MUC5B Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease.
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Abstract | BACKGROUND: Given the phenotypic similarities between rheumatoid arthritis (RA)-associated interstitial lung disease (ILD) (hereafter, RA-ILD) and idiopathic pulmonary fibrosis, we hypothesized that the strongest risk factor for the development of idiopathic pulmonary fibrosis, the gain-of-function MUC5B promoter variant rs35705950, would also contribute to the risk of ILD among patients with RA. METHODS: Using a discovery population and multiple validation populations, we tested the association of the MUC5B promoter variant rs35705950 in 620 patients with RA-ILD, 614 patients with RA without ILD, and 5448 unaffected controls. RESULTS: Analysis of the discovery population revealed an association of the minor allele of the MUC5B promoter variant with RA-ILD when patients with RA-ILD were compared with unaffected controls (adjusted odds ratio, 3.8; 95% confidence interval [CI], 2.8 to 5.2; P=9.7×10). The MUC5B promoter variant was also significantly overrepresented among patients with RA-ILD, as compared with unaffected controls, in an analysis of the multiethnic case series (adjusted odds ratio, 5.5; 95% CI, 4.2 to 7.3; P=4.7×10) and in a combined analysis of the discovery population and the multiethnic case series (adjusted odds ratio, 4.7; 95% CI, 3.9 to 5.8; P=1.3×10). In addition, the MUC5B promoter variant was associated with an increased risk of ILD among patients with RA (adjusted odds ratio in combined analysis, 3.1; 95% CI, 1.8 to 5.4; P=7.4×10), particularly among those with evidence of usual interstitial pneumonia on high-resolution computed tomography (adjusted odds ratio in combined analysis, 6.1; 95% CI, 2.9 to 13.1; P=2.5×10). However, no significant association with the MUC5B promoter variant was observed for the diagnosis of RA alone. CONCLUSIONS: We found that the MUC5B promoter variant was associated with RA-ILD and more specifically associated with evidence of usual interstitial pneumonia on imaging. (Funded by Société Française de Rhumatologie and others.). |
Year of Publication | 2018
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Journal | N Engl J Med
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Volume | 379
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Issue | 23
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Pages | 2209-2219
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Date Published | 2018 Dec 06
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ISSN | 1533-4406
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DOI | 10.1056/NEJMoa1801562
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PubMed ID | 30345907
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PubMed Central ID | PMC6371965
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Grant list | P01 HL092870 / HL / NHLBI NIH HHS / United States
KL2 TR000143 / TR / NCATS NIH HHS / United States
R21 HL120770 / HL / NHLBI NIH HHS / United States
K23 AR051461 / AR / NIAMS NIH HHS / United States
UH2 HL123442 / HL / NHLBI NIH HHS / United States
U01 AI101981 / AI / NIAID NIH HHS / United States
K23 HL138131 / HL / NHLBI NIH HHS / United States
Z01 AG000949 / Intramural NIH HHS / United States
R01 HL097163 / HL / NHLBI NIH HHS / United States
R33 HL120770 / HL / NHLBI NIH HHS / United States
UH3 HL123442 / HL / NHLBI NIH HHS / United States
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