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Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience
BACKGROUND: Bicyclol, the most commonly-used liver hepatoprotective drug in China, is often selected to control disease progression in CHB patients who refuse anti-viral treatment. However, data on histological changes after bicyclol treatment in these patients are scarce. Therefore, this study has...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567540/ https://www.ncbi.nlm.nih.gov/pubmed/31196030 http://dx.doi.org/10.1186/s12876-019-1005-1 |
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author | Chi, Xiaoling Xiao, Huanming Shi, Meijie Cai, Gaoshu Xie, Yubao Jiang, Junmin Tian, Guangjun Wu, Shuduo Zhang, Chaozhen Zhao, Pengtao Chen, Jiezhen |
author_facet | Chi, Xiaoling Xiao, Huanming Shi, Meijie Cai, Gaoshu Xie, Yubao Jiang, Junmin Tian, Guangjun Wu, Shuduo Zhang, Chaozhen Zhao, Pengtao Chen, Jiezhen |
author_sort | Chi, Xiaoling |
collection | PubMed |
description | BACKGROUND: Bicyclol, the most commonly-used liver hepatoprotective drug in China, is often selected to control disease progression in CHB patients who refuse anti-viral treatment. However, data on histological changes after bicyclol treatment in these patients are scarce. Therefore, this study has been conducted to find out whether bicyclol has good benefits of histological improvement in CHB patients who refuse anti-viral agents. METHODS: The demographic, clinical and pathological data were collected from CHB patients who received bicyclol from January 2010 to June 2016. Improvement in liver inflammation or fibrosis is defined as at least one-grade or one-stage decrease as measured by the Scheuer scoring system. Thirty patients treated with ETV for 48 weeks were chosen as a control group to compare the histological improvement between bicyclol and entecavir (ETV) after 48-week treatment. RESULTS: A total of 123 patients with CHB treated with bicyclol were included in this study. Paired liver biopsies were performed in 70 patients. Inter-biopsy interval was 17.44 ± 8.90 months (12–60 months). As shown by facts, 41.4% patients achieved liver inflammation improvement, while only 10.0% patients showed liver inflammation progression after bicyclol treatment. In regarding to liver fibrosis, as shown by facts, 28.6% patients achieved fibrosis improvement. More importantly, It was found that the proportions of patients with liver inflammation and fibrosis improvement were both not significantly lower than those in ETV group (53.3% vs 63.3 and 36.7% vs 43.4%). Most of patients (82.4%) with elevated baseline ALT became normal after bicyclol treatment. More importantly, as shown by the multi-variate analysis, the treatment course of bicyclol was an independent factor for liver inflammation improvement. With the HBeAg status adjusted, ALT and HBV-DNA quantity, the odds ratio (95% confidence interval) of patients with ≥48-week treatment was 5.756 (1.893,17.500) when compared with patients via < 48-week treatment. CONCLUSION: Bicyclol can improve liver inflammation and the ALT normalization rate of CHB patients, especially when the treatment course is prolonged. This has confirmed that bicyclol could control hepatitis activity, which might be a good choice for CHB patients who refuse anti-viral treatments. |
format | Online Article Text |
id | pubmed-6567540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65675402019-06-17 Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience Chi, Xiaoling Xiao, Huanming Shi, Meijie Cai, Gaoshu Xie, Yubao Jiang, Junmin Tian, Guangjun Wu, Shuduo Zhang, Chaozhen Zhao, Pengtao Chen, Jiezhen BMC Gastroenterol Research Article BACKGROUND: Bicyclol, the most commonly-used liver hepatoprotective drug in China, is often selected to control disease progression in CHB patients who refuse anti-viral treatment. However, data on histological changes after bicyclol treatment in these patients are scarce. Therefore, this study has been conducted to find out whether bicyclol has good benefits of histological improvement in CHB patients who refuse anti-viral agents. METHODS: The demographic, clinical and pathological data were collected from CHB patients who received bicyclol from January 2010 to June 2016. Improvement in liver inflammation or fibrosis is defined as at least one-grade or one-stage decrease as measured by the Scheuer scoring system. Thirty patients treated with ETV for 48 weeks were chosen as a control group to compare the histological improvement between bicyclol and entecavir (ETV) after 48-week treatment. RESULTS: A total of 123 patients with CHB treated with bicyclol were included in this study. Paired liver biopsies were performed in 70 patients. Inter-biopsy interval was 17.44 ± 8.90 months (12–60 months). As shown by facts, 41.4% patients achieved liver inflammation improvement, while only 10.0% patients showed liver inflammation progression after bicyclol treatment. In regarding to liver fibrosis, as shown by facts, 28.6% patients achieved fibrosis improvement. More importantly, It was found that the proportions of patients with liver inflammation and fibrosis improvement were both not significantly lower than those in ETV group (53.3% vs 63.3 and 36.7% vs 43.4%). Most of patients (82.4%) with elevated baseline ALT became normal after bicyclol treatment. More importantly, as shown by the multi-variate analysis, the treatment course of bicyclol was an independent factor for liver inflammation improvement. With the HBeAg status adjusted, ALT and HBV-DNA quantity, the odds ratio (95% confidence interval) of patients with ≥48-week treatment was 5.756 (1.893,17.500) when compared with patients via < 48-week treatment. CONCLUSION: Bicyclol can improve liver inflammation and the ALT normalization rate of CHB patients, especially when the treatment course is prolonged. This has confirmed that bicyclol could control hepatitis activity, which might be a good choice for CHB patients who refuse anti-viral treatments. BioMed Central 2019-06-13 /pmc/articles/PMC6567540/ /pubmed/31196030 http://dx.doi.org/10.1186/s12876-019-1005-1 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Chi, Xiaoling Xiao, Huanming Shi, Meijie Cai, Gaoshu Xie, Yubao Jiang, Junmin Tian, Guangjun Wu, Shuduo Zhang, Chaozhen Zhao, Pengtao Chen, Jiezhen Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience |
title | Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience |
title_full | Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience |
title_fullStr | Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience |
title_full_unstemmed | Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience |
title_short | Histological improvement in chronic hepatitis B patients treated with bicyclol: real world experience |
title_sort | histological improvement in chronic hepatitis b patients treated with bicyclol: real world experience |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6567540/ https://www.ncbi.nlm.nih.gov/pubmed/31196030 http://dx.doi.org/10.1186/s12876-019-1005-1 |
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