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Clinical course of lung physiology in patients with scleroderma and interstitial lung disease: Analysis of the Scleroderma Lung Study Placebo Group.

Authors :
Khanna, Dinesh
Tseng, Chi-Hong
Farmani, Niloofar
Steen, Virginia
Furst, Daniel E.
Clements, Philip J.
Roth, Michael D.
Goldin, Jonathan
Elashoff, Robert
Seibold, James R.
Saggar, Rajeev
Tashkin, Donald P.
Source :
Arthritis & Rheumatism. Oct2011, Vol. 63 Issue 10, p3078-3085. 8p.
Publication Year :
2011

Abstract

Objective Patients with systemic sclerosis-associated interstitial lung disease (SSc-ILD) are thought to have the greatest decline in lung function (forced vital capacity [FVC] % predicted) in the early years after disease onset. The aim of this study was to assess the natural history of the decline in FVC % predicted in patients receiving placebo in the Scleroderma Lung Study and to evaluate possible factors for cohort enrichment in future therapeutic trials. Methods Patients randomized to receive placebo (n = 79) were divided into 3 groups based on the duration of SSc (0-2 years, 2-4 years, and >4 years). Descriptive statistics and a mixed-effects model were used to analyze the rate of decline in the FVC % predicted over a 1-year period. Additional analyses stratified according to the severity of fibrosis on high-resolution computed tomography (HRCT) were performed, and interactions between disease severity and disease duration were explored. Results The mean ± SD decline in the unadjusted FVC % predicted during the 1-year period was 4.2 ± 12.8%. At baseline, 28.5%, 43.0%, and 28.5% of patients were in the groups with disease durations of 0-2 years, 2-4 years, and >4 years, respectively. The rate of decline in the FVC % predicted was not significantly different across the 3 disease groups ( P = 0.85). When stratified by baseline fibrosis on HRCT, the rate of decline in the FVC % predicted was statistically significantly greater in the group with severe fibrosis (mean annualized decline in the FVC % predicted 7.2% versus 2.7% in the groups with no or moderate fibrosis; P = 0.008). The decline observed in the group with severe fibrosis was most pronounced in those with a relatively short disease duration (0-2 years; annualized decline 7.0%). Conclusion Among patients with SSc-ILD in the Scleroderma Lung Study, the rates of progression of lung disease were similar irrespective of disease duration. The baseline HRCT fibrosis score is a predictor of a future decline in the FVC % predicted in the absence of effective treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00043591
Volume :
63
Issue :
10
Database :
Academic Search Index
Journal :
Arthritis & Rheumatism
Publication Type :
Academic Journal
Accession number :
65925537
Full Text :
https://doi.org/10.1002/art.30467