Multiregional Age-Associated Reduction of Brain Neuronal Reserve Without Association With Neurofibrillary Degeneration or β-Amyloidosis.

TitleMultiregional Age-Associated Reduction of Brain Neuronal Reserve Without Association With Neurofibrillary Degeneration or β-Amyloidosis.
Publication TypeJournal Article
Year of Publication2017
AuthorsWegiel J, Flory M, Kuchna I, Nowicki K, Ma SYong, Wegiel J, Badmaev E, Silverman WP, de Leon M, Reisberg B, Wisniewski T
JournalJ Neuropathol Exp Neurol
Volume76
Issue6
Pagination439-457
Date Published2017 Jun 01
ISSN1554-6578
KeywordsAdult, Aged, Aged, 80 and over, Aging, Alzheimer Disease, Amyloid beta-Peptides, Amyloidosis, Brain, Coloring Agents, Female, Humans, Immunohistochemistry, Male, Middle Aged, Neurofibrillary Tangles, Neurons, Tissue Embedding
Abstract

Increase in human life expectancy has resulted in the rapid growth of the elderly population with minimal or no intellectual deterioration. The aim of this stereological study of 10 structures and 5 subdivisions with and without neurofibrillary degeneration in the brains of 28 individuals 25-102-years-old was to establish the pattern of age-associated neurodegeneration and neuronal loss in the brains of nondemented adults and elderly. The study revealed the absence of significant neuronal loss in 7 regions and topographically selective reduction of neuronal reserve over 77 years in 8 brain structures including the entorhinal cortex (EC) (-33.3%), the second layer of the EC (-54%), cornu Ammonis sector 1 (CA1) (-28.5%), amygdala, (-45.8%), thalamus (-40.5%), caudate nucleus (-35%), Purkinje cells (-48.3%), and neurons in the dentate nucleus (40.1%). A similar rate of neuronal loss in adults and elderly, without signs of accelerating neuronal loss in agers or super-agers, appears to indicate age-associated brain remodeling with significant reduction of neuronal reserve in 8 brain regions. Multivariate analysis demonstrates the absence of a significant association between neuronal loss and the severity of neurofibrillary degeneration and β-amyloidosis, and a similar rate of age-associated neuronal loss in structures with and without neurofibrillary degeneration.

DOI10.1093/jnen/nlx027
Alternate JournalJ Neuropathol Exp Neurol
PubMed ID28505333
PubMed Central IDPMC5901097
Grant ListP30 AG008051 / AG / NIA NIH HHS / United States
R01 AG012101 / AG / NIA NIH HHS / United States
R01 AG022374 / AG / NIA NIH HHS / United States
R01 NS073502 / NS / NINDS NIH HHS / United States
Related Institute: 
Brain Health Imaging Institute (BHII)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065