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Hepatitis B Core-Related Antigen to Indicate High Viral Load: Systematic Review and Meta-Analysis of 10,397 Individual Participants

Authors :
Gian Paolo Caviglia
Maud Lemoine
Masao Honda
Enagnon Kazali Alidjinou
Maurizia Rossana Brunetto
Ivana Carey
Masatoshi Ishigami
Margo J. H. van Campenhout
Man-Fung Yuen
Benjamin Maasoumy
Shuhei Nishiguchi
Markus Cornberg
Eiji Tanaka
Akinobu Takaki
Sarah F. Feldman
Hwai I. Yang
Yasuhito Tanaka
Akihiro Matsumoto
Laurence Bocket
Sang Hoon Ahn
Alice Desbiolles
Hiroshi Yatsuhashi
Bo Wang
Pisit Tangkijvanich
En Qiang Chen
Lai Wei
Christoph Höner zu Siederdissen
Takeshi Matsui
Harry L.A. Janssen
Hidenori Toyoda
Masaru Enomoto
Kyoko Yoshida
Yoshihiko Yano
Yusuke Shimakawa
Mar Riveiro-Barciela
Masanori Atsukawa
Maria Buti
Gastroenterology & Hepatology
Source :
Clinical Gastroenterology and Hepatology, 19(1), 46-60.e8. W.B. Saunders
Publication Year :
2020

Abstract

Background & Aims: To eliminate hepatitis B virus (HBV) infection, scale-up of testing and treatment in resource-limited countries is crucial. However, access to nucleic acid testing to quantify HBV DNA, an essential test to examine treatment eligibility, remains severely limited. We assessed the performance of a novel immunoassay, HBV core-related antigen (HBcrAg), as a low-cost (less than US $15/assay) alternative to nucleic acid testing to indicate clinically important high viremia in chronic HBV patients infected with different genotypes. Methods: We searched Medline, Embase, Scopus, and Web of Science databases through June 27, 2018. Three reviewers independently selected studies measuring HBV DNA and HBcrAg in the same blood samples. We contacted authors to provide individual participant data (IPD). We randomly allocated each IPD to a derivation or validation cohort. We applied optimal HBcrAg cut-off values derived from the derivation set to the validation set to estimate sensitivity/specificity. Results: Of 74 eligible studies, IPD were obtained successfully for 60 studies (81%). Meta-analysis included 5591 IPD without antiviral therapy and 4806 treated with antivirals. In untreated patients, the pooled area under the receiver operating characteristic curve and optimal cut-off values were as follows: 0.88 (95% CI, 0.83–0.94) and 3.6 log U/mL to diagnose HBV DNA level of 2000 IU/mL or greater; and 0.96 (95% CI, 0.94–0.98) and 5.3 log U/mL for 200,000 IU/mL or greater, respectively. In the validation set, the sensitivity and specificity were 85.2% and 84.7% to diagnose HBV DNA level of 2000 IU/mL or greater, and 91.8% and 90.5% for 200,000 IU/mL or greater, respectively. The performance did not vary by HBV genotypes. In patients treated with anti-HBV therapy the correlation between HBcrAg and HBV DNA was poor. Conclusions: HBcrAg might be a useful serologic marker to indicate clinically important high viremia in treatment-naïve, HBV-infected patients.

Details

ISSN :
15427714 and 15423565
Volume :
19
Issue :
1
Database :
OpenAIRE
Journal :
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
Accession number :
edsair.doi.dedup.....ed61dec02ff427c3039b104a58d83a93