Journal of Lipid Research (Aug 1990)

Familial defective apolipoprotein B-100: a mutation of apolipoprotein B that causes hypercholesterolemia.

  • TL Innerarity,
  • RW Mahley,
  • KH Weisgraber,
  • TP Bersot,
  • RM Krauss,
  • GL Vega,
  • SM Grundy,
  • W Friedl,
  • J Davignon,
  • BJ McCarthy

Journal volume & issue
Vol. 31, no. 8
pp. 1337 – 1349

Abstract

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Familial defective apolipoprotein B-100 is a genetic disorder of apolipoprotein B-100 that causes moderate to severe hypercholesterolemia. A single amino acid mutation in apolipoprotein B diminishes the ability of low density lipoproteins to bind to the low density lipoprotein receptor. Low density lipoproteins accumulate in the plasma because their efficient receptor-mediated catabolism is disrupted. This mutation has been identified in the United States, Canada, and Europe and is estimated to occur at a frequency of approximately 1/500 in these populations. Thus, it appears that this newly described disorder may be a significant genetic cause of hypercholesterolemia in Western societies.