Circadian variation of sputum inflammatory cells in mild asthma

J Allergy Clin Immunol. 2003 Feb;111(2):308-12. doi: 10.1067/mai.2003.65.

Abstract

Background: Asthma, like many conditions, demonstrates a circadian rhythm with a worsening of lung function in the early morning hours compared with in the late afternoon.

Objective: Because eosinophilic airway inflammation is a proposed mechanism for worsening asthma, we characterized circadian variation in airway eosinophils and determined its relationship to variability in airway function.

Methods: Pulmonary function testing, sputum induction, and phlebotomy were performed at 7 am and 4 pm in 11 allergic subjects with mild asthma. Sputum was analyzed for cell viability, differential, and eosinophil-derived neurotoxin levels. IL-5 levels in serum were measured by means of ELISA.

Results: Subjects had a significant decrease in FEV(1) (median [interquartile range] = 80% [70%-86%] vs 85% [82%-94%], P =.009) and a greater beta-agonist reversibility (median [interquartile range] = 13% [7%-32%] vs 8% [5%-14%], P =.024) in the early morning compared with in the late afternoon. Sputum analysis showed an increase in early morning total sputum leukocytes (median [interquartile range] = 4.3 x 10(6) [2.3 x 10(6) to 6.1 x 10(6)] vs 2.6 x 10(6) [1.7 x 10(6) to 3.6 x 10(6)], P =.044) and eosinophils (median [interquartile range] = 7.0 x 10(4) [2.7 x 10(4) to 18.7 x 10(4)] vs 3.6 x 10(4) [1.0 x 10(4) to 8.2 x 10(4)], P =.024). Furthermore, sputum eosinophils correlated with beta-agonist reversibility (R (s) = 0.665, P =.019). Finally, levels of IL-5 in serum and eosinophil-derived neurotoxin in sputum were significantly increased at 7 am.

Conclusion: These data suggest that circadian variability in pulmonary function in asthma could be related to changes in airway eosinophil recruitment and activation.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Asthma / immunology
  • Asthma / pathology*
  • Asthma / physiopathology
  • Circadian Rhythm* / immunology
  • Circadian Rhythm* / physiology
  • Eosinophil-Derived Neurotoxin
  • Eosinophils / immunology
  • Eosinophils / pathology
  • Forced Expiratory Volume
  • Humans
  • Inflammation / immunology
  • Inflammation / pathology
  • Interleukin-5 / blood
  • Ribonucleases / metabolism
  • Sputum / cytology*
  • Sputum / immunology

Substances

  • Interleukin-5
  • Eosinophil-Derived Neurotoxin
  • Ribonucleases