Neurosciences Research Section, Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom.
Centre for Affective Disorders, Department of Psychological Medicine, Division of Academic Psychiatry, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, United Kingdom.
Magn Reson Med. 2022 Dec;88(6):2532-2547. doi: 10.1002/mrm.29420. Epub 2022 Aug 31.
Quasi-diffusion MRI (QDI) is a novel quantitative technique based on the continuous time random walk model of diffusion dynamics. QDI provides estimates of the diffusion coefficient, in mm s and a fractional exponent, , defining the non-Gaussianity of the diffusion signal decay. Here, the b-value selection for rapid clinical acquisition of QDI tensor imaging (QDTI) data is optimized.
Clinically appropriate QDTI acquisitions were optimized in healthy volunteers with respect to a multi-b-value reference (MbR) dataset comprising 29 diffusion-sensitized images arrayed between and 5000 s mm . The effects of varying maximum b-value ( ), number of b-value shells, and the effects of Rician noise were investigated.
QDTI measures showed dependence, most significantly for in white matter, which monotonically decreased with higher leading to improved tissue contrast. Optimized 2 b-value shell acquisitions showed small systematic differences in QDTI measures relative to MbR values, with overestimation of and underestimation of in white matter, and overestimation of and anisotropies in gray and white matter. Additional shells improved the accuracy, precision, and reliability of QDTI estimates with 3 and 4 shells at s mm , and 4 b-value shells at s mm , providing minimal bias in and compared to the MbR.
A highly detailed optimization of non-Gaussian dMRI for in vivo brain imaging was performed. QDI provided robust parameterization of non-Gaussian diffusion signal decay in clinically feasible imaging times with high reliability, accuracy, and precision of QDTI measures.
准扩散 MRI(QDI)是一种基于扩散动力学连续时间随机漫步模型的新型定量技术。QDI 提供了扩散系数 ,单位为 mm ²/s,以及分数指数 ,用于定义扩散信号衰减的非高斯性。这里,优化了快速临床采集 QDI 张量成像(QDTI)数据的 b 值选择。
在健康志愿者中,针对包含 29 张排列在 和 5000 之间的扩散敏感图像的多 b 值参考(MbR)数据集,优化了临床适宜的 QDTI 采集。研究了最大 b 值( )、b 值壳数量的变化以及瑞利噪声的影响。
QDTI 测量值表现出 依赖性,在白质中最为明显,随着 的增加, 单调下降,导致组织对比度提高。优化的 2 个 b 值壳采集相对于 MbR 值显示出 QDTI 测量值的小系统差异,白质中 和 高估,灰质和白质中 和各向异性高估。更多的壳增加了 QDTI 估计的准确性、精度和可靠性,在 3 个和 4 个壳时在 s ²/mm ² ,在 4 个 b 值壳时在 s ²/mm ² ,与 MbR 相比, 和 几乎没有偏差。
对体内脑成像的非高斯 dMRI 进行了高度详细的优化。QDI 以高可靠性、准确性和精度提供了对临床可行成像时间中非高斯扩散信号衰减的稳健参数化,用于 QDTI 测量。