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Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3

BACKGROUND: Genotype 3 increases fibrosis in chronic hepatitis C (CHC). AIM: To evaluate the effect of the hepatitis C virus (HCV) genotype on prevalence and severity of liver disease in CHC. MATERIALS AND METHODS: Nine hundred and forty-nine individuals with positive anti-HCV from June 2016 to May...

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Autores principales: Gupta, Tarana, Aggarwal, Hari K, Goyal, Sandeep, Singh, Virendra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Jaypee Brothers Medical Publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376599/
https://www.ncbi.nlm.nih.gov/pubmed/32742965
http://dx.doi.org/10.5005/jp-journals-10018-1311
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author Gupta, Tarana
Aggarwal, Hari K
Goyal, Sandeep
Singh, Virendra
author_facet Gupta, Tarana
Aggarwal, Hari K
Goyal, Sandeep
Singh, Virendra
author_sort Gupta, Tarana
collection PubMed
description BACKGROUND: Genotype 3 increases fibrosis in chronic hepatitis C (CHC). AIM: To evaluate the effect of the hepatitis C virus (HCV) genotype on prevalence and severity of liver disease in CHC. MATERIALS AND METHODS: Nine hundred and forty-nine individuals with positive anti-HCV from June 2016 to May 2017 were enrolled in the study. We compared biochemical and hematological parameters, HCV RNA load, transient elastography, and ultrasound, in genotype 3 and nongenotype 3 patients. Cirrhosis was diagnosed in patients with liver stiffness measurement (LSM) ≥13 kPa. RESULTS: Out of 835 CHC patients, overall, genotype 3 had higher LSM (11.3 vs 7.62, p = 0.01), higher aspartate aminotransferase (AST) (88.4 vs 68.6, p = 0.02), and low platelets (228.4 vs 261, p = 0.03) with higher prevalence of cirrhosis (115/415 vs 25/245, p = 0.01) than nongenotype 3. However, decompensation rates were not significantly different between two groups (32/115 vs 7/25, p = 0.98). The subgroup analysis revealed that cirrhotic genotype 3 had advanced age (50 vs 35, p < 0.01), male predominance, and higher AST (74.4 vs 57, p = 0.01) as compared to noncirrhotic genotype 3 patients. On multivariate analysis, age and AST values were higher in cirrhotic than noncirrhotic genotype 3 patients. CONCLUSION: Genotype 3 patients have higher prevalence of cirrhosis and fibrosis compared to nongenotype 3 patients; however, decompensation was not different between two groups. HOW TO CITE THIS ARTICLE: Gupta T, Aggarwal HK, Goyal S, et al. Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3. Euroasian J Hepato-Gastroenterol 2020;10(1):7–10.
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spelling pubmed-73765992020-07-31 Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3 Gupta, Tarana Aggarwal, Hari K Goyal, Sandeep Singh, Virendra Euroasian J Hepatogastroenterol Original Article BACKGROUND: Genotype 3 increases fibrosis in chronic hepatitis C (CHC). AIM: To evaluate the effect of the hepatitis C virus (HCV) genotype on prevalence and severity of liver disease in CHC. MATERIALS AND METHODS: Nine hundred and forty-nine individuals with positive anti-HCV from June 2016 to May 2017 were enrolled in the study. We compared biochemical and hematological parameters, HCV RNA load, transient elastography, and ultrasound, in genotype 3 and nongenotype 3 patients. Cirrhosis was diagnosed in patients with liver stiffness measurement (LSM) ≥13 kPa. RESULTS: Out of 835 CHC patients, overall, genotype 3 had higher LSM (11.3 vs 7.62, p = 0.01), higher aspartate aminotransferase (AST) (88.4 vs 68.6, p = 0.02), and low platelets (228.4 vs 261, p = 0.03) with higher prevalence of cirrhosis (115/415 vs 25/245, p = 0.01) than nongenotype 3. However, decompensation rates were not significantly different between two groups (32/115 vs 7/25, p = 0.98). The subgroup analysis revealed that cirrhotic genotype 3 had advanced age (50 vs 35, p < 0.01), male predominance, and higher AST (74.4 vs 57, p = 0.01) as compared to noncirrhotic genotype 3 patients. On multivariate analysis, age and AST values were higher in cirrhotic than noncirrhotic genotype 3 patients. CONCLUSION: Genotype 3 patients have higher prevalence of cirrhosis and fibrosis compared to nongenotype 3 patients; however, decompensation was not different between two groups. HOW TO CITE THIS ARTICLE: Gupta T, Aggarwal HK, Goyal S, et al. Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3. Euroasian J Hepato-Gastroenterol 2020;10(1):7–10. Jaypee Brothers Medical Publishers 2020 /pmc/articles/PMC7376599/ /pubmed/32742965 http://dx.doi.org/10.5005/jp-journals-10018-1311 Text en Copyright © 2020; Jaypee Brothers Medical Publishers (P) Ltd. © The Author(s). 2020 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/), which permits unrestricted use, distribution, and non-commercial 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 Original Article
Gupta, Tarana
Aggarwal, Hari K
Goyal, Sandeep
Singh, Virendra
Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3
title Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3
title_full Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3
title_fullStr Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3
title_full_unstemmed Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3
title_short Prediction of Cirrhosis in Patients with Chronic Hepatitis C by Genotype 3
title_sort prediction of cirrhosis in patients with chronic hepatitis c by genotype 3
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7376599/
https://www.ncbi.nlm.nih.gov/pubmed/32742965
http://dx.doi.org/10.5005/jp-journals-10018-1311
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