Mild exacerbations and eosinophilic inflammation in patients with stable, well-controlled asthma after 1 year of follow-up

Chest. 2001 Apr;119(4):1011-7. doi: 10.1378/chest.119.4.1011.

Abstract

Objectives: To determine the time to exacerbation and probability of a mild exacerbation of asthma, and the impact of eosinophilic inflammation on these parameters in patients with stable, well-controlled asthma.

Patients and methods: A cohort of 31 patients with stable, well-controlled asthma receiving inhaled steroid treatment regularly were followed up for 1 year or until a mild exacerbation occurred. Mild exacerbation was defined as symptoms of asthma lasting > 48 h with a fall in peak expiratory flow > 20%. FEV(1), provocative concentration of methacholine causing a 20% fall in FEV(1), eosinophil count, and eosinophilic cationic protein (ECP) levels in blood and in sputum were measured at the first visit and every 2 months.

Results: At baseline, the mean (SD) eosinophil count was 0.39 x 10(9)/L (0.21 x 10(9)/L) in blood and 13% (14%) in sputum; ECP was 30 microg/L (28 microg/L) in blood and 75 microg/L (85 microg/L) in sputum. Thirteen subjects experienced a mild exacerbation during the 1-year follow-up period. The mean time to mild exacerbation was 293 days (95% confidence interval [CI], 248 to 337 days), and the cumulative probability of not experiencing a mild exacerbation in 1 year was 49% (95% CI, 39 to 59%). An increased risk of mild exacerbation was associated with blood eosinophil count > 0.4 x 10(9)/L (relative risk 4.5; 95% CI of relative risk, 1.8 to 38.0), blood ECP > 20 microg/L (relative risk, 2.1; 95% CI of relative risk, 1.0 to 9.2), and sputum ECP > 40 microg/L (relative risk, 2.5; 95% CI of relative risk, 1.2 to 11.2), but was unassociated with other variables.

Conclusions: Patient with stable, well-controlled asthma are at risk of mild exacerbation during 1 year of follow-up despite regular inhaled steroid treatment. Eosinophilic inflammation expressed as eosinophil count and ECP is associated with higher risk of mild exacerbation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Inhalation
  • Administration, Topical
  • Adolescent
  • Adrenergic beta-Agonists / administration & dosage
  • Adult
  • Aged
  • Anti-Inflammatory Agents / administration & dosage
  • Asthma / blood
  • Asthma / drug therapy
  • Asthma / physiopathology*
  • Blood Proteins / analysis
  • Bronchial Provocation Tests
  • Bronchodilator Agents / administration & dosage
  • Budesonide / administration & dosage
  • Eosinophil Granule Proteins
  • Eosinophils / pathology*
  • Follow-Up Studies
  • Forced Expiratory Volume
  • Glucocorticoids
  • Humans
  • Inflammation
  • Leukocyte Count
  • Longitudinal Studies
  • Methacholine Chloride*
  • Middle Aged
  • Peak Expiratory Flow Rate
  • Ribonucleases*
  • Risk Factors

Substances

  • Adrenergic beta-Agonists
  • Anti-Inflammatory Agents
  • Blood Proteins
  • Bronchodilator Agents
  • Eosinophil Granule Proteins
  • Glucocorticoids
  • Methacholine Chloride
  • Budesonide
  • Ribonucleases