GCK gene-body hypomethylation is associated with the risk of coronary heart disease

Biomed Res Int. 2014:2014:151723. doi: 10.1155/2014/151723. Epub 2014 Feb 17.

Abstract

Objectives: Glucokinase encoded by GCK is a key enzyme that facilitates phosphorylation of glucose to glucose-6-phosphate. Variants of GCK gene were shown to be associated with type 2 diabetes (T2D) and coronary heart disease (CHD). The goal of this study was to investigate the contribution of GCK gene-body methylation to the risk of CHD.

Design and methods: 36 patients (18 males and 18 females) and 36 age- and sex-matched controls were collected for the current methylation research. DNA methylation level of the CpG island (CGI) region on the GCK gene-body was measured through the sodium bisulfite DNA conversion and pyrosequencing technology.

Results: Our results indicated that CHD cases have a much lower methylation level (49.77 ± 6.43%) compared with controls (54.47 ± 7.65%, P = 0.018). In addition, GCK gene-body methylation was found to be positively associated with aging in controls (r = 0.443, P = 0.010).

Conclusions: Our study indicated that the hypomethylation of GCK gene-body was significantly associated with the risk of CHD. Aging correlates with an elevation of GCK methylation in healthy controls.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Case-Control Studies
  • Coronary Disease / enzymology*
  • Coronary Disease / genetics*
  • CpG Islands
  • DNA Methylation / genetics*
  • Female
  • Genetic Association Studies*
  • Genetic Predisposition to Disease*
  • Glucokinase / genetics*
  • Humans
  • Male
  • Risk Factors

Substances

  • Glucokinase