Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/28202
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dc.contributor.authorStouffer, KM-
dc.contributor.authorGrande, X-
dc.contributor.authorDuezel, E-
dc.contributor.authorJohansson, M-
dc.contributor.authorCreese, B-
dc.contributor.authorWitter, MP-
dc.contributor.authorMiller, MI-
dc.contributor.authorWisse, LEM-
dc.contributor.authorBerron, D-
dc.date.accessioned2024-02-04T10:58:37Z-
dc.date.available2024-02-04T10:58:37Z-
dc.date.issued2023-12-18-
dc.identifierORCID iD: Kaitlin M. Stouffer https://orcid.org/0000-0003-4547-8836-
dc.identifierORCID iD: Emrah Duezel https://orcid.org/0000-0002-0139-5388-
dc.identifierORCID iD: Byron Creese https://orcid.org/0000-0001-6490-6037-
dc.identifierORCID iD: Menno P. Witter https://orcid.org/0000-0003-0285-1637-
dc.identifierORCID iD: David Berron https://orcid.org/0000-0003-1558-1883-
dc.identifierawad411-
dc.identifier.citationStouffer, 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.en_US
dc.identifier.issn0006-8950-
dc.identifier.urihttps://bura.brunel.ac.uk/handle/2438/28202-
dc.descriptionLaura 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.en_US
dc.descriptionSupplementary material: Supplementary material is available at Brain online at: https://doi.org/10.1093/brain/awad411 .-
dc.description.abstractThe 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.en_US
dc.description.sponsorshipThis work is supported by grants from the Swedish Research Council (2022-00900) and the Crafoord Foundation (LW). This study is supported by MultiPark - A Strategic Research Area at Lund University (LW). This work is supported by the National Institutes of Health: U19-AG033655, P30-AG066507, P41-EB031771, R01-EB020062, T32-GM13677, U19-MH114821, R01-NS074980-10S1, RF1MH126732, RF1MH128875, F30AG077736 (MM and KS) and the Kavli Neuroscience Discovery Institute (MM and KS) as well as the Kavli Foundation and the KG. Jebsen Foundation (MPW). This work is further supported by the Elly Bergren Foundation and regional research support by the Division of Psychiatry, Habilitation and Medical aid, Region Skåne (MJ). This work was partly supported by the National Institute for Health and Care Research 23 Exeter Biomedical Research Centre.en_US
dc.format.extent1 - [37]-
dc.format.mediumPrint-Electronic-
dc.languageEnglish-
dc.language.isoen_USen_US
dc.publisherOxford University Press on behalf of the Guarantors of Brainen_US
dc.rightsCopyright © 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.com-
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/-
dc.subjectAlzheimer’s diseaseen_US
dc.subjectamygdalaen_US
dc.subjecttau pathologyen_US
dc.subjectneuropsychiatric symptomsen_US
dc.subjectclinical imaging biomarkersen_US
dc.subjectmedial temporal lobe connectivityen_US
dc.titleAmidst an amygdala renaissance in Alzheimer’s diseaseen_US
dc.typeArticleen_US
dc.identifier.doihttps://doi.org/10.1093/brain/awad411-
dc.relation.isPartOfBrain-
pubs.issueahead of print-
pubs.publication-statusPublished online-
pubs.volume0-
dc.identifier.eissn1460-2156-
dc.rights.holderThe Author(s)-
Appears in Collections:Dept of Life Sciences Research Papers

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