Accelerated Microstructure Quantification by Q-Space Trajectory Imaging Using Machine Learning
Motivation: Tensor-encoded diffusion MRI (dMRI) methods for tissue microstructure elucidation typically require lengthy dMRI acquisitions and computationally costly, SNR-sensitive data analysis. Goal(s): Employing q-space trajectory imaging (QTI), we seek to greatly reduce both the number of required measurements and computational burden in analysis for robust estimation of parameters quantifying brain tissue microstructure. Approach: A machine learning-based estimator is trained on a 10-fold reduced subset of an extensive dMRI protocol acquired in 18 healthy volunteers. Results: The proposed method outperforms a state-of-the-art model fitting framework, yielding smoother parameter maps and showing lower deviation from the chosen ground truth, even at reduced SNR/increased resolution. Impact: Quantitative measures of brain microstructure are obtained by accelerated tensor-encoded diffusion MRI, employing a voxel-wise regression neural network. Observed resilience at reduced voxel size (1.7mm)3 appears promising regarding measurement of parameters such as microscopic fractional anisotropy in a clinical setting.
Authors
- Maximilian Rokuss (ORCID: https://orcid.org/0009-0004-4560-0760)
- Jan Martin (ORCID: https://orcid.org/0000-0002-7896-805X)
- Frederik Bernd Laun (ORCID: https://orcid.org/0000-0002-9269-5609)
- Julian Rauch
- Mark E. Ladd (ORCID: https://orcid.org/0000-0002-4128-9440)
- Tristan Anselm Kuder (ORCID: https://orcid.org/0000-0001-6439-8124)
- Peter Neher (ORCID: https://orcid.org/0000-0002-5285-7554)
- Oliver Goedicke
Publication Details
- Journal
- Proceedings 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 Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/3464
- Primary Topic
- Advanced X-ray and CT Imaging
- Type
- article
- Field-Weighted Citation Impact
- 0.00