Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B
Background/purpose: The predictors of off-therapy response in patients treated with neucleos(t)ide analogue (NA) have not been elucidated. It remained unexplored whether serum level of hepatitis B core antibody (anti-HBc) at the end of NA therapy was associated with relapse risks. Methods: This pros...
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doaj-5117a322ec164af5a64a9e496a5eecff2020-11-25T00:21:45ZengElsevierJournal of the Formosan Medical Association0929-66462018-10-0111710915921Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis BCheng-Hao Tseng0Yao-Chun Hsu1Chi-Yang Chang2Tai-Chung Tseng3Ming-Shiang Wu4Jaw-Town Lin5Jia-Horng Kao6Division of Gastroenterology and Hepatology, E-DA Cancer Hospital/I-Shou University, Kaohsiung, TaiwanDivision of Gastroenterology and Hepatology, Fu-Jen Catholic University Hospital, New Taipei, Taiwan; School of Medicine and Big Data Research Center, Fu-Jen Catholic University, New Taipei, Taiwan; Graduate Institute of Clinical Medicine, China Medical University, Taichung, TaiwanDivision of Gastroenterology and Hepatology, Fu-Jen Catholic University Hospital, New Taipei, Taiwan; School of Medicine and Big Data Research Center, Fu-Jen Catholic University, New Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, TaiwanDivision of Gastroenterology and Hepatology, Fu-Jen Catholic University Hospital, New Taipei, Taiwan; School of Medicine and Big Data Research Center, Fu-Jen Catholic University, New Taipei, TaiwanDivision of Gastroenterology and Hepatology, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan; Graduate Institute of Clinical Medicine, National Taiwan University, Taipei, Taiwan; Corresponding author. Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, 1 Chang-Te Street, Taipei 100, Taiwan. Fax: +886 2 23825962.Background/purpose: The predictors of off-therapy response in patients treated with neucleos(t)ide analogue (NA) have not been elucidated. It remained unexplored whether serum level of hepatitis B core antibody (anti-HBc) at the end of NA therapy was associated with relapse risks. Methods: This prospective study monitored 82 chronic hepatitis B (CHB) patients after discontinuing entecavir. All patients had been treated for 3 years or longer and serologically negative for viral DNA and HBeAg at treatment cessation. Patients were monitored for virological relapse (viral DNA > 2000 IU/mL), and clinical relapse (serum alanine aminotransferase > 80 U/L plus virological relapse). The association between anti-HBc levels and the risk of relapse was assessed by the Cox analysis. Results: Clinical and virological relapses occurred in 29 and 60 participants, respectively, with the cumulative incidences of 23.7% (95% CI, 15.8–34.6%) and 62.0% (95% CI, 51.5–72.5%) at 1 year, and 36.2% (95% CI, 26.2–48.4%) and 78.8% (95% CI, 68.2–87.8%) at 2 years, respectively. There was a trend for an inverse association between anti-HBc and clinical relapse (crude hazard ratio [HR], 0.50; 95% CI, 0.24–1.05). All 3 patients with the level <100 IU/mL had a rapid clinical relapse (P = 0.002). This trend remained after adjustment for HBsAg and age (adjusted HR 0.50, 95% CI, 0.24–1.03). On the other hand, anti-HBc quantity was unrelated to virological relapse (crude HR, 0.97; 95% CI, 0.58–1.62; adjusted HR, 0.97; 95% CI, 0.58–1.60). Conclusion: This pilot study suggests a trend for an inverse association between anti-HBc levels and clinical relapse in CHB patients off entecavir. Keywords: Chronic hepatitis B, Anti-HBc quantitation, Antiviral therapyhttp://www.sciencedirect.com/science/article/pii/S092966461730462X |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Cheng-Hao Tseng Yao-Chun Hsu Chi-Yang Chang Tai-Chung Tseng Ming-Shiang Wu Jaw-Town Lin Jia-Horng Kao |
spellingShingle |
Cheng-Hao Tseng Yao-Chun Hsu Chi-Yang Chang Tai-Chung Tseng Ming-Shiang Wu Jaw-Town Lin Jia-Horng Kao Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B Journal of the Formosan Medical Association |
author_facet |
Cheng-Hao Tseng Yao-Chun Hsu Chi-Yang Chang Tai-Chung Tseng Ming-Shiang Wu Jaw-Town Lin Jia-Horng Kao |
author_sort |
Cheng-Hao Tseng |
title |
Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B |
title_short |
Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B |
title_full |
Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B |
title_fullStr |
Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B |
title_full_unstemmed |
Quantification of serum hepatitis B core antibody to predict off-entecavir relapse in patients with chronic hepatitis B |
title_sort |
quantification of serum hepatitis b core antibody to predict off-entecavir relapse in patients with chronic hepatitis b |
publisher |
Elsevier |
series |
Journal of the Formosan Medical Association |
issn |
0929-6646 |
publishDate |
2018-10-01 |
description |
Background/purpose: The predictors of off-therapy response in patients treated with neucleos(t)ide analogue (NA) have not been elucidated. It remained unexplored whether serum level of hepatitis B core antibody (anti-HBc) at the end of NA therapy was associated with relapse risks. Methods: This prospective study monitored 82 chronic hepatitis B (CHB) patients after discontinuing entecavir. All patients had been treated for 3 years or longer and serologically negative for viral DNA and HBeAg at treatment cessation. Patients were monitored for virological relapse (viral DNA > 2000 IU/mL), and clinical relapse (serum alanine aminotransferase > 80 U/L plus virological relapse). The association between anti-HBc levels and the risk of relapse was assessed by the Cox analysis. Results: Clinical and virological relapses occurred in 29 and 60 participants, respectively, with the cumulative incidences of 23.7% (95% CI, 15.8–34.6%) and 62.0% (95% CI, 51.5–72.5%) at 1 year, and 36.2% (95% CI, 26.2–48.4%) and 78.8% (95% CI, 68.2–87.8%) at 2 years, respectively. There was a trend for an inverse association between anti-HBc and clinical relapse (crude hazard ratio [HR], 0.50; 95% CI, 0.24–1.05). All 3 patients with the level <100 IU/mL had a rapid clinical relapse (P = 0.002). This trend remained after adjustment for HBsAg and age (adjusted HR 0.50, 95% CI, 0.24–1.03). On the other hand, anti-HBc quantity was unrelated to virological relapse (crude HR, 0.97; 95% CI, 0.58–1.62; adjusted HR, 0.97; 95% CI, 0.58–1.60). Conclusion: This pilot study suggests a trend for an inverse association between anti-HBc levels and clinical relapse in CHB patients off entecavir. Keywords: Chronic hepatitis B, Anti-HBc quantitation, Antiviral therapy |
url |
http://www.sciencedirect.com/science/article/pii/S092966461730462X |
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