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Fast, accurate 2D-MR relaxation exchange spectroscopy (REXSY): Beyond compressed sensing

机译:快速,准确的2D-MR弛豫交换光谱(REXSY):超越压缩传感

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Previously, we showed that compressive or compressed sensing (CS) can be used to reduce significantly the data required to obtain 2D-NMR relaxation and diffusion spectra when they are sparse or well localized. In some cases, an order of magnitude fewer uniformly sampled data were required to reconstruct 2D-MR spectra of comparable quality. Nonetheless, this acceleration may still not be sufficient to make 2D-MR spectroscopy practicable for many important applications, such as studying time-varying exchange processes in swelling gels or drying paints, in living tissue in response to various biological or biochemical challenges, and particularly for in vivo MRI applications. A recently introduced framework, marginal distributions constrained optimization (MADCO), tremendously accelerates such 2D acquisitions by using a priori obtained 1D marginal distribution as powerful constraints when 2D spectra are reconstructed. Here we exploit one important intrinsic property of the 2D-MR relaxation exchange spectra: the fact that the 1D marginal distributions of each 2D-MR relaxation exchange spectrum in both dimensions are equal and can be rapidly estimated from a single Carr-Purcell-Meiboom-Gill (CPMG) or inversion recovery prepared CPMG measurement. We extend the MADCO framework by further proposing to use the 1D marginal distributions to inform the subsequent 2D data-sampling scheme, concentrating measurements where spectral peaks are present and reducing them where they are not. In this way we achieve compression or acceleration that is an order of magnitude greater than that in our previous CS method while providing data in reconstructed 2D-MR spectral maps of comparable quality, demonstrated using several simulated and real 2D T-2-T-2 experimental data. This method, which can be called "informed compressed sensing," is extendable to other 2D- and even ND-MR exchange spectroscopy.
机译:以前,我们表明压缩或压缩感测(CS)可用于显着减少稀疏或良好定位的获得2D-NMR弛豫和扩散谱所需的数据。在某些情况下,重建质量相当的2D-MR光谱所需的均匀采样数据要少一个数量级。然而,这种加速可能仍不足以使2D-MR光谱学在许多重要应用中切实可行,例如研究各种生物或生化挑战,尤其是研究活体组织中溶胀凝胶或干燥涂料,活组织中随时间变化的交换过程,特别是用于体内MRI应用。最近引入的框架,边际分布约束优化(MADCO),通过在重建2D光谱时使用先验获得的1D边际分布作为强大的约束条件,极大地加速了此类2D采集。在这里,我们利用2D-MR弛豫交换谱的一个重要内在特性:每个2D-MR弛豫交换谱在两个维度上的一维边际分布相等,并且可以通过单个Carr-Purcell-Meiboom-吉尔(CPMG)或反演恢复准备的CPMG测量。我们通过进一步建议使用1D边际分布来告知后续的2D数据采样方案,将测量集中在存在频谱峰值的地方以及在不存在频谱峰值的地方减少它们,来扩展MADCO框架。通过这种方式,我们实现了比以前的CS方法大一个数量级的压缩或加速,同时在重构的2D-MR频谱图中提供了可比较质量的数据,这通过使用多个模拟的和真实的2D T-2-T-2进行了演示。实验数据。这种方法可以称为“信息压缩传感”,它可以扩展到其他2D甚至ND-MR交换光谱。

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