A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease

Neurosci Lett. 2010 Jan 1;468(1):1-2. doi: 10.1016/j.neulet.2009.10.040. Epub 2009 Oct 22.

Abstract

Several observations suggest that neurotoxicity in Alzheimer's disease (AD) can be partly attributed to beta-amyloid (Abeta) and senile plaques. Recent work has suggested that the FISH (five SH3 domains) adapter protein and ADAM12 (a disintegrin and metalloprotease) may mediate the neurotoxic effect of Abeta. Both genes are located on chromosome 10, within a region linked to AD (for SH3PXD2A) or nearby (for ADAM12). A recent study reported a statistically significant interaction between 2 variants of these genes (rs3740473 for SH3PXD2A and rs11244787 for ADAM12) with respect to the risk of developing AD. With a view to replicating this observation, we genotyped the two SNPs in four European case-control cohorts of Caucasian origin (1913 cases and 1468 controls) but were unable to confirm the initial results.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / genetics*
  • ADAM12 Protein
  • Adaptor Proteins, Vesicular Transport / genetics*
  • Aged
  • Alzheimer Disease / genetics*
  • Case-Control Studies
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Polymorphism, Single Nucleotide
  • Risk Factors
  • White People

Substances

  • Adaptor Proteins, Vesicular Transport
  • Membrane Proteins
  • SH3PXD2A protein, human
  • ADAM Proteins
  • ADAM12 Protein
  • ADAM12 protein, human