Cleveland Clinic Foundation, Heart Vascular Institute, Department of Cardiology, Cleveland, OH, United States.
University of Miami, Department of Cardiology, Miami, FL, United States.
Eur J Intern Med. 2017 Dec;46:47-55. doi: 10.1016/j.ejim.2017.05.026. Epub 2017 Jul 29.
Risk stratification plays an important role in evaluating patients with no known cardiovascular disease (CVD). Few studies have investigated health-related quality of life questionnaires such as the Medical Outcomes Study Short Form-36 (SF-36®) as predictive tools for mortality, particularly in direct comparison with biomarkers. Our objective is to measure the relative effectiveness of SF-36® scores in predicting mortality when compared to traditional and novel biomarkers in a primary prevention population.
7056 patients evaluated for primary cardiac prevention between January 1996 and April 2011 were included in this study. Patient characteristics included medical history, SF-36® questionnaire and a laboratory panel (total cholesterol, triglycerides, HDL, LDL, ApoA, ApoB, ApoA1/ApoB ratio, homocysteine, lipoprotein (a), fibrinogen, hsCRP, uric acid and urine ACR). The primary outcome was all-cause mortality.
A low SF-36® physical score independently predicted a 6-fold increase in death at 8years (above vs. below median Hazard Ratio [95% confidence interval] 5.99 [3.86-9.35], p<0.001). In a univariate analysis, SF-36® physical score had a c-index of 0.75, which was superior to that of all the biomarkers. It also carried incremental predictive ability when added to non-laboratory risk factors (Net Reclassification Index=59.9%), as well as Framingham risk score components (Net Reclassification Index=61.1%). Biomarkers added no incremental predictive value to a non-laboratory risk factor model when combined to SF-36 physical score.
The SF-36® physical score is a reliable predictor of mortality in patients without CVD, and outperformed most studied traditional and novel biomarkers. In an era of rising healthcare costs, the SF-36® questionnaire could be used as an adjunct simple and cost-effective predictor of mortality to current predictors.
风险分层在评估无已知心血管疾病(CVD)的患者中起着重要作用。很少有研究将健康相关生活质量问卷(如医疗结局研究简表 36 项(SF-36®))作为死亡率的预测工具进行研究,特别是与生物标志物的直接比较。我们的目的是测量 SF-36®评分在预测死亡率方面的相对有效性,与传统和新型生物标志物在一级预防人群中的比较。
本研究纳入了 1996 年 1 月至 2011 年 4 月期间接受一级心脏预防评估的 7056 例患者。患者特征包括病史、SF-36®问卷和实验室检测(总胆固醇、甘油三酯、HDL、LDL、载脂蛋白 A、载脂蛋白 B、载脂蛋白 A1/载脂蛋白 B 比值、同型半胱氨酸、脂蛋白(a)、纤维蛋白原、hsCRP、尿酸和尿液 ACR)。主要结局为全因死亡率。
SF-36®身体评分低独立预测 8 年内死亡风险增加 6 倍(高于 vs. 低于中位数风险比[95%置信区间]5.99[3.86-9.35],p<0.001)。在单变量分析中,SF-36®身体评分的 c 指数为 0.75,优于所有生物标志物。当添加到非实验室危险因素时,它具有增量预测能力(净重新分类指数=59.9%),以及弗雷明汉风险评分成分(净重新分类指数=61.1%)。当与 SF-36 身体评分相结合时,生物标志物对非实验室风险因素模型没有增加预测价值。
SF-36®身体评分是无 CVD 患者死亡率的可靠预测指标,优于大多数研究的传统和新型生物标志物。在医疗保健成本不断上升的时代,SF-36®问卷可以作为一种简单、经济有效的死亡率预测指标,补充当前的预测指标。