Olivier A, Girerd N, Michel J B, Ketelslegers J M, Fay R, Vincent J, Bramlage P, Pitt B, Zannad F, Rossignol P
Inserm, CIC-P 14-33, U 116, CHU Nancy, France; University of Lorraine, France; F-CRIN INI-CRCT, Nancy, France; Department of Cardiovascular Disease, Institut Lorrain du Coeur et des Vaisseaux, Nancy University Hospital, Nancy, France.
Inserm, CIC-P 14-33, U 116, CHU Nancy, France; University of Lorraine, France; F-CRIN INI-CRCT, Nancy, France.
Int J Cardiol. 2017 Aug 15;241:344-350. doi: 10.1016/j.ijcard.2017.02.018. Epub 2017 Feb 8.
Increased levels of neuro-hormonal biomarkers predict poor prognosis in patients with acute myocardial infarction (AMI) complicated by left ventricular systolic dysfunction (LVSD). The predictive value of repeated (one-month interval) brain natriuretic peptides (BNP) and big-endothelin 1 (BigET-1) measurements were investigated in patients with LVSD after AMI.
In a sub-study of the Eplerenone Post-Acute Myocardial Infarction Heart Failure Efficacy and Survival Study (EPHESUS trial), BNP and BigET-1 were measured at baseline and at 1month in 476 patients.
When included in the same Cox regression model, baseline BNP (p=0.0003) and BigET-1 (p=0.026) as well as the relative changes (after 1month) from baseline in BNP (p=0.049) and BigET-1 (p=0.045) were predictive of the composite of cardiovascular death or hospitalization for worsening heart failure. Adding baseline and changes in BigET-1 to baseline and changes in BNP led to a significant increase in prognostic reclassification as assessed by integrated discrimination improvement index (5.0%, p=0.01 for the primary endpoint).
Both increased baseline and changes after one month in BigET-1 concentrations were shown to be associated with adverse clinical outcomes, independently from BNP baseline levels and one month changes, in patients after recent AMI complicated with LVSD. This novel result may be of clinical interest since such combined biomarker assessment could improve risk stratification and open new avenues for biomarker-guided targeted therapies.
In the present study, we report for the first time in a population of patients with reduced LVEF after AMI and signs or symptoms of congestive HF, that increased baseline values of BNP and BigET-1 as well as a further rise of these markers over the first month after AMI, were independently predictive of future cardiovascular events. This approach may therefore be of clinical interest with the potential of improving risk stratification after AMI with reduced LVEF while further opening new avenues for biomarker-guided targeted therapies.
神经激素生物标志物水平升高预示急性心肌梗死(AMI)合并左心室收缩功能障碍(LVSD)患者预后不良。本研究探讨了对AMI后LVSD患者重复(间隔1个月)检测脑钠肽(BNP)和大内皮素1(BigET-1)的预测价值。
依普利酮急性心肌梗死后心力衰竭疗效和生存研究(EPHESUS试验)的一项子研究中,对476例患者在基线和1个月时测量BNP和BigET-1。
当纳入同一Cox回归模型时,基线BNP(p=0.0003)、BigET-1(p=0.026)以及BNP(p=0.049)和BigET-1(p=0.045)从基线开始1个月后的相对变化可预测心血管死亡或因心力衰竭恶化住院的复合终点。将BigET-1的基线和变化值加入BNP的基线和变化值中,根据综合判别改善指数评估,预后重新分类有显著增加(主要终点为5.0%,p=0.01)。
在近期AMI合并LVSD的患者中,BigET-1浓度的基线升高和1个月后的变化均与不良临床结局相关,独立于BNP基线水平和1个月时的变化。这一新结果可能具有临床意义,因为这种联合生物标志物评估可改善风险分层,并为生物标志物指导的靶向治疗开辟新途径。
在本研究中,我们首次报道,在AMI后左心室射血分数降低且有充血性心力衰竭体征或症状的患者群体中,BNP和BigET-1的基线值升高以及AMI后第一个月这些标志物的进一步升高,可独立预测未来心血管事件。因此,这种方法可能具有临床意义,有可能改善AMI后左心室射血分数降低患者的风险分层,同时进一步为生物标志物指导的靶向治疗开辟新途径。