Methotrexate, leflunomide and tacrolimus use and the progression of rheumatoid arthritis-associated interstitial lung disease

Author:

Kim Ji-Won1ORCID,Chung Sang Wan2,Pyo Jung Yoon3,Chang Sung Hae4ORCID,Kim Min Uk5,Park Chan Ho6,Lee Ji Sung7ORCID,Lee Jeong Seok8,Ha You-Jung9,Kang Eun Ha9ORCID,Lee Yeon-Ah2,Park Yong-Beom3,Lee Eun Young10ORCID,Choe Jung-Yoon1

Affiliation:

1. Division of Rheumatology, Department of Internal Medicine, Daegu Catholic University School of Medicine , Daegu, Republic of Korea

2. Division of Rheumatology, Department of Internal Medicine, Kyung Hee University Medical Center , Seoul, Republic of Korea

3. Division of Rheumatology, Department of Internal Medicine, Yonsei University College of Medicine , Seoul, Republic of Korea

4. Division of Rheumatology, Department of Internal Medicine, Soonchunhyang University College of Medicine , Cheonan, Republic of Korea

5. Department of Radiology, Seoul Metropolitan Government-Seoul National University Boramae Medical Center , Seoul, Republic of Korea

6. Department of Radiology, Soonchunhyang University College of Medicine , Cheonan, Republic of Korea

7. Department of Medical Statistics, Clinical Research Center, Asan Institute for Life Sciences, Asan Medical Center , Seoul, Republic of Korea

8. Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST) , Daejeon, Republic of Korea

9. Division of Rheumatology, Department of Internal Medicine, Seoul National University Bundang Hospital , Seongnam, Republic of Korea

10. Division of Rheumatology, Department of Internal Medicine, Seoul National University College of Medicine , Seoul, Republic of Korea

Abstract

Abstract Objective To examine the association between MTX, LEF and tacrolimus use and the progression of RA-associated interstitial lung disease (ILD). Methods The Korean RA-ILD cohort prospectively enrolled patients with RA-associated ILD at multiple centres from 2015 to 2018 and followed up with them for 3 years. ILD progression was defined by any of the followings: a decrease of ≥10% in forced vital capacity, a decrease of ≥15% in the diffusing capacity of the lung for carbon monoxide, or death from respiratory failure. Results Of 143 patients, 64 patients experienced ILD progression during a median follow-up period of 33 months. The use of MTX [adjusted hazard ratio (aHR), 1.06; 95% CI, 0.59, 1.89], LEF (aHR, 1.75; 95% CI, 0.88, 3.46) and tacrolimus (aHR, 0.94; 95% CI, 0.52, 1.72) did not increase the risk of ILD progression. However, the association between LEF use and the risk of ILD progression was significant in subgroups with poor lung function (aHR, 8.42; 95% CI, 2.61, 27.15). Older age, male sex, a shorter RA duration, higher RA disease activity and extensive disease at baseline were independently associated with ILD progression. Conclusion None of the three treatments increased the risk of RA-associated ILD progression, except for LEF, which increased the risk of ILD progression in patients with severe ILD. The appropriate use of conventional synthetic disease-modifying antirheumatic drugs considering RA disease activity and ILD severity would be important for the management of RA-associated ILD.

Funder

Seoul National University Hospital

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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1. Research Progress of Progressive Pulmonary Fibrosis;Advances in Clinical Medicine;2024

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