Lp. Ho et al., NITRITE LEVELS IN BREATH CONDENSATE OF PATIENTS WITH CYSTIC-FIBROSIS IS ELEVATED IN CONTRAST TO EXHALED NITRIC-OXIDE, Thorax, 53(8), 1998, pp. 680-684
Background-Nitric oxide (NO) leased by activated macrophages, neutroph
ils, and stimulated bronchial epithelial cells. Exhaled NO has been sh
own to be increased in patients with asthma and has been put forward a
s a marker of airways inflammation. However, we have found that exhale
d NO is not raised in patients with cystic fibrosis, even during infec
tive pulmonary exacerbation. One reason for this may be that excess ai
rway secretions may prevent diffusion of gaseous NO into the airway lu
men. We hypothesised that exhaled NO may not reflect total NO producti
on in chronically suppurative airways and investigated nitrite as anot
her marker of NO production. Methods-Breath condensate nitrite concent
ration and exhaled NO levels were measured in 21 clinically stable pat
ients with cystic fibrosis of mean age 26 years and mean FEV1 57% and
12 healthy normal volunteers of mean age 31 years. Breath condensate w
as collected with a validated method which excluded saliva and nasal a
ir contamination and nitrite levels were measured using the Griess rea
ction. Exhaled NO was measured using a sensitive chemiluminescence ana
lyser (LR2000) at an exhalation rate of 250 ml/s. Fourteen patients wi
th cystic fibrosis had circulating plasma leucocyte levels and differe
ntial analysis performed on the day of breath collection. Results-Nitr
ite levels were significantly higher in patients with cystic fibrosis
than in normal subjects (median 1.93 mu M compared with 0.33 mu M). Th
is correlated positively with circulating plasma leucocytes and neutro
phils (r = 0.6). In contrast, exhaled NO values were not significantly
different from the normal range (median 3.8 ppb vs 4.4 ppb). There wa
s no correlation between breath condensate nitrite and lung function a
nd between breath condensate nitrite and exhaled NO. Conclusions-Nitri
te levels in breath condensate were raised in stable patients with cys
tic fibrosis in contrast to exhaled NO. This suggests that nitrite lev
els may be a more useful measure of NO production and possibly airways
inflammation in suppurative airways and that exhaled NO may not refle
ct total NO production.