Association of Airway Disease and Single-Nucleotide Variants in PTPN14 and IL9RP3 in Japanese Cases of Rheumatoid Arthritis

Objectives: Airway disease, commonly related to rheumatoid arthritis (RA), confers an inferior prognosis. Few genetic analyses in RA have investigated patient susceptibility to airway disease. We examined if single-nucleotide variants related to idiopathic pulmonary fibrosis susceptibility were related to airway disease in Japanese cases of RA. Methods: Genotyping for rs4233306 [C/T] in PTPN14 and rs3930589 [T/C] in IL9RP3 in 246 patients with RA and airway disease, and 425 with RA but without chronic lung disease was performed. Results:PTPN14 rs4233306C and IL9RP3 rs3930589T were significantly related to airway disease in RA under a dominant model for minor alleles (p = 0.0398; odds ratio [OR] 1.41; 95% confidence interval [CI] 1.02–1.96; p = 0.0462; OR 3.19; 95% CI 1.06–9.63, respectively). Stratification by male sex resulted in the remaining significant association of PTPN14 rs4233306 with airway disease in RA cases (p = 0.0028; OR 3.70; 95% CI 1.55–8.84). A significant relationship between IL9RP3 rs3930589 and airway disease in RA patients aged > 65 years was noted (p = 0.0135; OR 9.79; 95% CI 1.21–79.20). Conclusions: This is the first study to report associations of rs4233306 and rs3930589 with airway disease in Japanese RA cases.

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Journal
Journal of Personalized Medicine
Published
2026-09-25
DOI
https://doi.org/10.3390/jpm16100498
Primary Topic
Protein Tyrosine Phosphatases
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article
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article

Association of Airway Disease and Single-Nucleotide Variants in PTPN14 and IL9RP3 in Japanese Cases of Rheumatoid Arthritis

Shigeto Tohma, Takashi Higuchi, S Shinohara, Tadashi Nakamura et al.
Journal of Personalized Medicine
Protein Tyrosine Phosphatases
article

Association of Airway Disease and Single-Nucleotide Variants in PTPN14 and IL9RP3 in Japanese Cases of Rheumatoid Arthritis

Shigeto Tohma, Takashi Higuchi, S Shinohara, Tadashi Nakamura, Hiroshi Furukawa, Kiyoshi Migita, Kenji Itoh, Misuzu Fujimori, Toshihiro Matsui, Koichiro Saisho, Shomi Oka, Shouhei Nagaoka, Michita Suzuki, Satoshi Ito, Shinichiro Tsunoda, Kota Shimada
article en

Abstract

Objectives: Airway disease, commonly related to rheumatoid arthritis (RA), confers an inferior prognosis. Few genetic analyses in RA have investigated patient susceptibility to airway disease. We examined if single-nucleotide variants related to idiopathic pulmonary fibrosis susceptibility were related to airway disease in Japanese cases of RA. Methods: Genotyping for rs4233306 [C/T] in PTPN14 and rs3930589 [T/C] in IL9RP3 in 246 patients with RA and airway disease, and 425 with RA but without chronic lung disease was performed. Results:PTPN14 rs4233306C and IL9RP3 rs3930589T were significantly related to airway disease in RA under a dominant model for minor alleles (p = 0.0398; odds ratio [OR] 1.41; 95% confidence interval [CI] 1.02–1.96; p = 0.0462; OR 3.19; 95% CI 1.06–9.63, respectively). Stratification by male sex resulted in the remaining significant association of PTPN14 rs4233306 with airway disease in RA cases (p = 0.0028; OR 3.70; 95% CI 1.55–8.84). A significant relationship between IL9RP3 rs3930589 and airway disease in RA patients aged > 65 years was noted (p = 0.0135; OR 9.79; 95% CI 1.21–79.20). Conclusions: This is the first study to report associations of rs4233306 and rs3930589 with airway disease in Japanese RA cases.

Journal of Personalized MedicineVol. 16(10)
Fukushima Medical University (JP), Hyogo Medical University (JP), Yokohama Minami Kyosai Hospital (JP), Institute for Rheumatic Diseases (Japan) (JP), National Sagamihara Hospital (JP), Sumitomo Hospital (JP), Nagasaki Medical Center (JP), Imamura Hospital (JP), Uji 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), Sakurajyuji Hospital (JP), Niigata Rheumatic Center (JP)
Good health and well-being
Openalex Percentile: Top 19%
Protein Tyrosine Phosphatases
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