| Literature DB >> 29624802 |
P Zhang1,2, H B Du1,2, G D Tong3, X K Li1,2, X H Sun4, X L Chi5, Y F Xing3, Z H Zhou4, Q Li6, B Chen7, H Wang8, L Wang9, H Jin10, D W Mao11, X B Wang12, Q K Wu13, F P Li14, X Y Hu15, B J Lu16, Z Y Yang12, M X Zhang17, W B Shi18, Q He13, Y Li19, K P Jiang20, J D Xue14, X D Li21, J M Jiang5, W Lu22, G J Tian5, Z B Hu11, J C Guo23, C Z Li24, X Deng25, X L Luo21, F Y Li26, X W Zhang26, Y J Zheng3, G Zhao4, L C Wang27, J H Wu28, H Guo29, Y Q Mi22, Z J Gong30, C B Wang31, F Jiang1,2, P Guo32, X Z Yang2,33, W Q Shi34, H Z Yang35, Y Zhou36, N N Sun37, Y T Jiao38, Y Q Gao4, D Q Zhou3, Y A Ye1,2.
Abstract
The kinetics of serum hepatitis B surface antigen (HBsAg) during the natural history of hepatitis B virus (HBV) infection has been studied, but the factors affecting them remain unclear. We aimed to investigate the factors affecting HBsAg titres, using data from multicentre, large-sized clinical trials in China. The baseline data of 1795 patients in 3 multicentre trials were studied, and the patients were classified into 3 groups: hepatitis B early antigen (HBeAg)-positive chronic HBV infection (n = 588), HBeAg-positive chronic hepatitis B (n = 596), and HBeAg-negative chronic hepatitis B (n = 611). HBsAg titres in the different phases were compared, and multiple linear progression analyses were performed to investigate the implicated factors. HBsAg titres varied significantly in different phases (P = .000), with the highest (4.60 log10 IU/mL [10%-90% confidence interval: 3.52 log10 IU/mL-4.99 log10 IU/mL]) in patients with HBeAg-positive chronic HBV infection. In all phases, age and HBV DNA were correlated with serum HBsAg level. In HBeAg-positive chronic hepatitis B patients, a negative correlation between HBsAg titres and fibrosis stage was observed. Alanine amonitransferase or necroinflammatory activity was also correlated with HBsAg titres in HBeAg-negative chronic hepatitis B patients. In conclusion, decreased HBsAg titres may be associated with advancing fibrosis in HBeAg-positive chronic hepatitis B patients or increased necroinflammation in those with HBeAg-negative chronic hepatitis B. Our findings may help clinicians better understand the kinetics of HBsAg and provide useful insights into the management of this disease.Entities:
Keywords: HBV infection; HBsAg; affecting factor; multicentre trial; natural history
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Year: 2018 PMID: 29624802 DOI: 10.1111/jvh.12903
Source DB: PubMed Journal: J Viral Hepat ISSN: 1352-0504 Impact factor: 3.728