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. Author manuscript; available in PMC: 2017 Jun 10.
Published in final edited form as: Magn Reson Med. 2015 Mar 20;75(2):537–546. doi: 10.1002/mrm.25595

Gradient-Modulated SWIFT

Jinjin Zhang 1,2, Djaudat Idiyatullin 1, Curtis A Corum 1, Naoharu Kobayashi 1, Michael Garwood 1,*
PMCID: PMC5466705  NIHMSID: NIHMS862323  PMID: 25800547

Abstract

Purpose

Methods designed to image fast-relaxing spins, such as sweep imaging with Fourier transformation (SWIFT), often utilize high excitation bandwidth and duty cycle, and in some applications the optimal flip angle cannot be used without exceeding safe specific absorption rate (SAR) levels. The aim is to reduce SAR and increase the flexibility of SWIFT by applying time-varying gradient-modulation (GM). The modified sequence is called GM-SWIFT.

Theory and Methods

The method known as gradient-modulated offset independent adiabaticity was used to modulate the radiofrequency (RF) pulse and gradients. An expanded correlation algorithm was developed for GM-SWIFT to correct the phase and scale effects. Simulations and phantom and in vivo human experiments were performed to verify the correlation algorithm and to evaluate imaging performance.

Results

GM-SWIFT reduces SAR, RF amplitude, and acquisition time by up to 90%, 70%, and 45%, respectively, while maintaining image quality. The choice of GM parameter influences the lower limit of short T2* sensitivity, which can be exploited to suppress unwanted image haze from unresolvable ultrashort T2* signals originating from plastic materials in the coil housing and fixatives.

Conclusions

GM-SWIFT reduces peak and total RF power requirements and provides additional flexibility for optimizing SAR, RF amplitude, scan time, and image quality.

Keywords: SWIFT, frequency sweep, gradient modulation, SAR, GOIA, fast relaxing spins, ultrashort T2, VERSE

INTRODUCTION

The time elapsing between spin excitation and signal acquisition in gradient-echo and spin-echo MRI is typically too long to visualize nuclei with ultrashort effective transverse relaxation times (T2*) in the range of 1 millisecond or less. Such ultrashort relaxation times are found in highly ordered tissues (e.g., tendons and knee meniscus), highly mineralized tissues (e.g., bone and teeth), lung (1,2), and tissues containing a high concentration of magnetic nanoparticles (3). Ultrashort-T2*-sensitive sequences typically acquire the free induction decay (FID), and the k-space consists of frequency-encoded FIDs arranged in a radial manner. Common ultrashort-T2*-sensitive sequences include the ultrashort echo time (UTE) sequence (4,5), zero echo time sequences (68), and sweep imaging with Fourier transformation (SWIFT) (9,10). In addition, there are single point and hybrid methods (1113).

SWIFT uses swept radiofrequency (RF) excitation and nearly simultaneous signal acquisition in a time-shared mode. SWIFT captures signals from spins with ultrashort T2* down to the microsecond range and has found numerous applications (1421). A current limitation, however, is the high specific absorption rate (SAR) when using large excitation bandwidth (Bw) to maximally preserve signal from spins with ultrashort T2* and/or when using a large excitation flip angle to maximize signal from spins with short T1.

Attempts to enhance RF pulse performance using modulated gradients have been relatively successful as a means to reduce RF power deposition (2224). One example is the gradient-modulated offset independent adiabaticity (GOIA) approach, which transforms RF amplitude or frequency modulation to a corresponding gradient modulation while maintaining constant adiabaticity factor over the entire spectral Bw (23). Other approaches such as variable-rate selective excitation (VERSE) (22) can also be applied to modify the RF pattern in order to achieve the desired flat excitation profile. The implementation of such approaches in SWIFT is not trivial because the gradient modulation influences both the excitation and the phase evolution of the spins. As a consequence, the correlation procedure used in the original SWIFT method (9) is not capable of resolving the spatially and temporally varying phase of the spins that accumulates during the changing field gradients.

In this paper, we present an extension of the SWIFT method, which uses time-varying gradients during read-out. We call it gradient-modulated SWIFT (GM-SWIFT). We present theory, numerical simulations, and phantom and in-vivo human experiments. Image quality, RF amplitude, and SAR are compared between the standard SWIFT (constant gradient) and GM-SWIFT sequences.

THEORY

Generation of a GOIA Pulse

According to the GOIA approach (23), for given RF amplitude-modulation function F1(t) and gradient-modulation function G(t), the RF frequency-modulation function F2(t) can be solved from the constraint:

ddt(AF2(t)G(t))=2π(γB10F1(t))2KG(t), [1]

where the adiabatic factor K is held constant over time and frequency, B10 is the amplitude of the RF field, A is the amplitude of the frequency modulation, and c is the gyromagnetic ratio. G(t) can be any function without zero point and that is not linearly proportional to F2(t). Figure 1a schematically presents the standard SWIFT sequence, implemented with a constant gradient and a stretched hyperbolic secant pulse (HS2) (2528). Figure 1b shows the sequence diagram of GM-SWIFT with the frequency-modulation function calculated using Eq. [1], the amplitude-modulation function of the HS2 pulse, and the below HS-shaped gradient-modulation function:

G(t)=1gm·sech[β(2tTp1)np], [2]

where np is the HS modulation order (= 4 here for Fig. 1b), gm is the gradient-modulation factor, Tp is pulse length, and β = 7.6 is the truncation factor for truncation of the value of F1 to 0.001 at temporal edges. Although many different gradient shapes can in principle be used, the HS-shaped gradient-modulation function was chosen here based on its smoothness and continuity of derivatives.

FIG. 1.

FIG. 1

Pulse diagrams of (a) standard SWIFT and (b) GM-SWIFT with HS-shaped gradient modulation.

The GOIA principle was developed originally for inverting spins adiabatically. When exciting spins in a subadiabatic manner, as done in standard SWIFT and GM-SWIFT, the GOIA principle still produces a flat excitation profile (i.e., the flip angle is constant in the range of the frequency-swept bandwidth). The value of K needs to be adjusted in order to allow the frequency sweep given by AF2(t) to fall in the interval [−A,A] (23).

Correlation Procedures

In the SWIFT sequence, excitation and acquisition are nearly simultaneous. The acquisition happens in the gaps of the frequency-swept excitation pulse. The field gradient during this procedure plays the role of frequency encoding or readout. In standard SWIFT, G and Bw are constant, and projections of the spin density can be obtained using the correlation method described in the original SWIFT paper (9). In GM-SWIFT, G and Bw are time-dependent. As a result, spins excited at different times experience differing segments of the time-varying readout gradient and accumulate phase in a spatially and temporally dependent manner. Thus, the existing correlation procedure for standard SWIFT does not remove these additional phase variations; a different correlation procedure is needed for GM-SWIFT.

The first step is to derive the signal equation. The SWIFT sequence is operating in the linear, subadiabatic region (29). With the small tip-angle approximation (30), the evolution for a single isochromat at position x at time τ, Mxy(x,τ), can be derived by solving the Bloch equations (31) in the rotating frame

Mxy(x,τ)=iγM00τB1(t)eiγx·tτG(t)dtdt, [3]

where B1(t)=B10F1(t)eiAF2(t)dt is the modulation function of the RF pulse, and the bold G(t)=G(t)G^, represents a vector; therefore, it specifies the modulation function of the field gradient as well as its direction. Although Eq. [3] represents the solution for a continuous B1 field, it is also suitable for gapped excitation for the given bandwidth as long as the RF power and sampling requirements are met (32). The integral of Mxy(x,τ) over all spins at different positions gives the total signal response of the entire object,

r(τ)=iγM0x{ρ0(x)0τB1(t)eiγx·tτG(t)dtdt}dx, [4]

where ρ0(x) is the spin density. Recovering the spin density from the acquired signal is an inverse problem. The excitation k-space concept (31), which is defined as the integral of the time-varying gradient over time, can be used here to solve and provide further insight into the problem. By defining the excitation k-space k(t), the spatial frequency weighting function w(k) and the spatial frequency sampling function s(k) as follows:

k(t)=γtTacqG(t)dt, [5]
w(k(t)τ)=B1(t)/|γG(t)|, [6]
s(k,τ)=0δ(k(t)k)|k˙(t)|dt, [7]

the signal response can be rewritten as:

r(τ)=iγM0x{ρ0(x)kw(k)s(k,τ)eiγx·[kk(τ)]dk}dx. [8]

Both integrals of x and k are over the whole domains ([−∞, ∞]) in Eq. [8] and in the rest of the equations in this work. The integral in Eq. [5] starts at t, not zero, because spatial encoding does not commence until a spin isochromat has been excited by the frequency-swept pulse (29). Tacq is the acquisition time in one repetition period, TR (Fig. 1). Note that the spatial frequency sampling function s(k) is also explicitly time dependent through the acquisition time parameter τ. For almost all hardware designs, τ will be at equally spaced positions in the time domain, and s(k) maps τ to corresponding sample positions in k space. Both standard SWIFT and GM-SWIFT are radial k-space sampling sequences using the projection method so the excitation k-space trajectory follows center out “spokes” in 3D spherical k-space. More specifically, s(k, τ) = step (k(τ) − k) is a Heaviside step function describing signal existence only after a spin has been excited. Note that k-space sampling is uniform for standard SWIFT, but nonuniform for GM-SWIFT. After substituting s(k, τ) into Eq. [8] and integrating over x the signal response becomes

r(k(τ))=iγM0k{h(k(τ)k)}w(k)dk, [9]

with

h(k(τ)k)step(k(τ)k)xρ0(x)eiγx·[kk(τ)]dx. [10]

Here, h is the impulse response function (33). In the k domain, from Eq. [9] it can be seen that the signal response is the convolution of h(k) and w(k). By using the Fourier convolution theorem, the Fourier transform (FT) of r(k(t)) becomes:

R(x)=H(x)·W(x), [11]

where

H(x)=ρ0(x){step(t)} [12]

and

W(x)=kw(k(t))e-iγx·kdk={w(k(t))}. [13]

Note that the signal response r(τ) acquired with uniform sampling interval in the time domain τ should be resampled to uniformly sample in the domain of k(τ) (34). Then, the discrete FT can be used. The same applies for w(k(t)). The spectrum of the spin system H(x), which is actually the convolution of the spin density and the FT of the Heaviside step function as shown in Eq. [12], can be retrieved by

H(x)=R(x)·W(x)|W(x)|2. [14]

In a full set of radial acquisition data, each projection will have another corresponding projection acquired with the opposite gradient direction. In that case, the corresponding projections can be summed and the Heaviside step function will become a constant, with H(x) becoming the real valued spin density ρ0(x).

With constant gradient, G(t) = G0, the general analysis in equations [5–14] above, suitable for GM-SWIFT, reduces to the case of standard SWIFT. In that case, k(t) = γGt and kt. The FT of r(k(τ)) and w(k(t)) in the domain of k in Eq. [11] and Eq. [13] reduces to the direct FT on the signal r(t) and the RF pulse B1(t) in the familiar time domain t (9).

The generalized correlation step can also be treated as a time retransformation or variable substitution in which the k-space is transformed to a special time-modulated frame. In this case, the gradient appears “constant,” and B1 must be transformed into an effective B1 in this frame. Then the properties of linear response theory, as used for the time-independent system or standard SWIFT case, can be applied in this special time-modulated frame.

METHODS

Simulations of a one-dimensional (1D) object and experiments on phantoms and a human subject were performed. In both simulations and experiments, the acquisition was prolonged after the RF pulse to increase the k-space radius and thus the resolution. The fraction of signal acquired during the RF pulse is defined as the ratio of pulse duration and acquisition time, fRF = Tp/Tacq (Fig. 1a) (10). Before performing correlation and reconstruction, the signal acquired after the RF pulse were accordingly weighted to compensate for the difference in receiver duty cycle. All GM-SWIFT excitation pulses used in the simulations and experiments were based on the HS-shaped gradient modulations, as shown in Eq. [2] using np = 4 with different modulation factors gm. As mentioned, the excitation bandwidth Bw is also time dependent when using the time-dependent gradient. Thus, the parameter Bw-max is used to describe the maximum excitation bandwidth as per TR period.

Simulations

Numerical simulations were done based on the Bloch equations (35). The simulated 1D object was composed of 1,000 isochromats distributed evenly. The gapped HS2 RF pulse shape was oversampled by a factor of 16, as typically done in SWIFT (32). The frequency modulation of the RF pulse was calculated according to Eq. [1] for the given F1(t) and G(t). Simulations were carried out for different gm (from 0.1 to 0.9) and compared for gm equal to zero (standard SWIFT). The power spectral density of the pulses was calculated as the square of the FT of the RF pulses.

Simulations of the 1D point-spread function (PSF) were also performed. 1D spectral line broadening due to transverse relaxation was modeled in the simulations as an exponential decay between sampled data points. The procedures introduced in the Theory section were then used to transform the k-space data to the image domain to obtain the PSF.

Experiments

To validate the theory presented above and to evaluate image quality, GM-SWIFT with different gradient modulation factors were performed on a resolution phantom. The resolution phantom is a custom machined plastic (acrylic) container filled with MnCl2 solution (T1~280 ms). Images of the resolution phantom with different modulation factors (gm = 0, 0.8 and 0.9), different Bw-max (62.5 kHz and 31.25 kHz), and different fRF (0.5 and 0.25) were acquired.

A T2* phantom was also imaged. The T2* phantom was made of seven water-filled tubes, each doped with a different concentration of MnCl2, immersed in deionized water in a bigger container. The T2* values of the phantom were then determined individually by spectroscopy. To further evaluate the performance of GM-SWIFT on ultrashort T2* spins, a single human molar tooth was imaged. The tooth was immersed in fluorine fluid (Fluorinert, FC-770, 3M, St. Paul, MN) for matching magnetic susceptibilities.

Human studies were performed according to the procedure approved by the institutional review board of the University of Minnesota Medical School. The brain and ankle of a healthy volunteer were scanned using Bw-max = 62.5 kHz and 96 kHz, respectively, and at different gm and flip angles. Additionally for the ankle imaging, an off-resonance saturation pulse applied at +1 kHz from the central frequency was used as a magnetization preparation pulse to saturate signal from short T2* spins (10). Subtracting images acquired with and without the off-resonance pulse would yield an image dominated by short T2* signals.

Tooth imaging was performed using a 31-cm 9.4 T magnet interfaced to a DirectDrive console (Agilent Technologies, Santa Clara, CA) and a homemade surface coil. All other experiments were performed using a 90-cm 4T scanner (Oxford Magnet, Siemens SC72 gradient, Erlangen, Germany) interfaced to a DirectDrive (Agilent Technologies, Santa Clara, CA) console and a quadrature transverse electromagnetic volume coil.

The sound pressure level was also measured using an integrating sound level meter (model 2239A, Bruel & Kjaer, Naerum, Denmark).

RESULTS

Simulations

By visual inspection, negligible differences can be seen between simulated projections obtained with different levels of the gradient modulation (Fig. 2a). The case of gm = 0 corresponds to standard SWIFT. The power spectral density (Fig. 2b) shows that the power was distributed uniformly across the pulse excitation bandwidth in the gm = 0 case. As gm increases, more power is concentrated in the center frequency area where most spins are excited. The relationships between gm versus normalized SAR, RF amplitude, and acquisition time are shown in Figure 2c. SAR, RF amplitude, and Tacq all decrease as gm increases, while other sequence parameters are held constant. For example, when gm = 0.9, GM-SWIFT reduces SAR, RF amplitude, and Tacq by 90%, 70%, and 45%, respectively, as compared to standard SWIFT. The ability to decrease Tacq with GM-SWIFT is a direct consequence of the improved RF power efficiency of GOIA. That is, Tp decreases as gm increases, with any fixed set of values for flip angle, RF amplitude, and spatial resolution.

FIG. 2.

FIG. 2

Simulation results. (a) Reconstructed 1-D images (object profiles) for different gm values with the generalized (for gm ≠ 0) or original (for gm = 0) correlation procedures. (b) Power spectral density of the RF pulses with different gm. (c) Simulation results showing the relationships between the gradient-modulation factor gm and SAR, RF amplitude, or acquisition time. The flip angle was fixed in the simulation investigating the relationship between SAR or RF amplitude with gm. The RF amplitude, flip angle, and resolution were fixed in the simulation investigating the relationship between Tacq with gm.

Resolution Phantom Experiments

Images of the resolution phantom were acquired for the purpose of comparing the quality of images acquired with standard SWIFT versus GM-SWIFT. As shown in Figure 3a, GM-SWIFT images acquired with large gradient modulation in general have similar quality compared to standard SWIFT images. Intensity profiles (Fig. 3b) of the selected area confirm that standard SWIFT and GM-SWIFT provide similar image resolution. Notably, image intensity arising from the plastic container (red arrows in Figs. 3a,b) is more intense in the standard SWIFT image as compared to the GM-SWIFT images. The latter is due to the different sensitivity of the methods to the ultrashort T2* of the plastic container, as will be discussed later.

FIG. 3.

FIG. 3

Images and intensity profiles of the resolution phantom. (a) Phantom images obtained with different gm using fRF = 0.25 and Bw-max = 62.5 kHz. (b) Intensity profiles corresponding to the yellow dash lines in (a). (c) Phantom images with different gm and Bw-max using fRF = 0.5. Here, flip angles for all images were set to 4°. GM-SWIFT images acquired with large gradient modulation have comparable appearance when compared to standard SWIFT images. Standard SWIFT at Bw = 31.25 kHz has the same power efficiency with GM-SWIFT images with Bw-max = 62.5 kHz and gm = 0.8. When comparing the images of these two conditions, GM-SWIFT images appear sharper and susceptibility artifacts from the plastic and air bubbles are reduced (yellow arrows).

GM-SWIFT with gm= 0.8 can save about 50% of the RF amplitude, which can be accomplished in standard SWIFT by a 50% reduction in bandwidth. However, when comparing standard SWIFT images acquired with Bw = 31.25 kHz with GM-SWIFT images acquired with Bw-max = 62.5 kHz at same flip angle, the GM-SWIFT images appear sharper, and susceptibility artifacts from plastics and air bubbles are reduced (yellow arrows in Fig. 3c).

T2* Sensitive Range

Figure 4 presents plots of the signal-to-noise ratio (SNR) versus T2* for different gm values, along with the corresponding images of the T2* phantom. The noise signal was measured outside of the object (background signal). In general, the SNR is lower for shorter T2*s. The GM-SWIFT image with gm = 0.8 (blue line), when compared to the standard SWIFT image (see green line), has higher SNR for T2*>400 μs and lower SNR for T2*<400 μs, whereas the SNR is nearly zero for T2*<100 μs. The SNR improvement of GM-SWIFT for tubes containing spins with T2*>400 μs occurs due to reduced background signal from the poorly resolved tubes containing spins with extremely short T2* (<100 μs). Although GM-SWIFT lacks sensitivity to spins with T2*< 100 μs (marked as red region), it still preserves signal from spins with T2* ~200 μs (marked as blue region). This point is exemplified by the tooth images shown in Figures 5a–d, in which the T2* of dentin is known to be about 200 μs (36). GM-SWIFT with gm = 0.8 can still preserve the signal from dentin and can delineate the shape of dentin to a comparable level as SWIFT, although with slightly increased blur (yellow arrows). To demonstrate the insensitivity of GM-SWIFT to extremely short T2* spins, a piece of silicone rubber with T2*< 50 μs was placed on top of the phantom. As can be seen in Figures 5e and 5f, the rubber is visible and poorly resolved in the SWIFT image but is invisible in the GM-SWIFT image (red arrows). Due to the reduced visibility of the plastic containers in the GM-SWIFT case, the background is also much cleaner in the GM-SWIFT image than in the SWIFT image.

FIG. 4.

FIG. 4

(a) Plot of SNR (signal to background noise ratio) dependence on T2* using different modulation factors. (b) and (c) are images of the T2* phantom.

FIG. 5.

FIG. 5

(a, b, c, and d) Images of a tooth. (b) and (d) are images with increased intensity scaling. The signal from the dentin is sufficient in both SWIFT and GM-SWIFT cases. GM-SWIFT with gm = 0.8 is slightly more blurred (yellow arrows). (e) and (f) are images of the resolution phantom with a piece of silicone rubber placed on top of it (red arrows). The rubber is visible in the SWIFT image; however, due to the ultrashort T2* value, the rubber is not resolved well. Also, a halo over the whole image can be observed which comes from the plastic materials of the phantom. The image for GM-SWIFT (f) on the other hand is cleaner; the rubber and the container are both invisible.

Results from simulations investigating the PSF of GM-SWIFT are shown in Figure 6. The amplitude of the PSF decreases as gm increases due to the fast signal decay (Fig. 6a), whereas the full width at half maximum of the PSF increases only slightly as gm increases, despite the ultrashort T2* (400 μs) (Fig. 6b). When comparing the PSF of GM-SWIFT with that of standard SWIFT at lower Bw with the same RF power efficiency, it can be seen that GM-SWIFT has better resolution and higher signal level. This agrees well with the results of the phantom experiments (Fig. 3c).

FIG. 6.

FIG. 6

(a) PSF for standard SWIFT and GM-SWIFT with T1 = 1000 ms and T2 = 0.4 ms at different Bw or gradient modulation factor gm. (b) PSF in (a) with normalized amplitude. The standard SWIFT with Bw = 62.5 kHz has the same power-to-flip-angle efficiency as GM-SWIFT with Bw-max = 125 kHz and gm = 0.8.

Human In Vivo Experiment

Human brain images from standard SWIFT and GM-SWIFT are shown in Figure 7. The images in Figures 7a and 7b appear more like proton density-weighted images due to the low flip angle (2° for Fig. 7a; 4° for Fig. 7b) used. In comparison, the GM-SWIFT images acquired with matched RF power exhibit good T1-weighted contrast. The RF power delivered in these two cases (Figs. 7b,c) was identical. According to the Bloch simulation, the flip angle for GM-SWIFT with gm equal to 0.9 is about three-fold higher than in the standard SWIFT case. This high flip angle is frequently needed to obtain a good T1 contrast between the white and gray matter in the brain.

FIG. 7.

FIG. 7

In vivo human head images. (a) and (b) are standard SWIFT images with flip angle 2° and 4°. (c) is GM-SWIFT image with factor gm = 0.9. The RF power delivered in (b) and (c) are the same. Better T1 contrast is observed in the GM-SWIFT images because the flip angle achieved could be increased to as high as 12°.

Human ankle images acquired by standard SWIFT and GM-SWIFT are shown in Figure 8. In tendon, T2* is ~2ms and T1 is on the order of several hundred milliseconds (37). The Achilles tendon usually appears dark in gradient echo images (Fig. 8d). As in the phantom experiments, image quality of the ankle in Figure 8 is similar with GM-SWIFT and standard SWIFT acquisitions when performed with the same flip angle. The Achilles tendon is visible in all SWIFT and GM-SWIFT images. However, it is better delineated in the GM-SWIFT image with matched power than in the standard SWIFT image (red arrows) because the higher flip angle achieved is closer to the Ernst angle for tendon. With an off-resonance saturation pulse, the tendon spins with short T2 are saturated, whereas the surrounding slowly relaxing spins are minimally affected. Subtracting GM-SWIFT images acquired with and without the off-resonance pulse yields an image dominated by short T2* signals (Fig. 8e). In the subtraction image, a low level of intensity is also seen in the muscle, which is most likely due to a magnetization transfer effect.

FIG. 8.

FIG. 8

In vivo human ankle images. (a, b, and c) are standard SWIFT or GM-SWIFT with fat saturation. (d) GRE image. (e) Subtraction result between GM-SWIFT image without and with off resonance saturation.

The A-frequency-weighted equivalent continuous sound pressure level (Leq) of GM-SWIFT at different gm values is shown in Figure 9. Standard SWIFT without any gradient modulation is quiet and has Leq at around 52.5 dB. With gradient modulation, Leq increases with gm, but remains less than 75 dB. From Figure 9, it can be seen that the absolute sound pressure level is approximately linear with the gradient modulation. As compared with the typical Leq values of common fast MRI sequences in the range of 100 to 110 dB (38), GM-SWIFT is still much quieter.

FIG. 9.

FIG. 9

The frequency-weighted equivalent continuous sound pressure level Leq of GM-SWIFT with different gradient-modulation factors, gm.

DISCUSSION

In this work, a modified SWIFT sequence with gradient modulation called GM-SWIFT is introduced. The corresponding generalized correlation procedures to reconstruct images for GM-SWIFT are developed. Bloch simulations and experimental data verified the theory and demonstrate the imaging capabilities of GM-SWIFT.

The signal acquired in a SWIFT acquisition is contaminated by the RF pulse; therefore, it needs the correlation step to resolve the resonating signal from the RF pulse signal. As mentioned, some extra steps are needed in the correlation procedures for GM-SWIFT over the standard one, because in the case when the field gradient is time-varying, the original correlation procedure is not applicable. The changing gradient has an influence on the time when the spin gets excited and the evolution after excitation. The accumulated phase of a given spin is not only dependent on the time interval that it evolves but also on the specific time point when it is excited. Because the excitation phase is mixed along with the acquisition phase in the SWIFT scheme, the concept of excitation k-space as defined in Eq. [5] (31) is a good tool for dealing with the phase problem here.

The ability of GM-SWIFT to reduce SAR is beneficial for imaging of humans. Achieving T1-constrast requires high flip angle; therefore, it can be limited by hardware or SAR or requires a magnetization preparation module that reduces acquisition efficiency. Due to its increased flexibility in setting the flip angle, GM-SWIFT is capable of producing T1 contrast without magnetization preparation. Also, for imaging of fast relaxing spins, high excitation bandwidth is required but may not be attainable with standard SWIFT due to hardware (peak RF power) and SAR constraints. As a result, GM-SWIFT is a promising variation of SWIFT, particularly for human applications, by allowing reduced SAR, overcoming peak power limitations of the hardware, and producing often needed T1–weighted contrast. Furthermore, GM-SWIFT still produces much reduced sound level than conventional sequences (Fig. 9) because the gradient polarity need not be inverted quickly but instead is modulated smoothly below the gradient slew rate limit. Also, although the GOIA approach was used in this paper to generate RF pulses, other gradient modulation approaches such as VERSE (22) can also be applied to modify the RF pattern as long as they can achieve the desired flat excitation profile.

The simulations and phantom studies showed GM-SWIFT is able to achieve comparable image quality as standard SWIFT, even when using a gradient-modulation factor as high as 0.9. One consequence of gradient modulation is the reduced sensitivity of GM-SWIFT for ultrashort T2* spins as the gradient-modulation factor increases. However, the ability to alter the T2* sensitivity range with GM-SWIFT can be a benefit in certain cases. Standard SWIFT with constant gradient and large band-width is able to capture signal from spins with T2* as short as several microseconds; and as such, essentially all spins are present in SWIFT images, including plastic materials commonly used in coil construction. However, due to limited bandwidth, in practice these signals cannot be resolved and they manifest themselves as a halo over the whole image. With large gradient modulation, GM-SWIFT is less sensitive to spins with extremely short T2* (several to tens of microseconds); as a result, it generates images with a cleaner background. At the same time, GM-SWIFT with high gm = 0.9 still retains the ability to resolve spins with T2* longer than 200 μs but at the expense of some loss of image resolution (Fig. 6). The latter occurs in GM-SWIFT with HS-shaped gradient modulation because the fast decaying spins experience the low bandwidth portion of the GOIA pulse immediately after excitation. Compared to the constant gradient condition, some k-space information is lost in this process, which causes reduced sharpness in images of ultra-fast relaxing spins. Although most demonstrations in this article utilized high gradient modulation factor (gm = 0.8 or 0.9), GM-SWIFT can also work with a medium or small gm value. In practice, by increasing gm just enough to satisfy SAR, peak RF amplitude, and/or T1-weighting requirements, undesirable effects due to an increased T2*-sensitivity can be minimized.

In addition to reducing SAR, peak RF amplitude, and acquisition time over standard SWIFT, GM-SWIFT provides other flexibilities. For example, besides the HS-shape used herein, other gradient modulation shapes (e.g., a linearly increasing function) can be used in GM-SWIFT for other purposes, such as increasing the bandwidth of the acquisition period after the RF pulse. The generalized correlation procedures introduced here should also be suitable for other types of gradient modulation.

Of note, in the limit gm → 1, GM-SWIFT resembles UTE. However, the gradient in UTE always starts from zero amplitude, whereas GM-SWIFT offers flexibility to operate with an optimal gm value (i.e., the minimum value) that just satisfies some practical constraints (e.g., SAR, tolerated sound level, and unresolved background signal suppression), while minimizing image blur and SNR loss for short T2* spins. Compared with UTE, the requirement to switch fast between transmit and receive modes is more stringent with SWIFT, which currently limits its achievable bandwidth. However, GM-SWIFT reduces the bandwidth during excitation, which makes an increased switching time permissible such as in UTE. Hence, GM-SWIFT should be easier than SWIFT to implement on clinical scanners that cannot switch rapidly between transmit and receive modes.

As with most sequences that use gradient modulation, GM-SWIFT is sensitive to gradient performance. The gradient needs to be calibrated (39) so that the gradient timing error in different directions needs to be under several microseconds. A global delay in all directions can be compensated in the correlation step, but the occurrence of different delays in each direction introduces distortion on the shape of the gradient modulation, which produces bright/dark line artifacts at the edges of an object. A detailed discussion about the influence of gradient performance on GM-SWIFT is beyond the scope of this paper.

CONCLUSION

In summary, GM-SWIFT can achieve reductions of SAR, RF amplitude, or acquisition time, and provides control over the T2*-sensitive range for producing a clean background in images. The tradeoff is some reduction in the resolution of images of ultrafast relaxing spins, depending on the level of the gradient modulation used. By manipulating the gradient, GM-SWIFT can maximize the efficiency of RF power and provide a way to optimize the settings that balance RF amplitude, SAR, scan time, and image quality considerations.

Acknowledgments

Grant sponsors: National Institute of Biomedical Imaging and Bioengineering (NIBIB), National Center for Research Resources (NCRR), and National Center for Advancing Translational Sciences (NCATS) of the National Institutes of Health; Grant numbers: P41EB015894, S10RR023730, S10RR0027290, and KL2TR000113; Grant sponsor: WM KECK Foundation.

References

  • 1.Case TA, Durney CH, Ailion DC, Cutillo AG, Morris AH. A mathematical-model of diamagnetic line broadening in lung-tissue and similar heterogeneous systems - calculations and measurements. J Magn Reson. 1987;73:304–314. [Google Scholar]
  • 2.Kveder M, Zupancic I, Lahajnar G, Blinc R, Suput D, Ailion DC, Ganesan K, Goodrich C. Water proton nmr relaxation mechanisms in lung-tissue. Magn Reson Med. 1988;7:432–441. doi: 10.1002/mrm.1910070406. [DOI] [PubMed] [Google Scholar]
  • 3.Ferrucci JT, Stark DD. Iron oxide-enhanced MR imaging of the liver and spleen: review of the first 5 years. Am J Roentgenol. 1990;155:943–950. doi: 10.2214/ajr.155.5.2120963. [DOI] [PubMed] [Google Scholar]
  • 4.Bergin CJ, Pauly JM, Macovski A. Lung parenchyma–projection reconstruction MR imaging. Radiology. 1991;179:777–781. doi: 10.1148/radiology.179.3.2027991. [DOI] [PubMed] [Google Scholar]
  • 5.Robson MD, Gatehouse PD, Bydder M, Bydder GM. Magnetic resonance: an introduction to ultrashort TE (UTE) imaging. J Comput Assist Tomogr. 2003;27:825–846. doi: 10.1097/00004728-200311000-00001. [DOI] [PubMed] [Google Scholar]
  • 6.Hafner S. Fast imaging in liquids and solids with the back-projection low angle shot (BLAST) technique. Magn Reson Imag. 1994;12:1047–1051. doi: 10.1016/0730-725x(94)91236-p. [DOI] [PubMed] [Google Scholar]
  • 7.Madio DP, Lowe IJ. Ultra-fast imaging using low flip angles and FIDs. Magn Reson Med. 1995;34:525–529. doi: 10.1002/mrm.1910340407. [DOI] [PubMed] [Google Scholar]
  • 8.Weiger M, Brunner DO, Dietrich BE, Muller CF, Pruessmann KP. ZTE imaging in humans. Magn Reson Med. 2013;70:328–332. doi: 10.1002/mrm.24816. [DOI] [PubMed] [Google Scholar]
  • 9.Idiyatullin D, Corum C, Park JY, Garwood M. Fast and quiet MRI using a swept radiofrequency. J Magn Reson. 2006;181:342–349. doi: 10.1016/j.jmr.2006.05.014. [DOI] [PubMed] [Google Scholar]
  • 10.Garwood M, Idiyatullin D, Corum C, et al. Encycloepedia of Magnetic Resonance. New York, NY: John Wiley & Sons; 2012. Capturing signals from fast-relaxing spins with frequency-swept MRI: SWIFT. [Google Scholar]
  • 11.Emid S, Creyghton JHN. High-resolution NMR imaging in solids. Physica B & C. 1985;128:81–83. [Google Scholar]
  • 12.Balcom BJ, Macgregor RP, Beyea SD, Green DP, Armstrong RL, Bremner TW. Single-point ramped imaging with T1 enhancement (SPRITE) J Magn Reson A. 1996;123:131–134. doi: 10.1006/jmra.1996.0225. [DOI] [PubMed] [Google Scholar]
  • 13.Grodzki DM, Jakob PM, Heismann B. Ultrashort echo time imaging using pointwise encoding time reduction with radial acquisition (PETRA) Magn Reson Med. 2012;67:510–518. doi: 10.1002/mrm.23017. [DOI] [PubMed] [Google Scholar]
  • 14.Idiyatullin D, Corum C, Moeller S, Prasad HS, Garwood M, Nixdorf DR. Dental magnetic resonance imaging: making the invisible visible. J Endodontics. 2011;37:745–752. doi: 10.1016/j.joen.2011.02.022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Kendi AT, Khariwala SS, Zhang J, Idiyatullin DS, Corum CA, Michaeli S, Pambuccian SE, Garwood M, Yueh B. Transformation in mandibular imaging with sweep imaging with Fourier transform magnetic resonance imaging. Arch Otolaryngol Head Neck Surg. 2011;137:916–919. doi: 10.1001/archoto.2011.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Lehto LJ, Sierra A, Corum CA, Zhang J, Idiyatullin D, Pitkanen A, Garwood M, Grohn O. Detection of calcifications in vivo and ex vivo after brain injury in rat using SWIFT. Neuroimage. 2012;61(4):761–772. doi: 10.1016/j.neuroimage.2012.03.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Nelson MT, Benson JC, Prescott T, Corum CA, Snyder A, G M. Breast MRI using SWeep imaging with Fourier transform (SWIFT) Eur J Radiol. 2012;81:S109. doi: 10.1016/S0720-048X(12)70044-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Luhach I, Idiyatullin D, Lynch CC, Corum C, Martinez GV, Garwood M, Gillies RJ. Rapid ex vivo imaging of PAIII prostate to bone tumor with SWIFT-MRI. Magn Reson Med. 2013;72:858–863. doi: 10.1002/mrm.24979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Rautiainen J, Lehto LJ, Tiitu V, et al. Osteochondral repair: evaluation with sweep imaging with Fourier transform in an equine model. Radiology. 2013;269:113–121. doi: 10.1148/radiol.13121433. [DOI] [PubMed] [Google Scholar]
  • 20.Kobayashi N, Idiyatullin D, Corum C, Weber J, Garwood M, Sachdev D. SWIFT MRI enhances detection of breast cancer metastasis to the lung. Magn Reson Med. 2015;73:1812–1819. doi: 10.1002/mrm.25301. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Zhang J, Chamberlain R, Etheridge M, Idiyatullin D, Corum C, Bischof J, Garwood M. Quantifying iron-oxide nanoparticles at high concentration based on longitudinal relaxation using a three-dimensional SWIFT look-locker sequence. Magn Reson Med. 2014;71:1982–1988. doi: 10.1002/mrm.25181. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Conolly S, Nishimura D, Macovski A, Glover G. Variable-rate selective excitation. J Magn Reson. 1988;78:440–458. [Google Scholar]
  • 23.Tannus A, Garwood M. Adiabatic pulses. NMR Biomed. 1997;10:423–434. doi: 10.1002/(sici)1099-1492(199712)10:8<423::aid-nbm488>3.0.co;2-x. [DOI] [PubMed] [Google Scholar]
  • 24.Ordidge RJ, Wylezinska M, Hugg JW, Butterworth E, Franconi F. Frequency offset corrected inversion (FOCI) pulses for use in localized spectroscopy. Magn Reson Med. 1996;36:562–566. doi: 10.1002/mrm.1910360410. [DOI] [PubMed] [Google Scholar]
  • 25.Hioe FT. Solution of Bloch equations involving amplitude and frequency modulations. Phys Rev A. 1984;30:2100–2103. [Google Scholar]
  • 26.Silver MS, Joseph RI, Hoult DI. Highly selective π/2 and π-pulse generation. J Magn Reson. 1984;59:347–351. [Google Scholar]
  • 27.Silver MS, Joseph RI, Hoult DI. Selective spin inversion in nuclear magnetic-resonance and coherent optics through an exact solution of the Bloch-Riccati equation. Phys Rev A. 1985;31:2753–2755. doi: 10.1103/physreva.31.2753. [DOI] [PubMed] [Google Scholar]
  • 28.Tannus A, Garwood M. Improved performance of frequency-swept pulses using offset-independent adiabaticity. J Magn Reson Ser A. 1996;120:133–137. [Google Scholar]
  • 29.Garwood M, DelaBarre L. The return of the frequency sweep: designing adiabatic pulses for contemporary NMR. J Magn Reson. 2001;153:155–177. doi: 10.1006/jmre.2001.2340. [DOI] [PubMed] [Google Scholar]
  • 30.Hoult DI. Solution of the Bloch equations in the presence of a varying B1 field-approach to selective pulse analysis. J Magn Reson. 1979;35:69–86. [Google Scholar]
  • 31.Pauly J, Nishimura D, Macovski A. A k-space analysis of small-tip-angle excitation. J Magn Reson. 1989;81:43. doi: 10.1016/j.jmr.2011.09.023. [DOI] [PubMed] [Google Scholar]
  • 32.Idiyatullin D, Corum C, Moeller S, Garwood M. Gapped pulses for frequency-swept MRI. J Magn Reson. 2008;193:267–273. doi: 10.1016/j.jmr.2008.05.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Ernst R, Bodenhausen G, Wokaun A. Principles of Nuclear Magnetic Resonance in One and Two Dimensions. New York, NY: Oxford University Press; 1987. [Google Scholar]
  • 34.Frahm J, Hanicke W. Signal restoration for NMR imaging using time-dependent gradients. J Phys E: Sci Instrum. 1984;17:612. [Google Scholar]
  • 35.Idiyatullin D. NMR Kitchen. Available at: http://www.cmrr.umn.edu/~djaudat/nmrkitchen/index.html. Accessed on 2002.
  • 36.Schreiner LJ, Cameron IG, Funduk N, Miljkovic L, Pintar MM, Kydon DN. Proton NMR spin grouping and exchange in dentin. Biophys J. 1991;59:629–639. doi: 10.1016/S0006-3495(91)82278-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Filho GH, Du J, Pak BC, Statum S, Znamorowski R, Haghighi P, Bydder G, Chung CB. Quantitative characterization of the Achilles tendon in cadaveric specimens: T1 and T2* measurements using ultrashort-TE MRI at 3 T. Am J Roentgenol. 2009;192:W117–W124. doi: 10.2214/AJR.07.3990. [DOI] [PubMed] [Google Scholar]
  • 38.Price DL, De Wilde JP, Papadaki AM, Curran JS, Kitney RI. Investigation of acoustic noise on 15 MRI scanners from 0.2 T to 3 T. J Magn Reson Imag. 2001;13:288–293. doi: 10.1002/1522-2586(200102)13:2<288::aid-jmri1041>3.0.co;2-p. [DOI] [PubMed] [Google Scholar]
  • 39.Duyn JH, Yang YH, Frank JA, van der Veen JW. Simple correction method for k-space trajectory deviations in MRI. J Magn Reson. 1998;132:150–153. doi: 10.1006/jmre.1998.1396. [DOI] [PubMed] [Google Scholar]

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