Readout Gradient Research Articles

Two-parametric prescan calibration of gradient-induced sampling errors for rosette MRI.

The aim of this study was to develop a simple, robust, and easy-to-use calibration procedure for correcting misalignments in rosette MRI k-space sampling, with the objective of producing images with minimal artifacts. Quick automatic calibration scans were proposed for the beginning of the measurement to collect information on the time course of the rosette acquisition trajectory. A two-parameter model was devised to match the measured time-varying readout gradient delays and approximate the actual rosette sampling trajectory. The proposed calibration approach was implemented, and performance assessment was conducted on both phantoms and human subjects. The fidelity of phantom and in vivo images exhibited significant improvement compared with uncorrected rosette data. The two-parameter calibration approach also demonstrated enhanced precision and reliability, as evidenced by quantitative relaxometry analyses. Adequate correction of data sampling is a crucial step in rosette MRI. The presented experimental results underscore the robustness, ease of implementation, and suitability for routine experimental use of the proposed two-parameter rosette trajectory calibration approach.

Assessment of spectral ghost artifacts in echo-planar spectroscopic micro-imaging with flyback readout

In this work, echo-planar spectroscopic imaging (EPSI) with flyback readout gradient-echo train was implemented in a preclinical MR scanner. The aim of this study is to visualize and quantify the ghost spectral lines produced by two, three and four interleaved echo trains with different amplitudes of the readout gradients, and to investigate the feasibility of the flyback data acquisition in micro-imaging of small animals. Applied multi-slice EPSI sequence utilizes asymmetric gradient-echo train that combines the shortest possible rewind gradients with readout gradients. It simplifies data processing because all echoes are acquired with the same polarity of the readout gradient. The approach with four interleaved gradient-echo trains and with four echoes in each train provides broad spectral bandwidth in combination with narrow receiver bandwidth and a good water-fat signal separation. It improves signal-to-noise ratio without the undesired consequence of water-fat shift artifacts that are eliminated during data processing. Position, number, and intensity of the ghost spectral lines can be controlled by the suitable choice of spectral bandwidth, number of echo train interleaves, and the number of echoes in each interleave. This study demonstrates that high-spatial resolution EPSI with interleaved flyback readout gradient-echo trains is feasible on standard preclinical scanners.

Fuzzy ripple artifact in high resolution fMRI: identification, cause, and mitigation.

High resolution fMRI is a rapidly growing research field focused on capturing functional signal changes across cortical layers. However, the data acquisition is limited by low spatial frequency EPI artifacts; termed here as Fuzzy Ripples. These artifacts limit the practical applicability of acquisition protocols with higher spatial resolution, faster acquisition speed, and they challenge imaging in lower brain areas. We characterize Fuzzy Ripple artifacts across commonly used sequences and distinguish them from conventional EPI Nyquist ghosts, off-resonance effects, and GRAPPA artifacts. To investigate their origin, we employ dual polarity readouts. Our findings indicate that Fuzzy Ripples are primarily caused by readout-specific imperfections in k-space trajectories, which can be exacerbated by inductive coupling between third-order shims and readout gradients. We also find that these artifacts can be mitigated through complex-valued averaging of dual polarity EPI or by disconnecting the third-order shim coils. The proposed mitigation strategies allow overcoming current limitations in layer-fMRI protocols: (1)Achieving resolutions beyond 0.8mm is feasible, and even at 3T, we achieved 0.53mm voxel functional connectivity mapping.(2)Sub-millimeter sampling acceleration can be increased to allow sub-second TRs and laminar whole brain protocols with up to GRAPPA 8.(3)Sub-millimeter fMRI is achievable in lower brain areas, including the cerebellum.

Three-dimensional radial echo-planar spectroscopic imaging for hyperpolarized 13C MRSI in vivo.

To demonstrate the feasibility of 3D echo-planar spectroscopic imaging (EPSI) technique with rapid volumetric radial k-space sampling for hyperpolarized (HP) 13C magnetic resonance spectroscopic imaging (MRSI) in vivo. A radial EPSI (rEPSI) was implemented on a 3 T clinical PET/MR system. To enable volumetric coverage, the sinusoidal shaped readout gradients per k-t-spoke were rotated along the three spatial dimensions in a golden-angle like manner. A distance-weighted, density-compensated gridding reconstruction was used, also in cases with undersampling of spokes in k-space. Measurements without and with HP 13C-labeled substances were performed in phantoms and rats using a double-resonant 13C/1H volume resonator with 72 mm inner diameter. Phantom measurements demonstrated the feasibility of the implemented rEPSI sequence, as well as the robustness to undersampling in k-space up to a factor of 5 without advanced reconstruction techniques. Applied to measurements with HP [1-13C]pyruvate in a tumor-bearing rat, we obtained well-resolved MRSI datasets with a large matrix size of 123 voxels covering the whole imaging FOV of (180 mm)3 within 6.3 s, enabling to observe metabolism in dynamic acquisitions. After further optimization, the proposed rEPSI method may be useful in applications of HP 13C-tracers where unknown or varying metabolite resonances are expected, and the acquisition of dynamic, volumetric MRSI datasets with an adequate temporal resolution is a challenge.

Trajectory correction enables free-running chemical shift encoded imaging for accurate cardiac proton-density fat fraction quantification at 3T

BackgroundMetabolic diseases can negatively alter epicardial fat accumulation and composition, which can be probed using quantitative cardiac chemical shift encoded(CSE) MRI by mapping proton-density fat fraction (PDFF). To obtain motion-resolved high-resolution PDFF maps, we proposed a free-running cardiac CSE-MRI framework at 3T. To employ faster bipolar readout gradients, a correction for gradients imperfections was added using the gradient impulse response function (GIRF) and evaluated on intermediate images and PDFF quantification. MethodsTen minutes free-running cardiac 3D radial CSE-MRI acquisitions were compared in vitro and in vivo at 3T. Monopolar and bipolar readout gradients schemes provided 8 echoes (TE1/ΔTE = 1.16/1.96ms) and 13 echoes (TE1/ΔTE = 1.12/1.07ms), respectively. Bipolar-gradients free-running cardiac fat and water images and PDFF maps were reconstructed with or without GIRF-correction. PDFF values were evaluated in silico, in vitro on a fat/water phantom, and in vivo in 10 healthy volunteers and three diabetic patients. ResultsIn monopolar mode, fat-water swaps were demonstrated in silico and confirmed in vitro. Using bipolar readout gradients, PDFF quantification was reliable and accurate with GIRF correction with a mean bias of 0.03% in silico and 0.36% in vitro while it suffered from artifacts without correction, leading to a PDFF bias of 4.9% in vitro and swaps in vivo. Using bipolar readout gradients, in vivo PDFF of epicardial adipose tissue was significantly lower than in subcutaneous fat (80.4±7.1% vs 92.5±4.3%, P<0.0001). ConclusionAiming for an accurate PDFF quantification, high-resolution free-running cardiac CSE-MRI imaging proved to benefit from bipolar echoes with k-space trajectory correction at 3T. This free-breathing acquisition framework enables to investigate epicardial adipose tissue PDFF in metabolic diseases.

Three-Dimensional Variable Slab-Selective Projection Acquisition Imaging.

Three-dimensional (3D) projection acquisition (PA) imaging has recently gained attention because of its advantages, such as achievability of very short echo time, less sensitivity to motion, and undersampled acquisition of projections without sacrificing spatial resolution. However, larger subjects require a stronger Nyquist criterion and are more likely to be affected by outer-volume signals outside the field of view (FOV), which significantly degrades the image quality. Here, we proposed a variable slab-selective projection acquisition (VSS-PA) method to mitigate the Nyquist criterion and effectively suppress aliasing streak artifacts in 3D PA imaging. The proposed method involves maintaining the vertical orientation of the slab-selective gradient for frequency-selective spin excitation and the readout gradient for data acquisition. As VSS-PA can selectively excite spins only in the width of the desired FOV in the projection direction during data acquisition, the effective size of the scanned object that determines the Nyquist criterion can be reduced. Additionally, unwanted signals originating from outside the FOV (e.g., aliasing streak artifacts) can be effectively avoided. The mitigation of the Nyquist criterion owing to VSS-PA was theoretically described and confirmed through numerical simulations and phantom and human lung experiments. These experiments further showed that the aliasing streak artifacts were nearly suppressed.

Orthopedic implants affect the electric field induced by switching gradients in MRI.

To investigate whether the risk of peripheral nerve stimulation increases in the presence of bulky metallic prostheses implanted in a patient's body. A computational tool was used to calculate the electric field (E-field) induced in a realistic human model due to the action of gradient fields. The calculations were performed both on the original version of the anatomical model and on a version modified through "virtual surgery" to incorporate knee, hip, and shoulder prostheses. Five exam positions within a body gradient coil and one position using a head gradient coil were simulated, subjecting the human model to the readout gradient from an EPI sequence. The induced E-field in models with and without prostheses was compared, focusing on the nerves and all other tissues (both including and excluding the bones from the analysis). In the nerves, the most pronounced increase in the E-field (+24%) was observed around the knee implant during an abdominal MRI (Y axis readout). When extending the analysis to encompass all tissues (excluding bones), the greatest amplification (+360%) occurred around the knee implant during pelvic MRI (Z axis readout). Notable increases in E-field peaks were also identified around the shoulder and hip implants in multiple scenarios. Based on the presented results, further investigations aimed at quantifying the threshold of nerve stimulation in the presence of bulky implants are desirable.

Robust unenhanced peripheral magnetic resonance angiography using single-slab 3D chemical-shift-encoded GRASE.

Objective.To develop a novel, unenhanced magnetic resonance angiography (MRA) exploiting cardiac-gated, single-slab 3D chemical-shift-encoded gradient- and spin-echo (GRASE) imaging for robust background suppression.Approach.The proposed single-slab 3D GRASE employs variable-flip-angles (VFA) in the refocusing radio-frequency (RF) pulse train to promote sensitivity to blood flow as well as imaging encoding efficiency. Phase encoding blips are inserted between adjacent lobes of the switching readout gradients such that chemical shift-induced phase information is encoded into different locations in k-space. Based on the assumption that most background signals in the angiogram come from the fatty tissues, the proposed method directly separates angiograms from fatty background tissue signals from highly incomplete measurements by solving a constrained optimization problem with sparsity prior. Numerical simulations and experiments were performed to validate the effectiveness of the proposed method in healthy volunteers as compared with conventional fresh blood imaging (FBI).Main results.Compared with conventional FBI, the proposed method yields clearer delineation of small branching arteries and robust fatty background suppression without apparent loss of signals.Significance.We have successfully demonstrated the feasibility of the proposed, single-slab 3D VFA GRASE with chemical-shift-encoded reconstruction for the generation of robust unenhanced peripheral MRA.

Accounting for gradient non-uniformity in spatially-encoded diffusion-ordered NMR spectroscopy

Diffusion-ordered NMR spectroscopy (DOSY) is a powerful tool for the analysis of mixtures. Spatially-encoded (SPEN) DOSY makes it possible to collect a complete DOSY data set in a single scan, through spatial parallelisation of the gradient dimension. One limitation of current SPEN DOSY experiments is that the data is analysed assuming that the field gradient is uniform over the sample. This is usually not the case for high resolution NMR probes, and even less for triple-axis gradient probes. In this work, we have developed methods to account for gradient non-uniformity in the processing of SPEN DOSY experiment. We have first mapped the field gradient, using a stimulated echo (STE) NMR sequence with a weak readout gradient. We have then modified the calculation of the position-dependent effective gradient pulse area that is used in the analysis of SPEN DOSY data. The resulting model was validated through numerical simulations. A comparison of results obtained with and without inclusion of the effect of non-uniform gradients shows that the proposed approach increases the accuracy of SPEN DOSY experiments.

Experimental demonstration of diffusion limitations on resolution and SNR in MR microscopy

PurposeMR microscopy is in principle capable of producing images at cellular resolution (<10 µm), but various factors limit the quality achieved in practice. A recognized limit on the signal to noise ratio and spatial resolution is the dephasing of transverse magnetization caused by diffusion of spins in strong gradients. Such effects may be reduced by using phase encoding instead of frequency encoding read-out gradients. However, experimental demonstration of the quantitative benefits of phase encoding are lacking, and the exact conditions in which it is preferred are not clearly established. We quantify the conditions where phase encoding outperforms a readout gradient with emphasis on the detrimental effects of diffusion on SNR and resolution. MethodsA 15.2 T Bruker MRI scanner, with 1 T/m gradients, and micro solenoid RF coils < 1 mm in diameter, were used to quantify diffusion effects on resolution and the signal to noise ratio of frequency and phase encoded acquisitions. Frequency and phase encoding’s spatial resolution and SNR per square root time were calculated and measured for images at the diffusion limited resolution. The point spread function was calculated and measured for phase and frequency encoding using additional constant time phase gradients with voxels 3–15 µm in dimension. ResultsThe effect of diffusion during the readout gradient on SNR was experimentally demonstrated. The achieved resolutions of frequency and phase encoded acquisitions were measured via the point-spread-function and shown to be lower than the nominal resolution. SNR per square root time and actual resolution were calculated for a wide range of maximum gradient amplitudes, diffusion coefficients, and relaxation properties. The results provide a practical guide on how to choose between phase encoding and a conventional readout. Images of excised rat spinal cord at 10 µm × 10 µm in-plane resolution demonstrate phase encoding’s benefits in the form of higher measured resolution and higher SNR than the same image acquired with a conventional readout. ConclusionWe provide guidelines to determine the extent to which phase encoding outperforms frequency encoding in SNR and resolution given a wide range of voxel sizes, sample, and hardware properties.

T2* quantification using multi-echo gradient echo sequences: a comparative study of different readout gradients

To quantify T2*, multiple echoes are typically acquired with a multi-echo gradient echo sequence using either monopolar or bipolar readout gradients. The use of bipolar readout gradients achieves a shorter echo spacing time, enabling the acquisition of a larger number of echoes in the same scan time. However, despite their relative time efficiency and the potential for more accurate quantification, a comparative investigation of these readout gradients has not yet been addressed. This work aims to compare the performance of monopolar and bipolar readout gradients for T2* quantification. The differences in readout gradients were theoretically investigated with a Cramér-Rao lower bound and validated with computer simulations with respect to the various imaging parameters (e.g., flip angle, TR, TE, TE range, and BW). The readout gradients were then compared at 3 T using phantom and in vivo experiments. The bipolar readout gradients provided higher precision than monopolar readout gradients in both computer simulations and experimental results. The difference between the two readout gradients increased for a lower SNR and smaller TE range, consistent with the prediction made using Cramér-Rao lower bound. The use of bipolar readout gradients is advantageous for regions or situations where a lower SNR is expected or a shorter acquisition time is required.

Characterizing Off-center MRI with ZTE

PurposeTo maximize acquisition bandwidth in zero echo time (ZTE) sequences, readout gradients are already switched on during the RF pulse, creating unwanted slice selectivity. The resulting image distortions are amplified especially when the anatomy of interest is not located at the isocenter. We aim to characterize off-center ZTE MRI of extremities such as the shoulder, knee, and hip, adjusting the carrier frequency of the RF pulse excitation for each TR. MethodsIn ZTE MRI, radial encoding schemes are used, where the distorted slice profile due to the finite RF pulse length rotates with the k-space trajectory. To overcome these modulations for objects far away from the magnet isocenter, the frequency of the RF pulse is shifted for each gradient setting so that artifacts do not occur at a given off-center target position. The sharpness of the edges in the images were calculated and the ZTE acquisition with off-center excitation was compared to an acquisition with isocenter excitation both in phantom and in vivo off-center MRI of the shoulder, knee, and hip at 1.5 and 3T MRI systems. ResultsDistortion and blurriness artifacts on the off-center MRI images of the phantom, in vivo shoulder, knee, and hip images were mitigated with off-center excitation without time or noise penalty, at no additional computational cost. ConclusionThe off-center excitation allows ZTE MRI of the shoulder, knee, and hip for high-bandwidth image acquisitions for clinical settings, where positioning at the isocenter is not possible.

High-performance permanent magnet array design by a fast genetic algorithm (GA)-based optimization for low-field portable MRI

Lightweight and compact permanent magnet arrays (PMAs) are suitable for portable dedicated magnetic resonance imaging (MRI). It is worth exploring different PMA design possibilities and optimization methods with an adequate balance between weight, size, and performance, in addition to Halbach arrays and C-shaped/H-shaped magnets which are widely used. In this paper, the design and optimization of a sparse high-performance inward-outward ring-pair PMA consisting of magnet cuboids is presented for portable imaging of the brain. The design is lightweight (151kg) and compact (inner bore diameter: 270mm, outer diameter: 616mm, length: 480mm, 5-Gauss range: 1840×1840×2340mm3). The optimization framework is based on the genetic algorithm with a consideration of both field properties and simulated image quality. The resulting PMA design has an average field strength of 101.5 mT and a field pattern with a built-in linear readout gradient. Subtracting the best fit to the linear gradient target resulted in a residual deviation from the target field of 0.76mT and an average linear regression coefficient of 0.85 to the linear gradient. The required radiofrequency bandwidth is 6.9% within a field of view (FoV) with a diameter of 200mm and a length of 125mm. It has a magnetic field generation efficiency of 0.67mT/kg, which is high among the sparse PMAs that were designed for an FoV with a diameter of 200mm. The field can be used to supply gradients in one direction working with gradient coils in the other two directions, or can be rotated to encode signals for imaging with axial slice selection. The encoding capability of the designed PMA was examined through the simulated reconstructed images. The force experienced by each magnet in the design was calculated, and the feasibility of a physical implementation was confirmed. The design can offer an increased field strength, and thus, an increased signal-to-noise ratio. It has a longitudinal field direction that allows the application of technologies developed for solenoidal magnets. This proposed design can be a promising alternative to supplying the main and gradient fields in combination for dedicated portable MRI. Lastly, the design is resulted from a fast genetic algorithm-based optimization in which fast magnetic field calculation was applied and high design flexibility was feasible. Within optimization iterations, image quality metrics were used for the encoding field of a magnet configuration to guide the design of the magnet array.

An all-at-once 2D CEST by F1-spatial frequency encoding

In this work we present a 2D NMR experiment that provides insight into the full chemical exchange saturation transfer (CEST) network present in a sample. It yields all CEST profiles between any signals in a spectrum at once. The method relies on a combination of slice selective saturation during the preparation period, combined with an inverse read-out gradient applied during the evolution time. The resulting 2D spectrum yields gradient profiles in F1 with dips at the frequencies of signals that show a CEST to the corresponding signal in F2.

Quantum readout and gradient deep learning model for secure and sustainable data access in IWSN.

The industrial wireless sensor network (IWSN) is a surface-type of wireless sensor network (WSN) that suffers from high levels of security breaches and energy consumption. In modern complex industrial plants, it is essential to maintain the security, energy efficiency, and green sustainability of the network. In an IWSN, sensors are connected to the Internet in a non-monitored environment. Hence, non-authorized sensors can retrieve information from the IWSN. Therefore, to ensure that data access between sensors remains sustainable and secure, energy-efficient authentication and authorization are required. In this article, a novel Quantum Readout Gradient Secured Deep Learning (QR-GSDL) model is proposed to ensure that only trustworthy sensors can access IWSN data. The major objective of this QR-GSDL model is to create secure, energy-efficient IWSN to attain green sustainability and reduce the industrial impact on the environment. First, using the quantum readout and hash function, a registration method is designed to efficiently perform the registration process. Next, a gradient secured deep learning method is adopted to implement the authentication and authorization process in order to ensure energy-saving and secure data access. Simulations are conducted to evaluate the QR-GSDL model and compare its performance with that of three well-known models: online threshold anomaly detection, machine learning-based anomaly detection, and dynamic CNN. The simulation outcomes show that the proposed model is secure and energy-efficient for use in the IWSN. Moreover, the experimental results prove that the QR-SGDL model outperforms the existing models in terms of energy consumption, authentication rate, authentication time, and false acceptance rate.

Dual k-space and image-space post-processing for field-cycling MRI under low magnetic field stability and homogeneity conditions

We present a method to correct artifacts typically present in images acquired in field-cycled MRI experiments under poor magnetic field spatial-homogeneity and time-stability conditions. The proposed method was tested in both simulated and experimental data. The experiments were performed using a fast field-cycling MRI relaxometer of own design, based on a current-driven variable-geometry electromagnet. Current instability-induced artifacts in the images were mitigated through a phase correction array resulted from entropy and background minimization. Image distortions due to magnetic field inhomogeneity were compensated through two different approaches, involving a previous determination of the magnetic field homogeneity-map, or an experimental protocol where two images are acquired with inverted readout gradient polarity. Results show that images acquired at extreme conditions can be successfully improved, thus strengthening the possibilities for both low-cost MRI devices and faster field-switched MRI systems.

Echo planar imaging-induced errors in intracardiac 4D flow MRI quantification.

PurposeTo assess errors associated with EPI‐accelerated intracardiac 4D flow MRI (4DEPI) with EPI factor 5, compared with non‐EPI gradient echo (4DGRE).MethodsThree 3T MRI experiments were performed comparing 4DEPI to 4DGRE: steady flow through straight tubes, pulsatile flow in a left‐ventricle phantom, and intracardiac flow in 10 healthy volunteers. For each experiment, 4DEPI was repeated with readout and blip phase‐encoding gradient in different orientations, parallel or perpendicular to the flow direction. In vitro flow rates were compared with timed volumetric collection. In the left‐ventricle phantom and in vivo, voxel‐based speed and spatio‐temporal median speed were compared between sequences, as well as mitral and aortic transvalvular net forward volume.ResultsIn steady‐flow phantoms, the flow rate error was largest (12%) for high velocity (>2 m/s) with 4DEPI readout gradient parallel to the flow. Voxel‐based speed and median speed in the left‐ventricle phantom were ≤5.5% different between sequences. In vivo, mean net forward volume inconsistency was largest (6.4 ± 8.5%) for 4DEPI with nonblip phase‐encoding gradient parallel to the main flow. The difference in median speed for 4DEPI versus 4DGRE was largest (9%) when the 4DEPI readout gradient was parallel to the flow.ConclusionsVelocity and flow rate are inaccurate for 4DEPI with EPI factor 5 when flow is parallel to the readout or blip phase‐encoding gradient. However, mean differences in flow rate, voxel‐based speed, and spatio‐temporal median speed were acceptable (≤10%) when comparing 4DEPI to 4DGRE for intracardiac flow in healthy volunteers.

Multiple-echo steady-state (MESS): Extending DESS for joint T2 mapping and chemical-shift corrected water-fat separation.

PurposeTo extend the double echo steady‐state (DESS) sequence to enable chemical‐shift corrected water‐fat separation.MethodsThis study proposes multiple‐echo steady‐state (MESS), a sequence that modifies the readouts of the DESS sequence to acquire two echoes each with bipolar readout gradients with higher readout bandwidth. This enables water‐fat separation and eliminates the need for water‐selective excitation that is often used in combination with DESS, without increasing scan time. An iterative fitting approach was used to perform joint chemical‐shift corrected water‐fat separation and T2 estimation on all four MESS echoes simultaneously. MESS and water‐selective DESS images were acquired for five volunteers, and were compared qualitatively as well as quantitatively on cartilage T2 and thickness measurements. Signal‐to‐noise ratio (SNR) and T2 quantification were evaluated numerically using pseudo‐replications of the acquisition.ResultsThe water‐fat separation provided by MESS was robust and with quality comparable to water‐selective DESS. MESS T2 estimation was similar to DESS, albeit with slightly higher variability. Noise analysis showed that SNR in MESS was comparable to DESS on average, but did exhibit local variations caused by uncertainty in the water‐fat separation.ConclusionIn the same acquisition time as DESS, MESS provides water‐fat separation with comparable SNR in the reconstructed water and fat images. By providing additional image contrasts in addition to the water‐selective DESS images, MESS provides a promising alternative to DESS.

Investigating the effect of flow compensation and quantitative susceptibility mapping method on the accuracy of venous susceptibility measurement

Quantitative susceptibility mapping (QSM) is a promising non-invasive method for obtaining information relating to oxygen metabolism. However, the optimal acquisition sequence and QSM reconstruction method for reliable venous susceptibility measurements are unknown. Full flow compensation is generally recommended to correct for the influence of venous blood flow, although the effect of flow compensation on the accuracy of venous susceptibility values has not been systematically evaluated. In this study, we investigated the effect of different acquisition sequences, including different flow compensation schemes, and different QSM reconstruction methods on venous susceptibilities.Ten healthy subjects were scanned with five or six distinct QSM sequence designs using monopolar readout gradients and different flow compensation schemes. All data sets were processed using six different QSM pipelines and venous blood susceptibility was evaluated in whole-brain segmentations of the venous vasculature and single veins. The quality of vein segmentations and the accuracy of venous susceptibility values were analyzed and compared between all combinations of sequences and reconstruction methods.The influence of the QSM reconstruction method on average venous susceptibility values was found to be 2.7–11.6 times greater than the influence of the acquisition sequence, including flow compensation. The majority of the investigated QSM reconstruction methods tended to underestimate venous susceptibility values in the vein segmentations that were obtained.In summary, we found that multi-echo gradient-echo acquisition sequences without full flow compensation yielded venous susceptibility values comparable to sequences with full flow compensation. However, the QSM reconstruction method had a great influence on susceptibility values and thus needs to be selected carefully for accurate venous QSM.

Single-shot pseudo-centric EPI for magnetization-prepared imaging.

To implement a single-shot centric-reordered EPI (1sh-CenEPI), which reduces TE significantly, thus enabling to improve SNR for magnetization-prepared imaging. We proposed a 1sh-CenEPI in which grouped oscillating readout gradients, phase-encoding blips within each group, and big phase-encoding jumps between two consecutive groups are incorporated to encode whole k-space from the center to the edges in a single shot. The concept was tested on phantoms and human brains at 3 T. In addition, the proposed reordering scheme was applied to pseudo-continuous arterial spin labeling for evaluating the efficiency of the centric reordering in magnetization-prepared imaging. The proposed 1sh-CenEPI reduced TE from 50 ms to 1.4 ms for gradient-echo EPI, and from 100 ms to 7 ms for spin-echo EPI, while the elongation of readout duration was below 10% of the whole readout duration in most cases. The 1sh-CenEPI images exhibited no distinct geometric distortion both in phantom and human brain, comparable to the conventional two-shot center-out EPI. In pseudo-continuous arterial spin labeling results, 3-fold temporal SNR increase and 2-fold spatial SNR increase in the perfusion-weighted images were achieved with 1sh-CenEPI compared with the conventional linear ordering, whereas the cerebral blood flow values were consistent with previous studies. The proposed 1sh-CenEPI significantly reduced TE while maintaining similar readout window and providing images comparable to the conventional linear and multishot center-out EPI images. It can be a qualified candidate as a new readout for various magnetization-prepared imaging techniques.