Cargando…

Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels

Hepatitis C virus (HCV) infection causes chronic hepatitis, which frequently leads to hepatic fibrosis and hepatocellular carcinoma (HCC). Alanine aminotransferase (ALT) is a biomarker of hepatocyte injury and is associated with the progression of hepatic fibrosis. Advanced hepatic fibrosis also pre...

Descripción completa

Detalles Bibliográficos
Autores principales: Uto, Hirofumi, Mawatari, Seiich, Kumagai, Kotaro, Ido, Akio, Tsubouchi, Hirohito
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321325/
https://www.ncbi.nlm.nih.gov/pubmed/22509183
http://dx.doi.org/10.5812/hepatmon.829
_version_ 1782228935591854080
author Uto, Hirofumi
Mawatari, Seiich
Kumagai, Kotaro
Ido, Akio
Tsubouchi, Hirohito
author_facet Uto, Hirofumi
Mawatari, Seiich
Kumagai, Kotaro
Ido, Akio
Tsubouchi, Hirohito
author_sort Uto, Hirofumi
collection PubMed
description Hepatitis C virus (HCV) infection causes chronic hepatitis, which frequently leads to hepatic fibrosis and hepatocellular carcinoma (HCC). Alanine aminotransferase (ALT) is a biomarker of hepatocyte injury and is associated with the progression of hepatic fibrosis. Advanced hepatic fibrosis also predisposes HCV carriers to a risk of HCC. In contrast, some cases with persistent HCV infection have normal ALT levels that persist for a long time, and these HCV carriers have no or mild hepatitis and hepatic fibrosis. These HCV carriers are defined as persistent normal ALT (PNALT) cases and their risk of HCC is low compared to HCV carriers with abnormal ALT. However, there are various definitions of normal ALT and PNALT, and advanced hepatic fibrosis may be missed without a liver biopsy. In addition, there is also a risk of ALT elevation in HCV carriers with PNALT, which increases the risk of progression to hepatic fibrosis and HCC. Most HCV carriers with PNALT have asymptomatic or nonspecific symptoms. HCV carriers with PNALT are also considered to be responsive to interferon-based treatment. Thus, assessment of hepatic fibrosis is important in HCV carriers, and the eradication of HCV infection is more likely in HCV carriers with evidence of hepatic fibrosis, regardless of their ALT levels.
format Online
Article
Text
id pubmed-3321325
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Kowsar
record_format MEDLINE/PubMed
spelling pubmed-33213252012-04-16 Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels Uto, Hirofumi Mawatari, Seiich Kumagai, Kotaro Ido, Akio Tsubouchi, Hirohito Hepat Mon Review Article Hepatitis C virus (HCV) infection causes chronic hepatitis, which frequently leads to hepatic fibrosis and hepatocellular carcinoma (HCC). Alanine aminotransferase (ALT) is a biomarker of hepatocyte injury and is associated with the progression of hepatic fibrosis. Advanced hepatic fibrosis also predisposes HCV carriers to a risk of HCC. In contrast, some cases with persistent HCV infection have normal ALT levels that persist for a long time, and these HCV carriers have no or mild hepatitis and hepatic fibrosis. These HCV carriers are defined as persistent normal ALT (PNALT) cases and their risk of HCC is low compared to HCV carriers with abnormal ALT. However, there are various definitions of normal ALT and PNALT, and advanced hepatic fibrosis may be missed without a liver biopsy. In addition, there is also a risk of ALT elevation in HCV carriers with PNALT, which increases the risk of progression to hepatic fibrosis and HCC. Most HCV carriers with PNALT have asymptomatic or nonspecific symptoms. HCV carriers with PNALT are also considered to be responsive to interferon-based treatment. Thus, assessment of hepatic fibrosis is important in HCV carriers, and the eradication of HCV infection is more likely in HCV carriers with evidence of hepatic fibrosis, regardless of their ALT levels. Kowsar 2012-02 2012-02-29 /pmc/articles/PMC3321325/ /pubmed/22509183 http://dx.doi.org/10.5812/hepatmon.829 Text en Copyright © 2011, Kowsar M.P. Co. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Uto, Hirofumi
Mawatari, Seiich
Kumagai, Kotaro
Ido, Akio
Tsubouchi, Hirohito
Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels
title Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels
title_full Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels
title_fullStr Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels
title_full_unstemmed Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels
title_short Clinical Features of Hepatitis C Virus Carriers With Persistently Normal Alanine Aminotransferase Levels
title_sort clinical features of hepatitis c virus carriers with persistently normal alanine aminotransferase levels
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3321325/
https://www.ncbi.nlm.nih.gov/pubmed/22509183
http://dx.doi.org/10.5812/hepatmon.829
work_keys_str_mv AT utohirofumi clinicalfeaturesofhepatitiscviruscarrierswithpersistentlynormalalanineaminotransferaselevels
AT mawatariseiich clinicalfeaturesofhepatitiscviruscarrierswithpersistentlynormalalanineaminotransferaselevels
AT kumagaikotaro clinicalfeaturesofhepatitiscviruscarrierswithpersistentlynormalalanineaminotransferaselevels
AT idoakio clinicalfeaturesofhepatitiscviruscarrierswithpersistentlynormalalanineaminotransferaselevels
AT tsubouchihirohito clinicalfeaturesofhepatitiscviruscarrierswithpersistentlynormalalanineaminotransferaselevels