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多电极聚集法比血管扩张刺激磷蛋白磷酸化试验更能预测支架血栓形成。

Multiple electrode aggregometry predicts stent thrombosis better than the vasodilator-stimulated phosphoprotein phosphorylation assay.

机构信息

Department of Clinical Pharmacology, Medical University of Vienna, and 5th Medical Department, Kaiser-Franz-Josef Hospital, Vienna, Austria.

出版信息

J Thromb Haemost. 2010 Feb;8(2):351-9. doi: 10.1111/j.1538-7836.2009.03699.x. Epub 2009 Nov 23.

Abstract

BACKGROUND AND AIM

The prognostic value of the vasodilator-stimulated phosphoprotein (VASP) phosphorylation assay and multiple electrode aggregometry (MEA) for thrombotic adverse events has been shown in independent studies. As no direct comparison between the two methods has been made so far, we investigated which laboratory approach has a better predictive value for stent thrombosis.

METHODS

The VASP phosphorylation assay and MEA were performed in 416 patients with coronary artery disease undergoing percutaneous coronary intervention. The rate of stent thrombosis was recorded during a 6-month follow-up.

RESULTS

Definite stent thrombosis occurred in three patients (0.7%) and probable stent thrombosis in four (1%). Receiver operating characteristic (ROC) analysis demonstrated that MEA distinguishes between patients with or without subsequent stent thrombosis better than the VASP phosphorylation assay: the area under the ROC curve was higher for MEA (0.92; P=0.012) than for the VASP phosphorylation assay (0.60; P=0.55). At equal levels of sensitivity (100%), the specificity was greater for MEA than for the VASP phosphorylation assay (86% vs. 37%). Stent thrombosis occurred in 9% of patients with platelet hyperreactivity in MEA, who were simultaneously clopidogrel non-responders in the VASP phosphorylation assay. Interestingly, clopidogrel non-responders in the VASP phosphorylation assay without platelet hyperreactivity in MEA did not suffer from stent thrombosis.

CONCLUSIONS

Platelet hyperreactivity in MEA might be a better risk predictor for stent thrombosis than the assessment of the specific clopidogrel effect with the VASP phosphorylation assay.

摘要

背景与目的

已有独立研究表明,血管扩张刺激磷蛋白(VASP)磷酸化检测和多重电极聚集检测(MEA)对血栓不良事件具有预后价值。由于目前尚未对这两种方法进行直接比较,因此我们研究了哪种实验室方法对支架血栓形成具有更好的预测价值。

方法

对 416 例行经皮冠状动脉介入治疗的冠心病患者进行了 VASP 磷酸化检测和 MEA 检测。在 6 个月的随访期间记录支架血栓形成的发生率。

结果

3 例患者(0.7%)发生明确的支架血栓形成,4 例(1%)发生可能的支架血栓形成。受试者工作特征(ROC)分析表明,MEA 比 VASP 磷酸化检测更能区分有或无后续支架血栓形成的患者:MEA 的 ROC 曲线下面积更高(0.92;P=0.012),而 VASP 磷酸化检测的 ROC 曲线下面积较低(0.60;P=0.55)。在相同的灵敏度水平(100%)下,MEA 的特异性大于 VASP 磷酸化检测(86% vs. 37%)。在 MEA 中血小板高反应性的患者中,支架血栓形成发生率为 9%,同时在 VASP 磷酸化检测中这些患者对氯吡格雷无反应。有趣的是,在 MEA 中无血小板高反应性但在 VASP 磷酸化检测中对氯吡格雷无反应的患者并未发生支架血栓形成。

结论

MEA 中的血小板高反应性可能比 VASP 磷酸化检测评估氯吡格雷的特定作用更能预测支架血栓形成的风险。

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