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PMID: 14656067 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Neuropathology of cognitively normal elderly.

Journal of neuropathology and experimental neurology ·Vol. 62 ·No. 11 ·2003-11-00 ·Pages 1087-95

Knopman DS, Parisi JE, Salviati A, Floriach-Robert M, Boeve BF, Ivnik RJ, Smith GE, Dickson DW, Johnson KA, Petersen LE, McDonald WC, Braak H, Petersen RC

Abstract

Despite general agreement about the boundaries of Alzheimer disease (AD), establishing a maximum limit for Alzheimer-type pathology in cognitively intact individuals might aid in defining more precisely the point at which Alzheimer pathology becomes clinically relevant. In this study, we examined the neuropathological changes in the brains of 39 longitudinally followed. cognitively normal elderly individuals (24 women, 15 men; age range 74-95, median 85 years). Neuropathological changes of the Alzheimer type were quantified by determining neurofibrillary tangle (NFT) staging by the method of Braak and Braak and by quantification of the abundance of diffuse, cored, and neuritic plaque burden using the scheme developed by the Consortium to Establish a Registry for Alzheimer Disease (CERAD). Vascular, Lewy body, and argyrophilic grain pathology were also assessed. We found 34 subjects (87%) with a Braak stage <IV; 32 subjects (82%) with less than moderate numbers of cored plaques and 37 subjects (95%) with less than moderate numbers of tau-positive neuritic plaques. Many subjects had moderate or frequent diffuse plaques (n = 19, 49%). By the National Institute on Aging-Reagan Institute (NIA-RI) criteria, none of our cases met criteria for high "likelihood" of AD. Four met NIA-RI criteria for intermediate "likelihood." Seven cases met CERAD criteria for possible AD. Nineteen met Khachaturian criteria for AD. Only 1 subject had neocortical Lewy bodies. Small, old infarcts were common, but no subjects had more than 2 of these and none had a single large infarction. Thus, the majority of individuals who are cognitively normal near the time of their death have minimal amounts of tau-positive neuritic pathology (Braak stage <IV and neuritic plaques <6 per x100 field in the most affected neocortical region). The few subjects with more severe AD pathology can be expected based on incidence rates of AD in the very elderly.

MeSH Terms
Aged Aged, 80 and over Aging/pathology,psychology Apolipoproteins E/genetics Brain/pathology Brain Infarction/pathology Chi-Square Distribution Cognition/physiology Crystallins/metabolism Dementia, Vascular/pathology Female Geriatric Assessment Humans Immunohistochemistry Lewy Bodies/pathology Male Mental Status Schedule Neurofibrillary Tangles/pathology Neuropil/pathology Neuropil Threads/pathology Neuropsychological Tests Plaque, Amyloid/pathology Prospective Studies Reference Standards Severity of Illness Index tau Proteins/metabolism
Chemicals
Apolipoproteins E Crystallins tau Proteins
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Knopman D S
Department of Neurology, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA. [email protected]
Parisi J E
Salviati A
Floriach-Robert M
Boeve B F
Ivnik R J
Smith G E
Dickson D W
Johnson K A
Petersen L E
McDonald W C
Braak H
Petersen R C
Article Info
Journal
Journal of neuropathology and experimental neurology
Abbr.
J Neuropathol Exp Neurol
ISSN
0022-3069
Published
2003-11-00
Pages
1087-95
Language
English
Region
England
NLM ID
2985192R
Subset
IM
Grants
NIA NIH HHS · AG 06786 · United States
NIA NIH HHS · AG 16574 · United States
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