Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients

Background: The aim of this study is to investigate the association between hepatic activity index (HAI) and fibrosis score (FS) with inflammation biomarkers in non-uremic and uremic hepatitis C positive patients. Methods: Fifty chronic hepatitis C (cHepC) positive patients, having a liver biopsy we...

Full description

Bibliographic Details
Main Authors: Bengu Tatar, Sukran Kose, Emel Pala, Erhan Tatar
Format: Article
Language:English
Published: Karolinum Press 2017-10-01
Series:Acta Medica
Subjects:
Online Access:https://actamedica.lfhk.cuni.cz/60/2/0071/
_version_ 1811273012012384256
author Bengu Tatar
Sukran Kose
Emel Pala
Erhan Tatar
author_facet Bengu Tatar
Sukran Kose
Emel Pala
Erhan Tatar
author_sort Bengu Tatar
collection DOAJ
description Background: The aim of this study is to investigate the association between hepatic activity index (HAI) and fibrosis score (FS) with inflammation biomarkers in non-uremic and uremic hepatitis C positive patients. Methods: Fifty chronic hepatitis C (cHepC) positive patients, having a liver biopsy were included in this study. Liver biopsies were scored according to modified ISHAC scoring system. 25 healthy controls of similar age and gender were also enrolled as control group. Serum YKL-40, neutrophil/lymphocyte ratio (NLR), thrombocyte/lymphocyte ratio (PLR), CRP and Immunoglobulin (IgG, A and M) levels were used to determine inflammation. AST to Platelet Ratio Index (APRI) score was also evaluated. According to biopsy findings patients were divided into 2 groups: low (0–2) and severe (3–6) FS. Results: Patients with cHepC had increased inflammation compared to the healthy controls. End-stage renal disease (ESRD) patients had higher levels of inflammation markers (NLR, IgG, CRP and YKL-40) and lower HCV RNA levels, HAI and FS compared to non-uremic patients. When patients were grouped into 2 according to FS as mild and severe, IgG (p < 0.001), YKL-40 (p = 0.02) levels and APRI score (p = 0.002) were significantly higher compared to mild FS (p = 0.002). YKL-40 levels (t value: 3.48; p = 0.001) and APRI score (t value: 4.57, p < 0.001) were found as independent associated with FS in non-uremic patients. However, in adjusted models, only APRI score (t value: 3.98, p = 0.002) was an independent associated with FS in ESRD patients. Conclusion: In non-uremic cHepC patients, YKL-40 levels and APRI score may be valuable markers of FS. In ESRD patients, there is not sufficient data for prediction of HAI and FS. In these patients, APRI score may provide better information.
first_indexed 2024-04-12T22:51:32Z
format Article
id doaj.art-b31bc8d2114548adb4adbf37ae6ebfe7
institution Directory Open Access Journal
issn 1211-4286
1805-9694
language English
last_indexed 2024-04-12T22:51:32Z
publishDate 2017-10-01
publisher Karolinum Press
record_format Article
series Acta Medica
spelling doaj.art-b31bc8d2114548adb4adbf37ae6ebfe72022-12-22T03:13:20ZengKarolinum PressActa Medica1211-42861805-96942017-10-01602717510.14712/18059694.2017.965403Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C PatientsBengu TatarSukran KoseEmel PalaErhan TatarBackground: The aim of this study is to investigate the association between hepatic activity index (HAI) and fibrosis score (FS) with inflammation biomarkers in non-uremic and uremic hepatitis C positive patients. Methods: Fifty chronic hepatitis C (cHepC) positive patients, having a liver biopsy were included in this study. Liver biopsies were scored according to modified ISHAC scoring system. 25 healthy controls of similar age and gender were also enrolled as control group. Serum YKL-40, neutrophil/lymphocyte ratio (NLR), thrombocyte/lymphocyte ratio (PLR), CRP and Immunoglobulin (IgG, A and M) levels were used to determine inflammation. AST to Platelet Ratio Index (APRI) score was also evaluated. According to biopsy findings patients were divided into 2 groups: low (0–2) and severe (3–6) FS. Results: Patients with cHepC had increased inflammation compared to the healthy controls. End-stage renal disease (ESRD) patients had higher levels of inflammation markers (NLR, IgG, CRP and YKL-40) and lower HCV RNA levels, HAI and FS compared to non-uremic patients. When patients were grouped into 2 according to FS as mild and severe, IgG (p < 0.001), YKL-40 (p = 0.02) levels and APRI score (p = 0.002) were significantly higher compared to mild FS (p = 0.002). YKL-40 levels (t value: 3.48; p = 0.001) and APRI score (t value: 4.57, p < 0.001) were found as independent associated with FS in non-uremic patients. However, in adjusted models, only APRI score (t value: 3.98, p = 0.002) was an independent associated with FS in ESRD patients. Conclusion: In non-uremic cHepC patients, YKL-40 levels and APRI score may be valuable markers of FS. In ESRD patients, there is not sufficient data for prediction of HAI and FS. In these patients, APRI score may provide better information.https://actamedica.lfhk.cuni.cz/60/2/0071/APRI scorehepatitis Cend-stage renal diseaseinflammation biomarkersYKL-40liver histopathology
spellingShingle Bengu Tatar
Sukran Kose
Emel Pala
Erhan Tatar
Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients
Acta Medica
APRI score
hepatitis C
end-stage renal disease
inflammation biomarkers
YKL-40
liver histopathology
title Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients
title_full Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients
title_fullStr Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients
title_full_unstemmed Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients
title_short Inflammatory Biomarkers and Liver Histopathology in Non-Uremic and Uremic Chronic Hepatitis C Patients
title_sort inflammatory biomarkers and liver histopathology in non uremic and uremic chronic hepatitis c patients
topic APRI score
hepatitis C
end-stage renal disease
inflammation biomarkers
YKL-40
liver histopathology
url https://actamedica.lfhk.cuni.cz/60/2/0071/
work_keys_str_mv AT bengutatar inflammatorybiomarkersandliverhistopathologyinnonuremicanduremicchronichepatitiscpatients
AT sukrankose inflammatorybiomarkersandliverhistopathologyinnonuremicanduremicchronichepatitiscpatients
AT emelpala inflammatorybiomarkersandliverhistopathologyinnonuremicanduremicchronichepatitiscpatients
AT erhantatar inflammatorybiomarkersandliverhistopathologyinnonuremicanduremicchronichepatitiscpatients