MLXIPL variant in individuals with low and high triglyceridemia in white population in Central Europe

Hum Genet. 2008 Dec;124(5):553-5. doi: 10.1007/s00439-008-0577-6. Epub 2008 Oct 23.

Abstract

We tested the hypothesis that the MLXIPL rs3812316 variant predicts plasma triglyceride (TG) levels. We compared three groups of adult individuals: 162 persons with TG > 10 mmol/L, 266 persons with TG < 0.65 mmol/L, and 2,043 population-based controls (range of TG concentrations 0.7-8.7 mmol/L). We found a small difference in the frequency of the Gln allele carriers between population controls (20.4%) and persons with low TG (26.3%, P = 0.033). We found no difference between individuals with high TG and population controls, and there was no association between the MLXIPL variant and plasma TG levels among the population controls.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Amino Acid Substitution
  • Base Sequence
  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors / genetics*
  • Case-Control Studies
  • Czech Republic
  • DNA / genetics
  • Female
  • Gene Frequency
  • Genetic Variation
  • Genotype
  • Humans
  • Hypertriglyceridemia / blood
  • Hypertriglyceridemia / genetics*
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Triglycerides / blood*
  • White People / genetics

Substances

  • Basic Helix-Loop-Helix Leucine Zipper Transcription Factors
  • MLXIPL protein, human
  • Triglycerides
  • DNA