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Solving a Nonlinear Blind Inverse Problem for Tagged MRI with Physics and Deep Generative Priors

Zhangxing Bian, Shuwen Wei, Samuel W. Remedios, Junyu Chen, Aaron Carass, Blake E. Dewey, Jerry L. Prince

TL;DR

This work introduces a blind and nonlinear inverse framework for tagged MRI that unifies these tasks: anatomical image recovery, high-resolution cine image synthesis, and motion estimation, and demonstrates that the approach yields high-resolution anatomy images, cine images, and more accurate motion than specialized methods.

Abstract

Tagged MRI enables tracking internal tissue motion non-invasively. It encodes motion by modulating anatomy with periodic tags, which deform along with tissue. However, the entanglement between anatomy, tags and motion poses significant challenges for post-processing. The existence of tags and imaging blur hinders downstream tasks such as segmenting anatomy. Tag fading, due to T1-relaxation, disrupts the brightness constancy assumption for motion tracking. For decades, these challenges have been handled in isolation and sub-optimally. In contrast, we introduce a blind and nonlinear inverse framework for tagged MRI that, for the first time, unifies these tasks: anatomical image recovery, high-resolution cine image synthesis, and motion estimation. At its core, the synergy of MR physics and generative priors enables us to blindly estimate the unknown forward imaging models and high-resolution underlying anatomy, while simultaneously tracking 3D diffeomorphic Lagrangian motion over time. Experiments on tagged brain MRI demonstrate that our approach yields high-resolution anatomy images, cine images, and more accurate motion than specialized methods.

Solving a Nonlinear Blind Inverse Problem for Tagged MRI with Physics and Deep Generative Priors

TL;DR

This work introduces a blind and nonlinear inverse framework for tagged MRI that unifies these tasks: anatomical image recovery, high-resolution cine image synthesis, and motion estimation, and demonstrates that the approach yields high-resolution anatomy images, cine images, and more accurate motion than specialized methods.

Abstract

Tagged MRI enables tracking internal tissue motion non-invasively. It encodes motion by modulating anatomy with periodic tags, which deform along with tissue. However, the entanglement between anatomy, tags and motion poses significant challenges for post-processing. The existence of tags and imaging blur hinders downstream tasks such as segmenting anatomy. Tag fading, due to T1-relaxation, disrupts the brightness constancy assumption for motion tracking. For decades, these challenges have been handled in isolation and sub-optimally. In contrast, we introduce a blind and nonlinear inverse framework for tagged MRI that, for the first time, unifies these tasks: anatomical image recovery, high-resolution cine image synthesis, and motion estimation. At its core, the synergy of MR physics and generative priors enables us to blindly estimate the unknown forward imaging models and high-resolution underlying anatomy, while simultaneously tracking 3D diffeomorphic Lagrangian motion over time. Experiments on tagged brain MRI demonstrate that our approach yields high-resolution anatomy images, cine images, and more accurate motion than specialized methods.
Paper Structure (42 sections, 18 equations, 7 figures, 5 tables, 1 algorithm)

This paper contains 42 sections, 18 equations, 7 figures, 5 tables, 1 algorithm.

Figures (7)

  • Figure 1: We address a nonlinear blind inverse problem: given a time series of 3D tagged MRI volumes, we jointly estimate the imaging point spread functions responsible for image blurring, a sequence of high-resolution cine images, and the underlying motion fields. No additional training data are required.
  • Figure 2: Qualitative comparison of tag-to-cine synthesis. For two subjects, we show early ($t{=}1$) and late ($t{=}6$) frames. Left-most column shows input tagged MRI (other views and orientations are omitted) while right-most shows ground-truth cine. Fourier spectrum of input and ours are shown. Orange arrows indicate the faded and smeared harmonic peaks. Red arrows indicate the aliasing artifact.
  • Figure 3: Results of estimated point spread functions (PSFs) under different blurring settings and noise levels.
  • Figure 4: Motion magnitude comparison across methods. Cols. 1-2: input tagged MRI at two time points. Last column: ground-truth motion magnitude. Both sagittal and coronal views are shown.
  • Figure 5: Real tagged MRI: gel cylinder.
  • ...and 2 more figures