Eosinophil-derived neurotoxin in childhood asthma: correlation with disease severity

J Asthma. 2010 Jun;47(5):568-73. doi: 10.3109/02770901003792833.

Abstract

Background: Eosinophil numbers and eosinophil cationic protein (ECP) levels have been proposed as markers of disease activity; however, the usefulness of eosinophil-derived neurotoxin (EDN)--another eosinophil granular protein--as a marker in pediatric asthma has not been established.

Objective: The authors compared the concentrations of blood eosinophil counts (TECs), serum ECP, and serum EDN to asthma symptom severity in young children.

Methods: Forty-three young children with asthma (Asthma group: mean age, 2.9 years; range, 1.4-5.0 years) were evaluated during both the acute and stable phases of disease. Asthma severity was measured using a symptom-scoring technique, and serum eosinophil indices (EDN and ECP levels and TECs) were determined. Nineteen age-matched controls (Control group: mean age, 2.7 years; range, 1.0-5.0 years) were used for comparison.

Results: Levels of serum EDN, serum ECP, and TECs were significantly higher in children with acute asthma compared with Controls (p < .0001). However, in stable asthma only EDN and ECP levels differed significantly when compared to Controls (p < .0001 and p < .001, respectively). When comparing acute and stable phases, EDN and TECs differed significantly (p < .0001), whereas ECP did not. Symptom scores correlated significantly with EDN (r = 0.850, p < 0.0001), ECP (r = 0.374, p < 0.01) and TECs (r = 0.457, p < 0.01) in acute asthma patients. When symptom scores were divided into three subgroups based on severity, only EDN levels showed significant differences amongst the three groups.

Conclusion: These findings suggest that serum EDN is a useful marker for identifying disease activity in children with asthma. EDN levels may better reflect disease severity than ECP levels or total eosinophil counts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asthma / blood*
  • Asthma / diagnosis*
  • Biomarkers / blood
  • Case-Control Studies
  • Child, Preschool
  • Disease Progression
  • Enzyme-Linked Immunosorbent Assay
  • Eosinophil Cationic Protein / blood*
  • Eosinophil Cationic Protein / metabolism
  • Eosinophil-Derived Neurotoxin / blood*
  • Eosinophil-Derived Neurotoxin / metabolism
  • Female
  • Humans
  • Infant
  • Male
  • Predictive Value of Tests
  • Probability
  • Prognosis
  • Reference Values
  • Risk Assessment
  • Severity of Illness Index
  • Statistics, Nonparametric

Substances

  • Biomarkers
  • Eosinophil-Derived Neurotoxin
  • Eosinophil Cationic Protein