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Ophthalmic Genet ; 36(3): 224-8, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-24372405

RESUMEN

BACKGROUND: An association between LOC387715/ARMS2 (rs10490924) gene polymorphism and AMD has been reported. The aim of this study was to evaluate whether this polymorphism is associated with AMD in a Brazilian cohort. MATERIALS AND METHODS: In total, 126 unrelated AMD patients (mean age 74.17 ± 7.64) were compared with 86 healthy controls (mean age 71.82 ± 7.12). Study subjects were classified according to the International ARM Epidemiological Study Group definition for early and late-stage AMD. LOC387715/ARMS2 rs10490924 polymorphism was evaluated through polymerase chain reaction and direct sequencing. RESULTS: The T allele frequency was significantly higher in AMD patients than in controls (39.6% compared to 20.3%). The odds ratio (OR) for AMD was 2.05 (95% CI 1.13-3.71) for heterozygotes (TG) and 8.32 (95% CI 2.30-45.99) for homozygotes (TT). CONCLUSIONS: These results suggest that there is a contribution of the rs10490924 SNP of the LOC387715/ARMS2 gene to AMD susceptibility in this sample of the Brazilian population.


Asunto(s)
Atrofia Geográfica/genética , Polimorfismo de Nucleótido Simple , Proteínas/genética , Degeneración Macular Húmeda/genética , Anciano , Anciano de 80 o más Años , Brasil/epidemiología , Femenino , Predisposición Genética a la Enfermedad , Genotipo , Atrofia Geográfica/epidemiología , Humanos , Masculino , Reacción en Cadena de la Polimerasa , Factores de Riesgo , Análisis de Secuencia de ADN , Degeneración Macular Húmeda/epidemiología
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