The ATTRACT study: screening for the early identification of axial psoriatic arthritis in a cohort of Italian psoriatic patients

Author:

Luchetti Gentiloni Michele Maria1ORCID,Paci Valentino12,Cimaroli Ilaria12,Agostinelli Alice12,Giannoni Melania3,Campanati Anna3,Diotallevi Federico3,Carotti Marina4,Sessa Francesco5,Sordillo Raffaella12,Macchini Cristina12,Fiorini Federico12,Massaccesi Leonardo12,Ciferri Monia1,Gigli Marco12,Marconi Valentina12,Perini Lucia12,Marani Andrea3,Giovagnoni Andrea4,Polonara Gabriele5,Offidani Anna Maria3,Benfaremo Devis1,Proft Fabian6ORCID,Poddubnyy Denis6ORCID,Moroncini Gianluca1

Affiliation:

1. Medical Clinic, Department of Clinical and Molecular Sciences, Marche Polytechnic University , Ancona, Italy

2. Internal Medicine Residency Programme, Department of Clinical and Molecular Sciences, Marche Polytechnic University , Ancona, Italy

3. Dermatology Clinic, Department of Clinical and Molecular Sciences, Marche Polytechnic University , Ancona, Italy

4. Radiology Clinic, Department of Radiological Sciences, Polytechnic University of Marche , Ancona, Italy

5. Neuroradiology Clinic, Department of Radiological Sciences, Polytechnic University of Marche , Ancona, Italy

6. Department of Gastroenterology, Infectiology and Rheumatology (including Nutrition Medicine), Charité-Universitätsmedizin , Berlin, Germany

Abstract

Abstract Objective There is growing interest in the early identification of patients with axial PsA (axPsA). We aimed to evaluate whether a dermatology-based screening strategy could help to identify axPsA patients. Methods The dermatologist-centred screening (DCS) questionnaire was administrated by dermatologists to consecutive patients fulfilling the inclusion criteria [(i) age ≥18 years and (ii) clinical diagnosis of psoriasis made by a dermatologist] to identify patients eligible (affirmative answers 1–3c of the DCS) for rheumatological evaluation. Clinical, laboratory, genetic and imaging data were collected from all referred patients. Results Among the 365 patients screened, 265 fulfilled the inclusion criteria and 124/265 (46.8%) were eligible for rheumatological referral. Diagnosis of axPsA, with or without peripheral PsA (pPsA), was made in 36/124 (29.0%) patients; pPsA without axial involvement was found in 21/124 (16.9%) patients. Back pain at screening was recorded in 174 (66%) patients, with 158 (60%) reporting a back pain duration longer than 3 months and 140 (53%) reporting back pain onset before the age of 45 years. Active inflammatory and/or structural post-inflammatory changes in the sacroiliac joints and/or spine were observed in all axPsA patients. Patients with PsA showed a numerically longer duration of back pain and higher CRP levels in comparison with patients with psoriasis without PsA. Conclusion The DCS tool proved to be a valuable screening strategy for detecting and characterizing patients with axPsA in a real-life cohort of psoriasis patients in a dermatological setting and helped to identify a substantial number of patients affected by undiagnosed pPsA.

Funder

AbbVie Srl

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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