Nevirapine plasma exposure affects both durability of viral suppression and selection of Nevirapine primary resistance mutations in a clinical setting

被引:48
作者
de Requena, DG
Bonora, S
Garazzino, S
Sciandra, M
D'Avolio, A
Raiteri, R
Marrone, R
Boffito, M
De Rosa, FG
Sinicco, A
Di Perri, G
机构
[1] Univ Turin, Dept Infect Dis, I-10149 Turin, Italy
[2] Chelsea & Westminster Hosp, London, England
关键词
D O I
10.1128/AAC.49.9.3966-3969.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The relationship between nevirapine plasma concentrations and the durability of both viral suppression (VS) and selection of nevirapine primary resistance mutations (PRMs) was evaluated. A nevirapine trough concentration (C-trough) of > 4,300 ng/ml was found to predict longer VS. Patients with nevirapine C(trough)s ranging from 3,100 to 4,300 ng/ml had higher probabilities of developing PRMs than those with nevirapine Ctroughs below and above this concentration interval.
引用
收藏
页码:3966 / 3969
页数:4
相关论文
共 6 条
[1]   Determination of twelve antiretroviral agents in human plasma sample using reversed-phase high-performance liquid chromatography [J].
Aymard, G ;
Legrand, M ;
Trichereau, N ;
Diquet, B .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2000, 744 (02) :227-240
[2]  
MAINBERG MA, 2003, J ACQUIR IMMUNE D S1, V34, P3
[3]   BASIC PRINCIPLES OF ROC ANALYSIS [J].
METZ, CE .
SEMINARS IN NUCLEAR MEDICINE, 1978, 8 (04) :283-298
[4]   Natural variation of drug susceptibility in wild-type human immunodeficiency virus type 1 [J].
Parkin, NT ;
Hellmann, NS ;
Whitcomb, JM ;
Kiss, L ;
Chappey, C ;
Petropoulos, CJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (02) :437-443
[5]   High exposure to nevirapine in plasma is associated with an improved virological response in HIV-1-infected individuals [J].
Veldkamp, AI ;
Weverling, GJ ;
Lange, JMA ;
Montaner, JSG ;
Reiss, P ;
Cooper, DA ;
Vella, S ;
Hall, D ;
Beijnen, JH ;
Hoetelmans, RMW .
AIDS, 2001, 15 (09) :1089-1095
[6]   Restricting the selection of antibiotic-resistant mutants: A general strategy derived from fluoroquinolone studies [J].
Zhao, XL ;
Drlica, K .
CLINICAL INFECTIOUS DISEASES, 2001, 33 :S147-S156