4.4 Article

Involvement of miR-126 rs4636297 and miR-146a rs2910164 polymorphisms in the susceptibility for diabetic retinopathy: a case-control study in a type 1 diabetes population

Journal

ACTA OPHTHALMOLOGICA
Volume 99, Issue 4, Pages E461-E469

Publisher

WILEY
DOI: 10.1111/aos.14638

Keywords

diabetic retinopathy; microRNA; polymorphism; rs2910164; rs4636297; type 1 diabetes mellitus

Categories

Funding

  1. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)
  2. Fundo de Incentivo a Pesquisa e Eventos (FIPE) at Hospital de Clinicas de Porto Alegre [2018-0008]
  3. Fundacao de Amparo a Pesquisa do Estado do Rio Grande do Sul (FAPERGS)
  4. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES)
  5. Graduate Program in Medical Sciences: Endocrinology-Universidade Federal do Rio Grande do Sul
  6. CNPq
  7. CAPES

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The A allele of miR-126 rs4636297 miRSNP may be associated with protection against DR in a Southern Brazilian population, while miR-146a rs2910164 miRSNP is not associated with DR.
Background and purpose MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression. MiRNA-126 and miRNA-146a have been described as having abnormal expressions in diabetic retinopathy (DR) patients. Polymorphisms in genes codifying miRNAs (miRSNPs) may alter the expression of the corresponding miRNA and, thus, interfere with susceptibility to DR. Therefore, miRSNPs in miR-126 and miR-146a genes could be associated with DR susceptibility. The purpose of this study was to investigate the association between miR-126 rs4636297 (G/A) and miR-146a rs2910164 (G/C) miRSNPs and DR. Methods This case-control study included 195 type 1 diabetes mellitus (T1DM) patients with DR (cases) and 215 patients without DR and with >= 10 years of T1DM (controls). MiRSNPs were genotyped by real-time PCR. Results Genotype distributions of two analysed miRSNPs were in Hardy-Weinberg equilibrium in controls (p > 0.050). Frequencies of the miR-126 rs4636297 miRSNP were not significantly different between case and control groups (p = 0.169). However, after adjustment for age, glycated haemoglobin, triglycerides, estimated glomerular filtration rate and ethnicity, the A allele of this miRSNP was associated with protection for DR under additive [OR: 0.444 (95% CI: 0.211-0.936), p = 0.033] and dominant [OR: 0.512 (95% CI: 0.303-0.865), p = 0.012] inheritance models. Genotype and allele frequencies of miR-146a rs2910164 miRSNP did not differ between groups (p = 0.368 and p = 0.957), and this polymorphism was not associated with DR when assuming different inheritance models. Conclusion Our results suggest an association between the A allele of miR-126 rs4636297 miRSNP and protection for DR in a Southern Brazilian population.

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