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Open Forum Infect Dis . Blood Inflammatory Biomarkers Differentiate Inpatient and Outpatient Coronavirus Disease 2019 From Influenza

tetano

Editor, Senior Moderator
Open Forum Infect Dis


. 2023 Feb 21;10(3):ofad095.
doi: 10.1093/ofid/ofad095. eCollection 2023 Mar.
Blood Inflammatory Biomarkers Differentiate Inpatient and Outpatient Coronavirus Disease 2019 From Influenza


Lauren L Luciani[SUP] 1 [/SUP], Leigh M Miller[SUP] 2 3 [/SUP], Bo Zhai[SUP] 2 [/SUP], Karen Clarke[SUP] 4 [/SUP], Kailey Hughes Kramer[SUP] 5 [/SUP], Lucas J Schratz[SUP] 2 [/SUP], G K Balasubramani[SUP] 6 [/SUP], Klancie Dauer[SUP] 6 [/SUP], M Patricia Nowalk[SUP] 4 [/SUP], Richard K Zimmerman[SUP] 4 [/SUP], Jason E Shoemaker[SUP] 1 7 [/SUP], John F Alcorn[SUP] 2 3 [/SUP]



Affiliations

Abstract

Background: The ongoing circulation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) poses a diagnostic challenge because symptoms of coronavirus disease 2019 (COVID-19) are difficult to distinguish from other respiratory diseases. Our goal was to use statistical analyses and machine learning to identify biomarkers that distinguish patients with COVID-19 from patients with influenza.
Methods: Cytokine levels were analyzed in plasma and serum samples from patients with influenza and COVID-19, which were collected as part of the Centers for Disease Control and Prevention's Hospitalized Adult Influenza Vaccine Effectiveness Network (inpatient network) and the US Flu Vaccine Effectiveness (outpatient network).
Results: We determined that interleukin (IL)-10 family cytokines are significantly different between COVID-19 and influenza patients. The results suggest that the IL-10 family cytokines are a potential diagnostic biomarker to distinguish COVID-19 and influenza infection, especially for inpatients. We also demonstrate that cytokine combinations, consisting of up to 3 cytokines, can distinguish SARS-CoV-2 and influenza infection with high accuracy in both inpatient (area under the receiver operating characteristics curve [AUC] = 0.84) and outpatient (AUC = 0.81) groups, revealing another potential screening tool for SARS-CoV-2 infection.
Conclusions: This study not only reveals prospective screening tools for COVID-19 infections that are independent of polymerase chain reaction testing or clinical condition, but it also emphasizes potential pathways involved in disease pathogenesis that act as potential targets for future mechanistic studies.

Keywords: SARS-CoV-2; cytokine; human; machine learning; pneumonia.
 
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