High levels of adherence do not prevent accumulation of HIV drug resistance mutations

被引:182
作者
Bangsberg, DR
Charlebois, ED
Grant, RM
Holodniy, M
Deeks, SG
Perry, S
Conroy, KN
Clark, R
Guzman, D
Zolopa, A
Moss, A
机构
[1] Univ Calif San Francisco, San Francisco Gen Hosp, Epidemiol & Prevent Intervent Ctr, Div Infect Dis, San Francisco, CA 94110 USA
[2] Univ Calif San Francisco, San Francisco Gen Hosp, Posit Hlth Program, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Gladstone Inst Virol & Immunol, San Francisco, CA 94110 USA
[4] Univ Calif San Francisco, Dept Epidemiol & Biostat, San Francisco, CA 94110 USA
[5] VA Palo Alto Hlth Care Syst, Ctr AIDS Res, Palo Alto, CA USA
[6] Stanford Univ, Sch Med, Palo Alto, CA 94304 USA
关键词
adherence; resistance; HIV; viral suppression; viral evolution; health policy; homeless; injection drug user;
D O I
10.1097/00002030-200309050-00011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: To assess the relationship between development of antiretroviral drug resistance and adherence by measured treatment duration, virologic suppression, and the rate of accumulating new drug resistance mutations at different levels of adherence. Methods: Adherence was measured with unannounced pill counts performed at the participant's usual place of residence in a prospective cohort of HIV-positive urban poor individuals. Two genotypic resistance tests separated by 6 months (G1 and G2) were obtained in individuals on a stable regimen and with detectable viremia (> 50 copies/ml). The primary resistance outcome was the number of new HIV antiretroviral drug resistance mutations occurring over the 6 months between G1 and G2. Results: High levels of adherence were closely associated with greater time on treatment (P < 0.0001) and viral suppression (P < 0.0001) in 148 individuals. In a subset of 57 patients with a plasma viral load > 50 copies/ml on stable therapy, the accumulation of new drug resistance mutations was positively associated with the duration of prior treatment (P = 0.03) and pill count adherence (P = 0.002). Assuming fully suppressed individuals (< 50 copies/ml) do not develop resistance, it was estimated that 23% of all drug resistance occurs in the top quintile of adherence (92 - 100%), and over 50% of all drug resistance mutations occur in the top two quintiles of adherence (79 - 100%). Conclusion: Increasing rates of viral suppression at high levels of adherence is balanced by increasing rates of drug resistance among viremic patients. Exceptionally high levels of adherence will not prevent population levels of drug resistance. (C) 2003 Lippincott Williams Wilkins.
引用
收藏
页码:1925 / 1932
页数:8
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