Associations of the MUC5B promoter variant with timing of interstitial lung disease and rheumatoid arthritis onset.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
28 11 2022
Historique:
received: 15 12 2021
revised: 04 03 2022
pubmed: 16 3 2022
medline: 2 12 2022
entrez: 15 3 2022
Statut: ppublish

Résumé

To investigate the associations of the common MUC5B promoter variant with timing of RA-associated interstitial lung disease (RA-ILD) and RA onset. We identified patients with RA meeting 2010 ACR/EULAR criteria and available genotype information in the Mass General Brigham Biobank, a multihospital biospecimen and clinical data collection research study. We determined RA-ILD presence by reviewing all RA patients who had CT imaging, lung biopsy or autopsy results. We determined the dates of RA and RA-ILD diagnoses by manual records review. We examined the associations of the MUC5B promoter variant (G>T at rs35705950) with RA-ILD, RA-ILD occurring before or within 2 years of RA diagnosis and RA diagnosis at age >55 years. We used multivariable logistic regression to estimate odds ratios (ORs) for each outcome by MUC5B promoter variant status, adjusting for potential confounders including genetic ancestry and smoking. We identified 1005 RA patients with available genotype data for rs35705950 (mean age 45 years, 79% female, 81% European ancestry). The MUC5B promoter variant was present in 155 (15.4%) and was associated with RA-ILD [multivariable OR 3.34 (95% CI 1.97, 5.60)], RA-ILD before or within 2 years of RA diagnosis [OR 4.01 (95% CI 1.78, 8.80)] and RA onset after age 55 years [OR 1.52 (95% CI 1.08, 2.12)]. The common MUC5B promoter variant was associated with RA-ILD onset earlier in the RA disease course and older age of RA onset. These findings suggest that the MUC5B promoter variant may impact RA-ILD risk early in the RA disease course, particularly in patients with older-onset RA.

Identifiants

pubmed: 35289841
pii: 6548814
doi: 10.1093/rheumatology/keac152
pmc: PMC9707325
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

4915-4923

Subventions

Organisme : NIAMS NIH HHS
ID : R01 AR077607
Pays : United States
Organisme : NHLBI NIH HHS
ID : R03 HL148484
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR070253
Pays : United States
Organisme : NIAMS NIH HHS
ID : T32 AR055885
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR072577
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL155522
Pays : United States

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved. For permissions, please email: journals.permissions@oup.com.

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Auteurs

Gregory McDermott (G)

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

Ritu Gill (R)

Department of Medicine, Harvard Medical School.
Department of Radiology, Beth Israel Deaconess Medical Center.

Staci Gagne (S)

Department of Medicine, Harvard Medical School.
Department of Radiology, Brigham and Women's Hospital, Boston, MA.

Suzanne Byrne (S)

Department of Medicine, Harvard Medical School.
Department of Radiology, Brigham and Women's Hospital, Boston, MA.

Weixing Huang (W)

Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital.

Jing Cui (J)

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

Lauren Prisco (L)

Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital.

Alessandra Zaccardelli (A)

Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital.

Lily Martin (L)

Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital.

Vanessa L Kronzer (VL)

Division of Rheumatology, Mayo Clinic, Rochester, MN.

Matthew Moll (M)

Department of Medicine, Harvard Medical School.
Division of Pulmonary and Critical Care Medicine.
Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.

Michael H Cho (MH)

Department of Medicine, Harvard Medical School.
Division of Pulmonary and Critical Care Medicine.
Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, USA.

Nancy Shadick (N)

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

Paul F Dellaripa (PF)

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

Tracy Doyle (T)

Department of Medicine, Harvard Medical School.
Division of Pulmonary and Critical Care Medicine.

Jeffrey A Sparks (JA)

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

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