| Literature DB >> 25722197 |
Anne F Luetkemeyer1, Susan L Rosenkranz2, Darlene Lu2, Beatriz Grinsztejn3, Jorge Sanchez4, Michael Ssemmanda5, Ian Sanne6, Helen McIlleron7, Diane V Havlir1, David W Haas8.
Abstract
In STRIDE, slow metabolizer CYP2B6 and NAT2 genotypes were each associated with increased plasma efavirenz concentrations during antituberculosis therapy. Concentrations were greater on therapy than off therapy in 58% with CYP2B6 and 93% with NAT2 slow metabolizer genotypes. Individuals with slow metabolizer genotypes in both genes had markedly elevated concentrations.Entities:
Keywords: HIV/AIDS; efavirenz; pharmacogenetic; rifampin; tuberculosis
Mesh:
Substances:
Year: 2015 PMID: 25722197 PMCID: PMC4542662 DOI: 10.1093/cid/civ155
Source DB: PubMed Journal: Clin Infect Dis ISSN: 1058-4838 Impact factor: 9.079