Association between plasma HDL-cholesterol concentration and Taq1B CETP gene polymorphism in non-insulin-dependent diabetes mellitus

J Lipid Res. 1998 Jan;39(1):59-65.

Abstract

The effects of CETP gene Taq1B polymorphism on plasma lipoproteins were investigated in 176 patients with non-insulin-dependent diabetes mellitus. The distribution of CETP genotypes was similar to that previously described in the general population. A significant association was found between CETP genotype and both CETP and HDL cholesterol (HDL-c) concentrations. B1B1 had the highest CETP and the lowest HDL-c whereas B2B2 had the lowest CETP and the highest HDL-c. However, HDL-c was not correlated with CETP concentration, even when genetic groups were separately considered. By multivariate analysis, the determinants of HDL were body mass index, triglycerides concentration, net mass CE transfer, and CETP genotype. No association was found between CETP genetic groups and HDL or LDL size distribution. In contrast, net mass CET was positively and HDL and LDL sizes were negatively correlated with plasma triglyceride concentration. Overall, our work demonstrates that, in a population of diabetic patients where lipoprotein-related parameters vary over a large range, the association of CETP gene polymorphism with HDL-c is independent of plasma CETP concentration.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Carrier Proteins / blood
  • Carrier Proteins / genetics*
  • Cholesterol / blood
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL / blood*
  • Deoxyribonucleases, Type II Site-Specific / metabolism*
  • Diabetes Mellitus, Type 2 / genetics*
  • Female
  • Glycoproteins*
  • Humans
  • Lipoproteins, LDL / blood
  • Male
  • Middle Aged
  • Particle Size
  • Polymorphism, Restriction Fragment Length*
  • Triglycerides / blood

Substances

  • CETP protein, human
  • Carrier Proteins
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Glycoproteins
  • Lipoproteins, LDL
  • Triglycerides
  • Cholesterol
  • Deoxyribonucleases, Type II Site-Specific
  • TCGA-specific type II deoxyribonucleases