Identification and characteristics of patients with potential difficult-to-treat psoriatic arthritis: exploratory analyses of the Greek PsA registry

Author:

Vassilakis Konstantinos D1,Papagoras Charalampos2ORCID,Fytanidis Nikolaos2,Gazi Sousana3,Mole Evangelia3,Krikelis Michael3,Voulgari Paraskevi V4ORCID,Kaltsonoudis Evripidis4,Koletsos Nikolaos4ORCID,Boumpas Dimitrios5,Katsimpri Pelagia5,Katsifis-Nezis Dimitrios5,Dimitroulas Theodoros6ORCID,Kougkas Nikolaos6,Boutel Maria6,Sfikakis Petros P1ORCID,Tektonidou Maria G1ORCID,Gialouri Chrysoula1ORCID,Bogdanos Dimitrios7,Simopoulou Theodora7,Koutsianas Christos8,Mavrea Evgenia8,Katsifis Gkikas9,Kottas Konstantinos9,Konsta Maria10,Tziafalia Matthoula10,Kataxaki Evangelia11,Kalavri Eleni12,Klavdianou Kalliopi12,Grika Eleftheria P13,Sfontouris Charalampos13,Daoussis Dimitrios14ORCID,Iliopoulos George14,Bournazos Ilias15,Karokis Dimitrios15,Georganas Konstantinos15,Patrikos Dimos15,Vassilopoulos Dimitrios8ORCID,Fragoulis George E116ORCID

Affiliation:

1. Joint Academic Rheumatology Program, First Department of Propedeutic and Internal Medicine, National and Kapodistrian University of Athens , Athens, Greece

2. First Department of Internal Medicine, University Hospital of Alexandroupolis, Democritus University of Thrace , Alexandroupolis, Greece

3. Department of Rheumatology, KAT Hospital , Athens, Greece

4. Department of Rheumatology, School of Health Sciences, Faculty of Medicine, University of Ioannina , Ioannina, Greece

5. Joint Academic Rheumatology Program, 4th Department of Internal Medicine, Attikon University Hospital, National and Kapodistrian University of Athens Medical School , Athens, Greece

6. 4th Department of Medicine, Aristotle University , Thessaloniki, Greece

7. Department of Rheumatology and Clinical Immunology, University of Thessaly , Larissa, Greece

8. Joint Academic Rheumatology Program, Clinical Immunology, Rheumatology unit, 2nd Department of Medicine and Laboratory, National and Kapodistrian University of Athens Medical School, General Hospital of Athens “Hippokration” , Athens, Greece

9. Rheumatology Clinic, Naval Hospital of Athens , Athens, Greece

10. Rheumatology Unit, Sismanoglio Hospital , Athens, Greece

11. Rheumatology Department, General Hospital Elefsinas Thriaseio , Athens, Greece

12. Department of Rheumatology, “Asklepieion” General Hospital , Athens, Greece

13. Department of Rheumatology, Evaggelismos Athens General Hospital , Athens, Greece

14. Department of Rheumatology, Patras University Hospital, University of Patras Medical School , Patras, Greece

15. Private Practice , Athens, Greece

16. School of Infection and Immunity, University of Glasgow , Glasgow, UK

Abstract

Abstract Objective To present the characteristics of patients with potential difficult-to-treat (D2T) PsA. Methods We used data from the Greek multicentre registry of PsA patients. D2T PsA was defined as follows: patients with at least 6 months’ disease duration, who have failed to at least one conventional synthetic DMARD and at least two biologic DMARDs/targeted synthetic DMARDs with a different mechanism of action and have either at least moderate disease activity (MODA) defined as DAPSA (Disease Activity index in PSoriatic Arthritis) >14, and/or are not at minimal disease activity (MDA). Demographic and clinical characteristics were compared between D2T and non-D2T PsA patients. In two sensitivity analyses, patients classified as D2T solely according to the MODA or MDA criterion were examined separately. Results Among 467 patients included, 77 (16.5%) were considered D2T and 390 non-D2T PsA. Compared with non-D2T, patients with D2T PsA presented more commonly with extensive psoriasis (P < 0.0001) and were more likely to have higher BMI (P = 0.023) and a history of IBD (P = 0.026). In the MODA and MDA sensitivity analyses, 7.5% and 12.5% of patients were considered D2T, respectively. In both sensitivity analyses, extensive psoriasis was again identified as an independent variable for D2T PsA (P = 0.001 and P = 0.008, respectively). Moreover, female gender (P = 0.034) in the MODA analysis and axial disease (P = 0.040) in the MDA analysis were independent variables for D2T PsA. Conclusion Despite the availability of therapies, D2T PsA is common in real-life cohorts of patients with PsA and extensive psoriasis. High BMI, female gender, axial disease and history of IBD were also associated with D2T PsA.

Funder

Greek (Hellenic) Rheumatology Society

Publisher

Oxford University Press (OUP)

Reference28 articles.

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