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Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches

To explore potential biomarkers for amoxicillin/clavulanate‐induced liver injury (AC‐DILI), we conducted a clinical trial in 32 healthy subjects based on multi‐omics approaches. Every subject was administered amoxicillin/clavulanate for 14 days. The liver‐specific microRNA‐122 (miR‐122) level increa...

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Autores principales: Lee, J, Ji, SC, Kim, B, Yi, S, Shin, KH, Cho, JY, Lim, KS, Lee, SH, Yoon, SH, Chung, JY, Yu, KS, Park, HS, Kim, SH, Jang, IJ
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421739/
https://www.ncbi.nlm.nih.gov/pubmed/27785887
http://dx.doi.org/10.1111/cts.12425
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author Lee, J
Ji, SC
Kim, B
Yi, S
Shin, KH
Cho, JY
Lim, KS
Lee, SH
Yoon, SH
Chung, JY
Yu, KS
Park, HS
Kim, SH
Jang, IJ
author_facet Lee, J
Ji, SC
Kim, B
Yi, S
Shin, KH
Cho, JY
Lim, KS
Lee, SH
Yoon, SH
Chung, JY
Yu, KS
Park, HS
Kim, SH
Jang, IJ
author_sort Lee, J
collection PubMed
description To explore potential biomarkers for amoxicillin/clavulanate‐induced liver injury (AC‐DILI), we conducted a clinical trial in 32 healthy subjects based on multi‐omics approaches. Every subject was administered amoxicillin/clavulanate for 14 days. The liver‐specific microRNA‐122 (miR‐122) level increased prior to and correlated well with the observed alanine aminotransferase (ALT) level increase. This result indicates its potential as a sensitive early marker for AC‐DILI. We also identified urinary metabolites, such as azelaic acid and 7‐methylxanthine, with levels that significantly differed among the groups classified by ALT elevation level on day 8 after drug administration (P < 0.05). Lymphocyte proliferation in response to the drug was also observed. These findings demonstrate sequential changes in the process of AC‐DILI, including metabolic changes, increased miR‐122 level, increased liver enzyme activity, and enhanced lymphocyte proliferation after drug administration. In conclusion, this study provides potential biomarkers for AC‐DILI based on currently known mechanisms using comprehensive multi‐omics approaches.
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spelling pubmed-54217392017-05-23 Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches Lee, J Ji, SC Kim, B Yi, S Shin, KH Cho, JY Lim, KS Lee, SH Yoon, SH Chung, JY Yu, KS Park, HS Kim, SH Jang, IJ Clin Transl Sci Research To explore potential biomarkers for amoxicillin/clavulanate‐induced liver injury (AC‐DILI), we conducted a clinical trial in 32 healthy subjects based on multi‐omics approaches. Every subject was administered amoxicillin/clavulanate for 14 days. The liver‐specific microRNA‐122 (miR‐122) level increased prior to and correlated well with the observed alanine aminotransferase (ALT) level increase. This result indicates its potential as a sensitive early marker for AC‐DILI. We also identified urinary metabolites, such as azelaic acid and 7‐methylxanthine, with levels that significantly differed among the groups classified by ALT elevation level on day 8 after drug administration (P < 0.05). Lymphocyte proliferation in response to the drug was also observed. These findings demonstrate sequential changes in the process of AC‐DILI, including metabolic changes, increased miR‐122 level, increased liver enzyme activity, and enhanced lymphocyte proliferation after drug administration. In conclusion, this study provides potential biomarkers for AC‐DILI based on currently known mechanisms using comprehensive multi‐omics approaches. John Wiley and Sons Inc. 2016-10-26 2017-05 /pmc/articles/PMC5421739/ /pubmed/27785887 http://dx.doi.org/10.1111/cts.12425 Text en © 2016 The Authors. Clinical and Translational Science published by Wiley Periodicals, Inc. on behalf of American Society for Clinical Pharmacology and Therapeutics This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research
Lee, J
Ji, SC
Kim, B
Yi, S
Shin, KH
Cho, JY
Lim, KS
Lee, SH
Yoon, SH
Chung, JY
Yu, KS
Park, HS
Kim, SH
Jang, IJ
Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches
title Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches
title_full Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches
title_fullStr Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches
title_full_unstemmed Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches
title_short Exploration of Biomarkers for Amoxicillin/Clavulanate‐Induced Liver Injury: Multi‐Omics Approaches
title_sort exploration of biomarkers for amoxicillin/clavulanate‐induced liver injury: multi‐omics approaches
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421739/
https://www.ncbi.nlm.nih.gov/pubmed/27785887
http://dx.doi.org/10.1111/cts.12425
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