Lipoprotein profiles in children with two common cholesteryl ester transfer protein gene mutations, D442G and I14A, during the first year of life

Clin Chim Acta. 2009 Aug;406(1-2):52-6. doi: 10.1016/j.cca.2009.05.007. Epub 2009 May 19.

Abstract

Background: Hyperalphalipoproteinemia is associated with cholesteryl ester transfer protein (CETP) deficiency in adults but has unclear associations in children.

Methods: We measured lipoproteins in 19 heterozygotes (D442G, n=17; I14A, n=2), one D442G/I14A compound heterozygote, 13 non-affected siblings, and 30 healthy controls at birth, 3-4 months, and 12 months.

Results: CETP mass was 32-70% lower in heterozygotes than in controls throughout the year. Low-density lipoprotein-cholesterol (LDL-C) was lower in heterozygotes than in controls by 30, 20, and 15% at birth, 3-4 months, and 12 months, respectively. High-density lipoprotein-cholesterol (HDL-C) was similar among the groups at birth, but was 10% higher in heterozygotes compared with controls at 3-4 and 12 months. ApoE-rich HDL-C was similar between the two groups at birth, but was 50% higher in heterozygotes than in controls at 3-4 and 12 months. These lipoprotein profile characteristics were prominent in the compound heterozygote but were not found in non-affected siblings. In heterozygotes, CETP mass correlated positively with LDL-C but negatively with HDL-C at 3-4 and 12 months.

Conclusion: CETP is a determinant for LDL-C and HDL-C in CETP-deficient individuals in the first year of life.

MeSH terms

  • Apolipoproteins / metabolism
  • Cholesterol Ester Transfer Proteins / deficiency
  • Cholesterol Ester Transfer Proteins / genetics*
  • Cholesterol Ester Transfer Proteins / metabolism
  • Female
  • Humans
  • Infant, Newborn
  • Lipid Metabolism
  • Lipoproteins / metabolism*
  • Male
  • Mutation*

Substances

  • Apolipoproteins
  • Cholesterol Ester Transfer Proteins
  • Lipoproteins