Investigation Unit Don Benito-Villanueva, Fundesalud-Hospital Don Benito-Villanueva, Plaza de Conquistadores 49, Villanueva de la Serena, Badajoz, Spain.
Int J Cardiol. 2011 Jan 21;146(2):219-24. doi: 10.1016/j.ijcard.2010.04.016. Epub 2010 May 2.
Risk stratification of patients with unstable angina or non-ST-segment elevation myocardial infarction (UA/NSTEMI) is problematic given the heterogeneous presentation of the condition. This study was undertaken to compare, in UA/NSTEMI patients, the prognostic value of two clinical risk scores (RS) (i.e. Thrombolysis in Myocardial Infarction (TIMI) and physician's risk assessment (PRA)) and to assess whether serum biomarkers can increase the prognostic accuracy of these RS.
We prospectively assessed 610 consecutive UA/NSTEMI patients, 217 (36%) UA and 393 (64%) NSTEMI. In all patients RS, high sensitivity C-reactive protein, CD40 ligand, IL6, IL10, IL18, E-selectin, P-selectin, white blood cell count, neopterin, myeloperoxidase, fibrinogen and NT proBNP were assessed at study entry. The primary study endpoint was death and non-fatal MI at 30 and 360 days of follow-up.
At 1 year, 54 patients (8.9%) had reached the primary study endpoint (26 suffered a cardiac death (4.3%) and 34 (5.6%) a non-fatal MI). For both RS, the study endpoint occurred more commonly in patients at a "higher risk" compared to those classified as being at a "lower risk". Moreover, TIMI and PRA RS had similar discriminatory accuracy. TIMI RS, however, was a better predictor of events than PRA at both 30- and 360-day follow-up. The inflammatory biomarkers assessed in the study did not improve significantly the predictive value of RS.
Our study suggests both that TIMI RS is a better marker of risk than PRA RS and inflammatory biomarkers do not increase the predictive value of these clinical risk scores.
由于不稳定型心绞痛或非 ST 段抬高型心肌梗死(UA/NSTEMI)患者的临床表现存在异质性,因此对其进行风险分层存在问题。本研究旨在比较两种临床风险评分(即血栓形成溶栓治疗心肌梗死评分(TIMI)和医生风险评估(PRA))在 UA/NSTEMI 患者中的预后价值,并评估血清生物标志物是否可以提高这些 RS 的预后准确性。
我们前瞻性评估了 610 例连续的 UA/NSTEMI 患者,其中 217 例(36%)为 UA,393 例(64%)为 NSTEMI。在所有患者中,研究时均评估了 RS、高敏 C 反应蛋白、CD40 配体、IL6、IL10、IL18、E-选择素、P-选择素、白细胞计数、新蝶呤、髓过氧化物酶、纤维蛋白原和 NT proBNP。主要研究终点是 30 和 360 天随访期间的死亡和非致死性心肌梗死。
在 1 年时,54 例患者(8.9%)达到了主要研究终点(26 例发生心脏性死亡(4.3%),34 例发生非致死性心肌梗死(5.6%))。对于两种 RS,与低风险组相比,“高风险”患者发生研究终点的情况更为常见。此外,TIMI 和 PRA RS 的判别准确性相似。然而,TIMI RS 在 30 天和 360 天随访时均比 PRA RS 更能预测事件。研究中评估的炎症生物标志物并未显著提高 RS 的预测价值。
我们的研究表明,TIMI RS 是比 PRA RS 更好的风险标志物,炎症生物标志物不能提高这些临床风险评分的预测价值。