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Exhaled nitric oxide is elevated in patients with progressive systemic sclerosis without interstitial lung disease
1Respiratory Unit, Department of Medicine, University of Natal, Durban, South Africa.
Chest
|May 12, 2001
Summary
Exhaled nitric oxide (NO) is elevated in patients with progressive systemic sclerosis (PSS) even without lung disease, indicating subclinical inflammation. This noninvasive marker may help predict interstitial lung disease (ILD) progression in PSS patients.
Area of Science:
- Pulmonary Medicine
- Rheumatology
- Biomarker Discovery
Background:
- Progressive systemic sclerosis (PSS) is a multisystem disease where interstitial lung disease (ILD) is a leading cause of mortality.
- Identifying predictors of ILD onset or progression in PSS is crucial for patient management.
- Abnormal bronchoalveolar lavage fluid (BALF) cellularity has been observed in PSS patients without evident ILD.
Purpose of the Study:
- To evaluate exhaled nitric oxide (NO) as a noninvasive marker of pulmonary inflammation in PSS patients.
- To compare exhaled NO levels with bronchoalveolar lavage fluid (BALF) cellularity.
- To test the hypothesis that elevated exhaled NO correlates with abnormal BALF cellularity in PSS patients without ILD.
Main Methods:
- Exhaled NO was measured using chemiluminescence in 12 PSS patients with ILD, 12 PSS patients without ILD, and 30 healthy controls.
- Bronchoalveolar lavage (BAL) was performed on PSS patients (with and without ILD) and six healthy controls.
- Study conducted at a university-based, tertiary referral hospital in Durban, South Africa.
Main Results:
- Subclinical inflammation was confirmed by increased inflammatory cell counts in BALF of PSS patients without ILD.
- Exhaled NO levels were significantly higher in PSS patients without ILD (9.6 ppb) compared to those with ILD (6.2 ppb) and healthy controls (6.3 ppb).
- Elevated exhaled NO in PSS patients without ILD suggests underlying pulmonary inflammation.
Conclusions:
- Exhaled nitric oxide (NO) shows promise as a noninvasive surrogate marker for inflammation in PSS patients.
- This finding could aid in early detection and monitoring of pulmonary involvement in PSS.
- Further research may establish exhaled NO as a valuable tool in managing PSS-related lung complications.