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Abstract
To estimate the prevalence of Sjögren’s syndrome (SS) in the adult Spanish population we performed a population-based multicenter cross-sectional study. Cases were defined by the American-European Consensus Group criteria proposed in 2002. A total of 4,916 subjects aged 20 years or over were included. The estimated prevalence of SS (including primary and secondary forms) in the adult population in Spain was 0.33% (95% CI 0.21–0.53). Extrapolating to the total population of the country aged ≥ 20 years (around 37.7 million persons), there would be around 125,000 cases of SS in Spain. Considering only primary SS, the estimated prevalence was 0.25% (95% CI 0.15–0.43) or 1 person in 400. The prevalence of primary SS in Spain is comparable to that reported in other European studies with a similar design and diagnostic criteria. Based on these results, primary SS could not be considered a rare (orphan) disease. Only 50% of cases had already been diagnosed with SS prior EPISER 2016 study, confirming the existence of a non-negligible proportion of undiagnosed cases in the general population.
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1 Hospital Universitario de Bellvitge, Department of Rheumatology (Planta 10-2), Barcelona, Spain (GRID:grid.411129.e) (ISNI:0000 0000 8836 0780)
2 Complejo Hospitalario Mancha Centro, Rheumatology Unit, Alcázar de San Juan, Spain (GRID:grid.426047.3) (ISNI:0000 0001 1530 8903)
3 Sociedad Española de Reumatología, Unidad de Investigación, Madrid, Spain (GRID:grid.419354.e) (ISNI:0000 0000 9147 2636)
4 Hospital Universitario de Canarias, Department of Rheumatology, La Laguna, Spain (GRID:grid.411220.4) (ISNI:0000 0000 9826 9219)