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Article Abstract

Growth factor receptor-bound protein 2 (GRB2) is a negative regulator of insulin signaling and a positive regulator of angiogenesis. Its expression is increased in a mouse model of retinal neovascularization and in patients with type 2 diabetes mellitus (T2DM). This case-control study aimed to investigate the association between the rs9896052 polymorphism (A>C) upstream of and proliferative diabetic retinopathy (PDR) in patients with T2DM from Southern Brazil, taking into consideration self-reported skin color (white or non-white) and the known duration of diabetes (<10 years or ≥10 years). Genotypes were determined by real-time PCR in 838 patients with T2DM (284 cases with PDR and 554 controls without DR). In the total study group and in the analysis stratified by skin color, the genotype and allele frequencies were similar between cases and controls. However, among patients with less than 10 years of diabetes, the C allele was more frequent in cases than in controls (63.3% versus 51.8%, = 0.032), and the CC genotype was independently associated with an increased risk of PDR (adjusted OR = 2.82, 95% CI 1.17-6.75). In conclusion, our findings support the hypothesis that the rs9896052 polymorphism near is associated with PDR in Brazilian patients with T2DM.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11477274PMC
http://dx.doi.org/10.3390/ijms251910232DOI Listing

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Growth factor receptor-bound protein 2 (GRB2) is a negative regulator of insulin signaling and a positive regulator of angiogenesis. Its expression is increased in a mouse model of retinal neovascularization and in patients with type 2 diabetes mellitus (T2DM). This case-control study aimed to investigate the association between the rs9896052 polymorphism (A>C) upstream of and proliferative diabetic retinopathy (PDR) in patients with T2DM from Southern Brazil, taking into consideration self-reported skin color (white or non-white) and the known duration of diabetes (<10 years or ≥10 years).

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Article Synopsis
  • The study aims to identify genetic risk factors for diabetic retinopathy, a diabetes complication that can cause blindness, through a genome-wide association study.
  • The research involved comparing cases of sight-threatening diabetic retinopathy in white Australians with type 2 diabetes to diabetic controls without retinopathy and found a significant variant associated with the condition.
  • The findings suggest that the genetic variation near the GRB2 gene may be linked to increased risk for diabetic retinopathy, especially during conditions of retinal stress and new blood vessel formation.
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