Christ Michael, Laule Kirsten, Klima Theresia, Hochholzer Willibald, Breidthardt Tobias, Perruchoud Andre P, Mueller Christian
Department of Internal Medicine, University Hospital, Petersgraben 4, CH-4031 Basel, Switzerland.
Int J Cardiol. 2008 May 7;126(1):73-8. doi: 10.1016/j.ijcard.2007.03.119. Epub 2007 May 3.
Multimarker approaches improve risk prediction in patients presenting with acute coronary syndrome. We hypothesized that simultaneous assessment of B-type natriuretic peptide (BNP), cardiac troponin I (cTNI) and C-reactive protein (CRP) enables clinicians to better predict risk among patients with acute dyspnea presenting to the emergency department.
In this post-hoc analysis of the B-Type natriuretic peptide for Acute Shortness of Breath Evaluation (BASEL) study, above biomarkers were available in 305 patients. Death occurred in 123 (40%) patients within 24 months of follow-up. Using prospectively defined cut-off points (BNP>100 pg/mL; cTNI>0.8 microg/L; CRP>5 mg/L) and categorizing patients by the number of elevated cardiac biomarkers, the 24 months risk of death increased in proportion to the number of cardiac biomarkers elevated (p<0.001 for trend). Elevated biomarkers significantly predicted increased risk of death at 24 months of follow-up in univariate Cox models (BNP: RR 4.78, 95%CI: 2.51-9.14; p<0.001; cTNI: RR: 2.29, 95%CI: 1.61-3.26, p<0.001; CRP: RR 1.98, 95%CI: 1.28-3.08; p=0.002). Multivariable Cox regression analysis revealed that elevated levels of BNP (p<0.001) and TNI levels (p<0.002) indicated increased risk of death during long-term follow-up, while only a statistical trend was seen for elevated CRP (p=0.09). Comparably, risk of death or rehospitalization significantly increased with the number of elevated biomarkers.
Our findings suggest that a simple multimarker approach with simultaneous assessment of BNP, and cTNI demonstrates potential to assist clinicians in predicting risk of death and/or rehospitalization in patients presenting with acute dyspnea in the emergency department.
多标志物方法可改善急性冠状动脉综合征患者的风险预测。我们假设,同时评估B型利钠肽(BNP)、心肌肌钙蛋白I(cTNI)和C反应蛋白(CRP)能使临床医生更好地预测急诊科急性呼吸困难患者的风险。
在这项B型利钠肽用于急性呼吸急促评估(BASEL)研究的事后分析中,305例患者可获得上述生物标志物。123例(40%)患者在随访24个月内死亡。使用前瞻性定义的截断点(BNP>100 pg/mL;cTNI>0.8 μg/L;CRP>5 mg/L),并根据升高的心脏生物标志物数量对患者进行分类,24个月的死亡风险随升高的心脏生物标志物数量成比例增加(趋势p<0.001)。在单变量Cox模型中,升高的生物标志物显著预测随访24个月时死亡风险增加(BNP:RR 4.78,95%CI:2.51-9.14;p<0.001;cTNI:RR:2.29,95%CI:1.61-3.26,p<0.001;CRP:RR 1.98,95%CI:1.28-3.08;p=0.002)。多变量Cox回归分析显示,BNP水平升高(p<0.001)和TNI水平升高(p<0.002)表明长期随访期间死亡风险增加,而CRP升高仅显示出统计学趋势(p=0.09)。同样,死亡或再次住院的风险随升高的生物标志物数量显著增加。
我们的研究结果表明,一种简单的同时评估BNP和cTNI的多标志物方法有潜力帮助临床医生预测急诊科急性呼吸困难患者的死亡和/或再次住院风险。