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Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019
OBJECTIVES: Early and simple detection of high-risk groups is crucial for minimizing severe coronavirus disease 2019 (COVID-19)-related deaths. Soluble interleukin 2 receptors (sIL2R) have been suspected as being prognostic markers for infectious diseases. This study validated the usefulness of sIL2...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942057/ https://www.ncbi.nlm.nih.gov/pubmed/33711520 http://dx.doi.org/10.1016/j.ijid.2021.03.011 |
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author | Kaya, Hiroyasu Kaji, Masahide Usuda, Daisuke |
author_facet | Kaya, Hiroyasu Kaji, Masahide Usuda, Daisuke |
author_sort | Kaya, Hiroyasu |
collection | PubMed |
description | OBJECTIVES: Early and simple detection of high-risk groups is crucial for minimizing severe coronavirus disease 2019 (COVID-19)-related deaths. Soluble interleukin 2 receptors (sIL2R) have been suspected as being prognostic markers for infectious diseases. This study validated the usefulness of sIL2R as a marker for deaths related to COVID-19. METHODS: This retrospective observational study enrolled participants who showed positive results for severe acute respiratory syndrome coronavirus 2 RNA admitted to the current hospital between 01 April and 30 September 2020. Of the 102 patients enrolled in this study, sIL2R levels were measured in 87 patients. For comparisons between survival and non-survival groups, potential confounding variables were entered into univariate models, and variables showing significant correlations (p < 0.05) in those models were added to a multivariate model. RESULTS: Being aged ≥60 years and sIL2R levels ≥1060 U/ml were significantly associated with mortality on univariate analyses; only sIL2R levels significantly correlated with mortality on multivariate logistic regression analysis. Further, sequential sIL2R levels in three patients were increased at progression or death. CONCLUSION: SIL2R on admission and sequential monitoring of sIL2R might reflect disease severity. |
format | Online Article Text |
id | pubmed-7942057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79420572021-03-11 Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 Kaya, Hiroyasu Kaji, Masahide Usuda, Daisuke Int J Infect Dis Short Communication OBJECTIVES: Early and simple detection of high-risk groups is crucial for minimizing severe coronavirus disease 2019 (COVID-19)-related deaths. Soluble interleukin 2 receptors (sIL2R) have been suspected as being prognostic markers for infectious diseases. This study validated the usefulness of sIL2R as a marker for deaths related to COVID-19. METHODS: This retrospective observational study enrolled participants who showed positive results for severe acute respiratory syndrome coronavirus 2 RNA admitted to the current hospital between 01 April and 30 September 2020. Of the 102 patients enrolled in this study, sIL2R levels were measured in 87 patients. For comparisons between survival and non-survival groups, potential confounding variables were entered into univariate models, and variables showing significant correlations (p < 0.05) in those models were added to a multivariate model. RESULTS: Being aged ≥60 years and sIL2R levels ≥1060 U/ml were significantly associated with mortality on univariate analyses; only sIL2R levels significantly correlated with mortality on multivariate logistic regression analysis. Further, sequential sIL2R levels in three patients were increased at progression or death. CONCLUSION: SIL2R on admission and sequential monitoring of sIL2R might reflect disease severity. The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. 2021-04 2021-03-09 /pmc/articles/PMC7942057/ /pubmed/33711520 http://dx.doi.org/10.1016/j.ijid.2021.03.011 Text en © 2021 The Authors 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 | Short Communication Kaya, Hiroyasu Kaji, Masahide Usuda, Daisuke Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
title | Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
title_full | Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
title_fullStr | Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
title_full_unstemmed | Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
title_short | Soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
title_sort | soluble interleukin-2 receptor levels on admission associated with mortality in coronavirus disease 2019 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7942057/ https://www.ncbi.nlm.nih.gov/pubmed/33711520 http://dx.doi.org/10.1016/j.ijid.2021.03.011 |
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