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

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 (R)) as predictive tools for mortality, particularly in direct comparison with biomarkers. Our objective is to measure the relative effectiveness of SF-36 (R) 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 (R) 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 (R) physical score independently predicted a 6-fold increase in death at 8 years (above vs. below median Hazard Ratio [95% confidence interval] 5.99 [3.86-9.35], p < 0.001). In a univariate analysis, SF-36 (R) 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 (R) 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 (R) questionnaire could be used as an adjunct simple and cost-effective predictor of mortality to current predictors. (C) 2017 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.