Evidence map›Paper›PMID 41871052›Full record

ArticlePloS one2026

Reliability of durometry to assess firmness of calcinosis lesions in Juvenile and adult dermatomyositis.

Meghan Corrigan Nelson, Lisa G Rider, Hanna Kim, Scott Gillespie, Vy Do, Julie Fuller, Kelly Rouster-Stevens, Adam Schiffenbauer

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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No citing paper in PubMed yet.

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

8 authors.

Meghan Corrigan NelsonDivision of Pediatric Rheumatology, Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States of America.ORCID https://orcid.org/0000-0002-5320-4045
Lisa G RiderEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.
Hanna KimJuvenile Myositis Pathogenesis and Therapeutics Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH, Bethesda, Maryland, United States of America.
Scott GillespieEmory University, Atlanta, GeorgiaUnited States of America.
Vy DoTexas Scottish Rite Hospital for Children, Dallas, Texas, United States of America.
Julie FullerTexas Scottish Rite Hospital for Children, Dallas, Texas, United States of America.
Kelly Rouster-StevensDivision of Pediatric Rheumatology, Department of Pediatrics, Emory University School of Medicine, Atlanta, Georgia, United States of America.
Adam SchiffenbauerEnvironmental Autoimmunity Group, Clinical Research Branch, National Institute of Environmental Health Sciences, National Institutes of Health, Bethesda, Maryland, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectiveDermatomyositis (DM) and juvenile dermatomyositis (JDM) are inflammatory myopathies affecting multiple organs, including muscle and skin. Calcinosis is a complication of DM/JDM that causes significant morbidity; however, few tools exist to assess calcinosis in DM/JDM patients This study aimed to evaluate the reliability of durometry measurements to assess the firmness of calcinosis lesions in DM and JDM patients.

methodsCalcinosis firmness was measured using a handheld digital durometer. Six investigators across 3 institutions examined DM/JDM calcinosis lesions by durometry, as well as control readings in healthy unaffected skin/subcutaneous tissue in similar anatomic areas, recording three readings per site. Intra-rater and inter-rater intraclass correlations were evaluated.

resultsWe enrolled 57 patients and gathered 709 measurements (443 calcinosis lesions; 266 control lesions) over eleven anatomic regions. Intra-rater reliability was high across sites, while inter-rater reliability varied, being moderate to good in most areas, but poor in the thigh and anterior calf. Durometry readings were higher in calcinosis lesions than control sites overall. Measurements moderately correlated with qualitative physician assessments. Due to our study's cross-sectional nature, we could not assess calcinosis over time.

conclusionDurometry is a novel, reliable, quantitative measure in assessing and characterizing targeted calcinosis lesions of DM/JDM patients.

Indexed as

CalcinosisCalcinosis CutisDermatomyositisAdolescentAdultChildChild, PreschoolFemaleHumansMaleMiddle AgedReproducibility of ResultsSkinYoung Adult

Identifiers

PMID41871052
PMCPMC13008098

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