Zidan Yu’s research while affiliated with University of Hawaii System and other places

In our dynamic environments, predictive processing is vital for auditory perception and its associated behaviors. Predictive coding formalizes inferential processes by implementing them as information exchange across cortical layers and areas. With laminar-specific blood oxygenation level dependent we measured responses to a cascading oddball paradigm, to ground predictive auditory processes on the mesoscopic human cortical architecture. We show that the violation of predictions are potentially hierarchically organized and associated with responses in superficial layers of the planum polare and middle layers of the lateral temporal cortex. Moreover, we relate the updating of the brain’s internal model to changes in deep layers. Using a modeling approach, we derive putative changes in neural dynamics while accounting for draining effects. Our results support the role of temporal cortical architecture in the implementation of predictive coding and highlight the ability of laminar fMRI to investigate mesoscopic processes in a large extent of temporal areas.

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.

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.

Functional magnetic resonance imaging (fMRI) has emerged as an essential tool for exploring human brain function. Submillimeter fMRI, in particular, has emerged as a tool to study mesoscopic computations. The inherently low signal-to-noise ratio (SNR) at submillimeter resolutions warrants the use of denoising approaches tailored at reducing thermal noise—the dominant contributing noise component in high-resolution fMRI. NOise Reduction with DIstribution Corrected Principal Component Analysis (NORDIC PCA) is one of such approaches, and has been benchmarked against other approaches in several applications. Here, we investigate the effects that two versions of NORDIC denoising have on auditory submillimeter data. While investigating auditory functional responses poses unique challenges, we anticipated NORDIC to have a positive impact on the data on the basis of previous applications. Our results show that NORDIC denoising improves the detection sensitivity and the reliability of estimates in submillimeter auditory fMRI data. These effects can be explained by the reduction of the noise-induced signal variability. However, we did observe a reduction in the average response amplitude (percent signal change) within regions of interest, which may suggest that a portion of the signal of interest, which could not be distinguished from general i.i.d. noise, was also removed. We conclude that, while evaluating the effects of the signal reduction induced by NORDIC may be necessary for each application, using NORDIC in high-resolution auditory fMRI studies may be advantageous because of the large reduction in variability of the estimated responses.

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.

Functional magnetic resonance imaging (fMRI) has emerged as an essential tool for exploring human brain function. Submillimeter fMRI, in particular, has emerged as a tool to study mesoscopic computations. The inherently low signal to noise ratio (SNR) at submillimeter resolutions warrants the use of denoising approaches tailored at reducing thermal noise; the dominant contributing noise component in high resolution fMRI. NORDIC PCA is one of such approaches, and has been benchmarked against other approaches in several applications. Here, we investigate the effects that two versions of NORDIC denoising have on auditory submillimeter data. As investigating auditory functional responses poses unique challenges, we anticipated that the benefit of this technique would be especially pronounced. Our results show that NORDIC denoising improves the detection sensitivity and the reliability of estimates in submillimeter auditory fMRI data. These effects can be explained by the reduction of the noise-induced signal variability. However, we also observed a reduction in the average response amplitude (percent signal), which may suggest that a small amount of signal was also removed. We conclude that, while evaluating the effects of the signal reduction induced by NORDIC may be necessary for each application, using NORDIC in high resolution auditory fMRI studies may be advantageous because of the large reduction in variability of the estimated responses.

In this work, we introduce a super-resolution method that generates a high-resolution (HR) 23 Na image from simultaneously-acquired low-resolution (LR) 23 Na density-weighted MRI and HR proton density (PD), T1 , and T2 maps from 1 H MR fingerprinting (MRF) in the brain at 7 T. The core of our method is a partial least squares (PLS) regression between the HR (1 H) images and the LR (23 Na) image. An iterative loop and deconvolution with the point spread function (PSF) of each acquired image were included in the algorithm to generate a final HR 23 Na image without losing features from the LR 23 Na image. The method was applied to simultaneously-acquired HR proton and LR sodium data with in-plane resolution ratios between sodium and proton data of 3.8 and 1.9 and same slice thickness. Four volunteers were scanned to evaluate the method's performance. For the data with a resolution ratio of 3.8, the mean absolute difference between the generated and ground truth HR 23 Na images was in the range of 1.5-7.2% of the ground truth and a multi-scale structural similarity index (M-SSIM) of 0.93±0.03. For the data with a resolution ratio of 1.9, the mean absolute difference in the range of 4.8-6.3% and M-SSIM of 0.95±0.01.

Proton MRI can provide detailed morphological images, but it reveals little information about cell homeostasis. On the other hand, sodium MRI can provide metabolic information but cannot resolve fine structures. The complementary nature of proton and sodium MRI raises the prospect of their combined use in a single experiment. In this work, we assessed the repeatability of normalized proton density (PD), T1, T2, and normalized sodium density-weighted quantification measured with simultaneous 3D 1H MRF/23Na MRI in the brain at 7 T, from ten healthy volunteers who were scanned three times each. The coefficients of variation (CV) and the intra-class correlation (ICC) were calculated for the mean and standard deviation (SD) of these 4 parameters in grey matter, white matter, and cerebrospinal fluid. As result, the CVs were lower than 3.3% for the mean values and lower than 6.9% for the SD values. The ICCs were higher than 0.61 in all 24 measurements. We conclude that the measurements of normalized PD, T1, T2, and normalized sodium density-weighted from simultaneous 3D 1H MRF/23Na MRI in the brain at 7 T showed high repeatability. We estimate that changes > 6.6% (> 2 CVs) in mean values of both 1H and 23Na metrics could be detectable with this method.

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