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Sputum eosinophil counts and eosinophil cationic protein levels in cough‐variant asthma and in classic asthma, and their relationships to airway hypersensitivity or maximal airway response to methacholine
Author(s) -
Yoo Y.,
Koh Y. Y.,
Kang H.,
Yu J.,
Nah K. M.,
Kim C. K.
Publication year - 2004
Publication title -
allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.363
H-Index - 173
eISSN - 1398-9995
pISSN - 0105-4538
DOI - 10.1111/j.1398-9995.2004.00655.x
Subject(s) - methacholine , medicine , eosinophil cationic protein , asthma , sputum , eosinophil , airway , immunology , allergy , eosinophilic , respiratory disease , anesthesia , pathology , lung , tuberculosis
Background: The aims of this study were to compare the degree of airway inflammation in cough‐variant asthma (CVA) with that in classic asthma (CA), and to examine the relationship between airway inflammation and airway hypersensitivity or maximal airway response to methacholine in both conditions. Methods: Sputum was induced in 41 CVA patients, in 41 methacholine PC 20 ‐matched CA patients, and in 20 healthy children. The sputum samples were analyzed for total and differential cell counts, and for eosinophilic cationic protein (ECP). A high‐dose methacholine challenge test was performed in CVA and CA patients to determine PC 20 and maximal airway response. Results: Sputum eosinophil percentages and ECP levels were significantly elevated in CVA and CA vs the control, but no significant differences were found between the two asthma groups. In the two asthma groups, neither sputum parameters correlated significantly with methacholine PC 20 . However, the absence of a maximal response plateau or its higher level, when present, was associated with increased eosinophil percentages and ECP levels in the CVA group. Conclusions: The degree of eosinophilic inflammation may not be causally related to differences in presented asthma manifestations. The identification of a maximal response plateau and the level of this plateau in patients with CVA may provide information pertinent to airway eosinophilic inflammation.