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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: Results From the SONIC-B Study.

Authors :
Sonneveld, Milan J
Hansen, Bettina E
Brouwer, Willem P
Chan, Henry L-Y
Piratvisuth, Teerha
Jia, Ji-Dong
Zeuzem, Stefan
Chien, Rong-Nan
Knegt, Robert J de
Wat, Cynthia
Pavlovic, Vedran
Gaggar, Anuj
Xie, Qing
Buti, Maria
Man, Robert A de
Janssen, Harry L A
Group, SONIC-B Study
Chien, R N
de Knegt, R J
de Man, R A
Source :
Journal of Infectious Diseases; 6/1/2022, Vol. 225 Issue 11, p1967-1973, 7p
Publication Year :
2022

Abstract

<bold>Background: </bold>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.<bold>Methods: </bold>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.<bold>Results: </bold>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).<bold>Conclusions: </bold>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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
225
Issue :
11
Database :
Complementary Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
157236548
Full Text :
https://doi.org/10.1093/infdis/jiaa192