Division of Paediatric Cardiology, Department of Paediatrics, London Health Sciences Centre, University of Western Ontario, Canada.
Am Heart J. 2011 Jul;162(1):131-5. doi: 10.1016/j.ahj.2011.03.036.
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).
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.
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.
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.
许多患有先天性心脏病的年轻人尽管接受了矫正手术,但仍会发展为心力衰竭。生长分化因子 15(GDF-15)已被确立为急性心肌梗死后患者和心力衰竭患者风险分层和死亡率的标志物。我们的目的是确定 GDF-15 在接受手术的先天性心脏病(ACHD)患者中监测心力衰竭的作用。通过与最大摄氧量(VO(2max))和另一种生物标志物 N 端脑利钠肽前体(NT-proBNP)进行比较,验证了这种潜在的生物标志物。
共纳入 317 名 ACHD 患者(女性 129 名),平均年龄 26.5 ± 8.5 岁(均数 ± 标准差)。我们研究了 GDF-15 与 NT-proBNP 和 VO(2max)%(年龄和性别预测值)之间的关系。各组的截断值如下:NT-proBNP<100、100-300 和>300pg/ml;VO(2max)%<65%、65%-85%和>85%的预测正常。
在 NT-proBNP<100 组和 NT-proBNP>300 组之间,以及在 100-300 组和>300 组之间,GDF-15 水平存在显著差异。对于 VO(2max)%,在<65%和>85%组以及<65%和 65%-85%组之间,GDF-15 水平存在显著差异。NT-proBNP<100pg/ml 和 VO(2max)%>85%组的 GDF-15 均值最低。NT-proBNP>300pg/ml 和 VO(2max)%<65%组的 GDF-15 均值最高。包括 82 例接受法洛四联症手术的患者的亚组分析显示,纽约心脏协会(NYHA)心功能 I 级患者的 NT-proBNP 和 GDF-15 水平明显较低,VO(2max)明显较高,与 NYHA 更高等级的患者相比。
生长分化因子 15 可作为潜在心力衰竭的替代标志物,有助于识别有心力衰竭风险的 ACHD 患者,即使他们在临床上无症状。