Lichi Zhang

A first generation compact microbeam radiation therapy system based on carbon nanotube X-ray technology

We have developed a compact microbeam radiation therapy device using carbon nanotube cathodes to create a linear array of narrow focal line segments on a tungsten anode and a custom collimator assembly to select a slice of the resulting wedge-shaped radiation pattern. Effective focal line width was measured to be 131 μm, resulting in a microbeam width of ∼300 μm. The instantaneous dose rate was projected to be 2 Gy/s at full-power. Peak to valley dose ratio was measured to be >17 when a 1.4 mm microbeam separation was employed. Finally, multiple microbeams were delivered to a mouse with beam paths verified through histology.

Extraction of dynamic functional connectivity from brain grey matter and white matter for MCI classification

Brain functional connectivity (FC) extracted from resting‐state fMRI (RS‐fMRI) has become a popular approach for diagnosing various neurodegenerative diseases, including Alzheimers disease (AD) and its prodromal stage, mild cognitive impairment (MCI). Current studies mainly construct the FC networks between grey matter (GM) regions of the brain based on temporal co‐variations of the blood oxygenation level‐dependent (BOLD) signals, which reflects the synchronized neural activities. However, it was rarely investigated whether the FC detected within the white matter (WM) could provide useful information for diagnosis. Motivated by the recently proposed functional correlation tensors (FCT) computed from RS‐fMRI and used to characterize the structured pattern of local FC in the WM, we propose in this article a novel MCI classification method based on the information conveyed by both the FC between the GM regions and that within the WM regions. Specifically, in the WM, the tensor‐based metrics (e.g., fractional anisotropy [FA], similar to the metric calculated based on diffusion tensor imaging [DTI]) are first calculated based on the FCT and then summarized along each of the major WM fiber tracts connecting each pair of the brain GM regions. This could capture the functional information in the WM, in a similar network structure as the FC network constructed for the GM, based only on the same RS‐fMRI data. Moreover, a sliding window approach is further used to partition the voxel‐wise BOLD signal into multiple short overlapping segments. Then, both the FC and FCT between each pair of the brain regions can be calculated based on the BOLD signal segments in the GM and WM, respectively. In such a way, our method can generate dynamic FC and dynamic FCT to better capture functional information in both GM and WM and further integrate them together by using our developed feature extraction, selection, and ensemble learning algorithms. The experimental results verify that the dynamic FCT can provide valuable functional information in the WM; by combining it with the dynamic FC in the GM, the diagnosis accuracy for MCI subjects can be significantly improved even using RS‐fMRI data alone. Hum Brain Mapp 38:5019–5034, 2017.

Automatic labeling of MR brain images by hierarchical learning of atlas forests.

PURPOSE Automatic brain image labeling is highly demanded in the field of medical image analysis. Multiatlas-based approaches are widely used due to their simplicity and robustness in applications. Also, random forest technique is recognized as an efficient method for labeling, although there are several existing limitations. In this paper, the authors intend to address those limitations by proposing a novel framework based on the hierarchical learning of atlas forests. METHODS Their proposed framework aims to train a hierarchy of forests to better correlate voxels in the MR images with their corresponding labels. There are two specific novel strategies for improving brain image labeling. First, different from the conventional ways of using a single level of random forests for brain labeling, the authors design a hierarchical structure to incorporate multiple levels of forests. In particular, each atlas forest in the bottom level is trained in accordance with each individual atlas, and then the bottom-level forests are clustered based on their capabilities in labeling. For each clustered group, the authors retrain a new representative forest in the higher level by using all atlases associated with the lower-level atlas forests in the current group, as well as the tentative label maps yielded from the lower level. This clustering and retraining procedure is conducted iteratively to yield a hierarchical structure of forests. Second, in the testing stage, the authors also present a novel atlas forest selection method to determine an optimal set of atlas forests from the constructed hierarchical structure (by disabling those nonoptimal forests) for accurately labeling the test image. RESULTS For validating their proposed framework, the authors evaluate it on the public datasets, including Alzheimers disease neuroimaging initiative, Internet brain segmentation repository, and LONI LPBA40. The authors compare the results with the conventional approaches. The experiments show that the use of the two novel strategies can significantly improve the labeling performance. Note that when more levels are constructed in the hierarchy, the labeling performance can be further improved, but more computational time will be also required. CONCLUSIONS The authors have proposed a novel multiatlas-based framework for automatic and accurate labeling of brain anatomies, which can achieve accurate labeling results for MR brain images.

Concatenated spatially-localized random forests for hippocampus labeling in adult and infant MR brain images

Automatic labeling of the hippocampus in brain MR images is highly demanded, as it has played an important role in imaging-based brain studies. However, accurate labeling of the hippocampus is still challenging, partially due to the ambiguous intensity boundary between the hippocampus and surrounding anatomies. In this paper, we propose a concatenated set of spatially-localized random forests for multi-atlas-based hippocampus labeling of adult/infant brain MR images. The contribution in our work is two-fold. First, each forest classifier is trained to label just a specific sub-region of the hippocampus, thus enhancing the labeling accuracy. Second, a novel forest selection strategy is proposed, such that each voxel in the test image can automatically select a set of optimal forests, and then dynamically fuses their respective outputs for determining the final label. Furthermore, we enhance the spatially-localized random forests with the aid of the auto-context strategy. In this way, our proposed learning framework can gradually refine the tentative labeling result for better performance. Experiments show that, regarding the large datasets of both adult and infant brain MR images, our method owns satisfactory scalability by segmenting the hippocampus accurately and efficiently.

Brain atlas fusion from high-thickness diagnostic magnetic resonance images by learning-based super-resolution

It is fundamentally important to fuse the brain atlas from magnetic resonance (MR) images for many imaging-based studies. Most existing works focus on fusing the atlases from high-quality MR images. However, for low-quality diagnostic images (i.e., with high inter-slice thickness), the problem of atlas fusion has not been addressed yet. In this paper, we intend to fuse the brain atlas from the high-thickness diagnostic MR images that are prevalent for clinical routines. The main idea of our works is to extend the conventional groupwise registration by incorporating a novel super-resolution strategy. The contribution of the proposed super-resolution framework is two-fold. First, each high-thickness subject image is reconstructed to be isotropic by the patch-based sparsity learning. Then, the reconstructed isotropic image is enhanced for better quality through the random-forest-based regression model. In this way, the images obtained by the super-resolution strategy can be fused together by applying the groupwise registration method to construct the required atlas. Our experiments have shown that the proposed framework can effectively solve the problem of atlas fusion from the low-quality brain MR images.

Learning of Atlas Forest Hierarchy for Automatic Labeling of MR Brain Images

We propose a multi-atlas-based framework to label brain anatomies in magnetic resonance (MR) images, by constructing a hierarchical structure of atlas forests. We start by training the atlas forests in accordance to individual atlases, and then cluster atlas forests with similar labeling performances into several groups. For each group, a new representative forest is re-trained, based on all atlas images associated with the atlas forests in the group, as well as the tentative label maps output by the clustered atlas forests. This clustering and re-training procedure is conducted iteratively to obtain a hierarchical structure of atlas forests. When applied to an unlabeled image for testing, only the suitable trained atlas forests will be selected from the hierarchical structure. Hence the labeling result of the test image is fused from the outputs of selected atlas forests. Experimental results show that the proposed framework can significantly improve the labeling performance compared to the state-of-the-art method.

Deep embedding convolutional neural network for synthesizing CT image from T1-Weighted MR image

HighlightsWe propose a very deep network architecture for estimating CT images from MR images directly. It learns an end‐to‐end mapping between different imaging modalities, without any patch‐level pre‐ or post‐processing.We present a novel embedding strategy, to embed the tentatively synthesized CT image into the feature maps and further transform these features maps forward for better estimating the final CT image.The experimental results show that our method can be flexibly adapted to different applications. Moreover, our method outperforms the state‐of‐the‐art methods, regarding both the accuracy of estimated CT images and the speed of synthesis process. ABSTRACT Recently, more and more attention is drawn to the field of medical image synthesis across modalities. Among them, the synthesis of computed tomography (CT) image from T1‐weighted magnetic resonance (MR) image is of great importance, although the mapping between them is highly complex due to large gaps of appearances of the two modalities. In this work, we aim to tackle this MR‐to‐CT synthesis task by a novel deep embedding convolutional neural network (DECNN). Specifically, we generate the feature maps from MR images, and then transform these feature maps forward through convolutional layers in the network. We can further compute a tentative CT synthesis from the midway of the flow of feature maps, and then embed this tentative CT synthesis result back to the feature maps. This embedding operation results in better feature maps, which are further transformed forward in DECNN. After repeating this embedding procedure for several times in the network, we can eventually synthesize a final CT image in the end of the DECNN. We have validated our proposed method on both brain and prostate imaging datasets, by also comparing with the state‐of‐the‐art methods. Experimental results suggest that our DECNN (with repeated embedding operations) demonstrates its superior performances, in terms of both the perceptive quality of the synthesized CT image and the run‐time cost for synthesizing a CT image.

Learning-based structurally-guided construction of resting-state functional correlation tensors

Functional magnetic resonance imaging (fMRI) measures changes in blood-oxygenation-level-dependent (BOLD) signals to detect brain activities. It has been recently reported that the spatial correlation patterns of resting-state BOLD signals in the white matter (WM) also give WM information often measured by diffusion tensor imaging (DTI). These correlation patterns can be captured using functional correlation tensor (FCT), which is analogous to the diffusion tensor (DT) obtained from DTI. In this paper, we propose a noise-robust FCT method aiming at further improving its quality, and making it eligible for further neuroscience study. The novel FCT estimation method consists of three major steps: First, we estimate the initial FCT using a patch-based approach for BOLD signal correlation to improve the noise robustness. Second, by utilizing the relationship between functional and diffusion data, we employ a regression forest model to learn the mapping between the initial FCTs and the corresponding DTs using the training data. The learned forest can then be applied to predict the DTI-like tensors given the initial FCTs from the testing fMRI data. Third, we re-estimate the enhanced FCT by utilizing the DTI-like tensors as a feedback guidance to further improve FCT computation. We have demonstrated the utility of our enhanced FCTs in Alzheimers disease (AD) diagnosis by identifying mild cognitive impairment (MCI) patients from normal subjects.

Brain Image Labeling Using Multi-atlas Guided 3D Fully Convolutional Networks

Automatic labeling of anatomical structures in brain images plays an important role in neuroimaging analysis. Among all methods, multi-atlas based segmentation methods are widely used, due to their robustness in propagating prior label information. However, non-linear registration is always needed, which is time-consuming. Alternatively, the patch-based methods have been proposed to relax the requirement of image registration, but the labeling is often determined independently by the target image information, without getting direct assistance from the atlases. To address these limitations, in this paper, we propose a multi-atlas guided 3D fully convolutional networks (FCN) for brain image labeling. Specifically, multi-atlas based guidance is incorporated during the network learning. Based on this, the discriminative of the FCN is boosted, which eventually contribute to accurate prediction. Experiments show that the use of multi-atlas guidance improves the brain labeling performance.

Feature selection based on iterative canonical correlation analysis for automatic diagnosis of Parkinson’s disease

Parkinsons disease (PD) is a major progressive neurodegenerative disorder. Accurate diagnosis of PD is crucial to control the symptoms appropriately. However, its clinical diagnosis mostly relies on the subjective judgment of physicians and the clinical symptoms that often appear late. Recent neuroimaging techniques, along with machine learning methods, provide alternative solutions for PD screening. In this paper, we propose a novel feature selection technique, based on iterative canonical correlation analysis (ICCA), to investigate the roles of different brain regions in PD through T1-weighted MR images. First of all, gray matter and white matter tissue volumes in brain regions of interest are extracted as two feature vectors. Then, a small group of significant features were selected using the iterative structure of our proposed ICCA framework from both feature vectors. Finally, the selected features are used to build a robust classifier for automatic diagnosis of PD. Experimental results show that the proposed feature selection method results in better diagnosis accuracy, compared to the baseline and state-of-the-art methods.