Current Rheumatology Reports

, Volume 12, Issue 5, pp 363–369

Interstitial Lung Disease in Rheumatoid Arthritis


DOI: 10.1007/s11926-010-0116-z

Cite this article as:
Ascherman, D.P. Curr Rheumatol Rep (2010) 12: 363. doi:10.1007/s11926-010-0116-z


Rheumatoid arthritis (RA) is the most common systemic autoimmune disease in the United States, affecting 1% to 2% of the adult population. Although joints and synovium are the primary targets in this disorder, extra-articular manifestations involving the lungs can lead to significant morbidity and excess mortality. Among the various pulmonary complications that occur in RA, interstitial lung disease (ILD) is the most damaging, with effects ranging from subclinical inflammation/scarring to end-stage pulmonary fibrosis. New insights during the past several years have underscored the epidemiologic impact of clinically/functionally significant RA-associated ILD (RA-ILD) and have begun to identify factors contributing to the pathogenesis of this potentially devastating complication of RA. Despite these advancements, the complexity of RA-ILD and the lack of reliable predictors for disease progression highlight the need for improved biomarker development. Establishing such detailed molecular signatures will ultimately guide the application and timing of therapeutic agents that include immunomodulators as well as newly studied antifibrotic agents.


Rheumatoid arthritis (RA) Interstitial lung disease (ILD) Idiopathic pulmonary fibrosis (IPF) Usual interstitial pneumonia (UIP) Citrullination 

Copyright information

© Springer Science+Business Media, LLC 2010

Authors and Affiliations

  1. 1.Department of Medicine, Division of Rheumatology and Clinical ImmunologyUniversity of Pittsburgh School of MedicinePittsburghUSA