Interaction between a common variant of the cholesteryl ester transfer protein gene and the apolipoprotein E polymorphism: effects on plasma lipids and lipoproteins in a cohort of 7-year-old children

Nutr Metab Cardiovasc Dis. 2002 Dec;12(6):317-24.

Abstract

Background and aim: Common variations in genes, such as apolipoprotein E (apo E) and cholesteryl ester transfer protein (CETP), are major determinants of plasma lipid and lipoprotein levels. As both apo E and CETP contribute to the reverse transport of cholesterol to the liver, the effects of variations at the CETP locus may very well interact with the apo E genotype.

Methods and results: As part of an ongoing study, the combined effects of the apo E genotype and heterogeneity at the CETP gene locus on plasma lipids and lipoproteins were studied in a birth cohort sample of 257 Dutch prepubescent boys and girls (aged 6.7-8.1 years). The children with an apo E2E3 genotype (carrying the epsilon 2 allele; arg158-->cys) had lower concentrations of low-density lipoprotein cholesterol (LDL-C) and apolipoprotein B (apo B) than those with an apo E4E3 (carrying the epsilon 4 allele; cys112-->arg) or apo E3E3 genotype (homozygous for the parent epsilon 3 allele). These associations were statistically significant in children who were homozygous (p = 0.004 for LDL; p = 0.002 for apo B) or heterozygous (p < 0.0001 for LDL and apo B) for the absence of the Taq-IB polymorphism at the CETP gene locus (B2 allele), but not in those homozygous for the presence of this variant (B1B1). The highest plasma high-density lipoprotein cholesterol (HDL-C) concentrations were observed in children with the CETP B2B2 genotype. The difference in HDL-C levels between the CETP genotype groups was statistically significant only in E2E3 carriers (p = 0.01). The LDL/HDL ratio was significantly lower in E2E3 carriers, but not when combined with a CETP B1B1 genotype.

Conclusion: These findings indicate that the apo E genotype and heterogeneity at the CETP gene locus have an additive and interactive influence on plasma lipid and lipoprotein levels in children.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Apolipoproteins E / genetics*
  • Carrier Proteins / genetics*
  • Child
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL / genetics
  • Cholesterol, HDL / metabolism*
  • Cholesterol, LDL / genetics
  • Cholesterol, LDL / metabolism*
  • Cohort Studies
  • Coronary Disease / epidemiology
  • Coronary Disease / genetics*
  • Female
  • Genetic Predisposition to Disease*
  • Genotype
  • Glycoproteins*
  • Humans
  • Hyperlipidemias / epidemiology
  • Hyperlipidemias / genetics*
  • Incidence
  • Male
  • Netherlands / epidemiology
  • Polymorphism, Genetic*
  • Probability
  • Risk Assessment
  • Sensitivity and Specificity
  • Sex Distribution

Substances

  • Apolipoproteins E
  • CETP protein, human
  • Carrier Proteins
  • Cholesterol Ester Transfer Proteins
  • Cholesterol, HDL
  • Cholesterol, LDL
  • Glycoproteins