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MUC5B promoter variant rs35705950, rare but significant susceptibility locus in rheumatoid arthritis-interstitial lung disease with usual interstitial pneumonia in Asian populationsopen access

Authors
Joo, Young BinAhn, Soo MinBang, So-YoungPark, YounghoHong, Su JinLee, YoukyungCho, Soo-KyungChoi, Chan-BumSung, Yoon-KyoungKim, Tae-HwanJun, Jae-BumYoo, Dae HyunBae, Sang-CheolLee, Hye-Soon
Issue Date
Dec-2022
Publisher
EULAR | BMJ Publishing Group Ltd
Keywords
arthritis; rheumatoid; polymorphism; genetic
Citation
RMD Open, v.8, no.2, pp 1 - 7
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
RMD Open
Volume
8
Number
2
Start Page
1
End Page
7
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/182348
DOI
10.1136/rmdopen-2022-002790
ISSN
2056-5933
Abstract
Background MUC5B variant rs35705950 is the common and most significant risk variant for rheumatoid arthritis-interstitial lung disease (RA-ILD) in Western populations. However, little is known about its significant association with RA-ILD in Asian populations. We here investigate the association of rs35705950 with Korean patients with RA-ILD. Methods In this cross-sectional study, we genotyped rs35705950 in 2444 patients with RA. Among them, 683 patients with RA who have chest CT were divided into RA-ILD and RA-noILD. RA-ILD was classified as usual interstitial pneumonia (UIP) and other than UIP. The associations of rs35705950 with RA-ILD and its subtype were analysed using multivariable regression adjusted for age at RA diagnosis. Meta-analysis of a previously reported Japanese dataset and Korean dataset obtained for this study was conducted. Results The minor allele (T) frequency of rs35705950 was 0.37%, 1.43% and 2.38% in 2444 patients with RA, 105 patients with RA-ILD and 63 patients with UIP, respectively. Genotypic association of rs35705950 with RA-ILD was insignificant (OR 2.49, 95% CI 0.64 to 9.69, p=0.187), but showed significant association with UIP (OR 4.90, 95% CI 1.23 to 19.59, p=0.024) compared with RA-noILD. In meta-analysis (123 UIP and 878 RA-noILD) combining our data with previously reported Japanese data, this variant was found to be significantly associated with UIP (OR 3.51, 95% CI 1.19 to 10.37, p=0.023). Conclusion MUC5B variant rs35705950 is a rare but significant risk factor for Asian patients with RA-ILD with UIP, suggesting a sharing of the genetic background between Asian and Western populations.
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서울 의과대학 (DEPARTMENT OF INTERNAL MEDICINE)
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