Deep learning-based prediction of regional brain Tau PET burden from MRI.
4 affiliations
- 1Department of Radiology, Stanford University, Stanford, California, USA.
- 2Department of Radiology, Washington University in St. Louis, St. Louis, Missouri, USA.
- 3Department of Neurology and Neurological Sciences, Stanford University, Stanford, California, USA.
- 4Department of Epidemiology and Population Health, Stanford University, Stanford, California, USA.
Abstract
Introduction
Regional tau is strongly associated with Alzheimer's disease (AD) symptoms, but tau positron emission tomography (PET) is not routinely available, limiting early risk stratification.Methods
We trained a deep learning model to predict regional tau PET standardized uptake value ratios (SUVRs) from magnetic resonance imaging (MRI) with and without basic demographics using public cohorts (Alzheimer's Disease Neuroimaging Initiative [ADNI], Open Access Series of Imaging Studies 3 [OASIS3-tau], Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease Study [A4], Harvard Aging Brain Study [HABS]). Mean absolute error (MAE), Pearson r, area-under-the-receiver-operating-curve (AUC), and comparison with cognitive testing were assessed in external test sets (SCAN, Stanford University).Results
The model achieved an MAE of 0.14 (95% confidence interval [CI]: 0.12-0.16) and r = 0.72 for an early uptake region (Braak I-IV), and an MAE of 0.14 (95% CI: 0.12-0.17) and r = 0.71 for a late uptake region (Braak V-VI). AUCs for binary tau positivity in these regions were 0.87 (95% CI: 0.83-0.90) and 0.88 (95% CI: 0.84-0.91), respectively.Discussion
Predicting regional tau burden from magnetic resonance imaging (MRI) is feasible and may enable scalable tau-informed clinical AD care.
Related
- Quantitative MRI Characterization of Fluid-Related Phenotypes in Pediatric Epilepsy: Deep Learning-Assisted Assessment of Enlarged Perivascular Space Burden, Regional Distribution, and Clinical Associations
- Brain Amyloid Burden Mapping Using MR Fingerprinting Aided by Deep Learning
- A method for brain tumor detection and localization by means of deep learning and reliable prediction explainability
- Regional brain morphometric correlates of CT-defined metabolic dysfunction-associated steatotic liver disease and hepatic fat burden.
- Regional tau burden tracks with lower microglial HLA class II transcription in the human brain
BibTeX
@article{kim2026deep,
title = {{Deep learning-based prediction of regional brain Tau PET burden from MRI.}},
author = {Donghoon Kim and Brandon C Ho and Henk van Voorst and Yongkai Liu and Tammie L S Benzinger and Sharon Sha and Elizabeth Mormino and Victor W Henderson and Greg Zaharchuk},
journal = {Alzheimer's \& dementia : the journal of the Alzheimer's Association},
year = {2026},
month = oct,
doi = {10.1002/alz.71911},
url = {https://europepmc.org/article/MED/42963328},
note = {CC BY-NC-ND},
}
RIS
TY - JOUR
TI - Deep learning-based prediction of regional brain Tau PET burden from MRI.
AU - Donghoon Kim
AU - Brandon C Ho
AU - Henk van Voorst
AU - Yongkai Liu
AU - Tammie L S Benzinger
AU - Sharon Sha
AU - Elizabeth Mormino
AU - Victor W Henderson
AU - Greg Zaharchuk
PY - 2026
DA - 2026/10/01
JO - Alzheimer's & dementia : the journal of the Alzheimer's Association
DO - 10.1002/alz.71911
UR - https://europepmc.org/article/MED/42963328
AB - Introduction Regional tau is strongly associated with Alzheimer's disease (AD) symptoms, but tau positron emission tomography (PET) is not routinely available, limiting early risk stratification.Methods We trained a deep learning model to predict regional tau PET standardized uptake value ratios (SUVRs) from magnetic resonance imaging (MRI) with and without basic demographics using public cohorts (Alzheimer's Disease Neuroimaging Initiative [ADNI], Open Access Series of Imaging Studies 3 [OASIS3-tau], Anti-Amyloid Treatment in Asymptomatic Alzheimer's Disease Study [A4], Harvard Aging Brain Study [HABS]). Mean absolute error (MAE), Pearson r, area-under-the-receiver-operating-curve (AUC), and comparison with cognitive testing were assessed in external test sets (SCAN, Stanford University).Results The model achieved an MAE of 0.14 (95% confidence interval [CI]: 0.12-0.16) and r = 0.72 for an early uptake region (Braak I-IV), and an MAE of 0.14 (95% CI: 0.12-0.17) and r = 0.71 for a late uptake region (Braak V-VI). AUCs for binary tau positivity in these regions were 0.87 (95% CI: 0.83-0.90) and 0.88 (95% CI: 0.84-0.91), respectively.Discussion Predicting regional tau burden from magnetic resonance imaging (MRI) is feasible and may enable scalable tau-informed clinical AD care.
SN - 1552-5260
SN - 1552-5279
ER -