The effect of plasma drug concentrations on HIV-1 clearance rate during quadruple drug therapy

被引:98
作者
Hoetelmans, RMW
Reijers, MHE
Weverling, GJ
ten Kate, RW
Wit, FWNM
Mulder, JW
Weigel, HM
Frissen, PHJ
Roos, M
Jurriaans, S
Schuitemaker, H
de Wolf, F
Beijnen, JH
Lange, JMA
机构
[1] Slotervaart Hosp, Dept Pharm & Pharmacol, NL-1066 EC Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Internal Med, Natl AIDS Therapy Evaluat Ctr, NL-1105 AZ Amsterdam, Netherlands
[3] Onze Lieve Vrouwe Gasthuis, Dept Internal Med, Amsterdam, Netherlands
[4] Kennemer Gasthuis, Dept Internal Med, Haarlem, Netherlands
[5] Slotervaart Hosp, Dept Internal Med, Amsterdam, Netherlands
[6] Netherlands Red Cross, Blood Transfus Serv, Cent Lab, Dept Clin Viroimmunol, Amsterdam, Netherlands
[7] Univ Amsterdam, Acad Med Ctr, Dept Human Retrovirol, NL-1105 AZ Amsterdam, Netherlands
关键词
HIV-1 clearance rate; nelfinavir; pharmacokinetics; saquinavir; viral load;
D O I
10.1097/00002030-199811000-00002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To investigate the relationship between exposure to antiretroviral drugs and the initial decline of plasma HIV-1 RNA. Design: Open-label study in antiretroviral-naive HIV-1 infected patients using a quadruple drug regimen [nelfinavir (NFV), saquinavir (SQV), stavudine, and lamivudine]. Methods: The elimination rate constant (k) for HIV-1 clearance was calculated during the first 2 weeks of treatment in 29 patients. Exposure to NFV and SQV was quantified on each study visit. Observed NFV and SQV concentrations were related to those expected in a reference population and a concentration ratio was calculated. The median concentration ratios for NFV and SQV, the baseline CD4+ lymphocyte count and baseline log(10) HIV-1 RNA were correlated with k. Results: A significant positive correlation was observed between k and the median NFV (P = 0.001) or SQV concentration ratio (P = 0.016) in univariate analysis. In multivariate analyses, the median NFV concentration ratio remained significantly correlated with k. Conclusions: The variation in the rate of decline of plasma HIV-1 RNA between patients after the initiation of a quadruple drug regimen could be explained by differences in exposure to NFV or SQV. Determination of k could be used to optimise further antiretroviral drug therapy and may be a first tool to assess antiretroviral activities of new or increasing doses of drugs administered in combination regimens. Furthermore, our data suggest that exposure to antiretroviral drugs should be incorporated in mathematical models to describe HIV-1 dynamics in more detail. (C) 1998 Lippincott-Raven Publishers.
引用
收藏
页码:F111 / F115
页数:5
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