Drug induced liver injury classification
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rachita Navara, M.D. [2]
Overview
Drug induced liver injury may be classified into multiple subtypes based on clinical presentation, mechanism, or histologic findings.[1]
Classification
Drug induced liver injury may be classified into multiple subtypes based on clinical presentation, mechanism, or histologic findings.
Clinical presentation:
Hepatocellular injury
- Elevation of serum transaminases ≥ 2-5 times the upper limit of normal
- May have hyperbilirubinemia
- May have abnormal synthetic function tests (e.g. International Normalized Ratio, albumin)
Cholestatic injury
- Elevation of alkaline phosphatase ≥ 3 times the upper limit of normal
- May have hyperbilirubinemia
- May have abnormal synthetic function tests (e.g. International Normalized Ratio, albumin)
Mixed injury
- Both alkaline phosphatase and transaminases are elevated in roughly equal proportion, and/or an alanine aminotransferase to alkaline phosphatase ratio between 2-5
Mechanism:
Dose-dependent hepatotoxicity
- e.g. Acetaminophen-induced centrilobular necrosis
Idiosyncratic hepatotoxicity
- e.g. Stimulation of immune reponse by biologic agents, independent of dose, akin to drug hypersensitivity
- e.g. Altered host genes involved in drug metabolism
Histologic findings:
Histologic findings may be further subclassified into:
- Hepatitis (hepatocellular injury)
- Cholestasis
- Granulomatous
- Steatosis
- Fibrosis
References
- ↑ Fisher K, Vuppalanchi R, Saxena R (2015). "Drug-Induced Liver Injury". Arch Pathol Lab Med. 139 (7): 876–87. doi:10.5858/arpa.2014-0214-RA. PMID 26125428.