| Literature DB >> 26597697 |
Janna H Neltner1, Erin L Abner2, Gregory A Jicha3, Frederick A Schmitt3, Ela Patel4, Leonard W Poon5, Gearing Marla6, Robert C Green7, Adam Davey8, Mary Ann Johnson5, S Michal Jazwinski9, Sangkyu Kim9, Daron Davis10, John L Woodard11, Richard J Kryscio12, Linda J Van Eldik13, Peter T Nelson14.
Abstract
With an emphasis on evolving concepts in the field, we evaluated neuropathologic data from very old research volunteers whose brain autopsies were performed at the University of Kentucky Alzheimer's Disease Center, incorporating data from the Georgia Centenarian Study (n = 49 cases included), Nun Study (n = 17), and University of Kentucky Alzheimer's Disease Center (n = 11) cohorts. Average age of death was 102.0 (range: 98-107) years overall. Alzheimer's disease pathology was not universal (62% with "moderate" or "frequent" neuritic amyloid plaque densities), whereas frontotemporal lobar degeneration was absent. By contrast, some hippocampal neurofibrillary tangles (including primary age-related tauopathy) were observed in every case. Lewy body pathology was seen in 16.9% of subjects and hippocampal sclerosis of aging in 20.8%. We describe anatomic distributions of pigment-laden macrophages, expanded Virchow-Robin spaces, and arteriolosclerosis among Georgia Centenarians. Moderate or severe arteriolosclerosis pathology, throughout the brain, was associated with both hippocampal sclerosis of aging pathology and an ABCC9 gene variant. These results provide fresh insights into the complex cerebral multimorbidity, and a novel genetic risk factor, at the far end of the human aging spectrum.Entities:
Keywords: Arteriosclerosis; KATP; Lipohyalinosis; NFT; Neuropathology; Oldest-old; PART; SUR2; Stroke; Synucleinopathy; TDP-43; VCID
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Year: 2015 PMID: 26597697 PMCID: PMC4688098 DOI: 10.1016/j.neurobiolaging.2015.10.009
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673