Presenilin-1 mutation E318G and familial Alzheimer's disease in the Italian population

Neurobiol Aging. 2007 Nov;28(11):1682-8. doi: 10.1016/j.neurobiolaging.2006.07.003. Epub 2006 Sep 6.

Abstract

Presenilin-1 (PSEN-1) is a component of the gamma-secretase complex involved in beta-amyloid precursor protein (betaAPP) processing. To date about 140 pathogenic mutations in the PSEN-1 gene have been identified and their main biochemical effect is to increase the production of the fibrillogenic peptide Abeta(1-42). An exception is the PSEN-1 [E318G] mutation that does not alter Abeta(1-42) generation and is generally considered a non-pathogenic polymorphism. Nevertheless, this mutation was reported to be a genetic risk factor for familial Alzheimer's disease (FAD) in the Australian population. To independently confirm this indication, we performed a case-control association study in the Italian population. We found a significant association (p<0.05, Fisher's exact test) between the presence of PSEN-1 [E318G] and FAD. In addition, on measuring the Abeta(1-42) and Abeta(1-40) concentrations in fibroblast-conditioned media cultured from PSEN-1 [E318G] carriers and PSEN-1 [wild type] controls we noted a significant decrease (p<0.05, Mann-Whitney test) in the Abeta(1-42)/Abeta(1-40) ratio in PSEN-1 [E318G] carriers, suggesting a peculiar biochemical effect of this mutation.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / genetics*
  • Amino Acid Substitution / genetics
  • Case-Control Studies
  • Female
  • Genetic Carrier Screening
  • Glutamic Acid / genetics
  • Glycine / genetics
  • Humans
  • Italy
  • Male
  • Middle Aged
  • Mutation*
  • Pedigree
  • Presenilin-1 / genetics*

Substances

  • Presenilin-1
  • Glutamic Acid
  • Glycine