Dl. Bratton et al., Exhaled nitric oxide before and after montelukast sodium therapy in school-age children with chronic asthma: A preliminary study, PEDIAT PULM, 28(6), 1999, pp. 402-407
Exhaled nitric oxide (ENO) is a surrogate marker of airway inflammation in
asthma. In 12 children aged 6-11 years with mild to moderate persistent ast
hma, ENO concentrations were measured before and after 4 weeks of treatment
with montelukast sodium, a leukotriene receptor antagonist, and 2 weeks af
ter withdrawal of therapy.
Baseline ENO levels (mean and 95% confidence interval) were significantly e
levated in patients with asthma compared to age-matched nonasthmatic contro
l subjects, with levels of 83 (42-123) vs. 13 (11-15) ppb (P < 0.001). Afte
r treatment with montelukast sodium, there was a significant (P < 0.01) red
uction in ENO to 58 (27-89) ppb which again rose to 69 (38-99) ppb 2 weeks
after treatment was withdrawn. During treatment, the fail in ENO was accomp
anied by nonsignificant improvements in prebronchodilator forced expiratory
volume in 1 s (FEV1) from 81-85% predicted or reductions in use of albuter
ol from a mean of 2.5 to 1.6 puffs/day. Individual ENO measurements and cha
nge in ENO concentrations with treatment did not correlate with either pulm
onary function changes or use of bronchodilator.
These data show that ENO is elevated in children with relatively mild asthm
a treated with bronchodilator alone, and that treatment with montelukast so
dium for 4 weeks results in a significant reduction in ENO concentrations,
even in the absence of significant changes in pulmonary function. These fin
dings suggest an anti-inflammatory role for leukotriene D-4 receptor antago
nism in the treatment of children with mild to moderate asthma. (C) 1999 Wi
ley-Liss, Inc.