Abstract

Cross-scanner and cross-protocol variability of diffusion magnetic resonance imaging (dMRI) data are known to be major obstacles in multi-site clinical studies since they limit the ability to aggregate dMRI data and derived measures. Computational algorithms that harmonize the data and minimize such variability are critical to reliably combine datasets acquired from different scanners and/or protocols, thus improving the statistical power and sensitivity of multi-site studies. Different computational approaches have been proposed to harmonize diffusion MRI data or remove scanner-specific differences. To date, these methods have mostly been developed for or evaluated on single b-value diffusion MRI data. In this work, we present the evaluation results of 19 algorithms that are developed to harmonize the cross-scanner and cross-protocol variability of multi-shell diffusion MRI using a benchmark database. The proposed algorithms rely on various signal representation approaches and computational tools, such as rotational invariant spherical harmonics, deep neural networks and hybrid biophysical and statistical approaches. The benchmark database consists of data acquired from the same subjects on two scanners with different maximum gradient strength (80 and 300 ​mT/m) and with two protocols. We evaluated the performance of these algorithms for mapping multi-shell diffusion MRI data across scanners and across protocols using several state-of-the-art imaging measures. The results show that data harmonization algorithms can reduce the cross-scanner and cross-protocol variabilities to a similar level as scan-rescan variability using the same scanner and protocol. In particular, the LinearRISH algorithm based on adaptive linear mapping of rotational invariant spherical harmonics features yields the lowest variability for our data in predicting the fractional anisotropy (FA), mean diffusivity (MD), mean kurtosis (MK) and the rotationally invariant spherical harmonic (RISH) features. But other algorithms, such as DIAMOND, SHResNet, DIQT, CMResNet show further improvement in harmonizing the return-to-origin probability (RTOP). The performance of different approaches provides useful guidelines on data harmonization in future multi-site studies.

Highlights

  • Diffusion magnetic resonance imaging provides information to characterize tissue microstructure by probing the diffusive displacements of water molecules

  • We have evaluated the performance of 19 algorithms that have participated in an open competition on harmonization of multishell diffusion magnetic resonance imaging (dMRI) scans from different scanners and protocols

  • The LinearRISH approach achieved the best performance in almost all metrics except return-to-origin probability (RTOP) which may be caused by errors in relative signal decays along the radial direction of b-values of the predicted signals

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Summary

Introduction

Diffusion magnetic resonance imaging provides information to characterize tissue microstructure by probing the diffusive displacements of water molecules. Recent advances in acquisition protocols with multiple b-values provide imaging measures that are even more sensitive and/or specific than standard approaches based on single b-value data (Jensen et al, 2005; O€ zarslan et al, 2013; Ning et al, 2015). DMRI scans have intrinsic variability caused by various factors including but not limited to scanner field and gradient strength and acquisition protocols (Vollmar et al, 2010; Grech-Sollars et al, 2015; Veenith et al, 2013; Landman et al, 2011). It is imperative to reduce the cross-scanner and cross-protocol variability in order to reliably aggregate multi-site databases for increasing statistical power and sensitivity of studies

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