Detection of Soluble ED-A+Fibronectin and Evaluation as Novel Serum Biomarker for Cardiac Tissue Remodeling

Author:

Ziffels Barbara12ORCID,Ospel Johanna1,Grün Katja1ORCID,Neri Dario2,Pfeil Alexander3,Fritzenwanger Michael1,Figulla Hans R.1,Jung Christian14,Berndt Alexander5,Franz Marcus1ORCID

Affiliation:

1. Jena University Hospital, Department of Internal Medicine I, 07747 Jena, Germany

2. Swiss Federal Institute of Technology, Department of Chemistry and Applied Biosciences, 8093 Zurich, Switzerland

3. Jena University Hospital, Department of Internal Medicine III, 07747 Jena, Germany

4. Medical Faculty, Division of Cardiology, Pulmonology, and Vascular Medicine, University of Duesseldorf, 40225 Duesseldorf, Germany

5. Jena University Hospital, Institute of Pathology, 07743 Jena, Germany

Abstract

Background and Aims. Fibronectin containing the extra domain A (ED-A+Fn) was proven to serve as a valuable biomarker for cardiac remodeling. The study was aimed at establishing an ELISA to determine ED-A+Fn in serum of heart failure patients.Methods. ED-A+Fn was quantified in serum samples from 114 heart failure patients due to ischemic (ICM,n=44) and dilated (DCM,n=39) cardiomyopathy as well as hypertensive heart disease (HHD,n=31) compared to healthy controls (n=12).Results. In comparison to healthy volunteers, heart failure patients showed significantly increased levels of ED-A+Fn (p<0.001). In particular in ICM patients there were significant associations between ED-A+Fn serum levels and clinical parameters, for example, increased levels with rising NYHA class (p=0.013), a negative correlation with left ventricular ejection fraction (p=0.026,r: −0.353), a positive correlation with left atrial diameter (p=0.008,r: 0.431), and a strong positive correlation with systolic pulmonary artery pressure (p=0.002,r: 0.485). In multivariate analysis, ED-A+Fn was identified as an independent predictor of an ischemic heart failure etiology.Conclusions. The current study could clearly show that ED-A+Fn is a promising biomarker in cardiovascular diseases, especially in heart failure patients due to an ICM. We presented a valid ELISA method, which could be applied for further studies investigating the value of ED-A+Fn.

Funder

Seventh Framework Programme

Publisher

Hindawi Limited

Subject

Biochemistry (medical),Clinical Biochemistry,Genetics,Molecular Biology,General Medicine

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