Search
Browse
Statistics
Feeds

Disruption of temporo-parietal network in Alzheimer's disease and its association with memory impairment

[thumbnail of Original Article]
Preview
PDF (Original Article) - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
2MB
[thumbnail of Supplementary Information] MS Word (Supplementary Information)
268kB

Item Type:Article
Title:Disruption of temporo-parietal network in Alzheimer's disease and its association with memory impairment
Creators: Suksangkharn, Yanin, Schott, Björn Hendrik, Zeidman, Peter, Vockert, Niklas, Lattmann, René, Schütze, Hartmut, Yakupov, Renat, Peters, Oliver ORCID logoORCID: https://orcid.org/0000-0003-0568-2998, Hellmann-Regen, Julian ORCID logoORCID: https://orcid.org/0000-0003-0411-9204, Preis, Lukas ORCID logoORCID: https://orcid.org/0000-0001-7601-6410, Ersözlü, Ersin, Priller, Josef ORCID logoORCID: https://orcid.org/0000-0001-7596-0979, Spruth, Eike Jakob, Beckmann, Janna, Schneider, Anja, Fliessbach, Klaus, Wiltfang, Jens, Bartels, Claudia, Rostamzadeh, Ayda, Glanz, Wenzel, Incesoy, Enise I., Teipel, Stefan, Kilimann, Ingo, Goerss, Doreen, Laske, Christoph, Spottke, Annika, Kronmüller, Marie, Brosseron, Frederic, Lüsebrink, Falk, Schmid, Matthias, Kleineidam, Luca, Stark, Melina, Hetzer, Stefan, Dechent, Peter, Jessen, Frank, Maass, Anne, Düzel, Emrah and Ziegler, Gabriel
Abstract:Alzheimer's disease (AD) is characterised by the accumulation of β-amyloid (Aβ) and tau proteins, resulting in neurodegeneration and cognitive decline. Although Aβ and tau disrupt synaptic function, the association linking these molecular pathologies to network-level dysfunction and memory impairment remains poorly understood. Here, we investigated the effects of Aβ and tau pathology (CSF Aβ42/40 ratio and tau phosphorylated at position 181, p-tau-181, respectively) on effective connectivity related to memory encoding, which may provide a link between synaptic pathology and cognitive outcomes. Functional magnetic resonance imaging (fMRI) during visual memory encoding was acquired from 205 participants in the multicentric DZNE Longitudinal Cognitive Impairment and Dementia Study (DELCODE) across the AD spectrum. Effective connectivity was assessed using Dynamic Causal Modelling (DCM) of task-fMRI data, focusing on the parahippocampal place area (PPA), hippocampus (HC), and precuneus (PCU)-regions central to memory encoding. Disruptions in connectivity between temporal and parietal lobes were associated with both memory impairment and indices of AD pathology. Specifically, reduced positive effective connectivity from the PCU to the PPA and from the HC to the PCU were linked to higher p-tau-181 levels, with an amplification effect observed in the presence of amyloid accumulation for the latter connectivity. The disruption from the PCU to the PPA was found to be associated with decreased memory performance. Together, these findings indicate that temporo-parietal connectivity is associated with both AD molecular pathology and, for a subset of connections, with memory performance.
Keywords:Alzheimer's Disease, Memory Impairment, Synaptic Aberration, Beta-Amyloid, Tau, Neurodegeneration
Source:Alzheimer's Research & Therapy
ISSN:1758-9193
Publisher:BioMed Central
Volume:18
Number:1
Page Range:166
Date:16 July 2026
Official Publication:https://doi.org/10.1186/s13195-026-02138-w
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library