Serum hepatitis B core-related antigen predicts hepatocellular carcinoma in hepatitis B e antigen-negative patients
Background Hepatitis B core-related antigen (HBcrAg) is a novel serum viral marker. Recent studies showed that its level correlates with the risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). We aimed to evaluate the accuracy of serum HBsAg and HBcrAg levels at baseli...
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Published in | Journal of gastroenterology Vol. 55; no. 9; pp. 899 - 908 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Singapore
Springer Singapore
01.09.2020
Springer Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Hepatitis B core-related antigen (HBcrAg) is a novel serum viral marker. Recent studies showed that its level correlates with the risk of hepatocellular carcinoma (HCC) in patients with chronic hepatitis B (CHB). We aimed to evaluate the accuracy of serum HBsAg and HBcrAg levels at baseline to predict HCC.
Methods
1400 CHB patients who received nucleos(t)ide analogues (NA) treatment since December 2005 were included. Their stored serum samples at baseline were retrieved to measure HBsAg and HBcrAg levels. The primary endpoint was the cumulative incidence of HCC.
Results
85 (6.1%) patients developed HCC during a mean (± SD) follow-up duration of 45 ± 20 months. Serum HBcrAg level above 2.9 log10 U/mL at baseline was an independent factor for HCC in hepatitis B e antigen (HBeAg)-negative patients by multivariable analysis (adjusted hazard ratio 2.13, 95% CI 1.10–4.14,
P
= 0.025). HBcrAg above 2.9 log
10
U/mL stratified the risk of HCC in HBeAg-negative patients with high PAGE-B score (
P
= 0.024 by Kaplan–Meier analysis), and possibly in cirrhotic patients (
P
= 0.08). Serum HBsAg level did not show any correlation with the risk of HCC in all patients or any subgroups.
Conclusion
Serum HBcrAg level predicts the risk of HCC accurately in NA-treated HBeAg-negative CHB patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 0944-1174 1435-5922 1435-5922 |
DOI: | 10.1007/s00535-020-01700-z |