Original Article

The Association of Anti-Aminoacyl-Transfer Ribonucleic Acid Synthetase Antibodies in Patients With Rheumatoid Arthritis and Interstitial Lung Disease

Volume: 33 Issue: 1, March 2018 Publish Date: March 31, 2018
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Masakazu MATSUSHITA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan image/svg+xml
Naoto TAMURA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan image/svg+xml
Michihiro OGASAWARA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan image/svg+xml
Kurisu TADA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan image/svg+xml
Ken YAMAJI
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan image/svg+xml
Yoshinari TAKASAKI
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan image/svg+xml
Masakazu MATSUSHITA, Naoto TAMURA, Michihiro OGASAWARA, Kurisu TADA, Ken YAMAJI, & Yoshinari TAKASAKI. (2018). The Association of Anti-Aminoacyl-Transfer Ribonucleic Acid Synthetase Antibodies in Patients With Rheumatoid Arthritis and Interstitial Lung Disease. Archives of Rheumatology, 33(1), 026–032. https://doi.org/10.5606/ArchRheumatol.2018.6401
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Abstract

Objectives: This study aims to analyze the distribution and clinicopathological characteristics of anti-aminoacyl-transfer ribonucleic acid (tRNA) synthetase (ARS) antibodies in rheumatoid arthritis patients.

Patients and methods: We retrospectively studied the anti-ARS antibody levels in 228 RA patients’ (44 males, 184 females; mean age 62.9±14.0 years; range 23 to 88 years) sera from their medical charts. We determined the association with anti-cyclic citrullinated peptide antibody levels, interstitial lung disease (ILD), rheumatoid factor, and methotrexate or biological disease modifying antirheumatic drug treatments.

Results: Anti-ARS antibodies were detected in 14 RA patients (6.1%). ILD complications were significantly higher among anti-ARS antibody-positive patients (57.1% vs 22.4%, p<0.05). Levels of anti-threonyl-tRNA-synthetase (anti-PL-7) and anti-alanyl-tRNA-synthetase (anti-PL-12), two anti-ARS antibodies, were higher in RA patients with concurrent ILD (both p<0.05). Myositis and ILD worsening were not observed in three anti-ARS antibody- positive patients despite biological disease modifying antirheumatic drug administration. There was no difference in anti-cyclic citrullinated peptide and rheumatoid factor specificities between patients with or without ARS antibodies.

Conclusion: Anti-ARS antibodies were detected in RA patients, with higher prevalence in patients with concurrent ILD. RA patients, specifically those with ILD complications, should be tested for anti-ARS antibodies.

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Article Info
Published In
Journal Archives of Rheumatology
Volume / Issue Vol. 33 No. 1 (2018): The Archives of Rheumatology
Pages 026-032
History
Published Online March 31, 2018
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Affiliations
1
Masakazu MATSUSHITA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan
2
Naoto TAMURA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan
3
Michihiro OGASAWARA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan
4
Kurisu TADA
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan
5
Ken YAMAJI
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan
6
Yoshinari TAKASAKI
Department of Internal Medicine and Rheumatology, Juntendo University, School of Medicine, Tokyo, Japan
Cite this Article
Masakazu MATSUSHITA, Naoto TAMURA, Michihiro OGASAWARA, Kurisu TADA, Ken YAMAJI, & Yoshinari TAKASAKI. (2018). The Association of Anti-Aminoacyl-Transfer Ribonucleic Acid Synthetase Antibodies in Patients With Rheumatoid Arthritis and Interstitial Lung Disease. Archives of Rheumatology, 33(1), 026–032. https://doi.org/10.5606/ArchRheumatol.2018.6401
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