Evidence map›Paper›PMID 42856858›Full record

ArticleEULAR rheumatology open2026

Does articular and entheseal structural damage drive pain and patient-driven reported outcomes in patients with difficult-to-treat psoriatic arthritis? Results from a cross-sectional study.

Fabio Massimo Perrotta, Alen Zabotti, Mauro Fatica, Nicola Cabas, Andrea Guiotto, Nicoletta Franzolini, Ivan Giovannini, Maria De Martino, Cristina Di Nicola, Miriam Isola and 5 more

Abstract read
In one paragraph

Article in EULAR rheumatology 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.

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0cells of the map it votes in
0citing papers 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

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

15 authors.

Fabio Massimo PerrottaAcademic Rheumatology Unit, Dipartimento di Medicina e Scienze della Salute "Vincenzo Tiberio", Università degli Studi del Molise, Via Giovanni Paolo II, C/da Tappino, Campobasso, Italy.
Alen ZabottiDepartment of Medical and Biological Sciences, Rheumatology Clinic, University Hospital Santa Maria della Misericordia, Udine, Italy.
Mauro FaticaAcademic Rheumatology Unit, Dipartimento di Medicina e Scienze della Salute "Vincenzo Tiberio", Università degli Studi del Molise, Via Giovanni Paolo II, C/da Tappino, Campobasso, Italy.
Nicola CabasDepartment of Medical and Biological Sciences, Rheumatology Clinic, University Hospital Santa Maria della Misericordia, Udine, Italy.
Andrea GuiottoDepartment of Medical and Biological Sciences, Rheumatology Clinic, University Hospital Santa Maria della Misericordia, Udine, Italy.
Nicoletta FranzoliniPresidio Ospedaliero "S. Antonio", San Daniele (Udine), Italy.
Ivan GiovanniniDepartment of Medical and Biological Sciences, Rheumatology Clinic, University Hospital Santa Maria della Misericordia, Udine, Italy.
Maria De MartinoDepartment of Medicine, University of Udine, Udine, Italy.
Cristina Di NicolaEpidemiology Unit, Italian Society for Rheumatology, Milan, Italy.
Miriam IsolaDepartment of Medicine, University of Udine, Udine, Italy.
Andrea Di MatteoSection of Musculoskeletal Disease, NIHR Leeds Musculoskeletal Biomedical Research Centre, Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Chapel Allerton Hospital, Leeds, UK.
Gabriele De MarcoSection of Musculoskeletal Disease, NIHR Leeds Musculoskeletal Biomedical Research Centre, Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Chapel Allerton Hospital, Leeds, UK.
Dennis McGonagleSection of Musculoskeletal Disease, NIHR Leeds Musculoskeletal Biomedical Research Centre, Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Chapel Allerton Hospital, Leeds, UK.
Luca QuartuccioAcademic Rheumatology Unit, Dipartimento di Medicina e Scienze della Salute "Vincenzo Tiberio", Università degli Studi del Molise, Via Giovanni Paolo II, C/da Tappino, Campobasso, Italy.
Ennio LubranoAcademic Rheumatology Unit, Dipartimento di Medicina e Scienze della Salute "Vincenzo Tiberio", Università degli Studi del Molise, Via Giovanni Paolo II, C/da Tappino, Campobasso, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aims to assess difficult-to-treat psoriatic arthritis (D2T-PsA) and determine whether articular and entheseal structural damage, assessed by ultrasound (US), may drive pain and patient-driven outcomes in D2T-PsA. Methods: A multicentre cross-sectional study was conducted on patients with PsA treated with biologic/targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs). Eligible participants were required to meet the following inclusion criteria: age ≥18 years; diagnosis of PsA fulfilling the classification criteria for Psoriatic Arthritis (CASPAR); classification as D2T-PsA, defined by failure of ≥2 classes of b/tsDMARDs (with different mechanisms of action) following the failure or contraindication of ≥1 conventional synthetic DMARD, and persistently active disease (Disease Activity Index for PsA >14). Sonographic evaluation was performed by using the US damage score (ultrasound in psoriatic arthritis [UPsA]) from the Ultrasound in PSoriatic arthritis TREAtMent (UPSTREAM) study. We used Spearman rho correlation coefficient to evaluate correlations between UPsA damage score and clinical features. Results: 53 patients with PsA were included in the analysis. The median (IQR) UPsA damage score of the 53 D2T patients was 3.79 (1.28-5.45). The UPsA damage score negatively correlated with tender joint count (rho -0.27, Conclusions: Preliminary results of our study in patients with D2T PsA showed that articular damage could be associated with PhGA and swollen joints, but not with pain, suggesting that patient-driven outcomes may potentially be related to inflammation or noninflammatory mechanisms rather than damage itself.

Identifiers

PMID42856858
PMCPMC13650305

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