A Risk Score to Detect Subclinical Rheumatoid Arthritis-Associated Interstitial Lung Disease.


Journal

Arthritis & rheumatology (Hoboken, N.J.)
ISSN: 2326-5205
Titre abrégé: Arthritis Rheumatol
Pays: United States
ID NLM: 101623795

Informations de publication

Date de publication:
11 2022
Historique:
revised: 07 03 2022
received: 19 11 2021
accepted: 10 05 2022
pubmed: 19 5 2022
medline: 2 11 2022
entrez: 18 5 2022
Statut: ppublish

Résumé

Patients at high risk of rheumatoid arthritis-associated interstitial lung disease (RA-ILD) would benefit from being identified before the onset of respiratory symptoms; this can be done by screening patients with the use of chest high-resolution computed tomography (HRCT). Our objective was to develop and validate a risk score for patients who have subclinical RA-ILD. Our study included a discovery population and a replication population from 2 prospective RA cohorts (ESPOIR and TRANSLATE2, respectively) without pulmonary symptoms who had received chest HRCT scans. All patients were genotyped for MUC5B rs35705950. After multiple logistic regression, a risk score based on independent risk factors for subclinical RA-ILD was developed in the discovery population and tested for validation in the replication population. The discovery population included 163 patients with RA, and the replication population included 89 patients with RA. The prevalence of subclinical RA-ILD was 19.0% and 16.9%, respectively. In the discovery population, independent risk factors for subclinical RA-ILD were presence of the MUC5B rs35705950 T allele (odds ratio [OR] 3.74 [95% confidence interval (95% CI) 1.37, 10.39]), male sex (OR 3.93 [95% CI 1.40, 11.39]), older age at RA onset (for each year, OR 1.10 [95% CI 1.04, 1.16]), and increased mean Disease Activity Score in 28 joints using the erythrocyte sedimentation rate (for each unit, OR 2.03 [95% CI 1.24, 3.42]). We developed and validated a derived risk score with receiver operating characteristic areas under the curve of 0.82 (95% CI 0.70-0.94) for the discovery population and 0.78 (95% CI 0.65-0.92) for the replication population. Excluding MUC5B rs35705950 from the model provided a lower goodness of fit (likelihood ratio test, P = 0.01). We developed and validated a risk score that could help identify patients at high risk of subclinical RA-ILD. Our findings support an important contribution of MUC5B rs35705950 to subclinical RA-ILD risk.

Identifiants

pubmed: 35583934
doi: 10.1002/art.42162
pmc: PMC9828082
doi:

Substances chimiques

MUC5B protein, human 0
Mucin-5B 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

1755-1765

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR077607
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR070253
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR072577
Pays : United States

Informations de copyright

© 2022 The Authors. Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology.

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Auteurs

Pierre-Antoine Juge (PA)

Université de Paris, INSERM UMR 1152, F-75018, and Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

Benjamin Granger (B)

Sorbonne Université, Institut Pierre Louis d'Épidémiologie et de Santé Publique Département de Biostatistiques, INSERM UMR 1136, F-75013, and Santé Publique et Information Médicale, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, F-5013, Paris, France.

Marie-Pierre Debray (MP)

Université de Paris, INSERM UMR 1152, F-75018, and Service de Radiologie, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

Esther Ebstein (E)

Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

Fabienne Louis-Sidney (F)

Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

Joanna Kedra (J)

Sorbonne Université, Institut Pierre Louis d'Épidémiologie et de Santé Publique Département de Biostatistiques, INSERM UMR 1136, F-75013, and Service de Rhumatologie, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, F-75013, Paris, France.

Tracy J Doyle (TJ)

Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.

Raphaël Borie (R)

Université de Paris, INSERM UMR 1152, F-75018, Service de Pneumologie A, Centre de compétences maladies pulmonaires rares, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

Arnaud Constantin (A)

Université Toulouse III-Paul Sabatier, INSERM UMR 1043, F-31024, and Service de Rhumatologie, Hôpital Purpan, F-31024, Toulouse, France.

Bernard Combe (B)

Université de Montpellier and Departement de Rhumatologie, Hôpital Lapeyronie, F-34000, Montpellier, France.

René-Marc Flipo (RM)

Université de Lille, and Service de Rhumatologie, Hôpital Salengro, F-59000, Lille, France.

Xavier Mariette (X)

Université Paris-Saclay, INSERM UMR 1184, CEA, F-94270, and Service de Rhumatologie, Hôpital Bicêtre, AP-HP, F-94270, Le Kremlin Bicêtre, France.

Olivier Vittecoq (O)

Rouen University Hospital, Service de Rhumatologie, CIC-CRB 1404, F-76000, and Normandy University, UNIROUEN, INSERM, U1234, FR-76000, Rouen, France.

Alain Saraux (A)

Université de Bretagne Occidentale, INSERM UMR 1227, F-29200, and Service de Rhumatologie, Hôpital de la Cavale Blanche, F-2900, Brest, France.

Guillermo Carvajal-Alegria (G)

Université de Bretagne Occidentale, INSERM UMR 1227, F-29200, and Service de Rhumatologie, Hôpital de la Cavale Blanche, F-2900, Brest, France.

Jean Sibilia (J)

Université de Strasbourg, INSERM UMR S1109, F-67000, and Service de Rhumatologie, RESO: Centre de Reference des Maladies Autoimmunes Systémiques Rares Est Sud-Ouest, Hôpital De Hautepierre, F-67000, Strasbourg, France.

Francis Berenbaum (F)

Sorbonne Université, CRSA, INSERM UMR 938, F-75012, Service de Rhumatologie, Hôpital Saint-Antoine, AP-HP, F-75012, Paris, France.

Caroline Kannengiesser (C)

Université de Paris, INSERM UMR 1152, F-75018, Département de Génétique Moléculaire, Hôpital Bichat-Claude Bernard, AP-HP, FR-75018, Paris, France.

Catherine Boileau (C)

Département de Génétique Moléculaire, Hôpital Bichat-Claude Bernard, AP-HP, FR-75018, Université de Paris, INSERM UMR 1148, F-75018, Paris, France.

Jeffrey A Sparks (JA)

Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.

Bruno Crestani (B)

Université de Paris, INSERM UMR 1152, F-75018, Service de Pneumologie A, Centre de compétences maladies pulmonaires rares, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

Bruno Fautrel (B)

Sorbonne Université, Institut Pierre Louis d'Épidémiologie et de Santé Publique Département de Biostatistiques, INSERM UMR 1136, F-75013, and Service de Rhumatologie, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, F-75013, Paris, France.

Philippe Dieudé (P)

Université de Paris, INSERM UMR 1152, F-75018, and Service de Rhumatologie, Hôpital Bichat-Claude Bernard, AP-HP, F-75018, Paris, France.

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