Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury

Hepatitis C virus (HCV)-induced inflammation contributes to progressive liver disease. The chemoattractant protein chemerin is associated with systemic inflammation. We hypothesized that chemerin is a biomarker that predicts the severity of liver disease in HCV patients. Furthermore, we investigated...

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Main Authors: Georg Peschel, Jonathan Grimm, Karsten Gülow, Martina Müller, Christa Buechler, Kilian Weigand
Format: Article
Language:English
Published: MDPI AG 2020-11-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/10/11/974
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author Georg Peschel
Jonathan Grimm
Karsten Gülow
Martina Müller
Christa Buechler
Kilian Weigand
author_facet Georg Peschel
Jonathan Grimm
Karsten Gülow
Martina Müller
Christa Buechler
Kilian Weigand
author_sort Georg Peschel
collection DOAJ
description Hepatitis C virus (HCV)-induced inflammation contributes to progressive liver disease. The chemoattractant protein chemerin is associated with systemic inflammation. We hypothesized that chemerin is a biomarker that predicts the severity of liver disease in HCV patients. Furthermore, we investigated whether serum chemerin levels change during the course of HCV treatment using direct-acting antivirals (DAAs). Therefore, we measured serum concentration of chemerin in a cohort of 82 HCV-infected patients undergoing DAA treatment. Serum chemerin was positively associated with leukocyte count and negatively with markers of hepatic function and the model of end-stage liver disease (MELD) score. Low circulating chemerin levels significantly correlated with advanced liver fibrosis and cirrhosis as measured by the fibrosis-4 (FIB-4) score, the aminotransferase/platelet (AST/PLT) ratio index (APRI) score and the non-alcoholic fatty liver disease (NAFLD) score. Chemerin did not correlate with viral load or viral genotype. Treatment with DAAs did not improve MELD score and leukocyte count within the observation period, up to three months after the end of DAA treatment. Accordingly, chemerin levels remained unchanged during the treatment period. We conclude that low circulating chemerin is a noninvasive biomarker for hepatic dysfunction and advanced liver fibrosis and cirrhosis in HCV infection.
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spelling doaj.art-26648391467e49089714b26b666050d52023-11-20T21:35:42ZengMDPI AGDiagnostics2075-44182020-11-01101197410.3390/diagnostics10110974Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver InjuryGeorg Peschel0Jonathan Grimm1Karsten Gülow2Martina Müller3Christa Buechler4Kilian Weigand5Department of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, 93053 Regensburg, GermanyDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, 93053 Regensburg, GermanyDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, 93053 Regensburg, GermanyDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, 93053 Regensburg, GermanyDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, 93053 Regensburg, GermanyDepartment of Internal Medicine I, Gastroenterology, Hepatology, Endocrinology, Rheumatology and Infectious Diseases, University Hospital Regensburg, 93053 Regensburg, GermanyHepatitis C virus (HCV)-induced inflammation contributes to progressive liver disease. The chemoattractant protein chemerin is associated with systemic inflammation. We hypothesized that chemerin is a biomarker that predicts the severity of liver disease in HCV patients. Furthermore, we investigated whether serum chemerin levels change during the course of HCV treatment using direct-acting antivirals (DAAs). Therefore, we measured serum concentration of chemerin in a cohort of 82 HCV-infected patients undergoing DAA treatment. Serum chemerin was positively associated with leukocyte count and negatively with markers of hepatic function and the model of end-stage liver disease (MELD) score. Low circulating chemerin levels significantly correlated with advanced liver fibrosis and cirrhosis as measured by the fibrosis-4 (FIB-4) score, the aminotransferase/platelet (AST/PLT) ratio index (APRI) score and the non-alcoholic fatty liver disease (NAFLD) score. Chemerin did not correlate with viral load or viral genotype. Treatment with DAAs did not improve MELD score and leukocyte count within the observation period, up to three months after the end of DAA treatment. Accordingly, chemerin levels remained unchanged during the treatment period. We conclude that low circulating chemerin is a noninvasive biomarker for hepatic dysfunction and advanced liver fibrosis and cirrhosis in HCV infection.https://www.mdpi.com/2075-4418/10/11/974HCV infectionDAAbody mass indexMELD scoreliver fibrosis
spellingShingle Georg Peschel
Jonathan Grimm
Karsten Gülow
Martina Müller
Christa Buechler
Kilian Weigand
Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury
Diagnostics
HCV infection
DAA
body mass index
MELD score
liver fibrosis
title Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury
title_full Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury
title_fullStr Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury
title_full_unstemmed Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury
title_short Chemerin Is a Valuable Biomarker in Patients with HCV Infection and Correlates with Liver Injury
title_sort chemerin is a valuable biomarker in patients with hcv infection and correlates with liver injury
topic HCV infection
DAA
body mass index
MELD score
liver fibrosis
url https://www.mdpi.com/2075-4418/10/11/974
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