Association of a Single Nucleotide Variant in TERT with Airway Disease in Japanese Rheumatoid Arthritis Patients

Genes (Basel). 2023 Nov 16;14(11):2084. doi: 10.3390/genes14112084.

Abstract

Interstitial lung disease and airway disease (AD) are often complicated with rheumatoid arthritis (RA) and have a poor prognosis. Several studies reported genetic associations with interstitial lung disease in RA. However, few genetic studies have examined the susceptibility to AD in RA patients. Here, we investigated whether single nucleotide variants susceptible to idiopathic pulmonary fibrosis might be associated with interstitial lung disease or AD in Japanese RA patients. Genotyping of rs2736100 [C/A] in TERT and rs1278769 [G/A] in ATP11A was conducted in 98 RA patients with usual interstitial pneumonia, 120 with nonspecific interstitial pneumonia (NSIP), 227 with AD, and 422 without chronic lung disease using TaqMan assays. An association with AD in RA was found for rs2736100 (p = 0.0043, Pc = 0.0129, odds ratio [OR] 1.40, 95% confidence interval [CI] 1.11-1.77). ATP11A rs1278769 was significantly associated with NSIP in older RA patients (>65 years, p = 0.0010, OR 2.15, 95% CI 1.35-3.40). This study first reported an association of rs2736100 with AD in RA patients and ATP11A rs1278769 with NSIP in older RA patients.

Keywords: airway disease; genetic association; nonspecific interstitial pneumonia; rheumatoid arthritis; single nucleotide variant.

MeSH terms

  • Aged
  • Arthritis, Rheumatoid* / genetics
  • East Asian People
  • Humans
  • Idiopathic Pulmonary Fibrosis* / genetics
  • Lung Diseases, Interstitial* / complications
  • Lung Diseases, Interstitial* / genetics
  • Nucleotides
  • Telomerase* / genetics

Substances

  • Nucleotides
  • TERT protein, human
  • Telomerase