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PMID: 9330997 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Comparison of neuropathologic criteria for the diagnosis of Alzheimer's disease.

Neurobiology of aging ·Vol. 18 ·No. 4 Suppl ·1997-00-00 ·Pages S99-105

Geddes JW, Tekirian TL, Soultanian NS, Ashford JW, Davis DG, Markesbery WR

Abstract

The National Institute on Aging and Reagan Institute (NIA-RI) criteria, and other neuropathologic criteria for Alzheimer's disease (AD), were compared with the clinical diagnosis of dementia in a well defined population of Catholic sisters. The 47-participant subset examined in this study were college educated and lacked complicating conditions such as brain infarcts or diffuse Lewy body disease. Sixteen participants had a clinical diagnosis of dementia. The NIA-RI criteria imply a perfect correlation between neuritic plaque (NP) density and neurofibrillary tangle distribution. However, NP density often did not coincide with tangle distribution. As a result, it was not possible to categorize many of the participants using the NIA-RI guidelines. The 'high likelihood' category of the NIA-RI criteria for AD research settings (neocortical Braak stage and frequent neocortical NP) had relatively high specificity (90% of nondemented participants did not meet this criteria). However, only half of the demented participants were in this category. Neuropathologic criteria requiring the presence of neocortical tangles (rather than neocortical Braak stage) had relatively high sensitivity, accounting for 87-94% of participants with dementia, but also included 32-35% of nondemented participants. Criteria based on neocortical NP or senile plaques had 100% sensitivity, but a majority of nondemented participants also met these criteria. The results support consideration of both tangles and NP for the neuropathologic diagnosis of AD, but indicate that refinement of the NIA-RI criteria is necessary. A possible refinement is suggested for further consideration.

MeSH Terms
Aged Aged, 80 and over Aging/pathology Alzheimer Disease/diagnosis,pathology Brain/pathology Guidelines as Topic Humans Neocortex/pathology Neurofibrillary Tangles/pathology Plaque, Amyloid/pathology Severity of Illness Index
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Geddes J W
Sanders-Brown Center on Aging, University of Kentucky, Lexington 40536-0230, USA.
Tekirian T L
Soultanian N S
Ashford J W
Davis D G
Markesbery W R
Article Info
Journal
Neurobiology of aging
Abbr.
Neurobiol Aging
ISSN
0197-4580
Published
1997-00-00
Pages
S99-105
Language
English
Region
United States
NLM ID
8100437
Subset
IM
Grants
NIMH NIH HHS · F31MH11650 · United States
NIA NIH HHS · P50AG05144 · United States
NIA NIH HHS · R35 AG08974 · United States
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