使用内隐神经表征加速患者特异性非笛卡儿MRI重建。

IF 6.5 1区 医学 Q1 ONCOLOGY
Di Xu, Hengjie Liu, Xin Miao, Daniel O'Connor, Jessica E Scholey, Wensha Yang, Mary Feng, Michael Ohliger, Hui Lin, Dan Ruan, Yang Yang, Ke Sheng
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引用次数: 0

摘要

目的:加速MR采集对图像引导治疗应用至关重要。压缩感知(CS)是一种用于减少加速扫描中图像伪影的技术,但所需要的迭代重建计算复杂且难以推广。基于卷积神经网络(cnn)/变压器的深度学习(DL)方法作为一种更快的替代方法出现,但在连续k空间建模方面面临挑战,这一问题在加速采集中常用的非笛卡尔采样中被放大。相比之下,隐式神经表征可以在频域对连续信号进行建模,因此与任意k空间采样模式兼容。目前的研究开发了一种新的生成对抗训练的内隐神经表征(k-GINR),用于从头开始的欠采样非笛卡尔k空间重建。方法和材料:k-GINR包括两个阶段:1)对现有患者队列进行监督培训;2)自我监督的针对患者的优化。StarVIBE t1加权肝脏数据集由118个前瞻性扫描和相应的线圈数据组成,用于测试。k-GINR与两种基于INR的方法,NeRP和k-NeRP,展开深度学习方法,深度级联CNN和CS进行了比较。结果:k-GINR始终优于基线,在非常高的加速度下观察到更大的性能优势(PSNR: 3次时提高6.8%-15.2%,10次时提高15.1%-48.8%,20次时提高29.3%-60.5%)。k-GINR、NeRP、k-NeRP、CS和Deep Cascade CNN的重建时间分别约为3分钟、4-10分钟、3分钟、4分钟和3秒。结论:k-GINR是一种包含对抗训练的创新型两阶段INR网络,可用于新入院患者的直接非笛卡尔k空间重建。在很宽的加速比范围内,与CS和Deep Cascade CNN相比,它表现出了优越的图像质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Accelerated Patient-specific Non-Cartesian Magnetic Resonance Imaging Reconstruction Using Implicit Neural Representations.

Purpose: Accelerating magnetic resonance acquisition is essential for image guided therapeutic applications. Compressed sensing (CS) has been developed to minimize image artifacts in accelerated scans, but the required iterative reconstruction is computationally complex and difficult to generalize. Convolutional neural networks (CNNs)/Transformers-based deep learning methods emerged as a faster alternative but face challenges in modeling continuous k-space, a problem amplified with non-Cartesian sampling commonly used in accelerated acquisition. In comparison, implicit neural representations (INRs) can model continuous signals in the frequency domain and thus are compatible with arbitrary k-space sampling patterns. The current study developed novel k-space generative-adversarially trained INRs (k-GINR) for de novo undersampled non-Cartesian k-space reconstruction.

Methods and materials: k-GINR consists of 2 stages: 1) supervised training on an existing patient cohort; 2) self-supervised patient-specific optimization. The StarVIBE T1-weighted liver data set, consisting of 118 prospectively acquired scans and corresponding coil data, was employed for testing. k-GINR is compared with 2 INR-based methods, Neural Representation learning methodology with Prior embedding (NeRP) and k-space NeRP, an unrolled deep learning method, Deep Cascade CNN, and CS.

Results: k-GINR consistently outperformed the baselines with a larger performance advantage observed at very high accelerations (peak-signal-to-noise ratio: 6.8%-15.2% higher at 3 times, 15.1%-48.8% at 10 times, and 29.3%-60.5% higher at 20 times). The reconstruction times for k-GINR, NeRP, k-NeRP, CS, and Deep Cascade CNN were approximately 3 minutes, 4-10 minutes, 3 minutes, 4 minutes and 3 second, respectively.

Conclusions: k-GINR, an innovative 2-stage INR network incorporating adversarial training, was designed for direct non-Cartesian k-space reconstruction for new incoming patients. It demonstrated superior image quality compared to CS and Deep Cascade CNN across a wide range of acceleration ratios.

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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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