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An association study of a polymorphism in the heparan sulfate proteoglycan gene (perlecan, HSPG2) and 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

11 Scopus citations

Abstract

Accumulating evidence indicates that the heparan-sulfate-proteoglycan (perlecan, HSPG2), as well as other specific proteoglycans, are involved in amyloidogenesis and tau aggregation in Alzheimer's disease (AD). Moreover, the HSPG2 is located on chromosome 1p36, a region of linkage to late-onset AD (LOAD). These two criteria, pathological and positional, make the HSPG2 an interesting candidate for an association with AD. We performed a case-control association study between the common intron 6 BamHI polymorphism at a region of putative heparan-sulfate (HS) attachment sites in the HSPG2 gene and sporadic AD in Jews. No association was detected with AD, neither as a risk factor nor as a modifier gene affecting the age at disease onset and disease progression. In addition, no interactive effect was found with the known risk factor for AD, the apolipoprotein E (APOE) ε4. These findings show no evidence for association between HSPG2 intron 6 BamHI polymorphism and AD in our population.

Original languageEnglish
Pages (from-to)123-125
Number of pages3
JournalAmerican Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
Volume128 B
Issue number1
DOIs
StatePublished - 1 Jul 2004
Externally publishedYes

Keywords

  • Alzheimer's disease
  • Association study
  • HSPG2
  • Heparan-sulfate- proteoglycan
  • Perlecan
  • Polymorphism

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