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dc.contributor.authorVázquez-Comendador, José Manuel
dc.contributor.authorMateos Seirul-lo, María
dc.contributor.authorMartínez-Urbistondo, María
dc.contributor.authorMiguel-Ontañón, Nuria
dc.contributor.authorGonzález-Guzmán, Antonio
dc.contributor.authorFernández-Guitián, Román
dc.contributor.authorCastejón, Raquel
dc.contributor.authorDurán-del Campo, Pedro
dc.contributor.authorTutor, Pablo
dc.contributor.authorMellor-Pita, Susana
dc.contributor.authorMoreno-Torres, Víctor
dc.date2025
dc.date.accessioned2025-11-12T11:04:39Z
dc.date.available2025-11-12T11:04:39Z
dc.identifier.citationVázquez-Comendador, J. M., Mateos Seirul-Lo, M., Martínez-Urbistondo, M., Miguel-Ontañón, N., González-Guzmán, A., Fernández-Guitián, R., Castejón, R., Durán-Del Campo, P., Tutor, P., Mellor-Pita, S., & Moreno-Torres, V. (2025). Higher Mortality Risk From Ovarian Carcinomas, Small Bowel Neoplasms, and B-Cell and Mucosa-Associated Lymphoid Tissue Lymphomas in Sjögren Syndrome Patients. Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases, 31(2), 78–82. https://doi.org/10.1097/RHU.0000000000002169es_ES
dc.identifier.issn1076-1608
dc.identifier.issn1536-7355
dc.identifier.urihttps://reunir.unir.net/handle/123456789/18341
dc.description.abstractObjective To evaluate the impact of the different types of neoplasms and lineages on Sjögren syndrome (SjS) patient mortality. Methods Medical records review study based on the Spanish Hospital Discharge Database and the International Classification of Diseases, Tenth Revision, Clinical Modification coding list. The neoplasm-related deaths in SjS patients with the general population during the period 2016–2019 were compared. A binary logistic regression analysis considering age, sex, tobacco use, and alcohol use was performed to determine the impact of SjS on the risk of dying from each neoplasm group and lineage. Results In the period studied, 705,557 in-hospital deaths were certified in Spain, 139,531 (19.8%) from neoplasms. Neoplasms surpassed SjS activity as a cause of mortality in primary SjS patients (11.3% vs. 1.6%, p < 0.001). SjS patients presented higher mortality rates from small bowel carcinoma (0.3% vs. 1.8%; odds ratio [OR], 5.41; 95% confidence interval [CI], 1.33–22) and gynecological neoplasms (6.4% vs. 3%; OR, 2.13; 95% CI, 1.01–4.58), related to ovarian carcinomas (4.6% vs. 1.3%; OR, 3.65; 95% CI, 1.48–8.97), than the general population. Hematological neoplasm–related deaths were more prevalent in SjS patients than in the non-SjS population (18.3% vs. 8.9%; OR, 2.04; 95% CI, 1.25–3.31), mostly attributable to the higher proportion of deaths from B-cell non-Hodgkin lymphoma (8.3% vs. 2.5%; OR, 3.04; 95% CI, 1.54–6.03) and mucosa-associated lymphoid tissue lymphoma (1.8% vs. 0.1%; OR, 70.17; 95% CI, 16.61–296.36). Conclusion SjS patients face an elevated risk of mortality from small bowel neoplasms, ovarian carcinomas, and B-cell and mucosa-associated lymphoid tissue lymphoma compared with the general Spanish population. Apart from developing approaches to mitigate their occurrence, it is crucial to explore thoroughly and consider the implementation of targeted early-detection programs for these specific conditions.es_ES
dc.language.isoenges_ES
dc.publisherJournal of Clinical Rheumatologyes_ES
dc.relation.ispartofseries;vol. 31, nº 2
dc.relation.urihttps://journals.lww.com/jclinrheum/fulltext/2025/03000/higher_mortality_risk_from_ovarian_carcinomas,.6.aspxes_ES
dc.rightsopenAccesses_ES
dc.subjectSjögren syndromees_ES
dc.subjectmortalityes_ES
dc.subjectneoplasmes_ES
dc.subjectovarian neoplasmes_ES
dc.subjectsmall bowel carcinomaes_ES
dc.subjectB-cell lymphomaes_ES
dc.subjectMALT lymphomaes_ES
dc.titleHigher Mortality Risk From Ovarian Carcinomas, Small Bowel Neoplasms, and B-Cell and Mucosa-Associated Lymphoid Tissue Lymphomas in Sjögren Syndrome Patientses_ES
dc.typearticlees_ES
reunir.tag~OPUes_ES
dc.identifier.doihttps://doi.org/10.1097/rhu.0000000000002169


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