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Optimizing Sampling Patterns for Compressed Sensing MRI with Diffusion Generative Models

Sriram Ravula, Brett Levac, Yamin Arefeen, Ajil Jalal, Alexandros G. Dimakis, Jonathan I. Tamir

TL;DR

This work tackles the challenge of long MRI acquisition times by integrating diffusion-based priors into sampling pattern design. It introduces a one-step posterior mean objective that enables gradient-based learning of Cartesian k-space patterns without backpropagating through costly posterior sampling, and implements a greedy algorithm to construct informative, well-spaced sampling sets. A diffusion-model prior is used in a frozen form, with a Tweedie-extension loss that incorporates measurements to produce a tractable training signal for pattern optimization. Empirically, the approach yields higher reconstruction quality than fixed Poisson-disc or LOUPE-based baselines across multiple anatomies, contrasts, and acceleration factors, demonstrating robust gains and practical applicability in diffusion-based MRI pipelines. The method offers a flexible, non-end-to-end alternative to jointly training reconstruction and sampling, with potential extensions to pattern distributions and higher-dimensional sampling operators.

Abstract

Magnetic resonance imaging (MRI) is a powerful medical imaging modality, but long acquisition times limit throughput, patient comfort, and clinical accessibility. Diffusion-based generative models serve as strong image priors for reducing scan-time with accelerated MRI reconstruction and offer robustness across variations in the acquisition model. However, most existing diffusion-based approaches do not exploit the unique ability in MRI to jointly design both the sampling pattern and the reconstruction method. While prior learning-based approaches have optimized sampling patterns for end-to-end unrolled networks, analogous methods for diffusion-based reconstruction have not been established due to the computational burden of posterior sampling. In this work, we propose a method to optimize k-space sampling patterns for accelerated multi-coil MRI reconstruction using diffusion models as priors. We introduce a training objective based on a single-step posterior mean estimate that avoids backpropagation through an expensive iterative reconstruction process. Then we present a greedy strategy for learning Cartesian sampling patterns that selects informative k-space locations using gradient information from a pre-trained diffusion model while enforcing spatial diversity among samples. Experimental results across multiple anatomies and acceleration factors demonstrate that diffusion models using the optimized sampling patterns achieve higher-quality reconstructions in comparison to using fixed and learned baseline patterns.

Optimizing Sampling Patterns for Compressed Sensing MRI with Diffusion Generative Models

TL;DR

This work tackles the challenge of long MRI acquisition times by integrating diffusion-based priors into sampling pattern design. It introduces a one-step posterior mean objective that enables gradient-based learning of Cartesian k-space patterns without backpropagating through costly posterior sampling, and implements a greedy algorithm to construct informative, well-spaced sampling sets. A diffusion-model prior is used in a frozen form, with a Tweedie-extension loss that incorporates measurements to produce a tractable training signal for pattern optimization. Empirically, the approach yields higher reconstruction quality than fixed Poisson-disc or LOUPE-based baselines across multiple anatomies, contrasts, and acceleration factors, demonstrating robust gains and practical applicability in diffusion-based MRI pipelines. The method offers a flexible, non-end-to-end alternative to jointly training reconstruction and sampling, with potential extensions to pattern distributions and higher-dimensional sampling operators.

Abstract

Magnetic resonance imaging (MRI) is a powerful medical imaging modality, but long acquisition times limit throughput, patient comfort, and clinical accessibility. Diffusion-based generative models serve as strong image priors for reducing scan-time with accelerated MRI reconstruction and offer robustness across variations in the acquisition model. However, most existing diffusion-based approaches do not exploit the unique ability in MRI to jointly design both the sampling pattern and the reconstruction method. While prior learning-based approaches have optimized sampling patterns for end-to-end unrolled networks, analogous methods for diffusion-based reconstruction have not been established due to the computational burden of posterior sampling. In this work, we propose a method to optimize k-space sampling patterns for accelerated multi-coil MRI reconstruction using diffusion models as priors. We introduce a training objective based on a single-step posterior mean estimate that avoids backpropagation through an expensive iterative reconstruction process. Then we present a greedy strategy for learning Cartesian sampling patterns that selects informative k-space locations using gradient information from a pre-trained diffusion model while enforcing spatial diversity among samples. Experimental results across multiple anatomies and acceleration factors demonstrate that diffusion models using the optimized sampling patterns achieve higher-quality reconstructions in comparison to using fixed and learned baseline patterns.
Paper Structure (30 sections, 2 theorems, 23 equations, 10 figures, 1 algorithm)

This paper contains 30 sections, 2 theorems, 23 equations, 10 figures, 1 algorithm.

Key Result

Proposition 1

Let ${\mathbf x}_0 \sim p_0({\mathbf x}_0)$ be an unknown signal, ${\mathbf x}_t \sim p_t({\mathbf x}_t | {\mathbf x}_0) = {\cal N}({\mathbf x}_t; {\mathbf x}_0, \sigma^2_t {\mathbf I})$ a version of ${\mathbf x}_0$ corrupted by additive Gaussian noise, and ${\mathbf y} \sim p({\mathbf y} | {\mathbf

Figures (10)

  • Figure 1: Sampling patterns from different methods for T2 brain data. Optimized sampling patterns from our full proposed method used for reconstructing slices at acceleration factors $R$ in $\{4, 8, 16\}$ with the diffusion-based methods. Poisson Disc sampling tends to distribute samples more uniformly at high acceleration rates, while LOUPE concentrates many samples near the center of k-space. The proposed method balances these effects by maintaining spacing between samples while preferentially allocating measurements to informative central regions.
  • Figure 2: Overview of our method for learning sampling patterns. Starting with the autocalibration region, we greedily grow a set $\mathcal{H}$ (shown in green in the figure) of k-space sampling locations on the Cartesian grid. At each training iteration, we generate a pattern with proper acceleration $R=\frac{m}{n}$ using the previously selected points from $\mathcal{H}$ along with randomly chosen candidate points in k-space that have not yet been added to $\mathcal{H}$. Then, we use the generated pattern in our diffusion training objective to get a loss term and calculate the gradient of the loss at each candidate sampling location. Next, we isolate the $K$ candidate points with the smallest (i.e., largest negative) gradient values, select the point that is farthest away (in terms of Euclidean distance) from its nearest neighbor in $\mathcal{H}$, and finally add that point to $\mathcal{H}$. Our training proceeds, adding one k-space location at a time, until $|\mathcal{H}| = m$ and our desired acceleration is reached.
  • Figure 3: Example Reconstructions from different diffusion methods. We present reconstructions of PDFS knee slice, T2 brain slice, and PD knee slice, all from the test set at $R=20$. Each subfigure includes a zoomed-in region to show fine details (top-left corner) and quantitative metrics (lower-right corner). Reconstructions from our full method, which combines the proposed objective and sampling optimization strategy, achieves better quantitative and qualitative performance in comparison to the baseline diffusion methods.
  • Figure 4: Reconstructions from different diffusion methods for a PD knee slice from the test set at R=4 and R=16. We display the reconstructed slice along with the corresponding residual image (scaled 10$\times$). We present quantitative metrics for each reconstructed slice in the lower-right corner. Our full method produces reconstructions with fewer errors than reconstructions from baseline diffusion methods.
  • Figure 5: Reconstructions from different diffusion methods for a T2 brain slice from the test set at R=4 and R=16. We display the reconstructed slice along with the corresponding residual image (scaled 10$\times$). We present quantitative metrics for each reconstructed slice in the lower-right corner. Our full method produces reconstructions with fewer errors than reconstructions from baseline diffusion methods.
  • ...and 5 more figures

Theorems & Definitions (3)

  • Proposition 1: Tweedie's formula with additional measurements
  • Proposition 1: Tweedie's formula with additional measurements
  • proof