Abstract

PurposeDiffusion MRI has recently been used with detailed models to probe tissue microstructure. Much of this work has been performed ex vivo with powerful scanner hardware, to gain sensitivity to parameters such as axon radius. By contrast, performing microstructure imaging on clinical scanners is extremely challenging.MethodsWe use an optimized dual spin‐echo diffusion protocol, and a Bayesian fitting approach, to obtain reproducible contrast (histogram overlap of up to 92%) in estimated maps of axon radius index in healthy adults at a modest, widely‐available gradient strength (35 mT m −1). A key innovation is the use of influential priors.ResultsWe demonstrate that our priors can improve precision in axon radius estimates—a 7‐fold reduction in voxelwise coefficient of variation in vivo—without significant bias. Our results may reflect true axon radius differences between white matter regions, but this interpretation should be treated with caution due to the complexity of the tissue relative to our model.ConclusionsSome sensitivity to relatively large axons (3–15 μm) may be available at clinical field and gradient strengths. Future applications at higher gradient strength will benefit from the favorable eddy current properties of the dual spin‐echo sequence, and greater precision available with suitable priors. Magn Reson Med, 2015. © 2015 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance in Medicine. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. Magn Reson Med 75:1787–1796, 2016. © 2015 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. on behalf of International Society for Magnetic Resonance.

Highlights

  • Diffusion-weighted magnetic resonance imaging uses the random self-diffusion of water molecules as the basis for an endogenous contrast in biological tissues (Le Bihan, 2003)

  • A recent trend has been to use Diffusion-weighted magnetic resonance imaging (dMRI) in combination with detailed models of tissue microstructure to try to estimate characteristics which are generally more associated with invasive histology than clinical imaging, such as axon radius

  • We have explored the application of the ActiveAx approach to in vivo axon radius imaging using the popular dual spin-echo sequence (DSE) pulse sequence on a clinical scanner

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Summary

Introduction

Diffusion-weighted magnetic resonance imaging (dMRI) uses the random self-diffusion of water molecules as the basis for an endogenous contrast in biological tissues (Le Bihan, 2003). The tissue models are typically built up from simple geometric shapes such as cylinders and spheres, but despite their simplicity they may be able to provide more direct tissue microstructure parameters than can be obtained from traditional dMRI analysis (Alexander et al, 2010; Assaf & Basser, 2005; Stanisz et al, 1997). These model parameters may in turn offer greater interpretability and sensitivity as biomarkers. The strength of the magnetic gradients available has been shown to be a key limiting factor for these applications (Dyrby et al, 2013; Huang et al, 2015), and the lack of strong gradients at most sites is a major barrier to their widespread uptake

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