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

  • J. Lee
  • , S. C. Ji
  • , B. Kim
  • , S. Yi
  • , K. H. Shin
  • , J. Y. Cho
  • , K. S. Lim
  • , S. H. Lee
  • , S. H. Yoon
  • , J. Y. Chung
  • , K. S. Yu
  • , H. S. Park
  • , S. H. Kim
  • , I. J. Jang

Research output: Contribution to journalArticlepeer-review

26 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)163-171
Number of pages9
JournalClinical and Translational Science
Volume10
Issue number3
DOIs
StatePublished - May 2017

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