New Cardiovascular Biomarkers in Ischemic Heart Disease-GDF-15, A Probable Predictor for Ejection Fraction.

ejection fraction growth differentiation factor 15 (GDF-15) heart failure heart-type fatty acid-binding protein (H-FABP) soluble suppression of tumorigenicity 2 (sST2) soluble urokinase-type plasminogen activator receptor (suPAR)

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
27 Jun 2019
Historique:
received: 12 06 2019
revised: 21 06 2019
accepted: 24 06 2019
entrez: 30 6 2019
pubmed: 30 6 2019
medline: 30 6 2019
Statut: epublish

Résumé

Various biomarkers have been associated with coronary artery disease (CAD) and ischemic heart failure. The aim of this study was to investigate the correlation of serum levels of soluble urokinase-type plasminogen activator receptor (suPAR), growth differentiation factor 15 (GDF-15), heart-type fatty acid-binding protein (H-FABP), and soluble suppression of tumorigenicity 2 (sST2) with left ventricular ejection fraction (EF) in CAD patients and controls. CAD patients were divided into three groups according to their EF as measured by the biplane Simpson method (53-84%, 31-52%, ≤30%). Overall, 361 subjects were analyzed. In total, 155 CAD patients had an EF of 53-84%, 71 patients had an EF of 31-52%, and 23 patients had an EF of ≤30% as compared to 112 healthy controls (age 51.3 ± 9.0 years, 44.6% female). Mean ages according to EF were 62.1 ± 10.9, 65.2 ± 10.1, and 66.6 ± 8.2 years, respectively, with females representing 29.0, 29.6, and 13.0%. suPAR, GDF-15, H-FABP, and sST2 values were significantly higher in CAD patients and showed an exponential increase with decreasing EF. In a multiple logistic regression model, GDF-15 ( Biomarkers such as suPAR, GDF-15, H-FABP, and sST2 are increased in CAD patients, especially in highly impaired EF. Besides NT-proBNP as a well-known marker for risk prediction, GDF-15 may be an additional tool for diagnosis and clinical follow-up.

Sections du résumé

BACKGROUND BACKGROUND
Various biomarkers have been associated with coronary artery disease (CAD) and ischemic heart failure. The aim of this study was to investigate the correlation of serum levels of soluble urokinase-type plasminogen activator receptor (suPAR), growth differentiation factor 15 (GDF-15), heart-type fatty acid-binding protein (H-FABP), and soluble suppression of tumorigenicity 2 (sST2) with left ventricular ejection fraction (EF) in CAD patients and controls.
METHODS AND RESULTS RESULTS
CAD patients were divided into three groups according to their EF as measured by the biplane Simpson method (53-84%, 31-52%, ≤30%). Overall, 361 subjects were analyzed. In total, 155 CAD patients had an EF of 53-84%, 71 patients had an EF of 31-52%, and 23 patients had an EF of ≤30% as compared to 112 healthy controls (age 51.3 ± 9.0 years, 44.6% female). Mean ages according to EF were 62.1 ± 10.9, 65.2 ± 10.1, and 66.6 ± 8.2 years, respectively, with females representing 29.0, 29.6, and 13.0%. suPAR, GDF-15, H-FABP, and sST2 values were significantly higher in CAD patients and showed an exponential increase with decreasing EF. In a multiple logistic regression model, GDF-15 (
CONCLUSION CONCLUSIONS
Biomarkers such as suPAR, GDF-15, H-FABP, and sST2 are increased in CAD patients, especially in highly impaired EF. Besides NT-proBNP as a well-known marker for risk prediction, GDF-15 may be an additional tool for diagnosis and clinical follow-up.

Identifiants

pubmed: 31252588
pii: jcm8070924
doi: 10.3390/jcm8070924
pmc: PMC6678676
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Medical University of Vienna
ID : 1
Organisme : Paracelsus Medical University of Salzburg
ID : 1

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Auteurs

Daniel Dalos (D)

Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.

Georg Spinka (G)

Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.

Matthias Schneider (M)

Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.

Bernhard Wernly (B)

Division of Cardiology, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.

Vera Paar (V)

Division of Cardiology, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.

Uta Hoppe (U)

Division of Cardiology, Paracelsus Medical University of Salzburg, 5020 Salzburg, Austria.

Brigitte Litschauer (B)

Department of Pharmacology, Medical University of Vienna, 1090 Vienna, Austria.

Jeanette Strametz-Juranek (J)

Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.

Michael Sponder (M)

Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria. michael.sponder@meduniwien.ac.at.

Classifications MeSH