Axon Diameters and Myelin Content Modulate Microscopic Fractional Anisotropy at Short Diffusion Times in Fixed Rat Spinal Cord

Frontiers in Physics

Shemesh, Noam¹ 

[1] Champalimaud Neuroscience Programme, Champalimaud Centre for the Unknown, Lisbon, Portugal

关键词: microscopic anisotropy;    MRI;    microstructure;    diffusion MRI;    Myelin water fraction;    Spinal Cord;    axon diameter;    Double diffusion encoding;    myelin;   

DOI  :  10.3389/fphy.2018.00049

学科分类：物理（综合）

来源: Frontiers

【 摘 要 】

Mapping tissue microstructure accurately and noninvasively is one of the frontiers of biomedical imaging. Diffusion Magnetic Resonance Imaging (MRI) is at the forefront of such efforts, as it is capable of reporting on microscopic structures orders of magnitude smaller than the voxel size by probing restricted diffusion. Double Diffusion Encoding (DDE) and Double Oscillating Diffusion Encoding (DODE) in particular, are highly promising for their ability to report on microscopic fractional anisotropy (µFA), a measure of the pore anisotropy in its own eigenframe, irrespective of orientation distribution. However, the underlying correlates of µFA have insofar not been studied. Here, we extract µFA from DDE and DODE measurements at ultrahigh magnetic field of 16.4T in the aim to probe fixed rat spinal cord microstructure. We further endeavor to correlate µFA with Myelin Water Fraction (MWF) derived from multiexponential T2 relaxometry, as well as with literature-based spatially varying axonal diameters. In addition, a simple new method is presented for extracting unbiased µFA from three measurements at different b-values. Our findings reveal strong anticorrelations between µFA (derived from DODE) and axon diameter in the distinct spinal cord tracts; a moderate correlation was also observed between µFA derived from DODE and MWF. These findings suggest that axonal membranes strongly modulate µFA, which – owing to its robustness towards orientation dispersion effects – reflects axon diameter much better than its typical FA counterpart. The µFA exhibited modulations when measured via oscillating or blocked gradients, suggesting selective probing of different parallel path lengths and providing insight into how those modulate µFA metrics. Our findings thus shed light into the underlying microstructural correlates of µFA and are promising for future interpretations of this metric in health and disease.

【 授权许可】

CC BY