A New Strategy for Fast MRI-Based Quantification of the Myelin Water Fraction: Application to Brain Imaging in

Sofya Kulikova1, Lucie Hertz-Pannier1, Ghislaine Dehaene-Lambertz2

  • 1INSERM U1129, CEA/DRF/I2BM/Neurospin/UNIACT, Gif-sur-Yvette, France; Université Paris-Saclay, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.

Plos One
|October 14, 2016
PubMed

Insights

This study introduces a faster MRI method to measure brain myelination using myelin-related water fraction (fmy). The new technique significantly reduces scan and analysis times, enabling practical use in children and clinical settings.

Area of Science:

  • Neuroimaging
  • Biomedical Engineering
  • Radiology

Background:

  • Myelin-related water fraction (fmy) is a key MRI biomarker for assessing brain myelination.
  • Current fmy quantification methods are time-consuming, limiting clinical and pediatric research applications.
  • Developing rapid fmy mapping is crucial for advancing in vivo myelination studies.

Purpose of the Study:

  • To develop a novel, time-efficient strategy for quantifying fmy using multi-component T1 and T2 relaxometry.
  • To enable fast fmy mapping suitable for research on unsedated children and clinical use.
  • To validate the proposed method's accuracy and robustness.

Main Methods:

  • A 3-compartment model (myelin-related water, intra/extra-cellular water, unrestricted water) was employed.
  • Calibrated inherent relaxation times (T1c, T2c) were determined using a region contraction approach and non-negative least-square (NNLS) algorithm on adult data.
  • The method was tested using simulated data and applied to reduced acquisition time relaxometry datasets (acquisition <6 min, post-processing <5 min).

Main Results:

  • The novel strategy demonstrated robust estimation of T1c and T2c, comparable to voxel-wise fitting.
  • Fast fmy mapping was achieved with significantly reduced acquisition and post-processing times.
  • fmy maps in adults showed expected white matter variability, and in infants, revealed asynchronous myelination progression across white matter bundles.

Conclusions:

  • The proposed strategy offers a rapid and accurate method for fmy quantification.
  • This advancement facilitates in vivo brain myelination assessment in pediatric research and clinical settings.
  • The method provides valuable insights into myelination dynamics during early development.

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