Drug-Induced Liver Injury: Pattern Recognition and Future Directions

Gut Liver. 2016 Jan;10(1):27-36. doi: 10.5009/gnl15114.

Abstract

Drug-induced liver injury (DILI) remains a significant clinical challenge and is the leading cause of acute liver failure in most countries. An aging population that uses more medications, a constant influx of newly developed drugs and a growing risk from unfamiliar herbal and dietary supplements will make DILI an increasing part of clinical practice. Currently, the most effective strategy for disease management is rapid identification, withholding the inciting agents, supportive care and having a firm understanding of the expected natural history. There are resources available to aid the clinician, including a new online "textbook" as well as causality assessment tools, but a heightened awareness of risk and the disease's varying phenotypes and good history-taking remain cornerstones to diagnosis. Looking ahead, growing registries of cases, pharmacoepidemiology studies and translational research into the mechanisms of injury may produce better diagnostic tools, markers for risk and disease, and prevention and therapeutics.

Keywords: Diagnosis; Drug induced liver injury; Epidemiology; Hepatotoxicity; Herbal and dietary supplements.

Publication types

  • Review

MeSH terms

  • Age Factors
  • Anti-Infective Agents / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal / adverse effects
  • Anticonvulsants / adverse effects
  • Biopsy
  • Chemical and Drug Induced Liver Injury / diagnosis*
  • Chemical and Drug Induced Liver Injury / epidemiology
  • Dietary Supplements / adverse effects
  • Drugs, Chinese Herbal / adverse effects
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / adverse effects
  • Incidence
  • Liver / pathology
  • Liver Function Tests
  • Risk Factors
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors

Substances

  • Anti-Infective Agents
  • Anti-Inflammatory Agents, Non-Steroidal
  • Anticonvulsants
  • Drugs, Chinese Herbal
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Tumor Necrosis Factor-alpha