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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...

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Autores principales: de Vries, Judith J., Visser, Chantal, van Ommen, Maureen, Rokx, Casper, van Nood, Els, van Gorp, Eric C. M., Goeijenbier, Marco, van den Akker, Johannes P. C., Endeman, Henrik, Rijken, Dingeman C., Kruip, Marieke J. H. A., Weggeman, Miranda, Koopman, Jaap, de Maat, Moniek P. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Georg Thieme Verlag KG 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370639/
https://www.ncbi.nlm.nih.gov/pubmed/37501780
http://dx.doi.org/10.1055/a-2102-4521
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author de Vries, Judith J.
Visser, Chantal
van Ommen, Maureen
Rokx, Casper
van Nood, Els
van Gorp, Eric C. M.
Goeijenbier, Marco
van den Akker, Johannes P. C.
Endeman, Henrik
Rijken, Dingeman C.
Kruip, Marieke J. H. A.
Weggeman, Miranda
Koopman, Jaap
de Maat, Moniek P. M.
author_facet de Vries, Judith J.
Visser, Chantal
van Ommen, Maureen
Rokx, Casper
van Nood, Els
van Gorp, Eric C. M.
Goeijenbier, Marco
van den Akker, Johannes P. C.
Endeman, Henrik
Rijken, Dingeman C.
Kruip, Marieke J. H. A.
Weggeman, Miranda
Koopman, Jaap
de Maat, Moniek P. M.
author_sort de Vries, Judith J.
collection PubMed
description 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 γˊ 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 γˊ 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 γˊ 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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spelling pubmed-103706392023-07-27 Levels of Fibrinogen Variants Are Altered in Severe COVID-19 de Vries, Judith J. Visser, Chantal van Ommen, Maureen Rokx, Casper van Nood, Els van Gorp, Eric C. M. Goeijenbier, Marco van den Akker, Johannes P. C. Endeman, Henrik Rijken, Dingeman C. Kruip, Marieke J. H. A. Weggeman, Miranda Koopman, Jaap de Maat, Moniek P. M. TH Open 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 γˊ 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 γˊ 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 γˊ fibrinogen, which may be a cause or consequence of severe disease, but this is not associated with the development of thrombosis. Georg Thieme Verlag KG 2023-07-13 /pmc/articles/PMC10370639/ /pubmed/37501780 http://dx.doi.org/10.1055/a-2102-4521 Text en The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. ( https://creativecommons.org/licenses/by/4.0/ ) https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle de Vries, Judith J.
Visser, Chantal
van Ommen, Maureen
Rokx, Casper
van Nood, Els
van Gorp, Eric C. M.
Goeijenbier, Marco
van den Akker, Johannes P. C.
Endeman, Henrik
Rijken, Dingeman C.
Kruip, Marieke J. H. A.
Weggeman, Miranda
Koopman, Jaap
de Maat, Moniek P. M.
Levels of Fibrinogen Variants Are Altered in Severe COVID-19
title Levels of Fibrinogen Variants Are Altered in Severe COVID-19
title_full Levels of Fibrinogen Variants Are Altered in Severe COVID-19
title_fullStr Levels of Fibrinogen Variants Are Altered in Severe COVID-19
title_full_unstemmed Levels of Fibrinogen Variants Are Altered in Severe COVID-19
title_short Levels of Fibrinogen Variants Are Altered in Severe COVID-19
title_sort levels of fibrinogen variants are altered in severe covid-19
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10370639/
https://www.ncbi.nlm.nih.gov/pubmed/37501780
http://dx.doi.org/10.1055/a-2102-4521
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