Proceedings. IEEE International Symposium on Biomedical Imaging最新文献

Alzheimer's Disease (AD) is a neurodegenerative disorder characterized by progressive cognitive degeneration and motor impairment, affecting millions worldwide. Mapping the progression of AD is crucial for early detection of loss of brain function, timely intervention, and development of effective treatments. However, accurate measurements of disease progression are still challenging at present. This study presents a novel approach to understanding the heterogeneous pathways of AD through longitudinal biomarker data from medical imaging and other modalities. We propose an analytical pipeline adopting two popular machine learning methods from the single-cell transcriptomics domain, PHATE and Slingshot, to project multimodal biomarker trajectories to a low-dimensional space. These embeddings serve as our pseudotime estimates. We applied this pipeline to the Alzheimer's Disease Neuroimaging Initiative (ADNI) dataset to align longitudinal data across individuals at various disease stages. Our approach mirrors the technique used to cluster single-cell data into cell types based on developmental timelines. Our pseudotime estimates revealed distinct patterns of disease evolution and biomarker changes over time, providing a deeper understanding of the temporal dynamics of AD. The results show the potential of the approach in the clinical domain of neurodegenerative diseases, enabling more precise disease modeling and early diagnosis.

Physics-driven deep learning (PD-DL) has become a powerful tool for accelerated MRI. Recent developments have also developed unsupervised learning for PD-DL, including self-supervised learning. However, at very high acceleration rates, such approaches show performance deterioration. In this study, we propose to use cyclic-consistency (CC) to improve self-supervised learning for highly accelerated MRI. In our proposed CC, simulated measurements are obtained by undersampling the network output using patterns drawn from the same distribution as the true one. The reconstructions of these simulated measurements are obtained using the same network, which are then compared to the acquired data at the true sampling locations. This CC approach is used in conjunction with a masking-based self-supervised loss. Results show that the proposed method can substantially reduce aliasing artifacts at high acceleration rates, including rate 6 and 8 fastMRI knee imaging and 20-fold HCP-style fMRI.

Parkinson's Disease (PD) affects millions globally, impacting movement. Prior research utilized deep learning for PD prediction, primarily focusing on medical images, neglecting the data's underlying manifold structure. This work proposes a multimodal approach encompassing both image and non-image features, leveraging contrastive cross-view graph fusion for PD classification. We introduce a novel multimodal co-attention module, integrating embeddings from separate graph views derived from low-dimensional representations of images and clinical features. This enables more robust and structured feature extraction for improved multi-view data analysis. Additionally, a simplified contrastive loss-based fusion method is devised to enhance cross-view fusion learning. Our graph-view multimodal approach achieves an accuracy of 91% and an area under the receiver operating characteristic curve (AUC) of 92.8% in five-fold cross-validation. It also demonstrates superior predictive capabilities on non-image data compared to solely machine learning-based methods.

Alzheimer's disease (AD) is a neurodegenerative disorder, and timely diagnosis is crucial for early interventions. AD is known to have disruptive local and global brain neural connections that may be instrumental in understanding and extracting specific biomarkers. Existing machine-learning approaches are mostly based on convolutional neural network (CNN) and standard vision transformer (ViT) models, which may not sufficiently capture the multidimensional local and global patterns indicative of AD. Therefore, in this paper, we propose a novel approach called PVTAD to classify AD and cognitively normal (CN) cases using pretrained pyramid vision transformer (PVT) and white matter (WM) of T1-weighted structural MRI (sMRI) data. Our approach combines the advantages of CNN and standard ViT to extract both local and global features indicative of AD from the WM coronal middle slices. We performed experiments on subjects with T1-weighed MPRAGE sMRI scans from the ADNI dataset. Our results demonstrate that the PVTAD achieves an average accuracy of 97.7% and an F1-score of 97.6%, outperforming the single and parallel CNN and standard ViT based on sMRI data for AD vs. CN classification. Our code is available at https://github.com/pcdslab/PVTAD.

End-to-End (E2E) unrolled optimization frameworks show promise for Magnetic Resonance (MR) image recovery, but suffer from high memory usage during training. In addition, these deterministic approaches do not offer opportunities for sampling from the posterior distribution. In this paper, we introduce a memory-efficient approach for E2E learning of the posterior distribution. We represent this distribution as the combination of a data-consistency-induced likelihood term and an energy model for the prior, parameterized by a Convolutional Neural Network (CNN). The CNN weights are learned from training data in an E2E fashion using maximum likelihood optimization. The learned model enables the recovery of images from undersampled measurements using the Maximum A Posteriori (MAP) optimization. In addition, the posterior model can be sampled to derive uncertainty maps about the reconstruction. Experiments on parallel MR image reconstruction show that our approach performs comparable to the memory-intensive E2E unrolled algorithm, performs better than its memory-efficient counterpart, and can provide uncertainty maps. Our framework paves the way towards MR image reconstruction in 3D and higher dimensions.

High-resolution fMRI provides a window into the brain's mesoscale organization. Yet, higher spatial resolution increases scan times, to compensate for the low signal and contrast-to-noise ratio. This work introduces a deep learning-based 3D super-resolution (SR) method for fMRI. By incorporating a resolution-agnostic image augmentation framework, our method adapts to varying voxel sizes without retraining. We apply this innovative technique to localize fine-scale motion-selective sites in the early visual areas. Detection of these sites typically requires ≤ 1mm isotropic data, whereas here, we visualize them based on lower resolution (2-3mm isotropic) fMRI data. Remarkably, the super-resolved fMRI is able to recover high-frequency detail of the interdigitated organization of these sites (relative to the color-selective sites), even with training data sourced from different subjects and experimental paradigms - including non-visual resting-state fMRI, underscoring its robustness and versatility. Quantitative and qualitative results indicate that our method has the potential to enhance the spatial resolution of fMRI, leading to a drastic reduction in acquisition time.

Morphometricity examines the global statistical association between brain morphology and an observable trait, and is defined as the proportion of the trait variation attributable to brain morphology. In this work, we propose an accurate morphometricity estimator based on the generalized random effects (GRE) model, and perform morphometricity analyses on five cognitive traits in an Alzheimer's study. Our empirical study shows that the proposed GRE model outperforms the widely used LME model on both simulation and real data. In addition, we extend morphometricity estimation from the whole brain to the focal-brain level, and examine and quantify both global and regional neuroanatomical signatures of the cognitive traits. Our global analysis reveals 1) a relatively strong anatomical basis for ADAS13, 2) intermediate ones for MMSE, CDRSB and FAQ, and 3) a relatively weak one for RAVLT.learning. The top associations identified from our regional morphometricity analysis include those between all five cognitive traits and multiple regions such as hippocampus, amygdala, and inferior lateral ventricles. As expected, the identified regional associations are weaker than the global ones. While the whole brain analysis is more powerful in identifying higher morphometricity, the regional analysis could localize the neuroanatomical signatures of the studied cognitive traits and thus provide valuable information in imaging and cognitive biomarker discovery for normal and/or disordered brain research.

Real-time dynamic MRI is important for visualizing time-varying processes in several applications, including cardiac imaging, where it enables free-breathing images of the beating heart without ECG gating. However, current real-time MRI techniques commonly face challenges in achieving the required spatio-temporal resolutions due to limited acceleration rates. In this study, we propose a deep learning (DL) technique for improving the estimation of stationary outer-volume signal from shifted time-interleaved undersampling patterns. Our approach utilizes the pseudo-periodic nature of the ghosting artifacts arising from the moving organs. Subsequently, this estimated outer-volume signal is subtracted from individual timeframes of the real-time MR time series, and each timeframe is reconstructed individually using physics-driven DL methods. Results show improved image quality at high acceleration rates, where conventional methods fail.

High-quality training data are not always available in dynamic MRI. To address this, we propose a self-supervised deep learning method called deep image prior with structured sparsity (DISCUS) for reconstructing dynamic images. DISCUS is inspired by deep image prior (DIP) and recovers a series of images through joint optimization of network parameters and input code vectors. However, DISCUS additionally encourages group sparsity on frame-specific code vectors to discover the low-dimensional manifold that describes temporal variations across frames. Compared to prior work on manifold learning, DISCUS does not require specifying the manifold dimensionality. We validate DISCUS using three numerical studies. In the first study, we simulate a dynamic Shepp-Logan phantom with frames undergoing random rotations, translations, or both, and demonstrate that DISCUS can discover the dimensionality of the underlying manifold. In the second study, we use data from a realistic late gadolinium enhancement (LGE) phantom to compare DISCUS with compressed sensing (CS) and DIP, and to demonstrate the positive impact of group sparsity. In the third study, we use retrospectively undersampled single-shot LGE data from five patients to compare DISCUS with CS reconstructions. The results from these studies demonstrate that DISCUS outperforms CS and DIP, and that enforcing group sparsity on the code vectors helps discover true manifold dimensionality and provides additional performance gain.

Modern MRI scanners utilize one or more arrays of small receive-only coils to collect k-space data. The sensitivity maps of the coils, when estimated using traditional methods, differ from the true sensitivity maps, which are generally unknown. Consequently, the reconstructed MR images exhibit undesired spatial variation in intensity. These intensity variations can be at least partially corrected using pre-scan data. In this work, we propose an intensity correction method that utilizes pre-scan data. For demonstration, we apply our method to a digital phantom, as well as to cardiac MRI data collected from a commercial scanner by Siemens Healthineers. The code is available at https://github.com/OSU-MR/SCC.