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Reduced clot retraction rate and altered platelet energy production in patients with asthma

机译:降低哮喘患者的血块回缩率并改变血小板能量产生

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Objective: Asthma enhances the risk of pulmonary embolism. The mechanism of this phenomenon is unclear. Methods: We evaluated the kinetics of clot formation, clot retraction rate (CRR), clot volume at 40 min, the rate of lactate production (a marker of aerobic glycolysis in platelets in contracting clots), blood eosinophil count (EOS), nitric oxide in exhaled breath (FENO), and spirometry (FEV1) in 50 healthy controls and in 81 allergic asthmatics (41 subjects with steroid-naive asthma and 40 with steroid-treated asthma). Results: Thromboelastometry revealed that only steroid-treated asthmatics had slightly activated coagulation. Compared with healthy controls, whole asthmatics demonstrated (p < 0.05) reduced CRR, higher clot volume at 40 minutes, higher FENO, decreased FEV1, elevated EOS, and augmented lactate production in retracting clots. Reduced CRR was observed also in the absence of native plasma. In whole study population (asthmatics and healthy controls), CRR positively correlated with spirometry (r(S) = 0.668, p = < 0.001) and negatively with FENO (r(S) =-0.543; p < 0.001), EOS (r(S) =-0.367, p < 0.002), and lactate production (r(S) = -0.791; p<0.001). However, in steroid-treated asthmatics, the CRR did not correlate with FENO and EOS. In all study patients lactate production negatively correlated with FEV1 and positively with FENO. Conclusion: Collectively, this data is consistent with the hypothesis that, in asthmatics, reactive nitrogen species produced in the lungs may reduce platelet contractility (and CRR) through the diminution of platelet energy production. CRR inhibition would predispose asthmatics to pulmonary embolism.
机译:目的:哮喘会增加发生肺栓塞的风险。这种现象的机理尚不清楚。方法:我们评估了血凝块形成的动力学,血凝块收缩率(CRR),40分钟时的血凝块体积,乳酸生成速率(收缩性血凝块中血小板中有氧糖酵解的标志),血液嗜酸性粒细胞计数(EOS),一氧化氮50名健康对照者和81名过敏性哮喘患者(41名未接受类固醇的哮喘患者和40名接受类固醇治疗的哮喘患者)的呼气(FENO)和肺活量测定(FEV1)监测。结果:血栓弹力测定显示只有经类固醇治疗的哮喘患者的凝血功能轻微激活。与健康对照组相比,整个哮喘患者表现出(p <0.05)CRR降低,40分钟时血凝块体积增加,FENO升高,FEV1降低,EOS升高以及血凝块回缩中乳酸的产生增加。在没有天然血浆的情况下,也观察到CRR降低。在整个研究人群(哮喘和健康对照者)中,CRR与肺活量测定呈正相关(r(S)= 0.668,p = <0.001),与FENO呈负相关(r(S)= -0.543; p <0.001),EOS(r (S)=-0.367,p <0.002)和乳酸产生(r(S)=-0.791; p <0.001)。但是,在类固醇治疗的哮喘患者中,CRR与FENO和EOS不相关。在所有研究患者中,乳酸产生与FEV1负相关,与FENO正相关。结论:总体而言,该数据与以下假设一致:在哮喘患者中,肺中产生的反应性氮可能通过减少血小板能量产生而降低血小板收缩性(和CRR)。 CRR抑制会使哮喘患者容易发生肺栓塞。

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