Feinberg W M, Pearce L A, Hart R G, Cushman M, Cornell E S, Lip G Y, Bovill E G
Department of Neurology, the University of Arizona, Tucson, USA.
Stroke. 1999 Dec;30(12):2547-53. doi: 10.1161/01.str.30.12.2547.
Markers of thrombin generation and platelet activation are often elevated in patients with nonvalvular atrial fibrillation, but it is unclear whether such markers usefully predict stroke. Therefore, we undertook the present study to assess the relationship between prothrombin fragment F1.2 (F1.2), beta-thromboglobulin (BTG), fibrinogen, and the factor V Leiden mutation with stroke in atrial fibrillation.
Specimens were obtained from 1531 participants in the Stroke Prevention in Atrial Fibrillation III study. The results were correlated with patient features, antithrombotic therapy, and subsequent thromboembolism (ischemic stroke and systemic embolism) by multivariate analysis.
Increased F1.2 levels were associated with age (P<0.001), female sex (P<0.001), systolic blood pressure (P=0.006), and heart failure (P=0.001). F1.2 were not affected by aspirin use and were not associated with thromboembolism after adjustment for age (P=0. 18). BTG levels were higher with advanced age (P=0.006), coronary artery disease (P=0.05), carotid disease (P=0.005), and heart failure (P<0.001), lower in regular alcohol users (P=0.05), and not significantly associated with thromboembolism. Fibrinogen levels were not significantly related to thromboembolism but were associated with elevated BTG levels (P<0.001). The factor V Leiden mutation was not associated with thromboembolism (relative risk 0.5, 95% CI 0.1 to 3.8).
Elevated F1.2 levels were associated with clinical risk factors for stroke in atrial fibrillation, whereas increased BTG levels were linked to manifestations of atherosclerosis. In this large cohort of patients with atrial fibrillation who were receiving aspirin, F1.2, BTG, fibrinogen, and factor V Leiden were not independent, clinically useful predictors of stroke.
非瓣膜性心房颤动患者的凝血酶生成和血小板活化标志物常常升高,但尚不清楚这些标志物能否有效预测卒中。因此,我们开展了本研究,以评估凝血酶原片段F1.2(F1.2)、β-血小板球蛋白(BTG)、纤维蛋白原以及因子V莱顿突变与心房颤动患者卒中之间的关系。
从心房颤动卒中预防III研究的1531名参与者中获取样本。通过多变量分析将结果与患者特征、抗血栓治疗以及随后的血栓栓塞(缺血性卒中和全身性栓塞)相关联。
F1.2水平升高与年龄(P<0.001)、女性(P<0.001)、收缩压(P=0.006)和心力衰竭(P=0.001)相关。F1.2不受阿司匹林使用的影响,在调整年龄后与血栓栓塞无关(P=0.18)。BTG水平在高龄(P=0.006)、冠状动脉疾病(P=0.05)、颈动脉疾病(P=0.005)和心力衰竭(P<0.001)时较高,在经常饮酒者中较低(P=0.05),且与血栓栓塞无显著关联。纤维蛋白原水平与血栓栓塞无显著相关性,但与BTG水平升高相关(P<0.001)。因子V莱顿突变与血栓栓塞无关(相对风险0.5,95%可信区间0.1至3.8)。
F1.2水平升高与心房颤动患者卒中的临床危险因素相关,而BTG水平升高与动脉粥样硬化表现相关。在这个接受阿司匹林治疗的大型心房颤动患者队列中,F1.2、BTG、纤维蛋白原和因子V莱顿并非卒中的独立、临床有用预测指标。