Clinicopathologic Correlations in a Large Alzheimer Disease Center Autopsy Cohort: Neuritic Plaques and Neurofibrillary Tangles "Do Count" When Staging Disease Severity

• Published in: Journal of neuropathology and experimental neurology Vol. 66; no. 12; pp. 1136 - 1146
• Main Authors: Nelson, Peter T., Jicha, Gregory A., Schmitt, Frederick A., Liu, Huaichen, Davis, Daron G., Mendiondo, Marta S., Abner, Erin L., Markesbery, William R.
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD American Association of Neuropathologists, Inc 01.12.2007; Lippincott Williams & Wilkins; Oxford University Press
• Subjects: Aged; Aged, 80 and over; Alzheimer Disease - epidemiology; Alzheimer Disease - metabolism; Alzheimer Disease - pathology; Amyloid beta-Peptides - metabolism; Biological and medical sciences; Brain - pathology; Cohort Studies; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases; Disease Progression; Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes; Female; Humans; Male; Medical sciences; Mental Status Schedule; Nervous system (semeiology, syndromes); Neurofibrillary Tangles - pathology; Neurologic Examination; Neurology; Neuropil Threads; Neuropsychological Tests; Plaque, Amyloid - pathology; Postmortem Changes; Severity of Illness Index; Statistics as Topic; Nervous system diseases; Autopsy; Alzheimer disease; Neurofibrillary tangles (NFTs); Central nervous system disease; Degenerative disease; Amyloid; Cerebrovascular; Neurofibrillary tangle; Plaques; Cerebral disorder
• ISSN: 0022-3069; 1554-6578
• DOI: 10.1097/nen.0b013e31815c5efb

There is uncertainty regarding the association of cognitive decline in Alzheimer disease (AD) with classic histopathologic features- neurofibrillary tangles (NFTs) and "neuritic" amyloid plaques (NPs). This uncertainty fuels doubts about the diagnostic importance of NFTs and NPs and leads to confusion regarding hypotheses of AD pathogenesis. Three hundred ninety subjects who underwent longitudinal premortem clinical workup and postmortem quantitative neuropathologic assessment served as the group to address this issue. Subjects with concomitant brain disease(s) were analyzed independently to more accurately assess the contribution of distinct pathologies to cognitive decline. More than 60% of patients of all age groups had important non-AD brain pathologies. However, subjects without superimposed brain diseases showed strong correlations between AD-type pathology counts (NFTs > NPs) and premortem Mini-Mental State Examination scores. The observed correlation was stronger in isocortex than in allocortex and was maintained across age groups including patients older than 90 years. A theoretical model is proposed in which our results are interpreted to support the "amyloid cascade hypothesis" of AD pathogenesis. Our data show that there are many important contributory causes to cognitive decline in older persons. However, NFTs and NPs should not be dismissed as irrelevant in AD based on clinicopathologic correlation.