Urinary club cell protein 16 (CC16): Utility of its assay during acute bronchiolitis

Carole Egron1, André Labbé2, Emmanuelle Rochette3

  • 1Department of Pediatrics, CHU Clermont-Ferrand, Clermont-Ferrand, France.

Pediatric Pulmonology
|November 27, 2019
PubMed

Insights

Urinary Club Cell Protein 16 (CC16) levels, not serum, correlate with acute bronchiolitis severity in infants. This noninvasive biomarker shows promise for assessing illness severity, though further research is needed.

Area of Science:

  • Pediatrics
  • Pulmonology
  • Biomarkers

Background:

  • Acute bronchiolitis is a common cause of infant hospitalization.
  • Club Cell Protein 16 (CC16) is a lung epithelial biomarker, but its utility in bronchiolitis is unclear.
  • Urinary CC16 assay for bronchiolitis severity is not well-established.

Purpose of the Study:

  • To evaluate serum and urinary CC16 as biomarkers for acute bronchiolitis severity in infants.
  • To assess the correlation between CC16 levels and clinical severity scores, morbidity, and viral causes.
  • To investigate the association of CC16 with recurrent wheezing one year post-illness.

Main Methods:

  • Prospective observational study of 166 infants under one year hospitalized with bronchiolitis.
  • Analysis of serum and urinary CC16 levels, correlating them with the Wainwright score and clinical severity.
  • Multivariate analysis to identify factors influencing urinary CC16, including urinary retinol binding protein (RBP).

Main Results:

  • Serum CC16 did not correlate with bronchiolitis severity (P=.49).
  • Urinary CC16 significantly correlated with bronchiolitis severity (P<.001).
  • The ratio of urinary CC16 to urinary RBP (logCC16u/logRBPu) also correlated with severity (P=.02). CC16 levels were not linked to 1-year recurrent wheezing.

Conclusions:

  • Urinary CC16 is a potential noninvasive biomarker for acute bronchiolitis severity in infants.
  • Interpretation requires consideration of factors like renal tubular function.
  • Further studies are needed to validate urinary CC16 and refine its clinical application.