Evidence map›Paper›PMID 39504460›Full record

ArticleRheumatology (Oxford, England)2025

MUC5B promoter variant and survival in rheumatoid arthritis-associated interstitial lung disease.

Jacob Klein, Austin M Wheeler, Joshua F Baker, Yangyuna Yang, Punyasha Roul, Halie Frideres, Katherine D Wysham, Gail S Kerr, Andreas Reimold, Dana P Ascherman and 7 more

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Rheumatoid Lung Disease.Mediterranean journal of rheumatology · 2025
    Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Jacob KleinDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.
Austin M WheelerDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.ORCID 0000-0002-8816-7782
Joshua F BakerDepartment of Medicine, Division of Rheumatology, Corporal Michael J. Crescenz VA Medical Center and University of Pennsylvania, Philadelphia, PA, USA.
Yangyuna YangDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.
Punyasha RoulDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.
Halie FrideresDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.
Katherine D WyshamDepartment of Internal Medicine, Division of Rheumatology, VA Puget Sound Health Care System and University of Washington, Seattle, WA, USA.ORCID 0000-0001-8707-7649
Gail S KerrDepartment of Medicine, Division of Rheumatology, Washington D.C. VA, Howard University, & Georgetown University, Washington, DC, USA.
Andreas ReimoldDepartment of Internal Medicine, Rheumatic Diseases Division, Dallas VA & University of Texas Southwestern, Dallas, TX, USA.
Dana P AschermanDepartment of Medicine, Division of Rheumatology & Clinical Immunology, Pittsburgh VA & University of Pittsburgh, Pittsburgh, PA, USA.
Gary A KunkelDepartment of Internal Medicine, Division of Rheumatology, VA Salt Lake City Health Care System and University of Utah, Salt Lake City, UT, USA.
Grant W CannonDepartment of Internal Medicine, Division of Rheumatology, VA Salt Lake City Health Care System and University of Utah, Salt Lake City, UT, USA.ORCID 0000-0001-6640-9173
Paul A MonachBoston VA, Boston, MA, USA.
Jill A PooleDepartment of Internal Medicine, Division of Allergy & Immunology, University of Nebraska Medical Center, Omaha, NE, USA.
Geoffrey M ThieleDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.
Ted R MikulsDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.
Bryant R EnglandDepartment of Internal Medicine, Division of Rheumatology & Immunology, VA Nebraska Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, USA.ORCID 0000-0002-9649-3588

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RIZZO, MATTHEW · 2016 to 2025
$42.8M
BLRD VA I01 BX003635BLRD VA I01 BX004660Central States Center of Agricultural Safety and HealthCSRD VA I01 CX001703CSRD VA IK2 CX002203CSRD VA IK2 CX002351Department of Defence PR200793Department of Veterans Affairs Clinical Sciences Research & Development BX003635Department of Veterans Affairs Clinical Sciences Research & Development BX004660Department of Veterans Affairs Clinical Sciences Research & Development CX001703Department of Veterans Affairs Clinical Sciences Research & Development CX002203Department of Veterans Affairs Clinical Sciences Research & Development RX003644Department of Veterans Affairs Clinicl Sciences Research & Development CX002351National Institute for Occupational Safety R01OH012045NIGMS NIH HHS U54 GM115458NIOSH CDC HHS R01 OH012045NIOSH CDC HHS U54 OH010162Rheumatology Research FoundationRRD VA I01 RX003644U.S. Department of Defense PR200793
6 · The paper itself

Abstract

objectiveThe objective of this study was to investigate the association between the MUC5B rs35705950 promoter variant and survival in RA-associated interstitial lung disease (RA-ILD).

methodsWe studied participants in the Veteran Affairs Rheumatoid Arthritis (VARA) registry with validated ILD diagnoses. Participants were followed until death or till the end of the study period. The MUC5B rs35705950 promoter variant was measured using an Infinium genotyping array, assuming autosomal dominant inheritance. Survival and cause of death were determined from VA death records and the National Death Index. Associations of the MUC5B promoter variant with survival were tested in Cox regression models, adjusting for potential confounders.

resultsAmong 263 participants with RA-ILD (mean age 69 years, 95% male, 73% White, 85% smoking history), the MUC5B promoter variant was present in 33.5%. The mortality rate was similar between those with [12.2/100 PY (95% CI: 9.4, 15.8)] and without [11.1/100 PY (95% CI: 9.1, 13.5)] the variant. MUC5B status was not significantly associated with survival overall [aHR 0.97 (95% CI: 0.68, 1.37)] or when stratified by ILD pattern [clinical usual interstitial pneumonia (UIP) aHR 0.86 (95% CI: 0.55, 1.35); clinical non-UIP aHR 1.15 (95% CI: 0.63, 2.09)]. Further, MUC5B status was not significantly associated with respiratory-related [aHR 0.83 (95% CI: 0.42, 1.66)] or non-respiratory causes of death [aHR 1.08 (95% CI: 0.72, 1.62)].

conclusionWhile associated with RA-ILD risk, the MUC5B promoter variant was not predictive of survival among RA-ILD patients in this multicentre cohort. Further studies are needed to identify other genetic and non-genetic prognostic factors in RA-ILD to inform disease management.

Indexed as

Arthritis, RheumatoidLung Diseases, InterstitialMucin-5BPromoter Regions, GeneticAgedFemaleHumansMaleMiddle AgedRegistriesMUC5B protein, humanMucin-5Bgeneticsinterstitial lung diseaserheumatoid arthritissurvival

Identifiers

PMID39504460
PMCPMC12695044

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.