Magnetic Resonance Imaging (MRI) is widely utilized in medical imaging due to its high resolution and non-invasive nature. However, the prolonged acquisition time significantly limits its clinical applicability. Although traditional compressed sensing (CS) techniques can accelerate MRI acquisition, they often lead to degraded reconstruction quality under high undersampling rates. Deep learning-based methods, including CNN- and GAN-based approaches, have improved reconstruction performance, yet are limited by their local receptive fields, making it challenging to effectively capture long-range dependencies. Moreover, these models typically exhibit high computational complexity, which hinders their efficient deployment in practical scenarios. To address these challenges, we propose a lightweight Multi-scale Context-Aware Generative Adversarial Network (MCA-GAN), which enhances MRI reconstruction through dual-domain generators that collaboratively optimize both k-space and image-domain representations. MCA-GAN integrates several lightweight modules, including Depthwise Separable Local Attention (DWLA) for efficient local feature extraction, Adaptive Group Rearrangement Block (AGRB) for dynamic inter-group feature optimization, Multi-Scale Spatial Context Modulation Bridge (MSCMB) for multi-scale feature fusion in skip connections, and Channel-Spatial Multi-Scale Self-Attention (CSMS) for improved global context modeling. Extensive experiments conducted on the IXI, MICCAI 2013, and MRNet knee datasets demonstrate that MCA-GAN consistently outperforms existing methods in terms of PSNR and SSIM. Compared to SepGAN, the latest lightweight model, MCA-GAN achieves a 27.3% reduction in parameter size and a 19.6% reduction in computational complexity, while attaining the shortest reconstruction time among all compared methods. Furthermore, MCA-GAN exhibits robust performance across various undersampling masks and acceleration rates. Cross-dataset generalization experiments further confirm its ability to maintain competitive reconstruction quality, underscoring its strong generalization potential. Overall, MCA-GAN improves MRI reconstruction quality while significantly reducing computational cost through a lightweight architecture and multi-scale feature fusion, offering an efficient and accurate solution for accelerated MRI.

IntroductionStructural neuroimaging analyses require research quality images, acquired with costly MRI acquisitions. Isotropic (3D-T1) images are desirable for quantitative analyses, however a routine compromise in the clinical setting is to acquire anisotropic (2D-T1) analogues for qualitative visual inspection. ML (Machine learning-based) software have shown promise in addressing some of the limitations of 2D-T1 scans in research applications, yet their efficacy in quantitative research is generally poorly understood. Pathology-related abnormalities of the subcortical structures have previously been identified in idiopathic generalised epilepsy (IGE), which have been overlooked based on visual inspection, through the use of quantitative morphometric analyses. As such, IGE biomarkers present a suitable model in which to evaluate the applicability of image preprocessing methods. This study therefore explores subcortical structural biomarkers of IGE, first in our silver standard 3D-T1 scans, then in 2D-T1 scans that were either untransformed, resampled using a classical interpolation approach, or synthesised with a resolution and contrast agnostic ML model (the latter of which is compared to a separate model). Methods2D-T1 and 3D-T1 MRI scans were acquired during the same scanning session for 33 individuals with drug-responsive IGE (age mean 32.16 {+/-} SD = 14.20, male n = 14) and 42 individuals with drug-resistant IGE (31.76 {+/-} 11.12, 17), all diagnosed at the Walton Centre NHS Foundation Trust Liverpool, alongside 39 age- and sex-matched healthy controls (32.32 {+/-} 8.65, 16). The untransformed 2D-T1 scans were resampled into isotropic images using NiBabel (res-T1), and preprocessed into synthetic isotropic images using SynthSR (syn-T1). For the 3D-T1, 2D-T1, res-T1, and syn-T1 images, the recon-all command from FreeSurfer 8.0.0 was used to create parcellations of 174 anatomical regions (equivalent to the 174 regional parcellations provided as part of the DL+DiReCT pipeline), defined by the aseg and Destrieux atlases, and FSL run_first_all was used to segment subcortical surface shapes. The new ML FreeSurfer pipeline, recon-all-clinical, was also tested in the 2D-T1, 3D-T1, and res-T1 images. As a model comparison for SynthSR, the DL+DiReCT pipeline was used to provide segmentations of the 2D-T1 and res-T1 images, including estimates of regional volume and thickness. Spatial overlap and intraclass correlations between the morphometrics of the eight resulting parcellations were first determined, then subcortical surface shape abnormalities associated with IGE were identified by comparing the FSL run_first_all outputs of patients with controls. ResultsWhen standardised to the metrics derived from the 3D-T1 scans, cortical volume and thickness estimates trended lower for the 2D-T1, res-T1, syn-T1, and DL+DiReCT outputs, whereas subcortical volume estimates were more coherent. Dice coefficients revealed an acceptable spatial similarity between the cortices of the 3D-T1 scans and the other images overall, and was higher in the subcortical structures. Intraclass correlation coefficients were consistently lowest when metrics were computed for model-derived inputs, and estimates of thickness were less similar to the ground truth than those of volume. For the people with epilepsy, the 3D-T1 scans showed significant surface deflations across various subcortical structures when compared to healthy controls. Analysis of the 2D-T1 scans enabled the reliable detection of a subset of subcortical abnormalities, whereas analyses of the res-T1 and syn-T1 images were more prone to false-positive results. ConclusionsResampling and ML image synthesis methods do not currently attenuate partial volume effects resulting from low through plane resolution in anisotropic MRI scans, instead quantitative analyses using 2D-T1 scans should be interpreted with caution, and researchers should consider the potential implications of preprocessing. The recon-all-clinical pipeline is promising, but requires further evaluation, especially when considered as an alternative to the classical pipeline. Key PointsO_LISurface deviations indicative of regional atrophy and hypertrophy were identified in people with idiopathic generalised epilepsy. C_LIO_LIPartial volume effects are likely to attenuate subtle morphometric abnormalities, increasing the likelihood of erroneous inference. C_LIO_LIPriors in synthetic image creation models may render them insensitive to subtle biomarkers. C_LIO_LIResampling and machine-learning based image synthesis are not currently replacements for research quality acquisitions in quantitative MRI research. C_LIO_LIThe results of studies using synthetic images should be interpreted in a separate context to those using untransformed data. C_LI

Interpolating missing data in k-space is essential for accelerating imaging. However, existing methods, including convolutional neural network-based deep learning, primarily exploit local predictability while overlooking the inherent global dependencies in k-space. Recently, Transformers have demonstrated remarkable success in natural language processing and image analysis due to their ability to capture long-range dependencies. This inspires the use of Transformers for k-space interpolation to better exploit its global structure. However, their lack of interpretability raises concerns regarding the reliability of interpolated data. To address this limitation, we propose GPI-WT, a white-box Transformer framework based on Globally Predictable Interpolation (GPI) for k-space. Specifically, we formulate GPI from the perspective of annihilation as a novel k-space structured low-rank (SLR) model. The global annihilation filters in the SLR model are treated as learnable parameters, and the subgradients of the SLR model naturally induce a learnable attention mechanism. By unfolding the subgradient-based optimization algorithm of SLR into a cascaded network, we construct the first white-box Transformer specifically designed for accelerated MRI. Experimental results demonstrate that the proposed method significantly outperforms state-of-the-art approaches in k-space interpolation accuracy while providing superior interpretability.

Imaging inverse problems are commonly addressed by minimizing measurement consistency and signal prior terms. While huge attention has been paid to developing high-performance priors, even the most advanced signal prior may lose its effectiveness when paired with an ill-conditioned sensing matrix that hinders convergence and degrades reconstruction quality. In optimization theory, preconditioners allow improving the algorithm's convergence by transforming the gradient update. Traditional linear preconditioning techniques enhance convergence, but their performance remains limited due to their dependence on the structure of the sensing matrix. Learning-based linear preconditioners have been proposed, but they are optimized only for data-fidelity optimization, which may lead to solutions in the null-space of the sensing matrix. This paper employs knowledge distillation to design a nonlinear preconditioning operator. In our method, a teacher algorithm using a better-conditioned (synthetic) sensing matrix guides the student algorithm with an ill-conditioned sensing matrix through gradient matching via a preconditioning neural network. We validate our nonlinear preconditioner for plug-and-play FISTA in single-pixel, magnetic resonance, and super-resolution imaging tasks, showing consistent performance improvements and better empirical convergence.

This study aimed to explore whether an artificial intelligence iterative reconstruction (AIIR) algorithm combined with low-dose aortic computed tomography angiography (CTA) demonstrates clinical effectiveness in assessing preoperative access for transcatheter aortic valve implantation (TAVI). A total of 109 patients were prospectively recruited for aortic CTA scans and divided into two groups: group A (n = 51) with standard-dose CT examinations (SDCT) and group B (n = 58) with low-dose CT examinations (LDCT). Group B was further subdivided into groups B1 and B2. Groups A and B2 used the hybrid iterative algorithm (HIR: Karl 3D), whereas Group B1 used the AIIR algorithm. CT attenuation and noise of different vessel segments were measured, and the contrast-to-noise ratio (CNR) and signal-to-noise ratio (SNR) were calculated. Two radiologists, who were blinded to the study details, rated the subjective image quality on a 5-point scale. The effective radiation doses were also recorded for groups A and B. Group B1 demonstrated the highest CT attenuation, SNR, and CNR and the lowest image noise among the three groups (p < 0.05). The scores of subjective image noise, vessel and non-calcified plaque edge sharpness, and overall image quality in Group B1 were higher than those in groups A and B2 (p < 0.001). Group B2 had the highest artifacts scores compared with groups A and B1 (p < 0.05). The radiation dose in group B was reduced by 50.33% compared with that in group A (p < 0.001). The AIIR algorithm combined with low-dose CTA yielded better diagnostic images before TAVI than the Karl 3D algorithm.

To propose and evaluate an accelerated <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> quantification method that combines <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> -weighted fast spin echo (FSE) images and proton density (PD)-weighted anatomical FSE images, leveraging deep learning models for <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> mapping. The goal is to reduce scan time and facilitate integration into routine clinical workflows for osteoarthritis (OA) assessment. This retrospective study utilized MRI data from 40 participants (30 OA patients and 10 healthy volunteers). A volume of PD-weighted anatomical FSE images and a volume of <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> -weighted images acquired at a non-zero spin-lock time were used as input to train deep learning models, including a 2D U-Net and a multi-layer perceptron (MLP). <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> maps generated by these models were compared with ground truth maps derived from a traditional non-linear least squares (NLLS) fitting method using four <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> -weighted images. Evaluation metrics included mean absolute error (MAE), mean absolute percentage error (MAPE), regional error (RE), and regional percentage error (RPE). The best-performed deep learning models achieved RPEs below 5% across all evaluated scenarios. This performance was consistent even in reduced acquisition settings that included only one PD-weighted image and one <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> -weighted image, where NLLS methods cannot be applied. Furthermore, the results were comparable to those obtained with NLLS when longer acquisitions with four <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> -weighted images were used. The proposed approach enables efficient <math xmlns="http://www.w3.org/1998/Math/MathML"> <semantics> <mrow> <msub><mrow><mi>T</mi></mrow> <mrow><mn>1</mn> <mi>ρ</mi></mrow> </msub> </mrow> <annotation>$$ {T}_{1\rho } $$</annotation></semantics> </math> mapping using PD-weighted anatomical images, reducing scan time while maintaining clinical standards. This method has the potential to facilitate the integration of quantitative MRI techniques into routine clinical practice, benefiting OA diagnosis and monitoring.

Magnetic resonance imaging (MRI) typically utilizes multiple contrasts to assess different tissue features, but prolonged scanning increases the risk of motion artifacts. Compressive sensing MRI (CS-MRI) employs computational reconstruction algorithm to accelerate imaging. Full-sampled auxiliary MR images can effectively assist in the reconstruction of under-sampled target MR images. However, due to spatial offset and differences in imaging parameters, how to achieve cross-modal fusion is a key issue. In order to cope with this issue, we propose an end-to-end network integrating spatial registration and cascaded incremental reconstruction for multi-modal CS-MRI. Specifically, the proposed network comprises two stages: a coarse-to-fine spatial registration sub-network and a cascaded incremental reconstruction sub-network. The registration sub-network iteratively predicts deformation flow fields between under-sampled target images and full-sampled auxiliary images, gradually aligning them to mitigate spatial offsets. The cascaded incremental reconstruction sub-network adopts a new separated criss-cross window Transformer as the basic component and deploys them in dual-path to fuse inter-modal and intra-modal features from the registered auxiliary images and under-sampled target images. Through cascade learning, we can recover incremental details from fused features and continuously refine the target images. We validate our model using the IXI brain dataset, and the experimental results demonstrate that, compared to existing methods, our network exhibits superior performance.

In pelvic MRI, Turbo Spin Echo (TSE) pulse sequences are used for T2-weighted imaging. However, its lengthy acquisition time increases the potential for artifacts. Deep learning (DL) reconstruction achieves reduced scan times without the degradation in image quality associated with other accelerated techniques. Unfortunately, a comprehensive assessment of DL-reconstruction in pelvic MRI has not been performed. The objective of this prospective study was to compare the performance of DL-TSE and conventional TSE pulse sequences in a broad spectrum of pelvic MRI indications. Fifty-five subjects (33 females and 22 males) were scanned at 3 T using DL-TSE and conventional TSE sequences in axial and/or oblique acquisition planes. Two radiologists independently assessed image quality in 6 categories: edge definition, vessel margin sharpness, T2 Contrast Dynamic Range, artifacts, overall image quality, and lesion features. The contrast ratio was calculated for quantitative assessment. A two-tailed sign test was used for assessment. The 2 readers found DL-TSE to deliver equal or superior image quality than conventional TSE in most cases. There were only 3 instances out of 24 where conventional TSE was scored as providing better image quality. Readers agreed on DL-TSE superiority/inferiority/equivalence in 67% of categories in the axial plane and 75% in the oblique plane. DL-TSE also demonstrated a better contrast ratio in 75% of cases. DL-TSE reduced scan time by approximately 50%. DL-accelerated TSE sequences generally provide equal or better image quality in pelvic MRI than standard TSE with significantly reduced acquisition times.

Recently, large language models (LLMs) have driven promis ing progress in lossless image compression. However, di rectly adopting existing paradigms for medical images suf fers from an unsatisfactory trade-off between compression performance and efficiency. Moreover, existing LLM-based compressors often overlook the security of the compres sion process, which is critical in modern medical scenarios. To this end, we propose a novel joint lossless compression and steganography framework. Inspired by bit plane slicing (BPS), we find it feasible to securely embed privacy messages into medical images in an invisible manner. Based on this in sight, an adaptive modalities decomposition strategy is first devised to partition the entire image into two segments, pro viding global and local modalities for subsequent dual-path lossless compression. During this dual-path stage, we inno vatively propose a segmented message steganography algo rithm within the local modality path to ensure the security of the compression process. Coupled with the proposed anatom ical priors-based low-rank adaptation (A-LoRA) fine-tuning strategy, extensive experimental results demonstrate the su periority of our proposed method in terms of compression ra tios, efficiency, and security. The source code will be made publicly available.

This study explored the effects of using Intelligent Quick Magnetic Resonance (IQMR) image post-processing on image quality in Field of View Optimized and Constrained Single-Shot Diffusion-Weighted Imaging (FOCUS-DWI) sequences for prostate cancer detection, and assessed its efficacy in distinguishing malignant from benign lesions. The clinical data and MRI images from 62 patients with prostate masses (31 benign and 31 malignant) were retrospectively analyzed. Axial T2-weighted imaging with fat saturation (T2WI-FS) and FOCUS-DWI sequences were acquired, and the FOCUS-DWI images were processed using the IQMR post-processing system to generate IQMR-FOCUS-DWI images. Two independent radiologists undertook subjective scoring, grading using the Prostate Imaging Reporting and Data System (PI-RADS), diagnosis of benign and malignant lesions, and diagnostic confidence scoring for images from the FOCUS-DWI and IQMR-FOCUS-DWI sequences. Additionally, quantitative analyses, specifically, the peak signal-to-noise ratio (PSNR) and structural similarity index (SSIM), were conducted using T2WI-FS as the reference standard. The apparent diffusion coefficients (ADCs) of malignant and benign lesions were compared between the two imaging sequences. Spearman correlation coefficients were calculated to evaluate the associations between diagnostic confidence scores and diagnostic accuracy rates of the two sequence groups, as well as between the ADC values of malignant lesions and Gleason grading in the two sequence groups. Receiver operating characteristic (ROC) curves were utilized to assess the efficacy of ADC in distinguishing lesions. The qualitative analysis revealed that IQMR-FOCUS-DWI images showed significantly better noise suppression, reduced geometric distortion, and enhanced overall quality relative to the FOCUS-DWI images (P < 0.001). There was no significant difference in the PI-RADS scores between IQMR-FOCUS-DWI and FOCUS-DWI images (P = 0.0875), while the diagnostic confidence scores of IQMR-FOCUS-DWI sequences were markedly higher than those of FOCUS-DWI sequences (P = 0.0002). The diagnostic results of the FOCUS-DWI sequences for benign and malignant prostate lesions were consistent with those of the pathological results (P < 0.05), as were those of the IQMR-FOCUS-DWI sequences (P < 0.05). The quantitative analysis indicated that the PSNR, SSIM, and ADC values were markedly greater in IQMR-FOCUS-DWI images relative to FOCUS-DWI images (P < 0.01). In both imaging sequences, benign lesions exhibited ADC values markedly greater than those of malignant lesions (P < 0.001). The diagnostic confidence scores of both groups of sequences were significantly positively correlated with the diagnostic accuracy rate. In malignant lesions, the ADC values of the FOCUS-DWI sequences showed moderate negative correlations with the Gleason grading, while the ADC values of the IQMR-FOCUS-DWI sequences were strongly negatively associated with the Gleason grading. ROC curves indicated the superior diagnostic performance of IQMR-FOCUS-DWI (AUC = 0.941) compared to FOCUS-DWI (AUC = 0.832) for differentiating prostate lesions (P = 0.0487). IQMR-FOCUS-DWI significantly enhances image quality and improves diagnostic accuracy for benign and malignant prostate lesions compared to conventional FOCUS-DWI.