Plain Language Summary: Cholinergic neurons are a type of cell in the brain. Research suggests that cholinergic dysfunction is an early sign of Alzheimer's disease. However, there is currently no method for measuring cholinergic function. This project evaluated a new tool for imaging cholinergic function. Using the tool, we found that individuals at risk for disease exhibit cholinergic dysfunction. Background:
Alzheimer's disease (AD) staging models suggest that amyloid and tau pathologies do not emerge throughout the brain all at once. Rather, specific neurons exhibit early changes in function, which potentiate downstream pathophysiological events (Braak & Braak, 1991). The cholinergic neurons of the basal forebrain (BE) are among the first cell-types to exhibit pathology in AD (Schmitz et al., 2016). However, the lack of a cholinergic biomarker has prevented the evaluation of cholinergic function in early disease stages. PET imaging with [18F]FEOBV overcomes this obstacle (Mulholland et al., 1998). FEOBV targets VAChT, a protein found in cholinergic nerve terminals, making it well-suited for measuring changes in cholinergic function. Using FEOBV, we demonstrate the first molecular imaging evidence for cholinergic dysfunction in cognitively normal (CN) humans at-risk for AD. Methods:
We collected longitudinal MRI, cross-sectional FEOBV, and plasma ptaul81 data in 64 CN older adults atrisk for AD. Results:
Individuals were clustered into risk groups according to their longitudinal decline in B F volume: normal, low, and high-risk groups. Using FEOBV, we found that high-risk individuals exhibited greater molecular cholinergic dysfunction compared to low and normal risk groups. Increased cholinergic degeneration and dysfunction was also found to be associated with increased levels of plasma ptaul81. Conclusions:
We present the first evidence for molecular cholinergic dysfunction in CN humans at-risk for AD, highlighting the utility of FEOBV imaging for detecting at-risk individuals for preventative drug treatments. treatments.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2024. This work is published under https://creativecommons.org/licenses/by-nc-nd/2.5/ca/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Details
1 Western University
2 McGill University