Rheumatoid arthritis-associated interstitial lung disease: an overview

Rheumatoid arthritis (RA) is a chronic systemic autoimmune disorder characterized by synovial joint inflammation, leading to progressive joint damage, deformity, and disability. The lungs are the most common site for extra-articular manifestation, and significant Interstitial lung disease can occur in one in ten RA patients, leading to a significant increase in disability and mortality. This puts a substantial strain on patients and healthcare resources. The current understanding of RA and its manifestations remains limited. This review article explores the currently available data and literature.

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Publication Details

Journal
QJM
Published
2025-10-29
DOI
https://doi.org/10.1093/qjmed/hcaf260
Citations
2
Primary Topic
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
Type
article
Field-Weighted Citation Impact
3.04
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article

Rheumatoid arthritis-associated interstitial lung disease: an overview

Anne‐Michelle Noone, Orla Buckley, Khaled Musameh, S. O'Brien et al.
2 citations
QJM
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
3.04
article

Rheumatoid arthritis-associated interstitial lung disease: an overview

Anne‐Michelle Noone, Orla Buckley, Khaled Musameh, S. O'Brien, Thomas Bütler
article en
2 citations

Abstract

Rheumatoid arthritis (RA) is a chronic systemic autoimmune disorder characterized by synovial joint inflammation, leading to progressive joint damage, deformity, and disability. The lungs are the most common site for extra-articular manifestation, and significant Interstitial lung disease can occur in one in ten RA patients, leading to a significant increase in disability and mortality. This puts a substantial strain on patients and healthcare resources. The current understanding of RA and its manifestations remains limited. This review article explores the currently available data and literature.

QJMVol. 119(1)
Tallaght University Hospital (IE)
Openalex Percentile: Top 7%
Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
3.04
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