<i>MUC5B</i> Promoter Variant and Rheumatoid Arthritis with Interstitial Lung Disease

Pierre‐Antoine Juge(Inserm), Joyce Lee(Inserm), Esther Ebstein(Inserm), Hiroshi Furukawa(University of Tsukuba), Evgenia Dobrinskikh(Inserm), Steven Gazal(Broad Institute), Caroline Kannengiesser(Inserm), Sébastien Ottaviani(Inserm), Shomi Oka(University of Tsukuba), Shigeto Tohma(Inserm), Naoyuki Tsuchiya(University of Tsukuba), Jorge Rojas‐Serrano(Inserm), Montserrat I. González-Pérez(Inserm), Mayra Mejía(Inserm), Ivette Buendía-Roldán(Inserm), Ramcés Falfán‐Valencia(Inserm), Enrique Ambrocio-Ortiz(Inserm), Effrosyni D. Manali(Inserm), Spyros A. Papiris(Inserm), T. Karageorgas(Inserm), Dimitrios T. Boumpas(Inserm), Κατερίνα Αντωνίου(University of Crete), Coline H.M. van Moorsel(Inserm), Joanne van der Vis(Inserm), Yaël A de Man(Inserm), Jan C. Grutters(Inserm), Yaping Wang(Inserm), Raphaël Borie(Inserm), Lidwine Wémeau-Stervinou(Target (United States)), B. Wallaert(Target (United States)), René‐Marc Flipo(Inserm), Hilario Nunès(Inserm), Dominique Valeyre(Inserm), Nathalie Saidenberg-Kermanac’h(Inserm), Marie‐Christophe Boissier(Inserm), S. Marchand‐Adam(Inserm), Aline Frazier(Inserm), Pascal Richette(Inserm), Yannick Allanore(Inserm), Jean Sibilia(Inserm), Claire Dromer(Inserm), Christophe Richez(Inserm), Thierry Schaeverbeke(Inserm), H. Lioté(Inserm), Gabriel Thabut(Inserm), Nadia Nathan(Inserm), Serge Amselem(Inserm), Martin Soubrier(Inserm), Vincent Cottin(Université Claude Bernard Lyon 1), Annick Clément(Inserm), Kevin D. Deane(Inserm), Avram Walts(Inserm), Tasha E. Fingerlin(Inserm), Aryeh Fischer(Inserm), Jay H. Ryu(Inserm), Eric L. Matteson(Inserm), Timothy B. Niewold(Mayo Clinic), Deborah Assayag(Mayo Clinic), Andrew Gross(Mayo Clinic), Paul J. Wolters(Mayo Clinic), Marvin I. Schwarz(Inserm), Michael Holers(Inserm), Joshua J. Solomon(Inserm), Tracy J. Doyle(Brigham and Women's Hospital), Iván O. Rosas(Brigham and Women's Hospital), Cornelis Blauwendraat(Inserm), Mike A. Nalls(Inserm), Marie‐Pierre Debray(Inserm), Cathérine Boileau(Inserm), Bruno Crestani(Inserm), David A. Schwartz(Inserm), Philippe Dieudé(Inserm)
New England Journal of Medicine
October 20, 2018
Cited by 497Open Access
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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: ). 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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