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Bile acid indices as biomarkers for liver diseases I: Diagnostic markers
BACKGROUND: Hepatobiliary diseases result in the accumulation of toxic bile acids (BA) in the liver, blood, and other tissues which may contribute to an unfavorable prognosis. AIM: To discover and validate diagnostic biomarkers of cholestatic liver diseases based on the urinary BA profile. METHODS:...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080550/ https://www.ncbi.nlm.nih.gov/pubmed/33959226 http://dx.doi.org/10.4254/wjh.v13.i4.433 |
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author | Alamoudi, Jawaher Abdullah Li, Wenkuan Gautam, Nagsen Olivera, Marco Meza, Jane Mukherjee, Sandeep Alnouti, Yazen |
author_facet | Alamoudi, Jawaher Abdullah Li, Wenkuan Gautam, Nagsen Olivera, Marco Meza, Jane Mukherjee, Sandeep Alnouti, Yazen |
author_sort | Alamoudi, Jawaher Abdullah |
collection | PubMed |
description | BACKGROUND: Hepatobiliary diseases result in the accumulation of toxic bile acids (BA) in the liver, blood, and other tissues which may contribute to an unfavorable prognosis. AIM: To discover and validate diagnostic biomarkers of cholestatic liver diseases based on the urinary BA profile. METHODS: We analyzed urine samples by liquid chromatography-tandem mass spectrometry and compared the urinary BA profile between 300 patients with hepatobiliary diseases vs 103 healthy controls by statistical analysis. The BA profile was characterized using BA indices, which quantifies the composition, metabolism, hydrophilicity, and toxicity of the BA profile. BA indices have much lower inter- and intra-individual variability compared to absolute concentrations of BA. In addition, BA indices demonstrate high area under the receiver operating characteristic curves, and changes of BA indices are associated with the risk of having a liver disease, which demonstrates their use as diagnostic biomarkers for cholestatic liver diseases. RESULTS: Total and individual BA concentrations were higher in all patients. The percentage of secondary BA (lithocholic acid and deoxycholic acid) was significantly lower, while the percentage of primary BA (chenodeoxycholic acid, cholic acid, and hyocholic acid) was markedly higher in patients compared to controls. In addition, the percentage of taurine-amidation was higher in patients than controls. The increase in the non-12α-OH BA was more profound than 12α-OH BA (cholic acid and deoxycholic acid) causing a decrease in the 12α-OH/ non-12α-OH ratio in patients. This trend was stronger in patients with more advanced liver diseases as reflected by the model for end-stage liver disease score and the presence of hepatic decompensation. The percentage of sulfation was also higher in patients with more severe forms of liver diseases. CONCLUSION: BA indices have much lower inter- and intra-individual variability compared to absolute BA concentrations and changes of BA indices are associated with the risk of developing liver diseases. |
format | Online Article Text |
id | pubmed-8080550 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-80805502021-05-05 Bile acid indices as biomarkers for liver diseases I: Diagnostic markers Alamoudi, Jawaher Abdullah Li, Wenkuan Gautam, Nagsen Olivera, Marco Meza, Jane Mukherjee, Sandeep Alnouti, Yazen World J Hepatol Clinical and Translational Research BACKGROUND: Hepatobiliary diseases result in the accumulation of toxic bile acids (BA) in the liver, blood, and other tissues which may contribute to an unfavorable prognosis. AIM: To discover and validate diagnostic biomarkers of cholestatic liver diseases based on the urinary BA profile. METHODS: We analyzed urine samples by liquid chromatography-tandem mass spectrometry and compared the urinary BA profile between 300 patients with hepatobiliary diseases vs 103 healthy controls by statistical analysis. The BA profile was characterized using BA indices, which quantifies the composition, metabolism, hydrophilicity, and toxicity of the BA profile. BA indices have much lower inter- and intra-individual variability compared to absolute concentrations of BA. In addition, BA indices demonstrate high area under the receiver operating characteristic curves, and changes of BA indices are associated with the risk of having a liver disease, which demonstrates their use as diagnostic biomarkers for cholestatic liver diseases. RESULTS: Total and individual BA concentrations were higher in all patients. The percentage of secondary BA (lithocholic acid and deoxycholic acid) was significantly lower, while the percentage of primary BA (chenodeoxycholic acid, cholic acid, and hyocholic acid) was markedly higher in patients compared to controls. In addition, the percentage of taurine-amidation was higher in patients than controls. The increase in the non-12α-OH BA was more profound than 12α-OH BA (cholic acid and deoxycholic acid) causing a decrease in the 12α-OH/ non-12α-OH ratio in patients. This trend was stronger in patients with more advanced liver diseases as reflected by the model for end-stage liver disease score and the presence of hepatic decompensation. The percentage of sulfation was also higher in patients with more severe forms of liver diseases. CONCLUSION: BA indices have much lower inter- and intra-individual variability compared to absolute BA concentrations and changes of BA indices are associated with the risk of developing liver diseases. Baishideng Publishing Group Inc 2021-04-27 2021-04-27 /pmc/articles/PMC8080550/ /pubmed/33959226 http://dx.doi.org/10.4254/wjh.v13.i4.433 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Clinical and Translational Research Alamoudi, Jawaher Abdullah Li, Wenkuan Gautam, Nagsen Olivera, Marco Meza, Jane Mukherjee, Sandeep Alnouti, Yazen Bile acid indices as biomarkers for liver diseases I: Diagnostic markers |
title | Bile acid indices as biomarkers for liver diseases I: Diagnostic markers |
title_full | Bile acid indices as biomarkers for liver diseases I: Diagnostic markers |
title_fullStr | Bile acid indices as biomarkers for liver diseases I: Diagnostic markers |
title_full_unstemmed | Bile acid indices as biomarkers for liver diseases I: Diagnostic markers |
title_short | Bile acid indices as biomarkers for liver diseases I: Diagnostic markers |
title_sort | bile acid indices as biomarkers for liver diseases i: diagnostic markers |
topic | Clinical and Translational Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080550/ https://www.ncbi.nlm.nih.gov/pubmed/33959226 http://dx.doi.org/10.4254/wjh.v13.i4.433 |
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