AI Article Synopsis

  • Evaluating myelin using MRI is challenging but important for understanding diseases like multiple sclerosis (MS), and no definitive technique has been established yet.
  • This study investigates the relationship between a new method called synthetic MRI (SyMRI) and other established techniques for measuring myelin in MS patients, finding significant correlations between them.
  • SyMRI not only matched well with the other methods but also demonstrated greater sensitivity in detecting myelin damage, making it a promising tool for evaluating myelin in MS patients.

Article Abstract

Evaluation of myelin by magnetic resonance imaging (MRI) is a difficult challenge, but holds promise in demyelinating diseases, such as multiple sclerosis (MS). Although multiple techniques have been developed, no gold standard has been established. This study aims to evaluate the correlation between synthetic MRI myelin volume fraction (SyMRI) and myelin fraction estimated by other techniques, i.e., magnetization transfer saturation (MTsat), T1-weighted images divided by T2-weighted images (T1w/T2w), and radial diffusivity (RD) in patients with MS. We also compared the sensitivities of these techniques for detecting MS-related myelin damage. SyMRI, MTsat, T1w/T2w, and RD were averaged on plaque, periplaque white matter, and normal-appearing white matter (NAWM). Pairwise correlation was calculated using Spearman's correlation analysis. For all segmented regions, strong correlations were found between SyMRI and T1w/T2w (Rho = 0.89), MTsat (Rho = 0.82), or RD (Rho = -0.75). For each technique, the average estimated myelin differed significantly among regions, but the percentage change of NAWM from both periplaque white matter and plaque were highest in SyMRI. SyMRI might be suitable for myelin evaluation in MS patients, with relevant results as compared to other well-studied techniques. Moreover, it presented better sensitivity for the detection of the difference between plaque or periplaque white matter and NAWM.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7072333PMC
http://dx.doi.org/10.3390/cells9020393DOI Listing

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