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dc.contributor.authorGargallo, Carla J.
dc.contributor.authorRicart Gomez, Elena
dc.contributor.authorIglesias, Eva
dc.contributor.authorde Francisco, Ruth
dc.contributor.authorGisbert, Javier Pérez
dc.contributor.authorTaxonera, Carlos
dc.contributor.authorMañosa, Miriam
dc.contributor.authorAguas, Mariam
dc.contributor.authorNavarrete-Muñoz, Eva María
dc.contributor.authorSanahuja Martínez, Ana
dc.contributor.authorGuardiola, Jordi
dc.contributor.authorMesonero, Francisco
dc.contributor.authorRivero, Montserrat
dc.contributor.authorBARRIO, JESÚS
dc.contributor.authorVera Mendoza, Isabel
dc.contributor.authorDe Castro Parga, María Luisa
dc.contributor.authorGarcía-Planella, Esther
dc.contributor.authorCalvet, Xavier
dc.contributor.authorMartín Arranz, María Dolores
dc.contributor.authorGarcía, Santiago
dc.contributor.authorSicilia, Beatriz
dc.contributor.authorCarpio, Daniel
dc.contributor.authorDOMENECH, EUGENI
dc.contributor.authorGomollón, Fernando
dc.date.accessioned2026-05-06T10:35:38Z
dc.date.issued2024-11
dc.identifier.citationGargallo, C. J.; Ricart Gomez, E.; Iglesias, E. [et. al.]. Sex-Related Differences in the Phenotype and Course of Inflammatory Bowel Disease: SEXEII Study of ENEIDA. Clinical Gastroenterology and Hepatology, 2024, Volume 22, Issue 11, pp. 2280-2290. Disponible en: <https://www.cghjournal.org/article/S1542-3565(24)00487-7/fulltext>. Fecha de acceso: 6 May 2026. DOI: 10.1016/j.cgh.2024.05.013ca
dc.identifier.issn1542-3565ca
dc.identifier.urihttp://hdl.handle.net/20.500.12328/5311
dc.descriptionAcknowledgments: The authors are sincerely grateful to Erika Alfambra for administrative support. The authors also are grateful to Alberto Cebollada for statistical support. The Supplementary Appendix list the affiliations of the Estudio Nacional en Enfermedad Inflamatoria intestinal sobre Determinantes genéticos y Ambientales: Nationwide study on genetic and environmental determinants of inflammatory bowel disease-Grupo Español de trabajo en Enfermedad de Crohn y Colitis Ulcerosa investigators. Funding: The ENEIDA registry (Nationwide study on genetic and environmental determinants of inflammatory bowel disease) of Grupo Español de trabajo en Enfermedad de Crohn y Colitis Ulcerosa is supported by Takeda, Pfizer, Galápagos, AbbVie, and Biogen. None of them had access to the clinical information or were involved in the present analysis.ca
dc.description.abstractBackground & Aims: The impact of patient sex on the presentation of inflammatory bowel disease (IBD) has been poorly evaluated. Our aims were to assess potential disparities in IBD phenotype and progression between sexes. Methods: We performed an observational multicenter study that included patients with Crohn's disease (CD) or ulcerative colitis from the Spanish Estudio Nacional en Enfermedad Inflamatoria intestinal sobre Determinantes genéticos y Ambientales registry. Data extraction was conducted in July 2021. Results: A total of 51,595 patients with IBD were included, 52% were males and 25,947 had CD. The median follow-up period after diagnosis was 9 years in males and 10 years in females. In CD, female sex was an independent risk factor for medium disease onset (age, 17–40 y) (relative risk ratio, 1.45; 95% CI, 1.31–1.62), later disease onset (age, >40 y) (relative risk ratio, 1.55; 95% CI, 1.38–1.73), exclusive colonic involvement (odds ratio, 1.24; 95% CI, 1.14–1.34), inflammatory behavior (odds ratio, 1.14; 95% CI, 1.07–1.21), and extraintestinal manifestations (odds ratio, 1.48; 95% CI, 1.38–1.59). However, female sex was a protective factor for upper gastrointestinal involvement (odds ratio, 0.84; 95% CI, 0.79–0.90), penetrating behavior (odds ratio, 0.76; 95% CI, 0.70–0.82), perianal disease (odds ratio, 0.77; 95% CI, 0.71–0.82), and complications (odds ratio, 0.73; 95% CI, 0.66–0.80). In ulcerative colitis, female sex was an independent risk factor for extraintestinal manifestations (odds ratio, 1.48; 95% CI, 1.26–1.61). However, female sex was an independent protective factor for disease onset from age 40 onward (relative risk ratio, 0.76; 95% CI, 0.66–0.87), left-sided colonic involvement (relative risk ratio, 0.72; 95% CI, 0.67–0.78), extensive colonic involvement (relative risk ratio, 0.59; 95% CI, 0.55–0.64), and abdominal surgery (odds ratio, 0.78; 95% CI, 0.69–0.88). Conclusions: There is sexual dimorphism in IBD. The patient's sex should be taken into account in the clinical management of the disease.ca
dc.format.extentDesconocidoca
dc.language.isoengca
dc.publisherElsevierca
dc.relation.ispartofClinical Gastroenterology and Hepatologyca
dc.rights© 2024 by the AGA Instituteca
dc.subject.otherInflammatory Bowel Diseaseca
dc.subject.otherCrohn’s Diseaseca
dc.subject.otherUlcerative Colitisca
dc.subject.otherPatient Sexca
dc.subject.otherPhenotypeca
dc.subject.otherClinical Courseca
dc.subject.otherEnfermedad inflamatoria intestinalca
dc.subject.otherEnfermedad de Crohnca
dc.subject.otherColitis ulcerosaca
dc.subject.otherSexo del pacienteca
dc.subject.otherFenotipoca
dc.subject.otherCurso Clínicoca
dc.subject.otherMalaltia inflamatòria intestinalca
dc.subject.otherMalaltia de Crohnca
dc.subject.otherColitis ulcerosaca
dc.subject.otherSexe del pacientca
dc.subject.otherFenotipca
dc.subject.otherCurs Clínicca
dc.titleSex-Related Differences in the Phenotype and Course of Inflammatory Bowel Disease: SEXEII Study of ENEIDAca
dc.typeinfo:eu-repo/semantics/articleca
dc.description.versioninfo:eu-repo/semantics/publishedVersionca
dc.rights.accessLevelinfo:eu-repo/semantics/embargoedAccess
dc.embargo.termsforeverca
dc.subject.udc61ca
dc.identifier.doihttps://dx.doi.org/10.1016/j.cgh.2024.05.013ca
dc.date.embargoEnd9999-01-01


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