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Genetic factors for idiopathic choroidal neovascularization.
Cao, Xu-Sheng; Peng, Xiao-Yan; You, Qi-Sheng; Liu, Fen; Ding, Yuan-Jie; Yang, Hong-Li.
Afiliação
  • Cao XS; Department of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Science Key Lab , Beijing , China.
  • Peng XY; Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Science Key Lab , Beijing , China.
  • You QS; Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Science Key Lab , Beijing , China.
  • Liu F; Department of Epidemiology and Health Statistics, School of Public Health, Capital Medical University , Beijing , China.
  • Ding YJ; Department of Epidemiology and Health Statistics, School of Public Health, Capital Medical University , Beijing , China.
  • Yang HL; Beijing Institute of Ophthalmology, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University, Beijing Ophthalmology and Visual Science Key Lab , Beijing , China.
Ophthalmic Genet ; 40(4): 309-312, 2019 08.
Article em En | MEDLINE | ID: mdl-31512979
Objective: The aim of this study was to investigate genetic factors associated with idiopathic choroidal neovascularization (ICNV). Methods: We conducted a case-control study including 69 cases with ICNV and 114 controls who underwent cataract surgery. Single nucleotide polymorphisms (SNPs) from genes reported to be related to AMD, CNV and uveitis were selected for this study. Results: In an univariate analysis, the rs669676 SNP located in the COL8A1 gene was associated with the proportion of people who has idiopathic CNV ( X2 = 9.3453, corrected p-value = 0.1). For the rs669676 SNP, minor allele homozygotes, in the dominant model of genotype analysis (GG versus AA-GA), it showed significant differences in the ICNV group vs controls (p = .01, OR = 1.219 (95%CI: 1.04-1.429)). Conclusions: The rs669676 SNP located in the COL8A1 gene may contribute to a genetic susceptibility for ICNV.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neovascularização de Coroide / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Colágeno Tipo VIII Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neovascularização de Coroide / Predisposição Genética para Doença / Polimorfismo de Nucleotídeo Único / Colágeno Tipo VIII Idioma: En Ano de publicação: 2019 Tipo de documento: Article