Department of Pediatric Cardiology Center for Congenital Heart Diseases University Medical Center Groningen University of Groningen The Netherlands.
Department of Cardiothoracic Surgery Center for Congenital Heart Diseases University Medical Center Groningen University of Groningen The Netherlands.
J Am Heart Assoc. 2020 May 18;9(10):e015521. doi: 10.1161/JAHA.119.015521. Epub 2020 May 8.
Background We investigated serial serum levels of GDF-15 (growth differentiation factor 15) in Fontan patients and their relation to outcome. Methods and Results In this single-center prospective study of consecutive Fontan patients, serial serum GDF-15 measurement and clinical assessment was done at baseline (n=81) and after 2 years (n=51). The association between GDF-15 and the combined end point of all-cause mortality, heart transplant listing, and Fontan-related hospitalization was investigated. Median age at baseline was 21 years (interquartile range: 15-28 years). Median GDF-15 serum levels at baseline were 552 pg/mL (interquartile range: 453-729 pg/mL). GDF-15 serum levels correlated positively with age, age at Fontan initiation, New York Heart Association class, and serum levels of NT-proBNP (N-terminal pro-B-type natriuretic peptide) and ɣGT (γ-glutamyltransferase) and negatively with exercise capacity. During a median follow-up of 4.8 years (interquartile range: 3.3-5.5 years), the combined end point occurred in 30 patients (37%). Multivariate Cox regression showed that patients with the highest baseline GDF-15 (n=20, defined as the upper quartile) had a higher risk of hospitalization or death than the lowest 3 quartiles (hazard ratio [HR], 2.76; 95% CI, 1.27-6.00; =0.011). After 2 years of follow-up, patients in whom serum level of GDF-15 increased to >70 pg/mL (n=13) had a higher risk of hospitalization or death than the lowest 3 quartiles (HR, 2.69; 95% CI, 1.03-6.99; =0.043). Conclusions In Fontan patients, elevated serum levels of GDF-15 are associated with worse functional status and predict Fontan-related events. Furthermore, serial measurements showed that an increase in GDF-15 serum level was associated with increased risk for adverse outcome.
我们研究了 Fontan 患者的 GDF-15(生长分化因子 15)血清水平的变化及其与预后的关系。
在这项 Fontan 患者的单中心前瞻性研究中,我们在基线(n=81)和 2 年后(n=51)进行了连续的血清 GDF-15 测量和临床评估。研究了 GDF-15 与全因死亡率、心脏移植、Fontan 相关住院治疗的复合终点之间的关系。基线时的中位年龄为 21 岁(四分位距:15-28 岁)。基线时的中位 GDF-15 血清水平为 552 pg/ml(四分位距:453-729 pg/ml)。GDF-15 血清水平与年龄、Fontan 开始时的年龄、纽约心脏协会(NYHA)心功能分级、血清 NT-proBNP(N 末端 pro-B 型利钠肽)和 ɣGT(γ-谷氨酰转移酶)水平呈正相关,与运动能力呈负相关。在中位随访 4.8 年(四分位距:3.3-5.5 年)期间,30 例患者(37%)发生了复合终点事件。多变量 Cox 回归显示,基线时 GDF-15 最高的 20 例患者(定义为上四分位数)住院或死亡的风险高于最低的 3 个四分位数(风险比 [HR],2.76;95%可信区间,1.27-6.00;=0.011)。随访 2 年后,血清 GDF-15 水平升高至>70 pg/ml 的 13 例患者(n=13)住院或死亡的风险高于最低的 3 个四分位数(HR,2.69;95%可信区间,1.03-6.99;=0.043)。
在 Fontan 患者中,升高的血清 GDF-15 水平与功能状态恶化相关,并预测 Fontan 相关事件。此外,连续测量显示,GDF-15 血清水平升高与不良结局的风险增加相关。