# Correction of Partial Volume Effects in PET for Alzheimer's Disease Using Unsupervised Deep Learning

> **NIH NIH R21** · MASSACHUSETTS GENERAL HOSPITAL · 2020 · $452,956

## Abstract

Correction of Partial Volume Effects in PET for Alzheimer's Disease Using Unsupervised Deep
Learning
Abstract
Alzheimer's disease (AD), characterized by memory loss and cognitive impairments, affects
approximately 5.8 million people in the United States. It is a burden for patients, families and the
healthcare system. Post-mortem studies reveal that hyperphosphorylated Tau protein aggregates are
closely related with AD. With the developments of selective Tau tracers, Tau distributions can now be
characterized in vivo through Positron emission tomography (PET) imaging. According to the Braak
staging, Tau deposits start from the transentorhinal region of the temporal lobe at preclinical AD, then
spreading to other cortex regions at late stages. Regional Tau distribution pattern captured through
PET Tau imaging can thus provide important staging information, which is vital for early disease
diagnosis, progression tracking and treatment monitoring. However, accurate quantification of thin
cortex uptake is difficult due to partial volume effects (PVEs) in PET imaging. Besides, for the second-
generation Tau tracer, 18F-MK-6240, apart from higher uptakes observed in neocortical and medial
temporal brain regions for AD patients, nonspecific uptakes are also observed in areas such as the
meninges. Given the thin nature of the cortical ribbon and its close proximity to the meninges,
quantitative accuracy and detection precision of 18F-MK-6240 distributions are significantly impacted,
which in turn precludes finer localization of early tau accumulation associated with preclinical and
prodromal AD. This grant application proposes a novel partial volume correction (PVC) method through
unsupervised deep learning for Tau imaging. This new framework does not need high-quality training
labels and the network is specifically trained for each subject, with the training objective function
formulated based on the Poisson distribution assumption of the sinogram data. To further boost the
performance, the transfer learning and the kernel learning are integrated into this PVC framework. The
three specific aims of this exploratory proposal are (1) to develop a PET PVC framework based on
unsupervised deep learning, (2) to validate the proposed PVC framework using phantom studies and
(3) to apply the proposed PVC framework to 18F-MK-6240 imaging datasets. We expect that the
integrated outcome of the specific aims will be an efficient, practical and robust PVC method that can
better resolve the Tau distribution patterns for the early diagnosis of AD.

## Key facts

- **NIH application ID:** 9974892
- **Project number:** 1R21AG067422-01
- **Recipient organization:** MASSACHUSETTS GENERAL HOSPITAL
- **Principal Investigator:** Kuang Gong
- **Activity code:** R21 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2020
- **Award amount:** $452,956
- **Award type:** 1
- **Project period:** 2020-05-15 → 2023-04-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/9974892

## Citation

> US National Institutes of Health, RePORTER application 9974892, Correction of Partial Volume Effects in PET for Alzheimer's Disease Using Unsupervised Deep Learning (1R21AG067422-01). Retrieved via AI Analytics 2026-05-22 from https://api.ai-analytics.org/grant/nih/9974892. Licensed CC0.

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