Abstract
Limbic-predominant age-related TDP-43 encephalopathy neuropathologic changes (LATE-NC) often occur in aged brains that also contain appreciable Alzheimer disease neuropathologic changes (ADNC). Question has arisen as to whether LATE-NC can occur independently of ADNC. We evaluated data from the University of Kentucky Alzheimer's Disease Research Center autopsy cohort (383 included subjects) to address 2 questions: (i) Is LATE-NC seen in the absence of ADNC, outside of persons who had the frontotemporal dementia (FTD) clinical syndrome? and (ii) is LATE-NC associated with cognitive impairment across the full spectrum of ADNC severity? In the present study, the pathologic combination of LATE-NC (Stage >1) and low/no ADNC was common: 8.9% (34/383) of all subjects (including demented and non-demented individuals) showed this combination. There were no FTLD-TDP cases to be included from the community-based cohort. Across a broad range of ADNC severity, the presence of LATE-NC was associated with impaired cognition but was never associated with a FTD clinical syndrome.
Original language | English |
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Pages (from-to) | 649-651 |
Number of pages | 3 |
Journal | Journal of Neuropathology and Experimental Neurology |
Volume | 80 |
Issue number | 7 |
DOIs | |
State | Published - Jul 1 2021 |
Bibliographical note
Publisher Copyright:© 2021 Oxford University Press. All rights reserved.
Keywords
- Community-based
- Frontotemporal lobar degeneration (FTLD)
- Hippocampal sclerosis
- Human
- Lewy
- Neuropathology
ASJC Scopus subject areas
- General Medicine