Effect of highly active antiretroviral therapy on time to acquired immunodeficiency syndrome or death using marginal structural models

被引:212
作者
Cole, SR
Hernán, MA
Robins, JM
Anastos, K
Chmiel, J
Detels, R
Ervin, C
Feldman, J
Greenblatt, R
Kingsley, L
Lai, SH
Young, M
Cohen, M
Muñoz, A
机构
[1] Johns Hopkins Univ, Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD 21205 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[4] Lincoln Med & Mental Hlth Ctr, New York, NY USA
[5] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[6] Univ Calif Los Angeles, Sch Publ Hlth, Dept Epidemiol, Los Angeles, CA 90024 USA
[7] Kenneth Norris Jr Canc Hosp & Res Inst, Los Angeles, CA USA
[8] SUNY Hlth Sci Ctr, Dept Prevent Med & Community Hlth, Brooklyn, NY 11203 USA
[9] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[10] Univ Calif San Francisco, Dept Epidemiol, San Francisco, CA USA
[11] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Infect Dis & Microbiol, Pittsburgh, PA USA
[12] Georgetown Univ Hosp, Div Infect Dis, Washington, DC 20007 USA
[13] Cook Cty Hosp, Chicago, IL 60612 USA
关键词
acquired immunodeficiency syndrome; antiretroviral therapy; highly active; causality; confounding factors (epidemiology);
D O I
10.1093/aje/kwg206
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
To estimate the net (i.e., overall) effect of highly active antiretroviral therapy (HAART) on time to acquired immunodeficiency syndrome (AIDS) or death, the authors used inverse probability-of-treatment weighted estimation of a marginal structural model, which can appropriately adjust for time-varying confounders affected by prior treatment or exposure. Human immunodeficiency virus (HIV)-positive men and women (n = 1,498) were followed in two ongoing cohort studies between 1995 and 2002. Sixty-one percent (n = 918) of the participants initiated HAART during 6,763 person-years of follow-up, and 382 developed AIDS or died. Strong confounding by indication for HAART was apparent; the unadjusted hazard ratio for AIDS or death was 0.98. The hazard ratio from a standard time-dependent Cox model that included time-varying CD4 cell count, HIV RNA level, and other time-varying and fixed covariates as regressors was 0.81 (95% confidence interval: 0.61, 1.07). In contrast, the hazard ratio from a marginal structural survival model was 0.54 (robust 95% confidence interval: 0.38, 0.78), suggesting a clinically meaningful net benefit of HAART. Standard Cox analysis failed to detect a clear net benefit, because it does not appropriately adjust for time-dependent covariates, such as HIV RNA level and CD4 cell count, that are simultaneously confounders and intermediate variables.
引用
收藏
页码:687 / 694
页数:8
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