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dc.contributor.authorCoco Martín, María Begoña
dc.contributor.authorLeal Vega, Luis
dc.contributor.authorBlázquez Cabrera, José Antonio
dc.contributor.authorNavarro, Amalia
dc.contributor.authorMoro, María Jesús
dc.contributor.authorArranz García, Francisca
dc.contributor.authorAmérigo, María José
dc.contributor.authorSosa Henríquez, Manuel
dc.contributor.authorVázquez, María Ángeles
dc.contributor.authorMontoya, María José
dc.contributor.authorDíaz Curiel, Manuel
dc.contributor.authorOlmos, José Manuel
dc.contributor.authorPérez Castrillon, José Luis 
dc.contributor.authorFilgueira Rubio, José
dc.contributor.authorSánchez Molini, Pilar
dc.contributor.authorAguado Caballero, José María
dc.contributor.authorArmengol Sucarrats, Dolors
dc.contributor.authorCalero Bernal, María Luz
dc.contributor.authorde Escalante Yanguas, Begoña
dc.contributor.authorHernández de Sosa, Nerea
dc.contributor.authorHernández, José Luis
dc.contributor.authorJareño Chaumel, Julia
dc.contributor.authorMiranda García, María José
dc.contributor.authorGiner García, Mercedes
dc.contributor.authorMiranda Díaz, Cristina
dc.contributor.authorCotos Canca, Rafael
dc.contributor.authorCobeta García, Juan Carlos
dc.contributor.authorRodero Hernández, Francisco Javier
dc.contributor.authorTirado Miranda, Raimundo
dc.date.accessioned2024-01-31T09:44:04Z
dc.date.available2024-01-31T09:44:04Z
dc.date.issued2022
dc.identifier.citationAging Clin Exp Res. 2022 Sep;34(9):1997-2004es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/65419
dc.descriptionProducción Científicaes
dc.description.abstractPurpose To examine the response to anti-osteoporotic treatment, considered as incident fragility fractures after a minimum follow-up of 1 year, according to sex, age, and number of comorbidities of the patients. Methods For this retrospective observational study, data from baseline and follow-up visits on the number of comorbidities, prescribed anti-osteoporotic treatment and vertebral, humerus or hip fractures in 993 patients from the OSTEOMED registry were analyzed using logistic regression and an artificial network model. Results Logistic regression showed that the probability of reducing fractures for each anti-osteoporotic treatment considered was independent of sex, age, and the number of comorbidities, increasing significantly only in males taking vitamin D (OR = 7.918), patients without comorbidities taking vitamin D (OR = 4.197) and patients with ≥ 3 comorbidities taking calcium (OR = 9.412). Logistic regression correctly classified 96% of patients (Hosmer–Lemeshow = 0.492) compared with the artificial neural network model, which correctly classified 95% of patients (AUC = 0.6). Conclusion In general, sex, age and the number of comorbidities did not influence the likelihood that a given anti-osteoporotic treatment improved the risk of incident fragility fractures after 1 year, but this appeared to increase when patients had been treated with risedronate, strontium or teriparatide. The two models used classified patients similarly, but predicted differently in terms of the probability of improvement, with logistic regression being the better fit.es
dc.format.mimetypeapplication/pdfes
dc.language.isospaes
dc.publisherSpringer EEUUes
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.classificationOsteoporosis · Osteoporotic fractures · Anti-osteoporotic treatment · Comorbidities · Logistic regression · Artificial neural networkes
dc.titleComorbidity and osteoporotic fracture: approach through predictive modeling techniques using the OSTEOMED registryes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doi10.1007/s40520-022-02129-5es
dc.relation.publisherversionhttps://link.springer.com/es
dc.identifier.publicationfirstpage1997es
dc.identifier.publicationissue9es
dc.identifier.publicationlastpage2004es
dc.identifier.publicationtitleAging Clinical and Experimental Researches
dc.identifier.publicationvolume34es
dc.peerreviewedSIes
dc.identifier.essn1720-8319es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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