| Literature DB >> 33002767 |
David G Coughlin1, Jeffrey S Phillips2, Emily Roll2, Claire Peterson3, Rebecca Lobrovich3, Katya Rascovsky2, Molly Ungrady2, David A Wolk4, Sandhitsu Das4, Daniel Weintraub5, Edward B Lee6, John Q Trojanowski7, Leslie M Shaw8, Sanjeev Vaishnavi9, Andrew Siderowf9, Ilya M Nasrallah10, David J Irwin11, Corey T McMillan12.
Abstract
We compared regional retention of 18F-flortaucipir between 20 patients with Lewy body disorders (LBD), 12 Alzheimer's disease patients with positive amyloid positron emission tomography (PET) scans (AD+Aβ) and 15 healthy controls with negative amyloid PET scans (HC-Aβ). In LBD subjects, we compared the relationship between 18F-flortaucipir retention and cerebrospinal fluid (CSF) tau, cognitive performance, and neuropathological tau at autopsy. The LBD cohort was stratified using an Aβ42 cut-off of 192 pg/mL to enrich for groups likely harboring tau pathology (LBD+Aβ = 11, LBD-Aβ = 9). 18F-flortaucipir retention was higher in LBD+AB than HC-Aβ in five, largely temporal-parietal regions with sparing of medial temporal regions. Higher retention was associated with higher CSF total-tau levels (p = 0.04), poorer domain-specific cognitive performance (p = 0.02-0.04), and greater severity of neuropathological tau in corresponding regions. While 18F-flortaucipir retention in LBD is intermediate between healthy controls and AD, retention relates to cognitive impairment, CSF total-tau, and neuropathological tau. Future work in larger autopsy-validated cohorts is needed to define LBD-specific tau biomarker profiles.Entities:
Keywords: CSF; Cognition; Lewy body diseases; Neuropathology; PET imaging; Tau
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Year: 2020 PMID: 33002767 PMCID: PMC7819484 DOI: 10.1016/j.neurobiolaging.2020.08.003
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673