1. Regional differences in clinical phenotype of axial spondyloarthritis: results from the International Map of Axial Spondyloarthritis (IMAS).
- Author
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Poddubnyy, Denis, Sommerfleck, Fernando, Navarro-Compán, Victoria, Bundy, Christine, Makri, Souzi, Akerkar, Shashank, Wermskog, Lillann, Karam, Elie, Correa-Fernández, José, Siddiqui, Asif, and Garrido-Cumbrera, Marco
- Subjects
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CROSS-sectional method , *NONSTEROIDAL anti-inflammatory agents , *RESEARCH funding , *ANKYLOSIS , *POPULATION geography , *FAMILY history (Medicine) , *DESCRIPTIVE statistics , *ANTIRHEUMATIC agents , *WORLD health , *SPONDYLOARTHROPATHIES , *SUDDEN onset of disease , *DELAYED diagnosis , *PHENOTYPES , *HLA-B27 antigen , *COMORBIDITY - Abstract
Objectives To explore differences in axial spondyloarthritis (axSpA) clinical phenotype around the world in a large sample of patients included in the International Map of Axial Spondyloarthritis (IMAS). Method IMAS was a cross-sectional online survey (2017–2022) of 5557 unselected axSpA patients from 27 countries. We analysed across five geographic regions the age at symptom onset, diagnostic delay, gender, HLA-B27, family history, extra-musculoskeletal manifestations, presence of comorbidities, disease activity (BASDAI), level of spinal stiffness and treatments. Results Of 5557 IMAS participants, 3493 were from Europe, 770 from North America, 600 from Asia, 548 from Latin America and 146 from South Africa. Age at symptom onset ranged between 25 and 30 years and was higher in Latin America. Diagnostic delay was longest in South Africa and lowest in Asia. The lowest HLA-B27 positivity was observed in Latin America and the highest in Asia. Extra-musculoskeletal manifestations were the lowest in Europe. Mean disease activity (BASDAI) was 5.4, with highest values in South Africa and lowest in Asia. Most of the patients had used NSAIDs for their condition and less than half had ever taken conventional synthetic DMARDS; both were more frequent in Latin America and South Africa. Almost half of the patients had ever taken biologic DMARDs, more frequent use being in the Americas. Conclusion There is great heterogeneity of axSpA clinical phenotype presentation around the world. AxSpA manifests differently in different regions, so further understanding of these differences of phenotypes is needed to achieve early diagnosis and initiation of optimal disease treatment in axSpA in the different regions. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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