| Literature DB >> 33270870 |
Jerzy Wegiel, Michael Flory1, Izabela Kuchna2, Krzysztof Nowicki2, Shuang Yong Ma2, Jarek Wegiel2, Eulalia Badmaev2, Mony de Leon3, Thomas Wisniewski4, Barry Reisberg4.
Abstract
Clinical and neuropathological staging of Alzheimer disease (AD) neurodegeneration and neuronal loss dynamics is the baseline for identification of treatment targets and timing. The aim of this study of 14 brain regions in 25 subjects diagnosed with AD and 13 age-matched control subjects was to establish the pattern of neurodegeneration, and the severity and rate of neuronal loss in mild cognitive impairment/mild AD (Functional Assessment Staging [FAST] test 3-4), moderate to moderately severe AD (FAST 5-6), and severe AD (FAST 7). The study revealed (1) the most severe neuronal loss in FAST 3-4; (2) the highest rate of neuronal loss in FAST 5-6, to the "critical" point limiting further increase in neuronal loss; (3) progression of neurofibrillary degeneration, but decline of neuronal loss to a floor level in FAST 7; and (4) structure-specific rate of neuronal loss caused by neurofibrillary degeneration and a large pool of neuronal loss caused by other mechanisms. This study defines a range and speed of progression of AD pathology and functional decline that might potentially be prevented by the arrest of neuronal loss, both related and unrelated to neurofibrillary degeneration, during the 9-year duration of mild cognitive impairment/mild AD.Entities:
Keywords: Alzheimer disease; Clinicopathological staging; GDS/FAST; Neurofibrillary degeneration; Neuronal loss
Mesh:
Year: 2021 PMID: 33270870 PMCID: PMC7749716 DOI: 10.1093/jnen/nlaa140
Source DB: PubMed Journal: J Neuropathol Exp Neurol ISSN: 0022-3069 Impact factor: 3.685