Correlation between in vivo <sup>18</sup> F‐flortaucipir PET and whole‐brain postmortem histological tau signals in Alzheimer's disease

INTRODUCTION: F-flortaucipir (FTP) tau positron emission tomography (PET) signal but are limited by methods. We leveraged whole-brain, quantitative immunohistochemical (IHC) Alzheimer's Disease (AD) tau density maps to comprehensively evaluate the FTP tracer. METHODS: We generated IHC maps for three AD-tau antibodies-AT8, AT100, and MC1-using two human brains histologically staged at Braak IV and VI. FTP-PET scans were acquired 6 and 10 weeks prior to death. Using region-wise and voxelwise methods, we correlated FTP-PET with IHC signals. RESULTS: ] = 0.461, p < 0.001). FTP SUVRs failed to capture medial temporal lobe (MTL) tau burden, whereas neocortical regions showed lower IHC burden but more variability in FTP uptake. DISCUSSION: Although FTP signals correlate well with AT8-positive tau in the more advanced case, they underestimate the severity of MTL burden, potentially confounding assessments of tau-targeted therapies.

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Journal
Alzheimer s & Dementia
Published
2026-05-01
DOI
https://doi.org/10.1002/alz.71453
Primary Topic
Alzheimer's disease research and treatments
Type
article
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article

Correlation between in vivo 18 F‐flortaucipir PET and whole‐brain postmortem histological tau signals in Alzheimer's disease

Y. Chen, Yishu Chao, Lea T. Grinberg, Trevor A. Chadwick et al.
Alzheimer s & Dementia
Alzheimer's disease research and treatments
article

Correlation between in vivo 18 F‐flortaucipir PET and whole‐brain postmortem histological tau signals in Alzheimer's disease

Y. Chen, Yishu Chao, Lea T. Grinberg, Trevor A. Chadwick, Daniela Ushizima, Helmut Heinsen, William J. Jagust, Leonardo Iaccarino, Theresa M. Harrison, Duygu Tosun
article en

Abstract

INTRODUCTION: F-flortaucipir (FTP) tau positron emission tomography (PET) signal but are limited by methods. We leveraged whole-brain, quantitative immunohistochemical (IHC) Alzheimer's Disease (AD) tau density maps to comprehensively evaluate the FTP tracer. METHODS: We generated IHC maps for three AD-tau antibodies-AT8, AT100, and MC1-using two human brains histologically staged at Braak IV and VI. FTP-PET scans were acquired 6 and 10 weeks prior to death. Using region-wise and voxelwise methods, we correlated FTP-PET with IHC signals. RESULTS: ] = 0.461, p < 0.001). FTP SUVRs failed to capture medial temporal lobe (MTL) tau burden, whereas neocortical regions showed lower IHC burden but more variability in FTP uptake. DISCUSSION: Although FTP signals correlate well with AT8-positive tau in the more advanced case, they underestimate the severity of MTL burden, potentially confounding assessments of tau-targeted therapies.

Alzheimer s & DementiaVol. 22(5)
Lawrence Berkeley National Laboratory (US), Eli Lilly (United States) (US), Universidade de São Paulo (BR), University of California, San Francisco (US), University of Würzburg (DE), Jacksonville College (US), University Memory and Aging Center (US), Mayo Clinic in Florida (US), University of California, Berkeley (US)
Good health and well-being
Openalex Percentile: Top 4%
Alzheimer's disease research and treatments
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