Department of Gerontology and Geriatrics, C-2-R, Leiden University Medical Center, PO Box 9600, 2300 RC Leiden, The Netherlands.
J Gerontol A Biol Sci Med Sci. 2010 Jul;65(7):764-8. doi: 10.1093/gerona/glq004. Epub 2010 Jan 27.
White blood cell (WBC) count is, like C-reactive protein (CRP), a clinical marker of inflammation and predicts cardiovascular disease and mortality in middle-aged populations. Limited data exist on the association between WBC count and mortality in the oldest old. Moreover, because CRP and WBC count are closely linked, it is not known whether WBC count and CRP are independent risk factors for mortality. We assessed the independent predictive value of WBC count and CRP levels in relation to mortality, both vascular and nonvascular, in very old participants.
A total of 599 women and men were evaluated longitudinally in the Leiden 85-plus Study. Blood samples and medical information were collected at age 85, and all participants were visited annually until age 90 or death. Mortality risks were estimated with Cox proportional hazard models.
Increasing WBC count was associated with an increased risk for all-cause mortality (hazard ratio, HR [95% confidence interval, CI] = 1.26 [1.15-1.38]) after adjustment for sex and smoking status. CRP levels were also associated with an increased risk for mortality (HR [95% CI] = 1.22 [1.10-1.35]). The association between increasing WBC count and mortality remained significant after adjustment for CRP levels (HR [95% CI] = 1.20 [1.09-1.33]), whereas also the relation between increasing CRP levels and mortality remained significant after adjustment for WBC count (HR [95% CI] = 1.17 [1.05-1.30]).
Our results suggest that WBC count and CRP levels both independently predict mortality in the oldest old.
白细胞 (WBC) 计数与 C 反应蛋白 (CRP) 一样,是炎症的临床标志物,可预测中年人群的心血管疾病和死亡率。关于白细胞计数与最年长人群死亡率之间的关系,数据有限。此外,由于 CRP 和 WBC 计数密切相关,因此尚不清楚 WBC 计数和 CRP 是否是死亡率的独立危险因素。我们评估了白细胞计数和 CRP 水平与死亡率(包括血管性和非血管性)之间的独立预测价值,这些参与者都非常年长。
共有 599 名女性和男性在莱顿 85 岁以上研究中进行了纵向评估。在 85 岁时采集了血液样本和医疗信息,并在 90 岁或死亡之前每年对所有参与者进行一次随访。使用 Cox 比例风险模型估计死亡率风险。
在调整性别和吸烟状况后,白细胞计数增加与全因死亡率增加相关(风险比 [HR] [95%置信区间,CI] = 1.26 [1.15-1.38])。CRP 水平也与死亡率增加相关(HR [95% CI] = 1.22 [1.10-1.35])。在调整 CRP 水平后,白细胞计数增加与死亡率之间的关联仍然显著(HR [95% CI] = 1.20 [1.09-1.33]),而在调整白细胞计数后,CRP 水平增加与死亡率之间的关系仍然显著(HR [95% CI] = 1.17 [1.05-1.30])。
我们的研究结果表明,白细胞计数和 CRP 水平均可独立预测最年长人群的死亡率。