Estudio de polimorfismos de la Óxido Nítrico Sintasa Endotelial (NOSE) en pacientes con lupus eritematoso sistémico

dc.contributor.advisorDíaz Martínez, Luis Alfonso
dc.contributor.authorSerrano Díaz, Norma Cecilia
dc.contributor.authorPáez Leal, María Carolina
dc.contributor.authorAnaya C., Juan Manuel
dc.contributor.cvlacSerrano Diaz, Norma Cecilia [0000066613]spa
dc.contributor.cvlacPáez Leal, María Carolina [0000066656]spa
dc.contributor.cvlacDíaz Martínez, Luis Alfonso [0000066621]spa
dc.contributor.googlescholarSerrano Diaz, Norma Cecilia [iDn0AAAAAJ&hl=es&oi=ao]spa
dc.contributor.googlescholarPáez Leal, María Carolina [BAPR3-cAAAAJ]spa
dc.contributor.googlescholarDíaz Martínez, Luis Alfonso [ABarFDsAAAAJ]spa
dc.contributor.orcidSerrano Diaz, Norma Cecilia [0000-0003-3532-2002]spa
dc.contributor.orcidPáez Leal, María Carolina [0000-0002-0310-0125]spa
dc.contributor.orcidDíaz Martínez, Luis Alfonso [0000-0002-4498-6639]spa
dc.contributor.researchgatePáez Leal, María Carolina [Maria_Paez-Leal]spa
dc.contributor.scopusSerrano Diaz, Norma Cecilia [7003706613]spa
dc.contributor.scopusPáez Leal, María Carolina [12243485600]spa
dc.coverage.campusUNAB Campus Bucaramangaspa
dc.coverage.spatialBucaramanga (Santander, Colombia)spa
dc.coverage.temporal2005spa
dc.date.accessioned2023-11-20T15:56:17Z
dc.date.available2023-11-20T15:56:17Z
dc.date.issued2005
dc.description.abstractEl LES no es una enfermedad rara, pues su prevalencia en la población mundial fluctúa entre 2.9-206 casos x 100.000 habitantes, reportándose una mayor incidencia entre la población hispana y afroamericana, en cuyos grupos raciales suele presentar un curso más grave de la enfermedad. Este fenómeno ha sido atribuido por algunos expertos a factores socioeconómicos y ambientales, que colocan a países como Colombia como referentes para el estudio de esta entidad. Su etiología es aún desconocida, e involucra factores genéticos, hormonales y ambientales interactúan de una forma compleja en su génesis, representando el prototipo de las Enfermedades Complejas, donde la existencia de una predisposición genética en asociación con diferentes factores de riesgo medio ambientales, hacen que esa susceptibilidad genética se ponga de manifiesto y se desarrolle la enfermedad. Considerado el LES como una enfermedad compleja que cursa con disfunción endotelial en asociación con alteraciones en la biodisponibilidad del óxido nítrico, consideramos que el gen que codifica para la NOSe es un buen candidato que pudiera estar relacionado con el origen y desarrollo de la enfermedad, donde las variaciones genéticas representadas en polimorfismos del gen podrían comportarse como factor de riesgo independiente para el desarrollo de la misma. La importancia de determinar factores de riesgo genético asociados a la enfermedad permitiría en aquellas pacientes portadoras iniciar de manera temprana medidas terapéuticas que logren modificar el curso de la enfermedad.spa
dc.description.abstractenglishSLE is not a rare disease, since its prevalence in the world population fluctuates between 2.9-206 cases per 100,000 inhabitants, with a higher incidence reported among the Hispanic and African-American population, in whose racial groups usually presents a more severe course of the disease. This phenomenon has been attributed by some experts to socioeconomic and environmental factors, which place countries like Colombia as references for the study of this entity. Its etiology is still unknown, and it involves genetic, hormonal and environmental factors that interact in a complex way in its genesis, representing the prototype of Complex Diseases, where the existence of a genetic predisposition in association with different environmental risk factors, causes that genetic susceptibility becomes evident and the disease develops. Considering SLE as a complex disease that presents with endothelial dysfunction in association with alterations in the bioavailability of nitric oxide, we consider that the gene that codes for NOSe is a good candidate that could be related to the origin and development of the disease, where The genetic variations represented in gene polymorphisms could behave as an independent risk factor for its development. The importance of determining genetic risk factors associated with the disease would allow carrier patients to initiate therapeutic measures early that can modify the course of the disease.spa
dc.description.learningmodalityModalidad Presencialspa
dc.format.mimetypeapplication/pdfspa
dc.identifier.instnameinstname:Universidad Autónoma de Bucaramanga - UNABspa
dc.identifier.reponamereponame:Repositorio Institucional UNABspa
dc.identifier.repourlrepourl:https://repository.unab.edu.cospa
dc.identifier.urihttp://hdl.handle.net/20.500.12749/22850
dc.language.isospaspa
dc.publisher.facultyFacultad Ciencias de la Saludspa
dc.publisher.grantorUniversidad Autónoma de Bucaramanga UNABspa
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dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
dc.rights.creativecommonsAtribución-NoComercial-SinDerivadas 2.5 Colombia*
dc.rights.localAbierto (Texto Completo)spa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.5/co/*
dc.subject.keywordsComplex diseasesspa
dc.subject.keywordsGeneticsspa
dc.subject.keywordsLupusspa
dc.subject.keywordsSystemic lupus erythematosusspa
dc.subject.keywordsBiological developmentspa
dc.subject.keywordsPolymorphismspa
dc.subject.keywordsPathophysiologyspa
dc.subject.lembLupus eritematoso sistémicospa
dc.subject.lembDesarrollo biológicospa
dc.subject.lembPolimorfismospa
dc.subject.lembFisiopatologíaspa
dc.subject.proposalEnfermedades complejasspa
dc.subject.proposalGenéticaspa
dc.subject.proposalLupusspa
dc.titleEstudio de polimorfismos de la Óxido Nítrico Sintasa Endotelial (NOSE) en pacientes con lupus eritematoso sistémicospa
dc.title.translatedStudy of polymorphisms of Endothelial Nitric Oxide Synthase (NOSe) in patients with systemic lupus erythematosusspa
dc.typeResearch reporteng
dc.type.coarhttp://purl.org/coar/resource_type/c_18ws
dc.type.coarversionhttp://purl.org/coar/version/c_ab4af688f83e57aaspa
dc.type.driverinfo:eu-repo/semantics/workingPaperspa
dc.type.hasversioninfo:eu-repo/semantics/acceptedVersionspa
dc.type.localInforme de investigaciónspa
dc.type.redcolhttp://purl.org/redcol/resource_type/IFIspa

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