Department of Heart Disease, Haukeland University Hospital, Bergen, Norway.
Emergency Care Clinic, Haukeland University Hospital, Bergen, Norway.
Heart. 2024 Mar 12;110(7):508-516. doi: 10.1136/heartjnl-2023-323260.
Growth differentiation factor-15 (GDF-15) is a predictor of death and cardiovascular events when measured during index hospitalisation in patients with acute chest pain. This study investigated the prognostic utility of measuring GDF-15 3 months after an admission with suspected non-ST-elevation acute coronary syndrome (NSTE-ACS).
GDF-15 was measured at baseline and 3 months after admission in 758 patients admitted with suspected NSTE-ACS. Patients were followed for a median of 1540 (IQR: 1087-1776) days after the 3-month visit. The primary endpoint was all-cause mortality, while the secondary composite endpoint included all-cause mortality, incident myocardial infarction and heart failure hospitalisation during follow-up.
In patients with GDF-15 ≥1200 pg/mL (n=248), 18% died and 25% met the composite endpoint. In patients with GDF-15 <1200 pg/mL (n=510), 1.7% died and 4% met the composite endpoint. The GDF-15 concentration (log2 transformed) at 3 months was significantly associated with all-cause mortality (adjusted HR: 2.2, 95% CI: 1.4 to 3.3, p<0.001) and the composite endpoint (adjusted HR: 1.9, 95% CI: 1.4 to 2.7, p<0.001), independently of traditional risk factors and baseline troponin T. A 10% change in GDF-15 concentration from baseline to the 3-month visit was associated with increased risk of all-cause mortality (HR: 1.06, 95% CI: 1.01 to 1.13, p=0.031), adjusting for baseline GDF-15 concentrations.
High GDF-15 concentrations 3 months after admission for suspected NSTE-ACS are associated with long-term mortality and cardiovascular events, independent of traditional risk factors and troponin T. A change in GDF-15 concentration can provide prognostic information.
生长分化因子 15(GDF-15)在因急性胸痛住院的患者中,在住院期间测量时,是死亡和心血管事件的预测指标。本研究调查了在疑似非 ST 段抬高型急性冠状动脉综合征(NSTE-ACS)住院后 3 个月测量 GDF-15 的预后效用。
在 758 例疑似 NSTE-ACS 住院的患者中,在基线和住院后 3 个月测量 GDF-15。患者在第 3 个月就诊后中位数随访 1540(IQR:1087-1776)天。主要终点是全因死亡率,次要复合终点包括随访期间的全因死亡率、新发心肌梗死和心力衰竭住院。
在 GDF-15≥1200pg/ml(n=248)的患者中,18%死亡,25%符合复合终点。在 GDF-15<1200pg/ml(n=510)的患者中,1.7%死亡,4%符合复合终点。3 个月时的 GDF-15 浓度(对数 2 转换)与全因死亡率(调整后的 HR:2.2,95%CI:1.4 至 3.3,p<0.001)和复合终点(调整后的 HR:1.9,95%CI:1.4 至 2.7,p<0.001)显著相关,独立于传统危险因素和基线肌钙蛋白 T。从基线到 3 个月就诊时 GDF-15 浓度增加 10%,与全因死亡率增加相关(HR:1.06,95%CI:1.01 至 1.13,p=0.031),调整了基线 GDF-15 浓度。
疑似 NSTE-ACS 住院后 3 个月时的高 GDF-15 浓度与长期死亡率和心血管事件相关,独立于传统危险因素和肌钙蛋白 T。GDF-15 浓度的变化可提供预后信息。