Abstract
Keratins, a major component of epithelial cell intermediate filaments, provide structural support to the cell and are important for the maintenance of structural integrity. Beyond its role of structural integrity in hepatocytes, keratin 18 (K18) is a known marker of apoptosis and has been proposed as an indicator of progression in chronic liver diseases such as nonalcoholic fatty liver disease (NAFLD). NAFLD is the most common cause of chronic liver disease in children and adolescents in the United States and throughout the world and comprises a wide spectrum of diseases ranging from simple steatosis (fatty liver) to nonalcoholic steatohepatitis (NASH) and cirrhosis. While simple steatosis is typically benign in nature, NASH is a more serious condition that may progress to end-stage liver disease and liver failure. Currently, liver biopsy is considered the most reliable method of assessing the histological severity of disease and differentiating between simple steatosis and NASH. Because biopsy is invasive in nature, expensive, and subject to sampling error and/or variability in interpretation, it is not suitable as a screening test. Therefore, it is necessary to examine known mechanisms associated with the progression of liver disease, such as hepatocellular apoptosis, and identify potential biomarkers that could be used as a diagnostic tool in NASH. This review will focus on the 1) the role of keratins in health and disease, 2) K18 as a potential non invasive biomarker in liver disease, 3) overview of pediatric NAFLD and issues with diagnosis and 4) potential role for K18 in assessing pediatric nonalcoholic fatty liver disease.
Keywords: Apoptosis, biomarker, Children, keratin 18, Liver Disease, nonalcoholic fatty liver disease, hepatocyte, Fibrosis, nonalcoholic steatohepatitis, Biopsy
Current Pediatric Reviews
Title: Keratin 18, Apoptosis, and Liver Disease in Children
Volume: 7 Issue: 4
Author(s): Yanci O. Mannery, Craig J. McClain and Miriam B. Vos
Affiliation:
Keywords: Apoptosis, biomarker, Children, keratin 18, Liver Disease, nonalcoholic fatty liver disease, hepatocyte, Fibrosis, nonalcoholic steatohepatitis, Biopsy
Abstract: Keratins, a major component of epithelial cell intermediate filaments, provide structural support to the cell and are important for the maintenance of structural integrity. Beyond its role of structural integrity in hepatocytes, keratin 18 (K18) is a known marker of apoptosis and has been proposed as an indicator of progression in chronic liver diseases such as nonalcoholic fatty liver disease (NAFLD). NAFLD is the most common cause of chronic liver disease in children and adolescents in the United States and throughout the world and comprises a wide spectrum of diseases ranging from simple steatosis (fatty liver) to nonalcoholic steatohepatitis (NASH) and cirrhosis. While simple steatosis is typically benign in nature, NASH is a more serious condition that may progress to end-stage liver disease and liver failure. Currently, liver biopsy is considered the most reliable method of assessing the histological severity of disease and differentiating between simple steatosis and NASH. Because biopsy is invasive in nature, expensive, and subject to sampling error and/or variability in interpretation, it is not suitable as a screening test. Therefore, it is necessary to examine known mechanisms associated with the progression of liver disease, such as hepatocellular apoptosis, and identify potential biomarkers that could be used as a diagnostic tool in NASH. This review will focus on the 1) the role of keratins in health and disease, 2) K18 as a potential non invasive biomarker in liver disease, 3) overview of pediatric NAFLD and issues with diagnosis and 4) potential role for K18 in assessing pediatric nonalcoholic fatty liver disease.
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Cite this article as:
O. Mannery Yanci, J. McClain Craig and B. Vos Miriam, Keratin 18, Apoptosis, and Liver Disease in Children, Current Pediatric Reviews 2011; 7 (4) . https://dx.doi.org/10.2174/157339611796892364
DOI https://dx.doi.org/10.2174/157339611796892364 |
Print ISSN 1573-3963 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6336 |

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