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比较 SF-36® 评分与生物标志物预测初级心脏预防患者的死亡率。

Comparing SF-36® scores versus biomarkers to predict mortality in primary cardiac prevention patients.

机构信息

Cleveland Clinic Foundation, Heart Vascular Institute, Department of Cardiology, Cleveland, OH, United States.

University of Miami, Department of Cardiology, Miami, FL, United States.

出版信息

Eur J Intern Med. 2017 Dec;46:47-55. doi: 10.1016/j.ejim.2017.05.026. Epub 2017 Jul 29.

Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

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