Evidence map›Paper›PMID 36470416›Full record

Trial reportChest2023

Treatment Outcomes for Rheumatoid Arthritis-Associated Interstitial Lung Disease: A Real-World, Multisite Study of the Impact of Immunosuppression on Pulmonary Function Trajectory.

Scott M Matson, Misbah Baqir, Teng Moua, Michael Marll, Jessica Kent, Nicholas S Iannazzo, Ryan D Boente, John M Donatelli, Junqiang Dai, Francisco J Diaz and 7 more

Open access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Chest, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 6 pooled it
10.8field-weighted citation impact, top 1% of its field
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

57 citing papers in PubMed, 6 syntheses or guidelines pooled it, 79 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Pooled it
  5. Guideline
  6. Guideline
  7. Mycophenolate and azathioprine in fibrotic interstitial lung disease.American journal of respiratory and critical care medicine · 2026
    Observational
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. HE4: a potential diagnostic biomarker in autoimmune diseases.Central-European journal of immunology · 2026
    Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Rheumatoid Lung Disease.Mediterranean journal of rheumatology · 2025
    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 at 5 institutions in 1 country.

Scott M MatsonDivision of Pulmonary, Critical Care and Sleep Medicine, University of Kansas Medical Center, Kansas City, KS. Electronic address: smatson@kumc.edu.
Misbah BaqirDivision of Pulmonary, Critical Care Medicine, Mayo Clinic, Rochester, MN.
Teng MouaDivision of Pulmonary, Critical Care Medicine, Mayo Clinic, Rochester, MN.
Michael MarllDepartment of Medicine, University of Colorado School of Medicine, Aurora, CO.
Jessica KentDepartment of Internal Medicine, Baylor University Medical Center, Dallas, TX.
Nicholas S IannazzoDepartment of Pulmonary, Critical Care, Sleep and Occupational Medicine, Indiana University School of Medicine, Indianapolis, IN.
Ryan D BoenteDepartment of Pulmonary, Critical Care, Sleep and Occupational Medicine, Indiana University School of Medicine, Indianapolis, IN.
John M DonatelliDepartment of Radiology and Imaging Sciences, Indiana University School of Medicine, Indianapolis, IN.
Junqiang DaiDepartment of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS.
Francisco J DiazDepartment of Biostatistics and Data Science, University of Kansas Medical Center, Kansas City, KS.
M Kristen DemoruelleDivision of Rheumatology, University of Colorado School of Medicine, Aurora, CO.
Mark B HamblinDivision of Pulmonary, Critical Care and Sleep Medicine, University of Kansas Medical Center, Kansas City, KS.
Susan K MathaiCenter for Advanced Heart and Lung Disease and Baylor Scott & White Research Institute, Baylor University Medical Center, Dallas, TX.
Jay H RyuDivision of Pulmonary, Critical Care Medicine, Mayo Clinic, Rochester, MN.
Kristen PopeDepartment of Radiology, University of Kansas Medical Center, Kansas City, KS.
Christopher M WalkerDepartment of Radiology, University of Kansas Medical Center, Kansas City, KS.
Joyce S LeeDivision of Pulmonary Sciences and Critical Care Medicine, University of Colorado School of Medicine, Aurora, CO.
University of Kansas Medical Center · USIndiana University School of MedicineMayo Clinic in Arizona · USUniversity of Colorado Denver · USBaylor University Medical Center · US

Funding

Using Integrated Omics to Identify Dysfunctional Genetic Mechanisms Influencing Schizophrenia and Sleep DisturbancesP20GM130423 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI Kalyani Pyaram, Steven Allan Soper · 2019 to 2026
$21.5M
NIGMS NIH HHS P20 GM130423
6 · The paper itself

Abstract

backgroundRheumatoid arthritis (RA)-associated interstitial lung disease (ILD) is common in patients with RA and leads to significant morbidity and mortality. No randomized, placebo-controlled data are available that support the role of immunosuppression to treat RA-associated ILD, despite being widely used in clinical practice. RESEARCH QUESTION: How does immunosuppression impact pulmonary function trajectory in a multisite retrospective cohort of patients with RA-associated ILD? STUDY DESIGN AND

methodsPatients with RA who started treatment for ILD with mycophenolate, azathioprine, or rituximab were identified retrospectively from five ILD centers. Change in lung function before and after treatment was analyzed using a linear spline mixed-effect model with random intercept. Prespecified secondary analyses examined the impact of radiologic pattern of ILD (ie, usual interstitial pneumonia [UIP] vs non-UIP) on treatment trajectory.

resultsTwo hundred twelve patients were included in the analysis: 92 patients (43.4%) were treated with azathioprine, 77 patients (36.3%) were treated with mycophenolate mofetil, and 43 patients (20.3%) were treated with rituximab. In the combined analysis of all three agents, an improvement in FVC % predicted was found after 12 months of treatment compared with the potential 12-month response without treatment (+3.90%; P ≤ .001; 95% CI, 1.95-5.84). Diffusing capacity of the lungs for carbon monoxide (Dlco) % predicted also improved at 12 months (+4.53%; P ≤ .001; 95% CI, 2.12-6.94). Neither the UIP pattern of ILD nor choice of immunosuppressive agent significantly impacted the pulmonary function trajectory on immunosuppression.

interpretationImmunosuppression was associated with an improved trajectory in FVC and Dlco compared with the pretreatment pulmonary function trajectory. Prospective, randomized trials are required to validate these findings.

Indexed as

Arthritis, RheumatoidIdiopathic Pulmonary FibrosisLung Diseases, InterstitialAzathioprineHumansImmunosuppression TherapyImmunosuppressive AgentsLungProspective StudiesRetrospective StudiesRituximabTreatment OutcomeVital CapacityAzathioprineImmunosuppressive AgentsRituximabazathioprineinterstitial lung diseasemycophenolaterheumatoid arthritisrituximab

Identifiers

PMID36470416
PMCPMC10107057
OpenAlexW4310750632

What OpenQuestion 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 OpenQuestion graph.