High-resolution myelin-water fraction and quantitative relaxation mapping using 3D ViSTa-MR fingerprinting

TL;DR

This paper introduces a fast, high-resolution 3D MRI method combining ViSTa and MRF techniques to simultaneously map myelin-water fraction, T1, T2, and PD across the whole brain within clinically feasible scan times.

Contribution

The study develops a novel 3D ViSTa-MRF approach that enables rapid, high-fidelity multi-parametric brain mapping without multi-compartment fitting, suitable for clinical and research applications.

Findings

Achieved 1mm and 0.66mm resolution whole-brain mapping in 5 and 15 minutes.

MWF values are consistent with slower, standard ViSTa methods.

Enabled in-vivo and post-mortem brain assessments, including infant brain development.

Abstract

Purpose: This study aims to develop a high-resolution whole-brain multi-parametric quantitative MRI approach for simultaneous mapping of myelin-water fraction (MWF), T1, T2, and proton-density (PD), all within a clinically feasible scan time. Methods: We developed 3D ViSTa-MRF, which combined Visualization of Short Transverse relaxation time component (ViSTa) technique with MR Fingerprinting (MRF), to achieve high-fidelity whole-brain MWF and T1/T2/PD mapping on a clinical 3T scanner. To achieve fast acquisition and memory-efficient reconstruction, the ViSTa-MRF sequence leverages an optimized 3D tiny-golden-angle-shuffling spiral-projection acquisition and joint spatial-temporal subspace reconstruction with optimized preconditioning algorithm. With the proposed ViSTa-MRF approach, high-fidelity direct MWF mapping was achieved without a need for multi-compartment fitting that could introduce bias and/or noise from additional assumptions or priors. Results: The in-vivo results demonstrate the effectiveness of the proposed acquisition and reconstruction framework to provide fast multi-parametric mapping with high SNR and good quality. The in-vivo results of 1mm- and 0.66mm-iso datasets indicate that the MWF values measured by the proposed method are consistent with standard ViSTa results that are 30x slower with lower SNR. Furthermore, we applied the proposed method to enable 5-minute whole-brain 1mm-iso assessment of MWF and T1/T2/PD mappings for infant brain development and for post-mortem brain samples. Conclusions: In this work, we have developed a 3D ViSTa-MRF technique that enables the acquisition of whole-brain MWF, quantitative T1, T2, and PD maps at 1mm and 0.66mm isotropic resolution in 5 and 15 minutes, respectively. This advancement allows for quantitative investigations of myelination changes in the brain.