Genetic association between Alzheimer disease and the alpha-synuclein gene

Dement Geriatr Cogn Disord. 2001 Mar-Apr;12(2):106-9. doi: 10.1159/000051243.

Abstract

alpha-Synuclein has been isolated as a component of amyloid in addition to the major A beta peptide in Alzheimer disease (AD). However, there are conflicting reports regarding the association of alpha-synuclein gene polymorphism with AD. Using a novel and common polymorphism in intron 3, we examined the relationship between AD and alpha-synuclein and apolipoprotein E (ApoE) genes in 183 Japanese AD patients and 210 controls. Carriers of the alpha-synuclein deletion (D) allele had a 2.2-fold increased risk of developing AD than noncarriers in women. The odds ratio for the ApoE epsilon 4 and the alpha-synuclein D allele was 11.4 in women. The results showed that the alpha-synuclein gene is associated with sporadic AD in women, independent of ApoE epsilon 4 status.

MeSH terms

  • Aged
  • Alleles
  • Alzheimer Disease / genetics*
  • Alzheimer Disease / metabolism
  • Apolipoproteins E / genetics
  • Chromosomes, Human, Pair 4 / genetics
  • DNA Mutational Analysis
  • Female
  • Gene Deletion
  • Gene Expression
  • Humans
  • Male
  • Middle Aged
  • Nerve Tissue Proteins / genetics*
  • Point Mutation / genetics
  • Polymerase Chain Reaction
  • Polymorphism, Genetic / genetics
  • Risk Factors
  • Synucleins
  • alpha-Synuclein

Substances

  • Apolipoproteins E
  • Nerve Tissue Proteins
  • SNCA protein, human
  • Synucleins
  • alpha-Synuclein