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

被引:25
|
作者
Lee, J. [1 ]
Ji, S. C. [1 ]
Kim, B. [1 ]
Yi, S. [1 ]
Shin, K. H. [3 ,4 ]
Cho, J. Y. [1 ]
Lim, K. S. [5 ,6 ]
Lee, S. H. [1 ]
Yoon, S. H. [1 ]
Chung, J. Y. [7 ,8 ]
Yu, K. S. [1 ]
Park, H. S. [2 ]
Kim, S. H. [2 ]
Jang, I. J. [1 ]
机构
[1] Seoul Natl Univ, Coll Med & Hosp, Dept Clin Pharmacol & Therapeut, Seoul, South Korea
[2] Ajou Univ, Sch Med, Dept Allergy & Clin Immunol, Suwon, South Korea
[3] Kyungpook Natl Univ, Coll Pharm, Daegu, South Korea
[4] Kyungpook Natl Univ, Pharmaceut Sci Res Inst, Daegu, South Korea
[5] CHA Univ, Sch Med, Dept Clin Pharmacol & Therapeut, Seongnam, South Korea
[6] CHA Bundang Med Ctr, Seongnam, South Korea
[7] Seoul Natl Univ, Coll Med, Dept Clin Pharmacol & Therapeut, Seongnam, South Korea
[8] Bundang Hosp, Seongnam, South Korea
来源
关键词
SERUM ALANINE AMINOTRANSFERASE; CIRCULATING MICRORNAS; DRUG; HEPATOTOXICITY; SUSCEPTIBILITY; METABONOMICS; HEALTHY; OXIDOREDUCTASE; METABOLOMICS; SUPEROXIDE;
D O I
10.1111/cts.12425
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:163 / 171
页数:9
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