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Constructional apraxia in Alzheimer's disease correlates with neuritic neuropathology in occipital cortex. Brain Res 1996 Nov 25;741(1-2):284-93

Date

11/25/1996

Pubmed ID

9001734

DOI

10.1016/s0006-8993(96)00983-3

Scopus ID

2-s2.0-0030602038 (requires institutional sign-in at Scopus site)   32 Citations

Abstract

A variety of measures of neuropathology in Alzheimer's disease (AD) correlate with dementia severity. However, the role of beta-amyloid protein and abnormally phosphorylated tau protein in the decline of specific cognitive abilities is unknown. "Constructional praxis' (e.g., copying, constructing) is believed to require integrity of the parietal-occipital lobes. Unlike most other cognitive tasks, some AD patients are able to perform some constructional tasks even late in the disease course. Thus, it may be an ideal task to evaluate the relationship between various measures of AD neuropathology and cognitive performance. Fixed brain tissue was obtained from 16 AD patients who were cognitively assessed shortly before death. Parietal, frontal, entorhinal, and occipital cortices were examined by immunocytochemistry for beta-amyloid protein and abnormally phosphorylated tau protein at both early and later stages of neuropil thread and tangle formation. Constructional praxis in AD was strongly related to early-stage tau hyperphosphorylation in occipital cortex. Praxis ability was specific in that it was not significantly related to pathology in other areas and non-constructive tasks were not associated with occipital cortex pathology. In contrast, global dementia severity was related to beta-amyloid deposition in entorhinal, parietal, and frontal regions. These findings suggest that occipital cortex is critical for some constructional praxis tasks and that some regionally localizable tasks may be good indices of underlying pathology in corresponding brain regions.

Author List

Nielson KA, Cummings BJ, Cotman CW

Author

Kristy Nielson PhD Professor in the Psychology department at Marquette University




MESH terms used to index this publication - Major topics in bold

Aged
Aged, 80 and over
Alzheimer Disease
Amyloid beta-Peptides
Antibodies, Monoclonal
Apraxias
Female
Humans
Image Interpretation, Computer-Assisted
Immunohistochemistry
Male
Neurites
Neurofibrillary Tangles
Neuropsychological Tests
Occipital Lobe
tau Proteins