arXiv subjects

Zidan Yu

Publications and source records attributed to Zidan Yu.

6 recordsLinked to original sources

arXiv2026

Multinuclear fingerprinting

We developed a new magnetic resonance imaging method called multinuclear fingerprinting (MNF) which leverages simultaneously-acquired proton (1H) and sodium (23Na) data to generate seven quantitative maps of the whole brain: proton density (PD), T1 and T2 relaxation times from water, and tissue sodium concentration (TSC), T1, T2short and T2long from Na+ ions. MNF consists of two parts: (1) simultaneous 1H/23Na magnetic resonance fingerprinting (MRF), and (2) a super-resolution (SR) algorithm to increase the 23Na resolution to match the 1H resolution. It was tested on the brain of seven healthy subjects at 7 T, with a final resolution of 1.5x1.5x5 mm3 for all maps acquired in 13 min. MNF could provide new fundamental insights into the inter-relationship between morphology (i.e. tissue structure from the 1H maps) and physiology (i.e. ion homeostasis from the 23Na maps) in vivo to help improve our understanding of the human brain in general, and to study neuropathologies and their treatments. Since all 1H/23Na MRF data is acquired simultaneously, all images are exactly co-registered with identical spatial and temporal resolutions. MNF could be useful in future longitudinal studies for assessing local time-dependent and conjoint 1H/23Na MR changes during tasks or interventions. MNF was initially developed for neuroimaging, but it can be adapted to any other parts of the body.

physics.med-ph↗

arXiv2024

Correlation-weighted 23Na magnetic resonance fingerprinting in the brain

We developed a new sodium magnetic resonance fingerprinting ($^\text{23}\text{Na}$ MRF) method for the simultaneous mapping of $\text{T}_\text{1}$, $\text{T}_\text{2,long}^{*}$, $\text{T}_\text{2,short}^{*}$ and sodium density with built-in $\Delta\text{B}_{1}^{+}$ (radiofrequency transmission inhomogeneities) and $\Delta\text{f}_\text{0}$ corrections (frequency offsets). We based our $^\text{23}\text{Na}$ MRF implementation on a 3D FLORET sequence with 23 radiofrequency pulses. To capture the complex spin ${\frac{\text{3}}{\text{2}}}$ dynamics of the $^\text{23}\text{Na}$ nucleus, the fingerprint dictionary was simulated using the irreducible spherical tensor operators formalism. The dictionary contained 831,512 entries covering a wide range of $\text{T}_\text{1}$, $\text{T}_\text{2,long}^{*}$, $\text{T}_\text{2,short}^{*}$, $\Delta\text{B}_\text{1}^{+}$ factor and $\Delta\text{f}_\text{0}$ parameters. Fingerprint matching was performed using the Pearson correlation and the resulting relaxation maps were weighted with a subset of the highest correlation coefficients corresponding to signal matches for each voxel. Our $^\text{23}\text{Na}$ MRF method was compared against reference methods in a 7-compartment phantom, and applied in brain in five healthy volunteers at 7 T. In phantoms, $^\text{23}\text{Na}$ MRF produced values comparable to those obtained with reference methods. Average sodium relaxation time values in cerebrospinal fluid, gray matter and white matter across five healthy volunteers were in good agreement with values previously reported in the literature.

physics.med-ph↗

arXiv2024

Analysis of blurring due to short T2 decay at different resolutions in 23Na MRI

The nuclear magnetic resonance signal from sodium (23Na) nuclei demonstrates a fast bi-exponential T2 decay in biological tissues (T2,short = 0.5-5 ms and T2,long = 10-30 ms). Hence, blurring observed in sodium images acquired with center-out sequences is generally assumed to be dominated by signal attenuation at higher k-space frequencies. Most of the studies in the field primarily focus on the impact of readout duration on blurring but neglect the impact of resolution. In this paper, we examine the blurring effect of short T2 on images at different resolutions. A series of simulations, as well as phantom and in vivo scans were performed at varying resolutions and readout durations in order to evaluate progressive changes in image quality. We demonstrate that, given a fixed readout duration, T2 decay produces distinct blurring effects at different resolutions. Therefore, in addition to voxel size-dependent partial volume effects, the choice of resolution adds additional T2-dependent blurring.

physics.med-ph↗

arXiv2023

Non-Cartesian Self-Supervised Physics-Driven Deep Learning Reconstruction for Highly-Accelerated Multi-Echo Spiral fMRI

Functional MRI (fMRI) is an important tool for non-invasive studies of brain function. Over the past decade, multi-echo fMRI methods that sample multiple echo times has become popular with potential to improve quantification. While these acquisitions are typically performed with Cartesian trajectories, non-Cartesian trajectories, in particular spiral acquisitions, hold promise for denser sampling of echo times. However, such acquisitions require very high acceleration rates for sufficient spatiotemporal resolutions. In this work, we propose to use a physics-driven deep learning (PD-DL) reconstruction to accelerate multi-echo spiral fMRI by 10-fold. We modify a self-supervised learning algorithm for optimized training with non-Cartesian trajectories and use it to train the PD-DL network. Results show that the proposed self-supervised PD-DL reconstruction achieves high spatio-temporal resolution with meaningful BOLD analysis.

eess.IV↗

arXiv2020

Optimization of MR Fingerprinting for Free-Breathing Quantitative Abdominal Imaging

In this work, we propose a free-breathing magnetic resonance fingerprinting method that can be used to obtain $B_1^+$-robust quantitative maps of the abdomen in a clinically acceptable time. A three-dimensional MR fingerprinting sequence with a radial stack-of-stars trajectory was implemented for quantitative abdominal imaging. The k-space acquisition ordering was adjusted to improve motion-robustness. The flip angle pattern was optimized using the Cram\'er-Rao Lower Bound, and the encoding efficiency of sequences with 300, 600, 900, and 1800 flip angles was evaluated. To validate the sequence, a movable multicompartment phantom was developed. Reference multiparametric maps were acquired under stationary conditions using a previously validated MRF method. Periodic motion of the phantom was used to investigate the motion-robustness of the proposed sequence. The best performing sequence length (600 flip angles) was used to image the abdomen during a free-breathing volunteer scan. When using a series of 600 or more flip angles, the estimated $T_1$ values in the stationary phantom showed good agreement with the reference scan. Phantom experiments revealed that motion-related artefacts can appear in the quantitative maps, and confirmed that a motion-robust k-space ordering is essential in preventing these artefacts. The in vivo scan demonstrated that the proposed sequence can produce clean parameter maps while the subject breathes freely. Using this sequence, it is possible to generate $B_1^+$-robust quantitative maps of proton density, $T_1$, and $B_1^+$ under free-breathing conditions at a clinically usable resolution within 5 minutes.

physics.med-ph↗

arXiv2019

Magnetization Transfer in Magnetic Resonance Fingerprinting

Purpose: To study the effects of magnetization transfer (MT, in which a semisolid spin pool interacts with the free pool), in the context of magnetic resonance fingerprinting (MRF). Methods: Simulations and phantom experiments were performed to study the impact of MT on the MRF signal and its potential influence on T1 and T2 estimation. Subsequently, an MRF sequence implementing off-resonance MT pulses and a dictionary with an MT dimension by incorporating a two-pool model were used to estimate the fractional pool size in addition to the B1+, T1, and T2 values. The proposed method was evaluated in the human brain. Results: Simulations and phantom experiments showed that an MRF signal obtained from a cross-linked bovine serum sample is influenced by MT. Using a dictionary based on an MT model, a better match between simulations and acquired MR signals can be obtained (NRMSE 1.3% versus 4.7%). Adding off-resonance MT pulses can improve the differentiation of MT from T1 and T2. In-vivo results showed that MT affects the MRF signals from white matter (fractional pool-size ~16%) and gray matter (fractional pool-size ~10%). Furthermore, longer T1 (~1060 ms versus ~860 ms) and T2 values (~47 ms versus ~35 ms) can be observed in white matter if MT is accounted for. Conclusion: Our experiments demonstrated a potential influence of MT on the quantification of T1 and T2 with MRF. A model that encompasses MT effects can improve the accuracy of estimated relaxation parameters and allows quantification of the fractional pool size.

eess.IV↗