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Use of bile acids as potential markers of liver dysfunction in humans: A systematic review
OBJECTIVE: This study aimed to determine the effectiveness of using total, individual serum, or urinary bile acids (BA) as potential markers of liver dysfunction. METHODS: We searched the PubMed and Web of Science databases using the following keywords- “serum bile acids,” “liver dysfunction,” “live...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519223/ https://www.ncbi.nlm.nih.gov/pubmed/34731122 http://dx.doi.org/10.1097/MD.0000000000027464 |
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author | Azer, Samy A. Hasanato, Rana |
author_facet | Azer, Samy A. Hasanato, Rana |
author_sort | Azer, Samy A. |
collection | PubMed |
description | OBJECTIVE: This study aimed to determine the effectiveness of using total, individual serum, or urinary bile acids (BA) as potential markers of liver dysfunction. METHODS: We searched the PubMed and Web of Science databases using the following keywords- “serum bile acids,” “liver dysfunction,” “liver injury,” “liver disease,” “traditional liver function tests,” “Chronic liver disease,” “acute liver injury”. The search was complemented by manual screening of the list of references for relevant articles. We selected only English-language manuscripts for adult patients based on predetermined inclusion and exclusion criteria. Animal studies and studies on neonates and children were not included. OUTCOME MEASURES: Changes in BA concentrations or ratios at or prior to changes in liver function tests. RESULTS: A total of 547 studies were identified, of which 28 were included after reading the entire manuscript. These studies included 1630 patients and 836 controls published between 1990 and 2017. The methods used in BA assays varied significantly, and the studies did not agree. on specific individual BA or BA ratios as biomarkers of specific liver injury or dysfunction. Except for the prognostic value of BA in intrahepatic cholestasis of pregnancy (ICP), studies have failed to provide evidence for BA as a liver biomarker. CONCLUSIONS: Despite the research conducted on BA for over 27 years, there are inconsistencies in the reported results and a lack of solid evidence to support the use of individual BA or BA ratios as biomarkers of liver injury. Adequately conducted studies needed to resolve this limitation in the literature. |
format | Online Article Text |
id | pubmed-8519223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-85192232021-10-18 Use of bile acids as potential markers of liver dysfunction in humans: A systematic review Azer, Samy A. Hasanato, Rana Medicine (Baltimore) 4500 OBJECTIVE: This study aimed to determine the effectiveness of using total, individual serum, or urinary bile acids (BA) as potential markers of liver dysfunction. METHODS: We searched the PubMed and Web of Science databases using the following keywords- “serum bile acids,” “liver dysfunction,” “liver injury,” “liver disease,” “traditional liver function tests,” “Chronic liver disease,” “acute liver injury”. The search was complemented by manual screening of the list of references for relevant articles. We selected only English-language manuscripts for adult patients based on predetermined inclusion and exclusion criteria. Animal studies and studies on neonates and children were not included. OUTCOME MEASURES: Changes in BA concentrations or ratios at or prior to changes in liver function tests. RESULTS: A total of 547 studies were identified, of which 28 were included after reading the entire manuscript. These studies included 1630 patients and 836 controls published between 1990 and 2017. The methods used in BA assays varied significantly, and the studies did not agree. on specific individual BA or BA ratios as biomarkers of specific liver injury or dysfunction. Except for the prognostic value of BA in intrahepatic cholestasis of pregnancy (ICP), studies have failed to provide evidence for BA as a liver biomarker. CONCLUSIONS: Despite the research conducted on BA for over 27 years, there are inconsistencies in the reported results and a lack of solid evidence to support the use of individual BA or BA ratios as biomarkers of liver injury. Adequately conducted studies needed to resolve this limitation in the literature. Lippincott Williams & Wilkins 2021-10-15 /pmc/articles/PMC8519223/ /pubmed/34731122 http://dx.doi.org/10.1097/MD.0000000000027464 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | 4500 Azer, Samy A. Hasanato, Rana Use of bile acids as potential markers of liver dysfunction in humans: A systematic review |
title | Use of bile acids as potential markers of liver dysfunction in humans: A systematic review |
title_full | Use of bile acids as potential markers of liver dysfunction in humans: A systematic review |
title_fullStr | Use of bile acids as potential markers of liver dysfunction in humans: A systematic review |
title_full_unstemmed | Use of bile acids as potential markers of liver dysfunction in humans: A systematic review |
title_short | Use of bile acids as potential markers of liver dysfunction in humans: A systematic review |
title_sort | use of bile acids as potential markers of liver dysfunction in humans: a systematic review |
topic | 4500 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8519223/ https://www.ncbi.nlm.nih.gov/pubmed/34731122 http://dx.doi.org/10.1097/MD.0000000000027464 |
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