B. Pedersen et al., EOSINOPHIL AND NEUTROPHIL ACTIVITY IN ASTHMA IN A ONE-YEAR TRIAL WITHINHALED BUDESONIDE - THE IMPACT OF SMOKING, American journal of respiratory and critical care medicine, 153(5), 1996, pp. 1519-1529
Citations number
26
Categorie Soggetti
Emergency Medicine & Critical Care","Respiratory System
The object of this investigation was to study the long-term effects of
antiasthma treatment on blood markers of inflammation and lung functi
on in adult asthmatic subjects. For this purpose 85 allergic and nonal
lergic asthmatic subjects were randomized into three groups, which wer
e given high-dose; (1,600 mu g/d) inhaled budesonide, low-dose (400 mu
g/d) inhaled budesonide, and oral theophylline (600 mg/d), respective
ly, and were followed for 11 mo with testing of lung function and bloo
d sampling for the assay in serum of eosinophil cationic protein (ECP)
, eosinophil protein x/eosinophil derived neurotoxin (EPX/EDN) as eosi
nophil markers, and myeloperoxidase (MPO) and lactoferrin (LF) as neut
rophil markers. Lung functions (FEV(1)% predicted, and histamine PC20)
and the eosinophil markers ECP and EPX/EDN were improved and reduced,
respectively, by budesonide in a dose-dependent and temporally parall
el fashion. Theophylline did not alter lung functions but reduced ECP
and EPX/EDN after prolonged treatment. The treatment efficacy of budes
onide was attributed solely to an effect on nonsmoking asthmatic subje
cts, since neither lung functions nor eosinophil markers changed in sm
okers even with high-dose budesonide. MPO but not LF was reduced after
several months of treatment in all three groups, but only in nonsmoke
rs. We conclude that ECP and EPX/EDN may be used to monitor antiinflam
matory treatment in asthmatic patients, and that smoking asthmatic sub
jects are resistant to inhaled corticosteroids.