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Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure
Background and Aims: Recent accumulating evidence indicates the biological actions of autotaxin (ATX) in liver disease. However, the relationship between ATX and liver failure has not been reported. The present study aimed to examine alterations of serum ATX in acute-on-chronic liver failure (ACLF)...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
XIA & HE Publishing Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562802/ https://www.ncbi.nlm.nih.gov/pubmed/33083245 http://dx.doi.org/10.14218/JCTH.2020.00045 |
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author | Nie, Caiyun Zhang, Lei Chen, Xiaobing Li, Ying Ha, Fushuang Liu, Hua Han, Tao |
author_facet | Nie, Caiyun Zhang, Lei Chen, Xiaobing Li, Ying Ha, Fushuang Liu, Hua Han, Tao |
author_sort | Nie, Caiyun |
collection | PubMed |
description | Background and Aims: Recent accumulating evidence indicates the biological actions of autotaxin (ATX) in liver disease. However, the relationship between ATX and liver failure has not been reported. The present study aimed to examine alterations of serum ATX in acute-on-chronic liver failure (ACLF) and evaluate whether serum ATX could be useful as an early warning biomarker of ACLF. Methods: Serum ATX was measured in 50 patients with hepatitis B-related ACLF, 14 patients with alcohol-related ACLF, 11 patients with hepatitis B-related pre-ACLF, 11 patients with alcohol-related Child-Pugh A cirrhosis, 39 patients with hepatitis B-related Child-Pugh A cirrhosis, 26 patients with chronic hepatitis B, and 38 healthy volunteers by enzyme-linked immunosorbent assay. Results: Serum ATX level was significantly higher in the pre-ACLF group than in the Child-Pugh A cirrhosis and chronic hepatitis B groups but lower than in the ACLF group; furthermore, patients with pre-ACLF deteriorated to ACLF had significantly higher serum ATX levels than pre-ACLF patients that did not progress to ACLF. Serum ATX levels were significantly higher among male ACLF patients with preclinical infection, spontaneous bacterial peritonitis or pneumonia, as compared to patients with ACLF but no spontaneous bacterial peritonitis or pneumonia. Serum ATX levels were well correlated with serum biochemical parameters of liver function and model for end-stage liver disease score. Serum ATX ≥ 584.1 ng/mL was a poor prognostic factor for ACLF (hazard ratio of 4.750, 95% confidence interval of 1.106-20.392, p=0.036). Conclusions: Serum ATX level may be a useful early warning biomarker for ACLF. |
format | Online Article Text |
id | pubmed-7562802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | XIA & HE Publishing Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75628022020-10-19 Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure Nie, Caiyun Zhang, Lei Chen, Xiaobing Li, Ying Ha, Fushuang Liu, Hua Han, Tao J Clin Transl Hepatol Original Article Background and Aims: Recent accumulating evidence indicates the biological actions of autotaxin (ATX) in liver disease. However, the relationship between ATX and liver failure has not been reported. The present study aimed to examine alterations of serum ATX in acute-on-chronic liver failure (ACLF) and evaluate whether serum ATX could be useful as an early warning biomarker of ACLF. Methods: Serum ATX was measured in 50 patients with hepatitis B-related ACLF, 14 patients with alcohol-related ACLF, 11 patients with hepatitis B-related pre-ACLF, 11 patients with alcohol-related Child-Pugh A cirrhosis, 39 patients with hepatitis B-related Child-Pugh A cirrhosis, 26 patients with chronic hepatitis B, and 38 healthy volunteers by enzyme-linked immunosorbent assay. Results: Serum ATX level was significantly higher in the pre-ACLF group than in the Child-Pugh A cirrhosis and chronic hepatitis B groups but lower than in the ACLF group; furthermore, patients with pre-ACLF deteriorated to ACLF had significantly higher serum ATX levels than pre-ACLF patients that did not progress to ACLF. Serum ATX levels were significantly higher among male ACLF patients with preclinical infection, spontaneous bacterial peritonitis or pneumonia, as compared to patients with ACLF but no spontaneous bacterial peritonitis or pneumonia. Serum ATX levels were well correlated with serum biochemical parameters of liver function and model for end-stage liver disease score. Serum ATX ≥ 584.1 ng/mL was a poor prognostic factor for ACLF (hazard ratio of 4.750, 95% confidence interval of 1.106-20.392, p=0.036). Conclusions: Serum ATX level may be a useful early warning biomarker for ACLF. XIA & HE Publishing Inc. 2020-07-21 2020-09-28 /pmc/articles/PMC7562802/ /pubmed/33083245 http://dx.doi.org/10.14218/JCTH.2020.00045 Text en © 2020 Authors. http://creativecommons.org/licenses/by-nc/4.0/ This article has been published under the terms of Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0), which permits noncommercial unrestricted use, distribution, and reproduction in any medium, provided that the following statement is provided. “This article has been published in Journal of Clinical and Translational Hepatology at DOI: 10.14218/JCTH.2020.00045 and can also be viewed on the Journal’s website at http://www.jcthnet.com”. |
spellingShingle | Original Article Nie, Caiyun Zhang, Lei Chen, Xiaobing Li, Ying Ha, Fushuang Liu, Hua Han, Tao Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure |
title | Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure |
title_full | Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure |
title_fullStr | Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure |
title_full_unstemmed | Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure |
title_short | Autotaxin: An Early Warning Biomarker for Acute-on-chronic Liver Failure |
title_sort | autotaxin: an early warning biomarker for acute-on-chronic liver failure |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562802/ https://www.ncbi.nlm.nih.gov/pubmed/33083245 http://dx.doi.org/10.14218/JCTH.2020.00045 |
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