Two Italian kindreds carrying the Arg136-->Ser mutation of the Apo E gene: development of premature and severe atherosclerosis in the presence of epsilon 2 as second allele

Nutr Metab Cardiovasc Dis. 2003 Apr;13(2):93-9. doi: 10.1016/s0939-4753(03)80024-8.

Abstract

Background and aims: Type III hyperlipoproteinemia, or dysbetalipoproteinemia, is commonly associated with apolipoprotein E2 homozygosity (Cys112, Cys158). Apo E2-Christchurch (Arg136-->Ser), a rare mutation of the Apo E gene, located in the receptor-binding domain of the protein, has been found to be associated in the vast majority of cases of dysbetalipoproteinemia.

Methods and results: This is the first report of two Italian kindreds carrying the Arg136-->Ser mutation. One family is a four-generation kindred from Genoa (Liguria, Italy) with a high rate of mortality due to coronary artery disease: the proband was a 51-year-old woman with previous myocardial infarction and residual angina, severe carotid atherosclerosis, peripheral arterial vascular disease and arterial hypertension. The other family was identified in Palermo (Sicily, Italy): the proband was an overweight 62-year-old man with a mixed form of hyperlipidemia. The mutation, which was identified by means of Apo E genotyping followed by direct sequencing, co-segregated with the same haplotype in the two families.

Conclusions: The family histories and clinical examinations of these subjects clearly show that the Apo E Arg136-->Ser variant fully expresses a type III phenotype in association with a second allele coding for Apo E2, and only partially in association with a second allele coding for Apo E4.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Apolipoprotein E2
  • Apolipoproteins E / genetics*
  • Arteriosclerosis / etiology
  • Arteriosclerosis / genetics*
  • Base Sequence
  • Female
  • Genotype
  • Haplotypes
  • Humans
  • Hyperlipoproteinemia Type III / complications
  • Hyperlipoproteinemia Type III / genetics*
  • Lipids / blood
  • Male
  • Middle Aged
  • Mutation
  • Pedigree
  • Polymerase Chain Reaction
  • Sequence Homology

Substances

  • Apolipoprotein E2
  • Apolipoproteins E
  • Lipids