Open AccessDrug-induced liver injury: Is it somehow foreseeable?
Author(s) -
Giovanni Tarantino,
Matteo Nicola Dario Di Minno,
Domênico Capone
Publication year - 2009
Publication title -
world journal of gastroenterology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.427
H-Index - 155
eISSN - 2219-2840
pISSN - 1007-9327
DOI - 10.3748/wjg.15.2817
Subject(s) - liver injury , genotyping , drug , drug metabolism , medicine , pathogenesis , disease , liver disease , concomitant , adverse effect , pharmacology , bioinformatics , intensive care medicine , genotype , biology , gene , genetics
The classic view on the pathogenesis of drug-induced liver injury is that the so-called parent compounds are made hepatotoxic by metabolism (formation of neo-substances that react abnormally), mainly by cytochromes P-450 (CYP), with further pathways, such as mitochondrial dysfunction and apoptosis, also playing a role. Risk factors for drug-induced liver injury include concomitant hepatic diseases, age and genetic polymorphisms of CYP. However, some susceptibility can today be predicted before drug administration, working on the common substrate, by phenotyping and genotyping studies and by taking in consideration patients' health status. Physicians should always think of this adverse effect in the absence of other clear hepatic disease. Ethical and legal problems towards operators in the health care system are always matters to consider.