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糖蛋白 VI 作为有症状的冠心病患者心血管死亡的预后生物标志物。

Glycoprotein VI as a prognostic biomarker for cardiovascular death in patients with symptomatic coronary artery disease.

机构信息

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

出版信息

Clin Res Cardiol. 2010 Apr;99(4):227-33. doi: 10.1007/s00392-009-0109-y. Epub 2010 Jan 5.

Abstract

BACKGROUND

Platelets play a critical role in arterial thrombosis, acute coronary syndrome (ACS) and stroke. Platelet collagen receptor glycoprotein VI (GPVI) is associated with acute coronary events and a poor clinical outcome.

METHODS

Between January 2006 and March 2009, we evaluated 2,213 consecutive patients in a prospective study design, who presented with chest pain. Among 1,819 patients (82.2%) who underwent coronary angiography, 1,652 patients (90.8%) showed a coronary and 167 patients (9.2%) a non-coronary origin of chest pain. 901 patients (54.5%) presented with an ACS, 751 (45.5%) with a stable angina pectoris. Clinical outcome was performed by a predefined structured telephone interview after a 3-month follow-up (92.8%:1,533 of 1,652 patients).

RESULTS

Kaplan-Meier analysis for cumulative event-free survival revealed that patients with a elevated baseline GPVI expression had a poorer clinical outcome for cardiovascular death than patients with decreased GPVI levels (log rank; P = 0.040). These results were paralleled in composite cumulative survival that included myocardial infarction, stroke, and cardiovascular death (log rank; P = 0.002). Relative risk of cardiovascular death was found at 1.41 (95% CI 1.08-1.85) for platelet GPVI, 1.64 (95% CI 1.31-2.05) for brain natriuretic peptide, 1.16 (95% CI 0.81-1.64) for troponin-I and 1.33 (95% CI 0.97-1.82) for C-reactive protein.

CONCLUSIONS

Patients with CAD presenting increased levels of platelet GPVI had a poorer outcome and may profit from a dual antiplatelet therapy. Thus, GPVI may be a useful prognostic tool for adverse cardiovascular events. Future studies should substantiate GPVI for its potential role of risk prediction and consider its prognostic value to improve risk stratification.

摘要

背景

血小板在动脉血栓形成、急性冠状动脉综合征(ACS)和中风中起着关键作用。血小板胶原受体糖蛋白 VI(GPVI)与急性冠状动脉事件和不良临床结局相关。

方法

在 2006 年 1 月至 2009 年 3 月期间,我们对 2213 例连续胸痛患者进行了前瞻性研究设计评估。在 1819 例接受冠状动脉造影的患者中,1652 例(90.8%)显示冠状动脉病变,167 例(9.2%)显示非冠状动脉病变。901 例(54.5%)为 ACS,751 例(45.5%)为稳定型心绞痛。通过 3 个月的随访后进行预设的结构化电话访谈进行临床结局评估(92.8%:1652 例患者中有 1533 例)。

结果

累积无事件生存的 Kaplan-Meier 分析显示,基线 GPVI 表达升高的患者心血管死亡的临床结局较差,而 GPVI 水平降低的患者则较好(对数秩检验;P=0.040)。这一结果在包括心肌梗死、中风和心血管死亡的复合累积生存率中得到了印证(对数秩检验;P=0.002)。心血管死亡的相对风险为血小板 GPVI 为 1.41(95%可信区间 1.08-1.85),脑利钠肽为 1.64(95%可信区间 1.31-2.05),肌钙蛋白 I 为 1.16(95%可信区间 0.81-1.64),C 反应蛋白为 1.33(95%可信区间 0.97-1.82)。

结论

患有 CAD 的患者出现血小板 GPVI 水平升高时,结局较差,可能受益于双重抗血小板治疗。因此,GPVI 可能是一种有用的预测不良心血管事件的预后工具。未来的研究应证实 GPVI 对预测风险的潜在作用,并考虑其预后价值以改善风险分层。

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