Characteristics associated with poor COVID-19 outcomes in people with psoriasis, psoriatic arthritis and axial spondyloarthritis: data from the COVID-19 PsoProtect and Global Rheumatology Alliance physician-reported registries
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Published:2023-02-14
Issue:5
Volume:82
Page:698-709
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ISSN:0003-4967
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Container-title:Annals of the Rheumatic Diseases
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language:en
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Short-container-title:Ann Rheum Dis
Author:
Machado Pedro MORCID, Schäfer MartinORCID, Mahil Satveer K, Liew Jean, Gossec LaureORCID, Dand Nick, Pfeil AlexanderORCID, Strangfeld AnjaORCID, Regierer Anne ConstanzeORCID, Fautrel BrunoORCID, Alonso Carla Gimena, Saad Carla G S, Griffiths Christopher E M, Lomater Claudia, Miceli-Richard CorinneORCID, Wendling DanielORCID, Alpizar Rodriguez DeshireORCID, Wiek Dieter, Mateus Elsa FORCID, Sirotich EmilyORCID, Soriano Enrique RORCID, Ribeiro Francinne MachadoORCID, Omura Felipe, Rajão Martins FredericoORCID, Santos Helena, Dau Jonathan, Barker Jonathan N, Hausmann JonathanORCID, Hyrich Kimme LORCID, Gensler Lianne, Silva Ligia, Jacobsohn Lindsay, Carmona LoretoORCID, Pinheiro Marcelo MORCID, Zelaya Marcos David, Severina María de los Ángeles, Yates MarkORCID, Dubreuil Maureen, Gore-Massy Monique, Romeo Nicoletta, Haroon Nigil, Sufka Paul, Grainger Rebecca, Hasseli RebeccaORCID, Lawson-Tovey SaskiaORCID, Bhana Suleman, Pham ThaoORCID, Olofsson TorORCID, Bautista-Molano Wilson, Wallace Zachary S, Yiu Zenas Z N, Yazdany Jinoos, Robinson Philip CORCID, Smith Catherine H
Abstract
ObjectivesTo investigate factors associated with severe COVID-19 in people with psoriasis (PsO), psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA).MethodsDemographic data, clinical characteristics and COVID-19 outcome severity of adults with PsO, PsA and axSpA were obtained from two international physician-reported registries. A three-point ordinal COVID-19 severity scale was defined: no hospitalisation, hospitalisation (and no death) and death. ORs were estimated using multivariable ordinal logistic regression.ResultsOf 5045 cases, 18.3% had PsO, 45.5% PsA and 36.3% axSpA. Most (83.6%) were not hospitalised, 14.6% were hospitalised and 1.8% died. Older age was non-linearly associated with COVID-19 severity. Male sex (OR 1.54, 95% CI 1.30 to 1.83), cardiovascular, respiratory, renal, metabolic and cancer comorbidities (ORs 1.25–2.89), moderate/high disease activity and/or glucocorticoid use (ORs 1.39–2.23, vs remission/low disease activity and no glucocorticoids) were associated with increased odds of severe COVID-19. Later pandemic time periods (ORs 0.42–0.52, vs until 15 June 2020), PsO (OR 0.49, 95% CI 0.37 to 0.65, vs PsA) and baseline exposure to TNFi, IL17i and IL-23i/IL-12+23i (OR 0.57, 95% CI 0.44 to 0.73; OR 0.62, 95% CI 0.45 to 0.87; OR 0.67, 95% CI 0.45 to 0.98; respectively; vs no disease-modifying antirheumatic drug) were associated with reduced odds of severe COVID-19.ConclusionOlder age, male sex, comorbidity burden, higher disease activity and glucocorticoid intake were associated with more severe COVID-19. Later pandemic time periods, PsO and exposure to TNFi, IL17i and IL-23i/IL-12+23i were associated with less severe COVID-19. These findings will enable risk stratification and inform management decisions for patients with PsO, PsA and axSpA during COVID-19 waves or similar future respiratory pandemics.
Funder
European League Against Rheumatism American College of Rheumatology
Subject
General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Rheumatology
Cited by
12 articles.
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