Effect of cerebral amyloid angiopathy on brain iron, copper, and zinc in alzheimer's disease

Matthew Schrag, Andrew Crofton, Matthew Zabel, Arshad Jiffry, David Kirsch, April Dickson, Xiao Wen Mao, Harry V. Vinters, Dylan W. Domaille, Christopher J. Chang, Wolff Kirsch

Research output: Contribution to journalArticlepeer-review

67 Scopus citations

Abstract

Cerebral amyloid angiopathy (CAA) is a vascular lesion associated with Alzheimer's disease (AD) present in up to 95% of AD patients and produces MRI-detectable microbleeds in many of these patients. It is possible that CAA-related microbleeding is a source of pathological iron in the AD brain. Because the homeostasis of copper, iron, and zinc are so intimately linked, we determined whether CAA contributes to changes in the brain levels of these metals. We obtained brain tissue from AD patients with severe CAA to compare to AD patients without evidence of vascular amyloid-β. Patients with severe CAA had significantly higher non-heme iron levels. Histologically, iron was deposited in the walls of large CAA-affected vessels. Zinc levels were significantly elevated in grey matter in both the CAA and non-CAA AD tissue, but no vascular staining was noted in CAA cases. Copper levels were decreased in both CAA and non-CAA AD tissues and copper was found to be prominently deposited on the vasculature in CAA. Together, these findings demonstrate that CAA is a significant variable affecting transition metals in AD.

Original languageEnglish (US)
Pages (from-to)137-149
Number of pages13
JournalJournal of Alzheimer's Disease
Volume24
Issue number1
DOIs
StatePublished - 2011
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • General Neuroscience
  • Clinical Psychology
  • Geriatrics and Gerontology
  • Psychiatry and Mental health

Keywords

  • Atomic absorption
  • coppersensor 1 (CS1)
  • ferrous
  • non-heme iron

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