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The A allele of the rs759853 single nucleotide polymorphism in the AKR1B1 gene confers risk for diabetic kidney disease in patients with type 2 diabetes from a Brazilian population
Dieter, Cristine; Lemos, Natália Emerim; Corrêa, Nathalia Rodrigues de Faria; Pellenz, Felipe Mateus; Canani, Luís Henrique; Crispim, Daisy; Bauer, Andrea Carla.
  • Dieter, Cristine; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
  • Lemos, Natália Emerim; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
  • Corrêa, Nathalia Rodrigues de Faria; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
  • Pellenz, Felipe Mateus; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
  • Canani, Luís Henrique; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
  • Crispim, Daisy; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
  • Bauer, Andrea Carla; Hospital de Clínicas de Porto Alegre. Divisão Endócrina. Porto Alegre. BR
Arch. endocrinol. metab. (Online) ; 66(1): 12-18, Jan.-Feb. 2022. tab
Artículo en Inglés | LILACS | ID: biblio-1364310
ABSTRACT
ABSTRACT

Objective:

The AKR1B1 gene encodes an enzyme that catalyzes the reduction of glucose into sorbitol. Chronic hyperglycemia in patients with diabetes mellitus (DM) leads to increased AKR1B1 affinity for glucose and, consequently, sorbitol accumulation. Elevated sorbitol increases oxidative stress, which is one of the main pathways related to chronic complications of diabetes, including diabetic kidney disease (DKD). Accordingly, some studies have suggested the rs759853 polymorphism in the AKR1B1 gene is associated with DKD; however, findings are still contradictory. The aim was to investigate the association of the rs759853 polymorphism in the AKR1B1 gene and DKD. Materials and

methods:

The sample comprised 695 patients with type 2 DM (T2DM) and DKD (cases) and 310 patients with T2DM of more than 10 years' duration, but no DKD (controls). The polymorphism was genotyped by real-time PCR.

Results:

Allelic and genotype frequencies of this polymorphism did not differ significantly between groups. However, the A/A genotype was associated with risk for DKD after adjustment for gender, triglycerides, BMI, presence of hypertension and diabetic retinopathy, and duration of DM, under both recessive (P = 0.048) and additive (P = 0.037) inheritance models.

Conclusion:

Our data suggest an association between the AKR1B1 rs759853A/A genotype and risk for DKD in Brazilians T2DM patients.
Asunto(s)


Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Aldehído Reductasa / Diabetes Mellitus Tipo 2 / Nefropatías Diabéticas Tipo de estudio: Estudio de etiología / Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Humanos País/Región como asunto: America del Sur / Brasil Idioma: Inglés Revista: Arch. endocrinol. metab. (Online) Asunto de la revista: Endocrinologia / Metabolismo Año: 2022 Tipo del documento: Artículo País de afiliación: Brasil Institución/País de afiliación: Hospital de Clínicas de Porto Alegre/BR

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Texto completo: Disponible Índice: LILACS (Américas) Asunto principal: Aldehído Reductasa / Diabetes Mellitus Tipo 2 / Nefropatías Diabéticas Tipo de estudio: Estudio de etiología / Estudio observacional / Estudio pronóstico / Factores de riesgo Límite: Humanos País/Región como asunto: America del Sur / Brasil Idioma: Inglés Revista: Arch. endocrinol. metab. (Online) Asunto de la revista: Endocrinologia / Metabolismo Año: 2022 Tipo del documento: Artículo País de afiliación: Brasil Institución/País de afiliación: Hospital de Clínicas de Porto Alegre/BR