AIDS · 2010 · 49 citations · 9 references
PharmacyPharmacologyPharmacotherapyClinical PharmacologyMolecular VirologyVirologyAntiretroviral TherapyAntiviral AgentsAntiviral PharmacologyAntiviral PharmacotherapyAntiviral TherapyHuman Immunodeficiency Virus PharmacotherapyAntiviral TherapeuticsHiv Antiretroviral TherapyNon-nucleoside Reverse Transcriptase InhibitorsNucleoside Reverse Transcriptase InhibitorsUltrasensitive DetectionViral Disease SuppressionViral Load AssaysViral Load Assessment
OBJECTIVES: To compare the level of HIV-1 residual viremia, defined by a viral load below 50 copies/ml in patients receiving a tenofovir/emtricitabine and nevirapine (NVP) or efavirenz (EFV)-containing regimen. DESIGN: One hundred and sixty-five HIV-1-infected patients were retrospectively included since they achieved virological suppression (viral load <50 copies/ml) for at least 6 months with a tenofovir/emtricitabine and non-nucleoside reverse transcriptase inhibitor-containing regimen (NVP, n = 75 and EFV, n = 90). METHODS: Residual plasma viremia was measured using an ultrasensitive assay with a limit of quantification of 1 copy/ml. A Fisher's exact test was used to compare the percentage of patients with HIV-1 RNA below 1 copy/ml between the two treatment groups. Logistic regression was used to search for factors associated with a viral load below 1 copy/ml among the different patient characteristics. RESULTS: Patients in the NVP group had more frequently a viral load below 1 copy/ml than patients in the EFV group (81.3 vs. 55.6%, P < 0.001). In multivariate analysis, only NVP vs EFV (P = 0.005) and duration of viral suppression under antiretroviral treatment (P = 0.005) were independently associated with viral load below 1 copy/ml. CONCLUSIONS: It is well known that NVP has a good penetration in anatomic compartments that could explain a deep control of virus replication in some compartments and consequently decrease the residual level of viral load. The clinical relevance of having a viral load below 1 copy/ml has now to be studied for example on systemic inflammatory or immune activation markers.
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Sarah Palmer, Ann Wiegand, Frank Maldarelli et al. · Journal of Clinical Microbiology · 2003 · 611 citations · Full text
Andrea Antinori, Carlo Federico Perno, Maria Letizia Giancola et al. · Clinical Infectious Diseases · 2005 · 114 citations · Full text