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日本人群中基因座与类风湿关节炎合并间质性肺病的相关性研究。

Association of the locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese.

机构信息

Department of Statistical Genetics, Osaka University Graduate School of Medicine, Suita, Japan.

Department of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, Suita City, Japan.

出版信息

Ann Rheum Dis. 2020 Oct;79(10):1305-1309. doi: 10.1136/annrheumdis-2020-217256. Epub 2020 Jul 31.

DOI:10.1136/annrheumdis-2020-217256
PMID:32737115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7509520/
Abstract

OBJECTIVES

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.

METHODS

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.

RESULTS

We identified one novel RA-ILD risk locus at 7p21 that satisfied the genome-wide significance threshold (rs12702634 at , OR=2.04, 95% CI 1.59 to 2.60, p=1.5×10). 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).

CONCLUSION

We revealed one novel genetic association with RA-ILD in Japanese. The RA-ILD risk of the identified variant at was relatively high in the CT image patterns related to fibrosis. Our study should contribute to elucidation of the complicated aetiology of RA-ILD.

摘要

目的

类风湿关节炎-间质性肺病(RA-ILD)的遗传背景在欧洲人群中已得到评估,但在非欧洲人群中了解甚少。本研究旨在阐明非欧洲人群中 RA-ILD 的全基因组风险。

方法

我们在日本人群中进行了 RA-ILD 的全基因组关联研究(GWAS)的初步研究。通过对 RA 队列的三项 GWAS 数据集和日本生物库的荟萃分析,我们的研究纳入了 358 例 RA-ILD 病例和 4550 例无 ILD 的 RA 患者。然后,我们对每个 CT 图像模式的 GWAS 风险等位基因的分层分析进行了分析。

结果

我们在 7p21 上发现了一个新的 RA-ILD 风险位点,该位点达到了全基因组显著阈值(rs12702634 位于 ,OR=2.04,95%CI 1.59 至 2.60,p=1.5×10)。随后基于 CT 图像模式的分层分析表明,RA-ILD 风险等位基因(rs12702634-C)的效应大小较大,与 UIP 模式(OR=1.86,95%CI 0.97 至 3.58,p=0.062)和可能的 UIP 模式(OR=2.26,95%CI 1.36 至 3.73,p=0.0015)相关。

结论

我们在日本人群中发现了一个与 RA-ILD 相关的新的遗传关联。在与纤维化相关的 CT 图像模式中,鉴定出的位于 上的变体与 RA-ILD 的风险相关较高。我们的研究应有助于阐明 RA-ILD 的复杂病因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3c/7509520/866d70114887/annrheumdis-2020-217256f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3c/7509520/87e190cd6057/annrheumdis-2020-217256f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3c/7509520/866d70114887/annrheumdis-2020-217256f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3c/7509520/87e190cd6057/annrheumdis-2020-217256f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb3c/7509520/866d70114887/annrheumdis-2020-217256f02.jpg

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