Frontiers in Immunology (Aug 2024)

Predictive biomarkers of mortality in patients with severe COVID-19 hospitalized in intensive care unit

  • Sandrelli Meridiana de Fátima Ramos dos Santos Medeiros,
  • Sandrelli Meridiana de Fátima Ramos dos Santos Medeiros,
  • Bruna Maria Nepomuceno Sousa Lino,
  • Vinícius Pietta Perez,
  • Vinícius Pietta Perez,
  • Eduardo Sérgio Soares Sousa,
  • Eduardo Sérgio Soares Sousa,
  • Eloiza Helena Campana,
  • Eloiza Helena Campana,
  • Fábio Miyajima,
  • Wlisses Henrique Veloso Carvalho-Silva,
  • Naiara Naiana Dejani,
  • Naiara Naiana Dejani,
  • Matheus Santos de Sousa Fernandes,
  • Fatma Hilal Yagin,
  • Fahaid Al-Hashem,
  • Safaa M. Elkholi,
  • Hanan Alyami,
  • Fabrício Oliveira Souto

DOI
https://doi.org/10.3389/fimmu.2024.1416715
Journal volume & issue
Vol. 15

Abstract

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ObjectivesThis study was performed to identify predictive markers of worse outcomes in patients with severe COVID-19 in an intensive care unit.MethodsSixty patients with severe COVID-19, hospitalized in the Intensive Care Unit (ICU) between March and July 2021, were stratified into two groups according to the outcome survivors and non-survivors. After admission to the ICU, blood samples were collected directly for biomarker analysis. Routine hematological and biochemical biomarkers, as well as serum levels of cytokines, chemokines, and immunoglobulins, were investigated.ResultsLymphopenia, neutrophilia, and thrombocytopenia were more pronounced in non-surviving patients, while the levels of CRP, AST, creatinine, ferritin, AST, troponin I, urea, magnesium, and potassium were higher in the non-surviving group than the survival group. In addition, serum levels of IL-10, CCL2, CXCL9, and CXCL10 were significantly increased in patients who did not survive. These changes in the biomarkers evaluated were associated with increased mortality in patients with severe COVID-19.ConclusionThe present study confirmed and expanded the validity of laboratory biomarkers as indicators of mortality in severe COVID-19.

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