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

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dc.contributor.authorKim, Ji-Won-
dc.contributor.authorChung, Sang Wan-
dc.contributor.authorPyo, Jung Yoon-
dc.contributor.authorChang, Sung Hae-
dc.contributor.authorKim, Min Uk-
dc.contributor.authorPark, Chan Ho-
dc.contributor.authorLee, Ji Sung-
dc.contributor.authorLee, Jeong Seok-
dc.contributor.authorHa, You-Jung-
dc.contributor.authorKang, Eun Ha-
dc.contributor.authorLee, Yeon-Ah-
dc.contributor.authorPark, Yong Beom-
dc.contributor.authorLee, Eun Young-
dc.contributor.authorChoe, Jung-Yoon-
dc.date.accessioned2024-03-22T06:04:20Z-
dc.date.available2024-03-22T06:04:20Z-
dc.date.created2023-04-14-
dc.date.issued2023-07-
dc.identifier.issn1462-0324-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/198376-
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.description.statementOfResponsibilityrestriction-
dc.languageEnglish-
dc.publisherOxford University Press-
dc.relation.isPartOfRheumatology-
dc.relation.isPartOfRHEUMATOLOGY-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.titleMethotrexate, leflunomide and tacrolimus use and the progression of rheumatoid arthritis-associated interstitial lung disease-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorKim, Ji-Won-
dc.contributor.googleauthorChung, Sang Wan-
dc.contributor.googleauthorPyo, Jung Yoon-
dc.contributor.googleauthorChang, Sung Hae-
dc.contributor.googleauthorKim, Min Uk-
dc.contributor.googleauthorPark, Chan Ho-
dc.contributor.googleauthorLee, Ji Sung-
dc.contributor.googleauthorLee, Jeong Seok-
dc.contributor.googleauthorHa, You-Jung-
dc.contributor.googleauthorKang, Eun Ha-
dc.contributor.googleauthorLee, Yeon-Ah-
dc.contributor.googleauthorPark, Yong Beom-
dc.contributor.googleauthorLee, Eun Young-
dc.contributor.googleauthorChoe, Jung-Yoon-
dc.identifier.doi10.1093/rheumatology/keac651-
dc.relation.journalcodeJ03672-
dc.identifier.eissn1462-0332-
dc.identifier.pmid36394143-
dc.subject.keywordRA-
dc.subject.keywordinterstitial lung disease-
dc.subject.keywordMTX-
dc.subject.keywordLEF-
dc.subject.keywordtacrolimus-
dc.subject.keywordprogression-free survival-
dc.contributor.alternativeNamePark, Yong Beom-
dc.contributor.affiliatedAuthorPyo, Jung Yoon-
dc.contributor.affiliatedAuthorPark, Yong Beom-
dc.identifier.scopusid2-s2.0-85164240714-
dc.identifier.wosid000897732800001-
dc.citation.volume62-
dc.citation.number7-
dc.citation.startPage2377-
dc.citation.endPage2385-
dc.identifier.bibliographicCitationRheumatology, Vol.62(7) : 2377-2385, 2023-07-
dc.identifier.rimsid78605-
dc.type.rimsART-
dc.description.journalClass1-
dc.description.journalClass1-
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-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalWebOfScienceCategoryRheumatology-
dc.relation.journalResearchAreaRheumatology-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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