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Hippocampal sclerosis in the parkinsonism‐dementia complex of G uam: quantitative examination of neurons, neurofibrillary tangles, and TDP ‐43 immunoreactivity in CA1
Author(s) -
Oyanagi Kiyomitsu,
Yamazaki Mineo,
Hashimoto Tomoyo,
Asakawa Mika,
Wakabayashi Koichi,
Takahashi Hitoshi
Publication year - 2015
Publication title -
neuropathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.701
H-Index - 61
eISSN - 1440-1789
pISSN - 0919-6544
DOI - 10.1111/neup.12185
Subject(s) - hippocampal formation , hippocampus , parkinsonism , dementia , neuron , neuroscience , hippocampal sclerosis , pathology , chemistry , medicine , biology , endocrinology , temporal lobe , disease , epilepsy
The cornu ammonis 1 ( CA 1) area in the hippocampus of the parkinsonism‐dementia complex ( PDC ) of G uam was examined quantitatively with special references to the number of neurons, intraneuronal (i) and extracellular (e) neurofibirillary tangles ( NFT s), and TDP ‐43 (43‐kDa trans‐activation‐responsive region DNA ‐binding protein)‐immunopositive structures, in 24 C hamorro patients with PDC of G uam and seven control C hamorro G uamanians (both groups having no ischemic or anoxic complications). The results were that: (i) in the patients with mildly involved PDC , total numbers of neurons, iNFT s and eNFT s were almost the same as those of neurons of controls; (ii) in patients severely involved, total numbers of neurons, iNFT s and eNFT s decreased markedly; (iii) the decrease of the number of pyramidal neurons in CA1 with positive nuclear TDP ‐43 was intimately correlated with the decrease in total neuron numbers; (iv) whereas the numbers of neurons and TDP ‐43‐immunopositive intracytoplasmic aggregation in the CA1 area were inversely correlated; and (v) depression of nuclear TDP ‐43 immuonostainability was not affected by the presence or absence of NFT s. In conclusion, hippocampal sclerosis exists in PDC ; there is a possibility of elimination of eNFT s which appeared in the CA1 in patients with PDC and loss of the neurons correlates with disappearance of nuclear TDP ‐43, but not with appearance of intraneurocytoplasmic TDP ‐43 aggregation or iNFT s.