Resting-state global brain activity affects early β-amyloid accumulation in default mode network
Feng Han1, Xufu Liu1, Richard B Mailman2
1Department of Biomedical Engineering, The Pennsylvania State University, State College, PA, USA.
Nature Communications
|November 27, 2023
Summary
Early Alzheimer's disease shows beta-amyloid plaques accumulating in the default mode network. This coincides with reduced global brain activity in these areas, potentially due to impaired wave propagation, highlighting activity's role in plaque deposition.
Area of Science:
- Neuroscience
- Alzheimer's Disease Research
- Brain Imaging
Background:
- Alzheimer's disease (AD) is characterized by beta-amyloid (Aβ) plaques, particularly in the default mode network (DMN).
- The reasons for early Aβ deposition in the DMN remain unclear.
- Resting-state global brain activity, especially low-frequency (<0.1 Hz), has been linked to AD and may influence glymphatic clearance.
Purpose of the Study:
- To investigate the relationship between early Aβ plaque accumulation in the DMN and resting-state global brain activity in Alzheimer's disease.
- To explore the potential mechanisms, such as wave propagation, linking brain activity and Aβ deposition.
Main Methods:
- Analysis of Aβ plaque distribution in the cortex, focusing on the DMN.
- Measurement of resting-state low-frequency global brain activity.
- Correlation analysis between Aβ deposition and brain activity patterns.
- Modeling of wave propagation in the brain.
Main Results:
- Preferential accumulation of Aβ plaques in the DMN during early AD pathology was observed.
- This Aβ deposition was associated with a corresponding preferential reduction in global brain activity within the DMN.
- Impaired propagation of brain activity waves to these regions was identified as a potential contributing factor.
Conclusions:
- Resting-state global brain activity plays a significant role in the early, preferential deposition of Aβ in the DMN.
- Reduced brain activity and impaired wave propagation may contribute to the localized Aβ accumulation seen in early Alzheimer's disease.


