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可溶性CD40配体可预测非瓣膜性心房颤动患者的缺血性中风和心肌梗死。

Soluble CD40 ligand predicts ischemic stroke and myocardial infarction in patients with nonvalvular atrial fibrillation.

作者信息

Ferro Domenico, Loffredo Lorenzo, Polimeni Licia, Fimognari Filippo, Villari Paolo, Pignatelli Pasquale, Fuster Valentin, Violi Francesco

机构信息

Divisione di Medicina Interna H, Viale del Policlinico 155, Roma, 00161, Italy.

出版信息

Arterioscler Thromb Vasc Biol. 2007 Dec;27(12):2763-8. doi: 10.1161/ATVBAHA.107.152777. Epub 2007 Sep 27.

Abstract

OBJECTIVE

Atrial fibrillation (AF) is associated with a high incidence of vascular disease that may be related to a prothrombotic and inflammatory state. Soluble CD40 ligand (sCD40L), which stems essentially from platelet activation, possesses inflammatory and prothrombotic properties. The aim of the study was to assess whether sCD40L is a predictor of stroke or myocardial infarction (MI) in patients with nonvalvular AF.

METHODS AND RESULTS

Plasma levels of sCD40L were measured in 231 patients (177 [77%] had permanent or persistent AF, and 54 [23%] had paroxysmal AF). Patients were followed for a mean period of 27.8+/-8.8 months, and cardiovascular events such as fatal and nonfatal stroke and MI were recorded. AF population was divided in 2 groups according to sCD40L level above or below the median (4.76 ng/mL). The 2 patients' groups had similar distribution of cardiovascular risk factors, age, gender, medications, or serum C-reactive protein levels. During the follow-up period, vascular events occurred in 6 (2 nonfatal MI and 4 nonfatal ischemic strokes) of 116 patients with low levels of sCD40L (5.1%) and in 29 (11 fatal and 3 nonfatal MI; 3 fatal and 12 nonfatal ischemic strokes) of 115 patients with high levels (25.2%) (log-rank test: P<0.001). Using the COX proportional Hazards model, patients with sCD40L above the median were 4.63 times more likely to experience a vascular event (95% C.I.: 1.92 to 11.20).

CONCLUSIONS

This study shows that enhanced soluble CD40L level is a predictor of vascular events in patients with nonvalvular AF, thus suggesting that enhanced platelet activation may play a role in its clinical progression.

摘要

目的

房颤(AF)与血管疾病的高发病率相关,这可能与血栓形成前状态和炎症状态有关。可溶性CD40配体(sCD40L)主要源于血小板活化,具有炎症和促血栓形成特性。本研究的目的是评估sCD40L是否为非瓣膜性房颤患者发生中风或心肌梗死(MI)的预测指标。

方法与结果

对231例患者(177例[77%]为永久性或持续性房颤,54例[23%]为阵发性房颤)测定血浆sCD40L水平。患者平均随访27.8±8.8个月,记录心血管事件,如致命性和非致命性中风及心肌梗死。根据sCD40L水平高于或低于中位数(4.76 ng/mL)将房颤患者分为两组。两组患者的心血管危险因素、年龄、性别、用药情况或血清C反应蛋白水平分布相似。在随访期间,sCD40L水平较低的116例患者中有6例(2例非致命性心肌梗死和4例非致命性缺血性中风)发生血管事件(5.1%),sCD40L水平较高的115例患者中有29例(11例致命性和3例非致命性心肌梗死;3例致命性和12例非致命性缺血性中风)发生血管事件(25.2%)(对数秩检验:P<0.001)。使用COX比例风险模型,sCD40L高于中位数的患者发生血管事件的可能性高4.63倍(95%置信区间:1.92至11.20)。

结论

本研究表明,可溶性CD40L水平升高是非瓣膜性房颤患者血管事件的预测指标,提示血小板活化增强可能在其临床进展中起作用。

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