Do activities of cytochrome P450 (CYP)3A, CYP2D6 and P-glycoprotein differ between healthy volunteers and HIV-infected patients?
Author(s) -
Alexander Jetter,
Gerd Fätkenheuer,
Dorothee Frank,
Tobias Klaassen,
Angela Seeringer,
Oxana Doroshyenko,
Julia Kirchheiner,
W Hein,
Edgar Schömig,
Uwe Fuhr,
Christoph Wyen
Publication year - 2010
Publication title -
antiviral therapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.747
H-Index - 87
eISSN - 2040-2058
pISSN - 1359-6535
DOI - 10.3851/imp1648
Subject(s) - cyp3a , dextromethorphan , dextrorphan , medicine , cyp2d6 , pharmacokinetics , pharmacology , efavirenz , area under the curve , p glycoprotein , cyp3a5 , cyp2c9 , cyp3a4 , confidence interval , digoxin , cytochrome p450 , gastroenterology , immunology , viral load , biology , human immunodeficiency virus (hiv) , drug resistance , genotype , antiretroviral therapy , biochemistry , microbiology and biotechnology , metabolism , multiple drug resistance , gene , heart failure
In inflammation and infection, cytochrome P450 (CYP) enzyme activities are down-regulated. Information on possible discrepancies in activities of CYP enzymes and drug transporters between HIV-infected patients and healthy people is limited.
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