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

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dc.contributor.authorKim, Ji-Wonko
dc.contributor.authorChung, Sang Wanko
dc.contributor.authorPyo, Jung Yoonko
dc.contributor.authorChang, Sung Haeko
dc.contributor.authorKim, Min Ukko
dc.contributor.authorPark, Chan Hoko
dc.contributor.authorLee, Ji Sungko
dc.contributor.authorLee, Jeong Seokko
dc.contributor.authorHa, You-Jungko
dc.contributor.authorKang, Eun Hako
dc.contributor.authorLee, Yeon-Ahko
dc.contributor.authorPark, Yong-Beomko
dc.contributor.authorLee, Eun Youngko
dc.contributor.authorChoe, Jung-Yoonko
dc.date.accessioned2023-07-21T01:00:42Z-
dc.date.available2023-07-21T01:00:42Z-
dc.date.created2023-01-09-
dc.date.issued2023-07-
dc.identifier.citationRHEUMATOLOGY, v.62, no.7, pp.2377 - 2385-
dc.identifier.issn1462-0324-
dc.identifier.urihttp://hdl.handle.net/10203/310740-
dc.description.abstractObjective 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.-
dc.languageEnglish-
dc.publisherOXFORD UNIV PRESS-
dc.titleMethotrexate, leflunomide and tacrolimus use and the progression of rheumatoid arthritis-associated interstitial lung disease-
dc.typeArticle-
dc.identifier.wosid000897732800001-
dc.identifier.scopusid2-s2.0-85164240714-
dc.type.rimsART-
dc.citation.volume62-
dc.citation.issue7-
dc.citation.beginningpage2377-
dc.citation.endingpage2385-
dc.citation.publicationnameRHEUMATOLOGY-
dc.identifier.doi10.1093/rheumatology/keac651-
dc.contributor.localauthorLee, Jeong Seok-
dc.contributor.nonIdAuthorKim, Ji-Won-
dc.contributor.nonIdAuthorChung, Sang Wan-
dc.contributor.nonIdAuthorPyo, Jung Yoon-
dc.contributor.nonIdAuthorChang, Sung Hae-
dc.contributor.nonIdAuthorKim, Min Uk-
dc.contributor.nonIdAuthorPark, Chan Ho-
dc.contributor.nonIdAuthorLee, Ji Sung-
dc.contributor.nonIdAuthorHa, You-Jung-
dc.contributor.nonIdAuthorKang, Eun Ha-
dc.contributor.nonIdAuthorLee, Yeon-Ah-
dc.contributor.nonIdAuthorPark, Yong-Beom-
dc.contributor.nonIdAuthorLee, Eun Young-
dc.contributor.nonIdAuthorChoe, Jung-Yoon-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorRA-
dc.subject.keywordAuthorinterstitial lung disease-
dc.subject.keywordAuthorMTX-
dc.subject.keywordAuthorLEF-
dc.subject.keywordAuthortacrolimus-
dc.subject.keywordAuthorprogression-free survival-
dc.subject.keywordPlusIDIOPATHIC PULMONARY-FIBROSIS-
dc.subject.keywordPlusRISK-FACTORS-
dc.subject.keywordPlusACUTE EXACERBATION-
dc.subject.keywordPlusAMERICAN-COLLEGE-
dc.subject.keywordPlusINJURY-
dc.subject.keywordPlusCLASSIFICATION-
dc.subject.keywordPlusPNEUMONITIS-
dc.subject.keywordPlusMULTICENTER-
dc.subject.keywordPlusPROGNOSIS-
dc.subject.keywordPlusDIAGNOSIS-
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