Department of Cardiology, Thoraxcenter, Erasmus Medical Center, Rotterdam, the Netherlands; Cardiovascular Research School, Erasmus Medical Center (COEUR), Rotterdam, the Netherlands.
Department of Epidemiology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
J Am Coll Cardiol. 2017 Nov 7;70(19):2378-2388. doi: 10.1016/j.jacc.2017.09.026.
Several clinical studies have evaluated the association between ST2 and outcome in patients with heart failure (HF). However, little is known about the predictive value of frequently measured ST2 levels in patients with acute HF.
This study sought to describe the prognostic value of baseline and repeated ST2 measurements in patients with acute HF.
In the TRIUMPH (Translational Initiative on Unique and novel strategies for Management of Patients with Heart failure) clinical cohort study, 496 patients with acute HF were enrolled in 14 hospitals in the Netherlands between 2009 and 2014. Repeated blood samples (7) were drawn during 1-year follow-up. ST2 and N-terminal pro-B-type natriuretic peptide (NT-proBNP) levels were measured in a central laboratory. The primary endpoint was the composite of all-cause mortality and HF rehospitalization. Associations between repeated biomarker measurements and the primary endpoint were assessed using a joint model.
Median age was 74 years, and 37% of patients were women. The primary endpoint was reached in 188 patients (40%) during a median follow-up of 325 days (interquartile range: 85 to 401). The median baseline ST2 level was 71 ng/ml (interquartile range: 46 to 102). After adjustment for clinical factors and NT-proBNP, baseline ST2 was associated with an increased risk of the primary endpoint, and the hazard ratio per 1 SD increase of the baseline ST2 level (on the log scale) was 1.30 (95% confidence interval: 1.08 to 1.56; p = 0.005). When repeated measurements were taken into account, the adjusted hazard ratio per 1 SD increase of the ST2 level (on the log scale) during follow-up increased to 1.85 (95% confidence interval: 1.02 to 3.33; p = 0.044), adjusted for clinical factors and repeated measurements of NT-proBNP. Furthermore, ST2 levels appeared to elevate several weeks before the time of the primary endpoint.
Repeated ST2 measurements appeared to be a strong predictor of outcome in patients with acute HF, independent of repeatedly measured NT-proBNP. Hence ST2 may be helpful in clinical practice for prognostication and treatment monitoring. (TRanslational Initiative on Unique and novel strategies for Management of Patients with Heart failure [TRIUMPH]; NTR1893).
多项临床研究评估了 ST2 与心力衰竭(HF)患者结局之间的关联。然而,对于急性 HF 患者中频繁测量的 ST2 水平的预测价值知之甚少。
本研究旨在描述急性 HF 患者基线和重复 ST2 测量的预后价值。
在 TRIUMPH(用于管理心力衰竭患者的独特和新颖策略的转化倡议)临床队列研究中,2009 年至 2014 年期间,荷兰的 14 家医院共纳入了 496 名急性 HF 患者。在 1 年的随访期间采集了 7 次重复血样。在中心实验室测量 ST2 和 N 末端 pro-B 型利钠肽(NT-proBNP)水平。主要终点是全因死亡率和 HF 再住院的复合终点。使用联合模型评估重复生物标志物测量与主要终点之间的关联。
中位年龄为 74 岁,37%的患者为女性。在中位随访 325 天(四分位距:85 至 401)期间,188 例患者(40%)达到了主要终点。基线 ST2 中位数为 71ng/ml(四分位距:46 至 102)。在调整了临床因素和 NT-proBNP 后,基线 ST2 与主要终点风险增加相关,基线 ST2 水平每增加 1 SD(在对数标度上)的风险比为 1.30(95%置信区间:1.08 至 1.56;p=0.005)。当考虑重复测量时,在随访期间 ST2 水平每增加 1 SD(在对数标度上)的调整后风险比增加至 1.85(95%置信区间:1.02 至 3.33;p=0.044),调整了临床因素和 NT-proBNP 的重复测量。此外,ST2 水平似乎在主要终点时间前数周升高。
在急性 HF 患者中,重复 ST2 测量似乎是结局的强有力预测指标,独立于重复测量的 NT-proBNP。因此,ST2 可能有助于临床实践中的预后和治疗监测。(用于管理心力衰竭患者的独特和新颖策略的转化倡议 [TRIUMPH];NTR1893)。