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
{"title":"Levels of Fibrinogen Variants Are Altered in Severe COVID-19.","authors":"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","doi":"10.1055/a-2102-4521","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background</b> 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. <b>Aim</b> To investigate the levels of fibrinogen variants in plasma of patients with COVID-19. <b>Methods</b> 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 <sub>E</sub> ), 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). <b>Results</b> Healthy controls and ward patients with COVID-19 ( <i>n</i> = 10) showed similar fibrinogen (variant) levels. ICU patients with COVID-19 who later did ( <i>n</i> = 19) or did not develop thrombosis ( <i>n</i> = 18) and ICU patients with pneumococcal infection ( <i>n</i> = 6) had higher absolute levels of functional, total, intact, and α <sub>E</sub> fibrinogen than healthy controls ( <i>n</i> = 7). The relative α <sub>E</sub> 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. <b>Conclusion</b> Our results show that severe COVID-19 is associated with increased levels of α <sub>E</sub> 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.</p>","PeriodicalId":22238,"journal":{"name":"TH Open: Companion Journal to Thrombosis and Haemostasis","volume":"7 3","pages":"e217-e225"},"PeriodicalIF":0.0000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370639/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"TH Open: Companion Journal to Thrombosis and Haemostasis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2102-4521","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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.