TAU, UBIQUITIN, AND ALPHA-BETA-CRYSTALLIN IMMUNOHISTOCHEMISTRY DEFINETHE PRINCIPAL CAUSES OF DEGENERATIVE FRONTOTEMPORAL DEMENTIA

Citation
Pn. Cooper et al., TAU, UBIQUITIN, AND ALPHA-BETA-CRYSTALLIN IMMUNOHISTOCHEMISTRY DEFINETHE PRINCIPAL CAUSES OF DEGENERATIVE FRONTOTEMPORAL DEMENTIA, Archives of neurology, 52(10), 1995, pp. 1011-1015
Citations number
34
Categorie Soggetti
Clinical Neurology
Journal title
ISSN journal
00039942
Volume
52
Issue
10
Year of publication
1995
Pages
1011 - 1015
Database
ISI
SICI code
0003-9942(1995)52:10<1011:TUAAID>2.0.ZU;2-7
Abstract
Objective: We investigated the use of immunostaining with antibodies t o tau, ubiquitin, and alpha B-crystallin in defining a protocol for th e staged neuropathologic examination of brains from patients with a pr ogressive frontotemporal dementia. Design: Brains obtained from 50 pat ients dying with the clinical diagnosis of frontotemporal dementia wer e examined histopathologically to define pathologic distinctions. Sett ing: Two university hospital neuropathology departments. Results: Anti -tau immunostaining defined corticobasal degeneration, Alzheimer's dis ease, and Pick's disease; antiubiquitin defined motor neuron disease w ith dementia. The remaining brains have frontal lobe degeneration: the use of alpha B-crystallin immunostaining, on these, to detect balloon ed neurons may help to define two groups of patients, one of which we believe may represent a variant of Pick's disease. Conclusion: These f indings indicate that immunostaining with these antibodies is essentia l for the evaluation of frontal dementia.