Temporal lobar predominance of TDP-43 neuronal cytoplasmic inclusions in Alzheimer disease

被引:116
|
作者
Hu, William T. [1 ,2 ]
Josephs, Keith A. [2 ]
Knopman, David S. [2 ]
Boeve, Bradley F. [2 ]
Dickson, Dennis W. [3 ]
Petersen, Ronald C. [2 ]
Parisi, Joseph E. [1 ]
机构
[1] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Neurol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Neurosci, Jacksonville, FL USA
关键词
amygdala; FTLD-U; FTLD-MND; frontotemporal dementia; motor neuron disease;
D O I
10.1007/s00401-008-0400-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
TAR DNA binding protein-43 (TDP-43) immunoreactive neuronal inclusions are detected in 20-30% of Alzheimer disease (AD) brains, but the distribution of this pathology has not been rigorously studied. In this report, we describe region-specific distribution and density of TDP-43 positive neuronal cytoplasmic inclusions (NCIs) in clinically demented individuals with high probability AD pathology, all with Braak neurofibrillary tangle stages of V or VI. Sections of hippocampus, amygdala, as well as temporal, frontal, and parietal neocortex, were analyzed with TDP-43 immunohistochemistry, and the density of NCIs was assessed using a semiquantitative scoring method. Of the 29 cases, six had TDP-43 positive NCIs in the amygdala only and seven had TDP-43 inclusions restricted to amygdala and hippocampus. In 16 cases, TDP-43 immunoreactivity was more widespread, affecting temporal, frontal or parietal neocortex. These findings indicate that medial temporal lobe limbic structures are vulnerable to TDP-43 pathology in advanced AD, and that the amygdala appears to be the most susceptible region. The distribution of the lesions in this cross-sectional analysis may suggest a progression of TDP-43 pathology in AD, with limbic structures in the medial temporal lobe affected first, followed by higher order association cortices.
引用
收藏
页码:215 / 220
页数:6
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