4.4 Article

Disease specificity and pathologic progression of tau pathology in brainstem nuclei of Alzheimer's disease and progressive supranuclear palsy

Journal

NEUROSCIENCE LETTERS
Volume 491, Issue 2, Pages 122-126

Publisher

ELSEVIER IRELAND LTD
DOI: 10.1016/j.neulet.2011.01.020

Keywords

Colliculi; Geniculate bodies; Substantia nigra; Pedunculopontine nucleus; Alzheimer's disease; Progressive supranuclear palsy; Tau

Categories

Funding

  1. National Institutes of Health [P50 NS72187-01, P50 AG16574-11, P01 AG17216-11S1]
  2. society for Progressive Supranuclear Palsy (CurePSP, Inc.)
  3. Mayo Foundation

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Previous studies have shown tau pathology in the inferior colliculus (IC) and superior colliculus (SC) in Alzheimer's disease (AD); however, it has not been compared to other tauopathies, such as progressive supranuclear palsy (PSP), or characterized with respect to progression of tau pathology in AD. The main purpose of this study was to investigate frequency, neuroanatomical selectivity and disease specificity of tau pathology in visual and auditory nuclei (SC and lateral geniculate body (LGB); IC and medial geniculate body (MGB), respectively). We measured phospho-tau burden with immunohistochemistry and image analysis in 26 cases of AD, 37 PSP and 11 normal controls. Tau burden was also assessed in two unrelated brainstem nuclei (substantia nigra (SN) and pedunculopontine nucleus (PPN)) of the same cases. We found tau burden to be greater in the SC of PSP compared to AD and controls. Conversely, tau burden was greater in the IC of AD compared to PSP and controls. The MGB and LGB had sparse tau pathology in both AD and PSP. This disease selectivity parallels known deficits in visual reflexes in PSP and auditory reflexes in AD. Tau burden was greater in the SC, IC, and PPN in both PSP and AD compared to controls, and greater in the SN in PSP compared to AD and controls. Although present at early Braak neurofibrillary tangle stages, the SC, IC, PPN and SN did not accumulate tau consistently until later stages. These findings support a concept of tau pathology affecting the brainstem at mid-to-late stage AD. (C) 2011 Elsevier Ireland Ltd. All rights reserved.

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