Wang Zepeng, Sutton Bradley P, Lam Fan
Department of Bioengineering, University of Illinois Urbana-Champaign, Urbana, Illinois, USA.
Beckman Institute for Advanced Science and Technology, University of Illinois Urbana-Champaign, Urbana, Illinois, USA.
Magn Reson Med. 2025 Aug;94(2):450-469. doi: 10.1002/mrm.30479. Epub 2025 Mar 10.
To achieve high-resolution, three-dimensional (3D) quantitative diffusion-weighted MR spectroscopic imaging (DW-MRSI) for molecule-specific microstructural imaging of the brain.
We introduced and integrated several innovative acquisition and processing strategies for DW-MRSI: (a) a new double-spin-echo sequence combining selective excitation, bipolar diffusion encoding, rapid spatiospectral sampling, interleaved water spectroscopic imaging data, and a special sparsely sampled echo-volume-imaging (EVI)-based navigator, (b) a rank-constrained time-resolved reconstruction from the EVI data to capture spatially varying phases, (c) a model-based phase correction for DW-MRSI data, and (d) a multi-b-value subspace-based method for water/lipids removal and spatiospectral reconstruction using learned metabolite subspaces, and e) a hybrid subspace and parametric model-based parameter estimation strategy. Phantom and in vivo experiments were performed to validate the proposed method and demonstrate its ability to map metabolite-specific diffusion parameters in 3D.
The proposed method generated reproducible metabolite diffusion coefficient estimates, consistent with those from a standard single-voxel DW spectroscopy (SV-DWS) method. High-SNR multi-molecular mean diffusivity (MD) maps can be obtained at a 6.9 6.9 7.0 mm nominal resolution with large 3D brain coverage. High-resolution (4.4 4.4 5.6 mm ) metabolite and diffusion coefficient maps can be obtained within 20 mins for the first time. Tissue-dependent metabolite MDs were observed, i.e., larger MDs for NAA, creatine, and choline in white matter than gray matter, with region-specific differences.
We demonstrated an unprecedented capability of simultaneous, high-resolution metabolite and diffusion parameter mapping. This imaging capability has strong potential to offer richer molecular and tissue-compartment-specific microstructural information for various clinical and neuroscience applications.
实现用于大脑分子特异性微观结构成像的高分辨率三维(3D)定量扩散加权磁共振波谱成像(DW-MRSI)。
我们为DW-MRSI引入并整合了几种创新的采集和处理策略:(a)一种新的双自旋回波序列,结合选择性激发、双极扩散编码、快速空间谱采样、交错水磁共振波谱成像数据以及一种基于稀疏采样回波体积成像(EVI)的特殊导航器;(b)从EVI数据进行秩约束时间分辨重建以捕获空间变化的相位;(c)基于模型的DW-MRSI数据相位校正;(d)一种基于多b值子空间的方法,用于使用学习到的代谢物子空间去除水/脂质并进行空间谱重建;以及(e)一种基于混合子空间和参数模型的参数估计策略。进行了体模和体内实验以验证所提出的方法,并证明其在3D中绘制代谢物特异性扩散参数的能力。
所提出的方法生成了可重复的代谢物扩散系数估计值,与标准单体素DW波谱(SV-DWS)方法得到的结果一致。可以在标称分辨率为6.9×6.9×7.0 mm的情况下获得具有高信噪比的多分子平均扩散率(MD)图,且3D脑覆盖范围大。首次能够在20分钟内获得高分辨率(4.4×4.4×5.6 mm)的代谢物和扩散系数图。观察到了组织依赖性代谢物MD,即白质中NAA、肌酸和胆碱的MD大于灰质,且存在区域特异性差异。
我们展示了同时进行高分辨率代谢物和扩散参数映射的前所未有的能力。这种成像能力具有强大的潜力,可为各种临床和神经科学应用提供更丰富的分子和组织隔室特异性微观结构信息。