Role of SLMAP genetic variants in susceptibility of diabetes and diabetic retinopathy in Qatari population

J Transl Med. 2015 Feb 15:13:61. doi: 10.1186/s12967-015-0411-6.

Abstract

Background: Overexpression of SLMAP gene has been associated with diabetes and endothelial dysfunction of macro- and micro-blood vessels. In this study our primary objective is to explore the role of SLMAP gene polymorphisms in the susceptibility of type 2 diabetes (T2DM) with or without diabetic retinopathy (DR) in the Qatari population.

Methods: A total of 342 Qatari subjects (non-diabetic controls and T2DM patients with or without DR) were genotyped for SLMAP gene polymorphisms (rs17058639 C > T; rs1043045 C > T and rs1057719 A > G) using Taqman SNP genotyping assay.

Results: SLMAP rs17058639 C > T polymorphism was associated with the presence of DR among Qataris with T2DM. One-way ANOVA and multiple logistic regression analysis showed SLMAP SNP rs17058639 C > T as an independent risk factor for DR development. SLMAP rs17058639 C > T polymorphism also had a predictive role for the severity of DR. Haplotype Crs17058639Trs1043045Ars1057719 was associated with the increased risk for DR among Qataris with T2DM.

Conclusions: The data suggests the potential role of SLMAP SNPs as a risk factor for the susceptibility of DR among T2DM patients in the Qatari population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Demography
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetic Retinopathy / complications*
  • Diabetic Retinopathy / genetics*
  • Disease Progression
  • Female
  • Gene Frequency / genetics
  • Genetic Association Studies
  • Genetic Predisposition to Disease*
  • Haplotypes / genetics
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Phenotype
  • Polymorphism, Single Nucleotide / genetics*
  • Qatar
  • Regression Analysis

Substances

  • Membrane Proteins
  • SLMAP protein, human