Elevated cortical zinc in Alzheimer disease
Authors:
- D. ReligaDRD. Religa
- D. StrozykDSD. Strozyk
- R. A. ChernyRCR. A. Cherny
- I. VolitakisIVI. Volitakis
- V. HaroutunianVHV. Haroutunian
- B. WinbladBWB. Winblad
- J. NaslundJNJ. Naslund
- A. I. BushABA. I. Bush
- 11 July 2006
- journal article
- research article
- Published by Wolters Kluwer Health in Neurology
- Vol. 67 (1) , 69-75
Abstract
Objective: To determine whether changes in brain biometals in Alzheimer disease (AD) and in normal brain tissue are tandemly associated with amyloid β-peptide (Aβ) burden and dementia severity. Methods: The authors measured zinc, copper, iron, manganese, and aluminum and Aβ levels in postmortem neocortical tissue from patients with AD (n = 10), normal age-matched control subjects (n = 14), patients with schizophrenia (n = 26), and patients with schizophrenia with amyloid (n = 8). Severity of cognitive impairment was assessed with the Clinical Dementia Rating Scale (CDR). Results: There was a significant, more than twofold, increase of tissue zinc in the AD-affected cortex compared with the other groups. Zinc levels increased with tissue amyloid levels. Zinc levels were significantly elevated in the most severely demented cases (CDR 4 to 5) and in cases that had an amyloid burden greater than 8 plaques/mm2. Levels of other metals did not differ between groups. Conclusions: Brain zinc accumulation is a prominent feature of advanced Alzheimer disease (AD) and is biochemically linked to brain amyloid β-peptide accumulation and dementia severity in AD.Keywords
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