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Growth differentiation factor 15: an additional diagnostic tool for the risk stratification of developing heart
Kambiz Norozi1, Reiner Buchhorn, Abeer Yasin
1Division of Paediatric Cardiology, Department of Paediatrics, London Health Sciences Centre, University of Western Ontario, Canada. kambiz.norozi@lhsc.on.ca
Insights
Growth differentiation factor 15 (GDF-15) can monitor heart failure in adults with congenital heart defects (ACHD). GDF-15 identifies at-risk patients, even those without symptoms, aiding early intervention.
Area of Science:
- Cardiology
- Biomarker Discovery
- Congenital Heart Disease
Background:
- Adults with congenital heart defects (ACHD) often develop heart failure post-surgery.
- Growth differentiation factor 15 (GDF-15) is a known risk marker for heart failure and mortality.
- The role of GDF-15 in monitoring heart failure within the ACHD population requires further investigation.
Purpose of the Study:
- To evaluate Growth differentiation factor 15 (GDF-15) as a monitoring biomarker for heart failure in adults with operated congenital heart defects (ACHD).
- To validate GDF-15 by comparing it with maximal oxygen uptake (VO(2max)) and N-terminal pro-brain natriuretic peptide (NT-proBNP).
Main Methods:
- A cohort of 317 ACHD patients (mean age 26.5 ± 8.5 years) was studied.
- The relationship between GDF-15, NT-proBNP levels, and VO(2max%) was analyzed.
- Patients were categorized based on NT-proBNP (<100, 100-300, >300 pg/mL) and VO(2max%) (<65%, 65-85%, >85% predicted).
Main Results:
- Significant differences in GDF-15 levels were observed across NT-proBNP and VO(2max%) categories.
- Lowest GDF-15 levels correlated with lower NT-proBNP and higher VO(2max%).
- Highest GDF-15 levels correlated with higher NT-proBNP and lower VO(2max%).
- Subgroup analysis in operated tetralogy of Fallot patients showed lower GDF-15 and NT-proBNP with higher VO(2max) in NYHA class I.
Conclusions:
- Growth differentiation factor 15 (GDF-15) may serve as a surrogate marker for latent heart failure in ACHD patients.
- GDF-15 can potentially identify asymptomatic ACHD patients at risk of developing heart failure.
- This biomarker aids in risk stratification and monitoring of heart failure in ACHD.
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 (VO(2max)) 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 VO(2max%) (percent predicted for age and gender). The cutoffs for the groups were as follows: NT-proBNP <100, 100 to 300, and >300 pg/mL; VO(2max%) <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 VO(2max%), 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 VO(2max%) >85%. The highest mean GDF-15 was found in the groups with NT-proBNP >300 pg/mL and VO(2max%) <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 VO(2max) 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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