Evidence map›Paper›PMID 38709770›Full record

ArticlePloS one2024

External validation of a multi-biomarker-based score for predicting risk of cardiovascular disease in patients with rheumatoid arthritis.

Eric H Sasso, Brent Mabey, Darl D Flake, Elena Hitraya, Cheryl L Chin, Rotem Ben-Shachar, Alexander Gutin, Jerry S Lanchbury, Jeffrey R Curtis

Abstract readValidation Study
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Eric H SassoMedical and Scientific Affairs, Crescendo Bioscience, South San Francisco, CA, United States of America.
Brent MabeyMyriad Genetics Laboratories, Myriad, Salt Lake City, UT, United States of America.
Darl D FlakeMyriad Genetics Laboratories, Myriad, Salt Lake City, UT, United States of America.
Elena HitrayaMedical and Scientific Affairs, Crescendo Bioscience, South San Francisco, CA, United States of America.
Cheryl L ChinMedical and Scientific Affairs, Crescendo Bioscience, South San Francisco, CA, United States of America.
Rotem Ben-ShacharMyriad Genetics Laboratories, Myriad, Salt Lake City, UT, United States of America.
Alexander GutinMyriad Genetics Laboratories, Myriad, Salt Lake City, UT, United States of America.
Jerry S LanchburyMyriad Genetics Laboratories, Myriad, Salt Lake City, UT, United States of America.
Jeffrey R CurtisDivision of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, United States of America.ORCID 0000-0002-8907-8976

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA multi-biomarker disease activity (MBDA)-based cardiovascular disease (CVD) risk score was developed and internally validated in a Medicare cohort to predict 3-year risk for myocardial infarction (MI), stroke or CVD death in patients with rheumatoid arthritis (RA). It combines the MBDA score, leptin, MMP-3, TNF-R1, age and four clinical variables. We are now externally validating it in a younger RA cohort.

methodsClaims data from a private aggregator were linked to MBDA test data to create a cohort of RA patients ≥18 years old. A univariable Cox proportional hazards regression model was fit using the MBDA-based CVD risk score as sole predictor of time-to-a-CVD event (hospitalized MI or stroke). Hazard ratio (HR) estimate was determined for all patients and for clinically relevant subgroups. A multivariable Cox model evaluated whether the MBDA-based CVD risk score adds predictive information to clinical data.

results49,028 RA patients (340 CVD events) were studied. Mean age was 52.3 years; 18.3% were male. HR for predicting 3-year risk of a CVD event by the MBDA-based CVD risk score in the full cohort was 3.99 (95% CI: 3.51-4.49, p = 5.0×10-95). HR were also significant for subgroups based on age, comorbidities, disease activity, and drug use. In a multivariable model, the MBDA-based CVD risk score added significant information to hypertension, diabetes, tobacco use, history of CVD, age, sex and CRP (HR = 2.27, p = 1.7×10-7).

conclusionThe MBDA-based CVD risk score has been externally validated in an RA cohort that is younger than and independent of the Medicare cohort that was used for development and internal validation.

Indexed as

Arthritis, RheumatoidBiomarkersCardiovascular DiseasesAdultAgedCohort StudiesFemaleHumansMaleMiddle AgedMyocardial InfarctionProportional Hazards ModelsRisk AssessmentRisk FactorsBiomarkers

Identifiers

PMID38709770
PMCPMC11073667

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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.