Unité d'Épidémiologie des Maladies Émergentes, Institut Pasteur, Paris, France.
Global Hepatitis Programme, World Health Organization, Geneva, Switzerland.
Lancet Infect Dis. 2021 Jan;21(1):85-96. doi: 10.1016/S1473-3099(20)30593-4. Epub 2020 Aug 14.
Prevention of mother-to-child transmission (MTCT) of hepatitis B virus (HBV) involves neonatal immunoprophylaxis, with a birth dose of hepatitis B vaccine and immune globulin, and provision of peripartum antiviral prophylaxis in highly viraemic women. However, access to assays to quantify HBV DNA levels remains inadequate in resource-poor settings. This study was commissioned by WHO and aimed to identify the HBV DNA threshold for MTCT, to assess the sensitivity and specificity of hepatitis B e antigen (HBeAg) testing to identify pregnant women with HBV DNA levels above this threshold, and to predict MTCT of HBV infection on the basis of HBeAg testing.
For this systematic review and meta-analysis, we searched the PubMed, EMBASE, Scopus, CENTRAL, CNKI, and Wanfang databases for studies of pregnant women with chronic HBV infection without concurrent antiviral therapy, published between Jan 1, 2000, and April 3, 2019. Studies were eligible for inclusion if MTCT in mother-child pairs could be stratified by different levels of maternal HBV DNA during pregnancy, if maternal HBeAg status could be stratified by HBV DNA level, and if the MTCT status of infants could be stratified by maternal HBeAg status during pregnancy. Studies that selected pregnant women on the basis of HBeAg serostatus or HBV DNA levels were excluded. Aggregate data were extracted from eligible studies by use of a pre-piloted form; study authors were contacted to clarify any uncertainties about potential duplication or if crucial information was missing. To pool sensitivities and specificities of maternal HBeAg to identify highly viraemic women and to predict MTCT events, we used the DerSimonian-Laird bivariate random effects model. This study is registered with PROSPERO, CRD42019138227.
Of 9007 articles identified, 67 articles (comprising 66 studies) met the inclusion criteria. The risk of MTCT despite infant immunoprophylaxis was negligible (0·04%, 95% CI 0·00-0·25) below a maternal HBV DNA level of 5·30 log IU/mL (200 000 IU/mL) and increased above this threshold. The pooled sensitivity of HBeAg testing to identify HBV DNA levels of 5·30 log IU/mL or greater in pregnant women was 88·2% (83·9-91·5) and pooled specificity was 92·6% (90·0-94·5). The pooled sensitivity of HBeAg testing in predicting MTCT of HBV infection despite infant immunoprophylaxis was 99·5% (95% CI 91·7-100) and pooled specificity was 62·2% (55·2-68·7).
Maternal HBV DNA of 5·30 log IU/mL or greater appears to be the optimal threshold for MTCT of HBV infection despite infant immunoprophylaxis. HBeAg is accurate to identify women with HBV DNA levels above this threshold and has high sensitivity to predict cases of immunoprophylaxis failure. In areas where HBV DNA assays are unavailable, HBeAg can be used as an alternative to assess eligibility for antiviral prophylaxis.
World Health Organization.
乙型肝炎病毒(HBV)母婴传播(MTCT)的预防包括新生儿免疫预防,即出生时接种乙肝疫苗和免疫球蛋白,并为高病毒载量的女性提供围产期抗病毒预防。然而,在资源匮乏的环境中,HBV DNA 水平检测的应用仍然不足。本研究由世界卫生组织委托进行,旨在确定 MTCT 的 HBV DNA 阈值,评估乙型肝炎 e 抗原(HBeAg)检测识别 HBV DNA 水平超过此阈值的孕妇的敏感性和特异性,并基于 HBeAg 检测预测 HBV 感染的 MTCT。
本系统评价和荟萃分析检索了 2000 年 1 月 1 日至 2019 年 4 月 3 日期间发表的没有同时进行抗病毒治疗的慢性 HBV 感染孕妇的 PubMed、EMBASE、Scopus、CENTRAL、CNKI 和万方数据库,以筛选出符合条件的研究。如果母婴对可以根据孕妇怀孕期间不同水平的 HBV DNA 进行分层,如果 HBeAg 状态可以根据 HBV DNA 水平进行分层,并且如果婴儿的 MTCT 状态可以根据孕妇怀孕期间的 HBeAg 状态进行分层,那么研究就有资格纳入。排除了根据 HBeAg 血清学状态或 HBV DNA 水平选择孕妇的研究。使用预编制的表格从合格的研究中提取汇总数据;如果存在潜在的重复或关键信息缺失的不确定性,会联系研究作者进行澄清。为了汇总 HBeAg 识别高病毒载量女性和预测 MTCT 事件的敏感性和特异性,我们使用了 DerSimonian-Laird 双变量随机效应模型。本研究已在 PROSPERO 注册,CRD42019138227。
从 9007 篇文章中,有 67 篇文章(包括 66 项研究)符合纳入标准。尽管婴儿免疫预防,但在 HBV DNA 水平低于 5.30 log IU/mL(200000 IU/mL)时,MTCT 的风险可忽略不计(0.04%,95%CI 0.00-0.25),且风险随着阈值的升高而增加。HBeAg 检测识别孕妇 HBV DNA 水平为 5.30 log IU/mL 或更高的敏感性为 88.2%(83.9-91.5),特异性为 92.6%(90.0-94.5)。HBeAg 检测预测婴儿免疫预防后 HBV 感染 MTCT 的敏感性为 99.5%(95%CI 91.7-100),特异性为 62.2%(55.2-68.7)。
HBV DNA 水平为 5.30 log IU/mL 或更高似乎是 HBV 感染 MTCT 尽管婴儿免疫预防的最佳阈值。HBeAg 可准确识别 HBV DNA 水平超过此阈值的女性,并且具有预测免疫预防失败病例的高敏感性。在无法进行 HBV DNA 检测的地区,HBeAg 可作为评估抗病毒预防资格的替代方法。
世界卫生组织。