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dc.contributor.authorErazo Luna, Evelyn Vanesa-
dc.contributor.authorEchavarría Sierra, Claudia Janeth-
dc.contributor.authorCornejo Sánchez, Diana Marcela-
dc.contributor.authorSanclemente Mesa, Gloria-
dc.contributor.authorPineda Trujillo, Nicolás Guillermo-
dc.date.accessioned2024-11-10T19:18:32Z-
dc.date.available2024-11-10T19:18:32Z-
dc.date.issued2021-
dc.identifier.citationErazo Luna EV, Echavarría Sierra CJ, Cornejo-Sánchez DM, Sanclemente G, Pineda Trujillo NG. Protective association exhibited by a single nucleotide polymorphism of the IFIH1 gene in patients with psoriasis: A case-control study. Medwave. 2021 Dec 3;21(11):e8492. Spanish, English. doi: 10.5867/medwave.2021.11.002099.spa
dc.identifier.urihttps://hdl.handle.net/10495/43343-
dc.description.abstractABSTRACT: Introduction: Psoriasis is a chronic inflammatory dermatosis, a with variable clinical presentation and whose multifactorial etiology carries an essential genetic component. Multiple genetic variations associated with psoriasis have been described around the world. However, these variants are unknown among the Colombian population. This study aimed to evaluate the single nucleotide polymorphism rs10930046 (His460Arg) in the IFIH1 gene and its ssociation with the development of psoriasis in a Colombian population. Methods: An observational, unmatched, case-control study was performed, including 51 patients with psoriasis and 151 population controls, all with self-reported Paisa ancestry (from the Antioquia region). All individuals were genotyped for the single nucleotide polymorphism rs10930046 (His460Arg) in the IFIH1 gene, and its association with psoriasis was pursued. Both groups were demographically characterized, and cases were also assessed for clinical variables. Results: Through the allelic association analysis, cases were found to have a lower frequency of the single nucleotide polymorphism rs10930046 (His460Arg) in the IFIH1 gene than controls; 5% versus 22.67%, respectively. There were no significant differences in age or sex. We also found that psoriasis vulgaris was the most common variant (78%), that about half of the cases had nail psoriasis (56%), 19.6% had psoriatic arthritis, and that 45% had some comorbidity. Conclusions: The results obtained from this study confirm that carriers of the single nucleotide polymorphism rs10930046 (His460Arg) in the IFIH1 gene have a decreased risk of developing psoriasis.spa
dc.format.extent8 páginasspa
dc.format.mimetypeapplication/pdfspa
dc.language.isoengspa
dc.publisherMedwave Estudios Limitadaspa
dc.type.hasversioninfo:eu-repo/semantics/publishedVersionspa
dc.rightsinfo:eu-repo/semantics/openAccessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/2.5/co/*
dc.titleProtective association exhibited by a single nucleotide polymorphism of the IFIH1 gene in patients with psoriasis: A case-control studyspa
dc.typeinfo:eu-repo/semantics/articlespa
dc.publisher.groupGRID - Grupo de Investigación Dermatológicaspa
dc.publisher.groupGrupo Mapeo Genéticospa
dc.identifier.doi10.5867/medwave.2021.11.002099-
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85spa
dc.rights.accessrightshttp://purl.org/coar/access_right/c_abf2spa
dc.identifier.eissn0717-6384-
oaire.citationtitleMedwavespa
oaire.citationstartpage1spa
oaire.citationendpage8spa
oaire.citationvolume21spa
oaire.citationissue11spa
dc.rights.creativecommonshttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.publisher.placeSantiago, Chilespa
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1spa
dc.type.redcolhttps://purl.org/redcol/resource_type/ARTspa
dc.type.localArtículo de investigaciónspa
dc.subject.decsEstudios de Casos y Controles-
dc.subject.decsCase-Control Studies-
dc.subject.decsPredisposición Genética a la Enfermedad-
dc.subject.decsGenetic Predisposition to Disease-
dc.subject.decsPolimorfismo de Nucleótido Simple-
dc.subject.decsPolymorphism, Single Nucleotide-
dc.subject.decsPsoriasis-
dc.subject.decsHelicasa Inducida por Interferón IFIH1-
dc.subject.decsInterferon-Induced Helicase, IFIH1-
dc.description.researchgroupidCOL0050839spa
dc.description.researchgroupidCOL0057491spa
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D016022-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D020022-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D020641-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D011565-
dc.subject.meshurihttps://id.nlm.nih.gov/mesh/D000072640-
dc.relation.ispartofjournalabbrevMedwavespa
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