Accuracy and precision of statistical descriptors obtained from multidimensional diffusion signal inversion algorithms

Abstract

In biological tissues, typical MRI voxels comprise multiple microscopic environments, the local organization of which can be captured by microscopic diffusion tensors. The measured diffusion MRI signal can, therefore, be written as the multidimensional Laplace transform of an intravoxel diffusion tensor distribution (DTD). Tensor-valued diffusion encoding schemes have been designed to probe specific features of the DTD, and several algorithms have been introduced to invert such data and estimate statistical descriptors of the DTD, such as the mean diffusivity, the variance of isotropic diffusivities, and the mean squared diffusion anisotropy. However, the accuracy and precision of these estimations have not been assessed systematically and compared across methods. In this article, we perform and compare such estimations in silico for a one-dimensional Gamma fit, a generalized two-term cumulant approach, and two-dimensional and four-dimensional Monte-Carlo-based inversion techniques, using a clinically feasible tensor-valued acquisition scheme. In particular, we compare their performance at different signal-to-noise ratios (SNRs) for voxel contents varying in terms of the aforementioned statistical descriptors, orientational order, and fractions of isotropic and anisotropic components. We find that all inversion techniques share similar precision (except for a lower precision of the two-dimensional Monte Carlo inversion) but differ in terms of accuracy. While the Gamma fit exhibits infinite-SNR biases when the signal deviates strongly from monoexponentiality and is unaffected by orientational order, the generalized cumulant approach shows infinite-SNR biases when this deviation originates from the variance in isotropic diffusivities or from the low orientational order of anisotropic diffusion components. The two-dimensional Monte Carlo inversion shows remarkable accuracy in all systems studied, given that the acquisition scheme possesses enough directions to yield a rotationally invariant powder average. The four-dimensional Monte Carlo inversion presents no infinite-SNR bias, but suffers significantly from noise in the data, while preserving good contrast in most systems investigated.

Keywords: Laplace inversion; diffusion MRI; in silico validation; microstructure; tensor-valued diffusion encoding.