Horne Benjamin D, Muhlestein Joseph B, Bennett Sterling T, Muhlestein Joseph Boone, Ronnow Brianna S, May Heidi T, Bair Tami L, Anderson Jeffrey L
Intermountain Heart Institute, Intermountain Medical Center, Salt Lake City, UT, USA.
Genetic Epidemiology Division, Department of Medicine, University of Utah, Salt Lake City, UT, USA.
Eur J Clin Invest. 2015 Jun;45(6):541-9. doi: 10.1111/eci.12432. Epub 2015 May 13.
The red cell distribution width (RDW) predicts mortality among many populations. RDW is calculated as the standard deviation (SD) of the red blood cell (RBC) volume divided by mean corpuscular volume (MCV). Because higher MCV also predicts mortality, we hypothesized that the RDW numerator (one SD of RBC volume or 1SD-RDW) predicts mortality more strongly than the RDW.
Adult subjects hospitalized during a contemporary clinical era (10/2005-1/2014, N = 135,963) and a historical era (1/1999-9/2005, N = 119,530) were studied. The RDW was obtained from the complete blood count (CBC), while 1SD-RDW was calculated (RDW multiplied by MCV and divided by 100).
In univariable Cox regression (2005-2014 cohort), 1SD-RDW (quintile 5 vs. 1: hazard ratio [HR] = 8.38, 95% confidence interval [CI] = 7.94, 8.85; P < 0.001) was a superior predictor of mortality compared to RDW (quintile 5 vs. 1: HR = 4.78, CI = 4.57, 5.00; P < 0.001). This superiority remained after adjustment for age, sex, basic metabolic profile components and other CBC factors excluding MCV (1SD-RDW: HR = 2.41, CI = 2.28, 2.55; RDW: HR = 2.01, CI = 1.92, 2.11). Further adjustment for MCV strengthened the RDW association (HR = 2.14, CI = 2.04, 2.24; P < 0.001), becoming indistinct from 1SD-RDW (HR = 2.20, CI = 2.08, 2.33; P < 0.001). Findings were similar for the 1999-2005 cohort.
The 1SD-RDW predicted mortality more strongly than RDW, suggesting that 1SD-RDW is superior to RDW as an individual risk predictor. Further, these results indicate that the dispersion of RBC volume and its mean are independent risk markers. Further research is required to understand the clinical value and mechanistic basis of these associations.
红细胞分布宽度(RDW)可预测许多人群的死亡率。RDW的计算方法是红细胞(RBC)体积的标准差(SD)除以平均红细胞体积(MCV)。由于较高的MCV也可预测死亡率,我们推测RDW的分子(RBC体积的一个标准差或1SD-RDW)比RDW更能有力地预测死亡率。
对当代临床时期(2005年10月至2014年1月,N = 135,963)和历史时期(1999年1月至2005年9月,N = 119,530)住院的成年受试者进行研究。RDW通过全血细胞计数(CBC)获得,而1SD-RDW则通过计算得出(RDW乘以MCV再除以100)。
在单变量Cox回归分析(2005 - 2014年队列)中,与RDW相比,1SD-RDW(第5五分位数与第1五分位数:风险比[HR] = 8.38,95%置信区间[CI] = 7.94, 8.85;P < 0.001)是更优的死亡率预测指标(RDW:第5五分位数与第1五分位数:HR = 4.78,CI = 4.57, 5.00;P < 0.001)。在对年龄、性别、基本代谢指标成分以及排除MCV的其他CBC因素进行调整后,这种优越性依然存在(1SD-RDW:HR = 2.41,CI = 2.28, 2.55;RDW:HR = 2.01,CI = 1.92, 2.11)。对MCV进行进一步调整后,增强了RDW的关联性(HR = 2.14,CI = 2.04, 2.24;P < 0.001),与1SD-RDW的关联性变得难以区分(HR = 2.20,CI = 2.08, 2.33;P < 0.001)。1999 - 2005年队列的结果相似。
1SD-RDW比RDW更能有力地预测死亡率,这表明作为个体风险预测指标,1SD-RDW优于RDW。此外,这些结果表明RBC体积的离散度及其均值是独立的风险标志物。需要进一步研究以了解这些关联的临床价值和机制基础。