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Published Online First: 29 July 2005. doi:10.1136/thx.2004.039321
Thorax 2005;60:822-826
Copyright © 2005 BMJ Publishing Group Ltd & British Thoracic Society

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ASTHMA

Clinical and atopic parameters and airway inflammatory markers in childhood asthma: a factor analysis

T F Leung1, G W K Wong1, F W S Ko2, C W K Lam3, T F Fok1

1 Department of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong SAR, China
2 Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong SAR, China
3 Department of Chemical Pathology, The Chinese University of Hong Kong, Prince of Wales Hospital, Hong Kong SAR, China

Correspondence to:
Correspondence to:
Dr T F Leung
Department of Paediatrics, 6/F, Clinical Sciences Building, Prince of Wales Hospital, Shatin, NT, Hong Kong SAR, China; tfleung{at}cuhk.edu.hk

Background: Recent studies have repeatedly shown weak correlations among lung function parameters, atopy, exhaled nitric oxide level (FeNO), and airway inflammatory markers, suggesting that they are non-overlapping characteristics of asthma in adults. A study was undertaken to determine, using factor analysis, whether the above features represent separate dimensions of childhood asthma.

Methods: Clinically stable asthmatic patients aged 7–18 years underwent spirometric testing, methacholine bronchial challenge, blood sampling for atopy markers and chemokine levels (macrophage derived chemokine (MDC), thymus and activation regulated chemokine (TARC), and eotaxin), FeNO, and chemokines (MDC and eotaxin) and leukotriene B4 measurements in exhaled breath condensate (EBC).

Results: The mean (SD) forced expiratory volume in 1 second (FEV1) and FeNO of 92 patients were 92.1 (15.9)% predicted and 87.3 (65.7) ppb, respectively. 59% of patients received inhaled corticosteroids. Factor analysis selected four different factors, explaining 55.5% of total variance. The Kaiser-Meyer-Olkin measure of sampling adequacy was 0.587. Plasma total and specific IgE levels, peripheral blood eosinophil percentage, and FeNO loaded on factor 1; plasma TARC and MDC concentrations on factor 2; MDC, eotaxin and leukotriene B4 concentrations in EBC on factor 3; and plasma eotaxin concentration together with clinical indices including body mass index and disease severity score loaded on factor 4. Post hoc factor analyses revealed similar results when outliers were excluded.

Conclusions: The results suggest that atopy related indices and airway inflammation are separate dimensions in the assessment of childhood asthma, and inflammatory markers in peripheral blood and EBC are non-overlapping factors of asthma.


Abbreviations: BHR, bronchial hyperresponsiveness; BMI, body mass index; EBC, exhaled breath condensate; FENO, exhaled nitric oxide; FEV1, forced expiratory volume in 1 second; FVC, forced vital capacity; MDC, macrophage derived chemokine; NO, nitric oxide; TARC, thymus and activation regulated chemokine

Keywords: airway inflammation; asthma; exhaled breath condensate; factor analysis; lung function; children




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