The T111I mutation in the EL gene modulates the impact of dietary fat on the HDL profile in women

J Lipid Res. 2003 Oct;44(10):1902-8. doi: 10.1194/jlr.M300118-JLR200. Epub 2003 Jul 16.

Abstract

The objective of the present study was to examine the impact of the T111I missense mutation in exon 3 of the endothelial lipase (EL) gene on HDL and its potential interaction effect with dietary fat. The study sample included 281 women and 216 men aged between 17 and 76 years from the Québec Family Study. Plasma HDL3-C levels of I111I homozygote women were higher compared with those of women carrying the wild-type allele (P = 0.03). These differences were not attenuated when adjusted for levels of obesity and were not observed among men. Dietary PUFA interacted with the T111I mutation to modulate apolipoprotein A-I (apoA-I) and HDL3-C levels among women. Specifically, a diet rich in PUFA was associated with increased apoA-I levels among women carriers of the I111 allele and with decreased apoA-I among women homozygotes for the wild-type allele (P = 0.002). A similar interaction was observed with plasma HDL3-C levels (P = 0.003). These interactions were not observed among men. In conclusion, the EL T111I mutation appears to have a modest effect on plasma HDL levels. The gene-diet interaction among women, however, suggests that the T111I missense mutation may confer protection against the lowering effect of a high dietary PUFA intake on plasma apoA-I and HDL3-C levels.

Publication types

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

MeSH terms

  • Adipose Tissue / metabolism
  • Adolescent
  • Adult
  • Aged
  • Apolipoprotein A-I / blood
  • Apolipoprotein A-I / metabolism
  • Cholesterol, HDL / blood
  • Cholesterol, HDL / metabolism*
  • Dietary Fats / metabolism*
  • Endothelial Cells / metabolism
  • Energy Intake
  • Exons
  • Female
  • Genotype
  • Homozygote
  • Humans
  • Lipase / genetics*
  • Lipoprotein Lipase / genetics
  • Lipoprotein Lipase / metabolism*
  • Male
  • Middle Aged
  • Mutation, Missense / genetics*
  • Phenotype
  • Triglycerides / blood
  • Triglycerides / metabolism

Substances

  • Apolipoprotein A-I
  • Cholesterol, HDL
  • Dietary Fats
  • Triglycerides
  • LIPG protein, human
  • Lipase
  • Lipoprotein Lipase