Spatiotemporal Tau Accumulation and its Clinical Impact on Progressive Supranuclear Palsy: Longitudinal Florzolotau ( 18F ) Positron Emission T omography

BACKGROUND: Florzolotau (18F) positron emission tomography (florzolotau PET) enables high-contrast in vivo detection of four-repeat tau pathology in progressive supranuclear palsy (PSP), but whether longitudinal tau imaging reflects disease progression remains unclear. OBJECTIVES: To explore longitudinal tau accumulation using florzolotau PET and evaluate its association with clinical progression in PSP. METHODS: Twenty-six patients with PSP (18 Richardson's syndrome [PSP-RS], 8 non-RS) and 10 age- and sex-matched healthy controls (HCs) underwent florzolotau PET, magnetic resonance imaging, and clinical assessments at baseline and after 1 year. Regional standardized uptake value ratios (SUVRs) were extracted across 57 regions of interest. Partial least squares (PLS) multivariate analyses revealed regions with elevated baseline SUVR and longitudinal increase (ΔSUVR) in PSP relative to HCs, alongside regions where ΔSUVR was associated with changes in PSP Rating Scale scores. RESULTS: At baseline, tau deposition was most prominent in the globus pallidus (GP) and midbrain in patients with PSP. Longitudinal tau increases were observed in the GP, frontoparietal cortex, and cerebellar white matter, and minimal progression was observed in the midbrain. GP tau accumulation exhibited the strongest association with clinical progression in the PLS model among PSP-RS and a univariate correlation (Spearman's ρ = 0.688, P = 0.002). CONCLUSIONS: This study provides in vivo evidence of the spatiotemporal progression of tau pathology in PSP. In the GP, tau accumulation emerges early and continues to increase with clinical deterioration. These findings support the utility of florzolotau PET for monitoring disease progression and as a biological outcome measure in tau-targeted therapeutic trials. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Journal
Movement Disorders
Published
2026-09-04
DOI
https://doi.org/10.1002/mds.70468
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
0.00

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article

Spatiotemporal Tau Accumulation and its Clinical Impact on Progressive Supranuclear Palsy: Longitudinal Florzolotau ( 18F ) Positron Emission T omography

Yuki Komatsu, Makoto Higuchi, Yoshikazu Chishiki, Keisuke Takahata et al.
Movement Disorders
Parkinson's Disease Mechanisms and Treatments
article

Spatiotemporal Tau Accumulation and its Clinical Impact on Progressive Supranuclear Palsy: Longitudinal Florzolotau ( 18F ) Positron Emission T omography

Yuki Komatsu, Makoto Higuchi, Yoshikazu Chishiki, Keisuke Takahata, Shin Kurose, Ming‐Rong Zhang, Yuko Kataoka, Hironobu Endo, Asaka Oyama, Masanori Ichihashi, Ryoji Goto, Kiwamu Matsuoka, Yoshikazu Nakano, Chie Seki, Kazunori Kawamura, Shigeki Hirano, Kosei Hirata, Hitoshi Shimada, Kenji Tagai, Hitoshi Shinotoh, Hideki Matsumoto, Yasuharu Yamamoto, Tetsuji Kamada, Kenta Osawa, Tokahiko Tokuda, Hideo Kato, Sho Moriguchi, Yuki Momota
article en

Abstract

BACKGROUND: Florzolotau (18F) positron emission tomography (florzolotau PET) enables high-contrast in vivo detection of four-repeat tau pathology in progressive supranuclear palsy (PSP), but whether longitudinal tau imaging reflects disease progression remains unclear. OBJECTIVES: To explore longitudinal tau accumulation using florzolotau PET and evaluate its association with clinical progression in PSP. METHODS: Twenty-six patients with PSP (18 Richardson's syndrome [PSP-RS], 8 non-RS) and 10 age- and sex-matched healthy controls (HCs) underwent florzolotau PET, magnetic resonance imaging, and clinical assessments at baseline and after 1 year. Regional standardized uptake value ratios (SUVRs) were extracted across 57 regions of interest. Partial least squares (PLS) multivariate analyses revealed regions with elevated baseline SUVR and longitudinal increase (ΔSUVR) in PSP relative to HCs, alongside regions where ΔSUVR was associated with changes in PSP Rating Scale scores. RESULTS: At baseline, tau deposition was most prominent in the globus pallidus (GP) and midbrain in patients with PSP. Longitudinal tau increases were observed in the GP, frontoparietal cortex, and cerebellar white matter, and minimal progression was observed in the midbrain. GP tau accumulation exhibited the strongest association with clinical progression in the PLS model among PSP-RS and a univariate correlation (Spearman's ρ = 0.688, P = 0.002). CONCLUSIONS: This study provides in vivo evidence of the spatiotemporal progression of tau pathology in PSP. In the GP, tau accumulation emerges early and continues to increase with clinical deterioration. These findings support the utility of florzolotau PET for monitoring disease progression and as a biological outcome measure in tau-targeted therapeutic trials. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Movement Disorders
Tokyo Dental College (JP), Chiba University (JP), National Institutes for Quantum Science and Technology (JP), Chiba Hospital (JP), Niigata University (JP), The University of Osaka (JP)
Biogen, Japan Agency for Medical Research and Development, Keio University, Tokyo Medical and Dental University, Japan Society for the Promotion of Science, Core Research for Evolutional Science and Technology, Fusion Oriented REsearch for disruptive Science and Technology
Openalex Percentile: Top 11%
Parkinson's Disease Mechanisms and Treatments
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