Evidence map›Paper›PMID 40889898›Full record

ArticleRMD open2025

To optimise the diagnostic process of rheumatic diseases affecting the hands using fluorescence optical imaging (FOI).

Nele Stumper, Jörn Berger, Jens Klotsche, Egbert Gedat, Paula Hoff, Gabriela Schmittat, Gerd R Burmester, Gerhard Krönke, Marina Backhaus, Ida K Haugen and 1 more

Abstract read
In one paragraph

Article in RMD open, 2025. 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

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

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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

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5 · Who and what money

Authors and funding

11 authors.

Nele StumperDepartment of Rheumatology and Clinical Immunology, Charite-Universitatsmedizin Berlin, Berlin, BE, Germany n.stumper@web.de.ORCID 0009-0000-4298-9097
Jörn BergerXiralite GmbH, Berlin, Germany.
Jens KlotscheEpidemiology Unit, German Rheumatism Research Center Berlin, Berlin, Germany.ORCID 0000-0002-2954-5755
Egbert GedatFachbereich Ingenieur-und Naturwissenschaften, TH Wildau, Wildau, BB, Germany.
Paula HoffDepartment of Rheumatology and Clinical Immunology, Charite-Universitatsmedizin Berlin, Berlin, BE, Germany.ORCID 0000-0001-7494-0845
Gabriela SchmittatDepartment of Rheumatology and Clinical Immunology, Charite-Universitatsmedizin Berlin, Berlin, BE, Germany.
Gerd R BurmesterDepartment of Rheumatology and Clinical Immunology, Charite-Universitatsmedizin Berlin, Berlin, BE, Germany.ORCID 0000-0001-7518-1131
Gerhard KrönkeRheumatology and Clinical Immunology, Friedrich-Alexander University Erlangen-Nuremberg, Berlin, Germany.ORCID 0000-0002-7566-4325
Marina BackhausDepartment of Rheumatology and Clinical Immunology, Park-Klinik Weissensee, Berlin, BE, Germany.
Ida K HaugenDepartment of Rheumatology, Diakonhjemmet University College and Hospital, Oslo, Oslo, Norway.ORCID 0000-0001-7810-2216
Sarah OhrndorfDepartment of Rheumatology and Clinical Immunology, Charite-Universitatsmedizin Berlin, Berlin, BE, Germany.ORCID 0000-0001-5943-4688

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate and rapid diagnosis of rheumatic diseases is essential for further treatment decision. Different rheumatic diseases present characteristic patterns (image features) in fluorescence optical imaging (FOI). We developed an atlas of FOI image features and tested its ability to differentiate various rheumatic diseases.

methodsFOI images from patients with rheumatoid arthritis (RA), psoriatic arthritis (PsA), connective tissue diseases (CTD) and osteoarthritis (OA) were analysed by two readers blinded for diagnosis and calibrated against each other, using the prima vista mode (PVM) and an automated 5-phase model. Twenty-six different reoccurring typical signal enhancement patterns (features) indicating inflamed joints, nail or skin were defined and all FOI images were scored accordingly. The feature frequency in each patient cohort and phase (PVM, 5-phase) was counted. Contingency tables were created with categorical variable counts and diagnosis using common formulae.

findingsFour hundred thirty-eight patients with RA (n=117), PsA (n=110), CTD (n=121) and OA (n=90) were included. Once the data had been categorised, a two-step diagnostic pathway was developed: in the first step, OA was best distinguished from the other diseases with high specificity by five patterns (specificity >0.9, diagnostic OR between 2.34 and 8.24). In a second step, the remaining autoimmune diseases were differentiated from each other by a certain number of features (five for RA, 12 for PsA and four for CTD).

interpretationThis was the first study to show that feature analysis in FOI helps to differentiate typical rheumatic diseases from each other, potentially simplifying and speeding up the diagnostic process. Therefore, FOI could be considered an additional component of a wider range of imaging techniques used in rheumatology.

Indexed as

HandOptical ImagingRheumatic DiseasesAdultAgedArthritis, PsoriaticArthritis, RheumatoidFemaleHumansMaleMiddle AgedOsteoarthritisArthritis, PsoriaticArthritis, RheumatoidConnective Tissue DiseasesInflammationOsteoarthritis

Identifiers

PMID40889898
PMCPMC12406893

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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.