TY - JOUR
T1 - Advances in the development of tau PET radiotracers and their clinical applications
AU - Okamura, Nobuyuki
AU - Harada, Ryuichi
AU - Furukawa, Katsutoshi
AU - Furumoto, Shozo
AU - Tago, Tetsuro
AU - Yanai, Kazuhiko
AU - Arai, Hiroyuki
AU - Kudo, Yukitsuka
N1 - Funding Information:
N. Okamura, S. Furumoto, and Y. Kudo were funded by grants to study tau PET imaging from GE Healthcare, the SEI (Sumitomo Electric Industries, Ltd.) Group , and the CSR Foundation . They were also funded by the Health and Labor Sciences research grants from the Ministry of Health , Labor, and Welfare of Japan , and a Grant-in-Aid for Scientific Research (B) ( 15H04900 ) and a Grant-in-Aid for Scientific Research on Innovative Areas ( 26117003 ) from the Ministry of Education, Culture, Sports, Science and Technology (MEXT) , Japan.
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/9/1
Y1 - 2016/9/1
N2 - Alzheimer's disease and other neurodegenerative dementias belong to the family of tauopathies. These diseases are characterized by the deposition of insoluble tau aggregates possessing an enriched β-sheet structure. In vivo imaging of the tau deposits by positron emission tomography (PET) will facilitate the early and accurate diagnosis of these diseases, tracking of disease progression, assessment of disease severity, and prediction of disease prognosis. Furthermore, this technology is expected to play a vital role in the monitoring of treatment outcomes and in the selection of patients for the therapeutic trials of anti-dementia drugs. Recently, several tau PET tracers have been successfully developed and demonstrated as having high binding affinity and selectivity to tau protein deposits. Recent clinical studies using these tracers have demonstrated significant tracer retention in sites susceptible to tau deposition in Alzheimer's disease, as well as correlations with the disease severity and cognitive impairment in cases with dementia. These tracers, thus, have the potential to effectively diagnose the tauopathies. Further longitudinal assessment will clarify the effect of the tau deposition on the neurodegenerative process and cognitive decline and the interaction of tau with amyloid-β in the human brain.
AB - Alzheimer's disease and other neurodegenerative dementias belong to the family of tauopathies. These diseases are characterized by the deposition of insoluble tau aggregates possessing an enriched β-sheet structure. In vivo imaging of the tau deposits by positron emission tomography (PET) will facilitate the early and accurate diagnosis of these diseases, tracking of disease progression, assessment of disease severity, and prediction of disease prognosis. Furthermore, this technology is expected to play a vital role in the monitoring of treatment outcomes and in the selection of patients for the therapeutic trials of anti-dementia drugs. Recently, several tau PET tracers have been successfully developed and demonstrated as having high binding affinity and selectivity to tau protein deposits. Recent clinical studies using these tracers have demonstrated significant tracer retention in sites susceptible to tau deposition in Alzheimer's disease, as well as correlations with the disease severity and cognitive impairment in cases with dementia. These tracers, thus, have the potential to effectively diagnose the tauopathies. Further longitudinal assessment will clarify the effect of the tau deposition on the neurodegenerative process and cognitive decline and the interaction of tau with amyloid-β in the human brain.
KW - Alzheimer's disease
KW - Neurofibrillary tangles
KW - Neuroimaging
KW - Positron emission tomography
KW - Tau proteins
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U2 - 10.1016/j.arr.2015.12.010
DO - 10.1016/j.arr.2015.12.010
M3 - Review article
C2 - 26802556
AN - SCOPUS:84962052516
SN - 1568-1637
VL - 30
SP - 107
EP - 113
JO - Ageing Research Reviews
JF - Ageing Research Reviews
ER -