Elsevier

Journal of Hepatology

Volume 63, Issue 2, August 2015, Pages 503-514
Journal of Hepatology

Review
Drug-induced liver injury: Interactions between drug properties and host factors

https://doi.org/10.1016/j.jhep.2015.04.016Get rights and content
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open access

Summary

Idiosyncratic drug-induced liver injury (DILI) is a common cause for drug withdrawal from the market and although infrequent, DILI can result in serious clinical outcomes including acute liver failure and the need for liver transplantation. Eliminating the iatrogenic “harm” caused by a therapeutic intent is a priority in patient care. However, identifying culprit drugs and individuals at risk for DILI remains challenging. Apart from genetic factors predisposing individuals at risk, the role of the drugs’ physicochemical and toxicological properties and their interactions with host and environmental factors need to be considered. The influence of these factors on mechanisms involved in DILI is multi-layered. In this review, we summarize current knowledge on 1) drug properties associated with hepatotoxicity, 2) host factors considered to modify an individuals’ risk for DILI and clinical phenotypes, and 3) drug-host interactions. We aim at clarifying knowledge gaps needed to be filled in as to improve risk stratification in patient care. We therefore broadly discuss relevant areas of future research. Emerging insight will stimulate new investigational approaches to facilitate the discovery of clinical DILI risk modifiers in the context of disease complexity and associated interactions with drug properties, and hence will be able to move towards safety personalized medicine.

Abbreviations

DILI
drug-induced liver injury
HLA
human leucocyte antigen
DAMPs
the damage associated molecular pattern molecules
ADMET
absorption, distribution, metabolism, excretion and toxicity
GST
glutathione-S-transferase
ROS
reactive oxygen species
JNK
c-Jun N-terminal kinase
Nrf-2
nuclear factor erythroid 2-related factor 2
Keap-1
Kelch-like ECH-associated protein 1
mtDNA
mitochondrial DNA
MPT
mitochondrial permeability transition
BSEP
bile salt export pump
ATP
adenosine triphosphate
P-gp
P-glycoprotein
MRP
multidrug resistance-associated protein
NAT2
N-acetyltransferase 2
CYP450
cytochrome P450
GSTM1
glutathione S-transferase Mu 1
GSTT1
glutathione S-transferase theta 1
NSAIDs
non-steroidal anti-inflammatory drugs
GSH
gluthatione
POLG
polymerase (DNA directed), gamma
FXR
farnesoid X receptor
LPS
lipopolysaccharides
MELD
Model for end-stage liver disease
PARP-1
Poly-(ADP-Ribose) Polymerase-1
NAFLD
non-alcoholic fatty liver disease
SOD2
superoxide dismutase 2
GPX1
glutathione peroxidase
NASH
nonalcoholic steatohepatitis
UDPGT
UDP-glucuronosyltransferase
NRTIs
nucleoside reverse transcriptase Inhibitors
PPARγ
peroxisome proliferator-activated receptor gamma
APC
antigen-presenting cell
MHC
major histocompatibility complex

Keywords

Drug-induced liver injury
Drug physicochemical properties
Host factors
Drug-host Interaction
Pharmacogenetics
Drug metabolism
Drug clearance
Clinical toxicology

Cited by (0)

These authors equally contributed to the manuscript.