Alzheimer Disease Pathology in Middle Age Reveals a Spatial-Temporal Disconnect Between Amyloid-β and Phosphorylated Tau



Whitney Fornicola, Ari Pelcovits, Bei-Xu Li, Jonathan Heath, George Perry, Rudy J Castellani*
22 S. Greene Street, Baltimore, MD 21201


Article Metrics

CrossRef Citations:
3
Total Statistics:

Full-Text HTML Views: 317
Abstract HTML Views: 307
PDF Downloads: 76
Total Views/Downloads: 700
Unique Statistics:

Full-Text HTML Views: 194
Abstract HTML Views: 151
PDF Downloads: 57
Total Views/Downloads: 402



© Fornicola et al.; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.

* Address correspondence to this author at the 22 S. Greene Street, Baltimore, MD 21201, Tel: 1-410-328-5422; Fax: 1-410-328-5508; E-mail: rcastellani@som.umaryland.edu


Abstract

We studied the brain distribution of amyloid-β (Aβ) and phosphorylated tau (τ) in 20 consecutive autopsy cases between the ages of 51 and 65, with no history of neurologic disease during life. We note that early accumulations of Aβ and τ occur in distinct neuroanatomical distributions. In the locus ceruleus and medial temporal lobe allocortex τ often occurs in the absence of diffuse Aβ and that Aβ occurs in the neocortex in the absence of τ. In those cases with both Aβ and τ were present in the sections, there was no overlap at the microanatomical or cellular level. APOE genotype was also assessed, showing no specific relationship with the presence or distribution of Aβ and τ, although the numbers of cases were limited. These findings indicate that the early appearances of hallmark proteins of Alzheimer’s disease are disconnected both in time and in space, suggesting that both are reactive phenomena with no mechanistic relationship in aging or preclinical disease.

Keywords: Alzheimer’s disease, amyloid-beta, apoe genotyping , neurofibrillary degeneration, phospho-tau..