Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/28202
Title: Amidst an amygdala renaissance in Alzheimer’s disease
Authors: Stouffer, KM
Grande, X
Duezel, E
Johansson, M
Creese, B
Witter, MP
Miller, MI
Wisse, LEM
Berron, D
Keywords: Alzheimer’s disease;amygdala;tau pathology;neuropsychiatric symptoms;clinical imaging biomarkers;medial temporal lobe connectivity
Issue Date: 18-Dec-2023
Publisher: Oxford University Press on behalf of the Guarantors of Brain
Citation: Stouffer, K.M. et a. (2023) 'Amidst an amygdala renaissance in Alzheimer’s disease', Brain, 0 (ahead of print), awad411, pp. 1 - [37]. doi: 10.1093/brain/awad411.
Abstract: The amygdala was highlighted as an early site for neurofibrillary tau tangle pathology in Alzheimer’s disease in the seminal Braak & Braak article (1991). This knowledge has, however, only received traction recently with advances in imaging and image analysis techniques. Here, we provide a cross-disciplinary overview of pathology and neuroimaging studies on the amygdala. These studies provide strong support for an early role of the amygdala in Alzheimer’s disease and the utility of imaging biomarkers of the amygdala in detecting early changes and predicting decline in cognitive functions and neuropsychiatric symptoms in early stages. We summarize the animal literature on connectivity of the amygdala, demonstrating that amygdala nuclei that show the earliest and strongest accumulation of neurofibrillary tangle pathology are those that are connected to brain regions that also show early neurofibrillary tangle accumulation. Additionally, we propose an alternative pathway of neurofibrillary tangle spreading within the medial temporal lobe between the amygdala and the anterior hippocampus. The proposed existence of this pathway is strengthened by novel experimental data on human functional connectivity. Finally, we summarize the functional roles of the amygdala, highlighting the correspondence between neurofibrillary tangle accumulation and symptomatic profiles in Alzheimer’s disease. In summary, these findings provide a new impetus for studying the amygdala in Alzheimer’s disease and a unique perspective to guide further study on neurofibrillary tangle spreading and the occurrence of neuropsychiatric symptoms in Alzheimer’s disease.
Description: Laura E. M. Wisse and David Berron contributed equally to this work. Accepted manuscripts: Accepted manuscripts are PDF versions of the author’s final manuscript, as accepted for publication by the journal but prior to copyediting or typesetting. They can be cited using the author(s), article title, journal title, year of online publication, and DOI. They will be replaced by the final typeset articles, which may therefore contain changes. The DOI will remain the same throughout.
Supplementary material: Supplementary material is available at Brain online at: https://doi.org/10.1093/brain/awad411 .
URI: https://bura.brunel.ac.uk/handle/2438/28202
DOI: https://doi.org/10.1093/brain/awad411
ISSN: 0006-8950
Other Identifiers: ORCID iD: Kaitlin M. Stouffer https://orcid.org/0000-0003-4547-8836
ORCID iD: Emrah Duezel https://orcid.org/0000-0002-0139-5388
ORCID iD: Byron Creese https://orcid.org/0000-0001-6490-6037
ORCID iD: Menno P. Witter https://orcid.org/0000-0003-0285-1637
ORCID iD: David Berron https://orcid.org/0000-0003-1558-1883
awad411
Appears in Collections:Dept of Life Sciences Research Papers

Files in This Item:
File Description SizeFormat 
FullText.pdfCopyright © The Author(s) 2023. Published by Oxford University Press on behalf of the Guarantors of Brain. This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com838.85 kBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons