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高敏心肌肌钙蛋白 I 测定在非 ST 段抬高型急性冠状动脉综合征患者中的预后性能。

Prognostic performance of a high-sensitivity cardiac troponin I assay in patients with non-ST-elevation acute coronary syndrome.

机构信息

TIMI Study Group, Cardiovascular Division, Department of Medicine and.

出版信息

Clin Chem. 2014 Jan;60(1):158-64. doi: 10.1373/clinchem.2013.206441. Epub 2013 Sep 19.

Abstract

BACKGROUND

High-sensitivity assays for cardiac troponin enable more precise measurement of very low concentrations and improved diagnostic accuracy. However, the prognostic value of these measurements, particularly at low concentrations, is less well defined.

METHODS

We evaluated the prognostic performance of a new high-sensitivity cardiac troponin I (hs-cTnI) assay (Abbott ARCHITECT) compared with the commercial fourth generation cTnT assay in 4695 patients with non-ST-segment elevation acute coronary syndromes (NSTE-ACS) from the EARLY-ACS (Early Glycoprotein IIb/IIIa Inhibition in NSTE-ACS) and SEPIA-ACS1-TIMI 42 (Otamixaban for the Treatment of Patients with NSTE-ACS) trials. The primary endpoint was cardiovascular death or new myocardial infarction (MI) at 30 days. Baseline cardiac troponin was categorized at the 99th percentile reference limit (26 ng/L for hs-cTnI; 10 ng/L for cTnT) and at sex-specific 99th percentiles for hs-cTnI.

RESULTS

All patients at baseline had detectable hs-cTnI compared with 94.5% with detectable cTnT. With adjustment for all other elements of the TIMI risk score, patients with hs-cTnI ≥99th percentile had a 3.7-fold higher adjusted risk of cardiovascular death or MI at 30 days relative to patients with hs-cTnI <99th percentile (9.7% vs 3.0%; odds ratio, 3.7; 95% CI, 2.3-5.7; P < 0.001). Similarly, when stratified by categories of hs-cTnI, very low concentrations demonstrated a graded association with cardiovascular death or MI (P-trend < 0.001). Use of sex-specific cutpoints did not improve prognostic performance. Patients with negative fourth generation cTnT (<10 ng/L) but hs-cTnI ≥26 ng/L were at increased risk of cardiovascular death/MI compared to those with hs-cTnI <26 ng/L (9.2% vs 2.9%, P = 0.002).

CONCLUSIONS

Application of this hs-cTnI assay identified a clinically relevant higher risk of recurrent events among patients with NSTE-ACS, even at very low troponin concentrations.

摘要

背景

高敏肌钙蛋白检测可更精确地测量极低浓度的肌钙蛋白,提高诊断准确性。然而,这些检测,尤其是在低浓度下的预后价值,定义尚不明确。

方法

我们评估了一种新的高敏肌钙蛋白 I(hs-cTnI)检测(雅培 ARCHITECT)与商业第四代 cTnT 检测在非 ST 段抬高型急性冠脉综合征(NSTE-ACS)患者中的预后性能,这些患者来自 EARLY-ACS(NSTE-ACS 中早期糖蛋白 IIb/IIIa 抑制)和 SEPIA-ACS1-TIMI 42(NSTE-ACS 患者的 Otamixaban 治疗)试验,共 4695 例。主要终点为 30 天心血管死亡或新发心肌梗死(MI)。hs-cTnI 的参考上限第 99 百分位(26ng/L)和 hs-cTnI 的性别特异性第 99 百分位(男性 50ng/L,女性 45ng/L)对基线心脏肌钙蛋白进行分类。

结果

所有患者在基线时均检测到 hs-cTnI,而 cTnT 可检测到的患者为 94.5%。在调整 TIMI 风险评分的所有其他元素后,hs-cTnI >第 99 百分位的患者与 hs-cTnI <第 99 百分位的患者相比,30 天心血管死亡或 MI 的调整风险高 3.7 倍(9.7% vs 3.0%;比值比,3.7;95%CI,2.3-5.7;P<0.001)。同样,当按 hs-cTnI 类别分层时,较低浓度与心血管死亡或 MI 呈明显关联(P<0.001)。使用性别特异性截断值并不能提高预后性能。与 hs-cTnI <26ng/L 的患者相比,hs-cTnI≥26ng/L 且第四代 cTnT 阴性(<10ng/L)的患者心血管死亡/MI 风险增加(9.2% vs 2.9%,P=0.002)。

结论

应用该 hs-cTnI 检测方法可识别 NSTE-ACS 患者发生复发性事件的较高风险,即使在肌钙蛋白浓度较低时也是如此。

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