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Joseph Giorgio

2 papers in the library · publishing 2023-2026

Papers

Dopamine Compensates for Amyloid-Induced Default Mode Network Dysfunction to Support Learning

bioRxiv (Cold Spring Harbor Laboratory) July 10, 2026 Joseph Giorgio, Thomas Morin, Hsiang-Yu Chen et al.

In cognitively normal older adults, β-amyloid (Aβ) buildup in the default mode network impairs learning independently of tau, but higher dopamine synthesis capacity in the dorsolateral striatum can recover that learning performance. Aβ-positive individuals show reduced default mode network activity in response to error feedback, which relates to poorer learning. Computational modeling indicates that Aβ disinhibits the default mode network during error processing, and dopamine synthesis capacity in the dorsolateral striatum rebalances effective connectivity between the default mode network and frontostriatal network, counteracting Aβ-related disruption. These findings suggest that dopaminergic function can partially compensate for Aβ-related learning deficits through network rebalancing, offering a candidate mechanism for cognitive resilience in preclinical Alzheimer's disease.

Amyloid induced hyperexcitability in default mode network drives medial temporal hyperactivity and early tau accumulation.

Neuron December 1, 2023 Joseph Giorgio, Jenna N. Adams, A. Maass et al.

In early Alzheimer's disease, amyloid-beta deposits appear throughout association cortex while tau appears in the entorhinal cortex, but why these pathologies initially arise in different locations is unclear. Using task-based fMRI and multimodal PET imaging, the authors show that Alzheimer's pathologies flip interactions between the default mode network and the medial temporal lobe from inhibitory to excitatory. The default mode network becomes hyperexcited with increasing amyloid-beta levels, which drives hyperexcitability within the medial temporal lobe, and this directed hyperexcitation predicts the rate of tau accumulation within the entorhinal cortex. The results support a model where amyloid-beta-induced disruptions to local excitatory-inhibitory balance in the default mode network drive medial temporal lobe hyperexcitability, leading to tau accumulation.