Bazan-Socha S, Mastalerz L, Cybulska A, Zareba L, Kremers R, Zabczyk M, Pulka G, Iwaniec T, Hemker C, Undas A
Department of Internal Medicine, Jagiellonian University Medical College, Krakow, Poland.
Department of Differential Equations and Statistics, Faculty of Mathematics and Natural Sciences, University of Rzeszow, Rzeszow, Poland.
Clin Exp Allergy. 2016 Jul;46(7):932-44. doi: 10.1111/cea.12734. Epub 2016 May 3.
There is evidence that altered blood coagulation and fibrinolysis are involved in the pathogenesis of asthma. Increased thromboembolic risk has been reported in asthmatics.
To investigate whether enhanced thrombin generation and impaired fibrinolysis occur in asthmatics.
Plasma thrombin generation profile together with a computational assessment of thrombin dynamics and fibrinolytic capacity expressed as clot lysis time (CLT) were determined in 164 consecutive patients with stable asthma and 72 controls matched for age, gender, weight and smoking.
Asthma patients had 20.2% increased endogenous thrombin potential (ETP), 41.4% higher peak thrombin concentration, 61% higher maximal prothrombin conversion rate, 15.5% faster rate of thrombin formation (all, P < 0.0001) and 10% lower thrombin decay capacity (P = 0.0004) compared with controls. Asthmatics had also 14.4% longer CLT (P = 0.001) associated with 21.3% higher plasminogen activator inhibitor-1 (PAI-1) (P < 0.0001), and 13% higher plasma α2 -macroglobulin (P = 0.0002). Using ETP and CLT above 75th percentile of the control values as the cut-off levels, we found increased risks of enhanced thrombin generation and hypofibrinolysis in asthmatics, also after correction for potential confounders. ETP and CLT were associated inversely with forced expiratory volume in 1 s/vital capacity (FEV1 /VC) index, after adjustment for age and body mass index. Non-allergic asthma (n = 70, 42.6%) was characterized by 17.5% longer CLT (P = 0.02), which positively associated with PAI-1. Thrombin generation profile was not affected by allergy.
Asthma is associated with enhanced thrombin generation and impaired fibrinolysis, which might contribute to thromboembolic events in this disease.
有证据表明血液凝固和纤维蛋白溶解的改变参与了哮喘的发病机制。已有报道称哮喘患者的血栓栓塞风险增加。
研究哮喘患者是否存在凝血酶生成增强和纤维蛋白溶解受损的情况。
对164例连续的稳定期哮喘患者和72例年龄、性别、体重和吸烟情况相匹配的对照组进行血浆凝血酶生成曲线测定,并通过计算评估凝血酶动力学和以凝块溶解时间(CLT)表示的纤维蛋白溶解能力。
与对照组相比,哮喘患者的内源性凝血酶潜力(ETP)增加20.2%,凝血酶峰值浓度升高41.4%,最大凝血酶原转化率提高61%,凝血酶形成速率加快15.5%(均P<0.0001),凝血酶衰减能力降低10%(P = 0.0004)。哮喘患者的CLT也延长了14.4%(P = 0.001),同时纤溶酶原激活物抑制剂-1(PAI-1)升高21.3%(P<0.0001),血浆α2-巨球蛋白升高13%(P = 0.0002)。以ETP和CLT高于对照组值的第75百分位数作为截断水平,我们发现即使校正潜在混杂因素后,哮喘患者凝血酶生成增强和纤维蛋白溶解低下的风险仍增加。调整年龄和体重指数后,ETP和CLT与第1秒用力呼气量/肺活量(FEV1/VC)指数呈负相关。非过敏性哮喘(n = 70,42.6%)的特点是CLT延长17.5%(P = 0.02),且与PAI-1呈正相关。凝血酶生成曲线不受过敏影响。
哮喘与凝血酶生成增强和纤维蛋白溶解受损有关,这可能导致该疾病中的血栓栓塞事件。