Evidence map›Paper›PMID 42697585›Full record

ArticleRMD open2026

Comparative evaluation of disease activity measures for adult-onset Still's disease: a multicentre, retrospective, cohort study.

Stefan Vordenbäumen, Tim Filla, Rhea Friedrich, Norbert Blank, Diana Ernst, Jörg Henes, Gernot Keyßer, Philipp Klemm, Martin Krusche, Anna Meinecke and 10 more

Abstract readMulticenter StudyComparative Study
In one paragraph

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

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

0 citing papers in PubMed.

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

20 authors.

Stefan VordenbäumenDepartment of Rheumatology & Hiller Research Center, University Hospital of Düsseldorf, Düsseldorf, Germany Stefan.Vordenbaeumen@rrz-meerbusch.de.ORCID http://orcid.org/0000-0001-5725-5483
Tim FillaDepartment of Rheumatology & Hiller Research Center, University Hospital of Düsseldorf, Düsseldorf, Germany.ORCID http://orcid.org/0000-0001-5628-8398
Rhea FriedrichJustus Liebig University Giessen, Giessen, Germany.
Norbert BlankDepartment of Hematology, Oncology and Rheumatology, Internal Medicine V, University Hospital Heidelberg, Heidelberg, Germany.
Diana ErnstDepartment of Rheumatology and Immunology, Hannover Medical School, Hannover, Germany.
Jörg HenesDepartment of Internal Medicine II, Hematology, Oncology, Clinical Immunology, and Rheumatology, University Hospital Tübingen, Heidelberg, Germany.ORCID http://orcid.org/0000-0002-8385-6861
Gernot KeyßerClinic for Internal Medicine II, Department of Internal Medicine, University Hospital Halle (Saale), Martin Luther University Halle-Wittenberg, Halle (Saale), Germany.
Philipp KlemmDepartment of Rheumatology, Clinical Immunology, Osteology and Physical Medicine, Campus Kerckhoff, Justus-Liebig-Universitat Giessen, Giessen, Germany.
Martin KruscheDepartment Internal Medicine III, Division of Rheumatology and Inflammatory Systemic Autoimmune Diseases, University Hospital Eppendorf, Hamburg, Germany.
Anna MeineckeDepartment of Rheumatology and Immunology, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0009-0003-8517-616X
Jürgen RechDepartment of Internal Medicine 3 - Rheumatology and Immunology, Deutsches Zentrum Immuntherapie and Center for Rare Diseases Erlangen (ZSEER), Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany.ORCID http://orcid.org/0000-0002-2569-2029
Nils SchulzDepartment of Rheumatology, Clinical Immunology, Osteology and Physical Medicine, Campus Kerckhoff, Justus-Liebig-Universitat Giessen, Giessen, Germany.ORCID http://orcid.org/0009-0000-0378-3766
Simon Michael PetzinnaClinic of Internal Medicine III, Oncology, Hematology, Rheumatology and Clinical Immunology, University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-4686-1143
Anne PankowDepartment of Rheumatology and Clinical Immunology, Campus Charité Mitte, Berlin, Germany.
Valentin S SchäferClinic of Internal Medicine III, Oncology, Hematology, Rheumatology and Clinical Immunology, University Hospital Bonn, Bonn, Germany.
Alexander PfeilCenter of Rheumatology and Section Rheumatology and Osteology, Department of Internal Medicine III, Jena University Hospital-Friedrich Schiller University Jena, Jena, Germany.ORCID http://orcid.org/0000-0002-2709-6685
Sebastian KlapaInstitute of Experimental Medicine, Christian-Albrecht University Kiel, Kiel, Germany.ORCID http://orcid.org/0000-0002-0012-0163
Georg PongratzMedical Faculty, University of Regensburg, Regensburg, Germany.
Eugen FeistDepartment of Rheumatology and Immunology, Helios Clinic Vogelsang-Gommern, Gommern, Germany.ORCID http://orcid.org/0000-0002-9872-5282
Anna KernderDepartment of Rheumatology & Hiller Research Center, University Hospital of Düsseldorf, Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo comparatively evaluate recent adult-onset Still's disease (AOSD) activity measures-Development and Validation of Disease Activity in AOSD (DAVID), Still's Disease Activity Score (SDAS), Still Activity Score (SAS) with Pouchot's Systemic Score (PSS) in an independent multicentre cohort.

methodsDAVID and SDAS were modified (m) by omitting global assessments due to availability and to circumvent incorporation bias. Criterion validity was assessed by receiver operating characteristic (ROC) analysis against the treating physician's determination of disease activity (active vs inactive). Responsiveness was evaluated by comparing mean change in scores between remission and active disease, and Cohen's d. Longitudinal sensitivity to change was assessed using linear mixed-effects models with z-standardised scores and marginal R². Primary analysis uses imputed data, with complete-case sensitivity analysis.

resultsThe cohort comprised 86 patients with initially active AOSD (64% female; mean age 39.4±15.0 years). In ROC analyses, mSDAS, mDAVID and SAS showed comparable area under the curves (0.69, 0.68 and 0.68, respectively), whereas PSS had a lower AUC (0.60). Responsiveness was greatest for mDAVID (Cohen's d 0.76 (95% CI 0.30 to 1.20)), followed by mSDAS (0.61 (0.13 to 1.1)), SAS (0.46 (-0.01 to 0.90)) and PSS (0.22 (-0.30 to 0.68)). Longitudinal sensitivity to change, quantified by marginal R², was highest for mDAVID (0.65 (95% CI 0.59 to 0.70)), followed by mSDAS (0.61 (0.55 to 0.67)), PSS (0.61 (0.54 to 0.67)) and SAS (0.55 (0.45 to 0.64)). Sensitivity analyses using complete cases yielded similar results.

conclusionmDAVID and mSDAS demonstrated the most favourable and largely comparable performance profiles across the evaluated metrics, with mDAVID showing greater responsiveness and mSDAS demonstrating a stronger correlation with the articular disease domain. TRIAL REGISTRATION NUMBER: ISRCTN86135778.

Indexed as

Still's Disease, Adult-OnsetAdultBiomarkersFemaleHumansMaleMiddle AgedRetrospective StudiesROC CurveSeverity of Illness IndexBiomarkersBiomarkersInflammationStill's Disease, Adult-Onset

Identifiers

PMID42697585
PMCPMC13548246

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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.