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Low Rank plus Sparse Decomposition of ODFs for Improved Detection of Group-level Differences and Variable Correlations in White Matter

机译:ODF的低秩加稀疏分解可改进对白色物质中组水平差异和变量相关性的检测

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摘要

A novel approach is presented for group statistical analysis of diffusion weighted MRI datasets through voxelwise Orientation Distribution Functions (ODF).Recent advances in MRI acquisition make it possible to use high quality diffusion weighted protocols (multi-shell, large number of gradient directions) for routine in vivo study of white matter architecture. The dimensionality of these data sets is however often reduced to simplify statistical analysis. While these approaches may detect large group differences, they do not fully capitalize on all acquired image volumes. Incorporation of all available diffusion information in the analysis however risks biasing the outcome by outliers.Here we propose a statistical analysis method operating on the ODF, either the diffusion ODF or fiber ODF. To avoid outlier bias and reliably detect voxelwise group differences and correlations with demographic or behavioral variables, we apply the Low-Rank plus Sparse (L + S) matrix decomposition on the voxelwise ODFs which separates the sparse individual variability in the sparse matrix S whilst recovering the essential ODF features in the low-rank matrix L.We demonstrate the performance of this ODF L + S approach by replicating the established negative association between global white matter integrity and physical obesity in the Human Connectome dataset. The volume of positive findings (p < 0.01, 227cm3) agrees with and expands on the volume found by TBSS (17cm3), Connectivity based fixel enhancement (15cm3) and Connectometry (212cm3). In the same dataset we further localize the correlations of brain structure with neurocognitive measures such as fluid intelligence and episodic memory.The presented ODF L+S approach will aid in the full utilization of all acquired diffusion weightings leading to the detection of smaller group differences in clinically relevant settings as well as in neuroscience applications.
机译:提出了一种通过体素方向分布函数(ODF)对扩散加权MRI数据集进行组统计分析的新方法.MRI采集的最新进展使得可以使用高质量的扩散加权协议(多壳,大量梯度方向)常规体内研究白质结构。但是,通常会降低这些数据集的维数以简化统计分析。尽管这些方法可能会检测到较大的组差异,但它们并未完全利用所有获取的图像量。然而,将所有可用的扩散信息纳入分析中可能会使异常值偏向结果。在此,我们提出了一种基于ODF(扩散ODF或光纤ODF)的统计分析方法。为避免异常值偏差并可靠地检测人口统计学或行为变量与体素组的差异和相关性,我们在体素ODF上应用低秩加稀疏(L + S)矩阵分解,以在恢复时分离出稀疏矩阵S中的稀疏个体变异性通过在人类Connectome数据集中复制全球白质完整性和身体肥胖之间已建立的负相关性,我们证明了ODF L + S方法的性能。阳性结果的体积(p <0.01,227cm 3 )与TBSS发现的体积(17cm 3 )相符并扩大,基于连接性的固定增强(15cm 3 )和Connectometry(212cm 3 )。在同一数据集中,我们进一步将大脑结构与神经认知措施(如流体智力和情节性记忆)的相关性进行了定位。提出的ODF L + S方法将有助于充分利用所有获得的扩散权重,从而检测出较小的群体差异。临床相关设置以及在神经科学应用中。

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