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Protective effect of methotrexate on lung function and mortality in rheumatoid arthritis-related interstitial lung disease: a retrospective cohort study

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dc.contributor.author강영애-
dc.contributor.author김송이-
dc.contributor.author김영삼-
dc.contributor.author김은영-
dc.contributor.author박무석-
dc.contributor.author박영목-
dc.contributor.author용승현-
dc.contributor.author우아라-
dc.contributor.author이상훈-
dc.contributor.author이수환-
dc.contributor.author임아영-
dc.contributor.author정경수-
dc.contributor.author정지예-
dc.date.accessioned2023-03-03T02:06:48Z-
dc.date.available2023-03-03T02:06:48Z-
dc.date.issued2022-01-
dc.identifier.issn1753-4658-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/192739-
dc.description.abstractBackground: Studies on the risk and protective factors for lung function decline and mortality in rheumatoid arthritis-related interstitial lung disease (RA-ILD) are limited. Objectives: We aimed to investigate clinical factors and medication uses associated with lung function decline and mortality in RA-ILD. Methods: This retrospective cohort study examined the medical records of patients with RA-ILD who visited Severance Hospital between January 2006 and December 2019. We selected 170 patients with RA-ILD who had undergone at least one spirometry test and chest computed tomography scan. An absolute decline of ⩾10% in the functional vital capacity (FVC) was defined as significant decline in pulmonary function. Data for analysis were retrieved from electronic medical records. Results: Ninety patients (52.9%) were female; the mean age was 64.0 ± 10.2 years. Multivariate logistic regression showed that a high erythrocyte sediment rate level at baseline [odds ratio (OR) = 3.056; 95% confidence interval (CI) = 1.183-7.890] and methotrexate (MTX) use (OR = 0.269; 95% CI = 0.094-0.769) were risk and protective factors for lung function decline, respectively. Multivariate Cox regression analysis indicated that age ⩾65 years (OR = 2.723; 95% CI = 1.142-6.491), radiologic pattern of usual interstitial pneumonia (UIP) or probable UIP (OR = 3.948; 95% CI = 1.522-10.242), baseline functional vital capacity (FVC) % predicted (OR = 0.971; 95% CI = 0.948-0.994), and MTX use (OR = 0.284; 95% CI = 0.091-0.880) were predictive of mortality. Conclusion: We identified risk and protective factors for lung function decline and mortality in patients with RA-ILD. MTX use was associated with favorable outcome in terms of both lung function and mortality in our cohort.-
dc.description.statementOfResponsibilityopen-
dc.languageEnglish-
dc.publisherSAGE Publications-
dc.relation.isPartOfTHERAPEUTIC ADVANCES IN RESPIRATORY DISEASE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAged-
dc.subject.MESHArthritis, Rheumatoid* / complications-
dc.subject.MESHArthritis, Rheumatoid* / drug therapy-
dc.subject.MESHCohort Studies-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHIdiopathic Pulmonary Fibrosis*-
dc.subject.MESHLung / diagnostic imaging-
dc.subject.MESHLung Diseases, Interstitial* / drug therapy-
dc.subject.MESHLung Diseases, Interstitial* / etiology-
dc.subject.MESHMale-
dc.subject.MESHMethotrexate / therapeutic use-
dc.subject.MESHMiddle Aged-
dc.subject.MESHRetrospective Studies-
dc.titleProtective effect of methotrexate on lung function and mortality in rheumatoid arthritis-related interstitial lung disease: a retrospective cohort study-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Internal Medicine (내과학교실)-
dc.contributor.googleauthorKangjoon Kim-
dc.contributor.googleauthorAla Woo-
dc.contributor.googleauthorYoungmok Park-
dc.contributor.googleauthorSeung Hyun Yong-
dc.contributor.googleauthorSu Hwan Lee-
dc.contributor.googleauthorSang Hoon Lee-
dc.contributor.googleauthorAh Young Leem-
dc.contributor.googleauthorSong Yee Kim-
dc.contributor.googleauthorKyung Soo Chung-
dc.contributor.googleauthorEun Young Kim-
dc.contributor.googleauthorJi Ye Jung-
dc.contributor.googleauthorYoung Ae Kang-
dc.contributor.googleauthorYoung Sam Kim-
dc.contributor.googleauthorMoo Suk Park-
dc.identifier.doi10.1177/17534666221135314-
dc.contributor.localIdA00057-
dc.contributor.localIdA00626-
dc.contributor.localIdA00707-
dc.contributor.localIdA00811-
dc.contributor.localIdA01457-
dc.contributor.localIdA05828-
dc.contributor.localIdA06000-
dc.contributor.localIdA06223-
dc.contributor.localIdA02836-
dc.contributor.localIdA02904-
dc.contributor.localIdA03382-
dc.contributor.localIdA03570-
dc.contributor.localIdA03735-
dc.relation.journalcodeJ04378-
dc.identifier.eissn1753-4666-
dc.identifier.pmid36346076-
dc.subject.keywordinterstitial lung disease-
dc.subject.keywordmethotrexate-
dc.subject.keywordmortality-
dc.subject.keywordpulmonary function-
dc.subject.keywordrheumatoid arthritis-
dc.contributor.alternativeNameKang, Young Ae-
dc.contributor.affiliatedAuthor강영애-
dc.contributor.affiliatedAuthor김송이-
dc.contributor.affiliatedAuthor김영삼-
dc.contributor.affiliatedAuthor김은영-
dc.contributor.affiliatedAuthor박무석-
dc.contributor.affiliatedAuthor박영목-
dc.contributor.affiliatedAuthor용승현-
dc.contributor.affiliatedAuthor우아라-
dc.contributor.affiliatedAuthor이상훈-
dc.contributor.affiliatedAuthor이수환-
dc.contributor.affiliatedAuthor임아영-
dc.contributor.affiliatedAuthor정경수-
dc.contributor.affiliatedAuthor정지예-
dc.citation.volume16-
dc.citation.startPage17534666221135314-
dc.identifier.bibliographicCitationTHERAPEUTIC ADVANCES IN RESPIRATORY DISEASE, Vol.16 : 17534666221135314, 2022-01-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers

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