估算慢性乙型肝炎病毒感染免疫耐受期患者的主要结局和肝细胞癌风险:系统回顾和荟萃分析。

IF 9 2区 医学 Q1 VIROLOGY Reviews in Medical Virology Pub Date : 2024-07-01 DOI:10.1002/rmv.2570
Min Liu, Taixue Zhao, Jinyang Zhang, Bing Bu, Ruyi Zhang, Xueshan Xia, Jiawei Geng
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引用次数: 0

摘要

处于免疫耐受(IT)期的慢性乙型肝炎病毒(HBV)感染患者是否应该接受抗病毒治疗以及确定最佳治疗方案的问题仍不明确。我们对 PubMed、Embase、MEDLINE、Cochrane Library 和万方数据进行了全面检索,检索时间从开始到 2023 年 12 月 5 日。纳入了报告慢性 HBV 感染 IT 阶段患者 HBV DNA 检测不到、HBeAg 阳性减低或血清转换、HBsAg 阳性减低或血清转换以及肝细胞癌(HCC)发病率等关键结果的研究。总共纳入了 23 项研究。在 48 周的随访中,约有 4% 的 IT 期患者自发出现 HBeAg 消失。抗病毒治疗对 HBV DNA 阴性转阴产生了有利影响(儿童:风险比 [RR] = 6.83,95% CI:2.90-16.05;成人:风险比 [RR] = 25.84,95% CI:2.90-16.05):RR = 25.84,95% CI:6.47-103.31)和 HBsAg 消失率(儿童:RR = 9.49,95% CI:6.47-103.31):RR=9.49,95% CI:1.74-51.76;成人:IT阶段患者的HBsAg丢失率(儿童:RR=9.49,95% CI:1.74-51.76;成人:RR=7.35,95% CI:1.41-38.27)。亚组分析显示,在IT阶段的成人患者中,干扰素加核苷(t)ide类似物(NA)治疗患者的HBsAg丢失或血清转换率总和高于NA单药治疗患者(9%对0%)。此外,IT 阶段患者的汇总年度 HCC 发病率为每千人年 3.03 例(95% CI:0.99-5.88)。处于 IT 期的成人患者的 HCC 发病率风险明显低于 HBeAg 阳性的不确定期患者(RR = 0.46,95% CI:0.32-0.66),IT 期和免疫活性期之间未观察到显著差异。目前,仅从降低 HCC 发生风险的角度来看,还没有足够的证据建议对处于 IT 期的慢性 HBV 感染患者进行治疗。不过,处于 IT 期的成人和儿童患者对抗病毒治疗反应良好,HBsAg 下降或血清转换率较高。
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Estimating the key outcomes and hepatocellular carcinoma risk in patients in immune-tolerant phase of chronic hepatitis B virus infection: A systematic review and meta-analysis.

The question of whether patients in the immune-tolerant (IT) phase of chronic hepatitis B virus (HBV) infection should undergo antiviral therapy and determine the optimal regimen remains unclear. A comprehensive search of PubMed, Embase, MEDLINE, Cochrane Library, and Wanfang Data from inception to 5 December 2023, was conducted. Studies reporting on key outcomes such as HBV DNA undetectability, HBeAg loss or seroconversion, HBsAg loss or seroconversion, and hepatocellular carcinoma (HCC) incidence in patients in the IT phase of chronic HBV infection were included. In total, 23 studies were incorporated. Approximately 4% of patients in the IT phase achieved spontaneous HBeAg loss over 48 weeks of follow-up. Antiviral therapy demonstrated a favourable impact on HBV DNA negative conversion (Children: risk ratios [RR] = 6.83, 95% CI: 2.90-16.05; Adults: RR = 25.84, 95% CI: 6.47-103.31) and HBsAg loss rates (Children: RR = 9.49, 95% CI: 1.74-51.76; Adults: RR = 7.35, 95% CI: 1.41-38.27) for patients in the IT phase. Subgroup analysis revealed that in adult patients in the IT phase, interferon plus nucleos(t)ide analogues (NA)-treated patients exhibited a higher pooled rate of HBsAg loss or seroconversion than those treated with NA monotherapy (9% vs. 0%). Additionally, the pooled annual HCC incidence for patients in the IT phase was 3.03 cases per 1000 person-years (95% CI: 0.99-5.88). Adult patients in the IT phase had a significantly lower HCC incidence risk than HBeAg-positive indeterminate phase patients (RR = 0.46, 95% CI: 0.32-0.66), with no significant differences observed between IT and immune-active phases. Presently, there is insufficient evidence solely based on reducing the risk of HCC incidence, to recommend treating patients in the IT phase of chronic HBV infection. However, both adult and paediatric patients in the IT phase responded well to antiviral therapy, showing favourable rates of HBsAg loss or seroconversion.

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来源期刊
Reviews in Medical Virology
Reviews in Medical Virology 医学-病毒学
CiteScore
21.40
自引率
0.90%
发文量
88
期刊介绍: Reviews in Medical Virology aims to provide articles reviewing conceptual or technological advances in diverse areas of virology. The journal covers topics such as molecular biology, cell biology, replication, pathogenesis, immunology, immunization, epidemiology, diagnosis, treatment of viruses of medical importance, and COVID-19 research. The journal has an Impact Factor of 6.989 for the year 2020. The readership of the journal includes clinicians, virologists, medical microbiologists, molecular biologists, infectious disease specialists, and immunologists. Reviews in Medical Virology is indexed and abstracted in databases such as CABI, Abstracts in Anthropology, ProQuest, Embase, MEDLINE/PubMed, ProQuest Central K-494, SCOPUS, and Web of Science et,al.
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