Heeschen Christopher, Hamm Christian W, Mitrovic Veselin, Lantelme Nicte-Ha, White Harvey D
J.W. Goethe University, Department of Cardiology, Frankfurt, Theodor-Stern-Kai 7, 60590 Frankfurt, Germany.
Circulation. 2004 Nov 16;110(20):3206-12. doi: 10.1161/01.CIR.0000147611.92021.2B. Epub 2004 Nov 8.
Elevated baseline levels of B-type natriuretic peptide (BNP) and the N-terminal fragments of its prohormone, N-terminal-pro-BNP (NT-proBNP), have been associated with adverse long-term outcome in patients with acute coronary syndromes, whereas the prognostic implications of serial NT-proBNP measurements have not been investigated to date.
NT-proBNP, troponin T, and C-reactive protein were measured at baseline and at 48 and 72 hours in 1791 patients with non-ST-elevation acute coronary syndromes. Death and myocardial infarction were recorded during 30 days of follow-up. After adjustment for independent predictors of cardiac risk, baseline NT-proBNP levels >250 ng/L were associated with higher event rates (adjusted OR, 3.7; 95% CI, 2.3 to 5.7; P<0.001). In troponin T-negative patients, NT-proBNP identified a subgroup of high-risk patients (OR, 5.9; 95% CI, 2.6 to 13.3; P<0.001). The risk in those patients (7.2%) did not significantly differ from that in troponin T-positive patients (9.8%; P=0.25). Importantly, clinical stabilization without refractory ischemia was associated with a rapid (as soon as 48 hours after onset of symptoms) and significant (48 hours; -24%; 72 hours, -49%; both P<0.001) decline in NT-proBNP levels. In patients with high NT-proBNP baseline levels, lack of a rapid decline in NT-proBNP levels (< or =250 ng/L) was linked to an adverse short-term prognosis (OR, 33.7; 95% CI, 8.2 to 138.8; P<0.001). In patients with low NT-proBNP baseline levels, a rise in NT-proBNP levels over 72 hours to >250 ng/L was also linked to an adverse 30-day prognosis (OR, 24.0; 95% CI, 8.4 to 68.5; P<0.001).
Neurohumoral activation as evidenced by NT-proBNP appears as a unifying feature that is independent of other biochemical markers (myocardial necrosis, inflammation) and is a powerful and independent determinant of the short-term cardiac risk in patients with acute coronary syndromes. Whether serial measurements of NT-proBNP in patients with ACS may be used to more rapidly identify patients suitable for early discharge or more intensive therapy deserves future prospective studies.
B型利钠肽(BNP)及其前体激素的N端片段N末端B型利钠肽原(NT-proBNP)的基线水平升高与急性冠脉综合征患者的不良长期预后相关,而连续测量NT-proBNP的预后意义迄今尚未得到研究。
对1791例非ST段抬高型急性冠脉综合征患者在基线时、48小时和72小时测量NT-proBNP、肌钙蛋白T和C反应蛋白。在30天的随访期间记录死亡和心肌梗死情况。在对心脏风险的独立预测因素进行校正后,基线NT-proBNP水平>250 ng/L与较高的事件发生率相关(校正后的OR为3.7;95%CI为2.3至5.7;P<0.001)。在肌钙蛋白T阴性的患者中,NT-proBNP识别出一个高危患者亚组(OR为5.9;95%CI为2.6至13.3;P<0.001)。这些患者的风险(7.2%)与肌钙蛋白T阳性患者的风险(9.8%)无显著差异(P=0.25)。重要的是,无难治性缺血的临床稳定与NT-proBNP水平迅速(症状发作后48小时内)且显著下降(48小时时下降24%;72小时时下降49%;P均<0.001)相关。在NT-proBNP基线水平高的患者中,NT-proBNP水平未迅速下降(≤250 ng/L)与不良短期预后相关(OR为33.7;95%CI为8.2至138.8;P<0.001)。在NT-proBNP基线水平低的患者中,NT-proBNP水平在72小时内升高至>250 ng/L也与不良的30天预后相关(OR为24.0;95%CI为8.4至68.5;P<0.001)。
NT-proBNP所证明的神经体液激活似乎是一个统一特征,独立于其他生化标志物(心肌坏死、炎症),并且是急性冠脉综合征患者短期心脏风险的一个强大且独立的决定因素。急性冠脉综合征患者连续测量NT-proBNP是否可用于更快速地识别适合早期出院或强化治疗的患者,值得未来进行前瞻性研究。