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Drug-induced hyperbilirubinemia and the clinical influencing factors

Authors
Ah, Young-MiKim, Young-MiKim, Min-JungChoi,Young HeePark, Kyoung-HoSon, In-JaKim, Sang Geon
Issue Date
Oct-2008
Publisher
TAYLOR & FRANCIS INC
Keywords
Hyperbilirubinemia; UGT1A1; OATP1B1; Multidrug resistance-associated protein 2 (MRA2); Genetic polymorphisms; Annual occurrence indices; Adverse drug reactions
Citation
DRUG METABOLISM REVIEWS, v.40, no.4, pp 511 - 537
Pages
27
Indexed
SCIE
SCOPUS
Journal Title
DRUG METABOLISM REVIEWS
Volume
40
Number
4
Start Page
511
End Page
537
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/42154
DOI
10.1080/03602530802341133
ISSN
0360-2532
1097-9883
Abstract
Hyperbilirubinemia may accompany harmful effects such as jaundice, brain dysfunction, and pharmacokinetic alterations of drugs. Clinical drugs are the important causes of hyperbilirubinemia, especially for patients with certain pathologic conditions or with genetic variations. This article reviews hyperbilirubinemic pathophysiology with respect to the effects of clinical drugs. In addition, this review introduces a new formula that may be utilized to estimate the annual occurrences of drug-induced hyperbilirubinemia in a hospital. Variations in the genes of UDP-glucuronosyltransferases, organic anion-transporting polypeptides and multidrug resistance proteins are the predisposing factors for drug-induced hyperbilirubinemia; therefore, their genetic and ethnic polymorphisms are discussed.
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