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dc.creatorCharli-Joseph, Y.
dc.creatorCruz-Fuentes, C.
dc.creatorOrozco-Topete, R
dc.date.accessioned2017-06-30T03:58:08Z
dc.date.available2017-06-30T03:58:08Z
dc.date.issued2009es_ES
dc.identifier2417es_ES
dc.identifier.issn0926-9959es_ES
dc.identifier.urihttp://repositorio.inprf.gob.mx/handle/123456789/7059
dc.identifier.urihttps://doi.org/10.1111/j.1468-3083.2009.03173.xes_ES
dc.description.abstractBACKGROUND:Most adverse cutaneous drug reactions (ACDR) are mediated by delayed hypersensitivity (dh) with lymphocyte recruitment and inflammatory cytokines release, including tumour necrosis factor alpha (TNFalpha). Polymorphisms in the TNFalpha gene, such as the infrequentallele TNF2, predispose to certain inflammatory entities and enhance TNFalpha production. The incidence of the TNF2 allele is increased in British patients with severe ACDR, suggesting TNFalpha as a major contributor in the pathogenesis of ACDR. OBJECTIVE: We designed a prospective study to analyse the epidemiology of ACDR in a third-level Mexican hospital and explore the possibility of a relationship between the TNF2 allele and ACDR-dh. METHODS: A prospective study during 9 months allowed recognition of 34 ACDR-dh patients. The study included 33 paired patients, and 44 healthy volunteers. All subjects were genotyped for TNF2 by PCR DNA amplification and NcoI restriction endonuclease digestion. Results Incidence of ACDR was 0.95%. The TNF2 allele was detected in 9.9% of the sample population with no significant differences between healthy controls, and patients with or without ACDR-dh. Only 3 of the 34 ACDR-dh subjects presented severe reactions, with 1 having the TNF2 allele. Comorbidity analysis showed significance only with autoimmune thyroid disease, consistent with reports on Chinese and Tunisian patients. CONCLUSION: ACDR incidence and TNF2/TNFA heterozygosity were lower in Mexican than in Caucasian patients. ACDR-dh patients showed no increased frequency in the TNF2 allele.es_ES
dc.language.isoenges_ES
dc.publisherOxford : Wiley-Blackwelles_ES
dc.relation23 (7) 788-792 p.es_ES
dc.relationversión del editores_ES
dc.rightsacceso cerradoes_ES
dc.subject.meshAlleleses_ES
dc.subject.meshDermatologic Agents-Adverse effectses_ES
dc.subject.meshHumanses_ES
dc.subject.meshIncidencees_ES
dc.subject.meshMexicoes_ES
dc.subject.meshPolymerase Chain Reactiones_ES
dc.subject.meshProspective Studieses_ES
dc.subject.meshTumor Necrosis Factor-alpha-Geneticses_ES
dc.subject.meshDermatologic Agentses_ES
dc.subject.meshTNF protein, humanes_ES
dc.subject.meshTumor Necrosis Factor-alphaes_ES
dc.titleIncidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele.es_ES
dc.typearticlees_ES
dc.contributor.affiliationFacultad de Medicina, Universidad Nacional Autónoma de México, México DF, Méxicoes_ES
dc.contributor.emailrorozco@quetzal.innsz.mxes_ES
dc.relation.jnabreviadoJ EUR ACAD DERMATOL VENEREOLes_ES
dc.relation.journalJournal of the European Academy of Dermatology and Venereologyes_ES
dc.identifier.placeInglaterraes_ES
dc.date.published2009es_ES
dc.identifier.organizacionInstituto Nacional de Psiquiatría Ramón de la Fuente Muñizes_ES
dc.identifier.eissn1468-3083es_ES
dc.identifier.doi10.1111/j.1468-3083.2009.03173.xes_ES
dc.description.abstractotrodiomaBACKGROUND:Most adverse cutaneous drug reactions (ACDR) are mediated by delayed hypersensitivity (dh) with lymphocyte recruitment and inflammatory cytokines release, including tumour necrosis factor alpha (TNFalpha). Polymorphisms in the TNFalpha gene, such as the infrequentallele TNF2, predispose to certain inflammatory entities and enhance TNFalpha production. The incidence of the TNF2 allele is increased in British patients with severe ACDR, suggesting TNFalpha as a major contributor in the pathogenesis of ACDR. OBJECTIVE: We designed a prospective study to analyse the epidemiology of ACDR in a third-level Mexican hospital and explore the possibility of a relationship between the TNF2 allele and ACDR-dh. METHODS: A prospective study during 9 months allowed recognition of 34 ACDR-dh patients. The study included 33 paired patients, and 44 healthy volunteers. All subjects were genotyped for TNF2 by PCR DNA amplification and NcoI restriction endonuclease digestion. Results Incidence of ACDR was 0.95%. The TNF2 allele was detected in 9.9% of the sample population with no significant differences between healthy controls, and patients with or without ACDR-dh. Only 3 of the 34 ACDR-dh subjects presented severe reactions, with 1 having the TNF2 allele. Comorbidity analysis showed significance only with autoimmune thyroid disease, consistent with reports on Chinese and Tunisian patients. CONCLUSION: ACDR incidence and TNF2/TNFA heterozygosity were lower in Mexican than in Caucasian patients. ACDR-dh patients showed no increased frequency in the TNF2 allele.es_ES
dc.subject.kwReacción farmacológica adversa cutáneaes_ES
dc.subject.kwEnfermedad tiroidea autoinmunees_ES
dc.subject.kwHipersensibilidad retardadaes_ES
dc.subject.kwMéxicoes_ES
dc.subject.kwAlelo TNF2es_ES
dc.subject.kwFactor de necrosis tumoral alfaes_ES
dc.subject.koAdverse cutaneous drug reactiones_ES
dc.subject.koAutoimmune thyroid diseasees_ES
dc.subject.koDelayed hypersensitivityes_ES
dc.subject.koMexicoes_ES
dc.subject.koTNF2 allelees_ES
dc.subject.koTumour necrosis factor alphaes_ES


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