IEEE Trans Med Imaging. 2019 Oct;38(10):2364-2374. doi: 10.1109/TMI.2019.2899328. Epub 2019 Feb 13.
Magnetic resonance fingerprinting (MRF) is a quantitative imaging technique that can simultaneously measure multiple important tissue properties of human body. Although MRF has demonstrated improved scan efficiency as compared to conventional techniques, further acceleration is still desired for translation into routine clinical practice. The purpose of this paper is to accelerate MRF acquisition by developing a new tissue quantification method for MRF that allows accurate quantification with fewer sampling data. Most of the existing approaches use the MRF signal evolution at each individual pixel to estimate tissue properties, without considering the spatial association among neighboring pixels. In this paper, we propose a spatially constrained quantification method that uses the signals at multiple neighboring pixels to better estimate tissue properties at the central pixel. Specifically, we design a unique two-step deep learning model that learns the mapping from the observed signals to the desired properties for tissue quantification, i.e.: 1) with a feature extraction module for reducing the dimension of signals by extracting a low-dimensional feature vector from the high-dimensional signal evolution and 2) a spatially constrained quantification module for exploiting the spatial information from the extracted feature maps to generate the final tissue property map. A corresponding two-step training strategy is developed for network training. The proposed method is tested on highly undersampled MRF data acquired from human brains. Experimental results demonstrate that our method can achieve accurate quantification for T1 and T2 relaxation times by using only 1/4 time points of the original sequence (i.e., four times of acceleration for MRF acquisition).
磁共振指纹成像(MRF)是一种定量成像技术,可同时测量人体的多种重要组织特性。尽管与传统技术相比,MRF 已经证明了扫描效率的提高,但为了将其转化为常规临床实践,仍然需要进一步加速。本文的目的是通过开发一种新的 MRF 组织量化方法来加速 MRF 的采集,该方法允许使用更少的采样数据进行准确的量化。大多数现有的方法都使用每个像素的 MRF 信号演化来估计组织特性,而不考虑相邻像素之间的空间关联。在本文中,我们提出了一种空间约束量化方法,该方法使用多个相邻像素的信号来更好地估计中心像素处的组织特性。具体来说,我们设计了一个独特的两步深度学习模型,该模型从观察到的信号学习到所需的组织特性的映射,即:1)使用特征提取模块,通过从高维信号演化中提取低维特征向量来降低信号的维度,2)空间约束量化模块,用于从提取的特征图中利用空间信息生成最终的组织属性图。为网络训练开发了相应的两步训练策略。该方法在从人脑采集的高度欠采样的 MRF 数据上进行了测试。实验结果表明,我们的方法仅使用原始序列的四分之一时间点(即 MRF 采集的四倍加速)即可实现 T1 和 T2 弛豫时间的精确量化。