论文标题
3D-EPI Blip-up/down获取(BUDA),带有Caipi和关节Hankel结构性低级重建,用于快速无失真的高分辨率T2*映射
3D-EPI Blip-Up/Down Acquisition (BUDA) with CAIPI and Joint Hankel Structured Low-Rank Reconstruction for Rapid Distortion-Free High-Resolution T2* Mapping
论文作者
论文摘要
目的:这项工作旨在开发一种新型的无失真3D-EPI采集和图像重建技术,以实现快速,健壮,高分辨率,全脑成像以及定量T2*映射。方法:3D-Blip-UP和-Down采集(3D-BUDA)序列是为单echo和多回声3D GRE-EPI成像设计的,使用多个带有blip-up和-down读数的镜头来编码B0字段映射信息。互补的K空间覆盖范围是在整个镜头上平行成像(CAIPI)中的受控混叠来实现的。对于图像重建,采用了一种迭代硬质势算法来最大程度地减少将现场图信息通知的并行成像与多弹射3D-BUDA数据的结构性低率约束结合的成本函数。将3D-BUDA扩展到多回波成像允许T2*映射。为此,我们提出沿回声和射击尺寸构建关节汉克尔矩阵,以改善重建。结果:对体内多回波数据的实验结果表明,通过进行联合重建以及回声和射击尺寸,与标准3D-BUDA重建相比,重建精度可提高重建精度。 CAIPI采样进一步显示以增强图像质量。对于t2*映射,来自3D连接 - caipi-buda和参考多回声GRE的T2*值在Bland-Altman分析量化的一致性范围内。结论:所提出的技术使快速3D无失真的高分辨率成像和T2*映射。具体而言,3D-BUDA在22 s时在3 t和9 s的7 t扫描仪上启用1毫米各向同性的全脑成像。多回波3D-BUDA与Caipi采集和关节重建的组合可以使无失真的全脑T2*在47 s中以1.1x1.1x1.0 mmm3分辨率分辨率。
Purpose: This work aims to develop a novel distortion-free 3D-EPI acquisition and image reconstruction technique for fast and robust, high-resolution, whole-brain imaging as well as quantitative T2* mapping. Methods: 3D-Blip-Up and -Down Acquisition (3D-BUDA) sequence is designed for both single- and multi-echo 3D GRE-EPI imaging using multiple shots with blip-up and -down readouts to encode B0 field map information. Complementary k-space coverage is achieved using controlled aliasing in parallel imaging (CAIPI) sampling across the shots. For image reconstruction, an iterative hard-thresholding algorithm is employed to minimize the cost function that combines field map information informed parallel imaging with the structured low-rank constraint for multi-shot 3D-BUDA data. Extending 3D-BUDA to multi-echo imaging permits T2* mapping. For this, we propose constructing a joint Hankel matrix along both echo and shot dimensions to improve the reconstruction. Results: Experimental results on in vivo multi-echo data demonstrate that, by performing joint reconstruction along with both echo and shot dimensions, reconstruction accuracy is improved compared to standard 3D-BUDA reconstruction. CAIPI sampling is further shown to enhance the image quality. For T2* mapping, T2* values from 3D-Joint-CAIPI-BUDA and reference multi-echo GRE are within limits of agreement as quantified by Bland-Altman analysis. Conclusions: The proposed technique enables rapid 3D distortion-free high-resolution imaging and T2* mapping. Specifically, 3D-BUDA enables 1-mm isotropic whole-brain imaging in 22 s at 3 T and 9 s on a 7 T scanner. The combination of multi-echo 3D-BUDA with CAIPI acquisition and joint reconstruction enables distortion-free whole-brain T2* mapping in 47 s at 1.1x1.1x1.0 mm3 resolution.