KCNJ11 E23K polymorphism and diabetes mellitus with adult onset in Czech patients

Folia Biol (Praha). 2007;53(5):173-5.

Abstract

In this work, we studied the association of the E23K polymorphism of the Kir6.2 ATP-sensitive potassium channels in 212 Czech patients with diabetes mellitus who were diagnosed after the age of 35. Patients were classified into T1DM, LADA and T2DM groups based on C-peptide and GADA levels. Carriers of the predisposing Kir6.2 E23K K allele showed no increased risk of either type of diabetes mellitus development. On the other hand, we found a correlation between E23K SNP of the KCNJ11 gene and C-peptide levels, which may be considered a measure of pancreatic beta-cell activity, although this correlation was not statistically significant. In conclusion, we failed to confirm the Kir6.2 E23K as a genetic marker for T1DM, LADA and T2DM in the Central Bohemian population of the Czech Republic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Age of Onset
  • C-Peptide
  • Case-Control Studies
  • Czech Republic / epidemiology
  • Diabetes Mellitus / epidemiology*
  • Diabetes Mellitus / genetics*
  • Female
  • Gene Frequency
  • Genotype
  • Glutamic Acid / genetics*
  • Humans
  • Lysine / genetics*
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide / genetics*
  • Potassium Channels, Inwardly Rectifying / genetics*

Substances

  • C-Peptide
  • Kir6.2 channel
  • Potassium Channels, Inwardly Rectifying
  • Glutamic Acid
  • Lysine