Drug-induced liver injury

Curr Opin Gastroenterol. 2012 May;28(3):198-202. doi: 10.1097/MOG.0b013e3283528b5d.

Abstract

Purpose of review: Drug-induced liver injury (DILI) remains an important disease in clinical practice. It is difficult to predict, diagnose and manage. Studies in the peer-reviewed literature in the last 2 years, focusing on the diagnosis, prediction and management of DILI will be reviewed.

Recent findings: Antibiotics remain the most common drug causing DILI in the United States and Europe. Expert opinion may still be the better method of diagnosing DILI compared with an objective tool such as the Roussel-Uclaf Causality Assessment Method. Hepatitis E represents an alternative diagnosis to some cases of presumed drug hepatotoxicity. There is ongoing research into the genetics of the pathophysiology and susceptibility of DILI. A genome-wide association study confirmed the association between human leukocyte antigen (HLA) class II and susceptibility to coamoxiclav (amoxicillin-clavulanic acid) induced DILI. There is new information on the protective effect of HLA-DRB1*07 family of alleles. MicroRNAs are a potential marker of DILI. Keratin variants may predict outcome of acute liver failure. N-acetylcysteine may be protective against DILI while taking antituberculosis medication.

Summary: Recent findings in the genetics of pathophysiology and susceptibility of DILI can help with predicting and avoiding DILI in clinical practice and provide the foundation for ongoing research.

Publication types

  • Review

MeSH terms

  • Acetylcysteine / therapeutic use
  • Amoxicillin-Potassium Clavulanate Combination / adverse effects
  • Anti-Bacterial Agents / adverse effects*
  • Antitubercular Agents / adverse effects
  • Chemical and Drug Induced Liver Injury* / diagnosis
  • Chemical and Drug Induced Liver Injury* / drug therapy
  • Chemical and Drug Induced Liver Injury* / epidemiology
  • Chemical and Drug Induced Liver Injury* / physiopathology
  • Disease Susceptibility
  • Europe / epidemiology
  • Female
  • Genome-Wide Association Study
  • Genotype
  • HLA-DRB1 Chains
  • Humans
  • Male
  • Protective Agents / therapeutic use
  • Risk Factors
  • United States / epidemiology

Substances

  • Anti-Bacterial Agents
  • Antitubercular Agents
  • HLA-DRB1 Chains
  • Protective Agents
  • Amoxicillin-Potassium Clavulanate Combination
  • Acetylcysteine