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Medial Temporal Lobe Disconnection and Hyperexcitability Across Alzheimer's Disease Stages Publisher



Pasquini L1 ; Rahmani F2 ; Malekibalajoo S3, 4 ; La Joie R1 ; Zarei M4 ; Sorg C5, 6, 7 ; Drzezga A8 ; Tahmasian M4
Authors
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Authors Affiliations
  1. 1. Department of Neurology, Memory and Aging Center, University of California, San Francisco, San Francisco, CA, United States
  2. 2. School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Department of Biomedical Engineering, Electrical Engineering Faculty, K.N. Toosi University of Technology, Tehran, Iran
  4. 4. Institute of Medical Science and Technology, Shahid Beheshti University, Daneshjou Boulevard, Velenjak, P.O. Box 1983969411, Tehran, Iran
  5. 5. Departments of Neuroradiology, Klinikum Rechts der Isar, Technische Universitat Munchen, Munich, Germany
  6. 6. Departments of Psychiatry, Klinikum Rechts der Isar, Technische Universitat Munchen, Munich, Germany
  7. 7. TUM-Neuroimaging Center (TUM-NIC), Technische Universitat Munchen, Munich, Germany
  8. 8. Department of Nuclear Medicine, University Hospital of Cologne, Cologne, Germany

Source: Journal of Alzheimer's Disease Reports Published:2019


Abstract

The posteromedial cortex (PMC) and medial temporal lobes (MTL) are two brain regions particularly vulnerable in Alzheimer's disease (AD). We have reviewed the spatiotemporal patterns of amyloid-β and tau accumulation, local MTL functional alterations and MTL-PMC network reconfiguration, and propose a model to relate these elements to each other. Functional and structural MTL-PMC disconnection happen concomitant with amyloid-β plaques and neurofibrillary tau accumulation within these same regions. Ongoing disconnection is accompanied by dysfunctional intrinsic local MTL circuit hyperexcitability, which exacerbates across distinct clinical stages of AD. Our overarching model proposes a sequence of events relating the spatiotemporal patterns of amyloid-β and tau accumulation to MTL-PMC disconnection and local MTL hyperexcitability.We hypothesize that cortical PMC amyloid-β pathology induces long-range information processing deficits through functional and structural MTL-PMC dysconnectivity at early disease stages, which in turn drives local MTL circuit hyperexcitability. Intrinsic local MTL circuit hyperexcitability subsequently accelerates local age-related tau deposition, facilitating tau spread from the MTL to the PMC, eventually resulting in extensive structural degeneration of white and grey matter as the disease advances. We hope that the present model may inform future longitudinal studies needed to test the proposed sequence of events. © 2019 - IOS Press and the authors. All rights reserved.