<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Oka S</submitter><funding>Japan Research Foundation for Clinical Pharmacology</funding><funding>Astellas Pharma Inc.</funding><funding>the Japan Society for the Promotion of Science</funding><funding>National Hospital Organization</funding><funding>The Nakatomi Foundation</funding><funding>Abbott Japan Co., Ltd.</funding><funding>the Ministry of Health, Labour, and Welfare of Japan</funding><funding>Merck Sharp and Dohme Inc.</funding><funding>Chugai Pharmaceutical Co., Ltd.</funding><funding>Takeda Science Foundation</funding><funding>Mitsubishi Tanabe Pharma Corporation</funding><funding>Bristol-Myers Squibb Co.</funding><funding>Eisai Co., Ltd.</funding><funding>Japan Agency for Medical Research and Development</funding><funding>Mitsui Sumitomo Insurance Welfare Foundation</funding><funding>Daiwa Securities Health Foundation</funding><funding>Teijin Pharma Limited</funding><funding>Pfizer Japan Inc.</funding><funding>Takeda Pharmaceutical Company Limited</funding><pagination>363</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9962840</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>59(2)</volume><pubmed_abstract>Chronic lung diseases (CLD), including interstitial lung disease (ILD) and airway diseases (ADs), are common complications of rheumatoid arthritis (RA). Rheumatoid factor (RF) and anti-citrullinated peptide antibodies are reported to be associated with CLD in RA patients. The presence of anti-melanoma differentiation-associated gene 5 (MDA5) antibodies (Abs) is associated with clinically amyopathic dermatomyositis developing into rapidly progressive ILD. However, few studies on anti-MDA5 Abs in RA have been published. Here, we analyzed the association of anti-MDA5 Abs with CLD complications in RA. Anti-MDA5 Abs were quantified in sera from RA patients with or without CLD. Anti-MDA5 Ab levels were higher in RA patients with ADs than without (mean ± SDM, 4.4 ± 2.4 vs. 4.0 ± 4.2, &lt;i>p =&lt;/i> 0</pubmed_abstract><journal>Medicina (Kaunas, Lithuania)</journal><pubmed_title>Antibodies against Serum Anti-Melanoma Differentiation-Associated Gene 5 in Rheumatoid Arthritis Patients with Chronic Lung Diseases.</pubmed_title><pmcid>PMC9962840</pmcid><funding_grant_id>22591090, 26293123, 15K09543, 18K08402</funding_grant_id><pubmed_authors>Furukawa H</pubmed_authors><pubmed_authors>Komiya A</pubmed_authors><pubmed_authors>Hashimoto A</pubmed_authors><pubmed_authors>Okamoto A</pubmed_authors><pubmed_authors>Yoshikawa N</pubmed_authors><pubmed_authors>Fukui N</pubmed_authors><pubmed_authors>Higuchi T</pubmed_authors><pubmed_authors>Shimada K</pubmed_authors><pubmed_authors>Matsui T</pubmed_authors><pubmed_authors>Oka S</pubmed_authors><pubmed_authors>Tohma S</pubmed_authors><pubmed_authors>Katayama M</pubmed_authors><pubmed_authors>Saisho K</pubmed_authors><pubmed_authors>Migita K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antibodies against Serum Anti-Melanoma Differentiation-Associated Gene 5 in Rheumatoid Arthritis Patients with Chronic Lung Diseases.</name><description>Chronic lung diseases (CLD), including interstitial lung disease (ILD) and airway diseases (ADs), are common complications of rheumatoid arthritis (RA). Rheumatoid factor (RF) and anti-citrullinated peptide antibodies are reported to be associated with CLD in RA patients. The presence of anti-melanoma differentiation-associated gene 5 (MDA5) antibodies (Abs) is associated with clinically amyopathic dermatomyositis developing into rapidly progressive ILD. However, few studies on anti-MDA5 Abs in RA have been published. Here, we analyzed the association of anti-MDA5 Abs with CLD complications in RA. Anti-MDA5 Abs were quantified in sera from RA patients with or without CLD. Anti-MDA5 Ab levels were higher in RA patients with ADs than without (mean ± SDM, 4.4 ± 2.4 vs. 4.0 ± 4.2, &lt;i>p =&lt;/i> 0</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-04T21:43:15.555Z</modification><creation>2025-04-04T21:43:15.555Z</creation></dates><accession>S-EPMC9962840</accession><cross_references><pubmed>36837566</pubmed><doi>10.3390/medicina59020363</doi></cross_references></HashMap>