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The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease
The aim of the study was to detect the expression level of thymosin β4 (Tβ4) in serum and tissues of patients with chronic hepatitis B (CHB) combined nonalcoholic fatty liver disease (NAFLD). The effects of Tβ4 in hepatic steatosis, chronic inflammation, and fibrosis development in CHB combined NAFL...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5207590/ https://www.ncbi.nlm.nih.gov/pubmed/28033294 http://dx.doi.org/10.1097/MD.0000000000005763 |
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author | Liang, Jing Cai, Wenjuan Han, Tao Jing, Li Ma, Zhe Gao, Yingtang |
author_facet | Liang, Jing Cai, Wenjuan Han, Tao Jing, Li Ma, Zhe Gao, Yingtang |
author_sort | Liang, Jing |
collection | PubMed |
description | The aim of the study was to detect the expression level of thymosin β4 (Tβ4) in serum and tissues of patients with chronic hepatitis B (CHB) combined nonalcoholic fatty liver disease (NAFLD). The effects of Tβ4 in hepatic steatosis, chronic inflammation, and fibrosis development in CHB combined NAFLD patients were also discussed. The study included 46 patients in the case group with CHB and NAFLD and 42 patients in the control group with CHB. ELISA was applied to detect serum Tβ4 and TNF-α level. Furthermore, the correlation analysis of Tβ4 levels with biochemical index, pathological index, and TNF-α level was performed. The Tβ4 immunohistochemical levels of different inflammation fibrosis levels were compared, and the correlation analysis with TNF expression was performed. The Tβ4 levels in patients with CHB combined NAFLD showed no statistical difference when compared to the control group. In patients with CHB combined NAFLD group, the Tβ4 level had no correlation with ALT, AST, TG, FGP, hepatitis B virus (HBV)-DNA levels, and fat grading, but had negative correlation with inflammation score and fibrosis score (P <0.01). The immunohistochemical results of hepatic tissues showed that the expression intensity of severe inflammation fibrosis group had statistical significance compared with that of slight group, and the Tβ4 expression both in serum and in liver tissue negatively correlated with TNF-α expression. Tβ4 could be involved in the regulation of chronic inflammation and fibrosis and plays a defense role in the disease progression of CHB combined NAFLD patients. |
format | Online Article Text |
id | pubmed-5207590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-52075902017-01-09 The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease Liang, Jing Cai, Wenjuan Han, Tao Jing, Li Ma, Zhe Gao, Yingtang Medicine (Baltimore) 4500 The aim of the study was to detect the expression level of thymosin β4 (Tβ4) in serum and tissues of patients with chronic hepatitis B (CHB) combined nonalcoholic fatty liver disease (NAFLD). The effects of Tβ4 in hepatic steatosis, chronic inflammation, and fibrosis development in CHB combined NAFLD patients were also discussed. The study included 46 patients in the case group with CHB and NAFLD and 42 patients in the control group with CHB. ELISA was applied to detect serum Tβ4 and TNF-α level. Furthermore, the correlation analysis of Tβ4 levels with biochemical index, pathological index, and TNF-α level was performed. The Tβ4 immunohistochemical levels of different inflammation fibrosis levels were compared, and the correlation analysis with TNF expression was performed. The Tβ4 levels in patients with CHB combined NAFLD showed no statistical difference when compared to the control group. In patients with CHB combined NAFLD group, the Tβ4 level had no correlation with ALT, AST, TG, FGP, hepatitis B virus (HBV)-DNA levels, and fat grading, but had negative correlation with inflammation score and fibrosis score (P <0.01). The immunohistochemical results of hepatic tissues showed that the expression intensity of severe inflammation fibrosis group had statistical significance compared with that of slight group, and the Tβ4 expression both in serum and in liver tissue negatively correlated with TNF-α expression. Tβ4 could be involved in the regulation of chronic inflammation and fibrosis and plays a defense role in the disease progression of CHB combined NAFLD patients. Wolters Kluwer Health 2016-12-30 /pmc/articles/PMC5207590/ /pubmed/28033294 http://dx.doi.org/10.1097/MD.0000000000005763 Text en Copyright © 2016 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 4500 Liang, Jing Cai, Wenjuan Han, Tao Jing, Li Ma, Zhe Gao, Yingtang The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease |
title | The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease |
title_full | The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease |
title_fullStr | The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease |
title_full_unstemmed | The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease |
title_short | The expression of thymosin β4 in chronic hepatitis B combined nonalcoholic fatty liver disease |
title_sort | expression of thymosin β4 in chronic hepatitis b combined nonalcoholic fatty liver disease |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5207590/ https://www.ncbi.nlm.nih.gov/pubmed/28033294 http://dx.doi.org/10.1097/MD.0000000000005763 |
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