AIDS. 2014 Jun 1;28(9):1351-6. doi: 10.1097/QAD.0000000000000224.
Among antiretroviral therapy (ART)-naive individuals, viral load levels tend to increase and CD4(+) cell counts decline over time. We sought to explore the rate of change and influence of other factors associated with these markers of HIV progression.
An observational cohort collaboration study.
A total of 158 385 pairs of consecutive viral load and CD4(+) cell count simultaneously measured from 34 384 ART-naive individuals in the COHERE database were analysed. Annual changes and factors associated with these changes were estimated using generalized estimating equations.
Viral load continued to rise at a mean [95% confidence interval (CI)] rate of 0.091 (0.086-0.096) log10 copies/ml per year. A faster rise in viral load was significantly associated with older age, such that for every 10 years older, it was a mean 0.022 log10 copies/ml per year greater. The mean (95% CI) CD4(+) cell count change was -78.0 (-80.1 to -76.0) cell/μl per year and it was strongly associated with a higher current viral load: for every 1 log10 copies/ml higher, CD4(+) cell count declined by an additional 37.6 cells/μl per year (P < 0.001). Current viral load was a stronger predictor of CD4(+) cell count depletion than baseline viral load. Neither sex, race nor transmission by injecting drug use was associated with change in either the viral load or CD4(+) cell count.
We found that in ART-naive individuals, viral load continues to increase over time and more sharply in those who are older. Our results also suggest that higher current viral load is strongly associated with ongoing rate of CD4(+) cell count depletion.
在未曾接受抗逆转录病毒疗法(ART)的个体中,病毒载量水平往往会随时间推移而升高,CD4(+) 细胞计数则下降。我们试图探讨与 HIV 进展这些标志物相关的变化速度和其他因素的影响。
观察性队列合作研究。
我们分析了 COHERE 数据库中 34384 例未曾接受 ART 的个体中连续测量的 158385 对病毒载量和 CD4(+) 细胞计数,使用广义估计方程来估计这些标志物变化的年变化率和相关因素。
病毒载量以平均(95%置信区间(CI))[0.086-0.096]log10 拷贝/ml/年的速度持续升高。病毒载量的上升速度较快与年龄较大显著相关,即每增加 10 岁,每年的病毒载量就会增加 0.022log10 拷贝/ml。平均(95%CI)CD4(+) 细胞计数每年下降 78.0(-80.1 至 -76.0)个细胞/μl,与当前较高的病毒载量密切相关:每增加 1log10 拷贝/ml,CD4(+) 细胞计数每年下降 37.6 个细胞/μl(P < 0.001)。当前病毒载量是 CD4(+) 细胞计数消耗的更强预测因子,而基线病毒载量则不然。性别、种族或通过注射毒品传播均与病毒载量或 CD4(+) 细胞计数的变化无关。
我们发现,在未曾接受 ART 的个体中,病毒载量随时间推移持续升高,年龄较大者上升更为明显。我们的研究结果还表明,当前较高的病毒载量与 CD4(+) 细胞计数持续下降的速度密切相关。