Estimating HIV-1 drug resistance in antiretroviral-treated individuals in the United Kingdom

被引:0
作者
Pillay, D [1 ]
Green, H [1 ]
Matthias, R [1 ]
Dunn, D [1 ]
Phillips, A [1 ]
Sabin, C [1 ]
Evans, B [1 ]
Evans, B [1 ]
Cane, P [1 ]
Burns, S [1 ]
Cameron, S [1 ]
Chrystie, I [1 ]
Churchill, D [1 ]
Clarke, J [1 ]
Easterbrook, P [1 ]
Zuckerman, M [1 ]
Goldberg, D [1 ]
Gompels, M [1 ]
Hale, T [1 ]
Robb, G [1 ]
Leigh-Brown, A [1 ]
Geretti, AM [1 ]
Pillay, D [1 ]
Phillips, A [1 ]
Sabin, C [1 ]
Kellam, P [1 ]
Dunn, D [1 ]
Porter, K [1 ]
Matthias, R [1 ]
Orkin, C [1 ]
Pozniak, A [1 ]
Smit, R [1 ]
Tilston, P [1 ]
Williams, I [1 ]
机构
[1] UCL, Ctr Virol, Div Infect & Immun, Windeyer Inst, London W1T 4JF, England
基金
英国医学研究理事会;
关键词
THERAPY; TRANSMISSION; PREVALENCE; LAMIVUDINE; MUTATION; VIRUS;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Good estimates of the prevalence of human immunodeficiency virus drug resistance are important for assessing requirements for new drug classes and modeling the spread of resistance. However, little consensus exists on optimal methodologies to generate such data. To compare methodologies, we used the national data set of resistance tests from 14000 patients in the United Kingdom performed between 1998 and 2002. When single-time-point analysis ( method 1) was used, the proportion of tests with any form of resistance was similar to 80%, with little time trend. When a cumulative model of resistance ( method 2) was used and placed in the context of all treated patients, the prevalence of any resistance increased by year, reaching 17% of treated patients in 2002. Method 2 also nearly doubles estimates of numbers of individuals infected with multiclass drug-resistant virus. Our results identify an urgent need for new drugs within existing classes and new classes of antiretroviral therapy.
引用
收藏
页码:967 / 973
页数:7
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