Background: There is growing interest in the neuroscience community in estimating and mapping microscopic properties of brain tissue non-invasively using magnetic resonance measurements. Machine learning methods are actively investigated to predict the signals measured in diffusion magnetic resonance imaging (dMRI).
New Method: We applied the neural architecture search (NAS) to train a recurrent neural network to generate a multilayer perceptron to predict the dMRI data of unknown signals based on the different acquisition parameters and training data. The search space of NAS is the number of neurons in each layer of the multilayer perceptron network. To our best knowledge, this is the first time to apply NAS to solve the dMRI signal prediction problem.
Results: The experimental results demonstrate that the proposed NAS method can achieve fast training and predict dMRI signals accurately. For dMRI signals with four acquisition strategies of double diffusion encoding (DDE), double oscillating diffusion encoding (DODE), multi-shell and DSI-like pulsed gradient spin-echo (PGSE), the mean squared errors of the multilayer perceptron network designed by NAS are 0.0043, 0.0034, 0.0147 and 0.0199, respectively.
Comparison With Existing Method(s): We also compared NAS with other machine learning prediction methods, such as support vector regression (SVR), decision tree (DT) and random forest (RF), k-nearest neighbors (KNN), adaboost regressor (AR), gradient boosting regressor (GBR) and extra-trees regressor (ET). NAS achieved the better prediction performance in most cases.
Conclusion: In this study, NAS was developed for the prediction of dMRI signals and could become an effective prediction tool.
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http://dx.doi.org/10.1016/j.jneumeth.2021.109389 | DOI Listing |
Aging Cell
January 2025
Cardiff University Brain Research Imaging Centre (CUBRIC), School of Psychology, Cardiff University, Cardiff, UK.
Healthy brain aging involves changes in both brain structure and function, including alterations in cellular composition and microstructure across brain regions. Unlike diffusion-weighted MRI (dMRI), diffusion-weighted MR spectroscopy (dMRS) can assess cell-type specific microstructural changes, providing indirect information on both cell composition and microstructure through the quantification and interpretation of metabolites' diffusion properties. This work investigates age-related changes in the higher-order diffusion properties of total N-Acetyl-aspartate (neuronal biomarker), total choline (glial biomarker), and total creatine (both neuronal and glial biomarker) beyond the classical apparent diffusion coefficient in cerebral and cerebellar gray matter of healthy human brain.
View Article and Find Full Text PDFbioRxiv
December 2024
Athinoula A. Martinos Center for Biomedical Imaging, Charlestown, MA, United States.
Evaluating tissue microstructure and membrane integrity in the living human brain through diffusion-water exchange imaging is challenging due to requirements for a high signal-to-noise ratio and short diffusion times dictated by relatively fast exchange processes. The goal of this work was to demonstrate the feasibility of imaging of tissue micro-geometries and water exchange within the brain gray matter using the state-of-the-art Connectome 2.0 scanner equipped with an ultra-high-performance gradient system (maximum gradient strength=500 mT/m, maximum slew rate=600 T/m/s).
View Article and Find Full Text PDFNetw Neurosci
December 2024
Laufer Center for Physical and Quantitative Biology, Stony Brook University, Stony Brook, NY, USA.
The integration-segregation framework is a popular first step to understand brain dynamics because it simplifies brain dynamics into two states based on global versus local signaling patterns. However, there is no consensus for how to best define the two states. Here, we map integration and segregation to order and disorder states from the Ising model in physics to calculate state probabilities, and , from functional MRI data.
View Article and Find Full Text PDFDiffusion-weighted magnetic resonance imaging (dMRI) permits a detailed in-vivo analysis of neuroanatomical microstructure, invaluable for clinical and population studies. However, many measurements with different diffusion-encoding directions and possibly -values are necessary to infer the underlying tissue microstructure within different imaging voxels accurately. Two challenges particularly limit the utility of dMRI: limit feasible scans to only a few directional measurements, and the makes it difficult to combine datasets.
View Article and Find Full Text PDFMagn Reson Imaging
January 2025
Department of Radiology, Stanford University, Stanford, CA, USA; Department of Electrical Engineering, Stanford University, Stanford, CA, USA. Electronic address:
Purpose: BUDA-cEPI has been shown to achieve high-quality, high-resolution diffusion magnetic resonance imaging (dMRI) with fast acquisition time, particularly when used in conjunction with S-LORAKS reconstruction. However, this comes at a cost of more complex reconstruction that is computationally prohibitive. In this work we develop rapid reconstruction pipeline for BUDA-cEPI to pave the way for its deployment in routine clinical and neuroscientific applications.
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