INCREASED NITRIC-OXIDE IN EXHALED AIR OF PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS

Citation
G. Rolla et al., INCREASED NITRIC-OXIDE IN EXHALED AIR OF PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS, Journal of rheumatology, 24(6), 1997, pp. 1066-1071
Citations number
42
Categorie Soggetti
Rheumatology
Journal title
ISSN journal
0315162X
Volume
24
Issue
6
Year of publication
1997
Pages
1066 - 1071
Database
ISI
SICI code
0315-162X(1997)24:6<1066:INIEAO>2.0.ZU;2-5
Abstract
Objective, In experimental animals, elevated nitric oxide (NO) product ion has been implicated in the pathogenesis of a lupus-like syndrome. Abnormalities of lung function tests are reported in a high proportion of patients with systemic lupus erythematosus (SLE). We investigated whether NO output in exhaled air might be increased in patients with S LE and whether it is related to disease activity and to respiratory fu nction abnormalities. Methods. Lung volume, maximal expiratory flow at 50 and 25% of viral capacity (MEF50 MEF25), diffusion coefficient for carbon monoxide (K-CO), and NO in the exhaled air were measured in 27 outpatients with SLE (23 women, age 39.2 +/- 16.3). NO in exhaled air was also measured in 30 healthy control subjects. Disease activity wa s assessed by the European Consensus Lupus Activity Measurement (ECLAM ) scoring system. Results. Mean values of peak concentrations of NO ex haled air were 64.8 +/- 27.9 parts per billion (ppb) in patients and 3 1.6 +/- 7.7 ppb in controls, p < 0.001. Peak NO concentration was dire ctly related to ECLAM activity score (p < 0.05) and inversely related to MEF25 (p < 0.05). Conclusion, NO in exhaled air is significantly in creased and correlated with disease activity in patients with SLE. Whe ther increased NO output depends on respiratory tract inflammation, as the relationship with MEF25 may suggest, or on circulating cytokines produced elsewhere remains to be investigated.