In vivo visualization of tau deposits in corticobasal syndrome by 18F-THK5351 PET

被引:90
|
作者
Kikuchi, Akio [1 ]
Okamura, Nobuyuki [2 ]
Hasegawa, Takafumi [1 ]
Harada, Ryuichi [2 ]
Watanuki, Shoichi [4 ]
Funaki, Yoshihito [5 ]
Hiraoka, Kotaro [4 ]
Baba, Toru [1 ]
Sugeno, Naoto [1 ]
Oshima, Ryuji [1 ]
Yoshida, Shun [1 ]
Kobayashi, Junpei [1 ]
Ezura, Michinori [1 ]
Kobayashi, Michiko [8 ]
Tano, Ohito [9 ]
Mugikura, Shunji [3 ]
Iwata, Ren [5 ]
Ishiki, Aiko [6 ]
Furukawa, Katsutoshi [6 ]
Arai, Hiroyuki [6 ]
Furumoto, Shozo [5 ]
Tashiro, Manabu [4 ]
Yanai, Kazuhiko [2 ]
Kudo, Yukitsuka [7 ]
Takeda, Atsushi [10 ]
Aoki, Masashi [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Dept Neurol, Sendai, Miyagi, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Pharmacol, Sendai, Miyagi, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Diagnost Radiol, Sendai, Miyagi, Japan
[4] Tohoku Univ, Ctr Cyclotron & Radioisotope, Div Cyclotron Nucl Med, Sendai, Miyagi, Japan
[5] Tohoku Univ, Ctr Cyclotron & Radioisotope, Div Radiopharmaceut Chem, Sendai, Miyagi, Japan
[6] Tohoku Univ, Inst Dev Aging & Canc, Dept Geriatr & Resp Med, Sendai, Miyagi, Japan
[7] Tohoku Univ, Inst Dev Aging & Canc, Div Neuroimaging, Sendai, Miyagi, Japan
[8] Tohoku Pharmaceut Univ Hosp, Dept Neurol, Sendai, Miyagi, Japan
[9] Sendai Med Ctr, Dept Neurol, Sendai, Miyagi, Japan
[10] Natl Hosp Org, Sendai Nishitaga Hosp, Dept Neurol, Sendai, Miyagi, Japan
关键词
PROGRESSIVE SUPRANUCLEAR PALSY; BETA-AMYLOID BURDEN; ALZHEIMERS-DISEASE; NEUROFIBRILLARY PATHOLOGY; DEGENERATION; DEMENTIA; TAUOPATHIES; DIAGNOSIS;
D O I
10.1212/WNL.0000000000003375
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine whether F-18-THK5351 PET can be used to visualize tau deposits in brain lesions in live patients with corticobasal syndrome (CBS). Methods: We evaluated the in vitro binding of H-3-THK5351 in postmortem brain tissues from a patient with corticobasal degeneration (CBD). In clinical PET studies, F-18-THK5351 retention in 5 patients with CBS was compared to that in 8 age-matched normal controls and 8 patients with Alzheimer disease (AD). Results: H-3-THK5351 was able to bind to tau deposits in the postmortem brain with CBD. In clinical PET studies, the 5 patients with CBS showed significantly higher F-18-THK5351 retention in the frontal, parietal, and globus pallidus than the 8 age-matched normal controls and patients with AD. Higher F-18-THK5351 retention was observed contralaterally to the side associated with greater cortical dysfunction and parkinsonism. Conclusions: F-18-THK5351 PET demonstrated high tracer signal in sites susceptible to tau deposition in patients with CBS. F-18-THK5351 should be considered as a promising candidate radio-tracer for the in vivo imaging of tau deposits in CBS.
引用
收藏
页码:2309 / 2316
页数:8
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