Pulmonary involvement in juvenile dermatomyositis: a two-year longitudinalstudy

Citation
S. Trapani et al., Pulmonary involvement in juvenile dermatomyositis: a two-year longitudinalstudy, RHEUMATOLOG, 40(2), 2001, pp. 216-220
Citations number
27
Categorie Soggetti
Rheumatology
Journal title
RHEUMATOLOGY
ISSN journal
14620324 → ACNP
Volume
40
Issue
2
Year of publication
2001
Pages
216 - 220
Database
ISI
SICI code
1462-0324(200102)40:2<216:PIIJDA>2.0.ZU;2-G
Abstract
Objective. To investigate the prevalence and features of asymptomatic pulmo nary involvement in juvenile dermatomyositis (JDM). Methods. Twelve JDM patients underwent pulmonary function tests at baseline , 12 and 24 months. Disease activity, duration, serum lactate dehydrogenase (LDH) values and antinuclear antibody (ANA) titres were also evaluated. Results. Five patients showed lung impairment at baseline and four at 12 an d 24 months. Forced expiratory volume in 1 s, forced vital capacity (FVC), carbon monoxide diffusing capacity (DLCO) and alveolar volume were the most frequently altered variables, indicating a restrictive pattern and impairm ent of diffusion. The prevalence and features of pulmonary alterations did not change during follow-up. FVC values were significantly lower in active JDM patients and were inversely related to LDH. DLCO values were significan tly lower in ANA-positive patients. About half of the patients of this smal l case series of JDM had asymptomatic lung disease. Conclusions. We suggest that lung function should be evaluated at disease o nset and regularly during follow-up, as pulmonary function tests can detect otherwise unpredictable pulmonary involvement.