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

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 t...

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Veröffentlicht in:Rheumatology (Oxford, England) England), 2023-07, Vol.62 (7), p.2377-2385
Hauptverfasser: Kim, Ji-Won, Chung, Sang Wan, Pyo, Jung Yoon, Chang, Sung Hae, Kim, Min Uk, Park, Chan Ho, Lee, Ji Sung, Lee, Jeong Seok, Ha, You-Jung, Kang, Eun Ha, Lee, Yeon-Ah, Park, Yong-Beom, Lee, Eun Young, Choe, Jung-Yoon
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container_end_page 2385
container_issue 7
container_start_page 2377
container_title Rheumatology (Oxford, England)
container_volume 62
creator Kim, Ji-Won
Chung, Sang Wan
Pyo, Jung Yoon
Chang, Sung Hae
Kim, Min Uk
Park, Chan Ho
Lee, Ji Sung
Lee, Jeong Seok
Ha, You-Jung
Kang, Eun Ha
Lee, Yeon-Ah
Park, Yong-Beom
Lee, Eun Young
Choe, Jung-Yoon
description 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. Graphical Abstract
doi_str_mv 10.1093/rheumatology/keac651
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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. Graphical Abstract</description><identifier>ISSN: 1462-0324</identifier><identifier>EISSN: 1462-0332</identifier><identifier>DOI: 10.1093/rheumatology/keac651</identifier><identifier>PMID: 36394143</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Antirheumatic Agents - adverse effects ; Arthritis, Rheumatoid - chemically induced ; Arthritis, Rheumatoid - complications ; Arthritis, Rheumatoid - drug therapy ; Carbon monoxide ; Humans ; Immunomodulators ; Leflunomide ; Leflunomide - therapeutic use ; Lung diseases ; Lung Diseases, Interstitial - complications ; Lung Diseases, Interstitial - etiology ; Male ; Methotrexate ; Methotrexate - adverse effects ; Respiratory function ; Rheumatoid arthritis ; Tacrolimus ; Tacrolimus - adverse effects</subject><ispartof>Rheumatology (Oxford, England), 2023-07, Vol.62 (7), p.2377-2385</ispartof><rights>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 2022</rights><rights>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.</rights><rights>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</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-43a0a8b111cdf34dc4b053c6ae0a9d156375482b5d49a98106787ab7c19258be3</citedby><cites>FETCH-LOGICAL-c375t-43a0a8b111cdf34dc4b053c6ae0a9d156375482b5d49a98106787ab7c19258be3</cites><orcidid>0000-0002-0498-5762 ; 0000-0001-9697-1159 ; 0000-0001-8194-3462 ; 0000-0001-6975-8627 ; 0000-0002-7980-7194</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36394143$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Ji-Won</creatorcontrib><creatorcontrib>Chung, Sang Wan</creatorcontrib><creatorcontrib>Pyo, Jung Yoon</creatorcontrib><creatorcontrib>Chang, Sung Hae</creatorcontrib><creatorcontrib>Kim, Min Uk</creatorcontrib><creatorcontrib>Park, Chan Ho</creatorcontrib><creatorcontrib>Lee, Ji Sung</creatorcontrib><creatorcontrib>Lee, Jeong Seok</creatorcontrib><creatorcontrib>Ha, You-Jung</creatorcontrib><creatorcontrib>Kang, Eun Ha</creatorcontrib><creatorcontrib>Lee, Yeon-Ah</creatorcontrib><creatorcontrib>Park, Yong-Beom</creatorcontrib><creatorcontrib>Lee, Eun Young</creatorcontrib><creatorcontrib>Choe, Jung-Yoon</creatorcontrib><title>Methotrexate, leflunomide and tacrolimus use and the progression of rheumatoid arthritis-associated interstitial lung disease</title><title>Rheumatology (Oxford, England)</title><addtitle>Rheumatology (Oxford)</addtitle><description>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. 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Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Rheumatology (Oxford, England)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Ji-Won</au><au>Chung, Sang Wan</au><au>Pyo, Jung Yoon</au><au>Chang, Sung Hae</au><au>Kim, Min Uk</au><au>Park, Chan Ho</au><au>Lee, Ji Sung</au><au>Lee, Jeong Seok</au><au>Ha, You-Jung</au><au>Kang, Eun Ha</au><au>Lee, Yeon-Ah</au><au>Park, Yong-Beom</au><au>Lee, Eun Young</au><au>Choe, Jung-Yoon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methotrexate, leflunomide and tacrolimus use and the progression of rheumatoid arthritis-associated interstitial lung disease</atitle><jtitle>Rheumatology (Oxford, England)</jtitle><addtitle>Rheumatology (Oxford)</addtitle><date>2023-07-05</date><risdate>2023</risdate><volume>62</volume><issue>7</issue><spage>2377</spage><epage>2385</epage><pages>2377-2385</pages><issn>1462-0324</issn><eissn>1462-0332</eissn><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. Graphical Abstract</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>36394143</pmid><doi>10.1093/rheumatology/keac651</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-0498-5762</orcidid><orcidid>https://orcid.org/0000-0001-9697-1159</orcidid><orcidid>https://orcid.org/0000-0001-8194-3462</orcidid><orcidid>https://orcid.org/0000-0001-6975-8627</orcidid><orcidid>https://orcid.org/0000-0002-7980-7194</orcidid></addata></record>
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source Oxford University Press Journals All Titles (1996-Current); MEDLINE; Alma/SFX Local Collection
subjects Antirheumatic Agents - adverse effects
Arthritis, Rheumatoid - chemically induced
Arthritis, Rheumatoid - complications
Arthritis, Rheumatoid - drug therapy
Carbon monoxide
Humans
Immunomodulators
Leflunomide
Leflunomide - therapeutic use
Lung diseases
Lung Diseases, Interstitial - complications
Lung Diseases, Interstitial - etiology
Male
Methotrexate
Methotrexate - adverse effects
Respiratory function
Rheumatoid arthritis
Tacrolimus
Tacrolimus - adverse effects
title Methotrexate, leflunomide and tacrolimus use and the progression of rheumatoid arthritis-associated interstitial lung disease
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