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

Authors
 Ji-Won Kim  ;  Sang Wan Chung  ;  Jung Yoon Pyo  ;  Sung Hae Chang  ;  Min Uk Kim  ;  Chan Ho Park  ;  Ji Sung Lee  ;  Jeong Seok Lee  ;  You-Jung Ha  ;  Eun Ha Kang  ;  Yeon-Ah Lee  ;  Yong-Beom Park  ;  Eun Young Lee  ;  Jung-Yoon Choe 
Citation
 RHEUMATOLOGY, Vol.62(7) : 2377-2385, 2023-07 
Journal Title
RHEUMATOLOGY
ISSN
 1462-0324 
Issue Date
2023-07
MeSH
Antirheumatic Agents* / adverse effects ; Arthritis, Rheumatoid* / chemically induced ; Arthritis, Rheumatoid* / complications ; Arthritis, Rheumatoid* / drug therapy ; Humans ; Leflunomide / therapeutic use ; Lung Diseases, Interstitial* / complications ; Lung Diseases, Interstitial* / etiology ; Male ; Methotrexate / adverse effects ; Tacrolimus / adverse effects
Keywords
LEF ; MTX ; RA ; interstitial lung disease ; progression-free survival ; tacrolimus
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. © The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.
Full Text
https://academic.oup.com/rheumatology/article/62/7/2377/6832032
DOI
10.1093/rheumatology/keac651
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Park, Yong Beom(박용범)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/198376
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