Mid-dosing interval concentration of atazanavir and virological outcome in patients treated for HIV-1 infection

M. Fabbiani, S. Di Giambenedetto, E. Ragazzoni, M. Colafigli, M. Prosperi, R. Cauda, P. Navarra, A. De Luca

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Objectives: We investigated the clinical significance of monitoring the mid-dosing interval atazanavir (ATV) concentration (measured 12 ± 2 h after intake; C12 h) in patients taking this drug once daily in the evening. Methods: We retrospectively selected HIV-infected patients harbouring ATV-susceptible virus who underwent therapeutic drug monitoring (TDM) of ATV C12 h during routine out-patient visits, and we correlated C12 h to the 24-week virological response and toxicity. Results: A total of 115 plasma samples from 86 patients (76.7% with baseline HIV RNA0.23 mg/L showed virological failure in 14.3% of cases (P=0.021). In multivariate analysis, C12 h>0.23 mg/L was an independent predictor of virological response [odds ratio (OR) 4.23, P=0.031]. ATV levels correlated with concomitant unconjugated bilirubin levels (r=0.223, P=0.037), but a concentration cut-off predictive of moderate/severe hyperbilirubinaemia could not be identified. Conclusions: We identified a C12 h efficacy threshold that predicted virological response; this could be useful for morning TDM in selected subjects receiving ATV in the evening. Results must be interpreted with caution given the retrospective design of the study. © 2010 British HIV Association.
    Original languageEnglish
    Pages (from-to)326-333
    Number of pages7
    JournalHIV Medicine
    Volume11
    Issue number5
    Publication statusPublished - May 2010

    Keywords

    • Antiretroviral therapy
    • Atazanavir
    • HIV-1
    • Pharmacokinetic variability
    • Therapeutic drug monitoring

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