Increased Soluble ST2 Predicts Long-term Mortality in Patients with Stable Coronary Artery Disease: Results from the Ludwigshafen Risk and Cardiovascular Health Study

被引:101
作者
Dieplinger, Benjamin [1 ]
Egger, Margot [1 ]
Haltmayer, Meinhard [1 ]
Kleber, Marcus E. [2 ]
Scharnagl, Hubert [3 ]
Silbernagel, Guenther [4 ]
de Boer, Rudolf A. [5 ]
Maerz, Winfried [2 ,3 ,6 ]
Mueller, Thomas [1 ]
机构
[1] Konventhosp Barmherzige Brueder Linz, Dept Lab Med, Linz, Austria
[2] Heidelberg Univ, Inst Publ Hlth Social & Prevent Med, Mannheim Med Fac, Mannheim, Germany
[3] Med Univ Graz, Clin Inst Med & Chem Lab Diagnost, Graz, Austria
[4] Univ Bern, Inselspital, Dept Angiol, Swiss Cardiovasc Ctr, CH-3012 Bern, Switzerland
[5] Univ Groningen, Med Ctr Groningen, Dept Cardiol, Groningen, Netherlands
[6] Synlab Acad Mannheim, Mannheim, Germany
关键词
HIGH-SENSITIVITY ASSAY; FAMILY-MEMBER ST2; HEART-FAILURE; PROGNOSTIC UTILITY; TROPONIN-T; NATRIURETIC PEPTIDE; PROMOTER USAGE; RECEPTOR; IL-33; ATHEROSCLEROSIS;
D O I
10.1373/clinchem.2013.209858
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
BACKGROUND: Soluble suppression of tumorigenicity 2 (sST2) has emerged as a strong prognostic biomarker in patients with heart failure and myocardial infarction. The aim of this study was to evaluate the longterm prognostic value of sST2 in patients with stable coronary artery disease (CAD). METHODS: sST2 plasma concentrations were measured in 1345 patients with stable CAD referred for coronary angiography at a single tertiary care center. The primary endpoint was all-cause mortality. RESULTS: During a median follow-up time of 9.8 years, 477 (36%) patients died. The median sST2 plasma concentration at baseline was significantly higher among decedents than survivors (21.4 vs 18.5 ng/ mL; P < 0.001). In multivariate Cox proportional hazards regression analysis, sST2 was an independent predictor of all-cause mortality (risk ratio 1.16 per 1-SD increase in log-transformed values; 95% CI 1.05- 1.29; P = 0.004). In the same multivariate analysis, aminoterminal pro- B- type natriuretic peptide (NT- proBNP) and high- sensitivity cardiac troponin T (hs- cTnT) were also independent predictors, whereas galectin- 3 was not. Patients with sST2 in the highest quartile (> 24.6 ng/ mL) displayed a 2- fold increased risk of death in univariate analysis, which was attenuated but remained significant in a fully adjusted model (risk ratio 1.39; 95% CI 1.10-1.76; P = 0.006). Further analysis showed that the prognostic impact of sST2 was additive to NT- proBNP and hs- cTnT. Us-ing a multibiomarker approach combining these 3 complementary makers, we demonstrated that patients with all 3 biomarkers in the highest quartiles had the poorest outcome. CONCLUSIONS: In this cohort of patients with stable CAD, increased sST2 was an independent predictor of long-term all-cause mortality and provided complementary prognostic information to hs- cTnT and NT- proBNP. (C) 2013 American Association for Clinical Chemistry International
引用
收藏
页码:530 / 540
页数:11
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