Serum Anti-Aminoacyl-Transfer Ribonucleic Acid Synthetase Antibody Levels Are Involved in Rheumatoid Arthritis Complicated with Interstitial Lung Disease
<b>Objectives:</b> A common complication in patients with rheumatoid arthritis (RA) is interstitial lung disease (ILD). Antibodies (Abs) to anti-aminoacyl-transfer ribonucleic acid synthetase (ARS) are linked to ILD in patients with idiopathic inflammatory myopathies (IIM). There have been limited studies of anti-ARS Abs in RA. In this study, we examined anti-ARS Abs in ILD in patients with RA. <b>Methods:</b> Anti-ARS Abs in serum from patients with RA were measured. <b>Results:</b> There were higher anti-ARS Ab levels in RA patients with ILD (mean ± SDM, 16.3 ± 32.3 vs. 7.4 ± 7.0 (Index), <i>p</i> = 5.58 × 10<sup>-12</sup>), usual interstitial pneumonia (14.4 ± 24.4 vs. 7.4 ± 7.0 [Index], <i>p</i> = 3.14 × 10<sup>-12</sup>), and nonspecific interstitial pneumonia (17.9 ± 37.7 vs. 7.4 ± 7.0 (Index), <i>p</i> = 5.07 × 10<sup>-5</sup>) compared with patients without chronic lung disease. The area under the curve (AUC) of the receiver operating characteristic curve for anti-ARS Ab was too low to allow for discrimination among RA patients with/without chronic lung disease (0.608, 95% confidence interval (CI) 0.560-0.655, <i>p</i> = 8.69 × 10<sup>-6</sup>). Multiple logistic regression analyses of age, smoking status, anti-ARS Abs, as well as Steinbrocker stage generated an ARS-index with a high AUC value (0.707, 95%CI 0.662-0.752, <i>p</i> = 2.20 × 10<sup>-19</sup>). <b>Conclusions:</b> Anti-ARS Abs are related to ILD pathogenesis in RA and may be a biomarker for ILD.
Authors
- Shigeto Tohma (ORCID: https://orcid.org/0000-0003-4945-7629)
- Takashi Higuchi (ORCID: https://orcid.org/0000-0002-7489-1657)
- Akira Okamoto (ORCID: https://orcid.org/0000-0002-2057-6029)
- Kota Shimada (ORCID: https://orcid.org/0000-0002-2860-4266)
- Norie Yoshikawa
- Hiroshi Furukawa (ORCID: https://orcid.org/0000-0003-1353-8056)
- Kiyoshi Migita (ORCID: https://orcid.org/0000-0003-1339-5622)
- Naoshi Fukui (ORCID: https://orcid.org/0000-0002-8027-038X)
- Akiko Komiya
- Atsushi Hashimoto (ORCID: https://orcid.org/0000-0003-3559-7970)
- Misuzu Fujimori
- Toshihiro Matsui (ORCID: https://orcid.org/0000-0002-7686-3211)
- Masao Katayama
- Koichiro Saisho
- Shomi Oka
Institutions
- Fukushima Medical University (JP)
- Tokyo University of the Arts (JP)
- National Sagamihara Hospital (JP)
- Nagasaki Medical Center (JP)
- Imamura Hospital (JP)
- Himeji Medical Center (JP)
- National Institute of Technology, Miyakonojo College (JP)
- Tokyo Metropolitan Tama Medical Center (JP)
- Nagoya Medical Center (JP)
- Tokyo National Hospital (JP)
- The University of Tokyo (JP)
Publication Details
- Journal
- Journal of Clinical Medicine
- Published
- 2024-11-10
- DOI
- https://doi.org/10.3390/jcm13226761
- Primary Topic
- Viral Infections and Immunology Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Bristol-Myers Squibb
- Pfizer
- Takeda Science Foundation
- Japan Research Foundation for Clinical Pharmacology
- Nakatomi Foundation
- Mitsui Sumitomo Insurance Welfare Foundation
- Abbott Japan
- Japan Agency for Medical Research and Development
- Eisai
- Astellas Pharma
- Daiwa Securities Health Foundation
- Astellas Foundation for Research on Metabolic Disorders
- Teijin Pharma
- Mitsubishi Tanabe Pharma Corporation
- Pfizer Japan
- Chugai Pharmaceutical
- Japan Society for the Promotion of Science