Drug-Induced Liver Injury in Children: Clinical Observations, Animal Models, and Regulatory Status

• Published in: International journal of toxicology Vol. 36; no. 5; pp. 365 - 379
• Main Authors: Shi, Qiang, Yang, Xi, Greenhaw, James J., Salminen, Alec Thomas, Russotti, Gary M., Salminen, William F.
• Format: Journal Article
• Language: English
• Published: Los Angeles, CA SAGE Publications 01-09-2017
• Subjects: Animals; Chemical and Drug Induced Liver Injury - etiology; Child; Drug Approval; Humans; Models, Animal; Public Policy; United States; United States Government Agencies; drug-induced liver injury; children; hepatotoxicity; pediatric
• ISSN: 1091-5818; 1092-874X
• DOI: 10.1177/1091581817721675

Drug-induced liver injury in children (cDILI) accounts for about 1% of all reported adverse drug reactions throughout all age groups, less than 10% of all clinical DILI cases, and around 20% of all acute liver failure cases in children. The overall DILI susceptibility in children has been assumed to be lower than in adults. Nevertheless, controversial evidence is emerging about children’s sensitivity to DILI, with children’s relative susceptibility to DILI appearing to be highly drug-specific. The culprit drugs in cDILI are similar but not identical to DILI in adults (aDILI). This is demonstrated by recent findings that a drug frequently associated with aDILI (amoxicillin/clavulanate) was rarely associated with cDILI and that the drug basiliximab caused only cDILI but not aDILI. The fatality in reported cDILI studies ranged from 4% to 31%. According to the US Food and Drug Administration–approved drugs labels, valproic acid, dactinomycin, and ampicillin appear more likely to cause cDILI. In contrast, deferasirox, isoniazid, dantrolene, and levofloxacin appear more likely to cause aDILI. Animal models have been explored to mimic children’s increased susceptibility to valproic acid hepatotoxicity or decreased susceptibility to acetaminophen or halothane hepatotoxicity. However, for most drugs, animal models are not readily available, and the underlying mechanisms for the differential reactions to DILI between children and adults remain highly hypothetical. Diagnosis tools for cDILI are not yet available. A critical need exists to fill the knowledge gaps in cDILI. This review article provides an overview of cDILI and specific drugs associated with cDILI.