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Erschienen in: Clinical Rheumatology 1/2016

01.01.2016 | Original Article

Predictive factors of rapidly progressive-interstitial lung disease in patients with clinically amyopathic dermatomyositis

verfasst von: Y. Xu, C. S. Yang, Y. J. Li, X. D. Liu, J. N. Wang, Q. Zhao, W. G. Xiao, P. T. Yang

Erschienen in: Clinical Rheumatology | Ausgabe 1/2016

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Abstract

Clinically amyopathic dermatomyositis (CADM) is a unique subset of dermatomyositis, showing a high incidence of lung involvements. The aim of this study is to identify risk factors, other than melanoma differentiation-associated protein (MDA)-5, for developing rapidly progressive-interstitial lung disease (RP-ILD) in patients with CADM. Forty CADM patients, in whom 11 patients developed RP-ILD, were enrolled. Clinical features and laboratory findings were compared between the patients with and without RP-ILD. We found that skin ulceration, CRP, serum ferritin, anti-MDA5 Ab, and lymphocytopenia were significantly associated with ILD. Multivariate logistic regression analysis indicated that anti-MDA5 Ab+, elevated CRP, and decreased counts of lymphocyte were independent risk factors for RP-ILD, which can provide a precise predict for RP-ILD in CADM patients. When anti-MDA5 Ab+ was removed from the multivariate regression model, using skin ulcerations, elevated serum ferritin and decreased counts of lymphocyte can also precisely predict RP-ILD. Except for MDA-5, more commonly available clinical characteristics, such as skin ulcerations, serum ferritin, and count of lymphocyte may also help to predict prognosis in CADM.
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Metadaten
Titel
Predictive factors of rapidly progressive-interstitial lung disease in patients with clinically amyopathic dermatomyositis
verfasst von
Y. Xu
C. S. Yang
Y. J. Li
X. D. Liu
J. N. Wang
Q. Zhao
W. G. Xiao
P. T. Yang
Publikationsdatum
01.01.2016
Verlag
Springer London
Erschienen in
Clinical Rheumatology / Ausgabe 1/2016
Print ISSN: 0770-3198
Elektronische ISSN: 1434-9949
DOI
https://doi.org/10.1007/s10067-015-3139-z

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