Abstract

The effectiveness of interferon-free therapy during the course of HCV infection has already been confirmed. Liver fibrosis can be assessed in several ways, from biopsies to imaging tests. The present study evaluates the usefulness of non-invasive indirect biomarkers of liver fibrosis (APRI, GAPRI, FORNS, FIB-4, the AP index and HUI score) as markers of the effective treatment of HCV with the 3D regimen. Blood samples were collected from 70 patients suffering from chronic hepatitis C. Patients received the 3D AbbVie regimen for hepatitis C. All patients had HCV genotype 1b. The APRI, GAPRI, FIB-4, FORNS, HUI and AP index (age–platelet score) values were calculated with their respective algorithms. The stage of fibrosis was evaluated on the basis of a liver biopsy and confirmed by FibroScan-based transient elastography. An undetectable level of HCV RNA after 12 weeks of treatment with the 3D regimen indicates 100% eradication of hepatitis C virus. After the treatment, non-invasive indirect markers of liver fibrosis achieved levels below the limit for significant fibrosis, Thus, non-invasive indirect biomarkers of hepatic fibrosis failed to detect the presence of significant fibrosis, which was proved in histopathological examination. However, the eradication of hepatitis C virus by means of the 3D regimen treatment does not mean that patients were completely cured.

Highlights

  • The treatment of chronic hepatitis C virus (HCV) infection has been revolutionized in recent years [1]

  • We evaluated six indirect, non-invasive biomarkers of liver fibrosis (APRI, GAPRI, Forn’s, FIB-4, Age-Platelet and HUI score) as markers of the effective treatment of HCV with the 3D regimen

  • The study included 70 patients suffering from the hepatitis C virus: 32 women with a mean age of 54 and 38 men with a mean age of 48

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Summary

Introduction

The treatment of chronic hepatitis C virus (HCV) infection has been revolutionized in recent years [1]. The new therapeutic regimen for the treatment of chronic HCV infection consists of two pills: one tablet called. Viekirax/Exviera in Europe, comprising of the NS5A inhibitor ombitasvir, the protease inhibitor paritaprevir and cytochrome P3A inhibitor ritonavir; and a second tablet with non-nucleoside polymerase inhibitor dasabuvir (DSV) [3]. The combination of this threedrug regimen plus dasabuvir was developed by AbbVie and Enanta

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