Center for Molecular Imaging Technology and Translation (CMITT) Administrative Supplement #4

Information

  • Research Project
  • 10287986
  • ApplicationId
    10287986
  • Core Project Number
    P41EB022544
  • Full Project Number
    3P41EB022544-05S1
  • Serial Number
    022544
  • FOA Number
    PA-18-591
  • Sub Project Id
  • Project Start Date
    9/30/2017 - 7 years ago
  • Project End Date
    6/30/2022 - 2 years ago
  • Program Officer Name
    ATANASIJEVIC, TATJANA
  • Budget Start Date
    9/16/2021 - 3 years ago
  • Budget End Date
    6/30/2022 - 2 years ago
  • Fiscal Year
    2021
  • Support Year
    05
  • Suffix
    S1
  • Award Notice Date
    9/16/2021 - 3 years ago

Center for Molecular Imaging Technology and Translation (CMITT) Administrative Supplement #4

Abstract Alzheimer's Disease (AD) is characterized by the presence and distribution of intracellular neurofibrillary tangles tau and extracellular amyloid-?. Tau pathology is deeply associated with cognitive decline in AD in a region-specific manner. It will be highly valuable to predict how tau burden would spread in the future given a baseline tau PET measurement. Such approach can be used to predict how region-wise tau burden changes versus age and, therefore, stratify potential candidates for AD therapy based on their ?trajectory? of progression. It can also be used to determine how different a tau PET distribution is after a therapy from the predicted distribution if no therapy is applied. The recent availability of longitudinal tau PET data provides us a unique opportunity for technology development: to model tau-propagation using state-of-the-art deep learning methods. However, current available longitudinal tau PET datasets are relatively small, therefore, insufficient to train a deep neural network. To solve this problem, we propose a novel approach that incorporates a simple mathematical model in the training of the deep neural network. We first develop a simple network diffusion model that fits part of the available longitudinal tau PET data. We then generate a very large number of longitudinal tau PET datasets using the fitted model to pretrain a U-net-like autoencoder deep neural network. Finally, we further train the neural network by freezing all the parameters except those directly associated with the bottleneck layer of the neural network. This approach makes it possible to model tau propagation directly from measured longitudinal tau PET data while avoid overfitting caused by insufficient training data.

IC Name
NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING
  • Activity
    P41
  • Administering IC
    EB
  • Application Type
    3
  • Direct Cost Amount
    195815
  • Indirect Cost Amount
    133154
  • Total Cost
    328969
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    286
  • Ed Inst. Type
  • Funding ICs
    NIA:328969\
  • Funding Mechanism
    RESEARCH CENTERS
  • Study Section
    ZEB1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    MASSACHUSETTS GENERAL HOSPITAL
  • Organization Department
  • Organization DUNS
    073130411
  • Organization City
    BOSTON
  • Organization State
    MA
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    021142621
  • Organization District
    UNITED STATES