Possible association between genetic variability at the apolipoprotein(a) locus and Alzheimer's disease in apolipoprotein E2 carriers

Neurosci Lett. 2002 Oct 4;331(1):60-2. doi: 10.1016/s0304-3940(02)00703-6.

Abstract

Apolipoprotein(a) (Apo(a)) is a glycoprotein that is linked by a disulfide bond to apolipoprotein B on low density lipoprotein particles to form lipoprotein(a) (Lp(a)). High plasma levels of Lp(a) are thought to contribute directly to the development of atherosclerosis. We tested a variant (T3888P) located in the Kringle-IV region of Apo(a) in a case-control series. Overall, there were no differences between case and controls. However, in the apoE2 positive subgroup, we noticed that the mutant allele is over-represented in the cases (P=0.005). We suggest that this polymorphism and others at the Apo(a) locus be further studied in relation to Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alzheimer Disease / genetics*
  • Apolipoprotein E2
  • Apolipoproteins / genetics*
  • Apolipoproteins E / genetics*
  • Apoprotein(a)
  • Case-Control Studies
  • Genetic Variation*
  • Genotype
  • Humans
  • Kringles / genetics
  • Lipoprotein(a) / genetics*
  • Point Mutation

Substances

  • Apolipoprotein E2
  • Apolipoproteins
  • Apolipoproteins E
  • Lipoprotein(a)
  • Apoprotein(a)