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LATE Neuropathologic Changes with Little or No Alzheimer Disease is Common and is Associated with Cognitive Impairment but Not Frontotemporal Dementia

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

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 languageEnglish
Pages (from-to)649-651
Number of pages3
JournalJournal of Neuropathology and Experimental Neurology
Volume80
Issue number7
DOIs
StatePublished - Jul 1 2021

Bibliographical note

Publisher Copyright:
© 2021 Oxford University Press. All rights reserved.

Funding

Funding included NIH grants P30 AG028383, R01 AG057187, R01 AG042475, R01 AG054060, and RF1 NS118584.

FundersFunder number
National Institutes of Health (NIH)P30 AG028383, RF1 NS118584, R01 AG054060, R01 AG042475
National Institute on AgingR01AG057187

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Community-based
    • Frontotemporal lobar degeneration (FTLD)
    • Hippocampal sclerosis
    • Human
    • Lewy
    • Neuropathology

    ASJC Scopus subject areas

    • General Medicine

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