IEEE Trans Med Imaging. 2019 Aug;38(8):1801-1811. doi: 10.1109/TMI.2019.2896085. Epub 2019 Jan 31.
Quantitative magnetic resonance imaging (MRI) is of great value to both clinical diagnosis and scientific research. However, most MRI experiments remain qualitative, especially dynamic MRI, because repeated sampling with variable weighting parameter makes quantitative imaging time-consuming and sensitive to motion artifacts. A single-shot quantitative T mapping method based on multiple overlapping-echo acquisition (dubbed MOLED-4) was proposed to obtain reliable T mapping in milliseconds. Different from traditional MRI acceleration methods, such as compressed sensing and parallel imaging, MOLED-4 accelerates quantitative T mapping via synchronized multisampling and then deep learning to map the complex nonlinear relationship that is difficult to solve by traditional optimization-based methods. The results of simulation, phantom, and in vivo human brain experiments show the great performance of the proposed method. The principle of MOLED-4 may be extended to other ultrafast quantitative parameter mappings and potentially lead to new dynamic MRI with high efficiency to catch quantitative variation of tissue properties.
定量磁共振成像(MRI)对临床诊断和科学研究具有重要价值。然而,大多数 MRI 实验仍然是定性的,特别是动态 MRI,因为重复采样具有可变的加权参数使得定量成像既耗时又容易受到运动伪影的影响。提出了一种基于多次重叠回波采集的单次定量 T 映射方法(称为 MOLED-4),可在毫秒内获得可靠的 T 映射。与传统的 MRI 加速方法(如压缩感知和并行成像)不同,MOLED-4 通过同步多采样和深度学习来加速定量 T 映射,以映射传统基于优化的方法难以解决的复杂非线性关系。模拟、体模和活体人脑实验的结果表明了该方法的优异性能。MOLED-4 的原理可以扩展到其他超快速定量参数映射,并有可能导致具有高效率的新型动态 MRI,以捕捉组织特性的定量变化。