Immunodeficiency and the risk of serious clinical endpoints in a well studied cohort of treated HIV-infected patients

被引:69
作者
Achhra, Amit C. [1 ]
Amin, Janaki [1 ]
Law, Matthew G. [1 ]
Emery, Sean [1 ]
Gerstoft, Jan [2 ]
Gordin, Fred M. [3 ,4 ]
Vjecha, Michael J. [3 ,5 ]
Neaton, James D. [6 ]
Cooper, David A. [1 ]
机构
[1] Univ New S Wales, Natl Ctr HIV Epidemiol & Clin Res, Fac Med, Sydney, NSW 2034, Australia
[2] Univ Copenhagen, Rigshosp, Dept Infect Dis, DK-2100 Copenhagen, Denmark
[3] Vet Affairs Med Ctr, Washington, DC 20422 USA
[4] George Washington Univ, Sch Med, Washington, DC USA
[5] Inst Clin Res Inc, Washington, DC USA
[6] Univ Minnesota, Sch Publ Hlth, Div Biostat, Minneapolis, MN 55455 USA
关键词
AIDS; CD4(+); CD4(+) cell counts; immunodeficiency; serious non-AIDS events; ACTIVE ANTIRETROVIRAL THERAPY; CELL COUNTS; AIDS; MORTALITY; VIRUS; DEATH; ERA; INTERLEUKIN-2; INTERRUPTION; INCREASE;
D O I
10.1097/QAD.0b013e32833b1b26
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 relative predictive value of CD4(+) metrics for serious clinical endpoints. Design: Observational. Methods: Patients (3012; 20 317 person-years) from control arms of ESPRIT and SILCAAT were followed prospectively. We used Cox regression to identify CD4(+) metrics (latest, baseline and nadir CD4(+) cell count, latest CD4(+)%, time spent with CD4(+) count below certain thresholds and CD4(+) slopes) independently predictive of all-cause mortality, non-AIDS deaths, non-AIDS (cardiovascular, hepatic, renal and non-AIDS malignancy) and AIDS events. Akaike information criteria (AIC) were calculated for each model. Significant metrics (P < 0.05) were then additionally adjusted for latest CD4(+) cell count. Results: Non-AIDS deaths occurred at a higher rate than AIDS deaths [rate ratio: 6.48, 95% confidence interval (CI) 5.1 -8.1], and non-AIDS events likewise (rate ratio: 1.72, 95% CI 1.65-1.79). Latest CD4(+) cell count was strongly predictive of lower risk of death (hazard ratio per log(2) rise: 0.48, 95% CI 0.43-0.54), with lowest AIC of all metrics. CD4(+) slope over seven visits, after additional adjustment for latest CD4(+) cell count, was the onlymetric to be an independent predictor for all-cause (hazard ratio for slope < -10 cells/mu l per month vs. 0 +/- 10: 3.04, 95% CI 1.98 -4.67) and non-AIDS deaths (hazard ratio for slope < -10 cells/mu l per month vs. 0 +/- 10: 2.62, 95% CI 1.62-4.22). Latest CD4(+) cell count (per log(2) rise) was the best predictor across all four endpoints and predicted hepatic (hazard ratio 0.46, 95% CI 0.33-0.63) and renal events (hazard ratio 0.39, 95% CI 0.21-0.70), but not cardiovascular events (hazard ratio 1.05, 95% CI 0.77-1.43) or non-AIDS cancers (hazard ratio 0.78, 95% CI 0.59-1.03). Conclusion: Latest CD4(+) cell count is the best predictor of serious endpoints. CD4(+) slope independently predicts all-cause and non-AIDS deaths. (C) 2010 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins
引用
收藏
页码:1877 / 1886
页数:10
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