatitis B with Medium Hepatitis B Virus (HBV) DNA Levels.

机构信息

Department of Infectious Diseases, The Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou, Guangdong, China (mainland).

Department of Infectious Diseases, The Fifth Affiliated Hospital of Sun Yat-Sen University, Zhuhai, Guangdong, China (mainland).

出版信息

Med Sci Monit. 2017 Nov 2;23:5230-5236. doi: 10.12659/msm.903382.

DOI:10.12659/msm.903382
PMID:29095799
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5680675/
Abstract

BACKGROUND The antiviral effect of HBV in different nucleos (t) ide analogues is still not well known. This study was conducted to compare the effectiveness of lamivudine (LMV), adefovir dipivoxil (ADV), telbivudine (LdT), and entecavir (ETV) monotherapy in chronic HBeAg-negative hepatitis B patients with medium load of HBV DNA. MATERIAL AND METHODS The effective data of 207 patients treated by LMV (n=43), ADV (n=57), LdT (n=54) or ETV (n=53) were collected and analyzed during 144-week follow-up by retrospective analysis. RESULTS Serum HBV DNA levels were significantly lower in the ETV group 1.91±0.45 log10 IU/ml) than in the LdT group (2.09±0.62 log10 IU/ml), ADV group (2.26±0.73 log10 IU/ml), and LMV group (2.08±0.75 log10 IU/ml) at 12 weeks (P=0.0464). HBV DNA levels were maintained at lower levels in the ETV group compared to other 3 groups during follow-up (48 weeks, P<0.001; 96 weeks, P<0.001). Multivariate Cox regression analysis showed that LMV (P=0.001), ADV, (P<0.001), and LdT (P<0.001) were all negative predictors of HBV DNA-negative time, but ETV was not. Viral breakthrough occurred in 34.8% (15/43) of patients in the LMV group; 5.26% (3/57) in the ADV group, 7.4.0% (4/54) in the LdT group, and 0% (0/53) in the ETV group at the end of follow-up. No significant differences were found in mean ALT levels (all P>0.05) or in cumulative normalization rates (P=0.473). CONCLUSIONS ETV was more potent and faster for viral response and lower viral breakthrough in medium load of HBV DNA when compared to LMV, ADV, or LdT monotherapy in HBeAg-negative CHB.

摘要

背景

不同核苷(酸)类似物的抗乙肝病毒效果仍不明确。本研究旨在比较拉米夫定(LMV)、阿德福韦酯(ADV)、替比夫定(LdT)和恩替卡韦(ETV)单药治疗中载量中等的 HBV DNA 慢性 HBeAg 阴性乙型肝炎患者的疗效。

材料和方法

通过回顾性分析,收集并分析了 207 例接受 LMV(n=43)、ADV(n=57)、LdT(n=54)或 ETV(n=53)治疗的患者在 144 周随访期间的有效数据。

结果

治疗 12 周时,与 LdT 组(2.09±0.62 log10 IU/ml)、ADV 组(2.26±0.73 log10 IU/ml)和 LMV 组(2.08±0.75 log10 IU/ml)相比,ETV 组患者血清 HBV DNA 水平显著降低(1.91±0.45 log10 IU/ml)(P=0.0464)。与其他 3 组相比,ETV 组在随访期间(48 周,P<0.001;96 周,P<0.001)HBV DNA 水平保持较低水平。多变量 Cox 回归分析显示,LMV(P=0.001)、ADV(P<0.001)和 LdT(P<0.001)均为 HBV DNA 阴转时间的负预测因子,但 ETV 不是。治疗结束时,LMV 组有 34.8%(15/43)的患者发生病毒突破;ADV 组 5.26%(3/57)、LdT 组 7.4.0%(4/54)和 ETV 组 0%(0/53)。各组平均 ALT 水平(均 P>0.05)或累积正常化率(P=0.473)无显著差异。

结论

与 LMV、ADV 或 LdT 单药治疗相比,ETV 治疗 HBeAg 阴性 CHB 患者时,对中载量 HBV DNA 具有更强的病毒抑制作用,病毒学突破率更低。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5680675/dce10695096e/medscimonit-23-5230-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5680675/fff1c247efca/medscimonit-23-5230-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5680675/cfad343390b4/medscimonit-23-5230-g002.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5680675/fff1c247efca/medscimonit-23-5230-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5680675/cfad343390b4/medscimonit-23-5230-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9734/5680675/dce10695096e/medscimonit-23-5230-g003.jpg

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