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The fas promoter polymorphism at position -670 is not associated with late-onset sporadic Alzheimer's disease

  • Hanna Rosenmann*
  • , Zeev Meiner
  • , Esther Kahana
  • , Zoja Aladjem
  • , Gideon Friedman
  • , Arie Ben-Yehuda
  • , Tal Grenader
  • , Eli Wertman
  • , Oded Abramsky
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

9 Scopus citations

Abstract

The Fas antigen is a cell surface receptor-mediating cell apoptosis. Recent studies have demonstrated that Fasassociated apoptosis is involved in the pathogenesis of Alzheimer's disease (AD). Moreover, the Fas gene is located on chromosome 10q24.1, a region of linkage to late-onset AD (LOAD). These two criteria, pathobiological and positional, make the Fas antigen an interesting candidate for an association with AD. We performed a case-control association study between the common A/G polymorphism at position -670 in the Fas gene (TNFSRF6) promoter and sporadic AD in Jews, investigating whether this locus acts as a risk factor or whether it has a modifying effect. An association has recently been detected by Feuk et al. in the Scottish population between this locus and the risk of early-onset AD (EOAD), but not of LOAD. In agreement with Feuk et al., we found no association between this locus and the risk of LOAD (n = 86). However, in our small sample of patients with EOAD (n = 19), no association was found either. No interactive effect was found between the Fas promoter polymorphism at position -670 and the known risk factor of LOAD, apolipoprotein E ε4, and no association was detected with disease progression. These findings show no evidence for an association between the Fas promoter polymorphism at position -670 and AD in our population.

Original languageEnglish
Pages (from-to)143-146
Number of pages4
JournalDementia and Geriatric Cognitive Disorders
Volume17
Issue number3
DOIs
StatePublished - 2004
Externally publishedYes

Keywords

  • Alzheimer's disease
  • Apoptosis
  • Fas
  • Polymorphism
  • TNFSRF6

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