Stack-Sanchez Pablo, Beaulieu Christian, Gross Donald W
Department of Biomedical Engineering, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Department of Biomedical Engineering, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada; Department of Radiology and Diagnostic Imaging, Faculty of Medicine and Dentistry, University of Alberta, Edmonton, Alberta, Canada.
Magn Reson Imaging. 2025 Oct;122:110443. doi: 10.1016/j.mri.2025.110443. Epub 2025 Jun 2.
While high resolution diffusion tensor imaging (DTI) at 1 mm isotropic can detect focal lesions of the hippocampus in temporal lobe epilepsy (TLE), faster acquisition times would facilitate potential clinical implementation. The purpose here is to assess different published denoising algorithms to overcome the low signal-to-noise ratio and accelerate 1 mm isotropic DTI of the human hippocampus at 3 T while maintaining diffusivity metric accuracy and image quality for focal lesion detection in TLE. The previously published 5.5 min protocol of 110 diffusion images per slice (10 directions × 10 averages and 10 b = 0 s/mm) was assessed for subsets of 1-10 averages (same 10 directions) that were denoised using four algorithms that have been applied to other diffusion MRI datasets. In healthy controls, the variance-stabilizing transformation and optimal singular-value manipulation (VST) and Non-Local Spatial and Angular Matching (NLSAM) denoising greatly improved image quality while minimizing voxels with spurious extremes of fractional anisotropy (FA) or mean diffusivity (MD) down to 4 averages (i.e. 40 diffusion images and 4 b = 0 s/mm) in healthy controls. The identification of focal lesions indicated by elevated MD and alterations of internal micro-architecture with only 4 averages were comparable to the full data set of 10 averages. Therefore, denoising of 1 mm isotropic DTI of the hippocampus enables a clinically feasible scan time of 2.2 min at 3 T that can be used for the detection of focal hippocampal lesions in TLE, as well as other neurological disorders such as multiple sclerosis, dementia and Alzheimer's disease.
虽然1毫米各向同性的高分辨率扩散张量成像(DTI)能够检测颞叶癫痫(TLE)中海马体的局灶性病变,但更快的采集时间将有助于其在临床上的潜在应用。本文的目的是评估不同的已发表去噪算法,以克服低信噪比问题,并在3T磁场下加速对人类海马体进行1毫米各向同性DTI扫描,同时保持扩散指标的准确性和图像质量,用于检测TLE中的局灶性病变。对先前发表的每切片110幅扩散图像(10个方向×10次平均,10个b = 0 s/mm²)的5.5分钟扫描方案,评估了1至10次平均(相同的10个方向)的子集,这些子集使用已应用于其他扩散MRI数据集的四种算法进行去噪。在健康对照中,方差稳定变换和最优奇异值处理(VST)以及非局部空间和角度匹配(NLSAM)去噪极大地改善了图像质量,同时将具有伪极端分数各向异性(FA)或平均扩散率(MD)的体素数量降至最低,在健康对照中低至4次平均(即40幅扩散图像和4个b = 0 s/mm²)。由MD升高和内部微结构改变所指示的局灶性病变的识别,仅4次平均时与10次平均的完整数据集相当。因此,海马体1毫米各向同性DTI的去噪能够在3T磁场下实现2.2分钟的临床可行扫描时间,可用于检测TLE中的海马体局灶性病变,以及其他神经系统疾病,如多发性硬化症、痴呆症和阿尔茨海默病。