Detection of familial defective apoB (FDB) mutations in hypercholesterolemic children and adolescents by denaturing high performance liquid chromatography (DHPLC)

Clin Biochem. 2008 Apr;41(6):395-9. doi: 10.1016/j.clinbiochem.2007.12.018. Epub 2008 Jan 11.

Abstract

Objective: To seek apolipoprotein B (apoB) gene mutations in children and adolescents presenting to a lipid clinic with hypercholesterolemia and suspected of familial defective apoB (FDB), employing a new automated denaturing high performance liquid chromatography (DHPLC) method.

Design and methods: 131 patients between the ages of 3 and 18 years were screened for the presence of FDB mutations using DHPLC. Patients who exhibited aberrant DHPLC chromatograms were sequenced.

Results: Three patients were found to be positive for the R3500Q mutation in which a single nucleotide G-->A transition resulted in arginine to glutamine substitution at codon 3500 in exon 26 of the apoB-100 gene. All three subjects had elevated total cholesterol and LDL cholesterol levels, and high or borderline high plasma apoB levels. No R3500W or R3531C apoB mutations were found.

Conclusions: Automated DHPLC can be readily applied in rapid screening of hypercholesterolemic children presenting to a lipid clinic. Using DHPLC, this study revealed that the FDB mutation (R3500Q) is an important contributing factor to hypercholesterolemia observed in a pediatric lipid clinic population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Amino Acid Sequence
  • Apolipoproteins B / genetics*
  • Base Sequence
  • Child
  • Child, Preschool
  • Chromatography, High Pressure Liquid / methods*
  • DNA Mutational Analysis
  • Humans
  • Hypercholesterolemia / genetics*
  • Molecular Sequence Data
  • Point Mutation*

Substances

  • Apolipoproteins B