What influences patients' opinion of remission and low disease activity in psoriatic arthritis? Principal component analysis of an international study.


Journal

Rheumatology (Oxford, England)
ISSN: 1462-0332
Titre abrégé: Rheumatology (Oxford)
Pays: England
ID NLM: 100883501

Informations de publication

Date de publication:
03 11 2021
Historique:
received: 13 11 2020
accepted: 23 02 2021
pubmed: 23 3 2021
medline: 25 12 2021
entrez: 22 3 2021
Statut: ppublish

Résumé

In PsA, the treatment objective is remission or low disease activity (LDA), but patients' perception of remission is poorly studied. This analysis aimed to identify factors associated with patient-defined remission. This analysis uses ReFlaP data, an international PsA study, with remission defined as 'At this time, is your psoriatic arthritis in remission, if this means: you feel your disease is as good as gone?'. Variables associated with, first, patient-defined remission and, second, LDA were identified using multivariable logistic regression and principal component analysis (PCA) to explore correlated variables. Of 424 patients (50.2% male, mean age 52 years) with established disease, 94 (22.2%) reported themselves as being in remission and 191 (45.0%) as LDA alone. In multivariable analysis pain, psoriasis, impact of disease, physician opinion of symptoms from joint damage and Groll comorbidity index were independent predictors of remission. For LDA, results were similar. Using PCA, variance explained was 74% by five components for men and 80% by six components for women. The key component from PCA for remission was, for both sex, disease impact (Psoriatic Arthritis Impact of Disease, pain and HAQ) explaining 22.2-27.5% of variance. Other factors included musculoskeletal disease activity, chronicity/joint damage, psoriasis, enthesitis and CRP. For LDA, similar factors were identified but the variance explained was lower (64-68%). Many factors impact on patients' opinion of remission, dominated by disease impact. Disease activity in multiple domains, chronicity/age, comorbidities and symptoms due to other conditions contribute to a robust model highlighting that patient-defined remission is multifaceted. Clinicaltrials.gov, http://clinicaltrials.gov, NCT03119805.

Identifiants

pubmed: 33751029
pii: 6159629
doi: 10.1093/rheumatology/keab220
doi:

Substances chimiques

Antirheumatic Agents 0

Banques de données

ClinicalTrials.gov
['NCT03119805']

Types de publication

Journal Article Multicenter Study Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5292-5299

Subventions

Organisme : National Institute for Health Research
Organisme : Oxford Biomedical Research Centre
Organisme : NHS
Organisme : Department of Health
Pays : United Kingdom

Informations de copyright

© The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Rheumatology.

Auteurs

Laura C Coates (LC)

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.

Danielle E Robinson (DE)

Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.

Ana-Maria Orbai (AM)

Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Uta Kiltz (U)

Rheumazentrum Ruhrgebiet, Herne and Ruhr-Universität, Bochum, Germany.

Ying-Ying Leung (YY)

Rheumatology Department, Singapore General Hospital, Singapore, Singapore.

Penelope Palominos (P)

Serviço de Reumatologia, Hospital de Clínicas de Porto Alegre, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.

Juan D Cañete (JD)

Rheumatology Department, Hospital Clinic and Institut D'Investigacions Biomediques August Pi Sunyer, Barcelona, Spain.

Rossana Scrivo (R)

Rheumatology Unit, Department of Clinical Internal, Anaesthesiological and Cardiovascular Sciences, Sapienza Università di Roma, Rome, Italy.

Andra Balanescu (A)

Sf Maria Hospital, University of Medicine and Pharmacy Carol Davila, Bucharest, Romania.

Emmanuelle Dernis (E)

Rheumatology Department, Le Mans Central Hospital, Le Mans, France.

Sandra Meisalu (S)

Rheumatology Department, East-Tallinn Central Hospital, Tallinn, Estonia.

Adeline Ruyssen-Witrand (A)

Rheumatology Unit, Toulouse University Hospital, UMR 1027, INSERM, Université Paul Sabatier Toulouse III, Toulouse, France.

Lihi Eder (L)

Women's College Hospital, University of Toronto, Toronto, Ontario, Canada.

Maarten de Wit (M)

Patient Research Partner, Amsterdam, The Netherlands.

Josef S Smolen (JS)

Division of Rheumatology, Department of Medicine 3, Medical University of Vienna, Vienna, Austria.

Ennio Lubrano (E)

Academic Rheumatology Unit, Dipartimento di Medicina e Scienze della Salute 'Vincenzo Tiberio', University of Molise, Campobasso, Italy.

Laure Gossec (L)

Institut Pierre Louis d'Epidémiologie et de Santé Publique, INSERM, Sorbonne Université.
Rheumatology Department, Pitié Salpêtrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.

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