No Arabic abstract
Functional MRI (fMRI) is commonly used for interpreting neural activities across the brain. Numerous accelerated fMRI techniques aim to provide improved spatiotemporal resolutions. Among these, simultaneous multi-slice (SMS) imaging has emerged as a powerful strategy, becoming a part of large-scale studies, such as the Human Connectome Project. However, when SMS imaging is combined with in-plane acceleration for higher acceleration rates, conventional SMS reconstruction methods may suffer from noise amplification and other artifacts. Recently, deep learning (DL) techniques have gained interest for improving MRI reconstruction. However, these methods are typically trained in a supervised manner that necessitates fully-sampled reference data, which is not feasible in highly-accelerated fMRI acquisitions. Self-supervised learning that does not require fully-sampled data has recently been proposed and has shown similar performance to supervised learning. However, it has only been applied for in-plane acceleration. Furthermore the effect of DL reconstruction on subsequent fMRI analysis remains unclear. In this work, we extend self-supervised DL reconstruction to SMS imaging. Our results on prospectively 10-fold accelerated 7T fMRI data show that self-supervised DL reduces reconstruction noise and suppresses residual artifacts. Subsequent fMRI analysis remains unaltered by DL processing, while the improved temporal signal-to-noise ratio produces higher coherence estimates between task runs.
Deep learning (DL) has emerged as a tool for improving accelerated MRI reconstruction. A common strategy among DL methods is the physics-based approach, where a regularized iterative algorithm alternating between data consistency and a regularizer is unrolled for a finite number of iterations. This unrolled network is then trained end-to-end in a supervised manner, using fully-sampled data as ground truth for the network output. However, in a number of scenarios, it is difficult to obtain fully-sampled datasets, due to physiological constraints such as organ motion or physical constraints such as signal decay. In this work, we tackle this issue and propose a self-supervised learning strategy that enables physics-based DL reconstruction without fully-sampled data. Our approach is to divide the acquired sub-sampled points for each scan into training and validation subsets. During training, data consistency is enforced over the training subset, while the validation subset is used to define the loss function. Results show that the proposed self-supervised learning method successfully reconstructs images without fully-sampled data, performing similarly to the supervised approach that is trained with fully-sampled references. This has implications for physics-based inverse problem approaches for other settings, where fully-sampled data is not available or possible to acquire.
Deep learning (DL) has emerged as a powerful tool for accelerated MRI reconstruction, but these methods often necessitate a database of fully-sampled measurements for training. Recent self-supervised and unsupervised learning approaches enable training without fully-sampled data. However, a database of undersampled measurements may not be available in many scenarios, especially for scans involving contrast or recently developed translational acquisitions. Moreover, database-trained models may not generalize well when the unseen measurements differ in terms of sampling pattern, acceleration rate, SNR, image contrast, and anatomy. Such challenges necessitate a new methodology that can enable scan-specific DL MRI reconstruction without any external training datasets. In this work, we propose a zero-shot self-supervised learning approach to perform scan-specific accelerated MRI reconstruction to tackle these issues. The proposed approach splits available measurements for each scan into three disjoint sets. Two of these sets are used to enforce data consistency and define loss during training, while the last set is used to establish an early stopping criterion. In the presence of models pre-trained on a database with different image characteristics, we show that the proposed approach can be combined with transfer learning to further improve reconstruction quality.
Purpose: To develop an improved self-supervised learning strategy that efficiently uses the acquired data for training a physics-guided reconstruction network without a database of fully-sampled data. Methods: Currently self-supervised learning for physics-guided reconstruction networks splits acquired undersampled data into two disjoint sets, where one is used for data consistency (DC) in the unrolled network and the other to define the training loss. The proposed multi-mask self-supervised learning via data undersampling (SSDU) splits acquired measurements into multiple pairs of disjoint sets for each training sample, while using one of these sets for DC units and the other for defining loss, thereby more efficiently using the undersampled data. Multi-mask SSDU is applied on fully-sampled 3D knee and prospectively undersampled 3D brain MRI datasets, which are retrospectively subsampled to acceleration rate (R)=8, and compared to CG-SENSE and single-mask SSDU DL-MRI, as well as supervised DL-MRI when fully-sampled data is available. Results: Results on knee MRI show that the proposed multi-mask SSDU outperforms SSDU and performs closely with supervised DL-MRI, while significantly outperforming CG-SENSE. A clinical reader study further ranks the multi-mask SSDU higher than supervised DL-MRI in terms of SNR and aliasing artifacts. Results on brain MRI show that multi-mask SSDU achieves better reconstruction quality compared to SSDU and CG-SENSE. Reader study demonstrates that multi-mask SSDU at R=8 significantly improves reconstruction compared to single-mask SSDU at R=8, as well as CG-SENSE at R=2. Conclusion: The proposed multi-mask SSDU approach enables improved training of physics-guided neural networks without fully-sampled data, by enabling efficient use of the undersampled data with multiple masks.
Physics-guided deep learning (PG-DL) via algorithm unrolling has received significant interest for improved image reconstruction, including MRI applications. These methods unroll an iterative optimization algorithm into a series of regularizer and data consistency units. The unrolled networks are typically trained end-to-end using a supervised approach. Current supervised PG-DL approaches use all of the available sub-sampled measurements in their data consistency units. Thus, the network learns to fit the rest of the measurements. In this study, we propose to improve the performance and robustness of supervised training by utilizing randomness by retrospectively selecting only a subset of all the available measurements for data consistency units. The process is repeated multiple times using different random masks during training for further enhancement. Results on knee MRI show that the proposed multi-mask supervised PG-DL enhances reconstruction performance compared to conventional supervised PG-DL approaches.
Retrospectively gated cine (retro-cine) MRI is the clinical standard for cardiac functional analysis. Deep learning (DL) based methods have been proposed for the reconstruction of highly undersampled MRI data and show superior image quality and magnitude faster reconstruction time than CS-based methods. Nevertheless, it remains unclear whether DL reconstruction is suitable for cardiac function analysis. To address this question, in this study we evaluate and compare the cardiac functional values (EDV, ESV and EF for LV and RV, respectively) obtained from highly accelerated MRI acquisition using DL based reconstruction algorithm (DL-cine) with values from CS-cine and conventional retro-cine. To the best of our knowledge, this is the first work to evaluate the cine MRI with deep learning reconstruction for cardiac function analysis and compare it with other conventional methods. The cardiac functional values obtained from cine MRI with deep learning reconstruction are consistent with values from clinical standard retro-cine MRI.