Exhaled nitric oxide (NO) has attracted increasing interest as a non-invasi
ve marker of airway inflammation. The purpose of this study was to determin
e whether exhaled nitric oxide in subjects with asthma varied according to
their atopic status and to examine its correlation with airway hyperrespons
iveness and lung function measurements.
Forty patients with asthma and 13 controls participated in the study. Nitri
c oxide was measured on three occasions with intervals of at least 3 days,
using a chemiluminescence method. Airway responsiveness was assessed with m
ethacholine challenge and lung function measurements were made. All subject
s recorded peak expiratory flow and kept a symptom diary during a 17-day pe
riod. There was no significant difference in lung function measurements, pe
ak expiratory flow or symptom score between the two asthma groups. Atopic p
atients with asthma had a significantly higher mean amount of exhaled NO th
an non-atopic subjects with asthma (162+/-68 vs. 113+/-55 nl min(-1); P = 0
.03) and the control group (88+/-52 nl min(-1); P = 0.004). No significant
difference was found in the amount of exhaled NO between non-atopic patient
s with asthma and the controls. In atopic subjects with asthma the mean exh
aled NO was significantly correlated to the dose-response slope for methach
oline (r = -0.52; P = 0.02), while no such correlation was found in the non
-atopic group.
In conclusion; in this study, atopic subjects with asthma had higher levels
of exhaled NO than non-atopic subjects. Atopic status should be taken into
account when measuring levels of exhaled NO in subjects with asthma. (C) 1
999 Harcourt Publishers Ltd.