In a prospective study, Type III procollagen N-terminal peptide was measured in the sera of 38 subjects with biopsy-proven pulmonary sarcoidosis at 6-month intervals over a period of 5 yr. The subjects were divided into four groups according to their radiologic presentation and clinical course: Group A (n = 10) subjects with sarcoidosis Type I without radiologic progression over 5 yr; Group B (n = 5) subjects with sarcoidosis Type I with radiologic progression to Stage II or III; Group C (n = 9) subjects with sarcoidosis Types II and III without progression over 5 yr; and Group D (n = 14) subjects with sarcoidosis Types II and III with radiologic progression. Lung function tests (FVC, FEV1, and DL(CO)), chest roentgenograms, and measurements of serum angiotensin converting enzyme (S-ACE) were performed concurrently with the S-PCP-III levels. Significantly higher levels of S-PCP- III were found in group B (Type I, progressive) (18.2 ± 1.09 ng/ml) and in group D (Type II/III, progressive) (13.9 ± 1.2 ng/ml) compared with those of Group A (Type I, stable) (9.1 ± 1.09 ng/ml) and Group C (Type II/III, stable) (7.6 ± 1.1 ng/ml) or normal volunteers (9.4 ± 4 ng/ml) (p < 0.001 for all comparisons). Changes in S-PCP-III levels tended to parallel the clinical course, and steroid treatment resulted in a significant decrease in S-PCP-III concentrations (p < 0.001). In contrast, serum angiotensin converting enzyme (S-ACE) levels did not correlate with either the clinical course or radiologic changes. In conclusion, subjects with active sarcoidosis demonstrated significantly higher S-PCP-III levels than subjects with inactive disease. Additionally, increased S-PCP-III concentrations could be observed in subjects who deteriorated clinically and radiologically within the period of observation.
|Original language||English (US)|
|Number of pages||6|
|Journal||American Review of Respiratory Disease|
|Issue number||2 II SUPPL.|
|State||Published - Jan 1 1992|
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine