Abstract
Our incomplete understanding of the link between Alzheimer's Disease pathology and symptomatology is a crucial obstacle for therapeutic success. Recently, translational studies have begun to connect the dots between protein alterations and deposition, brain network dysfunction and cognitive deficits. Disturbance of neuronal activity, and in particular an imbalance in underlying excitation/inhibition (E/I), appears early in AD, and can be regarded as forming a central link between structural brain pathology and cognitive dysfunction. While there are emerging (non-)pharmacological options to influence this imbalance, the complexity of human brain dynamics has hindered identification of an optimal approach. We suggest that focusing on the integration of neurophysiological aspects of AD at the micro-, meso- and macroscale, with the support of computational network modeling, can unite fundamental and clinical knowledge, provide a general framework, and suggest rational therapeutic targets.
| Original language | English |
|---|---|
| Article number | 101372 |
| Journal | Ageing research reviews |
| Volume | 69 |
| DOIs | |
| Publication status | Published - 1 Aug 2021 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Alzheimer's disease
- Amyloid protein
- Animal models
- Computational neuroscience
- Excitation/inhibition imbalance
- Functional networks
- Hyperexcitability
- Hypersynchronization
- Macro scale
- Meso scale
- Microscale
- Tau protein
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