Common and rare alleles in apolipoprotein B contribute to plasma levels of low-density lipoprotein cholesterol in the general population

Marianne Benn, Maria Charlotte Aslaug Stene, Børge G Nordestgaard, Gorm B Jensen, Rolf Steffensen, Anne Tybjaerg-Hansen

33 Citations (Scopus)

Abstract

We have previously shown that rare mutations in the apolipoprotein B gene (APOB) may result in not only severe hypercholesterolemia and ischemic heart disease but also hypocholesterolemia. Despite this, common single-nucleotide polymorphisms (SNPs) in APOB have not convincingly been demonstrated to affect low-density lipoprotein (LDL) cholesterol levels.
Original languageEnglish
JournalJournal of Clinical Endocrinology and Metabolism
Volume93
Issue number3
Pages (from-to)1038-45
Number of pages8
ISSN0021-972X
DOIs
Publication statusPublished - 2008

Keywords

  • Adult
  • Aged
  • Aged, 80 and over
  • Alleles
  • Apolipoproteins B
  • Cholesterol, LDL
  • Female
  • Humans
  • Linkage Disequilibrium
  • Male
  • Middle Aged
  • Myocardial Infarction
  • Myocardial Ischemia
  • Polymorphism, Single Nucleotide
  • Prospective Studies

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