Quantitative magnetic resonance imaging (qMRI) offers tissue-specific physical parameters with significant potential for neuroscience research and clinical practice. However, lengthy scan times for 3D multiparametric qMRI acquisition limit its clinical utility. Here, we propose SUMMIT, an innovative imaging methodology that includes data acquisition and an unsupervised reconstruction for simultaneous multiparametric qMRI. SUMMIT first encodes multiple important quantitative properties into highly undersampled k-space. It further leverages implicit neural representation incorporated with a dedicated physics model to reconstruct the desired multiparametric maps without needing external training datasets. SUMMIT delivers co-registered T 1 , T 2 , T 2 ∗ , and subvoxel quantitative susceptibility mapping. Extensive simulations, phantom, and in vivo brain imaging demonstrate SUMMIT’s high accuracy. Notably, SUMMIT uniquely unravels microstructural alternations in patients with white matter hyperintense lesions with high sensitivity and specificity. Additionally, the proposed unsupervised approach for qMRI reconstruction also introduces a novel zero-shot learning paradigm for multiparametric imaging applicable to various medical imaging modalities .

Supervised Deep-Learning (DL)-based reconstruction algorithms have shown state-of-the-art results for highly-undersampled dynamic Magnetic Resonance Imaging (MRI) reconstruction. However, the requirement of excessive high-quality ground-truth data hinders their applications due to the generalization problem. Recently, Implicit Neural Representation (INR) has emerged as a powerful DL-based tool for solving the inverse problem by characterizing the attributes of a signal as a continuous function of corresponding coordinates in an unsupervised manner. In this work, we proposed an INR-based method to improve dynamic MRI reconstruction from highly undersampled $\boldsymbol {k}$ -space data, which only takes spatiotemporal coordinates as inputs and does not require any training on external datasets or transfer-learning from prior images. Specifically, the proposed method encodes the dynamic MRI images into neural networks as an implicit function, and the weights of the network are learned from sparsely-acquired ( $\boldsymbol {k}$ , t)-space data itself only. Benefiting from the strong implicit continuity regularization of INR together with explicit regularization for low-rankness and sparsity, our proposed method outperforms the compared state-of-the-art methods at various acceleration factors. E.g., experiments on retrospective cardiac cine datasets show an improvement of 0.6-2.0 dB in PSNR for high accelerations (up to $40.8\times $ ). The high-quality and inner continuity of the images provided by INR exhibit great potential to further improve the spatiotemporal resolution of dynamic MRI. The code is available at: https://github.com/AMRI-Lab/INR_for_DynamicMRI.

The process of brain aging is intricate, encompassing significant structural and functional changes, including myelination and iron deposition in the brain. Brain age could act as a quantitative marker to evaluate the degree of the individual's brain evolution. Quantitative susceptibility mapping (QSM) is sensitive to variations in magnetically responsive substances such as iron and myelin, making it a favorable tool for estimating brain age. In this study, we introduce an innovative 3D convolutional network named Segmentation-Transformer-Age-Network (STAN) to predict brain age based on QSM data. STAN employs a two-stage network architecture. The first-stage network learns to extract informative features from the QSM data through segmentation training, while the second-stage network predicts brain age by integrating the global and local features. We collected QSM images from 712 healthy participants, with 548 for training and 164 for testing. The results demonstrate that the proposed method achieved a high accuracy brain age prediction with a mean absolute error (MAE) of 4.124 years and a coefficient of determination (R2) of 0.933. Furthermore, the gaps between the predicted brain age and the chronological age of Parkinson's disease patients were significantly higher than those of healthy subjects (P<0.01). We thus believe that using QSM-based predicted brain age offers a more reliable and accurate phenotype, with the potentiality to serve as a biomarker to explore the process of advanced brain aging.

Parallel imaging is a commonly used technique to accelerate magnetic resonance imaging (MRI) data acquisition. Mathematically, parallel MRI reconstruction can be formulated as an inverse problem relating the sparsely sampled k-space measurements to the desired MRI image. Despite the success of many existing reconstruction algorithms, it remains a challenge to reliably reconstruct a high-quality image from highly reduced k-space measurements. Recently, implicit neural representation has emerged as a powerful paradigm to exploit the internal information and the physics of partially acquired data to generate the desired object. In this study, we introduced IMJENSE, a scan-specific implicit neural representation-based method for improving parallel MRI reconstruction. Specifically, the underlying MRI image and coil sensitivities were modeled as continuous functions of spatial coordinates, parameterized by neural networks and polynomials, respectively. The weights in the networks and coefficients in the polynomials were simultaneously learned directly from sparsely acquired k-space measurements, without fully sampled ground truth data for training. Benefiting from the powerful continuous representation and joint estimation of the MRI image and coil sensitivities, IMJENSE outperforms conventional image or k-space domain reconstruction algorithms. With extremely limited calibration data, IMJENSE is more stable than supervised calibrationless and calibration-based deep-learning methods. Results show that IMJENSE robustly reconstructs the images acquired at 5× and 6× accelerations with only 4 or 8 calibration lines in 2D Cartesian acquisitions, corresponding to 22.0% and 19.5% undersampling rates. The high-quality results and scanning specificity make the proposed method hold the potential for further accelerating the data acquisition of parallel MRI.

Susceptibility tensor imaging (STI) is a promising tool for studying orientation-dependent tissue magnetic susceptibility and for mapping white matter fiber orientations complementary to diffusion tensor imaging (DTI). However, the limited head rotation range within modern head coils for data acquisition makes in vivo STI reconstruction ill-conditioned. Conventional STI reconstruction method is usually vulnerable to noise and requires sufficiently large head rotations to solve this ill-conditioned inverse problem. In this study, based on the recently proposed asymmetric STI (aSTI) model, a new method termed aSTI+ was proposed to improve in vivo STI reconstruction by enforcing isotropic susceptibility tensor inside cerebrospinal fluid (CSF) and applying morphology constraint in white matter. Experimental results showed superior performance of the proposed method with reduced noise, improved tissue contrast and better fiber orientation estimation over previous methods. Thus aSTI+ may promote in vivo human brain STI studies on white matter and myelin-related brain diseases.