严重COVID-19患者纤维蛋白原变异水平发生改变

Judith J de Vries, Chantal Visser, Maureen van Ommen, Casper Rokx, Els van Nood, Eric C M van Gorp, Marco Goeijenbier, Johannes P C van den Akker, Henrik Endeman, Dingeman C Rijken, Marieke J H A Kruip, Miranda Weggeman, Jaap Koopman, Moniek P M de Maat
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引用次数: 0

摘要

纤维蛋白原变异是由信使RNA剪接或蛋白质降解引起的,可影响纤维蛋白(原)功能。在2019冠状病毒病(COVID-19)期间,这些变异的水平可能会改变,从而可能影响疾病的严重程度或血栓形成的风险。目的探讨新型冠状病毒肺炎患者血浆纤维蛋白原变异水平。方法在本病例对照研究中,我们使用Clauss法测量功能性纤维蛋白原的水平。采用酶联免疫吸附法测定健康对照组、重症监护病房(ICU)肺炎球菌感染患者、病区COVID-19患者和ICU COVID-19患者(有和无血栓形成,两个时间点)总抗原、完整(未降解的Aα链)、延伸Aα链(α E)和γ′纤维蛋白原水平。结果健康对照和病区新冠肺炎患者(n = 10)的纤维蛋白原(变异)水平相似。后来发生血栓形成(n = 19)或未发生血栓形成(n = 18)的COVID-19 ICU患者和肺炎球菌感染(n = 6) ICU患者的功能、总、完整和α E纤维蛋白原的绝对水平高于健康对照组(n = 7)。新冠肺炎ICU患者的相对α E纤维蛋白原水平高于健康对照组,而相对γ’纤维蛋白原水平低于健康对照组。在诊断为血栓形成后,只有合并COVID-19和血栓形成的ICU患者的功能性纤维蛋白原水平高于未合并血栓形成的ICU患者,而其他纤维蛋白原变异未见差异。结论重症COVID-19患者的α E纤维蛋白原水平升高,γ’纤维蛋白原水平相对降低,可能是重症的原因或结果,但与血栓形成无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Levels of Fibrinogen Variants Are Altered in Severe COVID-19.

Levels of Fibrinogen Variants Are Altered in Severe COVID-19.

Levels of Fibrinogen Variants Are Altered in Severe COVID-19.

Levels of Fibrinogen Variants Are Altered in Severe COVID-19.

Background  Fibrinogen variants as a result of alternative messenger RNA splicing or protein degradation can affect fibrin(ogen) functions. The levels of these variants might be altered during coronavirus disease 2019 (COVID-19), potentially affecting disease severity or the thrombosis risk. Aim  To investigate the levels of fibrinogen variants in plasma of patients with COVID-19. Methods  In this case-control study, we measured levels of functional fibrinogen using the Clauss assay. Enzyme-linked immunosorbent assays were used to measure antigen levels of total, intact (nondegraded Aα chain), extended Aα chain (α E ), and γ' fibrinogen in healthy controls, patients with pneumococcal infection in the intensive care unit (ICU), ward patients with COVID-19, and ICU patients with COVID-19 (with and without thrombosis, two time points). Results  Healthy controls and ward patients with COVID-19 ( n  = 10) showed similar fibrinogen (variant) levels. ICU patients with COVID-19 who later did ( n  = 19) or did not develop thrombosis ( n  = 18) and ICU patients with pneumococcal infection ( n  = 6) had higher absolute levels of functional, total, intact, and α E fibrinogen than healthy controls ( n  = 7). The relative α E fibrinogen levels were higher in ICU patients with COVID-19 than in healthy controls, while relative γ' fibrinogen levels were lower. After diagnosis of thrombosis, only the functional fibrinogen levels were higher in ICU patients with COVID-19 and thrombosis than in those without, while no differences were observed in the other fibrinogen variants. Conclusion  Our results show that severe COVID-19 is associated with increased levels of α E fibrinogen and decreased relative levels of γ' fibrinogen, which may be a cause or consequence of severe disease, but this is not associated with the development of thrombosis.

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