Evidence map›Paper›PMID 36831088›Full record

ArticleBiomedicines2023

The von Willebrand Factor Antigen Reflects the Juvenile Dermatomyositis Disease Activity Score.

Ellie Gibbs, Amer Khojah, Gabrielle Morgan, Louis Ehwerhemuepha, Lauren M Pachman

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  11. B Cell Lymphocytosis in Juvenile Dermatomyositis.Diagnostics (Basel, Switzerland) · 2023
    Article
  12. Article
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

5 authors at 5 institutions in 2 countries.

Ellie GibbsDepartment of Biological Sciences, Wellesley College, Wellesley, MA 02481, USA.ORCID 0000-0003-1381-8437
Amer KhojahDepartment of Pediatrics, College of Medicine, Umm Al-Qura University, Makkah 21421, Saudi Arabia.ORCID 0000-0003-3357-4863
Gabrielle MorganDivision of Pediatric Rheumatology, Ann & Robert H. Lurie Children's Hospital of Chicago, Cure-JM Center of Excellence in Juvenile Myositis Research and Care, Chicago, IL 60611, USA.ORCID 0000-0002-4058-7112
Louis EhwerhemuephaComputational Research, Children's Hospital of Orange County Research Institute, Orange, CA 92868, USA.ORCID 0000-0003-1369-7954
Lauren M PachmanDivision of Pediatric Rheumatology, Ann & Robert H. Lurie Children's Hospital of Chicago, Cure-JM Center of Excellence in Juvenile Myositis Research and Care, Chicago, IL 60611, USA.ORCID 0000-0001-8117-574X
Children's Hospital of Orange County · USLurie Children's Hospital · USNorthwestern University · USUmm al-Qura University · SAWellesley College · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Cure JM Foundation n/aNCATS NIH HHS UL1 TR001422NIH HHS UL1TR001422The DenUyl Family Fund n/aThe Vivian Allison and Daniel J. Pachman Fund n/a
6 · The paper itself

Abstract

objectiveThis study determined if an accessible, serologic indicator of vascular disease activity, the von Willebrand factor antigen (vWF:Ag), was useful to assess disease activity in children with juvenile dermatomyositis (JDM), a rare disease, but the most common of the pediatric inflammatory myopathies.

methodsA total of 305 children, median age 10 years, 72.5% female, 76.5% white, with definite/probable JDM at diagnosis, were enrolled in the Ann & Robert H. Lurie Cure JM Juvenile Myositis Repository, a longitudinal database. Disease Activity Score (DAS) and vWF:Ag data were obtained at each visit. These data were analyzed using generalized estimating equation (GEE) models (both linear and logistic) to determine if vWF:Ag reflects disease severity in children with JDM. A secondary analysis was performed for untreated active JDM to exclude the effect of medications on vWF:Ag.

resultThe vWF:Ag test was elevated in 25% of untreated JDM. We found that patients with elevated vWF:Ag had a 2.55-fold higher DAS total (CI

conclusionvWF:Ag elevation is a widely accessible concomitant of active disease in 25% of JDM.

Indexed as

disease activity scoresjuvenile dermatomyositisvon Willebrand factor antigen

Identifiers

PMID36831088
PMCPMC9953073
OpenAlexW4320729595

What OpenQuestion holds

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LicenceCC BY
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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.