Growth differentiation factor 15: An additional diagnostic tool for the risk stratification of developing heart failure in patients with operated congenital heart defects? - 06/08/11
Résumé |
Background |
Many young adults who have congenital heart defects develop heart failure despite corrective surgeries. Growth differentiation factor 15 (GDF-15) has an established role as a marker for risk stratification and mortality both in patients after acute myocardial infarction and in patients with heart failure. Our aim was to establish a role for GDF-15 for monitoring heart failure in operated congenital heart defects (ACHD). This potential biomarker was validated through comparison with maximal oxygen uptake (VO2max) and to another biomarker, N-terminal pro–brain natriuretic peptide (NT-proBNP).
Methods |
A total of 317 ACHD patients (129 females) with an average age of 26.5 ± 8.5 years (mean ± SD) enrolled in the study. We studied the relation between GDF-15 and NT-proBNP and VO2max% (percent predicted for age and gender). The cutoffs for the groups were as follows: NT-proBNP <100, 100 to 300, and >300 pg/mL; VO2max% <65%, 65% to 85%, and >85% of predicted normal.
Results |
Significant differences in mean GDF-15 levels were found between the NT-proBNP <100 and NT-proBNP >300 groups, as well as between the 100 to 300 and the >300 groups. For VO2max%, significant differences were found in GDF-15 levels between <65% and >85% and between <65% and 65% to 85%, respectively. The lowest mean GDF-15 was found in groups with NT-proBNP <100 pg/mL and VO2max% >85%. The highest mean GDF-15 was found in the groups with NT-proBNP >300 pg/mL and VO2max% <65%. A subgroup analysis, including 82 patients with operated tetralogy of Fallot, showed that patients in the New York Heart Association I class have significantly lower NT-proBNP and GDF-15 level and markedly higher VO2max compared with the patients in higher New York Heart Association class.
Conclusion |
Growth differentiation factor 15 might be used as a surrogate marker for latent heart failure and could help to identify patients with ACHD who are at risk for developing heart failure, even if they are clinically asymptomatic.
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This study was supported by grants from German Research Association to Professor A. Wessel (Nr. WE 2670/1-1) and Professor S. Geyer (Nr. GE 1167/3-1). |
Vol 162 - N° 1
P. 131-135 - juillet 2011 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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