In vivo PET classification of tau pathologies in patients with frontotemporal dementia

被引:6
作者
Kubota, Manabu [1 ,2 ,9 ]
Endo, Hironobu [1 ]
Takahata, Keisuke [1 ,3 ]
Tagai, Kenji [1 ,4 ]
Suzuki, Hisaomi [1 ,5 ]
Onaya, Mitsumoto [5 ]
Sano, Yasunori [1 ,3 ]
Yamamoto, Yasuharu [1 ,3 ]
Kurose, Shin [1 ,3 ]
Matsuoka, Kiwamu [1 ,6 ]
Seki, Chie [1 ]
Shinotoh, Hitoshi [1 ]
Kawamura, Kazunori [7 ]
Zhang, Ming-Rong [7 ]
Takado, Yuhei [1 ]
Shimada, Hitoshi [1 ,8 ]
Higuchi, Makoto [1 ]
机构
[1] Natl Inst Quantum Sci & Technol, Inst Quantum Med Sci, Dept Funct Brain Imaging, Quantum Life & Med Sci Directorate, Chiba 2638555, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Psychiat, Sakyo Ku, Kyoto 6068507, Japan
[3] Keio Univ, Sch Med, Dept Neuropsychiat, Tokyo 1608582, Japan
[4] Jikei Univ, Grad Sch Med, Dept Psychiat, Tokyo 1058461, Japan
[5] Shimofusa Psychiat Ctr, Chiba 2660007, Japan
[6] Nara Med Univ, Dept Psychiat, Nara 6348521, Japan
[7] Natl Inst Quantum Sci & Technol, Inst Quantum Med Sci, Dept Adv Nucl Med Sci, Quantum Life & Med Sci Directorate, Chiba 2638555, Japan
[8] Niigata Univ, Brain Res Inst, Ctr Integrated Human Brain Sci, Dept Funct Neurol & Neurosurg, Niigata 9518585, Japan
[9] Natl Inst Quantum Sci & Technol, Inst Quantum Med Sci, Dept Funct Brain Imaging, Quantum Life & Med Sci Directorate, Inage Ku, Chiba, Chiba 2638555, Japan
基金
日本学术振兴会;
关键词
frontotemporal lobar degeneration; PET; florzolotau; biomarker; tauopathy; PROGRESSIVE SUPRANUCLEAR PALSY; ALZHEIMERS-DISEASE; BEHAVIORAL VARIANT; LOBAR DEGENERATION; MOUSE MODEL; SEGMENTATION; VARIABILITY; DIAGNOSIS; ATROPHY;
D O I
10.1093/braincomms/fcae075
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Frontotemporal dementia refers to a group of neurodegenerative disorders with diverse clinical and neuropathological features. In vivo neuropathological assessments of frontotemporal dementia at an individual level have hitherto not been successful. In this study, we aim to classify patients with frontotemporal dementia based on topologies of tau protein aggregates captured by PET with 18F-florzolotau (aka 18F-APN-1607 and 18F-PM-PBB3), which allows high-contrast imaging of diverse tau fibrils in Alzheimer's disease as well as in non-Alzheimer's disease tauopathies. Twenty-six patients with frontotemporal dementia, 15 with behavioural variant frontotemporal dementia and 11 with other frontotemporal dementia phenotypes, and 20 age- and sex-matched healthy controls were included in this study. They underwent PET imaging of amyloid and tau depositions with 11C-PiB and 18F-florzolotau, respectively. By combining visual and quantitative analyses of PET images, the patients with behavioural variant frontotemporal dementia were classified into the following subgroups: (i) predominant tau accumulations in frontotemporal and frontolimbic cortices resembling three-repeat tauopathies (n = 3), (ii) predominant tau accumulations in posterior cortical and subcortical structures indicative of four-repeat tauopathies (n = 4); (iii) amyloid and tau accumulations consistent with Alzheimer's disease (n = 4); and (iv) no overt amyloid and tau pathologies (n = 4). Despite these distinctions, clinical symptoms and localizations of brain atrophy did not significantly differ among the identified behavioural variant frontotemporal dementia subgroups. The patients with other frontotemporal dementia phenotypes were also classified into similar subgroups. The results suggest that PET with 18F-florzolotau potentially allows the classification of each individual with frontotemporal dementia on a neuropathological basis, which might not be possible by symptomatic and volumetric assessments. Kubota et al. performed PET imaging with 18F-florzolotau in patients with frontotemporal dementia and categorized them into subgroups based on PET-assessed tau topologies. The proposed method may allow neuropathology-based classification of living individuals with this illness, which may not be feasible based on clinical symptoms and brain structural features. Graphical Abstract
引用
收藏
页数:15
相关论文
共 51 条
[1]   Autoradiography validation of novel tau PET tracer [F-18]-MK-6240 on human postmortem brain tissue [J].
Aguero, Cinthya ;
Dhaynaut, Maeva ;
Normandin, Marc D. ;
Amaral, Ana C. ;
Guehl, Nicolas J. ;
Neelamegam, Ramesh ;
Marquie, Marta ;
Johnson, Keith A. ;
El Fakhri, Georges ;
Frosch, Matthew P. ;
Gomez-Isla, Teresa .
ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2019, 7 (1) :37
[2]   Validation of the new consensus criteria for the diagnosis of corticobasal degeneration [J].
Alexander, S. K. ;
Rittman, T. ;
Xuereb, J. H. ;
Bak, T. H. ;
Hodges, J. R. ;
Rowe, J. B. .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2014, 85 (08) :923-927
[3]   STAGING OF ALZHEIMERS-DISEASE-RELATED NEUROFIBRILLARY CHANGES [J].
BRAAK, H ;
BRAAK, E .
NEUROBIOLOGY OF AGING, 1995, 16 (03) :271-278
[4]   Assessment of 18F-PI-2620 as a Biomarker in Progressive Supranuclear Palsy [J].
Brendel, Matthias ;
Barthel, Henryk ;
van Eimeren, Thilo ;
Marek, Ken ;
Beyer, Leonie ;
Song, Mengmeng ;
Palleis, Carla ;
Gehmeyr, Mona ;
Fietzek, Urban ;
Respondek, Gesine ;
Sauerbeck, Julia ;
Nitschmann, Alexander ;
Zach, Christian ;
Hammes, Jochen ;
Barbe, Michael T. ;
Onur, Oezguer ;
Jessen, Frank ;
Saur, Dorothee ;
Schroeter, Matthias L. ;
Rumpf, Jost-Julian ;
Rullmann, Michael ;
Schildan, Andreas ;
Patt, Marianne ;
Neumaier, Bernd ;
Barret, Olivier ;
Madonia, Jennifer ;
Russell, David S. ;
Stephens, Andrew ;
Roeber, Sigrun ;
Herms, Jochen ;
Boetzel, Kai ;
Classen, Joseph ;
Bartenstein, Peter ;
Villemagne, Victor ;
Levin, Johannes ;
Hoeglinger, Guenter U. ;
Drzezga, Alexander ;
Seibyl, John ;
Sabri, Osama .
JAMA NEUROLOGY, 2020, 77 (11) :1408-1419
[5]   Digital Histological Study of Neocortical Grey and White Matter Tau Burden Across Tauopathies [J].
Coughlin, David G. ;
Hiniker, Annie ;
Peterson, Claire ;
Kim, Yongya ;
Arezoumandan, Sanaz ;
Giannini, Lucia ;
Pizzo, Donald ;
Weintraub, Daniel ;
Siderowf, Andrew ;
Litvan, Irene ;
Rissman, Robert A. ;
Galasko, Douglas ;
Hansen, Lawrence ;
Trojanowski, John Q. ;
Lee, Edward ;
Grossman, Murray ;
Irwin, David .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2022, 81 (12) :953-964
[6]   Neuropathology of Frontotemporal Lobar Degeneration-Tau (FTLD-Tau) [J].
Dickson, Dennis W. ;
Kouri, Naomi ;
Murray, Melissa E. ;
Josephs, Keith A. .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2011, 45 (03) :384-389
[7]   A Machine Learning-Based Approach to Discrimination of Tauopathies Using [18F]PM-PBB3 PET Images [J].
Endo, Hironobu ;
Tagai, Kenji ;
Ono, Maiko ;
Ikoma, Yoko ;
Oyama, Asaka ;
Matsuoka, Kiwamu ;
Kokubo, Naomi ;
Hirata, Kosei ;
Sano, Yasunori ;
Oya, Masaki ;
Matsumoto, Hideki ;
Kurose, Shin ;
Seki, Chie ;
Shimizu, Hiroshi ;
Kakita, Akiyoshi ;
Takahata, Keisuke ;
Shinotoh, Hitoshi ;
Shimada, Hitoshi ;
Tokuda, Takahiko ;
Kawamura, Kazunori ;
Zhang, Ming-Rong ;
Oishi, Kenichi ;
Mori, Susumu ;
Takado, Yuhei ;
Higuchi, Makoto .
MOVEMENT DISORDERS, 2022, 37 (11) :2236-2246
[8]   In vivo binding of a tau imaging probe, [11C]PBB3, in patients with progressive supranuclear palsy [J].
Endo, Hironobu ;
Shimada, Hitoshi ;
Sahara, Naruhiko ;
Ono, Maiko ;
Koga, Shunsuke ;
Kitamura, Soichiro ;
Niwa, Fumitoshi ;
Hirano, Shigeki ;
Kimura, Yasuyuki ;
Ichise, Masanori ;
Shinotoh, Hitoshi ;
Zhang, Ming Rong ;
Kuwabara, Satoshi ;
Dickson, Dennis W. ;
Toda, Tatsushi ;
Suhara, Tetsuya ;
Higuchi, Makoto .
MOVEMENT DISORDERS, 2019, 34 (05) :744-754
[9]   Bayesian segmentation of brainstem structures in MRI [J].
Eugenio Iglesias, Juan ;
Van Leemput, Koen ;
Bhatt, Priyanka ;
Casillas, Christen ;
Dutt, Shubir ;
Schuff, Norbert ;
Truran-Sacrey, Diana ;
Boxer, Adam ;
Fischl, Bruce .
NEUROIMAGE, 2015, 113 :184-195
[10]   Whole brain segmentation: Automated labeling of neuroanatomical structures in the human brain [J].
Fischl, B ;
Salat, DH ;
Busa, E ;
Albert, M ;
Dieterich, M ;
Haselgrove, C ;
van der Kouwe, A ;
Killiany, R ;
Kennedy, D ;
Klaveness, S ;
Montillo, A ;
Makris, N ;
Rosen, B ;
Dale, AM .
NEURON, 2002, 33 (03) :341-355