Chest
Volume 102, Issue 3, September 1992, Pages 875-881
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Clinical Investigations
Small Airways Dysfunction in Systemic Sclerosis: A Controlled Study

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A debate exists regarding the importance of small airways disease in systemic sclerosis, while smoking seems to have a major effect on the exact prevalence. In order to evaluate small airways dysfunction (SAD) in a pure systemic sclerosis population, we performed pulmonary function studies in 31 nonsmoking patients and 31 age- and sex-matched nonsmoking control subjects. Patients’ FVC, TLC, and Dco mean values were significantly lower compared with the corresponding values of the controls (p<0.05), while there was no difference in MEF25, RV, and RV/TLC. Seven (22.6 percent) of 31 patients and four controls (a nonsignificant difference) had evidence of SAD, namely a maximum expiratory flow at 25 percent of vital capacity (MEF25) less than 60 percent of predicted. Positive correlation (p<0.001) was found between MEF25 and FEV1/FVC in the patients. Moreover, no differences were found in abnormal lung function patients with and those without SAD in demographic, clinical, roentgenologic, and serologic features and results of pulmonary function tests. These findings suggest that SAD in our patients is not a characteristic and early manifestation of systemic sclerosis and that, when present, it is not correlated with the severity of the pulmonary involvement in scleroderma.

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Materials and Methods

Thirty-one nonsmoking consecutive patients (28 female, three male) with definite progressive systemic sclerosis according to the American Rheumatism Association criteria13 were studied. All the patients satisfied the single major criterion for classification of definite progressive systemic sclerosis (proximal scleroderma). The 31 patients were classified as having diffuse cutaneous systemic sclerosis or the limited cutaneous form of the disease according to the classification of LeRoy.14 All

Results

Twenty-eight out of the 31 patients were women. The mean age ± SD of the patients was 51.5 ± 13.4 years (range, 18 to 64 years) and the mean duration of the disease was 6.4 ± 4.6 years (range, 1 to 20 years). Twenty (18 female, 2 males) of 31 patients were classified as having diffuse cutaneous systemic sclerosis, while the remaining 11 (10 female, 1 male) patients had the limited cutaneous form of the disease.

Thirteen (42 percent) of 31 patients had a history of dyspnea on exertion and/or

Discussion

Changes in pathologic findings of large and small airways have been reported in patients with scleroderma, but the prevalence and significance of functional abnormalities in the small airways have not been defined unequivocally. During the last years, high prevalence of SAD has been reported occasionally in scleroderma.7, 8, 10 However, most of the related studies are not controlled and include smoking patients, which probably affects the reported prevalence.11 Therefore, using the pulmonary

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