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Role of efavirenz plasma concentrations on long-term HIV suppression and immune restoration in HIV-infected children

BACKGROUND: To access the long term relationship between efavirenz plasma concentrations and evolution of HIV RNA loads and CD4 cell counts in children. METHODS: Retrospective analysis of data from HIV-infected children on first line efavirenz-containing regimen. A population pharmacokinetic-pharmac...

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Detalles Bibliográficos
Autores principales: Homkham, Nontiya, Cressey, Tim R., Bouazza, Naim, Ingsrisawang, Lily, Techakunakorn, Pornchai, Mekmullica, Jutarat, Borkird, Thitiporn, Puangsombat, Achara, Na-Rajsima, Sathaporn, Treluyer, Jean Marc, Urien, Saik, Jourdain, Gonzague
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521995/
https://www.ncbi.nlm.nih.gov/pubmed/31095608
http://dx.doi.org/10.1371/journal.pone.0216868
Descripción
Sumario:BACKGROUND: To access the long term relationship between efavirenz plasma concentrations and evolution of HIV RNA loads and CD4 cell counts in children. METHODS: Retrospective analysis of data from HIV-infected children on first line efavirenz-containing regimen. A population pharmacokinetic-pharmacodynamic (PK-PD) model was developed to describe the evolution of HIV RNA load and CD4 cell count (efficacy outcomes) in relation to efavirenz plasma concentration. Individual CYP2B6 516 G>T genotype data were not available for this analysis. A score (IS(EFV)) quantifying the effect of efavirenz concentrations on the long-term HIV replication was calculated from efavirenz concentrations and PD parameters and, a value of IS(EFV) below which HIV replication is likely not suppressed was determined. Cox proportional hazards regression models were used to assess the association of the risk of viral replication with IS(EFV), and with efavirenz mid-dose concentration(C(12)). RESULTS: At treatment initiation, median (interquartile range, IQR) age was 8 years (5 to 10), body weight 17 kg (14 to 23), HIV RNA load 5.1 log(10) copies/mL (4.6 to 5.4), and CD4 cell count 71 cells/mm(3). A model of PK-PD viral dynamics assuming that efavirenz decreases the rate of infected host cells adequately described the relationship of interest. After adjusting for age, baseline HIV RNA load and CD4 cell counts an IS(EFV) <85% was significantly associated with a higher risk of viral replication (p-value <0.001) while no significant association was observed with C(12) <1.0 mg/L. CONCLUSION: The IS(EFV) score was a good predictor of viral replication in children on efavirenz-based treatment.