Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, USA; Department of Radiology, Harvard Medical School, Boston, MA, USA; Center for Brain Imaging Science and Technology, Key Laboratory for Biomedical Engineering of Ministry of Education, College of Biomedical Engineering and Instrumental Science, Zhejiang University, Hangzhou, Zhejiang, China.
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, USA; Department of Radiology, Harvard Medical School, Boston, MA, USA.
Neuroimage. 2019 Jul 1;194:291-302. doi: 10.1016/j.neuroimage.2019.04.002. Epub 2019 Apr 3.
To propose a virtual coil (VC) acquisition/reconstruction framework to improve highly accelerated single-shot EPI (SS-EPI) and generalized slice dithered enhanced resolution (gSlider) acquisition in high-resolution diffusion imaging (DI).
For robust VC-GRAPPA reconstruction, a background phase correction scheme was developed to match the image phase of the reference data with the corrupted phase of the accelerated diffusion-weighted data, where the corrupted phase of the diffusion data varies from shot to shot. A G prewinding-blip was also added to the EPI acquisition, to create a shifted-k sampling strategy that allows for better exploitation of VC concept in the reconstruction. To evaluate the performance of the proposed methods, 1.5 mm isotropic whole-brain SS-EPI and 860 μm isotropic whole-brain gSlider-EPI diffusion data were acquired at an acceleration of 8-9 fold. Conventional and VC-GRAPPA reconstructions were performed and compared, and corresponding g-factors were calculated.
The proposed VC reconstruction substantially improves the image quality of both SS-EPI and gSlider-EPI, with reduced g-factor noise and reconstruction artifacts when compared to the conventional method. This has enabled high-quality low-noise diffusion imaging to be performed at 8-9 fold acceleration.
The proposed VC acquisition/reconstruction framework improves the reconstruction of DI at high accelerations. The ability to now employ such high accelerations will allow DI with EPI at reduced distortion and faster scan time, which should be beneficial for many clinical and neuroscience applications.
提出一种虚拟线圈(VC)采集/重建框架,以改善高分辨率扩散成像(DI)中高加速单次激发 EPI(SS-EPI)和广义切片抖动增强分辨率(gSlider)采集。
为了实现稳健的 VC-GRAPPA 重建,开发了一种背景相位校正方案,以匹配参考数据的图像相位与加速扩散加权数据的受扰相位,其中扩散数据的受扰相位随每个激发而变化。还在 EPI 采集过程中添加了 G 预绕射脉冲,以创建偏移-k 采样策略,从而在重建中更好地利用 VC 概念。为了评估所提出方法的性能,在 8-9 倍加速下采集了 1.5mm 各向同性全脑 SS-EPI 和 860μm 各向同性全脑 gSlider-EPI 扩散数据。进行了常规和 VC-GRAPPA 重建,并进行了比较,并计算了相应的 g 因子。
与常规方法相比,所提出的 VC 重建显著改善了 SS-EPI 和 gSlider-EPI 的图像质量,降低了 g 因子噪声和重建伪影。这使得在 8-9 倍加速下能够进行高质量、低噪声的扩散成像。
所提出的 VC 采集/重建框架提高了高加速下的 DI 重建质量。现在能够采用如此高的加速度,将使 EPI 扩散成像具有更低的失真和更快的扫描时间,这对于许多临床和神经科学应用应该是有益的。