Soluble ST2 for Predicting Sudden Cardiac Death in Patients With Chronic Heart Failure and Left Ventricular Systolic Dysfunction
Domingo A. Pascual-Figal, MD, PhD*,*,
Jordi Ordoñez-Llanos, MD, PhD ,
Pedro L. Tornel, PhD ,
Rafael Vázquez, MD, PhD||,
Teresa Puig, MD, PhD ,
Mariano Valdés, MD, PhD*,
Juan Cinca, MD, PhD ,
Antoni Bayes de Luna, MD, PhD¶,
Antoni Bayes-Genis, MD, PhD on behalf of the MUSIC Investigators
* Cardiology Service, Virgen de la Arrixaca Hospital and Department of Medicine, University of Murcia, Murcia, Spain
Biochemistry Service, Sant Pau Hospital and Department of Biochemistry and Molecular Biology, Universitat Autònoma de Barcelona, Barcelona, Spain
Cardiology Service, Sant Pau Hospital, Department of Medicine, Universitat Autònoma de Barcelona, Barcelona, Spain
Biochemistry Service, Virgen de la Arrixaca Hospital, Murcia, Spain
|| Cardiology Service, Hospital Universitario Puerta del Mar, Cádiz, Spain
¶ Institut Català de Ciències Cardiovasculars, Barcelona, Spain

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Figure 1 sST2 and NT-proBNP in Patients With SCD and Survivors
Box plots showing the baseline concentrations of soluble ST2 (sST2) (A) and N-terminal pro–B-type natriuretic peptide (NT-proBNP) (B) in patients experiencing sudden cardiac death (SCD) and the control survivor group.
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Figure 3 Events According to the Presence of None, Either, or Both sST2 >0.15 ng/ml and NT-proBNP >2,000 ng/l
Red bars = sudden cardiac death; open bars = survivors. Abbreviations as in Figure 1.
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