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

被引:26
作者
Shi, Qiang [1 ]
Yang, Xi [1 ]
Greenhaw, James J. [1 ]
Salminen, Alec Thomas [2 ]
Russotti, Gary M. [3 ]
Salminen, William F. [4 ]
机构
[1] US FDA, Div Syst Biol, Natl Ctr Toxicol Res, Jefferson, AR USA
[2] Univ Arkansas, Biomed Engn, Fayetteville, AR 72701 USA
[3] ProNat Brands LLC, Boca Raton, FL USA
[4] Gen X Tox LLC, Sarasota, FL 34241 USA
关键词
hepatotoxicity; pediatric; children; drug-induced liver injury; ACETAMINOPHEN-INDUCED HEPATOTOXICITY; HALOTHANE-ASSOCIATED HEPATOTOXICITY; AGE-RELATED-CHANGES; VALPROIC ACID; DEVELOPMENTAL PHARMACOLOGY; ANTITUBERCULOSIS DRUGS; GLUTATHIONE DEPLETION; METABOLIZING-ENZYMES; OXIDATIVE STRESS; HEPATIC-FAILURE;
D O I
10.1177/1091581817721675
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:365 / 379
页数:15
相关论文
共 156 条
[1]   Antiepileptic drugs and liver disease [J].
Ahmed, SN ;
Siddiqi, ZA .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2006, 15 (03) :156-164
[2]   Clinical diagnostic scale: a useful tool in the evaluation of suspected hepatotoxic adverse drug reactions [J].
Aithal, GP ;
Rawlins, MD ;
Day, CP .
JOURNAL OF HEPATOLOGY, 2000, 33 (06) :949-952
[3]   Determinants of Drug Metabolism in Early Neonatal Life [J].
Allegaert, Karel ;
van den Anker, John N. ;
Naulaers, Gunnar ;
de Hoon, Jan .
CURRENT CLINICAL PHARMACOLOGY, 2007, 2 (01) :23-29
[4]   Drug-induced liver injury in children [J].
Amin, Mansi D. ;
Harpavat, Sanjiv ;
Leung, Daniel H. .
CURRENT OPINION IN PEDIATRICS, 2015, 27 (05) :625-633
[5]   Using pharmacokinetics to predict the effects of pregnancy and maternal-infant transfer of drugs during lactation [J].
Anderson, Gail D. .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2006, 2 (06) :947-960
[6]  
[Anonymous], 2005, GUID IND NONCL STUD
[7]  
[Anonymous], 2002, DEV EMISSIONS INVENT, P1
[8]  
[Anonymous], 2009, Us Fda, V8, P1
[9]   Guidelines on paediatric dosing on the basis of developmental physiology and pharmacokinetic considerations [J].
Bartelink, Imke H. ;
Rademaker, Carin M. A. ;
Schobben, Alfred F. A. M. ;
van den Anker, John N. .
CLINICAL PHARMACOKINETICS, 2006, 45 (11) :1077-1097
[10]  
Bartkowska-Sniatkowska A, 2014, ANAESTH INTENSIVE TH, V46, P101, DOI [10.5603/AIT.2014.020, 10.5603/AIT.2014.0020]