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1.404000 重庆,重庆大学附属三峡医院肝病科
2.400038 重庆,陆军军医大学(第三军医大学)第一附属医院肝胆外科
[刘书宏, E-mail: 57485971@qq.com LIU Shuhong, E-mail: 57485971@qq.com
收稿:2021-07-18,
修回:2021-11-03,
纸质出版:2022-01-30
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安选, 刘书宏, 夏莉娜, 等. HBeAg/HBeAb双阳性慢性乙型肝炎患者不同抗病毒方案疗效及临床转归分析[J]. 陆军军医大学学报, 2022,44(2):162-167.
Xuan AN, Shuhong LIU, Lina XIA, et al. Efficacy and clinical outcomes of different antiviral regimens in HBeAg/HBeAb double-positive patients with chronic hepatitis B[J]. Journal of Army Medical University, 2022, 44(2): 162-167.
安选, 刘书宏, 夏莉娜, 等. HBeAg/HBeAb双阳性慢性乙型肝炎患者不同抗病毒方案疗效及临床转归分析[J]. 陆军军医大学学报, 2022,44(2):162-167. DOI: 10.16016/j.2097-0927.202107114.
Xuan AN, Shuhong LIU, Lina XIA, et al. Efficacy and clinical outcomes of different antiviral regimens in HBeAg/HBeAb double-positive patients with chronic hepatitis B[J]. Journal of Army Medical University, 2022, 44(2): 162-167. DOI: 10.16016/j.2097-0927.202107114.
目的
2
分析HBeAg/HBeAb双阳性慢乙肝患者的临床特征,并探讨其抗病毒疗效及临床转归。
方法
2
选取2014-2018年重庆三峡中心医院就诊的HBeAg及HBeAb双阳性慢性乙肝且符合抗病毒治疗标准的患者158例,按实际接收的治疗方案分为恩替卡韦抗病毒组(52例)、干扰素治疗组(49例)、未抗病毒治疗的对照组(57例),随访48周。观察不同处理组治疗前后疗效及患者的转归情况。
结果
2
基线HBeAg、HBeAb分布情况: 158例HBeAg/HBeAb双阳性慢乙肝患者中,HBeAg≥10患者79例,HBeAb
<
10的患者79例,各占50%;HBV DNA水平为(4.77±1.23)Lg;抗病毒疗效: 恩替卡韦组HBV DNA下降幅度及HBV DNA转阴率、ALT复常率方面均优于干扰素组(
P
<
0.05);而干扰素治疗组则在HBeAg下降幅度、HBeAb下降幅度以及HBeAg转阴率优于恩替卡韦组(
P
<
0.05);转归: 与未抗病毒治疗组相比,抗病毒治疗后转为HBeAg阴性的患者比例及转为“仅HBsAg及HBcAb阳性的慢乙肝”患者比例明显增高(
P
<
0.05);而未抗病毒治疗组持续“双阳性”的比例明显高于抗病毒治疗组(
P
<
0.05);治疗前后HBeAg-Lg/HBeAb下降幅度预测HBeAg转阴的价值最大。HBeAg/HBeAb双阳性慢乙肝患者HBeAg及HBeAb滴度处于偏低水平,HBV DNA处于相对较低水平;监测HBeAg-Lg/HBeAb下降幅度有助于判断阳性HBeAg转阴率。
结论
2
对于HBeAg/HBeAb双阳性慢性乙肝患者
应用干扰素在HBeAg转阴上具有较大优势;HBeAg-Lg/HBeAb下降幅度在临床转归方面具有良好的预测效能。
Objective
2
To analyze the clinical features of HBeAg and HBeAb double-positive patients with chronic hepatitis B
and explore the efficacy and outcomes of different antiviral regimens.
Methods
2
A total of 158 HBeAg and HBeAb double-positive patients with chronic hepatitis B who met the antiviral treatment criteria were selected from Chongqing Three Gorges Hospital from 2014 to 2018. They were divided into entecavir treatment group (
n
=52)
interferon treatment group (
n
=49)
and control group (without antiviral treatment
n
=57) according to the actual treatment regimen
and were followed up for 48 weeks. The efficacy and outcomes of patients were observed and compared among different groups.
Results
2
Baseline distribution of HBeAg and HBeAb: among 158 HBeAg/HBeAb double positive chronic hepatitrs B patients
79 patients had HBeAg≥10
and 79 patieats had HBeAg
<
10
each accounting for 50%; H
BV DNA level was 4.77±1.23 Lg. Antiviral efficacy: the decrease of HBV DNA level
the HBV DNA negative conversion rate
and the normalization rate of ALT were all better in the entecavir group than the interferon group (
P
<
0.05)
while the decline of HBeAg and HBeAb levels
as well as the HBeAg negative conversion rate were greater in the interferon group (
P
<
0.05). Clinical outcomes: the proportion of patients who became HBeAg negative or only presented HBsAg and HBcAb positive was significantly larger in the antiviral groups as compared with the control group (
P
<
0.05)
while the control group showed higher proportion of continuous "double-positive" (
P
<
0.05). In addition
the decrease range of HBeAg-Lg/HBeAb ratio before and after treatment had the greatest value in predicting HBeAg negative conversion.
Conclusion
2
For HBeAg and HBeAb double-positive patients with chronic hepatitis B
interferon treatment shows greater advantage in HBeAg negative conversion. Monitoring the decline of HBeAg-Lg/HBeAb is helpful to predict clinical outcome in the double-positive patients.
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