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Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection
BACKGROUND: HCV infection is characterized by a tendency towards chronicity. Acute HCV infection progresses to chronic infection in 70% of cases. Hepatitis C virus infection can cause progressive liver injury and lead to fibrosis and eventually cirrhosis. The degree of histologic fibrosis is an impo...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
AVICENA, d.o.o., Sarajevo
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4130668/ https://www.ncbi.nlm.nih.gov/pubmed/25126010 http://dx.doi.org/10.5455/msm.2014.26.172-176 |
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author | Vukobrat-Bijedic, Zora Husic-Selimovic, Azra Mehinovic, Lejla Mehmedovic, Amila Junuzovic, Dzelaludin Bjelogrlic, Ivana Sofic, Amela Djurovic, Aleksandra |
author_facet | Vukobrat-Bijedic, Zora Husic-Selimovic, Azra Mehinovic, Lejla Mehmedovic, Amila Junuzovic, Dzelaludin Bjelogrlic, Ivana Sofic, Amela Djurovic, Aleksandra |
author_sort | Vukobrat-Bijedic, Zora |
collection | PubMed |
description | BACKGROUND: HCV infection is characterized by a tendency towards chronicity. Acute HCV infection progresses to chronic infection in 70% of cases. Hepatitis C virus infection can cause progressive liver injury and lead to fibrosis and eventually cirrhosis. The degree of histologic fibrosis is an important marker of the stage of the disease. One of current standard treatment for CHC infection is the combination of PEG-IFN α and ribavirin. OBJECTIVES: The aim of the study was to investigate the effect of the therapy with Peginterferon alfa-2a or alfa-2b plus Ribavirin on evolution of liver fibrosis in patients with chronic hepatitis C. Also, our aim was to examine whether there was a difference between the genders in the efficacy of these antiviral therapy. Our goal also was to determine effect of the therapy with Peginterferon alfa-2a or alfa-2b plus Ribavirin on evolution of liver steatosis in patients with chronic hepatitis C. PATIENTS AND METHODS: A retrospective study was made of chronic hepatitis C patients who had been treated from 2005 to April 2014 at the Clinic of Gastroenterohepatology, Clinical Center University of Sarajevo. We reviewed 40 patient medical records to collect demographic, epidemiological and clinical information, as information on liver biopsies that was performed prior to the antiviral therapy and FibroScan(®) test that was performed after the antiviral therapy. For the processing of data SPSS (Statistical Package for the Social Sciences Program) for Windows, ver. 21.0 statistical software was used. Comparisons between qualitative and quantitative variables were performed using the Student t-test. Mann Whitney U test was used to compare differences in variables such as fibrosis stage and steatosis grade. A value of p<0.05 was considered as statistically significant. RESULTS: After treatment, there was a statistically significant increase in the number of patients with no fibrosis (p<0.05). There was no statistically significant reduction in the number of patients with cirrhosis (F4) (p>0.05). There was significantly higher decrease of fibrosis progression at the patients that were in an mild-to-moderate fibrosis (F1/F2/F3), patients that were in advanced stage of fibrosis (F4) at the time of the pre-treatment did not have a statistically significant fibrosis reduction. We found significant association in evolution of fibrosis after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2a (12,5) kD with ribavirin (p< 0.05). We also found significant association in evolution of steatosis after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2a (12,5) kD with ribavirin (p < 0.05). There was statistically significant differences (p<0.05) between genders within fibrosis qualitative evolution. CONCLUSIONS: There were significant regression of fibrosis especially at the patients that were in an mild-to-moderate fibrosis (F1/F2/F3), patients that were in advanced stage of fibrosis (F4) at the time of the pre-treatment did not have a statistically significant fibrosis reduction after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2b (12,5) kD with ribavirin. Our results showed significant improvement in steatosis in patients infected with HCV after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2b (12,5) kD with ribavirin. Those results provides further evidence for direct involvement of HCV and antiviral therapy in the pathogenesis of hepatic steatosis. Female gender showed a higher degree of fibrosis reduction. |
format | Online Article Text |
id | pubmed-4130668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | AVICENA, d.o.o., Sarajevo |
record_format | MEDLINE/PubMed |
spelling | pubmed-41306682014-08-14 Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection Vukobrat-Bijedic, Zora Husic-Selimovic, Azra Mehinovic, Lejla Mehmedovic, Amila Junuzovic, Dzelaludin Bjelogrlic, Ivana Sofic, Amela Djurovic, Aleksandra Mater Sociomed Original Paper BACKGROUND: HCV infection is characterized by a tendency towards chronicity. Acute HCV infection progresses to chronic infection in 70% of cases. Hepatitis C virus infection can cause progressive liver injury and lead to fibrosis and eventually cirrhosis. The degree of histologic fibrosis is an important marker of the stage of the disease. One of current standard treatment for CHC infection is the combination of PEG-IFN α and ribavirin. OBJECTIVES: The aim of the study was to investigate the effect of the therapy with Peginterferon alfa-2a or alfa-2b plus Ribavirin on evolution of liver fibrosis in patients with chronic hepatitis C. Also, our aim was to examine whether there was a difference between the genders in the efficacy of these antiviral therapy. Our goal also was to determine effect of the therapy with Peginterferon alfa-2a or alfa-2b plus Ribavirin on evolution of liver steatosis in patients with chronic hepatitis C. PATIENTS AND METHODS: A retrospective study was made of chronic hepatitis C patients who had been treated from 2005 to April 2014 at the Clinic of Gastroenterohepatology, Clinical Center University of Sarajevo. We reviewed 40 patient medical records to collect demographic, epidemiological and clinical information, as information on liver biopsies that was performed prior to the antiviral therapy and FibroScan(®) test that was performed after the antiviral therapy. For the processing of data SPSS (Statistical Package for the Social Sciences Program) for Windows, ver. 21.0 statistical software was used. Comparisons between qualitative and quantitative variables were performed using the Student t-test. Mann Whitney U test was used to compare differences in variables such as fibrosis stage and steatosis grade. A value of p<0.05 was considered as statistically significant. RESULTS: After treatment, there was a statistically significant increase in the number of patients with no fibrosis (p<0.05). There was no statistically significant reduction in the number of patients with cirrhosis (F4) (p>0.05). There was significantly higher decrease of fibrosis progression at the patients that were in an mild-to-moderate fibrosis (F1/F2/F3), patients that were in advanced stage of fibrosis (F4) at the time of the pre-treatment did not have a statistically significant fibrosis reduction. We found significant association in evolution of fibrosis after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2a (12,5) kD with ribavirin (p< 0.05). We also found significant association in evolution of steatosis after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2a (12,5) kD with ribavirin (p < 0.05). There was statistically significant differences (p<0.05) between genders within fibrosis qualitative evolution. CONCLUSIONS: There were significant regression of fibrosis especially at the patients that were in an mild-to-moderate fibrosis (F1/F2/F3), patients that were in advanced stage of fibrosis (F4) at the time of the pre-treatment did not have a statistically significant fibrosis reduction after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2b (12,5) kD with ribavirin. Our results showed significant improvement in steatosis in patients infected with HCV after treatment with PEG-IFN α2a (40) kD and PEG-IFNα2b (12,5) kD with ribavirin. Those results provides further evidence for direct involvement of HCV and antiviral therapy in the pathogenesis of hepatic steatosis. Female gender showed a higher degree of fibrosis reduction. AVICENA, d.o.o., Sarajevo 2014-06-21 2014-06 /pmc/articles/PMC4130668/ /pubmed/25126010 http://dx.doi.org/10.5455/msm.2014.26.172-176 Text en Copyright: © AVICENA http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Vukobrat-Bijedic, Zora Husic-Selimovic, Azra Mehinovic, Lejla Mehmedovic, Amila Junuzovic, Dzelaludin Bjelogrlic, Ivana Sofic, Amela Djurovic, Aleksandra Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection |
title | Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection |
title_full | Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection |
title_fullStr | Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection |
title_full_unstemmed | Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection |
title_short | Analysis of Effect of Antiviral Therapy on Regression of Liver Fibrosis in Patient with HCV Infection |
title_sort | analysis of effect of antiviral therapy on regression of liver fibrosis in patient with hcv infection |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4130668/ https://www.ncbi.nlm.nih.gov/pubmed/25126010 http://dx.doi.org/10.5455/msm.2014.26.172-176 |
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