| Literature DB >> 29972789 |
Taylor W Schmitz1, Marieke Mur2, Meghmik Aghourian3, Marc-Andre Bedard3, R Nathan Spreng4.
Abstract
The cholinergic neurons of the basal forebrain (BF) provide virtually all of the brain's cortical and amygdalar cholinergic input. They are particularly vulnerable to neuropathology in early Alzheimer's disease (AD) and may trigger the emergence of neuropathology in their cortico-amygdalar projection system through cholinergic denervation and trans-synaptic spreading of misfolded proteins. We examined whether longitudinal degeneration within the BF can explain longitudinal cortico-amygdalar degeneration in older human adults with abnormal cerebrospinal fluid biomarkers of AD neuropathology. We focused on two BF subregions, which are known to innervate cortico-amygdalar regions via two distinct macroscopic cholinergic projections. To further assess whether structural degeneration of these regions in AD reflects cholinergic denervation, we used the [18F] FEOBV radiotracer, which binds to cortico-amygdalar cholinergic terminals. We found that the two BF subregions explain spatially distinct patterns of cortico-amygdalar degeneration, which closely reflect their cholinergic projections, and overlap with [18F] FEOBV indices of cholinergic denervation.Entities:
Keywords: Alzheimer’s disease; [18F] FEOBV PET; aging; amyloid beta; basal forebrain; cerebrospinal fluid biomarker; cholinergic system; longitudinal analysis; structural MRI; tau
Mesh:
Year: 2018 PMID: 29972789 PMCID: PMC8840819 DOI: 10.1016/j.celrep.2018.06.001
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423