Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows

Rheumatoid arthritis (RA) is a chronic and systemic inflammatory disease affecting 0.5–1% of the population worldwide. Interstitial lung disease (ILD) is a serious pulmonary complication of RA and it is responsible for 10–20% of mortality, with a mean survival of 5–8 years. However, nowadays there a...

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Main Authors: Giulia Cassone, Andreina Manfredi, Caterina Vacchi, Fabrizio Luppi, Francesca Coppi, Carlo Salvarani, Marco Sebastiani
Format: Article
Language:English
Published: MDPI AG 2020-04-01
Series:Journal of Clinical Medicine
Subjects:
Online Access:https://www.mdpi.com/2077-0383/9/4/1082
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author Giulia Cassone
Andreina Manfredi
Caterina Vacchi
Fabrizio Luppi
Francesca Coppi
Carlo Salvarani
Marco Sebastiani
author_facet Giulia Cassone
Andreina Manfredi
Caterina Vacchi
Fabrizio Luppi
Francesca Coppi
Carlo Salvarani
Marco Sebastiani
author_sort Giulia Cassone
collection DOAJ
description Rheumatoid arthritis (RA) is a chronic and systemic inflammatory disease affecting 0.5–1% of the population worldwide. Interstitial lung disease (ILD) is a serious pulmonary complication of RA and it is responsible for 10–20% of mortality, with a mean survival of 5–8 years. However, nowadays there are no therapeutic recommendations for the treatment of RA-ILD. Therapeutic options for RA-ILD are complicated by the possible pulmonary toxicity of many disease modifying anti-rheumatic drugs (DMARDs) and by their unclear efficacy on pulmonary disease. Therefore, joint and lung involvement should be evaluated independently of each other for treatment purposes. On the other hand, some similarities between RA-ILD and idiopathic pulmonary fibrosis and the results of the recent INBIULD trial suggest a possible future role for antifibrotic agents. From this perspective, we review the current literature describing the pulmonary effects of drugs (immunosuppressants, conventional, biological and target synthetic DMARDs and antifibrotic agents) in patients with RA and ILD. In addition, we suggest a framework for the management of RA-ILD patients and outline a research agenda to fill the gaps in knowledge about this challenging patient cohort.
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spelling doaj.art-25ff3a57500a43dcbe0c5d5df05108582023-11-19T21:16:08ZengMDPI AGJournal of Clinical Medicine2077-03832020-04-0194108210.3390/jcm9041082Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and ShadowsGiulia Cassone0Andreina Manfredi1Caterina Vacchi2Fabrizio Luppi3Francesca Coppi4Carlo Salvarani5Marco Sebastiani6Clinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, 41124 Modena, ItalyChair and Rheumatology Unit, University of Modena and Reggio Emilia, Azienda Ospedaliero-Universitaria Policlinico di Modena, 41124 Modena, ItalyClinical and Experimental Medicine PhD Program, University of Modena and Reggio Emilia, 41124 Modena, ItalyRespiratory Unit, University of Milano Bicocca, S. Gerardo Hospital, 20900 Monza, ItalyDepartment of Cardiology, University of Modena and Reggio Emilia, Azienda Ospedaliero-Univesitaria Policlinico di Modena, 41124 Modena, ItalyChair and Rheumatology Unit, University of Modena and Reggio Emilia, Azienda Ospedaliero-Universitaria Policlinico di Modena, 41124 Modena, ItalyChair and Rheumatology Unit, University of Modena and Reggio Emilia, Azienda Ospedaliero-Universitaria Policlinico di Modena, 41124 Modena, ItalyRheumatoid arthritis (RA) is a chronic and systemic inflammatory disease affecting 0.5–1% of the population worldwide. Interstitial lung disease (ILD) is a serious pulmonary complication of RA and it is responsible for 10–20% of mortality, with a mean survival of 5–8 years. However, nowadays there are no therapeutic recommendations for the treatment of RA-ILD. Therapeutic options for RA-ILD are complicated by the possible pulmonary toxicity of many disease modifying anti-rheumatic drugs (DMARDs) and by their unclear efficacy on pulmonary disease. Therefore, joint and lung involvement should be evaluated independently of each other for treatment purposes. On the other hand, some similarities between RA-ILD and idiopathic pulmonary fibrosis and the results of the recent INBIULD trial suggest a possible future role for antifibrotic agents. From this perspective, we review the current literature describing the pulmonary effects of drugs (immunosuppressants, conventional, biological and target synthetic DMARDs and antifibrotic agents) in patients with RA and ILD. In addition, we suggest a framework for the management of RA-ILD patients and outline a research agenda to fill the gaps in knowledge about this challenging patient cohort.https://www.mdpi.com/2077-0383/9/4/1082rheumatoid arthritisinterstitial lung diseasetherapyDMARDsantifibrotic agents
spellingShingle Giulia Cassone
Andreina Manfredi
Caterina Vacchi
Fabrizio Luppi
Francesca Coppi
Carlo Salvarani
Marco Sebastiani
Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows
Journal of Clinical Medicine
rheumatoid arthritis
interstitial lung disease
therapy
DMARDs
antifibrotic agents
title Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows
title_full Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows
title_fullStr Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows
title_full_unstemmed Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows
title_short Treatment of Rheumatoid Arthritis-Associated Interstitial Lung Disease: Lights and Shadows
title_sort treatment of rheumatoid arthritis associated interstitial lung disease lights and shadows
topic rheumatoid arthritis
interstitial lung disease
therapy
DMARDs
antifibrotic agents
url https://www.mdpi.com/2077-0383/9/4/1082
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AT fabrizioluppi treatmentofrheumatoidarthritisassociatedinterstitiallungdiseaselightsandshadows
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