Andre van der Kouwe

Zihui Wu, Tianwei Yin, Yu Sun et al.

Compressed sensing magnetic resonance imaging (CS-MRI) seeks to recover visual information from subsampled measurements for diagnostic tasks. Traditional CS-MRI methods often separately address measurement subsampling, image reconstruction, and task prediction, resulting in a suboptimal end-to-end performance. In this work, we propose TACKLE as a unified co-design framework for jointly optimizing subsampling, reconstruction, and prediction strategies for the performance on downstream tasks. The naïve approach of simply appending a task prediction module and training with a task-specific loss leads to suboptimal downstream performance. Instead, we develop a training procedure where a backbone architecture is first trained for a generic pre-training task (image reconstruction in our case), and then fine-tuned for different downstream tasks with a prediction head. Experimental results on multiple public MRI datasets show that TACKLE achieves an improved performance on various tasks over traditional CS-MRI methods. We also demonstrate that TACKLE is robust to distribution shifts by showing that it generalizes to a new dataset we experimentally collected using different acquisition setups from the training data. Without additional fine-tuning, TACKLE leads to both numerical and visual improvements compared to existing baselines. We have further implemented a learned 4$\times$-accelerated sequence on a Siemens 3T MRI Skyra scanner. Compared to the fully-sampling scan that takes 335 seconds, our optimized sequence only takes 84 seconds, achieving a four-fold time reduction as desired, while maintaining high performance.

Jingting Yao, Artan Kaso, Nikhil Patel et al.

Current magnetic resonance imaging (MRI) requires the subject to remain stationary to limit motion artifacts and avoid unwanted field-induced brain stimulation. However, imaging during large-scale motion could enable studies in which motion itself is central. One example is the study of brain networks involved in vestibular function, which senses head motion. Here, we demonstrate Moving MRI (mMRI), a system that enables imaging during large-scale motion by moving the subject and scanner together to minimize relative motion. We implemented a proof-of-concept platform using a compact, cryogen-free superconducting magnet mounted on a pneumatically actuated tilt mechanism that moves the magnet, gradients, and RF coil as a unit during scanning. Phantom and in vivo rat brain scans were acquired during repetitive tilting. We characterized artifacts arising from tilt-induced field shifts and residual subject-scanner motion, and partially reduced these effects. mMRI enables imaging during large-scale movement and may broaden access to naturalistic vestibular paradigms while providing a foundation for future human systems.

Divya Varadarajan, Katherine L. Bouman, Andre van der Kouwe et al.

In neuroimaging, MRI tissue properties characterize underlying neurobiology, provide quantitative biomarkers for neurological disease detection and analysis, and can be used to synthesize arbitrary MRI contrasts. Estimating tissue properties from a single scan session using a protocol available on all clinical scanners promises to reduce scan time and cost, enable quantitative analysis in routine clinical scans and provide scan-independent biomarkers of disease. However, existing tissue properties estimation methods - most often $\mathbf{T_1}$ relaxation, $\mathbf{T_2^*}$ relaxation, and proton density ($\mathbf{PD}$) - require data from multiple scan sessions and cannot estimate all properties from a single clinically available MRI protocol such as the multiecho MRI scan. In addition, the widespread use of non-standard acquisition parameters across clinical imaging sites require estimation methods that can generalize across varying scanner parameters. However, existing learning methods are acquisition protocol specific and cannot estimate from heterogenous clinical data from different imaging sites. In this work we propose an unsupervised deep-learning strategy that employs MRI physics to estimate all three tissue properties from a single multiecho MRI scan session, and generalizes across varying acquisition parameters. The proposed strategy optimizes accurate synthesis of new MRI contrasts from estimated latent tissue properties, enabling unsupervised training, we also employ random acquisition parameters during training to achieve acquisition generalization. We provide the first demonstration of estimating all tissue properties from a single multiecho scan session. We demonstrate improved accuracy and generalizability for tissue property estimation and MRI synthesis.

Amod Jog, P. Ellen Grant, Joseph L. Jacobson et al.

Skullstripping is defined as the task of segmenting brain tissue from a full head magnetic resonance image~(MRI). It is a critical component in neuroimage processing pipelines. Downstream deformable registration and whole brain segmentation performance is highly dependent on accurate skullstripping. Skullstripping is an especially challenging task for infant~(age range 0--18 months) head MRI images due to the significant size and shape variability of the head and the brain in that age range. Infant brain tissue development also changes the $T_1$-weighted image contrast over time, making consistent skullstripping a difficult task. Existing tools for adult brain MRI skullstripping are ill equipped to handle these variations and a specialized infant MRI skullstripping algorithm is necessary. In this paper, we describe a supervised skullstripping algorithm that utilizes three trained fully convolutional neural networks~(CNN), each of which segments 2D $T_1$-weighted slices in axial, coronal, and sagittal views respectively. The three probabilistic segmentations in the three views are linearly fused and thresholded to produce a final brain mask. We compared our method to existing adult and infant skullstripping algorithms and showed significant improvement based on Dice overlap metric~(average Dice of 0.97) with a manually labeled ground truth data set. Label fusion experiments on multiple, unlabeled data sets show that our method is consistent and has fewer failure modes. In addition, our method is computationally very fast with a run time of 30 seconds per image on NVidia P40/P100/Quadro 4000 GPUs.

Juan Eugenio Iglesias, Ricardo Insausti, Garikoitz Lerma-Usabiaga et al.

The human thalamus is a brain structure that comprises numerous, highly specific nuclei. Since these nuclei are known to have different functions and to be connected to different areas of the cerebral cortex, it is of great interest for the neuroimaging community to study their volume, shape and connectivity in vivo with MRI. In this study, we present a probabilistic atlas of the thalamic nuclei built using ex vivo brain MRI scans and histological data, as well as the application of the atlas to in vivo MRI segmentation. The atlas was built using manual delineation of 26 thalamic nuclei on the serial histology of 12 whole thalami from six autopsy samples, combined with manual segmentations of the whole thalamus and surrounding structures (caudate, putamen, hippocampus, etc.) made on in vivo brain MR data from 39 subjects. The 3D structure of the histological data and corresponding manual segmentations was recovered using the ex vivo MRI as reference frame, and stacks of blockface photographs acquired during the sectioning as intermediate target. The atlas, which was encoded as an adaptive tetrahedral mesh, shows a good agreement with with previous histological studies of the thalamus in terms of volumes of representative nuclei. When applied to segmentation of in vivo scans using Bayesian inference, the atlas shows excellent test-retest reliability, robustness to changes in input MRI contrast, and ability to detect differential thalamic effects in subjects with Alzheimer's disease. The probabilistic atlas and companion segmentation tool are publicly available as part of the neuroimaging package FreeSurfer.