Common and rare single nucleotide polymorphisms in the LDLR gene are present in a black South African population and associate with low-density lipoprotein cholesterol levels

J Hum Genet. 2014 Feb;59(2):88-94. doi: 10.1038/jhg.2013.123. Epub 2013 Nov 28.

Abstract

The LDL receptor has an essential role in regulating plasma LDL-C levels. Genetic variation in the LDLR gene can be associated with either lower or moderately raised plasma levels of LDL-C, or may cause familial hypercholesterolemia. The prevalence of single-nucleotide polymorphisms (SNPs) in the LDLR in the black South African population is not known and therefore, we aimed to determine the genotypic variation of the LDLR in the study population as well as to define the association of the different genotypes with plasma LDL-C levels. A random selection of 1860 apparently healthy black South African volunteers aged 35-60 years was made in a cross-sectional study. Novel SNPs were identified in a subset of 30 individuals by means of automated sequencing before screening the entire cohort by means of the Illumina VeraCode GoldenGate Genotyping Assay on a BeadXpress Reader system. Twenty-five SNPs were genotyped, two of which were novel. A very rare SNP, rs17249141, in the promoter region was significantly associated with lower levels of LDL-C. Four other SNPs (rs2738447, rs14158, rs2738465 and rs3180023) were significantly associated with increased levels of LDL-C. We can conclude that some of the various SNPs identified do indeed associate with LDL-C levels.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Black People / genetics*
  • Cholesterol, LDL / blood*
  • Cholesterol, LDL / genetics
  • Cholic Acids / blood*
  • Cholic Acids / genetics
  • Cross-Sectional Studies
  • Female
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Prospective Studies
  • Receptors, LDL / genetics*
  • Receptors, LDL / metabolism
  • South Africa
  • Steroid Metabolism, Inborn Errors / blood*
  • Steroid Metabolism, Inborn Errors / genetics*

Substances

  • Cholesterol, LDL
  • Cholic Acids
  • LDLR protein, human
  • Receptors, LDL

Supplementary concepts

  • Hypercholanemia, Familial