Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/1092
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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP-
dc.contributor.authorCAPPI, Carolina-
dc.contributor.authorMUNIZ, Renan Kawano-
dc.contributor.authorSAMPAIO, Aline Santos-
dc.contributor.authorCORDEIRO, Quirino-
dc.contributor.authorBRENTANI, Helena-
dc.contributor.authorPALACIOS, Selma A.-
dc.contributor.authorMARQUES, Andrea H.-
dc.contributor.authorVALLADA, Homero-
dc.contributor.authorMIGUEL, Euripedes Constantino-
dc.contributor.authorGUILHERME, Luiza-
dc.contributor.authorHOUNIE, Ana Gabriela-
dc.date.accessioned2013-07-30T15:18:57Z-
dc.date.available2013-07-30T15:18:57Z-
dc.date.issued2012-
dc.identifier.citationARQUIVOS DE NEURO-PSIQUIATRIA, v.70, n.2, p.87-90, 2012-
dc.identifier.issn0004-282X-
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/1092-
dc.description.abstractObsessive-compulsive disorder (OCD) is a prevalent psychiatric disorder of unknown etiology. However, there is some evidence that the immune system may play an important role in its pathogenesis. In the present study, two polymorphisms (rs1800795 and rs361525) in the promoter region of the cytokine tumor necrosis factor-alpha (TNFA) gene were genotyped in 183 OCD patients and in 249 healthy controls. The statistical tests were performed using the PLINK (R) software. We found that the A allele of the TNFA rs361525 polymorphism was significantly associated with OCD subjects, according to the allelic x association test (p=0.007). The presence of genetic markers, such as inflammatory cytokines genes linked to OCD, may represent additional evidence supporting the rote of the immune system in its pathogenesis.-
dc.description.abstractO transtorno obsessivo-compulsivo (TOC) é um quadro psiquiátrico de prevalência considerável na população e de etiologia desconhecida. No entanto, há evidências de que o sistema imunológico pode desempenhar um papel importante em sua patogênese. No presente estudo, dois polimorfismos (rs1800795 e rs361525), localizados na região promotora do gene que codifica a citocina conhecida como fator de necrose tumoral alfa (TNFA), foram genotipados em 183 pacientes com TOC e 249 controles saudáveis. Os testes estatísticos foram realizados utilizando-se o software PLINK®. Assim, evidenciou-se que o alelo A do polimorfismo rs361525 apresentava associação estatisticamente significante com o TOC (p=0,007). A presença de marcadores genéticos, tais como genes que codificam citocinas inflamatórias, associados com TOC, confere suporte adicional ao papel do sistema imunológico na patogênese desse transtorno.-
dc.description.sponsorshipCAPES/PRODOC-
dc.description.sponsorshipFAPESP [98/15-013-9, 2005/55628-8]-
dc.description.sponsorshipCNPq-
dc.language.isoeng-
dc.publisherASSOC ARQUIVOS NEURO- PSIQUIATRIA-
dc.relation.ispartofArquivos de Neuro-Psiquiatria-
dc.rightsopenAccess-
dc.subjectcytokines-
dc.subjectgenetic markers-
dc.subjectmental disorder-
dc.subjectpolymorphism-
dc.subjectcitocinas-
dc.subjectmarcadores genéticos-
dc.subjecttranstorno mental-
dc.subjectpolimorfismo-
dc.subject.othernecrosis-factor-alpha-
dc.subject.otherpromoter polymorphism-
dc.subject.otherdepressive symptoms-
dc.subject.otherrheumatic-fever-
dc.subject.otherstress-
dc.subject.otherbrain-
dc.subject.otheridentification-
dc.subject.otherepidemiology-
dc.subject.otherpopulation-
dc.subject.othermechanisms-
dc.titleAssociation study between functional polymorphisms in the TNF-alpha gene and obsessive-compulsive disorder-
dc.title.alternativeEstudo de associação entre polimorfismos funcionais do gene do TNF-alfa e transtorno obsessivo-compulsivo-
dc.typearticle-
dc.rights.holderCopyright ASSOC ARQUIVOS NEURO- PSIQUIATRIA-
dc.identifier.doi10.1590/S0004-282X2012000200003-
dc.identifier.pmid22311210-
dc.subject.wosNeurosciences-
dc.subject.wosPsychiatry-
dc.type.categoryoriginal article-
dc.type.versionpublishedVersion-
hcfmusp.author.externalCORDEIRO, Quirino:Santa Casa Med Sch, Dept Psychiat & Psychol Med, Sao Paulo, Brazil-
hcfmusp.description.beginpage87-
hcfmusp.description.endpage90-
hcfmusp.description.issue2-
hcfmusp.description.volume70-
hcfmusp.origemWOS-
hcfmusp.origem.id2-s2.0-84857136589-
hcfmusp.origem.idWOS:000300650300003-
hcfmusp.origem.idSCIELO:S0004-282X2012000200003-
hcfmusp.publisher.citySAO PAULO SP-
hcfmusp.publisher.countryBRAZIL-
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dc.description.indexMEDLINE-
hcfmusp.remissive.sponsorshipCAPES-
hcfmusp.remissive.sponsorshipCNPq-
hcfmusp.remissive.sponsorshipFAPESP-
hcfmusp.lim.ref2012-
hcfmusp.citation.scopus24-
hcfmusp.scopus.lastupdate2024-04-12-
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Artigos e Materiais de Revistas Científicas - FM/MPS
Departamento de Psiquiatria - FM/MPS

Artigos e Materiais de Revistas Científicas - HC/InCor
Instituto do Coração - HC/InCor

Artigos e Materiais de Revistas Científicas - HC/IPq
Instituto de Psiquiatria - HC/IPq

Artigos e Materiais de Revistas Científicas - LIM/19
LIM/19 - Laboratório de Histocompatibilidade e Imunidade Celular

Artigos e Materiais de Revistas Científicas - LIM/21
LIM/21 - Laboratório de Neuroimagem em Psiquiatria

Artigos e Materiais de Revistas Científicas - LIM/23
LIM/23 - Laboratório de Psicopatologia e Terapêutica Psiquiátrica


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