4.4 Article

High-resolution neural network-driven mapping of multiple diffusion metrics leveraging asymmetries in the balanced steady-state free precession frequency profile

期刊

NMR IN BIOMEDICINE
卷 35, 期 6, 页码 -

出版社

WILEY
DOI: 10.1002/nbm.4669

关键词

diffusion metrics; high resolution; multiparametric quantitative MRI; neural networks; phase-cycled bSSFP; probabilistic uncertainty estimation

资金

  1. German Research Foundation
  2. Max Planck Society

向作者/读者索取更多资源

The study proposed using neural network to estimate multiple diffusion metrics, utilizing high-resolution bSSFP phase-cycling scheme as NN input and deriving low-resolution target diffusion data through SE-EPI scans. The results showed that the NN predictions were highly reliable in MD for both white matter and gray matter structures, but there was some bias in the dependence on WM anisotropy.
We propose to utilize the rich information content about microstructural tissue properties entangled in asymmetric balanced steady-state free precession (bSSFP) profiles to estimate multiple diffusion metrics simultaneously by neural network (NN) parameter quantification. A 12-point bSSFP phase-cycling scheme with high-resolution whole-brain coverage is employed at 3 and 9.4 T for NN input. Low-resolution target diffusion data are derived based on diffusion-weighted spin-echo echo-planar-imaging (SE-EPI) scans, that is, mean, axial, and radial diffusivity (MD, AD, and RD), fractional anisotropy (FA), as well as the spherical coordinates (azimuth phi and inclination circle minus) of the principal diffusion eigenvector. A feedforward NN is trained with incorporated probabilistic uncertainty estimation. The NN predictions yielded highly reliable results in white matter (WM) and gray matter structures for MD. The quantification of FA, AD, and RD was overall in good agreement with the reference but the dependence of these parameters on WM anisotropy was somewhat biased (e.g. in corpus callosum). The inclination circle minus was well predicted for anisotropic WM structures, while the azimuth phi was overall poorly predicted. The findings were highly consistent across both field strengths. Application of the optimized NN to high-resolution input data provided whole-brain maps with rich structural details. In conclusion, the proposed NN-driven approach showed potential to provide distortion-free high-resolution whole-brain maps of multiple diffusion metrics at high to ultrahigh field strengths in clinically relevant scan times.

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