Serum eosinophil cationic protein and bronchial responsiveness in pediatric and adolescent asthma patients

Citation
W. Gruber et al., Serum eosinophil cationic protein and bronchial responsiveness in pediatric and adolescent asthma patients, CHEST, 116(2), 1999, pp. 301-305
Citations number
35
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CHEST
ISSN journal
00123692 → ACNP
Volume
116
Issue
2
Year of publication
1999
Pages
301 - 305
Database
ISI
SICI code
0012-3692(199908)116:2<301:SECPAB>2.0.ZU;2-D
Abstract
Background: Serum eosinophil cationic protein (ECP) has been promoted as a marker of inflammatory activity in bronchial asthma. Bronchial responsivene ss, measured either by inhaling pharmacologically active substances such as histamine or methacholine, or by applying physical stimuli such as the hyp erventilation of cold dry air, is also considered to be an indirect marker of bronchial inflammation. Objectives: In this study, we investigated the possible relationship betwee n serum ECP and bronchial responsiveness to both cold dry air and histamine in presently symptom- and medication-free pediatric and adolescent asthma patients. Subjects: Thirty-six children and adolescents with atopic asthma were studi ed. Methods: On 2 consecutive days, bronchial responsiveness was assessed nonph armacologically by cold dry air and pharmacologically by histamine in rando m order, Blood samples for determination of ECP were collected before each challenge, Results: Serum ECP levels correlated with neither cold dry air-induced chan ges in FEV1 nor the provocation concentrations of histamine causing a 20% f all in FEV1. Subjects with bronchial hyperresponsiveness to cold dry air an d histamine had somewhat higher levels of serum ECP than subjects with norm al responses, but these differences were insignificant, Conclusions: Our results indicate a lack of relationship both between serum ECP and bronchial responsiveness to cold dry air and between serum ECP and bronchial responsiveness to histamine.