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γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity
Coronavirus disease 2019 (COVID-19) is characterized by a pro-inflammatory state associated with organ failure, thrombosis, and death. We investigated a novel inflammatory biomarker, γ′ fibrinogen (GPF), in 103 hospitalized patients with COVID-19 and 19 healthy controls. We found significant associa...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147444/ https://www.ncbi.nlm.nih.gov/pubmed/37150704 http://dx.doi.org/10.1016/j.bcmd.2023.102746 |
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author | Kornblith, Lucy Z. Sadhanandhan, Bindhya Arun, Sreepriya Long, Rebecca Johnson, Alicia J. Noll, Jamie Ramchand, C.N. Olynyk, John K. Farrell, David H. |
author_facet | Kornblith, Lucy Z. Sadhanandhan, Bindhya Arun, Sreepriya Long, Rebecca Johnson, Alicia J. Noll, Jamie Ramchand, C.N. Olynyk, John K. Farrell, David H. |
author_sort | Kornblith, Lucy Z. |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) is characterized by a pro-inflammatory state associated with organ failure, thrombosis, and death. We investigated a novel inflammatory biomarker, γ′ fibrinogen (GPF), in 103 hospitalized patients with COVID-19 and 19 healthy controls. We found significant associations between GPF levels and the severity of COVID-19 as judged by blood oxygen saturation (SpO(2)). The mean level of GPF in the patients with COVID-19 was significantly higher than in controls (69.8 (95 % CI 64.8–74.8) mg/dL compared with 36.9 (95 % CI 31.4–42.4) mg/dL, p < 0.0001), whereas C-reactive protein (CRP), lactate dehydrogenase (LDH), and total fibrinogen levels were not significantly different between groups. Mean GPF levels were significantly highest in patients with severe COVID-19 (SpO(2) ≤ 93 %, GPF 75.2 (95 % CI 68.7–81.8) mg/dL), compared to mild/moderate COVID-19 (SpO(2) > 93 %, GPF 62.5 (95 % CI 55.0–70.0) mg/dL, p = 0.01, AUC of 0.68, 95 % CI 0.57–0.78; Youden's index cutpoint 62.9 mg/dL, sensitivity 0.64, specificity 0.63). In contrast, CRP, interleukin-6, ferritin, LDH, D-dimers, and total fibrinogen had weaker associations with COVID-19 disease severity (all ROC curves with lower AUCs). Thus, GPF may be a useful inflammatory marker of COVID-19 respiratory disease severity. |
format | Online Article Text |
id | pubmed-10147444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-101474442023-05-01 γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity Kornblith, Lucy Z. Sadhanandhan, Bindhya Arun, Sreepriya Long, Rebecca Johnson, Alicia J. Noll, Jamie Ramchand, C.N. Olynyk, John K. Farrell, David H. Blood Cells Mol Dis Article Coronavirus disease 2019 (COVID-19) is characterized by a pro-inflammatory state associated with organ failure, thrombosis, and death. We investigated a novel inflammatory biomarker, γ′ fibrinogen (GPF), in 103 hospitalized patients with COVID-19 and 19 healthy controls. We found significant associations between GPF levels and the severity of COVID-19 as judged by blood oxygen saturation (SpO(2)). The mean level of GPF in the patients with COVID-19 was significantly higher than in controls (69.8 (95 % CI 64.8–74.8) mg/dL compared with 36.9 (95 % CI 31.4–42.4) mg/dL, p < 0.0001), whereas C-reactive protein (CRP), lactate dehydrogenase (LDH), and total fibrinogen levels were not significantly different between groups. Mean GPF levels were significantly highest in patients with severe COVID-19 (SpO(2) ≤ 93 %, GPF 75.2 (95 % CI 68.7–81.8) mg/dL), compared to mild/moderate COVID-19 (SpO(2) > 93 %, GPF 62.5 (95 % CI 55.0–70.0) mg/dL, p = 0.01, AUC of 0.68, 95 % CI 0.57–0.78; Youden's index cutpoint 62.9 mg/dL, sensitivity 0.64, specificity 0.63). In contrast, CRP, interleukin-6, ferritin, LDH, D-dimers, and total fibrinogen had weaker associations with COVID-19 disease severity (all ROC curves with lower AUCs). Thus, GPF may be a useful inflammatory marker of COVID-19 respiratory disease severity. Elsevier Inc. 2023-07 2023-04-28 /pmc/articles/PMC10147444/ /pubmed/37150704 http://dx.doi.org/10.1016/j.bcmd.2023.102746 Text en © 2023 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Kornblith, Lucy Z. Sadhanandhan, Bindhya Arun, Sreepriya Long, Rebecca Johnson, Alicia J. Noll, Jamie Ramchand, C.N. Olynyk, John K. Farrell, David H. γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity |
title | γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity |
title_full | γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity |
title_fullStr | γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity |
title_full_unstemmed | γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity |
title_short | γ′ fibrinogen levels as a biomarker of COVID-19 respiratory disease severity |
title_sort | γ′ fibrinogen levels as a biomarker of covid-19 respiratory disease severity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10147444/ https://www.ncbi.nlm.nih.gov/pubmed/37150704 http://dx.doi.org/10.1016/j.bcmd.2023.102746 |
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