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Cir Cir ; 83(6): 467-72, 2015.
Artigo em Espanhol | MEDLINE | ID: mdl-26188706

RESUMO

BACKGROUND: Intracranial aneurysms are abnormal dilations of the cerebral arteries of unknown origin. However, some genes have been linked to their formation, as in the case of NOS3 gene which encodes the endothelial nitric oxide synthase responsible for producing nitric oxide. Several polymorphisms in this gene, in association with a variable number tandem repeat located in intron 4 from eNOS4 gene, can influence the formation of aneurysms. Therefore, the purpose of this study is to determine the genotype frequencies of eNOS3 and eNOS4 genes, and their relationship with intracranial aneurysms. MATERIAL AND METHODS: A prospective case-control study was performed on 79 cases with ruptured intracranial aneurysm and 93 healthy controls. DNA was obtained from all subjects for the study of the eNOS3 and eNOS4 genes by molecular techniques. RESULTS: The GG genotype of eNOS3 gene showed the largest number of patients (n=29) with a large aneurysm. While the intracranial aneurysms of medium size were found in a higher percentage (50%) in patients with genotype GT. In terms of patient outcomes, it was observed that those with genotype GG had the highest percentage (43.13%) recovery, compared to genotype GT (27.27%). CONCLUSIONS: The present study shows that there is a tendency of an association between genotypes of eNOS3 gene with the mean size of the aneurysm, as well as clinical sequelae of the disease in patients with intracranial aneurysms.


Assuntos
Aneurisma Intracraniano/genética , Óxido Nítrico Sintase Tipo III/genética , Adulto , Idoso , Aneurisma Roto/genética , Antropometria , Dano Encefálico Crônico/etiologia , Dano Encefálico Crônico/genética , Estudos de Casos e Controles , Artérias Cerebrais/patologia , Feminino , Frequência do Gene , Predisposição Genética para Doença , Genótipo , Humanos , Aneurisma Intracraniano/complicações , Aneurisma Intracraniano/patologia , Íntrons/genética , Masculino , Pessoa de Meia-Idade , Repetições Minissatélites , Polimorfismo de Nucleotídeo Único , Estudos Prospectivos , Fatores de Risco
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