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Cir Cir ; 83(6): 467-72, 2015.
Article in Spanish | MEDLINE | ID: mdl-26188706

ABSTRACT

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.


Subject(s)
Intracranial Aneurysm/genetics , Nitric Oxide Synthase Type III/genetics , Adult , Aged , Aneurysm, Ruptured/genetics , Anthropometry , Brain Damage, Chronic/etiology , Brain Damage, Chronic/genetics , Case-Control Studies , Cerebral Arteries/pathology , Female , Gene Frequency , Genetic Predisposition to Disease , Genotype , Humans , Intracranial Aneurysm/complications , Intracranial Aneurysm/pathology , Introns/genetics , Male , Middle Aged , Minisatellite Repeats , Polymorphism, Single Nucleotide , Prospective Studies , Risk Factors
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