Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Clinical Division of Haematology and Haemostaseology, Department of Medicine I, Medical University of Vienna, Vienna, Austria.
Eur J Intern Med. 2021 Jun;88:35-42. doi: 10.1016/j.ejim.2021.02.011. Epub 2021 Mar 9.
Growth-differentiation factor-15 (GDF-15) has recently been described as a potential biomarker for predicting risk of mortality and cardiovascular events in patients with atrial fibrillation (AF) but requires validation in clinical practice.
The study population consisted of 362 patients (mean age: 71 years, 37% women) with non-valvular AF included in a prospective cohort study. Relationship of GDF-15 with all-cause mortality and major adverse cardiac events (MACE) was analyzed using Cox regression. Survival analysis stratified by GDF-15 was based on national death records, while MACE was recorded at personal follow-up. Further, we evaluated the recently developed GDF-15 based prognostic score towards prediction of all-cause mortality (ABC-death score).
Over a median observation period of 4.3 years, 81 (23.3%) patients died, and over a median personal follow-up of 316 days 47 MACE occurred. GDF-15 was independently associated with all-cause mortality (adjusted HR per double increase 2.33, 95%CI 1.74-3.13) and MACE (adjusted HR per double increase 2.33, 95%CI 1.60-3.39). GDF-15 levels, measured at follow-up, were similarly associated with mortality, and longitudinal measurements of GDF-15 did not significantly differ. Six-year survival probability of patients above vs. below the median GDF-15 level was 44% (95%CI 34-57) and 84% (95%CI 76-93), respectively. The ABC-death score revealed a C-statistic of 0.80.
GDF-15 predicts risk of all-cause mortality and MACE in patients with non-valvular AF. Further, the ABC-death score showed good predictive accuracy in a "real-world" cohort. Therefore, introduction of GDF-15 into clinical practice would enhance risk prediction of morbidity and mortality in AF patients.
生长分化因子 15(GDF-15)最近被描述为预测非瓣膜性心房颤动(AF)患者死亡和心血管事件风险的潜在生物标志物,但需要在临床实践中验证。
研究人群包括纳入前瞻性队列研究的 362 名非瓣膜性 AF 患者(平均年龄:71 岁,37%为女性)。使用 Cox 回归分析 GDF-15 与全因死亡率和主要不良心脏事件(MACE)的关系。基于全国死亡记录对 GDF-15 分层的生存分析,而 MACE 在个人随访时记录。此外,我们评估了最近开发的基于 GDF-15 的预后评分(ABC-死亡评分)对全因死亡率的预测能力。
在中位观察期 4.3 年期间,81 名(23.3%)患者死亡,在中位个人随访 316 天期间,47 名患者发生 MACE。GDF-15 与全因死亡率(每增加一倍的调整 HR 为 2.33,95%CI 为 1.74-3.13)和 MACE(每增加一倍的调整 HR 为 2.33,95%CI 为 1.60-3.39)独立相关。在随访时测量的 GDF-15 水平与死亡率也具有相似的相关性,且 GDF-15 的纵向测量并无显著差异。GDF-15 中位数以上和以下的患者 6 年生存率分别为 44%(95%CI 34-57)和 84%(95%CI 76-93)。ABC-死亡评分的 C 统计量为 0.80。
GDF-15 可预测非瓣膜性 AF 患者的全因死亡率和 MACE。此外,ABC-死亡评分在“真实世界”队列中显示出良好的预测准确性。因此,将 GDF-15 引入临床实践将提高 AF 患者的发病率和死亡率风险预测。