Ultrafast low-angle RARE: U-FLARE

The subsecond application of the RARE technique is described. Two possible methods of implementation are discussed, one in which T2 contrast is manipulated by temporal reordering of the phase-encoding gradient, and the other in which the phase-encoding order is held constant and the contrast is manipulated by means of a spin-echo preparation experiment. In vivo images obtained with the latter method are presented and applications of the sequence discussed.     

RASER: a new ultrafast magnetic resonance imaging method.

A new MRI method is described to acquire a T(2)-weighted image from a single slice in a single shot. The technique is based on rapid acquisition by sequential excitation and refocusing (RASER). RASER avoids relaxation-related blurring because the magnetization is sequentially refocused in a manner that effectively creates a series of spin echoes with a constant echo time. RASER uses the quadratic phase produced by a frequency-swept chirp pulse to time-encode one dimension of the image. In another implementation the pulse can be used to excite multiple slices with phase-encoding and frequency-encoding in the other two dimensions. The RASER imaging sequence is presented along with single-shot and multislice images, and is compared to conventional spin-echo and echo-planar imaging sequences. A theoretical and empirical analysis of the spatial resolution is presented, and factors in choosing the spatial resolution for different applications are discussed. RASER produces high-quality single-shot images that are expected to be advantageous for a wide range of applications.     

Sequence design for magnetic resonance spectroscopic imaging of prostate cancer at 3 T.

Magnetic resonance spectroscopic imaging (MRSI) has proven to be a powerful tool for the metabolic characterization of prostate cancer in patients before and following therapy. The metabolites that are of particular interest are citrate and choline because an increased choline-to-citrate ratio can be used as a marker for cancer. High-field systems offer the advantage of improved spectral resolution as well as increased magnetization. Initial attempts at extending MRSI methods to 3 T have been confounded by the J-modulation of the citrate resonances. A new pulse sequence is presented that controls the J-modulation of citrate at 3 T such that citrate is upright, with high amplitude, at a practical echo time. The design of short (14 ms) spectral-spatial refocusing pulses and trains of nonselective refocusing pulses are described. Phantom studies and simulations showed that upright citrate with negligible sidebands is observed at an echo time of 85 ms. Studies in a human subject verified that this behavior is reproduced in vivo and demonstrated that the water and lipid suppression of the new pulse sequence are sufficient for application in prostate cancer patients.     

An analysis of fast imaging sequences with steady-state transverse magnetization refocusing

Recently, several groups have proposed and demonstrated the use of rapid imaging methods, using short pulse repetition times and gradient-reversal echoes. Here, we analyze the behavior of the magnetization and the resulting image contrasts in such sequences for the case where the pulse repetition time TR is of the order of, or shorter than, the transverse relaxation time T2, and the transverse magnetization is not destroyed between phase-encoding cycles. Exact analytical expressions describing the signal evolution between the pulses are derived, taking into account the effects of resonance offsets and flip angles, and examining the influence of constant-phase or alternate-phase RF pulse trains. It is shown that for typical imaging sequences two distinct echo signals will develop between pulses, which may have a detrimental effect on image quality if they partially overlap within the sampling window. It is shown that artifact-free images can be obtained only if the two echo signals overlap precisely, which seems technically close to impossible to achieve, or if they are sufficiently separated in time to allow sampling of only one of the signals.     

Single-shot GRASE imaging with short effective TEs

A new phase-encoding scheme for gradient- and spin-echo (GRASE) imaging giving a short effective TE is described. Unlike previous orders, phase encoding is centric rather than sequential. The sequence is a development of k-banded GRASE that uses different time segments of the echo train to encode different bands of k space. This phase-encoding order has been implemented in single-shot sequences on an imager with high performance gradients. Approximately 144 phase-encoding lines can be acquired in an echo train time of 390 ms. With centric phase encoding, the effective TE is 8 ms, compared with 75 ms for sequential encoding, and signal-to-noise ratios (SNRs) in brain tissue are 50 to 70% higher. The sequence can be employed in, for example, diffusion and velocity imaging.     

Sliding multislice (SMS): a new technique for minimum FOV usage in axial continuously moving-table acquisitions.

A novel technique for axial continuously moving-table scans is described that minimizes the required extension of the scanner's field of view (FOV) along the direction of table motion (z) by applying a segmented multislice acquisition technique. Any anatomical slice is acquired by applying the same phase-encoding steps at the same spatial positions along the scanner FOV. The full k-space data set of any anatomical slice is collected while the slice moves through the scanner from one scan position to the next. Simultaneous acquisition of multiple slices is realized by shifting the acquisition trajectories of different slices in time. It is demonstrated how the image artifact behavior that relates to varying imaging properties along the distance the table traverses during the acquisition of any given anatomical slice can be optimized simultaneously for all images. Discontinuities between the images along the slice axis are avoided because all z-dependent scan properties are encoded identically for all slices. Flexible spatial acquisition patterns are proposed to enable data oversampling and overlapping slice acquisitions at reduced table speeds. A framework of equations is presented by which matched parameter combinations for sliding multislice acquisitions can be applied to both single- and multiecho sequences. The new technique is validated on phantom and in vivo measurements using a T1-weighted fast low-angle shot (FLASH) sequence as well as a T2-weighted multi-spin-echo sequence of variable echo train lengths.     

High field localized proton spectroscopy in small volumes: greatly improved localization and shimming using shielded strong gradients

The availability of shielded gradients facilitates accurate single-voxel spectroscopy. Exact localization (90-99%) of volumes as small as 2 x 2 x 2 mm is demonstrated using a modified stimulated echo sequence. Strong gradient pulses (up to 200 mT/m) are employed to clear the stimulated echo of unwanted magnetization, enabling superior (single-scan) shimming of the selected volume. In vivo and in vitro proton NMR results at 4.7 T are presented.     

Single breath-hold volumetric imaging of the heart using magnetization-prepared 3-dimensional segmented echo planar imaging

We show the feasibility of single breath-hold volumetric imaging of the heart using a three-dimensional (3D) segmented echo planar Imaging (EPI) pulse sequence. Fifteen healthy subjects were evaluated using three magnetization preparation schemes: (a) a driven equilibrium T2-weighted preparation for bright blood and dark myocardium; (b) a STEAM magnetization preparation for dark blood; and (c) fat suppression for coronary artery Imaging. An interleaved EPI trajectory encoding six echoes per Interleave with a 1090 Hz/pixel readout bandwidth was used to collect a 126 × 256 matrix in 22 heartbeats with data acquisition windows per cardiac cycle of 71–285 msec for 8–32 sections. Multiplanar reconstructions could be used if thin (1–3 mm) sections were acquired. Breath-hold volumetric imaging with 3D segmented EPI holds promise for rapid volumetric evaluation of cardiac anatomy.     

Optimized inversion-prepared gradient echo imaging

Purpose:

To implement a method using an extended phase graph (EPG)‐based simulation to optimize inversion‐prepared gradient echo sequences with respect to signal and contrast within the shortest acquisition time.

Materials and Methods:

A critical issue in rapid gradient‐echo imaging is the effect of residual transverse magnetization between consecutive data acquisition windows. Various spoiling schemes have been proposed to mitigate this problem, and while spoiling is often considered to be perfect, imaging can be more truthfully described using the EPG. An EPG‐based simulation is used to analyze and predict the image signal and contrast to serve as a basis for sequence optimization.

Results:

Fourteen biological phantom experiments and five brain imaging experiments on each of five healthy volunteers was performed to validate and verify the accuracy of the EPG‐based simulation. In addition, two experiments on an in‐cranial cadaver brain were performed to show the ability of the proposed method for improving overall image quality.

Conclusion:

From the experiment results, it is demonstrated that optimization of 3D magnetization‐prepared rapid gradient‐echo imaging sequences can be performed with an EPG‐based simulation to manipulate the sequence parameters for generating images with highly specific signal and contrast characteristics for quantitative T1‐weighted human brain imaging. J. Magn. Reson. Imaging 2012;36:748–755. © 2012 Wiley Periodicals, Inc.     

T2 quantitation of articular cartilage at 1.5 T

PURPOSE: To evaluate sources of error when using a multiecho sequence for quantitative T2 mapping of articular cartilage at 1.5 T. MATERIALS AND METHODS: Phantom measurements were used to assess the contribution of stimulated echoes to inaccuracy of T2 measurements in cartilage using a multiecho sequence. Five volunteer studies compared in vivo single-echo spin echo results to multiecho, single-slice and multiecho, multislice acquisitions for assessment of both the stimulated echo and magnetization transfer contrast (MTC) contributions to T2 measurement inaccuracy. RESULTS: Phantom experiments demonstrated that substantial inaccuracy (10%-13% longer T2 values) is introduced from stimulated echoes with a multiecho sequence with slice-selective refocusing pulses. The in vivo volunteer studies also demonstrated increases in measured T2 by up to 48% with a multiecho sequence. Use of the multiecho sequence in the multislice mode resulted in T2 values closer to the single-echo standards for the volunteer studies. However, this apparent increased accuracy should be regarded as circumstantial, as it only occurs because the error due to MTC has the opposite sign compared to the error due to the stimulated echo contribution. CONCLUSION: Use of a multiecho, multislice sequence for cartilage T2 measurements should be undertaken with the caution that substantial inaccuracy is introduced from stimulated echoes and MTC.     

RARE imaging: a fast imaging method for clinical MR

Based on the principles of echo imaging, we present a method to acquire sufficient data for a 256 X 256 image in from 2 to 40 s. The image contrast is dominated by the transverse relaxation time T2. Sampling all projections for 2D FT image reconstruction in one (or a few) echo trains leads to image artifacts due to the different T2 weighting of the echo. These artifacts cannot be described by a simple smearing out of the image in the phase direction. Proper distribution of the phase-encoding steps on the echoes can be used to minimize artifacts and even lead to resolution enhancement. In spite of the short data acquisition times, the signal amplitudes of structures with long T2 are nearly the same as those in a conventional 2D FT experiment. Our method, therefore, is an ideal screening technique for lesions with long T2.     

Optimizing the sequence parameters for double-quantum CRAZED imaging.

The evolution of magnetization during repeated application of the double-quantum-(DQ)-CRAZED sequence is analyzed, with the aim of identifying sequence parameters that maximize sensitivity to signal produced by the distant dipole field (DDF). Phase cycling schemes that allow cancellation of signals following undesired coherence pathways are also described. Simulations and imaging experiments carried out at 3 T on phantoms and the human head were used to verify the analysis. The results indicate that in the absence of phase cycling, the DDF-related signal-to-noise ratio (SNR) per unit time is maximized using TR=2.05 T1, along with values of the RF flip angles (alpha approximately 90 degrees and beta approximately 60 degrees ), and echo time (TE=T2) that have previously been shown to maximize the DDF-related signal at long TR. However, with TR=2.05 T1 there can also be a significant signal contribution due to stimulated echo effects (up to 40% of the signal for water at 3 T and TE=70 ms). Using a two-step phase cycle, the stimulated echo signal is eliminated and the maximum SNR per unit time occurs for TR=2.76 T1. It is also demonstrated that sensitivity to signal changes caused by small variations in T2 is maximized by setting TE=2T2.     

Reduced power multislice MDEFT imaging

A novel method is presented for acquiring multislice T1-weighted images. The method utilizes non-slice-selective inversion pulses followed by a series of slice-selective excitations. k-space is divided into a number of segments equal to the number of slices. Successive segments of k-space are assigned to successive slice-selective pulses, and the order in which the slices are excited is manipulated to ensure that images of each slice have identical contrast and point spread function (PSF). This method is applied to the MDEFT experiment, a particular version of the inversion recovery experiment. The implications of this acquisition scheme on the PSF are examined, and it is shown that, provided the k-space modulation function does not change sign, a good PSF is achieved. For a given maximum number of slices, the total experimental duration depends only on TR and the number of phase-encoding steps. A method of accelerating the experiment by multiply exciting each slice is described. An experimental demonstration of the proposed sequences is given by imaging the human head at 3 T.     

A generalized k-sampling scheme for 3D fast spin echo

The phase-encoding scheme can significantly affect the quality of fast spin-echo (FSE) images because the echo amplitude is modulated as a function of the echo position in k-space. The effects of the modulation in two-dimensional FSE imaging include ghosting and blurring artifacts and resolution loss in the phase-encoding (PE) direction. In 3D FSE imaging, the use of two PE directions presents the opportunity for improved PE schemes. A new scheme for assignment of echoes to views in 3D FSE, termed generalized, has been developed. This scheme distributes T(2) effects along both PE directions, allowing considerable flexibility in the selection of blurring artifact appearance. In a set of simulations, phantom experiments, and in vivo experiments, the performance of the generalized PE scheme for 3D FSE imaging was compared with the performance of existing PE schemes. The results demonstrate that the generalized PE scheme can be used to reduce blurring artifacts greatly relative to other PE techniques that are presently in use. This approach to PE can be used to manipulate the blurring artifact appearance and to optimize acquisition time.     

Multiecho sequences with variable refocusing flip angles: optimization of signal behavior using smooth transitions between pseudo steady states (TRAPS).

A variation of the rapid acquisition with relaxation enhancement (RARE) sequence (also called turbo spin-echo (TSE) or fast spin-echo (FSE)) is presented. This technique uses variable flip angles along the echo train such that magnetization is initially prepared into the static pseudo steady state (PSS) for a low refocusing flip angle (alpha < 180 degrees ). It is shown that after such a preparation, magnetization will always stay very close to the static PSS even after significant variation of the subsequent refocusing flip angles. This allows the design of TSE sequences in which high refocusing flip angles yielding 100% of the attainable signal are applied only for the important echoes encoding for the center of k-space. It is demonstrated that a reduction of the RF power (RFP) by a factor of 2.5-6 can be achieved without any loss in signal intensity. The contribution of stimulated-echo pathways leads to a reduction of the effective TE by a factor f(t), which for typical implementations is on the order of 0.5-0.8. This allows the use of longer echo readout times, and thus longer echo trains, for acquiring images with a given T(2) contrast.     

Method for quantitative imaging of the macromolecular 1H fraction in tissues.

A new method was developed for mapping the relative density of the macromolecular protons involved in magnetization transfer (MT). This method employs a stimulated echo preparation scheme in order to modulate the phase distribution within a spin ensemble. This labeled spin ensemble is then used as an intrinsic indicator, which is diluted due to magnetization exchange with macromolecular protons. A pulse sequence is presented which compensates for longitudinal relaxation, allows observation of the dilution effect only, and provides for calculation of parameter maps using indicator dilution theory. Compared to other quantitative MT techniques, neither additional relaxation time measurements nor knowledge regarding the lineshape of the macromolecular proton pool are required. Moreover, the inherent low specific absorption rate and the low sensitivity for B(1) errors make this method favorable in a clinical setting. This sequence was used to measure the macromolecular proton density in cross-linked bovine serum albumin. Using a navigated echo planar readout, the sequence was also employed to visualize the macromolecular content of human brain in vivo.     

Homogeneous preparation encoding (HoPE) in multislice imaging.

Fast magnetization preparation techniques acquire a series of echoes after a single magnetization preparation. If these echoes are acquired from different slices using a multislice technique the change in the preparation state of the echoes due to relaxation effects leads to different contrast modification for each slice. Encoding different preparation states along the phase-encoding direction of each slice instead of acquiring each slice in a different preparation state is introduced as a general concept to obtain images of identical contrast and point-spread function. This can be realized either by cycling the slice excitation order several times over the total number of repetitions or by moving the point of time at which the preparation is applied within each repetition. One possible application of this method is chemical shift selective fat saturation imaging. A homogeneous fat suppression across a multislice volume could be achieved using a FLASH sequence at a repetition time of TR = 145 ms, including a single fat saturation preparation. Conventional fat saturated spin-echo imaging at any TR can be accelerated significantly by reducing the number of applied preparations per repetition. A further application of the homogeneous preparation encoding (HoPE) method is described that encodes the spatial self-saturation of the multislice excitation order homogeneously in all slices. Only a reduced number of slices of the total volume are excited in each repetition and the slice excitation order is continuously moved along the imaging volume. This method is applied for time of flight (TOF) imaging. Using a TONE-like series of flip angles for the slice excitations of each repetition homogeneous TOF images can be obtained on the basis of a multislice acquisition.     

Phase insensitive preparation of single-shot RARE: Application to diffusion imaging in humans

Although RARE and GRASE can produce single-shot images of excellent quality, their utility has been restricted because preparation of the magnetization with interesting contrast before imaging can cause severe artifacts. These artifacts relate to the strong sensitivity of multiple spin echo sequences to the phase of the prepared magnetization. Modifications of the RARE sequence to eliminate these artifacts are discussed, and an approach that eliminates the artifact producing signals from the very first echo is presented. The approach is applied to diffusion imaging of the human brain in normal volunteers and one patient.     

Triple contrast technique for black blood imaging with double inversion preparation.

This work reports on the development of a pulse sequence to simultaneously acquire proton density, T(1), and T(2) weighted images in a single magnetization prepared fast spin echo acquisition. The technique is based upon the application of a magnetization preparation consisting of a global inversion followed by slice-selective 180 degrees and 90 degrees pulses to prepare the signal of specific slices. Slices are acquired in an interleaved manner with time delays appropriate for the desired image contrasts. Data acquisition is repeated for all combinations of slice interleaving covering the region of interest until images from all slice locations have been acquired with all desired image contrasts. The multiple image contrasts obtained with this technique should be useful in applications where discrimination between different types of tissue components is desired, such as in the analysis of plaque in cervical carotid artery disease.     

Improved three-dimensional GRASE imaging with the SORT phase-encoding strategy

The phase-encoding strategy plays a critical role in determining the quality of gradient- and spin-echo (GRASE) images. Phase-encoding methods developed for two-dimensional GRASE imaging strive to achieve a balance between artifacts from T2-dependent signal amplitude modulations and off-resonance-dependent signal phase shifts, although no current method provides smooth and nonperiodic evolutions for both of these signal changes. In three-dimensional GRASE imaging, the use of two phase-encoding directions presents the opportunity for improved phase-encoding strategies. In this report a phase-encoding strategy for three-dimensional GRASE, termed SORT, is described; this strategy separates off-resonance and T2 effects, mapping one along each of the two phase-encoding directions. Thus, off-resonance-induced artifacts can be minimized while eliminating T2-dependent periodic signal modulations and allowing complete flexibility in the selection of echo time. The performance of the SORT phase-encoding method for T2-weighted GRASE imaging was compared with that of existing methods based on calculated point spread functions and simulated images. The predicted performance of SORT phase encoding was verified experimentally using T2-weighted three-dimensional GRASE imaging of the brain. Generally artifact-free images were obtained even in the presence of fat, susceptibility interfaces, and a wide range of T2 values.