We introduce MRF-DiPh, a novel physics informed denoising diffusion approach for multiparametric tissue mapping from highly accelerated, transient-state quantitative MRI acquisitions like Magnetic Resonance Fingerprinting (MRF). Our method is derived from a proximal splitting formulation, incorporating a pretrained denoising diffusion model as an effective image prior to regularize the MRF inverse problem. Further, during reconstruction it simultaneously enforces two key physical constraints: (1) k-space measurement consistency and (2) adherence to the Bloch response model. Numerical experiments on in-vivo brain scans data show that MRF-DiPh outperforms deep learning and compressed sensing MRF baselines, providing more accurate parameter maps while better preserving measurement fidelity and physical model consistency-critical for solving reliably inverse problems in medical imaging.

Segmentation of brain structures from MRI is crucial for evaluating brain morphology, yet existing CNN and transformer-based methods struggle to delineate complex structures accurately. While current diffusion models have shown promise in image segmentation, they are inadequate when applied directly to brain MRI due to neglecting anatomical information. To address this, we propose Collaborative Anatomy Diffusion (CA-Diff), a framework integrating spatial anatomical features to enhance segmentation accuracy of the diffusion model. Specifically, we introduce distance field as an auxiliary anatomical condition to provide global spatial context, alongside a collaborative diffusion process to model its joint distribution with anatomical structures, enabling effective utilization of anatomical features for segmentation. Furthermore, we introduce a consistency loss to refine relationships between the distance field and anatomical structures and design a time adapted channel attention module to enhance the U-Net feature fusion procedure. Extensive experiments show that CA-Diff outperforms state-of-the-art (SOTA) methods.

Understanding brain dynamics through functional Magnetic Resonance Imaging (fMRI) remains a fundamental challenge in neuroscience, particularly in capturing how the brain transitions between various functional states. Recently, metastability, which refers to temporarily stable brain states, has offered a promising paradigm to quantify complex brain signals into interpretable, discretized representations. In particular, compared to cluster-based machine learning approaches, tokenization approaches leveraging vector quantization have shown promise in representation learning with powerful reconstruction and predictive capabilities. However, most existing methods ignore brain transition dependencies and lack a quantification of brain dynamics into representative and stable embeddings. In this study, we propose a Hierarchical State space-based Tokenization network, termed HST, which quantizes brain states and transitions in a hierarchical structure based on a state space-based model. We introduce a refined clustered Vector-Quantization Variational AutoEncoder (VQ-VAE) that incorporates quantization error feedback and clustering to improve quantization performance while facilitating metastability with representative and stable token representations. We validate our HST on two public fMRI datasets, demonstrating its effectiveness in quantifying the hierarchical dynamics of the brain and its potential in disease diagnosis and reconstruction performance. Our method offers a promising framework for the characterization of brain dynamics, facilitating the analysis of metastability.

Brain tumor (BT) is a rapid growth of brain cells. If the BT is not identified and treated in the first stage, it could cause death. Despite several methods and efforts being developed for segmenting and identifying BT, the detection of BT is complicated due to the distinct position of the tumor and its size. To solve such issues, this paper proposes the Conditional Autoregressive Value-at-Risk_Xception Maxout-Network (Caviar_XM-Net) for BT detection utilizing magnetic resonance imaging (MRI) images. The input MRI image gathered from the dataset is denoised using the adaptive bilateral filter (ABF), and tumor region segmentation is done using BFC-MRFNet-RVSeg. Here, the segmentation is done by the Bayesian fuzzy clustering (BFC) and multi-branch residual fusion network (MRF-Net) separately. Subsequently, outputs from both segmentation techniques are combined using the RV coefficient. Image augmentation is performed to boost the quantity of images in the training process. Afterwards, feature extraction is done, where features, like local optimal oriented pattern (LOOP), convolutional neural network (CNN) features, median binary pattern (MBP) with statistical features, and local Gabor XOR pattern (LGXP), are extracted. Lastly, BT detection is carried out by employing Caviar_XM-Net, which is acquired by the assimilation of the Xception model and deep Maxout network (DMN) with the CAViaR approach. Furthermore, the effectiveness of Caviar_XM-Net is examined using the parameters, namely sensitivity, accuracy, specificity, precision, and F1-score, and the corresponding values of 91.59%, 91.36%, 90.83%, 90.99%, and 91.29% are attained. Hence, the Caviar_XM-Net performs better than the traditional methods with high efficiency.

Identifying amyloid-beta (Aβ)-positive patients is essential for Alzheimer's disease (AD) clinical trials and disease-modifying treatments but currently requires PET or cerebrospinal fluid sampling. Previous MRI-based deep learning models, using only T1-weighted (T1w) images, have shown moderate performance. Multi-contrast MRI and PET-based quantitative Aβ deposition were retrospectively obtained from three public datasets: ADNI, OASIS3, and A4. Aβ positivity was defined using each dataset's recommended centiloid threshold. Two EfficientNet models were trained to predict amyloid positivity: one using only T1w images and another incorporating both T1w and T2-FLAIR. Model performance was assessed using an internal held-out test set, evaluating AUC, accuracy, sensitivity, and specificity. External validation was conducted using an independent cohort from Stanford Alzheimer's Disease Research Center. DeLong's and McNemar's tests were used to compare AUC and accuracy, respectively. A total of 4,056 exams (mean [SD] age: 71.6 [6.3] years; 55% female; 55% amyloid-positive) were used for network development, and 149 exams were used for external testing (mean [SD] age: 72.1 [9.6] years; 58% female; 56% amyloid-positive). The multi-contrast model outperformed the single-modality model in the internal held-out test set (AUC: 0.67, 95% CI: 0.65-0.70, <i>P</i> < 0.001; accuracy: 0.63, 95% CI: 0.62-0.65, <i>P</i> < 0.001) compared to the T1w-only model (AUC: 0.61; accuracy: 0.59). Among cognitive subgroups, the highest performance (AUC: 0.71) was observed in mild cognitive impairment. The multi-contrast model also demonstrated consistent performance in the external test set (AUC: 0.65, 95% CI: 0.60-0.71, <i>P</i> = 0.014; accuracy: 0.62, 95% CI: 0.58- 0.65, <i>P</i> < 0.001). The use of multi-contrast MRI, specifically incorporating T2-FLAIR in addition to T1w images, significantly improved the predictive accuracy of PET-determined amyloid status from MRI scans using a deep learning approach. Aβ＝ amyloid-beta; AD＝ Alzheimer's disease; AUC＝ area under the receiver operating characteristic curve; CN＝ cognitively normal; MCI＝ mild cognitive impairment; T1w = T1-wegithed; T2-FLAIR = T2-weighted fluid attenuated inversion recovery; FBP＝¹⁸F-florbetapir; FBB＝¹⁸F-florbetaben; SUVR＝ standard uptake value ratio.

White matter hyperintensities (WMH) are radiological markers of small vessel disease and neurodegeneration, whose accurate segmentation and spatial localization are crucial for diagnosis and monitoring. While multimodal MRI offers complementary contrasts for detecting and contextualizing WM lesions, existing approaches often lack flexibility in handling missing modalities and fail to integrate anatomical localization efficiently. We propose a deep learning framework for WM lesion segmentation and localization that operates directly in native space using single- and multi-modal MRI inputs. Our study evaluates four input configurations: FLAIR-only, T1-only, concatenated FLAIR and T1, and a modality-interchangeable setup. It further introduces a multi-task model for jointly predicting lesion and anatomical region masks to estimate region-wise lesion burden. Experiments conducted on the MICCAI WMH Segmentation Challenge dataset demonstrate that multimodal input significantly improves the segmentation performance, outperforming unimodal models. While the modality-interchangeable setting trades accuracy for robustness, it enables inference in cases with missing modalities. Joint lesion-region segmentation using multi-task learning was less effective than separate models, suggesting representational conflict between tasks. Our findings highlight the utility of multimodal fusion for accurate and robust WMH analysis, and the potential of joint modeling for integrated predictions.

Background: Conventional cardiovascular magnetic resonance (CMR) in paediatric and congenital heart disease uses 2D, breath-hold, balanced steady state free precession (bSSFP) cine imaging for assessment of function and cardiac-gated, respiratory-navigated, static 3D bSSFP whole-heart imaging for anatomical assessment. Our aim is to concatenate a stack 2D free-breathing real-time cines and use Deep Learning (DL) to create an isotropic a fully segmented 3D cine dataset from these images. Methods: Four DL models were trained on open-source data that performed: a) Interslice contrast correction; b) Interslice respiratory motion correction; c) Super-resolution (slice direction); and d) Segmentation of right and left atria and ventricles (RA, LA, RV, and LV), thoracic aorta (Ao) and pulmonary arteries (PA). In 10 patients undergoing routine cardiovascular examination, our method was validated on prospectively acquired sagittal stacks of real-time cine images. Quantitative metrics (ventricular volumes and vessel diameters) and image quality of the 3D cines were compared to conventional breath hold cine and whole heart imaging. Results: All real-time data were successfully transformed into 3D cines with a total post-processing time of <1 min in all cases. There were no significant biases in any LV or RV metrics with reasonable limits of agreement and correlation. There is also reasonable agreement for all vessel diameters, although there was a small but significant overestimation of RPA diameter. Conclusion: We have demonstrated the potential of creating a 3D-cine data from concatenated 2D real-time cine images using a series of DL models. Our method has short acquisition and reconstruction times with fully segmented data being available within 2 minutes. The good agreement with conventional imaging suggests that our method could help to significantly speed up CMR in clinical practice.

Recent advances in deep learning have made it possible to predict phenotypic measures directly from functional magnetic resonance imaging (fMRI) brain volumes, sparking significant interest in the neuroimaging community. However, existing approaches, primarily based on convolutional neural networks or transformer architectures, often struggle to model the complex relationships inherent in fMRI data, limited by their inability to capture long-range spatial and temporal dependencies. To overcome these shortcomings, we introduce BrainMT, a novel hybrid framework designed to efficiently learn and integrate long-range spatiotemporal attributes in fMRI data. Our framework operates in two stages: (1) a bidirectional Mamba block with a temporal-first scanning mechanism to capture global temporal interactions in a computationally efficient manner; and (2) a transformer block leveraging self-attention to model global spatial relationships across the deep features processed by the Mamba block. Extensive experiments on two large-scale public datasets, UKBioBank and the Human Connectome Project, demonstrate that BrainMT achieves state-of-the-art performance on both classification (sex prediction) and regression (cognitive intelligence prediction) tasks, outperforming existing methods by a significant margin. Our code and implementation details will be made publicly available at this https://github.com/arunkumar-kannan/BrainMT-fMRI

To review the latest developments in self-supervised deep learning (DL) techniques for magnetic resonance imaging (MRI) reconstruction, emphasizing their potential to overcome the limitations of supervised methods dependent on fully sampled k-space data. While DL has significantly advanced MRI, supervised approaches require large amounts of fully sampled k-space data for training-a major limitation given the impracticality and expense of acquiring such data clinically. Self-supervised learning has emerged as a promising alternative, enabling model training using only undersampled k-space data, thereby enhancing feasibility and driving research interest. We conducted a comprehensive literature review to synthesize recent progress in self-supervised DL for MRI reconstruction. The analysis focused on methods and architectures designed to improve image quality, reduce scanning time, and address data scarcity challenges, drawing from peer-reviewed publications and technical innovations in the field. Self-supervised DL holds transformative potential for MRI reconstruction, offering solutions to data limitations while maintaining image quality and accelerating scans. Key challenges include robustness across diverse anatomies, standardization of validation, and clinical integration. Future research should prioritize hybrid methodologies, domain-specific adaptations, and rigorous clinical validation. This review consolidates advancements and unresolved issues, providing a foundation for next-generation medical imaging technologies.

Magnetic resonance imaging (MRI) is a crucial tool for visualizing orbital structures and detecting eye pathologies. However, manual segmentation of orbital anatomy is challenging due to the complexity and variability of the structures. Recent advancements in deep learning (DL), particularly convolutional neural networks (CNNs), offer promising solutions for automated segmentation in medical imaging. This study aimed to train and evaluate a U-Net-based model for the automated segmentation of key orbital structures. This retrospective study included 117 patients with various orbital pathologies who underwent orbital MRI. Manual segmentation was performed on four anatomical structures: the ocular bulb, ocular tumors, retinal detachment, and the optic nerve. Following the UNet autoconfiguration by nnUNet, we conducted a five-fold cross-validation and evaluated the model's performances using Dice Similarity Coefficient (DSC) and Relative Absolute Volume Difference (RAVD) as metrics. nnU-Net achieved high segmentation performance for the ocular bulb (mean DSC: 0.931) and the optic nerve (mean DSC: 0.820). Segmentation of ocular tumors (mean DSC: 0.788) and retinal detachment (mean DSC: 0.550) showed greater variability, with performance declining in more challenging cases. Despite these challenges, the model achieved high detection rates, with ROC AUCs of 0.90 for ocular tumors and 0.78 for retinal detachment. This study demonstrates nnU-Net's capability for accurate segmentation of orbital structures, particularly the ocular bulb and optic nerve. However, challenges remain in the segmentation of tumors and retinal detachment due to variability and artifacts. Future improvements in deep learning models and broader, more diverse datasets may enhance segmentation performance, ultimately aiding in the diagnosis and treatment of orbital pathologies.