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Association of the rs9896052 Polymorphism Upstream of GRB2 with Proliferative Diabetic Retinopathy in Patients with Less than 10 Years of Diabetes.
Bastos, Caroline Moura Cardoso; da Silva Machado, Lucas Marcelo; Crispim, Daisy; Canani, Luís Henrique; Dos Santos, Kátia Gonçalves.
Afiliação
  • Bastos CMC; Laboratory of Human Molecular Genetics, Lutheran University of Brazil (ULBRA), Av. Farroupilha 8001, Canoas 92425-900, RS, Brazil.
  • da Silva Machado LM; Laboratory of Human Molecular Genetics, Lutheran University of Brazil (ULBRA), Av. Farroupilha 8001, Canoas 92425-900, RS, Brazil.
  • Crispim D; Endocrine Division, Clinical Hospital of Porto Alegre (HCPA), R. Ramiro Barcelos 2350, Porto Alegre 90035-903, RS, Brazil.
  • Canani LH; Department of Internal Medicine, Federal University of Rio Grande do Sul (UFRGS), R. Ramiro Barcelos 2400, Porto Alegre 90035-003, RS, Brazil.
  • Dos Santos KG; Laboratory of Human Molecular Genetics, Lutheran University of Brazil (ULBRA), Av. Farroupilha 8001, Canoas 92425-900, RS, Brazil.
Int J Mol Sci ; 25(19)2024 Sep 24.
Article em En | MEDLINE | ID: mdl-39408563
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 GRB2 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%, p = 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 GRB2 is associated with PDR in Brazilian patients with T2DM.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Diabetes Mellitus Tipo 2 / Retinopatia Diabética / Proteína Adaptadora GRB2 Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Brasil Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Polimorfismo de Nucleotídeo Único / Diabetes Mellitus Tipo 2 / Retinopatia Diabética / Proteína Adaptadora GRB2 Limite: Aged / Female / Humans / Male / Middle aged País/Região como assunto: America do sul / Brasil Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Brasil País de publicação: Suíça