Diagnostics (Aug 2024)

Club Cell Secretory Protein-16 (CC16) as a Prognostic Biomarker for COVID-19 and H1N1 Viral Infections

  • Shane Moore,
  • Keerthana Gopichandran,
  • Elizabeth Sevier,
  • Siddhika Gamare,
  • Sultan Almuntashiri,
  • Gustavo Ramírez,
  • Nora Regino,
  • Luis Jiménez-Alvarez,
  • Alfredo Cruz-Lagunas,
  • Tatiana S. Rodriguez-Reyna,
  • Joaquin Zuñiga,
  • Caroline A. Owen,
  • Xiaoyun Wang,
  • Duo Zhang

DOI
https://doi.org/10.3390/diagnostics14161720
Journal volume & issue
Vol. 14, no. 16
p. 1720

Abstract

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Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) and H1N1 viruses are inflammatory lung pathogens that can lead to acute lung injury (ALI) and acute respiratory distress syndrome (ARDS). ALI/ARDS are still life-threatening diseases in critically ill patients with 30–40% mortality in the last decade. Currently, there are no laboratory tests for the early diagnosis or prognosis of ALI/ARDS. Club cell secretory protein (CC16) has been investigated as a potential biomarker of lung epithelial damage in various lung diseases. In this study, we evaluated whether plasma CC16 reflects the severity of COVID-19 and H1N1 infections. The plasma CC16 levels showed no significant differences between H1N1 and COVID-19 groups (p = 0.09). Among all subjects, CC16 levels were significantly higher in non-survivors than in survivors (p = 0.001). Upon the area under the receiver operating characteristic (AUROC) analysis, CC16 had an acceptable value to distinguish survivors and non-survivors (p = 0.002). In the COVID-19 group, plasma CC16 levels moderately correlated with the Acute Physiology and Chronic Health Evaluation II (APACHE II) score (r = 0.374, p = 0.003) and Sequential Organ Failure Assessment (SOFA) score (r = 0.474, p p = 0.022). Among all the patients, weak correlations between plasma CC16 levels with the SOFA score (r = 0.328, p p < 0.001) were observed. Thus, circulating CC16 might reflect the severity of COVID-19 and H1N1 infections.

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