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September 17, 2025Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition0 citations

Prediction of amyloid positivity based on white matter structural integrity in non-demented individuals using 3D CNN

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PGPavithran Pattiam GiriprakashZYZhengshi YangDCDietmar Cordes

Key Points

  • White matter microstructure predicts amyloid burden with a mean validation AUC of 0.7.
  • The study uses deep learning techniques to analyze spatial and temporal features of white matter.
  • The goal is early detection of amyloid burden in non-demented individuals to improve clinical outcomes.
  • Findings indicate that diffusion MRI can help stratify patients at high risk for developing Alzheimer's disease.

Abstract

Motivation: There exists a nonmonotonic relationship between water molecule diffusion in white matter and cerebral amyloid deposition. Goal(s): The primary goal of this study is to use deep learning to simultaneously learn spatial and temporal features of white matter microstructure for prediction of amyloid positivity. Approach: (2+1)D convolutional neural networks (CNNs) with different pooling layers are used to learn independent spatiotemporal features from various aspects of diffusion (free water fraction, neurite density index and orientation dispersion). Collective information from these features are then utilized for amyloid positivity prediction. Results: White matter microstructure predicts amyloid burden with a mean validation AUC of 0.7. Impact: Early detection of elevated amyloid burden in non-demented patients using diffusion MRI can stratify patients with a high risk of developing Alzheimer's disease. It could potentially serve a prognostic biomarker for recommending early clinical intervention.

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Cite This Study

Giriprakash et al. (2025) studied this question.

synapsesocial.com/papers/68d45b0b31b076d99fa5d17fhttps://doi.org/10.58530/2025/3902
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