Association of the <i>RPA3-UMAD1</i> locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese.
cross_sectional · Level IV
Where this comes from
- Record sourced from PubMed, PMID 32737115.
- Also identified by DOI 10.1136/annrheumdis-2020-217256 and PMC identifier 7509520.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The genetic background of rheumatoid arthritis-interstitial lung disease (RA-ILD) has been evaluated in Europeans, but little knowledge has been obtained in non-Europeans. This study aimed to elucidate genome-wide risk of RA-ILD in non-Europeans. We performed an initial genome-wide association study (GWAS) of RA-ILD in the Japanese population. By conducting the meta-analysis of the three GWAS datasets of the RA cohorts and biobank of Japanese, our study included 358 RA-ILD cases and 4550 RA subjects without ILD. We then conducted the stratified analysis of the effect of the GWAS risk allele in each CT image pattern. We identified one novel RA-ILD risk locus at 7p21 that satisfied the genome-wide significance threshold (rs12702634 at <i>RPA3-UMAD1</i>, OR=2.04, 95% CI 1.59 to 2.60, p=1.5×10<sup>-8</sup>). Subsequent stratified analysis based on the CT image patterns demonstrated that the effect size of the RA-ILD risk allele (rs12702634-C) was large with the UIP pattern (OR=1.86, 95% CI 0.97 to 3.58, p=0.062) and the probable UIP pattern (OR=2.26, 95% CI 1.36 to 3.73, p=0.0015). We revealed one novel genetic association with RA-ILD in Japanese. The RA-ILD risk of the identified variant at <i>RPA3-UMAD1</i> was relatively high in the CT image patterns related to fibrosis. Our study should contribute to elucidation of the complicated aetiology of RA-ILD.
Medical subject headings
- Arthritis, Rheumatoid
- DNA-Binding Proteins
- Lung Diseases, Interstitial