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血小板糖蛋白 VI(GPVI)用于胸痛患者急性冠状动脉综合征的早期识别。

Platelet glycoprotein VI (GPVI) for early identification of acute coronary syndrome in patients with chest pain.

机构信息

Medizinische Klinik III, Kardiologie und Kreislauferkrankungen, Eberhard-Karls-Universität Tübingen, Germany.

出版信息

Thromb Res. 2010 May;125(5):e184-9. doi: 10.1016/j.thromres.2010.01.005. Epub 2010 Feb 1.

Abstract

BACKGROUND

Platelet glycoprotein VI (GPVI) is elevated in patients with acute coronary syndrome (ACS), stroke and associated with acute coronary events. GPVI may be helpful to distinguish an imminent ACS from non-coronary (NC) causes in patients with chest pain who were transferred to chest pain unit, before the myocardial necrosis is evident with classical biomarkers.

METHODS

Based on the findings of our previous studies, we consecutively examined 1004 patients with chest pain in a prospective study design. ACS was found in 416 (41.4%), stable angina pectoris (SAP) in 233 (23.2%), and NC causes of chest pain (hypertension, musculoskeletal disease, pulmonary embolism, myocarditis, cardiophobia) in 355 patients (35.4%). Platelet surface expression of GPVI was measured by flow cytometry.

RESULTS

Patients with ACS showed significantly enhanced GPVI expression levels compared to patients with SAP or NC causes of chest pain (ACSvs.SAP(mean fluorescence intensity (MFI)+/-SD):18.9+/-7.4vs.17.9+/-9.5;P=0.028;ACSvs.NC:15.4+/-6.9;P=0.002). Elevated GPVI expression was associated with ACS independent of markers of myocardial necrosis like troponin and creatine kinase-MB. Patients with an elevated GPVI expression (MFI>or=18.6) had a poorer clinical outcome than patients with baseline GPVI expression in regard to composite cumulative survival that included myocardial infarction, stroke, and cardiovascular death at three months (Log rank;P=0.025).

DISCUSSION

Platelet GPVI surface expression is enhanced in patients at risk for an ACS and is an early marker for imminent acute coronary events in patients with chest pain.

摘要

背景

血小板糖蛋白 VI(GPVI)在急性冠脉综合征(ACS)、中风患者中升高,并与急性冠脉事件相关。在心肌坏死标志物明显升高之前,GPVI 可能有助于区分胸痛患者中即将发生的 ACS 与非冠脉(NC)原因。

方法

基于我们之前研究的结果,我们在一项前瞻性研究设计中连续检查了 1004 例胸痛患者。ACS 患者 416 例(41.4%),稳定型心绞痛(SAP)患者 233 例(23.2%),NC 胸痛原因(高血压、肌肉骨骼疾病、肺栓塞、心肌炎、心脏恐惧症)患者 355 例(35.4%)。通过流式细胞术测量血小板表面 GPVI 的表达。

结果

与 SAP 或 NC 胸痛患者相比,ACS 患者的 GPVI 表达水平显著升高(ACS 与 SAP(平均荧光强度(MFI)+/-SD):18.9+/-7.4 比 17.9+/-9.5;P=0.028;ACS 与 NC:15.4+/-6.9;P=0.002)。升高的 GPVI 表达与 ACS 相关,独立于心肌坏死标志物,如肌钙蛋白和肌酸激酶-MB。与基线 GPVI 表达相比,GPVI 表达升高(MFI>或=18.6)的患者在三个月时的复合累积生存率(包括心肌梗死、中风和心血管死亡)方面预后较差(Log 秩;P=0.025)。

讨论

处于 ACS 风险中的患者血小板 GPVI 表面表达增强,是胸痛患者即将发生急性冠脉事件的早期标志物。

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