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Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients
BACKGROUND: Cysteinyl leukotrienes (CysLT) are potent inflammation-promoting mediators, but remain scarcely explored in COVID-19. We evaluated urinary CysLT (U-CysLT) relationship with disease severity and their usefulness for prognostication in hospitalized COVID-19 patients. The impact on U-CysLT...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826622/ https://www.ncbi.nlm.nih.gov/pubmed/36617343 http://dx.doi.org/10.1007/s00011-022-01682-z |
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author | Reina-Couto, Marta Roboredo-Madeira, Mariana Pereira-Terra, Patrícia Silva-Pereira, Carolina Martins, Sandra Teixeira-Santos, Luísa Pinho, Dora Dias, Andreia Cordeiro, Gonçalo Dias, Cláudia Camila Sarmento, António Tavares, Margarida Guimarães, João T. Roncon-Albuquerque, Roberto Paiva, José-Artur Albino-Teixeira, António Sousa, Teresa |
author_facet | Reina-Couto, Marta Roboredo-Madeira, Mariana Pereira-Terra, Patrícia Silva-Pereira, Carolina Martins, Sandra Teixeira-Santos, Luísa Pinho, Dora Dias, Andreia Cordeiro, Gonçalo Dias, Cláudia Camila Sarmento, António Tavares, Margarida Guimarães, João T. Roncon-Albuquerque, Roberto Paiva, José-Artur Albino-Teixeira, António Sousa, Teresa |
author_sort | Reina-Couto, Marta |
collection | PubMed |
description | BACKGROUND: Cysteinyl leukotrienes (CysLT) are potent inflammation-promoting mediators, but remain scarcely explored in COVID-19. We evaluated urinary CysLT (U-CysLT) relationship with disease severity and their usefulness for prognostication in hospitalized COVID-19 patients. The impact on U-CysLT of veno-venous extracorporeal membrane oxygenation (VV-ECMO) and of comorbidities such as hypertension and obesity was also assessed. METHODS: Blood and spot urine were collected in “severe” (n = 26), “critically ill” (n = 17) and “critically ill on VV-ECMO” (n = 17) patients with COVID-19 at days 1–2 (admission), 3–4, 5–8 and weekly thereafter, and in controls (n = 23) at a single time point. U-CysLT were measured by ELISA. Routine markers, prognostic scores and outcomes were also evaluated. RESULTS: U-CysLT did not differ between groups at admission, but significantly increased along hospitalization only in critical groups, being markedly higher in VV-ECMO patients, especially in hypertensives. U-CysLT values during the first week were positively associated with ICU and total hospital length of stay in critical groups and showed acceptable area under curve (AUC) for prediction of 30-day mortality (AUC: 0.734, p = 0.001) among all patients. CONCLUSIONS: U-CysLT increase during hospitalization in critical COVID-19 patients, especially in hypertensives on VV-ECMO. U-CysLT association with severe outcomes suggests their usefulness for prognostication and as therapeutic targets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00011-022-01682-z. |
format | Online Article Text |
id | pubmed-9826622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-98266222023-01-09 Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients Reina-Couto, Marta Roboredo-Madeira, Mariana Pereira-Terra, Patrícia Silva-Pereira, Carolina Martins, Sandra Teixeira-Santos, Luísa Pinho, Dora Dias, Andreia Cordeiro, Gonçalo Dias, Cláudia Camila Sarmento, António Tavares, Margarida Guimarães, João T. Roncon-Albuquerque, Roberto Paiva, José-Artur Albino-Teixeira, António Sousa, Teresa Inflamm Res Original Research Paper BACKGROUND: Cysteinyl leukotrienes (CysLT) are potent inflammation-promoting mediators, but remain scarcely explored in COVID-19. We evaluated urinary CysLT (U-CysLT) relationship with disease severity and their usefulness for prognostication in hospitalized COVID-19 patients. The impact on U-CysLT of veno-venous extracorporeal membrane oxygenation (VV-ECMO) and of comorbidities such as hypertension and obesity was also assessed. METHODS: Blood and spot urine were collected in “severe” (n = 26), “critically ill” (n = 17) and “critically ill on VV-ECMO” (n = 17) patients with COVID-19 at days 1–2 (admission), 3–4, 5–8 and weekly thereafter, and in controls (n = 23) at a single time point. U-CysLT were measured by ELISA. Routine markers, prognostic scores and outcomes were also evaluated. RESULTS: U-CysLT did not differ between groups at admission, but significantly increased along hospitalization only in critical groups, being markedly higher in VV-ECMO patients, especially in hypertensives. U-CysLT values during the first week were positively associated with ICU and total hospital length of stay in critical groups and showed acceptable area under curve (AUC) for prediction of 30-day mortality (AUC: 0.734, p = 0.001) among all patients. CONCLUSIONS: U-CysLT increase during hospitalization in critical COVID-19 patients, especially in hypertensives on VV-ECMO. U-CysLT association with severe outcomes suggests their usefulness for prognostication and as therapeutic targets. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00011-022-01682-z. Springer International Publishing 2023-01-08 2023 /pmc/articles/PMC9826622/ /pubmed/36617343 http://dx.doi.org/10.1007/s00011-022-01682-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Research Paper Reina-Couto, Marta Roboredo-Madeira, Mariana Pereira-Terra, Patrícia Silva-Pereira, Carolina Martins, Sandra Teixeira-Santos, Luísa Pinho, Dora Dias, Andreia Cordeiro, Gonçalo Dias, Cláudia Camila Sarmento, António Tavares, Margarida Guimarães, João T. Roncon-Albuquerque, Roberto Paiva, José-Artur Albino-Teixeira, António Sousa, Teresa Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients |
title | Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients |
title_full | Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients |
title_fullStr | Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients |
title_full_unstemmed | Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients |
title_short | Evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in COVID-19 patients |
title_sort | evaluation of urinary cysteinyl leukotrienes as biomarkers of severity and putative therapeutic targets in covid-19 patients |
topic | Original Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9826622/ https://www.ncbi.nlm.nih.gov/pubmed/36617343 http://dx.doi.org/10.1007/s00011-022-01682-z |
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