AIDS Research and Human Retroviruses · 2003 · 28 citations · 11 references
PharmacyPharmacokineticsPharmacologyDrug ClearanceHepatic PharmacokineticsVirologyAntiretroviral TherapyAntiviral PharmacologyAntiviral PharmacotherapyAntiviral TherapyPharmacokinetics In Liver DiseaseViral HepatitisAntiretroviral InteractionsChronic Viral HepatitisHepatic Toxicity Of AntiretroviralsHepatitis C InfectionHighly Active Antiretroviral TherapyHiv Antiretroviral TherapyLiver Toxicity MechanismsTrough Concentrations
Both chronic hepatitis C and nevirapine (NVP) use are risk factors for transaminase elevation under highly active antiretroviral therapy. NVP is metabolized in the liver and its clearance could be altered in the presence of chronic hepatitis C virus (HCV) infection, enhancing the risk of liver toxicity. We examined NVP plasma levels in 70 HIV-infected subjects receiving NVP-containing triple combinations. The median (range) NVP plasma trough concentrations were similar in 32 HCV antibody-positive and 38 HCV antibody-negative patients (5.8 [0.7-29] vs. 6.1 [0.9-9.6] microg/ml). Thus, HCV coinfection itself does not seem to influence significantly the pharmacokinetics of NVP in HIV-infected subjects.
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Liver toxicity caused by nevirapine
Daniel González de Requena, Marina Núñez, Inmaculada Jiménez‐Nácher et al. · AIDS · 2002 · 177 citations