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Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity
BACKGROUND/AIMS: Growth differentiation factor 15 (GDF-15) belongs to the transforming growth factor-β superfamily. GDF-15 is emerging as a biomarker for several diseases. The aim of this study was to determine the clinical performances of GDF-15 for the prediction of liver fibrosis and severity in...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Editorial Office of Gut and Liver
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347653/ https://www.ncbi.nlm.nih.gov/pubmed/27728964 http://dx.doi.org/10.5009/gnl16049 |
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author | Lee, Eaum Seok Kim, Seok Hyun Kim, Hyun Jin Kim, Kyung Hee Lee, Byung Seok Ku, Bon Jeong |
author_facet | Lee, Eaum Seok Kim, Seok Hyun Kim, Hyun Jin Kim, Kyung Hee Lee, Byung Seok Ku, Bon Jeong |
author_sort | Lee, Eaum Seok |
collection | PubMed |
description | BACKGROUND/AIMS: Growth differentiation factor 15 (GDF-15) belongs to the transforming growth factor-β superfamily. GDF-15 is emerging as a biomarker for several diseases. The aim of this study was to determine the clinical performances of GDF-15 for the prediction of liver fibrosis and severity in chronic liver disease. METHODS: The serum GDF-15 levels were examined via enzyme immunoassay in 145 patients with chronic liver disease and 101 healthy individuals. The patients with chronic liver disease consisted of 54 patients with chronic hepatitis, 44 patients with compensated liver cirrhosis, and 47 patients with decompensated liver cirrhosis. RESULTS: Of the patients with chronic liver diseases, the decompensated liver cirrhosis patients had an increased serum GDF-15 (3,483 ng/L) level compared with the patients with compensated liver cirrhosis (1,861 ng/L) and chronic hepatitis (1,232 ng/L). The overall diagnostic accuracies of GDF-15, as determined by the area under the receiver operating characteristic curves, were as follows: chronic hepatitis=0.656 (>574 ng/L, sensitivity, 53.7%; specificity, 79.2%), compensated liver cirrhosis=0.886 (>760 ng/L, sensitivity, 75.6%; specificity, 92.1%), and decompensated liver cirrhosis=0.984 (>869 ng/L, sensitivity, 97.9%; specificity, 94.1%). CONCLUSIONS: This investigation represents the first study to demonstrate the availability of GDF-15 in chronic liver disease. GDF-15 comprised a useful biomarker for the prediction of liver fibrosis and severity in chronic liver disease. |
format | Online Article Text |
id | pubmed-5347653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Editorial Office of Gut and Liver |
record_format | MEDLINE/PubMed |
spelling | pubmed-53476532017-04-06 Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity Lee, Eaum Seok Kim, Seok Hyun Kim, Hyun Jin Kim, Kyung Hee Lee, Byung Seok Ku, Bon Jeong Gut Liver Original Article BACKGROUND/AIMS: Growth differentiation factor 15 (GDF-15) belongs to the transforming growth factor-β superfamily. GDF-15 is emerging as a biomarker for several diseases. The aim of this study was to determine the clinical performances of GDF-15 for the prediction of liver fibrosis and severity in chronic liver disease. METHODS: The serum GDF-15 levels were examined via enzyme immunoassay in 145 patients with chronic liver disease and 101 healthy individuals. The patients with chronic liver disease consisted of 54 patients with chronic hepatitis, 44 patients with compensated liver cirrhosis, and 47 patients with decompensated liver cirrhosis. RESULTS: Of the patients with chronic liver diseases, the decompensated liver cirrhosis patients had an increased serum GDF-15 (3,483 ng/L) level compared with the patients with compensated liver cirrhosis (1,861 ng/L) and chronic hepatitis (1,232 ng/L). The overall diagnostic accuracies of GDF-15, as determined by the area under the receiver operating characteristic curves, were as follows: chronic hepatitis=0.656 (>574 ng/L, sensitivity, 53.7%; specificity, 79.2%), compensated liver cirrhosis=0.886 (>760 ng/L, sensitivity, 75.6%; specificity, 92.1%), and decompensated liver cirrhosis=0.984 (>869 ng/L, sensitivity, 97.9%; specificity, 94.1%). CONCLUSIONS: This investigation represents the first study to demonstrate the availability of GDF-15 in chronic liver disease. GDF-15 comprised a useful biomarker for the prediction of liver fibrosis and severity in chronic liver disease. Editorial Office of Gut and Liver 2017-03 2016-10-13 /pmc/articles/PMC5347653/ /pubmed/27728964 http://dx.doi.org/10.5009/gnl16049 Text en Copyright © 2017 by The Korean Society of Gastroenterology, the Korean Society of Gastrointestinal Endoscopy, the Korean Society of Neurogastroenterology and Motility, Korean College of Helicobacter and Upper Gastrointestinal Research, Korean Association the Study of Intestinal Diseases, the Korean Association for the Study of the Liver, Korean Pancreatobiliary Association, and Korean Society of Gastrointestinal Cancer. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Eaum Seok Kim, Seok Hyun Kim, Hyun Jin Kim, Kyung Hee Lee, Byung Seok Ku, Bon Jeong Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity |
title | Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity |
title_full | Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity |
title_fullStr | Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity |
title_full_unstemmed | Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity |
title_short | Growth Differentiation Factor 15 Predicts Chronic Liver Disease Severity |
title_sort | growth differentiation factor 15 predicts chronic liver disease severity |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5347653/ https://www.ncbi.nlm.nih.gov/pubmed/27728964 http://dx.doi.org/10.5009/gnl16049 |
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