Literature DB >> 28505333

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

Jerzy Wegiel1, Michael Flory1, Izabela Kuchna1, Krzysztof Nowicki1, Shuang Yong Ma1, Jarek Wegiel1, Eulalia Badmaev1, Wayne P Silverman1, Mony de Leon1, Barry Reisberg1, Thomas Wisniewski1.   

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.
© 2017 American Association of Neuropathologists, Inc. All rights reserved.

Entities:  

Keywords:  Brain aging; Neurofibrillary degeneration; Neuronal loss; Neuronal reserve; β-Amyloidosis

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Substances:

Year:  2017        PMID: 28505333      PMCID: PMC5901097          DOI: 10.1093/jnen/nlx027

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


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