Neural network algorithms predict new diffusion MRI data for multi-compartmental analysis of brain microstructure in a clinical setting

人类连接体项目 磁共振弥散成像 卷积神经网络 扩散成像 计算机科学 模式识别(心理学) 人工智能 人工神经网络 磁共振成像 医学 神经科学 功能连接 放射科 生物
作者
Cayden Murray,Olayinka Oladosu,Manish Joshi,Shannon Kolind,Jiwon Oh,Yunyan Zhang
出处
期刊:Magnetic Resonance Imaging [Elsevier BV]
卷期号:102: 9-19
标识
DOI:10.1016/j.mri.2023.03.023
摘要

High angular resolution diffusion imaging (HARDI) is a promising method for advanced analysis of brain microstructure. However, comprehensive HARDI analysis requires multiple acquisitions of diffusion images (multi-shell HARDI), which is time consuming and often impractical in clinical settings. This study aimed to establish neural network models that can predict new diffusion datasets from clinically feasible brain diffusion MRI for multi-shell HARDI. The development included 2 algorithms: multi-layer perceptron (MLP) and convolutional neural network (CNN). Both followed a voxel-based approach for model training (70%), validation (15%), and testing (15%). The investigations involved 2 multi-shell HARDI datasets: 1) 11 healthy subjects from the Human Connectome Project (HCP); and 2) 10 local subjects with multiple sclerosis (MS). To assess outcomes, we conducted neurite orientation dispersion and density imaging using both predicted and original data and compared their orientation dispersion index (ODI) and neurite density index (NDI) in different brain tissues with 2 measures: peak signal-to-noise ratio (PSNR) and structural similarity index measure (SSIM). Results showed that both models achieved robust predictions, which provided competitive ODI and NDI, especially in brain white matter. The CNN outperformed MLP with the HCP data on both PSNR (p < 0.001) and SSIM (p < 0.01). With the MS data, the models performed similarly. Overall, the optimized neural networks can help generate non-acquired brain diffusion MRI, which will make advanced HARDI analysis possible in clinical practice following further validation. Enabling detailed characterization of brain microstructure will allow enhanced understanding of brain function in both health and disease.

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