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Association of hepatitis B core antibody level and hepatitis B surface antigen clearance in HBeAg-negative patients with chronic hepatitis B.

Authors :
Wang J
Zhang Z
Zhu L
Zhang Q
Zhang S
Pan Y
Liu J
Cao F
Fan T
Xiong Y
Yin S
Yan X
Chen Y
Zhu C
Li J
Liu X
Wu C
Huang R
Source :
Virulence [Virulence] 2024 Dec; Vol. 15 (1), pp. 2404965. Date of Electronic Publication: 2024 Sep 24.
Publication Year :
2024

Abstract

Predicting hepatitis B surface antigen (HBsAg) clearance is important for chronic hepatitis B (CHB) patients receiving pegylated interferon-alfa (Peg-IFN) therapy. We aimed to determine the predictive value of serum hepatitis B core antibody (anti-HBc) for HBsAg clearance. A total of 189 HBeAg-negative CHB patients who received Peg-IFN based therapy were retrospectively included and classified into two groups: nucleos(t)ide analogues (NAs) add-on Peg-IFN group (add-on group, n  = 94) and Peg-IFN combined with NAs or Peg-IFN monotherapy group (combination or monotherapy group, n  = 95). After 48 weeks of treatment, 27.5% (52/189) and 15.9% (30/189) of patients achieved HBsAg clearance and seroconversion, respectively. Patients in the combination or monotherapy group tended to achieve relatively higher HBsAg clearance (31.6% vs. 23.4%, p  = 0.208) and seroconversion (21.1% vs. 10.6%, p  = 0.050) rates than those in the add-on group. In combination or monotherapy group, anti-HBc levels at week 12 were lower in patients with HBsAg clearance (9.0 S/CO vs. 9.9 S/CO, p  < 0.001) and seroconversion (8.8 S/CO vs. 9.8 S/CO, p  < 0.001) than those without. Anti-HBc level at week 12 was an independent predictor of HBsAg clearance and seroconversion. Patients with lower anti-HBc levels at week 12 showed a more significant decline in HBsAg levels during treatment. Combination of anti-HBc at week 12 and baseline HBsAg could identify over 70% of patients who achieved HBsAg clearance after 48 weeks of treatment. In addition to HBsAg, anti-HBc level could be used as a promising marker for selecting HBeAg-negative CHB patients who are more likely to respond to Peg-IFN-based therapy.

Details

Language :
English
ISSN :
2150-5608
Volume :
15
Issue :
1
Database :
MEDLINE
Journal :
Virulence
Publication Type :
Academic Journal
Accession number :
39317345
Full Text :
https://doi.org/10.1080/21505594.2024.2404965