Correlations of 18F-THK5351 PET with Postmortem Burden of Tau and Astrogliosis in Alzheimer Disease
Open accessAbstract
Clinical PET studies using 18F-THK5351 have demonstrated significant tracer retention in sites susceptible to tau burden in Alzheimer disease (AD). However, the in vivo PET signal to reflect tau aggregates remains controversial. Methods: We examined the spatial pattern of tracer binding, amyloid-β, tau, and gliosis in an autopsy-confirmed AD patient who underwent 18F-THK5351 and 11C-Pittsburgh compound B PET before death. Results: Regional in vivo 18F-THK5351 retention was significantly correlated with the density of tau aggregates in the neocortex and monoamine oxidase-B in the whole brain, but not correlated with that of insoluble amyloid-β. Furthermore, significant association was observed between the density of tau aggregates, monoamine oxidase-B, and glial fibrillary acidic protein, suggesting that neocortical tau would strongly influence the formation of reactive astrocytes. Conclusion:18F-THK5351 PET may have limited utility as a biomarker of tau pathology in AD; however, it could be used to monitor the neuroinflammatory processes in the living brain.
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THK is known to trace not only neurofibrillary tangles but a combination of neurofibrillary tangles and astrocytosis.
“THK is known to trace not only neurofibrillary tangles but a combination of neurofibrillary tangles and astrocytosis (Ng et al., 2017; Harada et al., 2018).”
From Effects of Alzheimer’s and Vascular Pathologies on Structural Connectivity in Early- and Late-Onset Alzheimer’s Disease (2021) · cites this paper as Harada et al., 2018
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Cites
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Reactive Glia not only Associates with Plaques but also Parallels Tangles in Alzheimer’s Disease
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- Authors
- Harada, R., Ishiki, A., Kai, H., Sato, N., Furukawa, K., Furumoto, S., Tago, T., Tomita, N., Watanuki, S., Hiraoka, K., Ishikawa, Y., Funaki, Y., Nakamura, T., Yoshikawa, T., Iwata, R., Tashiro, M., Sasano, H., Kitamoto, T., Yanai, K., Arai, H., Kudo, Y., & Okamura, N.
- Affiliations
- Tohoku University (JP)
- Tokyo Metropolitan Institute of Gerontology (JP)
- Tohoku Medical and Pharmaceutical University (JP)
- ORCID
- Venue
- Journal of Nuclear Medicine
- Publisher
- Society of Nuclear Medicine
- Published
- 2017-09-01
- Volume
- 59
- Issue
- 4
- Pages
- 671-674
- ISSN
- 0161-5505 (ISSN-L)
- 2159-662X
- OpenAlex
- W2750990748
- Cited by
- 168
- References
- 5
- Citations by year
- 2026: 9 · 2025: 8 · 2024: 12 · 2023: 20 · 2022: 14 · 2021: 20 · 2020: 35 · 2019: 24 · 2018: 24 · 2017: 2
- FWCI
- 17.21
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Nuclear Medicine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Japan Society for the Promotion of Science (15K08127, 16H07486, 16H05383, 26253016)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Medical Imaging Techniques and Applications
- Keywords
- 18F-THK5351, tau PET imaging, Alzheimer's disease, tau pathology, astrocyte activation, reactive astrocytes, amyloid-beta, monoamine oxidase B, glial fibrillary acidic protein, neuroinflammation, biomarkers, neocortex
- MeSH terms
- Aged, 80 and over, Alzheimer Disease, Aminopyridines, Gliosis, Humans, Male, Postmortem Changes, Quinolines, tau Proteins, Positron-Emission Tomography
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