Navigator-Free Submillimeter Diffusion Imaging using Multishot-encoded Simultaneous Multi-slice (MUSIUM)
Authors:
Wei-Tang Chang,
Khoi Minh Huynh,
Pew-Thian Yap,
Weili Lin
Abstract:
The ability to achieve submillimter isotropic resolution diffusion MR imaging (dMRI) is critically important to study fine-scale brain structures, particularly in the cortex. One of the major challenges in performing submillimeter dMRI is the inherently low signal-to-noise ratio (SNR). While approaches capable of mitigating the low SNR in high resolution dMRI have been proposed, namely simultaneou…
▽ More
The ability to achieve submillimter isotropic resolution diffusion MR imaging (dMRI) is critically important to study fine-scale brain structures, particularly in the cortex. One of the major challenges in performing submillimeter dMRI is the inherently low signal-to-noise ratio (SNR). While approaches capable of mitigating the low SNR in high resolution dMRI have been proposed, namely simultaneous multi-slab (SMSlab) and generalized slice dithered enhanced resolution with simultaneous multislice (gSlider-SMS), limitations are associated with these approaches. The SMSlab sequences suffer from the slab boundary artifacts and require additional navigators for phase estimation. On the other hand, gSlider sequences require relatively high RF power and peak amplitude, which increase the SAR and complicate the RF excitation. In this work, we developed a navigator-free multishot-encoded simultaneous multi-slice (MUSIUM) imaging approach on a 3T MR scanner, achieving enhanced SNR, low RF power and peak amplitude, and being free from slab boundary artifacts. The dMRI with ultrahigh resolution (0.86 mm isotropic resolution), whole brain coverage and ~12.5 minute acquisition time were achieved, revealing detailed structures at cortical and white matter areas. The simulated and in vivo results also demonstrated that the MUSIUM imaging was minimally affected by the motion. Taken together, the MUSIUM imaging is a promising approach to achieve submillimeter diffusion imaging on 3T MR scanners within clinically feasible scan time.
△ Less
Submitted 7 December, 2020; v1 submitted 1 December, 2020;
originally announced December 2020.
Probing Tissue Microarchitecture of the Baby Brain via Spherical Mean Spectrum Imaging
Authors:
Khoi Minh Huynh,
Tiantian Xu,
Ye Wu,
Geng Chen,
Xifeng Wang,
Kim-Han Thung,
Haiyong Wu,
Weili Lin,
Dinggang Shen,
Pew-Thian Yap
Abstract:
During the first years of life, the human brain undergoes dynamic spatially-heterogeneous changes, involving differentiation of neuronal types, dendritic arborization, axonal ingrowth, outgrowth and retraction, synaptogenesis, and myelination. To better quantify these changes, this article presents a method for probing tissue microarchitecture by characterizing water diffusion in a spectrum of len…
▽ More
During the first years of life, the human brain undergoes dynamic spatially-heterogeneous changes, involving differentiation of neuronal types, dendritic arborization, axonal ingrowth, outgrowth and retraction, synaptogenesis, and myelination. To better quantify these changes, this article presents a method for probing tissue microarchitecture by characterizing water diffusion in a spectrum of length scales, factoring out the effects of intra-voxel orientation heterogeneity. Our method is based on the spherical means of the diffusion signal, computed over gradient directions for a fixed set of diffusion weightings (i.e., b-values). We decompose the spherical mean series at each voxel into a spherical mean spectrum (SMS), which essentially encodes the fractions of spin packets undergoing fine- to coarse-scale diffusion processes, characterizing hindered and restricted diffusion stemming respectively from extra- and intra-neurite water compartments. From the SMS, multiple orientation distribution invariant indices can be computed, allowing for example the quantification of neurite density, microscopic fractional anisotropy ($μ$FA), per-axon axial/radial diffusivity, and free/restricted isotropic diffusivity. We show maps of these indices for baby brains, demonstrating that microscopic tissue features can be extracted from the developing brain for greater sensitivity and specificity to development related changes. Also, we demonstrate that our method, called spherical mean spectrum imaging (SMSI), is fast, accurate, and can overcome the biases associated with other state-of-the-art microstructure models.
△ Less
Submitted 7 June, 2020; v1 submitted 13 August, 2019;
originally announced August 2019.