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A New Strategy for Fast MRI-Based Quantification of the Myelin Water Fraction: Application to Brain Imaging in Infants

机译:一种基于MRI的髓磷脂水成分快速定量的新策略:在婴儿脑成像中的应用

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摘要

The volume fraction of water related to myelin (fmy) is a promising MRI index for in vivo assessment of brain myelination, that can be derived from multi-component analysis of T1 and T2 relaxometry signals. However, existing quantification methods require rather long acquisition and/or post-processing times, making implementation difficult both in research studies on healthy unsedated children and in clinical examinations. The goal of this work was to propose a novel strategy for fmy quantification within acceptable acquisition and post-processing times. Our approach is based on a 3-compartment model (myelin-related water, intra/extra-cellular water and unrestricted water), and uses calibrated values of inherent relaxation times (T1c and T2c) for each compartment c. Calibration was first performed on adult relaxometry datasets (N = 3) acquired with large numbers of inversion times (TI) and echo times (TE), using an original combination of a region contraction approach and a non-negative least-square (NNLS) algorithm. This strategy was compared with voxel-wise fitting, and showed robust estimation of T1c and T2c. The accuracy of fmy calculations depending on multiple factors was investigated using simulated data. In the testing stage, our strategy enabled fast fmy mapping, based on relaxometry datasets acquired with reduced TI and TE numbers (acquisition <6 min), and analyzed with NNLS algorithm (post-processing <5min). In adults (N = 13, mean age 22.4±1.6 years), fmy maps showed variability across white matter regions, in agreement with previous studies. In healthy infants (N = 18, aged 3 to 34 weeks), asynchronous changes in fmy values were demonstrated across bundles, confirming the well-known progression of myelination.
机译:与髓磷脂(fmy)有关的水的体积分数是用于体内评估脑髓鞘形成的有希望的MRI指数,可以从T1和T2弛张测量信号的多成分分析中得出。然而,现有的定量方法需要相当长的采集和/或后处理时间,这使得在对健康的非镇静儿童的研究和临床检查中都难以实施。这项工作的目标是提出一种在可接受的采集和后处理时间内进行fmy定量的新策略。我们的方法基于三室模型(髓磷脂相关水,细胞内/细胞外水和非限制性水),并使用每个室c的固有弛豫时间(T1c和T2c)的校准值。首先使用区域收缩方法和非负最小二乘法(NNLS)的原始组合,对以大量反转时间(TI)和回波时间(TE)获取的成人弛张测量数据集(N = 3)进行校准算法。将该策略与按体素拟合进行了比较,并显示了对T1c和T2c的可靠估计。使用模拟数据研究了取决于多个因素的fmy计算的准确性。在测试阶段,我们的策略基于以减少的TI和TE值(采集<6分钟)获取的弛豫测量数据集并使用NNLS算法进行分析,从而实现了快速的 f my 映射(后处理<5分钟)。在成年人(N = 13,平均年龄22.4±1.6岁)中, f my 图谱显示白质区域之间存在差异,与先前的研究一致。在健康婴儿(N = 18,年龄3至34周)中,跨束显示了 f my 值的异步变化,证实了众所周知的髓鞘形成进展。

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