Disrupted Sleep Cycles and Alzheimer's Disease Risk
About the Research Project
Program
Award Type
Standard
Award Amount
$300,000
Active Dates
July 01, 2023 - June 30, 2026
Grant ID
A2023011S
Goals
The aim of this project is to evaluate disrupted sleep as an Alzheimer’s disease risk factor.
Summary
Studies in animals have highlighted sleep disruption as a factor in the development of Alzheimer’s disease. Sleep–wake cycles are associated with proper signaling between nerve cells using a region called synapses. In this first-of-its kind series of experiments, Jingyuan Chen, PhD, and her colleagues will use cutting-edge imaging to track metabolic markers of sleep–wake disruption at synapses.
The study will include people with and without known risk for Alzheimer’s disease. They will be imaged in real time so that Dr. Chen and her colleagues can follow how metabolism changes in the synapses during sleep–wake cycles. The researchers will assess these patterns in association with Alzheimer’s disease risk. In addition, they will home in on how the use of glucose, the brain’s molecular fuel, tracks with brain waves that have been previously associated with Alzheimer’s disease.
The results of this study will yield a trove of potential imaging patterns related to risk for the condition and uncover more of the picture of how Alzheimer’s disease and sleep are linked.
Unique and Innovative
This proposal features a series of first-of-its-kind experiments on cutting-edge human imaging facilities. The multi-modal imaging framework pioneered by our team has provided a unique opportunity to track brain-wide, sleep-wake metabolic dynamics non-invasively in humans. We will apply this technique to perform the first human validation of the role of sleep-wake synaptic activity in promoting AD.
Foreseeable Benefits
Findings of this study will help advance our understanding of the fundamental mechanisms underlying AD and the influence of generic factors for AD. Imaging markers identified in the current proposal also hold great promise in facilitating the prognosis of AD.
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