Estimating tau onset age from tau PET imaging in two longitudinal cohorts using sampled iterative local approximation

Understanding the time course of Alzheimer's disease biomarkers of amyloid and tau pathology and their temporal relation to clinical symptoms is key to identifying optimal windows for disease intervention and planning future drug trials. The goal of this work was to determine the extent to which Sampled Iterative Local Approximation (SILA), an algorithm extensively validated for amyloid PET, is capable of modeling longitudinal tau (T) PET trajectories and estimating person-level tau positivity onset ages in two commonly analyzed brain regions and two tracers from two different cohorts. Methods: carriers and non-carriers, as well as differences in time T+ between levels of cognitive impairment. Results: carriers (p <0.05) and those with dementia (p <0.05). Conclusions: Our results suggest SILA can be used to accurately model longitudinal tau PET trajectories and retrospectively estimate individual T+ onset ages in the meta-temporal region. The accuracy of SILA time estimates in entorhinal cortex worsened amongst those with dementia in ADNI suggesting entorhinal cortex may only be suitable for studying the temporal progression of tau during the preclinical time frame.

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Publication Details

Journal
medRxiv
Published
2026-04-03
DOI
https://doi.org/10.64898/2026.04.01.26349872
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
0.00

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article

Estimating tau onset age from tau PET imaging in two longitudinal cohorts using sampled iterative local approximation

Margo B. Heston, Tobey J. Betthauser, William Coath, Hailey Bruzzone et al.
medRxiv
Dementia and Cognitive Impairment Research
article

Estimating tau onset age from tau PET imaging in two longitudinal cohorts using sampled iterative local approximation

Margo B. Heston, Tobey J. Betthauser, William Coath, Hailey Bruzzone, Jordan P Teague
article en

Abstract

Understanding the time course of Alzheimer's disease biomarkers of amyloid and tau pathology and their temporal relation to clinical symptoms is key to identifying optimal windows for disease intervention and planning future drug trials. The goal of this work was to determine the extent to which Sampled Iterative Local Approximation (SILA), an algorithm extensively validated for amyloid PET, is capable of modeling longitudinal tau (T) PET trajectories and estimating person-level tau positivity onset ages in two commonly analyzed brain regions and two tracers from two different cohorts. Methods: carriers and non-carriers, as well as differences in time T+ between levels of cognitive impairment. Results: carriers (p <0.05) and those with dementia (p <0.05). Conclusions: Our results suggest SILA can be used to accurately model longitudinal tau PET trajectories and retrospectively estimate individual T+ onset ages in the meta-temporal region. The accuracy of SILA time estimates in entorhinal cortex worsened amongst those with dementia in ADNI suggesting entorhinal cortex may only be suitable for studying the temporal progression of tau during the preclinical time frame.

medRxiv
University of Wisconsin–Madison (US), Stanford University (US)
U.S. Department of Defense, Alzheimer's Association, Bristol-Myers Squibb, Eli Lilly and Company, Biogen, Alzheimer's Disease Neuroimaging Initiative, BioClinica, Eisai, H. Lundbeck A/S, IXICO, National Institutes of Health, Genentech, National Institute on Aging
Good health and well-being
Openalex Percentile: Top 32%
Dementia and Cognitive Impairment Research
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