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Brain CommunicationsNeurosciencePeer-reviewed journal article

Amyloid-beta relates to default and attention network connectivity during working memory retrieval

Hengda HeiD, Christian Georg HabeckiD, Yaakov SterniD

PDFDOIPreprint

Abstract

As one of the earliest pathological events in Alzheimers disease, amyloid-beta accumulation has been linked to alterations in large-scale brain networks, especially the default mode network. While most prior work has focused on resting-state functional connectivity or task-evoked activation, how amyloid-beta relates to task-modulated connectivity that directly supports behavior is less explored. Here, we examined the relationship between amyloid-beta burden and task-modulated connectivity during a Letter Sternberg verbal working-memory task in eighty-four cognitively normal older adults from an ongoing longitudinal cohort (age 56-71 years; 41 female). To further understand these connectivity alterations, we tested whether these connections were associated with task performance or with cognitive reserve factors. We found that higher amyloid-beta burden was associated with reduced connectivity specifically during the probe phase of working-memory retrieval. At the regional scale, lower node strength in posterior-medial regions of the default mode network was related to worse task performance and mediated the amyloid-behavior relationship. At the network scale, altered coupling between the default mode and dorsal attention networks was related to task performance but did not mediate the amyloid-behavior relationship. Moreover, physical activity was associated with network-level coupling but not with regional node strength. These findings suggest that amyloid-beta burden disrupts retrieval-related working-memory systems, particularly regions of the default mode network that are vulnerable to amyloid-beta, while coupling between the default mode and dorsal attention networks indexes resilience. Collectively, task-modulated connectivity provides insight into pathways through which early Alzheimers disease pathology influences working-memory performance and resilience and may inform targeted lifestyle or neuromodulation interventions for older adults.

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