Drug-induced liver injury
- PMID: 20020257
- DOI: 10.1007/978-3-642-00663-0_1
Drug-induced liver injury
Abstract
Many drugs and environmental chemicals are capable of evoking some degree of liver injury. The liver represents a primary target for adverse drug reactions due to its central role in biotransformation and excretion of foreign compounds, its portal location within the circulation exposing it to a wide variety of substances, and its anatomic and physiologic structure. Drug-induced liver injury (DILI) remains the single most common adverse indication leading to drug candidate failure or withdrawal from the market. However, the absolute incidence of DILI is low, and this presents a challenge to mechanistic studies. DILI remains unpredictable making prevention very difficult. In this chapter, we focus on the current understanding of DILI. We begin with an overview regarding the significance and epidemiology of DILI and then examine the clinical presentation and susceptibility factors related to DILI. This is followed by a review of the current literature regarding the proposed pathogenesis of DILI, which involves the participation of a drug, or most often a reactive metabolite of the drug, that either directly affects cellular function or elicits an immune response. It is our hope that this chapter will shed light on the major problems associated with DILI in regards to the pharmaceutical industry, drug regulatory agencies, physicians and pharmacists, and patients.
Similar articles
-
Idiosyncratic drug-induced liver injury: an update on the 2007 overview.Expert Opin Drug Saf. 2014 Jan;13(1):67-81. doi: 10.1517/14740338.2013.828032. Epub 2013 Sep 27. Expert Opin Drug Saf. 2014. PMID: 24073714 Review.
-
Review article: drug-induced liver injury in clinical practice.Aliment Pharmacol Ther. 2010 Jul;32(1):3-13. doi: 10.1111/j.1365-2036.2010.04320.x. Epub 2010 Mar 31. Aliment Pharmacol Ther. 2010. PMID: 20374223 Review.
-
Signal transduction pathways involved in drug-induced liver injury.Handb Exp Pharmacol. 2010;(196):267-310. doi: 10.1007/978-3-642-00663-0_10. Handb Exp Pharmacol. 2010. PMID: 20020266 Review.
-
Evidence-based selection of training compounds for use in the mechanism-based integrated prediction of drug-induced liver injury in man.Arch Toxicol. 2016 Dec;90(12):2979-3003. doi: 10.1007/s00204-016-1845-1. Epub 2016 Sep 22. Arch Toxicol. 2016. PMID: 27659300 Free PMC article. Review.
-
Utilization of causal reasoning of hepatic gene expression in rats to identify molecular pathways of idiosyncratic drug-induced liver injury.Toxicol Sci. 2014 Jan;137(1):234-48. doi: 10.1093/toxsci/kft232. Epub 2013 Oct 17. Toxicol Sci. 2014. PMID: 24136188
Cited by
-
Regulation of drug-induced liver injury by signal transduction pathways: critical role of mitochondria.Trends Pharmacol Sci. 2013 Apr;34(4):243-53. doi: 10.1016/j.tips.2013.01.009. Epub 2013 Feb 28. Trends Pharmacol Sci. 2013. PMID: 23453390 Free PMC article. Review.
-
MetaPredictor: in silico prediction of drug metabolites based on deep language models with prompt engineering.Brief Bioinform. 2024 Jul 25;25(5):bbae374. doi: 10.1093/bib/bbae374. Brief Bioinform. 2024. PMID: 39082648 Free PMC article.
-
Research Progress on the Animal Models of Drug-Induced Liver Injury: Current Status and Further Perspectives.Biomed Res Int. 2019 Apr 15;2019:1283824. doi: 10.1155/2019/1283824. eCollection 2019. Biomed Res Int. 2019. PMID: 31119149 Free PMC article. Review.
-
Mechanism Investigation of Rifampicin-Induced Liver Injury Using Comparative Toxicoproteomics in Mice.Int J Mol Sci. 2017 Jul 2;18(7):1417. doi: 10.3390/ijms18071417. Int J Mol Sci. 2017. PMID: 28671602 Free PMC article.
-
Low-dose isotretinoin therapy and blood lipid abnormality: A case series with sixty patients.J Family Med Prim Care. 2018 Jan-Feb;7(1):171-174. doi: 10.4103/jfmpc.jfmpc_104_16. J Family Med Prim Care. 2018. PMID: 29915754 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical