Evidence map›Paper›PMID 35377443›Full record

ArticleRheumatology (Oxford, England)2022

The impact of disease severity measures on survival in U.S. veterans with rheumatoid arthritis-associated interstitial lung disease.

Rebecca Brooks, Joshua F Baker, Yangyuna Yang, Punyasha Roul, Gail S Kerr, Andreas M Reimold, Gary Kunkel, Katherine D Wysham, Namrata Singh, Deana Lazaro and 5 more

Open access · greenAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 2 pooled it
7.4field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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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

15 authors at 8 institutions in 1 country.

Rebecca BrooksVA Nebraska-Western Iowa Health Care System and Division of Rheumatology & Immunology, University of Nebraska Medical Center, Omaha, NE.
Joshua F BakerCorporal Michael J. Crescenz VA and Division of Rheumatology, University of Pennsylvania, Philadelphia, PA.
Yangyuna YangVA Nebraska-Western Iowa Health Care System and Division of Rheumatology & Immunology, University of Nebraska Medical Center, Omaha, NE.
Punyasha RoulVA Nebraska-Western Iowa Health Care System and Division of Rheumatology & Immunology, University of Nebraska Medical Center, Omaha, NE.
Gail S KerrDivision of Rheumatology, Washington DC VA, Howard University and Georgetown University, Washington, DC.
Andreas M ReimoldDallas VA and Division of Rheumatic Diseases, University of Texas Southwestern, Dallas, TX.
Gary KunkelVA Salt Lake City and Division of Rheumatology, University of Utah, Salt Lake City, UT.
Katherine D WyshamVA Puget Sound Health Care System and Division of Rheumatology, University of Washington, Seattle, WA.ORCID 0000-0001-8707-7649
Namrata SinghVA Puget Sound Health Care System and Division of Rheumatology, University of Washington, Seattle, WA.
Deana LazaroBrooklyn VA, Brooklyn, NY.
Paul A MonachBoston VA, Boston, MA.
Jill A PooleDivision of Allergy & Immunology, University of Nebraska Medical Center, Omaha, NE.
Dana P AschermanPittsburgh VA and Division of Rheumatology and Clinical Immunology, University of Pittsburgh, Pittsburgh, PA, USA.
Ted R MikulsVA Nebraska-Western Iowa Health Care System and Division of Rheumatology & Immunology, University of Nebraska Medical Center, Omaha, NE.
Bryant R EnglandVA Nebraska-Western Iowa Health Care System and Division of Rheumatology & Immunology, University of Nebraska Medical Center, Omaha, NE.ORCID 0000-0002-9649-3588
VA Nebraska Western Iowa Health Care System · USUniversity of Washington · USBoston VA Research Institute · USHoward University · USPhiladelphia VA Medical Center · USUniversity of Nebraska Medical Center · USUniversity of Pittsburgh · USUniversity of Utah · US

Funding

Tracking and Evaluation CoreU54GM115458 · NIGMS · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI HOLSTEIN, SARAH A · 2016 to 2025
$42.8M
Surveillance of Agricultural Injuries in the Central States RegionsU54OH010162 · OH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI RAUTIAINEN, RISTO HEIKKI · 2011 to 2025
$23.6M
Resolving Occupational Exposure-Induced Lung DiseaseR01OH012045 · OH · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI POOLE, JILL A · 2021 to 2024
$2.3M
Pathogenic Role of Malondialdehyde-Acetaldehyde Adducts in Rheumatoid ArthritisI01BX004660 · VA · OMAHA VA MEDICAL CENTER · PI MIKULS, TED RICHARD · 2020 to 2023
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Adipokines as Biomarkers of Cachexia and High-Risk Rheumatoid ArthritisI01CX001703 · VA · PHILADELPHIA VA MEDICAL CENTER · PI BAKER, JOSHUA F. · 2019 to 2023
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Improving the Management of Rheumatoid Arthritis-Associated Lung Disease in Veterans Using Real-World DataIK2CX002203 · VA · OMAHA VA MEDICAL CENTER · PI Bryant R England · 2021 to 2026
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ACL HHS U54OH010162BLRD VA I01 BX004660CSRD VA I01 CX001703CSRD VA IK2 CX002203NIGMS NIH HHS U54 GM115458NIOSH CDC HHS R01 OH012045NIOSH CDC HHS R01OH012045NIOSH CDC HHS U54 OH010162
6 · The paper itself

Abstract

objectivesTo determine whether RA and interstitial lung disease (ILD) severity measures are associated with survival in patients with RA-ILD.

methodsWe studied US veterans with RA-ILD participating in a multicentre, prospective RA cohort study. RA disease activity (28-joint DAS [DAS28-ESR]) and functional status (multidimensional HAQ [MDHAQ]) were collected longitudinally while pulmonary function tests (forced vital capacity [FVC], diffusing capacity for carbon monoxide) were obtained from medical records. Vital status and cause of death were determined from the National Death Index and administrative data. Predictors of death were assessed using multivariable Cox regression models adjusting for age, sex, smoking status, ILD duration, comorbidity burden and medications.

resultsWe followed 227 RA-ILD participants (93% male and mean age of 69 years) over 1073 person-years. Median survival after RA-ILD diagnosis was 8.5 years. Respiratory diseases (28%) were the leading cause of death, with ILD accounting for 58% of respiratory deaths. Time-varying DAS28-ESR (adjusted hazard ratio [aHR] 1.21; 95% CI: 1.03, 1.41) and MDHAQ (aHR 1.85; 95% CI: 1.29, 2.65) were separately associated with mortality independent of FVC and other confounders. Modelled together, the presence of either uncontrolled disease activity (moderate/high DAS28-ESR) or FVC impairment (<80% predicted) was significantly associated with mortality risk. Those with a combination of moderate/high disease activity and FVC <80% predicted had the highest risk of death (aHR 4.43; 95% CI: 1.70, 11.55).

conclusionBoth RA and ILD disease severity measures are independent predictors of survival in RA-ILD. These findings demonstrate the prognostic value of monitoring the systemic features of RA-ILD.

Indexed as

Arthritis, RheumatoidLung Diseases, InterstitialVeteransAgedCohort StudiesFemaleHumansMaleProspective StudiesSeverity of Illness Indexdisease activityinterstitial lung diseasemortalityRA

Identifiers

PMID35377443
PMCPMC9960484
OpenAlexW4225619998

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.