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RPA3-UMAD1 rs12702634 and rheumatoid arthritis-associated interstitial lung disease in European ancestry.
Juge, Pierre-Antoine; Sparks, Jeffrey A; Gazal, Steven; Ebstein, Esther; Borie, Raphaël; Debray, Marie-Pierre; Kannengiesser, Caroline; McDermott, Gregory C; Cui, Jing; Hayashi, Keigo; Doyle, Tracy J; van Moorsel, Coline H M; van der Vis, Joanne J; Grutters, Jan C; Knevel, Rachel; Heckert, Sascha L; Vasarmidi, Eirini; Antoniou, Katerina M; van der Helm van Mil, Annette H M; Boileau, Catherine; Crestani, Bruno; Dieudé, Philippe.
Affiliation
  • Juge PA; Université de Paris Cité, INSERM UMR 1152, Paris, France.
  • Sparks JA; Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.
  • Gazal S; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.
  • Ebstein E; Harvard Medical School, Boston, MA, USA.
  • Borie R; Department of Population and Public Health Sciences, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Debray MP; Center for Genetic Epidemiology, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Kannengiesser C; Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.
  • McDermott GC; Université de Paris Cité, INSERM UMR 1152, Paris, France.
  • Cui J; Service de Pneumologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.
  • Hayashi K; Service de Radiologie, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.
  • Doyle TJ; Université de Paris Cité, INSERM UMR 1152, Paris, France.
  • van Moorsel CHM; Service de Génétique, Hôpital Bichat-Claude Bernard, AP-HP, Paris, France.
  • van der Vis JJ; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.
  • Grutters JC; Harvard Medical School, Boston, MA, USA.
  • Knevel R; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.
  • Heckert SL; Harvard Medical School, Boston, MA, USA.
  • Vasarmidi E; Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA, USA.
  • Antoniou KM; Harvard Medical School, Boston, MA, USA.
  • van der Helm van Mil AHM; Harvard Medical School, Boston, MA, USA.
  • Boileau C; Division of Pulmonary and Critical Care, Brigham and Women's Hospital, Boston, MA, USA.
  • Crestani B; Interstitial Lung Disease Center of Excellence, Department of Pulmonology, St Antonius Hospital, Nieuwegein, The Netherlands.
  • Dieudé P; Division of Heart and Lungs, University Medical Center Utrecht, Utrecht, The Netherlands.
Rheumatol Adv Pract ; 8(2): rkae059, 2024.
Article in En | MEDLINE | ID: mdl-38854416
ABSTRACT

Objective:

Recently, a genome-wide association study identified an association between RA-associated interstitial lung disease (ILD) and RPA3-UMAD1 rs12702634 in the Japanese population, especially for patients with a usual interstitial pneumonia (UIP) pattern. We aimed to replicate this association in a European population and test for interaction with MUC5B rs35705950.

Methods:

In this genetic case-control association study, patients with RA and ILD and controls with RA and no ILD were included from France, the USA and the Netherlands. Only cases and controls from European genetic ancestries determined by principal components analysis were included in the analyses. RA was defined by the 1987 ACR or 2010 ACR/EULAR criteria and ILD by chest high-resolution CT scan, except in the control dataset from the Netherlands, where the absence of ILD was determined by chart review. Patients were genotyped for RPA3-UMAD1 rs12702634 and MUC5B rs35705950. Associations were tested using logistic regression adjusted for sex, age at RA onset, age at ILD onset or at certified absence of ILD, tobacco smoking status and country of origin.

Results:

Among the 883 patients included, 322 were RA-ILD cases (36.5%). MUC5B rs35705950 was strongly associated with RA-ILD in all datasets {combined adjusted odds ratio [OR] 2.9 [95% CI 2.1, 3.9], P = 1.1 × 10-11. No association between RPA3-UMAD1 rs12702634 and RA-ILD was observed [combined OR 1.2 (95% CI 0.8, 1.6), P = 0.31. No interaction was found between RPA3-UMAD1 rs12702634 and MUC5B rs35705950 (P = 0.70).

Conclusion:

Our findings did not support a contribution of RPA3-UMAD1 rs12702634 to the overall RA-ILD susceptibility in the European population.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Rheumatol Adv Pract Year: 2024 Document type: Article Affiliation country: Francia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Rheumatol Adv Pract Year: 2024 Document type: Article Affiliation country: Francia