Ace variants and association with brain aβ levels in alzheimer's disease

J. Scott Miners, Zoë Van Helmond, Merryn Raiker, Seth Love, Patrick G. Kehoe

Research output: Contribution to journalArticle (Academic Journal)peer-review

40 Citations (Scopus)

Abstract

ACE is a candidate gene for Alzheimer's disease (AD) and associations have been reported between ACE variants and plasma ACE levels, AD risk, AD age at onset of disease and cerebrospinal fluid levels of Aβ. Despite evidence that ACE can degrade Aβ, the relationships between ACE variants and the levels of different types of Aβ in the brain are not known. We have investigated the relationship between AD-associated ACE variants, for which the associations with brain activity of ACE were previously analysed, and brain homogenate levels of soluble, insoluble and oligomeric Aβ. Reported AD risk variants in the ACE indel (rs1799752) and its 'proxy' rs4343 were significantly associated with soluble Aβ level in AD only (p=0.001), as was rs1800764 but less so (p=0.014). In contrast, insoluble Aβ was associated with ACE indel and rs4343 variants in controls only (p < 0.01). No associations were found for oligomeric Aβ. These data indicate a complex relationship between ACE and Aβ that differs between AD and control brains.

Original languageEnglish
Pages (from-to)73-80
Number of pages8
JournalAmerican Journal of Translational Research
Volume3
Issue number1
Publication statusPublished - 1 Jan 2011

Bibliographical note

Publisher: e-Century Publishing Corporation

Research Groups and Themes

  • Cerebrovascular and Dementia Research Group

Keywords

  • ACE
  • Alzheimer's disease
  • Amyloid
  • Angiotensin
  • Association
  • Cerebral blood flow
  • Degrading enzyme
  • Hypertension
  • Insoluble Aβ
  • Neuropathology
  • SNP
  • Soluble Aβ

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