Horne Benjamin D, Anderson Jeffrey L, Muhlestein Joseph B, Ridker Paul M, Paynter Nina P
Intermountain Medical Center, Salt Lake City, USA University of Utah, Salt Lake City, USA
Intermountain Medical Center, Salt Lake City, USA University of Utah, Salt Lake City, USA.
Eur J Prev Cardiol. 2015 Apr;22(4):519-26. doi: 10.1177/2047487313519347. Epub 2014 Jan 8.
Previously, we showed that sex-specific complete blood count (CBC) risk scores strongly predicted risk of all-cause mortality in multiple sets of general medical patients. This study evaluated the CBC risk score in an independent, well-studied international primary risk population of lower-risk individuals initially free from cardiovascular (CV) disease.
Observational secondary analysis of a randomized trial population.
The previously derived and validated CBC score was evaluated for association with all-cause mortality among CV disease-free females (n = 6568) and males (n = 10,629) enrolled for up to 5 years in the Justification for the Use of Statins in Prevention: an Intervention Trial Evaluating Rosuvastatin (JUPITER) trial. Associations of the CBC score with CV mortality and with major CV disease were also tested.
The CBC score predicted all-cause mortality, with univariable hazard ratio (HR) 4.83 (95% CI 3.70-6.31) for the third CBC score tertile vs. the first tertile, and HR 2.31 (CI 1.75-3.05) for the second tertile (p trend < 0.001). The CBC score retained significance after adjustment: HR 1.97 (CI 1.46-2.67) and 1.51 (CI 1.13-2.00) for tertiles 3 and 2 vs. 1, respectively (p trend < 0.001). The CBC score also predicted CV mortality (p trend = 0.025) and the primary JUPITER endpoint (p trend = 0.015). c-statistics for mortality were 0.729 among all, and 0.722 and 0.750 for females and males, respectively.
The CBC risk score was strongly associated with all-cause mortality among JUPITER trial participants and had good discrimination. It also predicted CV-specific outcomes. This CBC score may be useful in identifying cardiac disease-free individuals at increased risk of mortality.
此前,我们发现特定性别的全血细胞计数(CBC)风险评分能有力地预测多组普通内科患者的全因死亡率。本研究在一个独立的、经过充分研究的国际低风险个体初级风险人群中评估了CBC风险评分,这些个体最初无心血管(CV)疾病。
对一项随机试验人群进行观察性二次分析。
在“他汀类药物用于预防的合理性:一项评估瑞舒伐他汀的干预试验”(JUPITER试验)中,对先前得出并验证的CBC评分进行评估,以确定其与入选长达5年的无CV疾病女性(n = 6568)和男性(n = 10629)的全因死亡率之间的关联。还测试了CBC评分与CV死亡率及主要CV疾病之间的关联。
CBC评分可预测全因死亡率,第三CBC评分三分位数与第一三分位数相比,单变量风险比(HR)为4.83(95%置信区间3.70 - 6.31),第二三分位数的HR为2.31(置信区间1.75 - 3.05)(p趋势<0.001)。调整后CBC评分仍具有显著性:第三和第二三分位数与第一三分位数相比,HR分别为1.97(置信区间1.46 - 2.67)和1.51(置信区间1.13 - 2.00)(p趋势<0.001)。CBC评分还可预测CV死亡率(p趋势 = 0.025)和JUPITER试验的主要终点(p趋势 = 0.015)。全因死亡率的c统计量在所有人群中为0.729,女性和男性分别为0.722和0.750。
CBC风险评分与JUPITER试验参与者的全因死亡率密切相关且具有良好的区分度。它还能预测特定CV结局。该CBC评分可能有助于识别无心脏病但死亡风险增加的个体。