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The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis
AIM: The objective of this work is to find out whether there is a relation between the expression of TLR4 and fibrosis progression in chronic HCV patients. BACKGROUND: Toll-like Receptor 4 (TLR4) is a pattern recognition receptor whose activation results in the production of several pro-inflammatory...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shaheed Beheshti University of Medical Sciences
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758735/ https://www.ncbi.nlm.nih.gov/pubmed/29379592 |
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author | Mohamed, Salem Youssef Mostafa, Ehab Fawzy Hanafy, Amr Shaaban Atia, Hesham Metwally, Ashraf Marei, Ayman M. |
author_facet | Mohamed, Salem Youssef Mostafa, Ehab Fawzy Hanafy, Amr Shaaban Atia, Hesham Metwally, Ashraf Marei, Ayman M. |
author_sort | Mohamed, Salem Youssef |
collection | PubMed |
description | AIM: The objective of this work is to find out whether there is a relation between the expression of TLR4 and fibrosis progression in chronic HCV patients. BACKGROUND: Toll-like Receptor 4 (TLR4) is a pattern recognition receptor whose activation results in the production of several pro-inflammatory cytokines. METHODS: Fifty patients with chronic HCV were included. They were divided into group A: 40 patients (F1-F4) and group B (control group) which included ten patients (F0) based on fibroscan value. All patients were exposed to clinical and laboratory evaluations preliminary to antiviral therapy, assessment of TLR4 mRNA by Real Time- PCR. RESULTS: Twenty-eight males and 22 females with a mean age 28.9±6.1 years. The mean TLR4 expression is 11.2±7.4 folds, TLR4 expression in F0 group is 2.8±1.9, in F1 group 4.8±1.5, F2 group 10.2±2.5, F3 group 16.8±1.5 and in F4 21.3±3.6 folds (p<0.001). TLR4 showed a positive correlation with age, fibrosis stage, HCV RNA, serum transaminases, total bilirubin and prothrombin time, a negative correlation with platelet count and serum albumin. Fibrosis progression was independently associated with TLR4 expression (β=0. 648, P<0.0001), RNA (β= 0.160, P =0.001) and platelet count (β= -0.248, P = 0.004). CONCLUSION: The expression of TLR4 is highly correlated with the fibrosis progression; TLR4 may be a potential target for drugs to limit the progression of fibrosis. |
format | Online Article Text |
id | pubmed-5758735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Shaheed Beheshti University of Medical Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-57587352018-01-29 The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis Mohamed, Salem Youssef Mostafa, Ehab Fawzy Hanafy, Amr Shaaban Atia, Hesham Metwally, Ashraf Marei, Ayman M. Gastroenterol Hepatol Bed Bench Original Article AIM: The objective of this work is to find out whether there is a relation between the expression of TLR4 and fibrosis progression in chronic HCV patients. BACKGROUND: Toll-like Receptor 4 (TLR4) is a pattern recognition receptor whose activation results in the production of several pro-inflammatory cytokines. METHODS: Fifty patients with chronic HCV were included. They were divided into group A: 40 patients (F1-F4) and group B (control group) which included ten patients (F0) based on fibroscan value. All patients were exposed to clinical and laboratory evaluations preliminary to antiviral therapy, assessment of TLR4 mRNA by Real Time- PCR. RESULTS: Twenty-eight males and 22 females with a mean age 28.9±6.1 years. The mean TLR4 expression is 11.2±7.4 folds, TLR4 expression in F0 group is 2.8±1.9, in F1 group 4.8±1.5, F2 group 10.2±2.5, F3 group 16.8±1.5 and in F4 21.3±3.6 folds (p<0.001). TLR4 showed a positive correlation with age, fibrosis stage, HCV RNA, serum transaminases, total bilirubin and prothrombin time, a negative correlation with platelet count and serum albumin. Fibrosis progression was independently associated with TLR4 expression (β=0. 648, P<0.0001), RNA (β= 0.160, P =0.001) and platelet count (β= -0.248, P = 0.004). CONCLUSION: The expression of TLR4 is highly correlated with the fibrosis progression; TLR4 may be a potential target for drugs to limit the progression of fibrosis. Shaheed Beheshti University of Medical Sciences 2017 /pmc/articles/PMC5758735/ /pubmed/29379592 Text en ©2017 RIGLD, Research Institute for Gastroenterology and Liver Diseases This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Mohamed, Salem Youssef Mostafa, Ehab Fawzy Hanafy, Amr Shaaban Atia, Hesham Metwally, Ashraf Marei, Ayman M. The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis |
title | The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis |
title_full | The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis |
title_fullStr | The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis |
title_full_unstemmed | The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis |
title_short | The relationship between expression of Toll-like receptor 4 in chronic hepatitis C patients and different stages of liver fibrosis |
title_sort | relationship between expression of toll-like receptor 4 in chronic hepatitis c patients and different stages of liver fibrosis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758735/ https://www.ncbi.nlm.nih.gov/pubmed/29379592 |
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