Bedell Richard, Heath Katherine V, Hogg Robert S, Wood Evan, Press Natasha, Yip Benita, O'Shaughnessy Michael V, Montaner Julio S G
Centre for Excellence in HIV/AIDS, University of British Columbia, Vancouver, British Columbia, Canada.
Antivir Ther. 2003 Oct;8(5):379-84.
To characterize the value of total lymphocyte counts in predicting risk of death among patients initiating triple combination antiretroviral therapy.
Study subjects included antiretroviral-naive persons aged 18 years or older who initiated treatment with triple combination therapy between August 1 1996 and September 30 1999 in a population-based observational cohort of HIV-infected individuals. Total lymphocyte counts as well as CD4 count and plasma viral load were assessed at baseline. Separate Cox proportional hazards models were devised to evaluate the effect on survival of total lymphocyte count in lieu of or with CD4 count after adjustment for other prognostic factors including plasma viral load.
A total of 733 antiretroviral-naive persons initiated triple drug combination antiretroviral therapy over the study period with a median follow-up of 29.5 months. In the first analysis, only baseline CD4 cell counts of 50-199 cells/microl or less than 50 microl were associated with an increased risk of mortality [adjusted relative risk (ARR) 2.90; 95% CI: 1.40, 5.98] and (ARR 6.30; 95% CI: 2.93, 13.54), respectively. When CD4 counts were excluded from the analysis as if unavailable, total lymphocyte count of between 0.8 and 1.4 G/I, and less than 0.8 G/I were both significantly associated with an increased risk of mortality (ARR 2.36; 95% CI: 1.16, 4.78) and (ARR 6.17; 95% CI: 2.93, 13.01), respectively.
Total lymphocyte count may provide a simple and cost-effective alternative for prioritizing therapy initiation in resource-limited settings. Our results suggest that, if appropriately validated, judicious application of total lymphocyte counts could overcome one of the practical obstacles to more widespread provision of antiretroviral therapy in resource-poor settings.
评估在开始接受三联抗逆转录病毒治疗的患者中,总淋巴细胞计数对于预测死亡风险的价值。
研究对象包括1996年8月1日至1999年9月30日期间,在一个基于人群的HIV感染个体观察队列中开始接受三联疗法治疗的、未曾接受过抗逆转录病毒治疗的18岁及以上人群。在基线时评估总淋巴细胞计数、CD4细胞计数和血浆病毒载量。设计了单独的Cox比例风险模型,以评估在调整包括血浆病毒载量在内的其他预后因素后,总淋巴细胞计数代替CD4细胞计数或与CD4细胞计数一起对生存的影响。
在研究期间,共有733名未曾接受过抗逆转录病毒治疗的患者开始接受三联药物联合抗逆转录病毒治疗,中位随访时间为29.5个月。在首次分析中,只有基线CD4细胞计数为50 - 199个/微升或低于50个/微升与死亡风险增加相关[调整后相对风险(ARR)2.90;95%置信区间:1.40,5.98]和(ARR 6.30;95%置信区间:2.93,13.54)。当在分析中排除CD4细胞计数(如同无法获得一样)时,总淋巴细胞计数在0.8至1.4 G/L之间以及低于0.8 G/L均与死亡风险增加显著相关(ARR 2.36;95%置信区间:1.16,4.78)和(ARR 6.17;95%置信区间:2.93,13.01)。
在资源有限的环境中,总淋巴细胞计数可为优先启动治疗提供一种简单且具有成本效益的替代方法。我们的结果表明,如果经过适当验证,明智地应用总淋巴细胞计数可以克服资源匮乏环境中更广泛提供抗逆转录病毒治疗的一个实际障碍。