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

J. W. Geddes, T. L. Tekirian, N. S. Soultanian, J. W. Ashford, D. G. Davis, W. R. Markesbery

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91 Scopus citations

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.

Original languageEnglish
Pages (from-to)S99-S105
JournalNeurobiology of Aging
Volume18
Issue number4 SUPPL.
DOIs
StatePublished - 1997

Bibliographical note

Funding Information:
We thank Ela Patel for excellent technical assistance and Dr. Huaichen Liu for quantitative assessment of AD pathology. This study would not have been possible without the support of the members, leaders, and health care providers of the School Sisters of Notre Dame. This study was funded by grants R35 AG08974 (J. W. G.), P50AG05144 (W. R. M.) and F31MH11650 (T. L. T.), and a grant from the Abercrombie Foundation.

Funding

We thank Ela Patel for excellent technical assistance and Dr. Huaichen Liu for quantitative assessment of AD pathology. This study would not have been possible without the support of the members, leaders, and health care providers of the School Sisters of Notre Dame. This study was funded by grants R35 AG08974 (J. W. G.), P50AG05144 (W. R. M.) and F31MH11650 (T. L. T.), and a grant from the Abercrombie Foundation.

FundersFunder number
National Institute of Mental HealthF31MH011650
Abercrombie Foundation

    Keywords

    • Alzheimer's disease
    • Cerebral cortex
    • Cognition disorders
    • Diagnosis
    • Epidemiology
    • Neurofibrillary tangles
    • Pathology
    • Prospective studies
    • Psychological tests

    ASJC Scopus subject areas

    • General Neuroscience
    • Aging
    • Developmental Biology
    • Clinical Neurology
    • Geriatrics and Gerontology

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