A LRRC37A2 single nucleotide variant is associated with emphysema in Japanese patients with rheumatoid arthritis
Year: 2026
Type: article
Study design: Observational Study
Abstract: Objective Extra-articular manifestations commonly complicate rheumatoid arthritis (RA) and include chronic lung diseases (CLD), for example, interstitial lung disease or emphysema (EMP). These confer a poor prognosis. Genetic studies of idiopathic pulmonary fibrosis (IPF) or EMP were conducted. However, there are limited genetic studies on EMP in RA. We examined whether a single nucleotide variant associated with susceptibility to IPF was associated to EMP in Japanese RA patients. Methods rs199526 [C/G] genotyping of LRRC37A2 in samples from 88 RA patients with EMP and 425 RA lacking CLD was conducted. Results LRRC37A2 rs199526C was significantly associated to EMP in RA according to an allele model (p = 0.0083, odds ratio [OR] 1.72, 95% confidence interval [CI] 1.14-2.59) or recessive model for major alleles (p = 0.0139, OR 1.82, 95% CI 1.13-2.94), although it was protectively associated against IPF in European populations. Multiple logistic regression analyses revealed an independent association with age, Steinbrocker stage, and Steinbrocker class. An association between LRRC37A2 rs199526 and RA per se was detected. Conclusion An association between rs199526 and EMP was noted in Japanese RA. Differential roles of the single nucleotide variant between EMP in RA and IPF were suggested.
DOI: 10.1093/rap/rkag133
Institutions: Tokyo National Hospital, National Sagamihara Hospital, Tokyo Metropolitan Tama Medical Center, Hyogo Medical University, Sumitomo Hospital, Niigata Rheumatic Center, Himeji Medical Center, Sakurajyuji Hospital, Nagoya Medical Center, National Hospital Organization Miyakonojo Medical Center, Fukushima Medical University, Nagasaki Medical Center, Yokohama Minami Kyosai Hospital
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,974
Funders: Bristol-Myers Squibb, Pfizer, Takeda Pharmaceuticals U.S.A., Japan Research Foundation for Clinical Pharmacology, Nakatomi Foundation, Mitsui Sumitomo Insurance Welfare Foundation, Abbott Japan, Asahi Kasei Pharma Corporation, Dainippon Sumitomo Pharma, Eisai, Astellas Pharma, Daiwa Securities Health Foundation, Teijin Pharma, Mitsubishi Tanabe Pharma Corporation, Ono Pharmaceutical, Pfizer Japan, Chugai Pharmaceutical, Japan Society for the Promotion of Science, Daiichi Sankyo Europe
Awards: Genetic factors of interstitial lung disease associated with polymyositis and dermatomyositis., Genetic Association Study on HLA with Interstitial Lung Diseases in Rheumatoid Arthritis Patients., Elucidation of the genetic factors and the mechanisms of adverse effects by anti-rheumatic drugs., The regulation of the expression of SH2D1A gene in systemic lupus erythematosus., The important roles of a common protective allele HLA-DRB1*13:02 in collagen diseases.
OpenAlex ID: W7224129012
