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
{"title":"使用内隐神经表征加速患者特异性非笛卡儿MRI重建。","authors":"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","doi":"10.1016/j.ijrobp.2025.08.059","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>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.</p><p><strong>Methods and materials: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":14215,"journal":{"name":"International Journal of Radiation Oncology Biology Physics","volume":" ","pages":""},"PeriodicalIF":6.5000,"publicationDate":"2025-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Accelerated Patient-specific Non-Cartesian Magnetic Resonance Imaging Reconstruction Using Implicit Neural Representations.\",\"authors\":\"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\",\"doi\":\"10.1016/j.ijrobp.2025.08.059\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Purpose: </strong>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.</p><p><strong>Methods and materials: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>k-GINR, an innovative 2-stage INR network incorporating adversarial training, was designed for direct non-Cartesian k-space reconstruction for new incoming patients. 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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.
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.