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The Potential Role of Metabolomics in Drug-Induced Liver Injury (DILI) Assessment
Abstract
Drug-induced liver injury (DILI) is one of the most frequent adverse clinical reactions and a relevant cause of morbidity and mortality. Hepatotoxicity is among the major reasons for drug withdrawal during post-market and late development stages, representing a major concern to the pharmaceutical industry. The current biochemical parameters for the detection of DILI are based on enzymes (alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transpeptidase (GGT), alkaline phosphatase (ALP)) and bilirubin serum levels that are not specific of DILI and therefore there is an increasing interest on novel, specific, DILI biomarkers discovery. Metabolomics has emerged as a tool with a great potential for biomarker discovery, especially in disease diagnosis, and assessment of drug toxicity or efficacy. This review summarizes the multistep approaches in DILI biomarker research and discovery based on metabolomics and the principal outcomes from the research performed in this field. For that purpose, we have reviewed the recent scientific literature from PubMed, Web of Science, EMBASE, and PubTator using the terms “metabolomics”, “DILI”, and “humans”. Despite the undoubted contribution of metabolomics to our understanding of the underlying mechanisms of DILI and the identification of promising novel metabolite biomarkers, there are still some inconsistencies and limitations that hinder the translation of these research findings into general clinical practice, probably due to the variability of the methods used as well to the different mechanisms elicited by the DILI causing agent.
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“but there are still limitations preventing these research findings from being translated into general clinical practice”
From Metabolomic Analysis of Pediatric Patients with Idiosyncratic Drug-Induced Liver Injury According to the Updated RUCAM (2023) · cites this paper as [60]
In the citing paper
“Metabolomics has undoubtedly contributed to the understanding of the underlying mechanisms of DILI”
From Metabolomic Analysis of Pediatric Patients with Idiosyncratic Drug-Induced Liver Injury According to the Updated RUCAM (2023) · cites this paper as [60]
In the citing paper
“and has allowed the identification of metabolites as potential biomarkers”
From Metabolomic Analysis of Pediatric Patients with Idiosyncratic Drug-Induced Liver Injury According to the Updated RUCAM (2023) · cites this paper as [60]
In the citing paper
“Moreno-Torres et al. in a recent review (June 2022) recognized that the current diagnosis of drug-induced liver injury is based on determination of transaminases and serum bilirubin levels that are not specific for DILI”
From Metabolomic Analysis of Pediatric Patients with Idiosyncratic Drug-Induced Liver Injury According to the Updated RUCAM (2023) · cites this paper as Moreno-Torres et al. in a recent review (June 2022)
In the citing paper
“probably due to the variability of the methods used in the different studies, as well as due to the different mechanisms caused by the agent that causes or prevents DILI [60].”
From Metabolomic Analysis of Pediatric Patients with Idiosyncratic Drug-Induced Liver Injury According to the Updated RUCAM (2023) · cites this paper as [60]
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Wesseler, M. F., Taebnia, N., Harrison, S., Youhanna, S., Preiss, L. C., Kemas, A. M., Vegvari, A., Mokry, J., Sullivan, G. J., Lauschke, V. M., et al. (2023) · Acta Biomaterialia · doi:10.1016/j.actbio.2023.09.022 · Cited by 39
Andújar-Vera, F., Alés-Palmer, M. L., Muñoz-de-Rueda, P., Iglesias-Baena, I., & Ocete-Hita, E. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241713562 · Cited by 10
Metadata
- Authors
- Moreno-Torres, M., Quintás, G., & Castell, J. V.
- Venue
- Metabolites
- Publisher
- MDPI AG
- Published
- 2022-06-19
- Volume
- 12
- Issue
- 6
- Pages
- 564
- ISSN
- 2218-1989
- PMC
- PMC9227129
- Cited by
- 50
- References
- 1
- Language
- en
- Funders
- European Consortium EU-ToxRisk (681002, IJC2018-036209-I, FP7-HEALTH-2013-INNOVATION-1, CP-IP 602156-1)
- Ministerio de Ciencia e Innovación (681002, IJC2018-036209-I, FP7-HEALTH-2013-INNOVATION-1, CP-IP 602156-1)
- EU project HeCaTos (681002, IJC2018-036209-I, FP7-HEALTH-2013-INNOVATION-1, CP-IP 602156-1)
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