Abstract

Despite recent advancements in MR imaging, non-invasive mapping of myelin in the brain still remains an open issue. Here we attempted to provide a potential solution. Specifically, we developed a processing workflow based on T1-w and T2-w MR data to generate an optimized myelin enhanced contrast image. The workflow allows whole brain mapping using the T1-w/T2-w technique, which was originally introduced as a non-invasive method for assessing cortical myelin content. The hallmark of our approach is a retrospective calibration algorithm, applied to bias-corrected T1-w and T2-w images, that relies on image intensities outside the brain. This permits standardizing the intensity histogram of the ratio image, thereby allowing for across-subject statistical analyses. Quantitative comparisons of image histograms within and across different datasets confirmed the effectiveness of our normalization procedure. Not only did the calibrated T1-w/T2-w images exhibit a comparable intensity range, but also the shape of the intensity histograms was largely corresponding. We also assessed the reliability and specificity of the ratio image compared to other MR-based techniques, such as magnetization transfer ratio (MTR), fractional anisotropy (FA), and fluid-attenuated inversion recovery (FLAIR). With respect to these other techniques, T1-w/T2-w had consistently high values, as well as low inter-subject variability, in brain structures where myelin is most abundant. Overall, our results suggested that the T1-w/T2-w technique may be a valid tool supporting the non-invasive mapping of myelin in the brain. Therefore, it might find important applications in the study of brain development, aging and disease.

Highlights

  • Myelin, the dielectric sheath surrounding neuronal axons, is an essential component for efficient brain functioning

  • Non-invasive imaging tools based on magnetic resonance imaging (MRI) were proposed for myelin mapping (Barkovich, 2000; Paus et al, 2001): conventional T1-weighted (T1-w) and T2weighted (T2-w) imaging, magnetization transfer imaging, diffusion tensor imaging (DTI), fluid-attenuated inversion recovery (FLAIR), multi-component T2-relaxation imaging (MCRI), and multi-component Driven Equilibrium Single Pulse Observation of T1 and T2

  • We evaluated the variability in image histograms across datasets when no calibration procedure was applied (Figure 5)

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Summary

Introduction

The dielectric sheath surrounding neuronal axons, is an essential component for efficient brain functioning. Histopathological investigations are typically conducted for only a limited number of regions, rather than for the whole brain. To address this problem, non-invasive imaging tools based on magnetic resonance imaging (MRI) were proposed for myelin mapping (Barkovich, 2000; Paus et al, 2001): conventional T1-weighted (T1-w) and T2weighted (T2-w) imaging, magnetization transfer imaging, diffusion tensor imaging (DTI), fluid-attenuated inversion recovery (FLAIR), multi-component T2-relaxation imaging (MCRI), and multi-component Driven Equilibrium Single Pulse Observation of T1 and T2 (mcDESPOT)

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