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Pretreatment CD4 cell slope and progression to AIDS or death in HIV-infected patients initiating antiretroviral therapy--the CASCADE collaboration: a collaboration of 23 cohort studies.

机译:在开始抗逆转录病毒治疗的HIV感染患者中,CD4细胞的斜率预处理和发展为AIDS或死亡或死亡的研究-CASCADE合作:一项23个队列研究的合作。

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摘要

BACKGROUND: CD4 cell count is a strong predictor of the subsequent risk of AIDS or death in HIV-infected patients initiating combination antiretroviral therapy (cART). It is not known whether the rate of CD4 cell decline prior to therapy is related to prognosis and should, therefore, influence the decision on when to initiate cART. METHODS AND FINDINGS: We carried out survival analyses of patients from the 23 cohorts of the CASCADE (Concerted Action on SeroConversion to AIDS and Death in Europe) collaboration with a known date of HIV seroconversion and with at least two CD4 measurements prior to initiating cART. For each patient, a pre-cART CD4 slope was estimated using a linear mixed effects model. Our primary outcome was time from initiating cART to a first new AIDS event or death. We included 2,820 treatment-naïve patients initiating cART with a median (interquartile range) pre-cART CD4 cell decline of 61 (46-81) cells/microl per year; 255 patients subsequently experienced a new AIDS event or death and 125 patients died. In an analysis adjusted for established risk factors, the hazard ratio for AIDS or death was 1.01 (95% confidence interval 0.97-1.04) for each 10 cells/microl per year reduction in pre-cART CD4 cell decline. There was also no association between pre-cART CD4 cell slope and survival. Alternative estimates of CD4 cell slope gave similar results. In 1,731 AIDS-free patients with >350 CD4 cells/microl from the pre-cART era, the rate of CD4 cell decline was also not significantly associated with progression to AIDS or death (hazard ratio 0.99, 95% confidence interval 0.94-1.03, for each 10 cells/microl per year reduction in CD4 cell decline). CONCLUSIONS: The CD4 cell slope does not improve the prediction of clinical outcome in patients with a CD4 cell count above 350 cells/microl. Knowledge of the current CD4 cell count is sufficient when deciding whether to initiate cART in asymptomatic patients. Please see later in the article for the Editors' Summary.
机译:背景:CD4细胞计数是开始联合抗逆转录病毒治疗(cART)的HIV感染患者继发艾滋病或死亡风险的有力预测指标。尚不知道治疗前CD4细胞下降的速度是否与预后有关,因此是否会影响何时启动cART的决定。方法和研究结果:我们对23名CASCADE(欧洲公认的针对血清转化为AIDS和死亡的证据行动)与已知的HIV血清转化日期进行了生存分析,并在开始cART之前至少进行了两次CD4测量。对于每个患者,使用线性混合效应模型估计了cART之前的CD4斜率。我们的主要结果是从启动cART到第一次新的AIDS事件或死亡的时间。我们纳入了2,820名未接受过cART治疗的患者,这些患者开始接受cART治疗前每年的cART CD4细胞下降中位数为61(46-81)个细胞/微升。 255名患者随后发生了新的艾滋病事件或死亡,另有125名患者死亡。在对已确定的危险因素进行调整的分析中,每年每减少10个细胞/μl,cART pre CD4细胞下降的AIDS或死亡的风险比为1.01(95%置信区间0.97-1.04)。 cART之前的CD4细胞斜率与存活率之间也没有关联。 CD4细胞斜率的替代估计给出了相似的结果。在从cART前时代开始的1,731例无AIDS且CD4细胞> 350微克/微升的患者中,CD4细胞下降的速率也与进展为AIDS或死亡无关(危险比0.99,95%置信区间0.94-1.03,每年每10个细胞/微升减少CD4细胞下降)。结论:CD4细胞计数高于350细胞/微升的患者,CD4细胞斜率不能改善临床预后的预测。在决定是否在无症状患者中启动cART时,对当前CD4细胞计数的了解就足够了。请参阅本文后面的“编辑摘要”。

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