Transferrin C2 variant does confer a risk for Alzheimer's disease in caucasians

J Alzheimers Dis. 2003 Dec;5(6):423-7. doi: 10.3233/jad-2003-5601.

Abstract

Several gene mutations are associated with an increased risk of Alzheimer's disease. Previous studies reported higher transferrin C2 allele frequencies in Alzheimer's disease compared with normal controls. However, potential interactions between transferrin C2 and APOE (epsilon 4), have not been extensively investigated and have been the subject of controversial reports from several laboratories. We have carried out a case-control study on the association between Alzheimer's disease and transferrin C2 and APOE epsilon 4 alleles. epsilon 4 allele was associated with a four fold increase in the risk of disease, and transferrin C2 allele was significantly associated with Alzheimer's disease only in epsilon 4 negative subjects. These results suggest that apoE and transferrin may be part of a complex mechanism in the pathogenesis of Alzheimer's disease.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alleles
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / metabolism*
  • Apolipoproteins E / metabolism
  • Diagnostic and Statistical Manual of Mental Disorders
  • Female
  • Globus Pallidus / metabolism
  • Humans
  • Iron / metabolism
  • Male
  • Middle Aged
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics
  • Transferrin / genetics*
  • Transferrin / metabolism*
  • White People*

Substances

  • Apolipoproteins E
  • Transferrin
  • Iron