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Variable flip angle echo planar time-resolved imaging (vFA-EPTI) for fast high-resolution gradient echo myelin water imaging
被引:15
|作者:
Dong, Zijing
[1
,2
]
Wang, Fuyixue
[1
,3
]
Chan, Kwok-Shing
[4
]
Reese, Timothy G.
[1
]
Bilgic, Berkin
[1
,3
]
Marques, Jose P.
[4
]
Setsompop, Kawin
[1
,3
]
机构:
[1] Massachusetts Gen Hosp, Athinoula A Martins Ctr Biomed Imaging, Charlestown, MA 02129 USA
[2] MIT, Dept Elect Engn & Comp Sci, Cambridge, MA 02139 USA
[3] MIT, Harvard MIT Hlth Sci & Technol, 77 Massachusetts Ave, Cambridge, MA 02139 USA
[4] Radhoud Univ, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
来源:
关键词:
Myelin water imaging;
Fast imaging;
High resolution;
Multi-compartment;
Myeloarchitecture;
Cortical layers;
PROSPECTIVE MOTION CORRECTION;
MULTIPLE-SCLEROSIS;
HUMAN BRAIN;
RECONSTRUCTION;
VISUALIZATION;
RELAXATION;
FIELD;
D O I:
10.1016/j.neuroimage.2021.117897
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Myelin water imaging techniques based on multi-compartment relaxometry have been developed as an important tool to measure myelin concentration in vivo, but are limited by the long scan time of multi-contrast multi-echo acquisition. In this work, a fast imaging technique, termed variable flip angle Echo Planar Time-Resolved Imaging (vFA-EPTI), is developed to acquire multi-echo and multi-flip-angle gradient-echo data with significantly reduced acquisition time, providing rich information for multi-compartment analysis of gradient-echo myelin water imaging (GRE-MWI). The proposed vFA-EPTI method achieved 26 folds acceleration with good accuracy by utilizing an efficient continuous readout, optimized spatiotemporal encoding across echoes and flip angles, as well as a joint subspace reconstruction. An approach to estimate off-resonance field changes between different flip-angle acquisitions was also developed to ensure high-quality joint reconstruction across flip angles. The accuracy of myelin water fraction (MWF) estimate under high acceleration was first validated by a retrospective undersampling experiment using a lengthy fully-sampled data as reference. Prospective experiments were then performed where whole-brain MWF and multi-compartment quantitative maps were obtained in 5 min at 1.5 mm isotropic resolution and 24 min at 1 mm isotropic resolution at 3T. Additionally, ultra-high resolution data at 600 mu m isotropic resolution were acquired at 7T, which show detailed structures within the cortex such as the line of Gennari, demonstrating the ability of the proposed method for submillimeter GRE-MWI that can be used to study cortical myeloarchitecture in vivo
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