Rothwell Peter M, Howard Sally C, Power Dermot A, Gutnikov Sergei A, Algra Ale, van Gijn Jan, Clark Tanne G, Murphy Michael F G, Warlow Charles P
Stroke Prevention Research Unit, University of Oxford, UK.
Stroke. 2004 Oct;35(10):2300-5. doi: 10.1161/01.STR.0000141701.36371.d1. Epub 2004 Sep 2.
Fibrinogen is an independent risk factor for coronary events in population-based studies and in patients with coronary heart disease, but there is uncertainty about prediction of stroke, particularly in secondary prevention.
We studied unpublished data from 3 prospective studies of patients with recent transient ischemic attack (TIA) or minor ischemic stroke: the United Kingdom TIA Aspirin (UK-TIA) trial (n=1860); the Dutch TIA trial (n=2960); and the Oxford TIA Study (n=293). By separate and pooled analysis, we used Cox models to determine the relationship between fibrinogen and risk of ischemic stroke and other vascular events during 23,272 patient-years of follow-up and adjusted for other risk factors.
There was no significant heterogeneity in fibrinogen risk associations between studies. Fibrinogen predicted subsequent ischemic stroke, with a pooled hazard ratio (HR) for values above the median of 1.34 (95% CI, 1.13 to 1.60; P=0.001). The association tended to be stronger in patients with nonlacunar (HR=1.42; 95% CI, 1.13 to 1.78; P=0.002) than lacunar syndromes (HR=1.09; 95% CI, 0.80 to 1.49; P=0.58), but was not significantly so (P=0.18). There was no association with hemorrhagic stroke (adjusted HR=1.09; 95% CI, 0.55 to 2.17; P=0.81). Fibrinogen predicted acute coronary events (adjusted HR=1.42; 95% CI, 1.18 to 1.70; P<0.001) and all ischemic vascular events (adjusted HR=1.31; 95% CI, 1.15 to 1.49; P<0.001), but not nonvascular death (adjusted HR=1.24; 95% CI, 0.90 to 1.70; P=0.19).
In patients with a previous TIA or ischemic stroke, risks of recurrent ischemic stroke and acute coronary events increase linearly with fibrinogen levels, but the relationships are weaker than in some previous population-based studies.
在基于人群的研究以及冠心病患者中,纤维蛋白原是冠状动脉事件的独立危险因素,但对于中风的预测存在不确定性,尤其是在二级预防中。
我们研究了来自3项针对近期短暂性脑缺血发作(TIA)或轻度缺血性中风患者的前瞻性研究的未发表数据:英国TIA阿司匹林试验(UK-TIA)(n = 1860);荷兰TIA试验(n = 2960);以及牛津TIA研究(n = 293)。通过单独分析和汇总分析,我们使用Cox模型来确定纤维蛋白原与23272患者年随访期间缺血性中风及其他血管事件风险之间的关系,并对其他危险因素进行了校正。
各研究之间纤维蛋白原风险关联无显著异质性。纤维蛋白原可预测随后的缺血性中风,纤维蛋白原值高于中位数时的合并风险比(HR)为1.34(95%CI,1.13至1.60;P = 0.001)。在非腔隙性综合征患者中这种关联往往更强(HR = 1.42;95%CI,1.13至1.78;P = 0.002),而在腔隙性综合征患者中则较弱(HR = 1.09;95%CI,0.80至1.49;P = 0.58),但差异无统计学意义(P = 0.18)。与出血性中风无关联(校正HR = 1.09;95%CI,0.55至2.17;P = 0.81)。纤维蛋白原可预测急性冠状动脉事件(校正HR = 1.42;95%CI,1.18至1.70;P < 0.001)和所有缺血性血管事件(校正HR = 1.31;95%CI,1.15至1.49;P < 0.001),但与非血管性死亡无关联(校正HR = 1.24;95%CI,0.90至1.70;P = 0.19)。
在既往有TIA或缺血性中风的患者中,复发性缺血性中风和急性冠状动脉事件的风险随纤维蛋白原水平呈线性增加,但这种关系比一些既往基于人群的研究中要弱。