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Early effects of paroxysmal atrial fibrillation on plasma markers of fibrinolysis

机译:阵发性心房颤动对纤维蛋白溶解血浆标志物的早期影响

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There are no studies to date on the early changes in the hemostasis profile of patients with paroxysmal atrial fibrillation (PAF). Given the key role of the fibrinolytic system in maintaining blood fluidity, our aim was to examine its activity in patients with clinical manifestation of the disease We studied 51 nonanticoagulated patients with a first episode of the disease (26 men, 25 women; mean age 59.84?±?1.60 years) and 52 controls (26 men, 26 women; mean age 59.50?±?1.46 years) who matched the patients in terms of gender, age, comorbidities, and conducted treatment. Using enzyme-linked immunoassays and colorimetric assays we assessed the plasminogen activity, tissue plasminogen activator level (t-PA), plasminogen activator inhibitor 1 activity (PAI-1), α2-antiplasmin activity (α2-AP), D-dimer level, and vitronectin level. Blood samples were collected immediately after hospitalization. Patients were hospitalized between the second and twenty fourth hours (mean 8.14?±?0.76?hours) after the onset of PAF. Compared to controls, plasminogen (159.40?±?4.81 vs 100.2?±?2.88%, P??0.001) and t-PA levels (11.25?±?0.35 vs 6.05?±?0.31?ng/mL, P??0.001) were significantly higher in the patient group. PAI-1 activity (7.33?±?0.37 vs 15.15?±?0.52?AU/mL, P??0.001) and α2-AP (112.9?±?2.80 vs 125.60?±?3.74%, P??0.05) as well as vitronectin plasma levels (134.7?±?5.83 vs 287.3?±?10.44?mcg/mL, P??0.001) were lower in the PAF group. Conversely, the levels of D-dimer in patients were significantly higher (0.53?±?0.07 vs 0.33?±?0.02?ng/mL, P??0.05). Early changes in the fibrinolytic system occur in PAF, suggesting their close relationship with the manifestation of the disease. There is high plasma fibrinolytic activity, during the very first 24 hours of the disease, which is most likely a pathophysiological response to the intensified procoagulation process.
机译:迄今为止没有关于阵发性心房颤动(PAF)患者止血型材的早期变化的研究。鉴于纤维蛋白溶解系统在维持血液流动性方面的关键作用,我们的目的是研究其在患有疾病的临床表现患者中的活动,我们研究了51例疾病的第一个发作(26名男子,25名女性;平均年龄59.84 ?±1.60岁)和52个控件(26名男子,26名女性;平均59.50岁?±1.46岁),患者在性别,年龄,可用性和进行治疗方面与患者相匹配。使用酶联免疫测定和比色测定评估纤溶酶原活性,组织纤溶酶原激活剂水平(T-PA),纤溶酶原激活剂抑制剂1活性(PAI-1),α2-抗蛋白活性(α2-AP),D-二聚体水平,和vitronectin水平。住院后立即收集血样。在PAF发作后,患者在第二和二十四小时(平均8.14Ω±0.76℃)之间住院。与对照组相比,纤溶酶原(159.40?±4.81 Vs 100.2?±2.88%,p ?? 0.001)和T-PA水平(11.25?±0.35 Vs 6.05?±0.31?Ng / ml,p ?? 0.001 )患者组显着较高。 PAI-1活性(7.33?±0.37 Vs 15.15?±0.52?Au / ml,p ?? 0.001)和α2-AP(112.9?±α?2.80与125.60?±3.74%,p ?? 0.05)与vitronectin等离子体水平(134.7?±5.83 vs 287.3?±10.44?mcg / ml,p ?? 0.001)在PAF组中较低。相反,患者D-二聚体的水平显着更高(0.53?±0.07 Vs 0.33?±0.02?ng / ml,p ?? 0.05)。纤维蛋白溶解系统的早期变化发生在PAF中,表明他们与疾病的表现密切相关。在疾病的前24小时内,存在高的血浆纤维蛋白溶解活性,这最有可能对增殖的促成过程的病理生理反应。

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