Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/200936
Type: Artigo de periódico
Title: Association Of Loc387715/arms2 (rs10490924) Gene Polymorphism With Age-related Macular Degeneration In The Brazilian Population.
Author: Hirata, Fabio Endo
Vasconcellos, José Paulo Cabral de
Medina, Flávio MacCord
Rim, Priscila Hae Hyun
Fulco, Enzo Augusto Medeiros
Melo, Mônica Barbosa de
Abstract: Abstract 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.
Subject: Amd
Loc387715/arms2
Macular Degeneration
Polymorphism
Rs10490924
Rights: fechado
Identifier DOI: 10.3109/13816810.2013.867449
Address: http://www.ncbi.nlm.nih.gov/pubmed/24372405
Date Issue: 2013
Appears in Collections:Unicamp - Artigos e Outros Documentos

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