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Hepatitis B Surface Antigen Levels Can Be Used to Rule Out Cirrhosis in Hepatitis B e Antigen-Positive Chronic Hepatitis B

Authors :
Milan J. Sonneveld
Maria Buti
R.A. de Man
Rong-Nan Chien
R.J. de Knegt
Qing Xie
Bettina E. Hansen
Anuj Gaggar
Teerha Piratvisuth
Harry L.A. Janssen
Vedran Pavlovic
Stefan Zeuzem
H.L. Chan
Jidong Jia
Willem P. Brouwer
Cynthia Wat
Gastroenterology & Hepatology
Source :
Journal of Infectious Diseases, 225(11), 1967-1973. Oxford University Press
Publication Year :
2022
Publisher :
Oxford University Press, 2022.

Abstract

Background Serum hepatitis B surface antigen (HBsAg) levels correlate with the duration of chronic hepatitis B virus (HBV) infection and may predict the extent of hepatic fibrosis. Methods We analyzed data from the SONIC-B database, which contains data from 8 global randomized trials and 2 large hepatology centers. Relationship between HBsAg levels and presence of significant fibrosis (Ishak 3–4) or cirrhosis (Ishak 5–6) were explored, and clinically relevant cutoffs were identified to rule out cirrhosis. Results The dataset included 2779 patients: 1866 hepatitis B e antigen (HBeAg)-positive; 322 with cirrhosis. Among HBeAg-positive patients, lower HBsAg levels were associated with higher rates of significant fibrosis (odds ratio [OR], 0.419; P < .001) and cirrhosis (OR, 0.435; P < .001). No relationship was observed among HBeAg-negative patients. Among HBeAg-positive patients, genotype-specific HBsAg cutoffs had excellent negative predictive values (>97%) and low misclassification rates (≤7.1%) and may therefore have utility in ruling out cirrhosis. Diagnostic performance of the HBsAg cutoffs was comparable among patients in whom cirrhosis could not be ruled out with fibrosis 4 (FIB-4). Conclusions Hepatitis B virus genotype-specific HBsAg cutoffs may have utility in ruling out presence of cirrhosis in HBeAg-positive patients with genotypes B, C, and D and can be an adjunct to FIB-4 to reduce the need for further testing.

Details

Language :
English
ISSN :
15376613 and 00221899
Volume :
225
Issue :
11
Database :
OpenAIRE
Journal :
Journal of Infectious Diseases
Accession number :
edsair.doi.dedup.....b95dfd0542e2a3f0550e5f34e7c07d9d