Associations Between Blood Biomarkers, Cardiac Function, and Adverse Outcome in a Young Fontan Cohort

Author:

van den Bosch Eva123ORCID,Bossers Sjoerd S. M.12,Kamphuis Vivian P.34,Boersma Eric5ORCID,Roos‐Hesselink Jolien W.5ORCID,Breur Johannes M. P. J.6,Ten Harkel Arend D. J.4,Kapusta Livia78,Bartelds Beatrijs1ORCID,Roest Arno A. W.4ORCID,Kuipers Irene M.9,Blom Nico A.49,Koopman Laurens P.1,Helbing Willem A.128ORCID

Affiliation:

1. Division of Pediatric Cardiology Department of Pediatrics Erasmus University Medical Center Rotterdam The Netherlands

2. Department of Radiology Erasmus University Medical Center Rotterdam The Netherlands

3. Netherlands Heart Institute Utrecht The Netherlands

4. Division of Pediatric Cardiology Department of Pediatrics Leiden University Medical Center The Netherlands

5. Department of Cardiology Erasmus University Medical Center Rotterdam The Netherlands

6. Department of Pediatric Cardiology University Medical Center Utrecht Utrecht The Netherlands

7. Department of Pediatric Cardiology Sourasky Medical Center Tel Aviv University Tel Aviv Israel

8. Division of Pediatric Cardiology Department of Pediatrics Radboud University Medical Center Nijmegen The Netherlands

9. Division of Pediatric Cardiology Department of Pediatrics Academic Medical Center Amsterdam The Netherlands

Abstract

Background Patients who have undergone the Fontan procedure are at high risk of circulatory failure. In an exploratory analysis we aimed to determine the prognostic value of blood biomarkers in a young cohort who have undergone the Fontan procedure. Methods and Results In multicenter prospective studies patients who have undergone the Fontan procedure underwent blood sampling, cardiopulmonary exercise testing, and stress cardiac magnetic resonance imaging. Several biomarkers including NT‐proBNP (N‐terminal pro‐B‐type natriuretic peptide), GDF‐15 (growth differentiation factor 15), Gal‐3 (galectin‐3), ST2 (suppression of tumorigenicity 2), DLK‐1 (protein delta homolog 1), FABP‐4 (fatty acid‐binding protein 4), IGFBP‐1 (insulin‐like growth factor‐binding protein 1), IGFBP‐7, MMP‐2 (matrix metalloproteinase 2), and vWF (von Willebrand factor) were assessed in blood at 9.6 (7.1–12.1) years after Fontan completion. After this baseline study measurement, follow‐up information was collected on the incidence of adverse cardiac events, including cardiac death, out of hospital cardiac arrest, heart transplantation (listing), cardiac reintervention (severe events), hospitalization, and cardioversion/ablation for arrhythmias was collected and the relation with blood biomarkers was assessed by Cox proportional hazard analyses. The correlation between biomarkers and other clinical parameters was evaluated. We included 133 patients who have undergone the Fontan procedure, median age 13.2 (25th, 75th percentile 10.4–15.9) years, median age at Fontan 3.2 (2.5–3.9) years. After a median follow‐up of 6.2 (4.9–6.9) years, 36 (27.1%) patients experienced an event of whom 13 (9.8%) had a severe event. NT‐proBNP was associated with (all) events during follow‐up and remained predictive after correction for age, sex, and dominant ventricle (hazard ratio, 1.89; CI, 1.32–2.68). The severe event‐free survival was better in patients with low levels of GDF‐15 ( P =0.005) and vWF ( P =0.008) and high levels of DLK‐1 ( P =0.041). There was a positive correlation (β=0.33, P =0.003) between DLK‐1 and stress cardiac magnetic resonance imaging functional reserve. Conclusions NT‐proBNP, GDF‐15, vWF, DLK‐1, ST‐2 FABP‐4, and IGFBP‐7 levels relate to long‐term outcome in young patients who have undergone the Fontan procedure.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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