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Published on: July 22, 2022
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.
Abstract:
The volume fraction of water related to myelin (fmy) is a promising MRI index for in vivo assessment of brain myelination, that can be derived from multi-component analysis of T1 and T2 relaxometry signals. However, existing quantification methods require rather long acquisition and/or post-processing times, making implementation difficult both in research studies on healthy unsedated children and in clinical examinations. The goal of this work was to propose a novel strategy for fmy quantification within acceptable acquisition and post-processing times. Our approach is based on a 3-compartment model (myelin-related water, intra/extra-cellular water and unrestricted water), and uses calibrated values of inherent relaxation times (T1c and T2c) for each compartment c. Calibration was first performed on adult relaxometry datasets (N = 3) acquired with large numbers of inversion times (TI) and echo times (TE), using an original combination of a region contraction approach and a non-negative least-square (NNLS) algorithm. This strategy was compared with voxel-wise fitting, and showed robust estimation of T1c and T2c. The accuracy of fmy calculations depending on multiple factors was investigated using simulated data. In the testing stage, our strategy enabled fast fmy mapping, based on relaxometry datasets acquired with reduced TI and TE numbers (acquisition <6 min), and analyzed with NNLS algorithm (post-processing <5min). In adults (N = 13, mean age 22.4±1.6 years), fmy maps showed variability across white matter regions, in agreement with previous studies. In healthy infants (N = 18, aged 3 to 34 weeks), asynchronous changes in fmy values were demonstrated across bundles, confirming the well-known progression of myelination.
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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