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Updated: Jun 11, 2026

Human Liver Microphysiological System for Assessing Drug-Induced Liver Toxicity In Vitro
Published on: January 31, 2022
Predicting and preventing acute drug-induced liver injury: what's new in 2010?
Gordon Liss1, Sushil Rattan, James H Lewis
1Georgetown University Medical Center, 3800 Reservoir Road, NW, Washington, DC 20007, USA.
Importance Of The Field:
The field of drug-induced liver injury (DILI) continues to expand in terms of global registries and with new agents added every year. Given the need to improve on our current methods of preclinical testing and monitoring for DILI during both clinical trials and in the post-approval setting, there is increasing research aimed at better understanding why injury occurs and who is most susceptible. To this end, the active pursuit of biomarkers that will predict injury prior to its occurrence and genetic testing that can identify individuals at risk of DILI continue to be at the forefront.
Areas Covered In This Review:
While alanine aminotransferase (ALT) testing remains the workhorse of biochemical monitoring, it only detects hepatic injury after it has occurred and, therefore, is not a true predictor. The utility and shortcomings of ALT and other liver tests are reviewed along with a synopsis of several other candidate biomarkers that are being studied. In addition, we review the recent data supporting testing for genetic predisposition to DILI and how identifying clinical risk factors may translate into better means for preventing DILI.
What The Reader Will Gain:
We update the basis on which age and gender are considered risk factors for DILI, and review the latest reports detailing the association of several candidate genes and the development of DILI in a susceptible patient. Human leukocyte antigen-B*5701 is closely linked to the hypersensitivity reaction seen with abacavir, and such screening has been successfully incorporated into HIV treatment around the globe and offers the promise that testing for other genetic markers will soon become a routine part of clinical practice. At present, candidate genes conferring specific susceptibility to DILI have been identified for a relatively few agents (e.g., flucloxacillin, amoxicillin-clavulanate, ximelagatran and isoniazid), but many more are under study. Preventing DILI often comes down to avoiding the use of potentially hepatotoxic drugs in certain situations, and we review the clinical scenarios in which this is most relevant.
Take Home Message:
Given the number and range of studies aimed at identifying predictors of DILI, the focus of this review is to summarize what we consider to be the most relevant new information published on the topics of clinical and genetic factors that predispose to DILI, the use of biomarkers as predictors of acute DILI, along with advances in prevention strategies.
Insights
Identifying predictors for drug-induced liver injury (DILI) is crucial. This review summarizes new information on clinical and genetic factors, biomarkers, and prevention strategies for DILI.
Area of Science:
- Hepatology
- Pharmacology
- Genetics
Background:
- Drug-induced liver injury (DILI) is a growing concern with increasing global registries and new causative agents annually.
- Improved preclinical testing and monitoring methods are needed for DILI during clinical trials and post-approval.
- Research focuses on understanding DILI mechanisms and identifying susceptible individuals, with a strong emphasis on predictive biomarkers and genetic testing.
Purpose of the Study:
- To review the latest advancements in predicting and preventing drug-induced liver injury (DILI).
- To summarize new findings on clinical and genetic factors predisposing individuals to DILI.
- To discuss the utility of biomarkers for predicting acute DILI and highlight progress in prevention strategies.
Main Methods:
- Review of current literature on DILI, including preclinical and clinical studies.
- Analysis of alanine aminotransferase (ALT) testing utility and limitations.
- Synopsis of candidate biomarkers and genetic testing data for DILI risk assessment.
- Examination of clinical risk factors and scenarios relevant to DILI prevention.
Main Results:
- Age and gender are confirmed risk factors for DILI.
- Specific genetic markers, such as Human Leukocyte Antigen-B*5701 for abacavir hypersensitivity, show promise for routine screening.
- Candidate genes conferring susceptibility to DILI have been identified for several drugs, with more under investigation.
- Prevention strategies often involve avoiding specific hepatotoxic drugs in at-risk individuals.
Conclusions:
- Significant progress has been made in identifying predictors of DILI.
- Biomarkers and genetic testing hold promise for early DILI detection and risk stratification.
- Advances in understanding risk factors are leading to improved DILI prevention strategies.
Related Concept Videos
Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment
Drug Toxicity: Risk factors
Effect of Hepatic Disease on Pharmacokinetics: Active Drug, Metabolite and Fraction of Metabolized Drug
