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Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation

Background: Brain (18)F-AV-45 amyloid positron emission tomography (PET) in Taiwanese patients with familial Alzheimer's disease with the amyloid precursor protein (APP) p.D678H mutation tends to involve occipital and cerebellar cortical areas. However, tau pathology in patients with this speci...

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Autores principales: Huang, Chin-Chang, Hsiao, Ing-Tsung, Huang, Chu-Yun, Weng, Yi-Ching, Huang, Kuo-Lun, Liu, Chi-Hung, Chang, Ting-Yu, Wu, Hsiu-Chuan, Yen, Tzu-Chen, Lin, Kun-Ju
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538951/
https://www.ncbi.nlm.nih.gov/pubmed/31191427
http://dx.doi.org/10.3389/fneur.2019.00503
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author Huang, Chin-Chang
Hsiao, Ing-Tsung
Huang, Chu-Yun
Weng, Yi-Ching
Huang, Kuo-Lun
Liu, Chi-Hung
Chang, Ting-Yu
Wu, Hsiu-Chuan
Yen, Tzu-Chen
Lin, Kun-Ju
author_facet Huang, Chin-Chang
Hsiao, Ing-Tsung
Huang, Chu-Yun
Weng, Yi-Ching
Huang, Kuo-Lun
Liu, Chi-Hung
Chang, Ting-Yu
Wu, Hsiu-Chuan
Yen, Tzu-Chen
Lin, Kun-Ju
author_sort Huang, Chin-Chang
collection PubMed
description Background: Brain (18)F-AV-45 amyloid positron emission tomography (PET) in Taiwanese patients with familial Alzheimer's disease with the amyloid precursor protein (APP) p.D678H mutation tends to involve occipital and cerebellar cortical areas. However, tau pathology in patients with this specific Taiwan mutation remains unknown. In this study, we aimed to study the Tau PET images in these patients. Methods: Clinical features, brain magnetic resonance imaging/computed tomography (MRI/CT), and brain (18)F-THK-5351 PET were recorded in five patients with the APP p.D678H mutation and correlated with brain (18)F-AV-45 PET images. We also compared the tau deposition patterns among five patients with familial mild cognitive impairment (fMCI), six patients with sporadic amnestic mild cognitive impairment (sMCI), nine patients with mild to moderate dementia due to Alzheimer's disease (AD), and 12 healthy controls (HCs). All of the subjects also received brain (18)F-AV-45 PET. Results: The nine patients with sAD and six patients with sMCI had a positive brain AV-45 PET scans, while the 12 HCs had negative brain AV-45 PET scans. All five patients with fMCI received a tau PET scan with the age at onset ranging from 46 to 53 years, in whom increased standard uptake value ratio (SUVR) of (18)F-THK-5351 was noted in all seven brain cortical areas compared with the HCs. In addition, the SUVRs of (18)F-THK-5351 were increased in the frontal, medial parietal, lateral parietal, lateral temporal, and occipital areas (P < 0.001) in the patients with sAD compared with the HCs. The patients with fMCI had a significant higher SUVR of (18)F-THK-5351 in the cerebellar cortex compared to the patients with sMCI. The correlations between regional SUVR and Mini-Mental State Examination score and between regional SUVR and clinical dementia rating (sum box) scores within volumes of interest of Braak stage were statistically significant. Conclusion: Tau deposition was increased in the patients with fMCI compared to the HCs. Increased regional SUVR in the cerebellar cortical area was a characteristic finding in the patients with fMCI. As compared between amyloid and tau PET, the amyloid deposition is diffuse, but tau deposition is limited to the temporal lobe in the patients with fMCI.
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spelling pubmed-65389512019-06-12 Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation Huang, Chin-Chang Hsiao, Ing-Tsung Huang, Chu-Yun Weng, Yi-Ching Huang, Kuo-Lun Liu, Chi-Hung Chang, Ting-Yu Wu, Hsiu-Chuan Yen, Tzu-Chen Lin, Kun-Ju Front Neurol Neurology Background: Brain (18)F-AV-45 amyloid positron emission tomography (PET) in Taiwanese patients with familial Alzheimer's disease with the amyloid precursor protein (APP) p.D678H mutation tends to involve occipital and cerebellar cortical areas. However, tau pathology in patients with this specific Taiwan mutation remains unknown. In this study, we aimed to study the Tau PET images in these patients. Methods: Clinical features, brain magnetic resonance imaging/computed tomography (MRI/CT), and brain (18)F-THK-5351 PET were recorded in five patients with the APP p.D678H mutation and correlated with brain (18)F-AV-45 PET images. We also compared the tau deposition patterns among five patients with familial mild cognitive impairment (fMCI), six patients with sporadic amnestic mild cognitive impairment (sMCI), nine patients with mild to moderate dementia due to Alzheimer's disease (AD), and 12 healthy controls (HCs). All of the subjects also received brain (18)F-AV-45 PET. Results: The nine patients with sAD and six patients with sMCI had a positive brain AV-45 PET scans, while the 12 HCs had negative brain AV-45 PET scans. All five patients with fMCI received a tau PET scan with the age at onset ranging from 46 to 53 years, in whom increased standard uptake value ratio (SUVR) of (18)F-THK-5351 was noted in all seven brain cortical areas compared with the HCs. In addition, the SUVRs of (18)F-THK-5351 were increased in the frontal, medial parietal, lateral parietal, lateral temporal, and occipital areas (P < 0.001) in the patients with sAD compared with the HCs. The patients with fMCI had a significant higher SUVR of (18)F-THK-5351 in the cerebellar cortex compared to the patients with sMCI. The correlations between regional SUVR and Mini-Mental State Examination score and between regional SUVR and clinical dementia rating (sum box) scores within volumes of interest of Braak stage were statistically significant. Conclusion: Tau deposition was increased in the patients with fMCI compared to the HCs. Increased regional SUVR in the cerebellar cortical area was a characteristic finding in the patients with fMCI. As compared between amyloid and tau PET, the amyloid deposition is diffuse, but tau deposition is limited to the temporal lobe in the patients with fMCI. Frontiers Media S.A. 2019-05-22 /pmc/articles/PMC6538951/ /pubmed/31191427 http://dx.doi.org/10.3389/fneur.2019.00503 Text en Copyright © 2019 Huang, Hsiao, Huang, Weng, Huang, Liu, Chang, Wu, Yen and Lin. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Huang, Chin-Chang
Hsiao, Ing-Tsung
Huang, Chu-Yun
Weng, Yi-Ching
Huang, Kuo-Lun
Liu, Chi-Hung
Chang, Ting-Yu
Wu, Hsiu-Chuan
Yen, Tzu-Chen
Lin, Kun-Ju
Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation
title Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation
title_full Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation
title_fullStr Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation
title_full_unstemmed Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation
title_short Tau PET With (18)F-THK-5351 Taiwan Patients With Familial Alzheimer's Disease With the APP p.D678H Mutation
title_sort tau pet with (18)f-thk-5351 taiwan patients with familial alzheimer's disease with the app p.d678h mutation
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6538951/
https://www.ncbi.nlm.nih.gov/pubmed/31191427
http://dx.doi.org/10.3389/fneur.2019.00503
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