MRI-based Deep Learning Assessment of Amyloid, Tau, and Neurodegeneration Biomarker Status across the Alzheimer

Christopher O Lew1, Longfei Zhou1, Maciej A Mazurowski1

  • 1From the Department of Radiology, Division of Neuroradiology, Alzheimer Disease Imaging Research Laboratory (C.O.L., J.R.P.), and Neurocognitive Disorders Program, Departments of Psychiatry and Medicine (P.M.D.), Duke University Medical Center, DUMC-Box 3808, Durham, NC 27710-3808; and Duke Institute for Brain Sciences (P.M.D.) and Department of Electrical and Computer Engineering, Department of Computer Science, Department of Biostatistics and Bioinformatics (L.Z., M.A.M.), Duke University, Durham, NC.

Radiology
|October 10, 2023
PubMed

Insights

Deep learning models can predict Alzheimer's disease biomarkers using MRI scans and patient data, offering a non-invasive alternative to PET scans. This approach aids in amyloid, tau, and neurodegeneration classification.

Area of Science:

  • Neuroimaging and Artificial Intelligence
  • Biomarker Discovery for Alzheimer's Disease

Background:

  • Positron Emission Tomography (PET) is crucial for Alzheimer's disease (AD) amyloid-tau-neurodegeneration (ATN) classification but is costly and involves radiation.
  • Magnetic Resonance Imaging (MRI) has limited current utility in characterizing ATN status.
  • Deep learning (DL) excels at identifying complex patterns in MRI, offering potential for noninvasive ATN assessment.

Purpose of the Study:

  • To develop and validate a DL algorithm for predicting PET-determined ATN biomarker status.
  • To utilize MRI and routinely available diagnostic data for noninvasive ATN classification.

Main Methods:

  • Retrospective analysis of MRI and PET data from the Alzheimer's Disease Imaging Initiative.
  • A convolutional neural network (CNN) processed MRI data to extract imaging features.
  • Features were integrated with demographics, APOE status, cognitive scores, hippocampal volumes, and clinical diagnoses in a logistic regression model for ATN classification.

Main Results:

  • The DL model achieved AUCs of 0.79 for amyloid, 0.73 for tau, and 0.86 for neurodegeneration in the test set.
  • Key brain regions identified by the model included temporal, parietal, frontal, and occipital cortices.
  • Cognitive scores, hippocampal volumes, and APOE status were the most influential predictors.

Conclusions:

  • A DL algorithm effectively predicts individual ATN biomarker components using MRI and standard diagnostic data.
  • This approach shows promise for noninvasive and accessible ATN status classification in Alzheimer's disease.