New England Journal of Medicine · 2018 · 502 citations · 33 references
Life SciencesGeneticsMolecular GeneticsAutoimmunityMedical GeneticsRheumatologyAutoimmune Disease Susceptibility GenesDisease Susceptibility LociFibrosisImmune-mediated Inflammatory DiseasesInterstitial Lung DiseaseRheumatoid ArthritisAutoimmune-associated Interstitial Lung DiseaseConnective Tissue Disease - Associated Interstitial Lung DiseaseConnective Tissue Disease-associated Interstitial Lung DiseaseFibrotic Interstitial Lung DiseaseInterstitital Lung DiseasePulmonary Fibrosis Progression
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: ). 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.).
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