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慢性乙肝病毒携带者抗病毒治疗有效性与安全性研究现状

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目的:通过检索国内外数据库,对慢性乙型肝炎病毒携带者(chronic hepatitis B virus carriers,CHBVC)抗病毒治疗的有效性与安全性进行系统评价.方法:采用计算机检索PubMed、Embase、Cochrane Library、Web of Science、知网、万方、维普和中国生物医学文献数据库,筛选关于CHBVC抗病毒治疗核苷类似物(nucleoside analogue,NA)单用方案,α干扰素(interferon alpha,IFNα)单用方案及NA+IFNα联合方案的临床随机对照研究或队列研究文献,并使用Stata17进行Meta分析.结果:共纳入28篇文献,涉及1 623例CHBVC患者接受抗病毒治疗.有效性分析:HBsAg血清清除率为20%(338/1 421),其中HBeAg阴性组HBsAg清除率高达52.9%,阳性组仅为1.5%;HBeAg阴性组中HBV DNA<2 000 IU/mL组的HBsAg清除率为45.6%,HBV DNA<20 IU/mL组的HBsAg清除率可达59.9%.HBsAg血清转化率为15.3%(196/946),其中HBeAg阴性组HBsAg转化率较高(38.2%),阳性组未见明显变化;HBeAg阴性组中HBV DNA<2 000 IU/mL组的HBsAg转化率为34.5%,而HBV DNA<20 IU/mL组的HBsAg血清转化率可达49.4%.HBeAg血清阴转率为6.6%(34/465),随着治疗时间延长呈逐渐上升趋势,在192周时可达8.8%.HBeAg血清转化率为8%(63/700),在96周时最高(24%),同时NA+IFNα联合方案比NA单用更具优势(8.1%vs.5.4%).HBV DNA血清阴转率总体达到70.1%(500/738).安全性分析:共有494例患者被纳入8篇文献进行不良事件发生情况统计,总体不良事件发生率约为5.4%(28/494).结论:CHBVC抗病毒治疗有较高的有效性和安全性,NA+IFNα联合方案及长期治疗方案对改善CHBVC效益更为明显.
Efficacy and safety of antiviral therapy in chronic hepatitis B virus carriers
Objective:To investigate the efficacy and safety of antiviral therapy in chronic hepatitis B virus carriers(CHBVCs)through a systematical review by searching the databases in China and globally.Methods:PubMed,Embase,the Cochrane Library,Web of Science,CNKI,Wanfang Data,VIP,and CMB were searched for randomized controlled clinical trials or cohort studies on antiviral therapy for CHBVC,with the regimens of nucleos(t)ide analogue(NA)alone,interferon-α(IFNα)alone,and NA combined with IFNα,and Stata17 was used to perform the meta-analysis.Results:A total of 28 articles were included,involving 1623 CHBVCs who received antiviral therapy.As for the analysis of efficacy,serum HBsAg clearance rate was 20%(338/1421),and the HBeAg negative group had an HBsAg clearance rate as high as 52.9%,while the HBeAg positive group had a clearance of 1.5%;in the HBeAg negative group,the HBV DNA<2000 IU/mL group had an HBsAg clearance rate of 45.6%,while the HBV DNA<20 IU/mL group had an HBsAg clearance rate of 59.9%.The HBsAg seroconversion rate was 15.3%(196/946),and the HBeAg negative group had a relatively high HBsAg seroconversion rate of 38.2%,while no significant change was observed in the HBeAg positive group;in the HBeAg negative group,the HBV DNA<2000 IU/mL group had an HBsAg seroconversion rate of 34.5%,while the HBV DNA<20 IU/mL group had an HBsAg seroconversion rate of 49.4%.The serum HBeAg clearance rate was 6.6%(34/465),which gradually increased over the course of treatment and reached 8.8%at week 192.The HBeAg seroconversion rate was 8%(63/700),with the highest rate of 24%at week 96,and the combination of NA and IFNα was superior to NA alone(8.1%vs.5.4%).The overall serum HBV DNA clearance rate reached 70.1%(500/738).In the analysis of safety,a statistical analysis of adverse events was performed among 494 patients in 8 articles,and the results showed that the overall incidence rate of adverse events was about 5.4%(28/494).Conclusion:Antiviral therapy has good efficacy and safety in CHBVCs,and the NA+IFNαregimen and the long-term treatment regimen have significant benefits in CHBVCs.

chronic hepatitis B virus carriersantiviral therapynucleos(t)ide analogueinterferon-αmeta-analysis

李芮、唐霓、游子杰、姚云清

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重庆医科大学附属第一医院感染科,重庆 400016

重庆医科大学感染性疾病分子生物学教育部重点实验室,重庆 400016

慢性乙型肝炎病毒携带者 抗病毒治疗 核苷类似物 α干扰素 Meta分析

国家自然科学基金资助项目

82272975

2024

重庆医科大学学报
重庆医科大学

重庆医科大学学报

CSTPCD北大核心
影响因子:0.724
ISSN:0253-3626
年,卷(期):2024.49(8)
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