EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients
BackgroundThe coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and has evoked a pandemic that challenges public health-care systems worldwide. Endothelial cell dysfunction plays a key role in pathophysiology, and simple prognosticators may...
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doaj-4b85aab98f1f4f79b81dd0b27c5e6c452021-06-23T06:37:11ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-06-011210.3389/fimmu.2021.634416634416EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected PatientsThomas Luft0Clemens-Martin Wendtner1Florentina Kosely2Aleksandar Radujkovic3Axel Benner4Felix Korell5Lars Kihm6Matthias F. Bauer7Peter Dreger8Uta Merle9Department of Internal Medicine V, University of Heidelberg, Heidelberg, GermanyMunich Clinic Schwabing, Academic Teaching Hospital, Ludwig-Maximilians University (LMU), Munich, GermanyMedical Department B, Hospital Ludwigshafen, Ludwigshafen, GermanyDepartment of Internal Medicine V, University of Heidelberg, Heidelberg, GermanyDivision of Biostatistics, German Cancer Research Center, Heidelberg, GermanyDepartment of Internal Medicine V, University of Heidelberg, Heidelberg, GermanyDepartment of Internal Medicine I, University of Heidelberg, Heidelberg, GermanyInstitute of Laboratory Diagnostics, Hygiene and Transfusion Medicine, Hospital Ludwigshafen, Ludwigshafen, GermanyDepartment of Internal Medicine V, University of Heidelberg, Heidelberg, GermanyDepartment of Internal Medicine IV, University of Heidelberg, Heidelberg, GermanyBackgroundThe coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and has evoked a pandemic that challenges public health-care systems worldwide. Endothelial cell dysfunction plays a key role in pathophysiology, and simple prognosticators may help to optimize allocation of limited resources. Endothelial activation and stress index (EASIX) is a validated predictor of endothelial complications and outcome after allogeneic stem cell transplantation. Aim of this study was to test if EASIX could predict life-threatening complications in patients with COVID-19.MethodsSARS-CoV-2-positive, hospitalized patients were enrolled onto a prospective non-interventional register study (n=100). Biomarkers were assessed at hospital admission. Primary endpoint was severe course of disease (mechanical ventilation and/or death, V/D). Results were validated in 126 patients treated in two independent institutions.ResultsEASIX at admission was a strong predictor of severe course of the disease (odds ratio for a two-fold change 3.4, 95%CI 1.8-6.3, p<0.001), time to V/D (hazard ratio (HR) for a two-fold change 2.0, 95%CI 1.5-2.6, p<0.001) as well as survival (HR for a two-fold change 1.7, 95%CI 1.2-2.5, p=0.006). The effect was retained in multivariable analysis adjusting for age, gender, and comorbidities and could be validated in the independent cohort. At hospital admission EASIX correlated with increased suppressor of tumorigenicity-2, soluble thrombomodulin, angiopoietin-2, CXCL8, CXCL9 and interleukin-18, but not interferon-alpha.ConclusionEASIX is a validated predictor of COVID19 outcome and an easy-to-access tool to segregate patients in need for intensive surveillance.https://www.frontiersin.org/articles/10.3389/fimmu.2021.634416/fullendothelial activation and stress indexEASIXSARS-CoV2 (COVID- 19)suppressor of tumorigenicity 2 (ST2)soluble thrombomodulinangiopoietin-2 (Ang-2) |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Thomas Luft Clemens-Martin Wendtner Florentina Kosely Aleksandar Radujkovic Axel Benner Felix Korell Lars Kihm Matthias F. Bauer Peter Dreger Uta Merle |
spellingShingle |
Thomas Luft Clemens-Martin Wendtner Florentina Kosely Aleksandar Radujkovic Axel Benner Felix Korell Lars Kihm Matthias F. Bauer Peter Dreger Uta Merle EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients Frontiers in Immunology endothelial activation and stress index EASIX SARS-CoV2 (COVID- 19) suppressor of tumorigenicity 2 (ST2) soluble thrombomodulin angiopoietin-2 (Ang-2) |
author_facet |
Thomas Luft Clemens-Martin Wendtner Florentina Kosely Aleksandar Radujkovic Axel Benner Felix Korell Lars Kihm Matthias F. Bauer Peter Dreger Uta Merle |
author_sort |
Thomas Luft |
title |
EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients |
title_short |
EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients |
title_full |
EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients |
title_fullStr |
EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients |
title_full_unstemmed |
EASIX for Prediction of Outcome in Hospitalized SARS-CoV-2 Infected Patients |
title_sort |
easix for prediction of outcome in hospitalized sars-cov-2 infected patients |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2021-06-01 |
description |
BackgroundThe coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) and has evoked a pandemic that challenges public health-care systems worldwide. Endothelial cell dysfunction plays a key role in pathophysiology, and simple prognosticators may help to optimize allocation of limited resources. Endothelial activation and stress index (EASIX) is a validated predictor of endothelial complications and outcome after allogeneic stem cell transplantation. Aim of this study was to test if EASIX could predict life-threatening complications in patients with COVID-19.MethodsSARS-CoV-2-positive, hospitalized patients were enrolled onto a prospective non-interventional register study (n=100). Biomarkers were assessed at hospital admission. Primary endpoint was severe course of disease (mechanical ventilation and/or death, V/D). Results were validated in 126 patients treated in two independent institutions.ResultsEASIX at admission was a strong predictor of severe course of the disease (odds ratio for a two-fold change 3.4, 95%CI 1.8-6.3, p<0.001), time to V/D (hazard ratio (HR) for a two-fold change 2.0, 95%CI 1.5-2.6, p<0.001) as well as survival (HR for a two-fold change 1.7, 95%CI 1.2-2.5, p=0.006). The effect was retained in multivariable analysis adjusting for age, gender, and comorbidities and could be validated in the independent cohort. At hospital admission EASIX correlated with increased suppressor of tumorigenicity-2, soluble thrombomodulin, angiopoietin-2, CXCL8, CXCL9 and interleukin-18, but not interferon-alpha.ConclusionEASIX is a validated predictor of COVID19 outcome and an easy-to-access tool to segregate patients in need for intensive surveillance. |
topic |
endothelial activation and stress index EASIX SARS-CoV2 (COVID- 19) suppressor of tumorigenicity 2 (ST2) soluble thrombomodulin angiopoietin-2 (Ang-2) |
url |
https://www.frontiersin.org/articles/10.3389/fimmu.2021.634416/full |
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