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Soluble IL-2R Levels at Baseline Predict the Development of Severe Respiratory Failure and Mortality in COVID-19 Patients

Authors :
Nikolaos K. Gatselis
Vasiliki Lygoura
Aggeliki Lyberopoulou
George Giannoulis
Anna Samakidou
Antonia Vaiou
George Vatidis
Katerina Antoniou
Aggelos Stefos
Sarah Georgiadou
Dimitrios Sagris
Dafni Sveroni
Despoina Stergioula
Stella Gabeta
George Ntaios
George N. Dalekos
Source :
Viruses; Volume 14; Issue 4; Pages: 787
Publication Year :
2022

Abstract

Risk stratification of coronavirus disease-19 (COVID-19) patients by simple markers is critical to guide treatment. We studied the predictive value of soluble interleukin-2 receptor (sIL-2R) for the early identification of patients at risk of developing severe clinical outcomes. sIL-2R levels were measured in 197 patients (60.9% males; median age 61 years; moderate disease, n = 65; severe, n = 132, intubated and/or died, n = 42). All patients received combined immunotherapies (anakinra ± corticosteroids ± intravenous immunoglobulin ± tocilizumab) according to our local treatment algorithm. The endpoint was the composite event of intubation due to severe respiratory failure (SRF) or mortality. Median (interquartile range) sIL-2R levels were significantly higher in patients with severe disease, compared with those with moderate disease (6 (6.2) vs. 5.2 (3.4) ng/mL, p = 0.017). sIL-2R was the strongest laboratory predictive factor for intubation/death (hazard ratio 1.749, 95%CI 1.041–2.939, p = 0.035) after adjustment for other known risk factors. Youden’s index revealed optimal sIL-2R cut-off for predicting intubation/death at 9 ng/mL (sensitivity: 67%; specificity: 86%; positive and negative predictive value: 57% and 91%, respectively). Delta sIL-2R between the day of event or discharge minus admission date was higher in patients that intubated/died than in those who did not experience an event (2.91 (10.42) vs. 0.44 (2.88) ng/mL; p = 0.08)). sIL-2R on admission and its dynamic changes during follow-up may reflect disease severity and predict the development of SRF and mortality.

Details

ISSN :
19994915
Volume :
14
Issue :
4
Database :
OpenAIRE
Journal :
Viruses
Accession number :
edsair.doi.dedup.....c34bb3ed8efdfb07d7a11f1a07cd8989