TY - JOUR T1 - <sup>18</sup>F-THK5351: A Novel PET Radiotracer for Imaging Neurofibrillary Pathology in Alzheimer Disease JF - Journal of Nuclear Medicine JO - J Nucl Med SP - 208 LP - 214 DO - 10.2967/jnumed.115.164848 VL - 57 IS - 2 AU - Ryuichi Harada AU - Nobuyuki Okamura AU - Shozo Furumoto AU - Katsutoshi Furukawa AU - Aiko Ishiki AU - Naoki Tomita AU - Tetsuro Tago AU - Kotaro Hiraoka AU - Shoichi Watanuki AU - Miho Shidahara AU - Masayasu Miyake AU - Yoichi Ishikawa AU - Rin Matsuda AU - Akie Inami AU - Takeo Yoshikawa AU - Yoshihito Funaki AU - Ren Iwata AU - Manabu Tashiro AU - Kazuhiko Yanai AU - Hiroyuki Arai AU - Yukitsuka Kudo Y1 - 2016/02/01 UR - http://jnm.snmjournals.org/content/57/2/208.abstract N2 - Imaging of neurofibrillary pathology in the brain helps in diagnosing dementia, tracking disease progression, and evaluating the therapeutic efficacy of antidementia drugs. The radiotracers used in this imaging must be highly sensitive and specific for tau protein fibrils in the human brain. We developed a novel tau PET tracer, 18F-THK5351, through compound optimization of arylquinoline derivatives. Methods: The in vitro binding properties, pharmacokinetics, and safety of 18F-THK5351 were investigated, and a clinical study on Alzheimer disease (AD) patients was performed. Results: 18F-THK5351 demonstrated higher binding affinity for hippocampal homogenates from AD brains and faster dissociation from white-matter tissue than did 18F-THK5117. The THK5351 binding amount correlated with the amount of tau deposits in human brain samples. Autoradiography of brain sections revealed that THK5351 bound to neurofibrillary tangles selectively and with a higher signal-to-background ratio than did THK5117. THK5351 exhibited favorable pharmacokinetics and no defluorination in mice. In first-in-human PET studies in AD patients, 18F-THK5351 demonstrated faster kinetics, higher contrast, and lower retention in subcortical white matter than18F-THK5117. Conclusion: 18F-THK5351 is a useful PET tracer for the early detection of neurofibrillary pathology in AD patients. ER -