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
Machado, P.M.; Schäfer, M.; Mahil, S.K.; Liew, J.; Gossec, L.; Dand, N.; Pfeil, A.; Strangfeld, A.; Regierer, A.C.; Fautrel, B.; Alonso, C.G.; Saad, C.G.S.; Griffiths, C.E.M.; Lomater, C.; Miceli-Richard, C.; Wendling, D.; Alpizar Rodriguez, D.; Wiek, D.; Mateus, E.F.; Sirotich, E.; Soriano, E.R.; Ribeiro, F.M.; Omura, F.; Rajão Martins, F.; Santos, H.; Dau, J.; Barker, J.N.; Hausmann, J.; Hyrich, K.L.; Gensler, L.; Silva, L.; Jacobsohn, L.; Carmona Ortells, Loreto; Pinheiro, M.M.; Zelaya, M.D.; Severina, M.L.Á.; Yates, M.; Dubreuil, M.; Gore-Massy, M.; Romeo, N.; Haroon, N.; Sufka, P.; Grainger, R.; Hasseli, R.; Lawson-Tovey, S.; Bhana, S.; Pham, T.; Olofsson, T.; Bautista-Molano, W.; Wallace, Z.S.; Yiu, Z.Z.N.; Yazdany, J.; Robinson, P.C.; Smith, C.H.
Identificadores
Identificadores
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Visualización o descarga de ficheros
Fecha de publicación
2023Título de revista
Annals of the rheumatic diseases
Tipo de contenido
Artigo
MeSH
Adult | Humans | Male | Arthritis, Psoriatic | Rheumatology | COVID-19 | Psoriasis | Axial Spondyloarthritis | Physicians | Glucocorticoids | Interleukin-12 | RegistriesResumen
OBJECTIVES: To investigate factors associated with severe COVID-19 in people with psoriasis (PsO), psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA). METHODS: Demographic 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. RESULTS: Of 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. CONCLUSION: Older 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.
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