Influence of VEGF-C936T genetic variant in age-related macular degeneration

• Grant number: 12/12063-4
• Support Opportunities: Scholarships in Brazil - Scientific Initiation
• Effective date (Start): September 01, 2012
• Effective date (End): August 31, 2013
• Field of knowledge: Health Sciences - Medicine
• Principal Investigator: Rubens Camargo Siqueira
• Grantee: Fernanda Tanaka Iasbeck Gonçalves
• Host Institution: Faculdade de Medicina de São José do Rio Preto (FAMERP). Secretaria de Desenvolvimento Econômico (São Paulo - Estado). São José do Rio Preto , SP, Brazil

Abstract

Age-related macular degeneration (AMD) is a complex disorder of multifactorial eye that affects the elderly, being the third leading cause of blindness worldwide. AMD results in progressive and irreversible loss of central vision that affects the macula of the eye and involves the retinal pigment epithelium (RPE), Bruch's membrane (BM), coriocapilares. Genetic risk factors have been associated with the disease, including high expression of the gene variants and polymorphisms of vascular endothelial growth factor (VEGF), apolipoprotein E4 (APOE*4), and a member of the A subfamily of ABC transporters adenosine triphosphate-binding cassette (ABCA4). Objectives: Evaluate the influence of polymorphisms VEGF-C936T, APOE-HhaI and ABCA4 in patients with age-related macular degeneration (ARMD); evaluate the gene expression of VEGF, ABCA4, and APOE in peripheral blood of patients with AMD (exudative form) and verify the existence of a correlation between the expression of the different genes proposed for each group, separately. Methods: 240 individuals will be selected, regardless of gender, ethnicity and age in three groups. Group 1 (G1) - 80 individuals diagnosed with age-related macular degeneration in dry form, Group 2 (G2) - 80 individuals with macular degeneration related to age as exudative and Group 3 (G3) - 80 individuals with macular degeneration not related with age. Nucleic acids (DNA and RNA) are extracted from peripheral blood and glass, respectively. Conventional PCR will be performed in real time for analysis of samples. The biochemical analysis are carried out using enzyme immunoassay (EIA) and by ELISA . Statistical analysis will include the Fisher exact test, multivariate regression, with significance level P <0.05.(AU)