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. 2022 Mar 10;88(1):180–194. doi: 10.1002/mrm.29199

Parallel transmit pulse design for saturation homogeneity (PUSH) for magnetization transfer imaging at 7T

David Leitão 1,, Raphael Tomi‐Tricot 2, Pip Bridgen 1, Tom Wilkinson 1, Patrick Liebig 3, Rene Gumbrecht 3, Dieter Ritter 3, Sharon L Giles 1, Ana Baburamani 4, Jan Sedlacik 1,4, Joseph V Hajnal 1,4, Shaihan J Malik 1,4
PMCID: PMC9315051  PMID: 35266204

Abstract

Purpose

This work proposes a novel RF pulse design for parallel transmit (pTx) systems to obtain uniform saturation of semisolid magnetization for magnetization transfer (MT) contrast in the presence of transmit field B1+ inhomogeneities. The semisolid magnetization is usually modeled as being purely longitudinal, with the applied B1+ field saturating but not rotating its magnetization; thus, standard pTx pulse design methods do not apply.

Theory and Methods

Pulse design for saturation homogeneity (PUSH) optimizes pTx RF pulses by considering uniformity of root‐mean squared B1+, B1rms, which relates to the rate of semisolid saturation. Here we considered designs consisting of a small number of spatially non‐selective sub‐pulses optimized over either a single 2D plane or 3D. Simulations and in vivo experiments on a 7T Terra system with an 8‐TX Nova head coil in five subjects were carried out to study the homogenization of B1rms and of the MT contrast by acquiring MT ratio maps.

Results

Simulations and in vivo experiments showed up to six and two times more uniform B1rms compared to circular polarized (CP) mode for 2D and 3D optimizations, respectively. This translated into 4 and 1.25 times more uniform MT contrast, consistently for all subjects, where two sub‐pulses were enough for the implementation and coil used.

Conclusion

The proposed PUSH method obtains more uniform and higher MT contrast than CP mode within the same specific absorption rate (SAR) budget.

Keywords: B1+ inhomogeneity, magnetization transfer, parallel transmit, RF pulse design, ultrahigh‐field

1. INTRODUCTION

Imaging at ultrahigh‐field benefits from increased SNR 1 but is also hampered by larger transmit field (B1+) inhomogeneity. This can lead to non‐uniform excitation of the magnetization and undesired spatially varying contrast. Various hardware 2 , 3 and pulse design 4 , 5 solutions have been proposed and one of the most flexible is parallel transmit 6 , 7 , 8 , 9 (pTx), which uses multiple transmit channels to enable spatial and temporal manipulation of the B1+ field. Its most basic form, “static” B1+ shimming, 10 , 11 , 12 attempts to create a more homogeneous B1+ field by applying amplitude and phase weightings to the individual transmit channels without changing the RF pulse waveforms themselves. Much greater control can be achieved if we instead consider the magnetization rotation using both RF and gradients; in this case a desired “flip angle” distribution is usually designed by tailoring the RF pulse waveforms on each channel. This is often achieved using the small tip angle approximation in which case the design problem can be considered using the excitation k‐space concept. 13 For larger rotations this concept breaks down but various methods still exist to design RF pulses by considering the rotation of magnetization directly. 14 , 15 , 16

Although a great diversity of RF pulse design methods exist, they typically have in common the use of the Bloch equation 17 to model the effect of the applied RF and/or gradient fields. Assuming short duration pulses, the effect of applying these fields is to rotate the magnetization. The Bloch equation can successfully model the magnetization dynamics of free water, but in biological tissues there is usually also a significant pool of semisolid magnetization. 18 , 19 This latter pool is affected differently by RF fields and can exchange magnetization with the free water, a phenomenon usually referred to as magnetization transfer 20 , 21 (MT). Two common assumptions of the semisolid pool are: (1) it can be modeled as having no transverse magnetization due to its very short T2s10μs; (2) its longitudinal magnetization directly saturates at a rate proportional to the applied RF power 22 (i.e., B1+2). These properties and the coupling with free water magnetization can be modeled using the so‐called binary‐spin‐bath model. 20

Since the saturation of semisolid magnetization depends on B1+2 and not simply B1+, the effect of B1+ inhomogeneities is more severe. Existing RF pulse design methods that might be used to correct for non‐uniform flip angles in free water magnetization will fail if used for designing semisolid saturation pulses because: (i) the semisolid has no transverse component that can be rotated by any applied gradients that are often used to improve excitation properties 23 , 24 and (ii) the saturation rate of its longitudinal magnetization depends on B1+2 and not B1+. 20 , 22

An important distinction here must be drawn between the saturation of semisolids, which is the subject of this work, and general ‘saturation’ pulses that are used (often with spoiler gradients) to suppress magnetization from free water and/or solutes. For the latter type, there are examples using standard pTx pulse design methods, 25 , 26 as there is transverse magnetization amenable to rotation from the RF pulses and gradients. For the remainder of this article, the term “saturation” is used to refer to semisolid saturation, unless otherwise specified.

In this work, we propose a novel RF pulse design framework for semisolid saturation, called pulse design for saturation homogeneity (PUSH). We first explore a general case of RF pulse design in the presence of semisolids, and then propose a simple exemplar method using trains of short sub‐pulses with pTx and demonstrate the efficacy of this approach for MT‐weighted imaging at 7 T.

2. THEORY

2.1. Physics models

The dynamics of free water (f) magnetization Mf=MxfMyfMzfT are described by the Bloch equation 17 :

dMfdt=0γΔBzγB1,yγΔBz0γB1,xγB1,yγB1,x0+R2f000R2f000R1fMf+00R1fM0f=(A+E)Mf+c (1)

where A comprises RF (B1+=B1,x+iB1,y) and B0 field variations (ΔBz=ΔB0+G·r) at coordinates r induced by off‐resonance ΔB0 and gradients G. Operators E and c contain relaxation effects through the relaxation rates R1f (=1/T1f) and R2f (=1/T2f), and M0f is the equilibrium magnetization.

On the other hand, systems with MT can be described by the binary‐spin‐bath model, 22 which contains two pools corresponding to free water (f) and semisolid (s) magnetization:

ddtMfMzs=A00W+R2f0000R2f0000kfsR1fksf00kfsksfR1sMfMzs+cR1sM0s=(A˜+E˜)MfMzs+c˜. (2)

The operators A˜, E˜ and c˜ include the effects of RF, gradients, relaxation, and exchange. In these expressions R1s (=1/T1s) is the semisolid longitudinal relaxation rate, M0s is the semisolid equilibrium magnetization, kfs is the exchange rate from Mzf to Mzs (vice‐versa for ksf), and W is the average saturation rate 22 that models the semisolid response to RF. In case of RF irradiation at a single off‐resonance frequency ω, then W is given by 22

W=πγ2gωγΔBz,T2s1τ0τB1+(t)2dt=πγ2gωγΔBz,T2sB1+2 (3)

where B1+2 is the mean squared B1+ over pulse duration τ, and g is the semisolid absorption lineshape that depends on its transverse relaxation time T2s and on the frequency shift ωγΔBz. Typically, the absorption lineshape has much broader bandwidth 21 than the RF or B0 field variations in the absence of gradients, such that gωγΔBz,T2sgω,T2s. It has also been observed that g may have a chemical shift away from water (e.g., Jiang et al. 27 observed 2.6 ppm in white matter)—this shift should be considered part of the definition of g. Although Equation (3) defines W for single frequency irradiation, it can also be calculated in some cases for RF pulses with multiple frequencies (e.g., multiband pulses 28 ).

2.2. RF pulse design

In solving the Bloch equation (Equation 1) for a short RF pulse, matrix E and vector c can be neglected as relaxation typically occurs over a longer timescale, hence the magnetization dynamics comprises of rotations determined by A. This can be solved by discretizing the sequence parameters in Nt constant piecewise timesteps of duration Δt, each producing a rotation R(t):

Mf(t+Δt)=exp(A(t)Δt)Mf(t)=R(t)Mf(t) (4)

whereas the full rotation Rfull of the magnetization can be calculated by taking left‐wise multiplication over all R(t).

Similarly, in the binary‐spin‐bath model (Equation 2) relaxation and exchange can be assumed to occur over a longer timescale than the typical RF pulse allowing them to be neglected for RF pulse design. The magnetization response is thus determined by A˜ and can also be solved by discretizing time:

MfMzs(t+Δt)=expA(t)00WΔtMfMzs(t) (5)

In the absence of exchange, the response of the free water and semisolid pools is decoupled (A˜ is block diagonal); thus, the matrix exponential is the exponential of its diagonal terms. The full magnetization response to an RF pulse can then be calculated by taking the product of the matrix exponentials from all Nt timesteps over the duration τ of the RF:

MfMzs(t+τ)=t=1NtR(t)00eWΔtMfMzs(t)=Rfull00eWτMfMzs(t) (6)

where the free water and semisolid pools responses are independent from each other. Design of RF pulses for free water magnetization usually target a desired flip angle αdes from rotation matrix Rfull. On the other hand, to control saturation of semisolid magnetization we can target a desired average saturation rate Wdes. Thus, the RF pulse design for both pools can be cast as a joint optimization:

{b^,G^}argminb,G(1λ)ααdes22+λWWdes22 (7)

where λ[0,1] balances the error between the two terms and b and G are the RF and gradient waveforms, respectively.

2.3. Pulse design for saturation homogeneity

In this work, we explored design of RF pulses to achieve uniform semisolid saturation, using pTx systems. To this end, we have considered single frequency high power saturation pulses 29 , 30 (Figure 1A) applied at large offset frequency ω. We assume that ω is much larger than the saturation pulse bandwidth such that we can neglect the effect on the free water magnetization, that is, it has null flip angle (α0)—effectively performing the pulse design in Equation (7) with λ=1. Furthermore, according to Equation (3) for single frequency irradiation we can control semisolid saturation using B1+2 instead of W in the pulse design.

FIGURE 1.

MRM-29199-FIG-0001-b

(A) Sequence diagram for one TR of the MT‐weighted spoiled gradient‐recalled‐echo sequence used (here shown for 3D imaging but adaptable for 2D imaging). (B) In this work, the saturation pulse can be composed of several sub‐pulses applied at large offset frequency as shown with three sub‐pulses. These are individually scaled with complex weights per channel, where the weights are calculated with PUSH (Equation 12) or with CP mode. The excitation pulse is always applied in CP mode

For a pTx system, the applied B1+ field is the linear superposition of the fields from its Nch channels:

B1+(r,t)=j=1Nchsj(r)bj(t) (8)

where sj(r) are the transmit sensitivity maps (units of μT/V) and bj(t) are the RF waveforms for each channel (units of V). In this implementation, we used short TR sequences in which saturation depends on the cumulative effect over many TR periods, scaling with the mean squared B1+ (Equation 3) averaged over the TR 31 , 32 instead of the pulse duration τ:

B1+2(r)=1TR0τB1+(r,t)2dt=1TR0τj=1Nchsj(r)bj(t)2dt (9)

Here, the contribution from any other pulses during the same TR period (e.g., excitation pulse as described in Methods) is neglected as they typically have much less power than the designed saturation pulse. The advantage of designing for B1rms (=B1+2) at the sequence rather than pulse level is that the former is typically the limiting factor for an MT‐weighted sequence since it scales with the SAR; exposing this limit allows more flexibility to optimize the sequence within this constraint.

In this work, we applied the same normalized waveform b(t) (arbitrary units) in each channel scaled by a complex weight wj (units of V), moving the sum outside the integral:

B1+2r,wj=j=1Nchsj(r)wj21TR0τ|b(t)|2dt=j=1Nchsj(r)wj2b2 (10)

where b2 is the mean squared B1+ of the normalized waveform. Similarly to spokes 33 , 34 /kT‐points, 23 the pulse can be extended by concatenating Nsp sub‐pulses, designated as PUSH‐Nsp, with each sub‐pulse weighted differently:

B1+2r,wjp=p=1Nspj=1Nchsj(r)wjp2b2 (11)

where p is the sub‐pulse index. Each sub‐pulse produces its own spatial mean squared B1+, such that the total B1+2 is the sum of the contributions from all sub‐pulses (example in Supporting Information Figure S1, which is available online). Finally, the RF complex weights wjp can be designed to achieve a desired saturation by solving the optimization:

w^jpargminwjpB1+2r,wjpβ(r)22SAR10g,vSAR10g,max,1vNVOP,s.t.PjwjpPmax,1jNch,wjpVmax,1pNsp,1jNch. (12)

where β(r) specifies the desired spatial B1+2=W/πγ2gω,T2s. Note that the optimization has been rewritten in terms of the square root of B1+2—doing so does not change the global optima. This was done so that the special case of a saturation pulse consisting of a single sub‐pulse would reduce to magnitude least‐squares (MLS) B1+ shimming 11 , 12 , 35 of the saturation pulse. The terms “PUSH‐1 (1 sub‐pulse)” and “static shimming” will be used interchangeably from here onward. Optimization was constrained to be within local SAR limits for a total of NVOP virtual observation points (VOPs), 36 as well as average power per channel Pj and maximum voltage Vmax per sub‐pulse and per channel. 37 In the case of using the circular polarized (CP) mode, the complex weights are defined as wj=wCPexpi2π(j1)/Nch, where wCP was determined by minimizing the cost function (Equation 12) and i2=1 denotes the imaginary unit.

3. METHODS

All experiments were performed using a 7T scanner (MAGNETOM Terra, Siemens Healthcare, Erlangen, Germany) in prototype research configuration, with an 8Tx/32Rx head coil (Nova Medical, Wilmington MA, USA).

3.1. Pulse sequence setup

To illustrate the PUSH concept, we used a simple MT‐weighted spoiled gradient‐recalled echo (SPGR) sequence containing one saturation and one excitation pulse per TR (Figure 1A). The saturation sub‐pulses (Figure 1B) applied at offset frequency ω=2kHz had a Gaussian waveform (time bandwidth product =2.27,τ=4ms) and its complex weights were determined using Equation (12). Pulse optimization was solved in Matlab (Mathworks Inc., Natick, MA) using the interior‐point algorithm from the fmincon routine, providing first and second order derivatives; constraints (SAR10g,max=20W/kg over eight VOPs provided by the vendor and in first level SAR mode, 38 Vmax=207V,Pmax=24W) were evaluated within the vendor pulse design framework included in the scanner console software (release Syngo.MR VE12U). A multi‐start strategy with 10 random seeds proved to obtain consistent solutions.

As we focused on the saturation pulse design, the excitation was always in CP mode. To minimize the impact of the excitation pulse on the MT contrast, the flip angle was minimized balancing SNR and its inhomogeneity profile (Supporting Information Figure S2). This way the excitation pulse also had negligible power compared to the saturation pulse such that B1+2 in Equation (12) can be assumed equivalent to the sequence B1rms.

3.2. Simulations

To explore the pulse design performance, saturation pulses with different number of sub‐pulses (1, 2, and 3) were designed offline for a spatially invariant β ranging from 0.1μT to 2μT in steps of 0.1μT. The optimizations were performed for both 2D axial slices and 3D volume of brain transmit maps from an eight‐channel pTx system (details below), with each 2D single slice/3D optimization taking 7/22 s in Matlab R2020b (Mathworks Inc., Natick, MA) on a desktop computer (Intel i9‐10900X @ 3.70GHz, 64GB of RAM, not parallelized). The solutions were analyzed in terms of their B1rms maps and normalized RMS error (NRMSE).

To predict the impact of spatial variation in mean squared B1+ on the MT contrast, magnetization transfer ratio (MTR) maps were simulated using the definition:

MTR(%)=100×MrefMsatMref (13)

where Msat and Mref are the steady‐state signals acquired with and without the saturation pulse, respectively. For the MTR simulations, the steady state of an SPGR sequence was calculated by solving Equation (2) assuming the whole brain to have uniform tissue parameters similar to white matter 39 , 40 : R1f=0.4s1,T2f=60ms,f=M0s/M0s+M0f=0.1357,k=ksf/(1f)=kfs/f=32.79s1,R1s=1.85s1,T2s=9.6μs, and a Super‐Lorentzian absorption lineshape (centered at ‐773 Hz). 27 Different saturation pulses optimized offline forβ=1μT were applied combined with a small excitation flip angle of αexc=5.

3.3. Experiments

In vivo scanning of five healthy volunteers was performed in accordance with local ethical approval. MTR maps were acquired for 2D and 3D imaging, as described in the subsections below. The saturation pulse was designed online as described in subsection 2.3 with calculation fully scanner‐integrated within a Matlab R2012b (Mathworks Inc., Natick, MA) framework from the vendor, taking 30 s. Prior to pulse design off‐resonance ΔB0 mapping was performed using a dual‐echo SPGR sequence and B1+ mapping was performed using a pre‐saturation turbo‐FLASH sequence 41 (both with resolution 4×4×6mm3); B1+ was corrected for bias using an empirically determined correction factor. 42 The reference voltage (Vref) determined by the scanner's built‐in adjustment steps was also recorded: a higher reference Vref indicates lower efficiency in generating B1+, and, hence, lower achieved B1+ for a given SAR level. A signal intensity‐based mask from the vendor's framework was used to not impair the workflow but was pre‐processed to remove non‐brain tissue voxels by eroding each axial slice with a three‐pixel (12 mm) radius disk and cropping axial slices that included voxels from the mouth and jaw.

Prior to MTR maps calculation (Equation 13), images were registered together using FSL BET 43 and FSL FLIRT, 44 and white matter (WM) segmentation was performed using FSL FAST, 45 further eroded with a 1‐pixel radius disk to reduce partial volume effects. B1rms maps were simulated retrospectively using the B1+ maps and the pulses optimized online (during the scan).

3.3.1. 2D imaging

2D MTR maps were acquired in all subjects for a single axial slice in the middle of the brain (resolution 1×1×5mm3, matrix size 220×220, TR = 22 ms, TE = 4 ms, BW=220Hz/Px, four averages). Data were acquired using three different saturation pulses (CP mode, PUSH‐1, PUSH‐2) and for four β (0.7μT, 1.0μT, 1.3μT, 1.6μT). For each MTR map a set of Msat and Mref images were acquired, firstly Msat with 30 s of dummy pulses (to stabilize the RF output) followed immediately by Mref with 10 s of dummy pulses, resulting in Tacq=1:19 s per MTR map. Fewer dummy cycles were required for Mref since it was acquired immediately after Msat. White matter segmentation for further analysis was performed using the MTR map obtained with PUSH‐2 at β=1.3μT due to its uniform contrast (as shown later).

3.3.2. 3D imaging

The 3D whole brain MTR maps (resolution 1×1×1mm3, matrix size 220×220×176, TR = 22 ms, TE = 4 ms, BW=220Hz/Px, GRAPPA 46 acceleration factor of 2×2, and elliptical shutter) were acquired in two subjects with β=1μT using three different saturation pulses (CP mode, PUSH‐1, PUSH‐2). A single Mref volume was acquired plus three Msat volumes, one for each saturation pulse. All volumes were acquired with 30 s of dummy pulses, resulting in Tacq=4:26 s per volume. An additional MP2RAGE 47 acquired at the same resolution was used for segmentation.

3.3.3. Gradient blip experiment

To explore the impact of applying gradients between RF sub‐pulses on the semisolid saturation, we carried an experiment adding gradient blips to the PUSH saturation pulse trains. These gradients would affect the “flip angle” if this pulse was applied to free water magnetization, but not the semisolid saturation if it behaves as modeled with longitudinal magnetization only. The 2D MTR maps (same protocol as in 3.3.1 with TR = 27 ms) were acquired in one subject with saturation pulses designed using PUSH‐3 for β=1μT, both excluding and including gradient blips between the sub‐pulses. For the latter, the gradient blips were 100μs in duration in the x and y‐directions, each producing a 4π phase roll across the FOV. The B1rms and flip angle maps of each pulse were computed (flip angle calculated at the RF offset frequency with Equation 6) and compared to the measured MTR maps.

4. RESULTS

4.1. Simulations

Figure 2 examines the error in B1rms as a function of the target β for 2D optimization on a middle axial slice (Figure 2A) and 3D whole‐brain optimization (Figure 2B). Supporting Information Figure S3 further expands on Figure 2A for other axial slices. In all cases, CP mode has a constant NRMSE until reaching the local SAR limits when the error increases as the voltage is capped. On the other hand, PUSH‐1, ‐2, and ‐3 perform better than CP mode across all β for both 2D and 3D imaging. For the 2D case, PUSH‐1 (i.e., static shimming) gives an NRMSE two times smaller than CP mode for β0.4μT in the middle slice (Figure 2A), but its performance worsens as β increases. PUSH‐2 and ‐3 perform equally well, with a constant NRMSE six times smaller than CP mode (for β1μT) in the middle slice. Remarkably, PUSH‐2 and ‐3 still perform well for β1μT, beyond where CP mode reached the local SAR limits. Generally, in 2D the performance gain offered by PUSH was larger for middle and inferior slices while superior slices had less inhomogeneity to begin with.

FIGURE 2.

MRM-29199-FIG-0002-c

NRMSE of the B1rms for 2D middle axial slice (A) and 3D (B) volume, comparing CP mode with optimized PUSH solutions using one, two, and three sub‐pulses (curves for two and three sub‐pulses are superimposed due to nearly identical performance). The gray area represents β where CP mode reached the local SAR limits and its voltage capped

For 3D imaging (Figure 2B) similar trends were observed, but with overall larger NRMSE. For β1μT, PUSH‐1 obtains an NRMSE 17% smaller than CP mode, whereas PUSH‐2 and ‐3 perform again equally well and still achieve an NRMSE two times smaller than CP mode.

Figures 3 and 4 show computed B1rms maps for 2D and 3D imaging, respectively, for some of the solutions in Figure 2. Note that in Figure 4 some stripes are visible in the sagittal and coronal planes; these were found to be caused by artifacts in the acquired B1+ maps. In Figure 3, the B1rms for CP mode scales up with β and caps after reaching the local SAR limits. PUSH‐1 achieves more uniform B1rms for β0.7μT but gets progressively less homogeneous with increasing β, producing solutions with “holes”. PUSH‐2 and ‐3 achieve B1rms maps similar to one another that are more uniform up to larger β. For 3D imaging, Figure 4 shows that CP mode produces a B1rms pattern with center brightening. The B1rms produced by PUSH‐1 is very similar to CP mode with slight improvements for β0.7μT. With PUSH‐2 and ‐3 the B1rms is more uniform in the middle slices and up to larger β; however, both solutions underdeliver in the superior and inferior slices of the brain.

FIGURE 3.

MRM-29199-FIG-0003-c

2D B1rms maps for some solutions in Figure 2. Columns contain maps for different β, increasing from left to right. Rows contain different saturation pulses: CP mode (top), PUSH‐1—that is, static shimming—(second from top), PUSH‐2 (second from bottom) and PUSH‐3 (bottom). For each combination, the mean ± SD of B1rms is shown below the respective maps

FIGURE 4.

MRM-29199-FIG-0004-c

Transverse, coronal, and sagittal planes of the 3D B1rms maps for some β and solutions in Figure 2. Columns contain maps for different β, increasing from left to right. Rows contain different saturation pulses: CP mode (top), PUSH‐1—that is, static shimming—(second from top), PUSH‐2 (second from bottom), and PUSH‐3 (bottom). For each combination, the mean ± SD of B1rms is shown below the respective maps

Figure 5 shows simulated 2D and 3D MTR maps for β = 1μT solutions from Figure 2. Note that all simulated MTR maps have been calculated using white matter properties over the whole brain: they are intended to visualize the spatial variations of saturation rather than the actual MTR contrast that will be seen in a scan. Both CP mode and PUSH‐1 solutions yield similar MTR maps with center brightening for both 2D and 3D. However, for 2D imaging PUSH‐1 can also yield solutions with contrast “holes” for some slices. On the other hand, PUSH‐2 and ‐3 achieve similar strong improvement in 2D and 3D, with an SD 2 times smaller than CP mode. A drop in achieved MTR toward the superior and inferior slices is seen in 3D. For all cases, the MTR maps have a good correlation with the respective B1rms in Figures 3 and 4.

FIGURE 5.

MRM-29199-FIG-0005-c

Simulated 2D (A) and 3D (B) MTR maps using solutions (CP mode, PUSH‐1, PUSH‐2, and PUSH‐3) from Figure 2 for β = 1μT as the saturation pulses. For 2D slices 6, 10, 12 (slice in Figure 3), 14, and 18 (from left to right) that were individually optimized are shown. (A) The green arrow points to a contrast “hole” seen in some slices optimized with PUSH‐1. The mean ± SD of MTR over the whole volume is shown below the respective maps

4.2. Experiments

4.2.1. 2D imaging

2D MTR maps from one subject are shown in Figure 6 for different pulses and β. CP mode shows a constant contrast pattern brighter in the center, that scales up with the β until it reaches the local SAR limits, after which the voltage is capped and no more RF power is delivered with increasing β. PUSH‐1 achieves more uniform contrast for the smallest β but then resembles CP mode up to the largest β where it has a “hole” in the contrast, while increasing the contrast everywhere else. PUSH‐2 yields uniform contrast for all β with up to 4 times smaller dispersion except for β=1.6μT, where it is slightly less bright in the center. The MTR maps correlate very well with the corresponding B1rms maps in Supporting Information Figure S4.

FIGURE 6.

MRM-29199-FIG-0006-c

The 2D MTR maps from one subject (subject A in Figure 7) using different saturation pulses (top row: CP mode; middle row: PUSH‐1; bottom row: PUSH‐2) and different β (across the columns, increasing from left to right). Below each is the mean ± SD of MTR over the white matter mask

Figure 7 illustrates the MTR distribution in white matter for five subjects as a function of the saturation pulse and β; the subjects are arranged in order of increasing Vref. The MTR distributions are consistent across all subjects, with PUSH‐2 yielding narrower distributions for all β. PUSH‐1 has narrower distributions for the smallest β, but at 1.6μT, its distribution exhibits a heavy tail toward low MTR values as its maps have “holes” (Figure 6). Nevertheless, both PUSH‐1 and ‐2 can achieve higher mean MTR than CP mode for the largest β, as in all subjects CP mode reached the local SAR limits below 1.3μT. The MTR in Figure 7 correlates well with the corresponding B1rms distributions in Supporting Information Figure S5. The subjects are ordered by increasing Vref, showing an expected negative correlation between MTR and Vref for the largest β (also illustrated by Supporting Information Figure S6), as higher Vref means lower maximum B1+ peak.

FIGURE 7.

MRM-29199-FIG-0007-c

Violin plots of the MTR distribution in white matter for all five subjects scanned with the 2D imaging protocol. MTR distributions for saturation pulses designed using β of 0.7μT (A), 1μT (B), 1.3μT (C), and 1.6μT (D). The black line represents the mean MTR. Subjects are sorted in increasing order of reference voltage (Vref={245,254,259,260,272}V), which is inversely proportional to the maximum β achievable with CP mode

4.2.2. 3D imaging

Figure 8 shows the 3D MTR maps (β=1μT) and their distribution in WM for one subject. CP mode and PUSH‐1 show similar contrast with center brightening. On the other hand, PUSH‐2 yields approximately 25% more uniform MTR (SD over WM mask), as indicated by the narrower and taller histograms, especially in the middle and bottom slabs. The MTR maps and histograms correlate well with the corresponding B1rms in Supporting Information Figure S7. MTR and B1rms maps for a second subject are given in Supporting Information Figures S8 and S9, which show similar results.

FIGURE 8.

MRM-29199-FIG-0008-c

(A) Transverse, coronal, and sagittal planes of the 3D MTR maps for subject C (β=1μT). The left column contains the MTR maps acquired using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± SD of MTR over the white matter mask. B–D, Histograms of the MTR distribution in white matter over three slabs: top slab (B), middle slab (C), and bottom slab (D), as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend

4.2.3. Gradient blip experiment

Figure 9 shows results from PUSH‐3 pulses without (Figure 9A) and with (Figure 9E) gradient blips between sub‐pulses; MTR maps were acquired while B1rms and flip angle maps were simulated from acquired B1+ and ΔB0 maps. The MTR maps (Figure 9D,H) are virtually identical and very uniform, in agreement with their respective B1rms maps (Figure 9B,F). The flip angle maps (Figure 9C,G) computed by also considering rotation induced by the gradients have a very different appearance and are both non‐uniform.

FIGURE 9.

MRM-29199-FIG-0009-c

(A–H) Experiment using the same PUSH‐3 pulses without (A–D) and with (E–H) gradient blips between sub‐pulses, each blip producing a dephasing of 4π across the x‐ and y‐FOV. Corresponding (B,F) B1rms, (C,G) flip angle at the RF offset frequency and (D,H) MTR maps

5. DISCUSSION

This work presents a novel pTx pulse design to overcome B1+ inhomogeneity in MT imaging at ultrahigh field by controlling semisolid saturation through the mean squared B1+. This can be performed either instead of or in addition to controlling the excitation properties of water for a given RF pulse; in this work we focused on testing the former case, which is relevant to application of off‐resonance saturation pulses. PUSH was tested in simulations and in vivo, yielding more uniform MT contrast.

Current pTx pulse design methods 23 , 24 , 33 , 34 usually use a combination of RF and B0 gradients to optimize the flip angle of the resulting excitation. These methods are unsuitable for designing semisolid saturation pulses for MT imaging since the semisolid pool has no transverse magnetization and instead saturates directly with B1+2. This was experimentally confirmed (Figure 9) by applying the same RF pulse twice, with and without gradient blips in‐between its sub‐pulses. The gradients blips do not change B1+2 but drastically alter the flip angle if applied to free water magnetization. The measured MTR maps show no difference in the MT contrast, supporting the fact that ‘flip angle’ is not a useful metric to use when designing or describing semisolid saturation pulses.

A simpler alternative to “dynamic pTx” pulse design is B1+ shimming, 11 , 12 , 35 which aims to create a spatially uniform B1+ distribution. An optimal B1+ shimming solution would also achieve a uniform B1+2 meaning that in principle B1+ shimming is a special case of PUSH where the RF pulse is “static” (i.e., pTx degrees of freedom are not modulated through the pulse). To connect PUSH with B1+ shimming, the optimization (Equation 12) is formulated in terms of the square‐root of B1+2, such that, with one sub‐pulse, it simplifies to a magnitude least‐squares 11 , 12 , 35 B1+ shimming design.

A related alternative approach is the MIMOSA 48 pTx design proposed to homogenize saturation in pulsed CEST. In that case, a train of saturation pulses interleaved with spoiling gradients can be approximated by an equivalent continuous wave saturation whose effective B1+ is better described by the B1rms 49 over the pulse train. Hence, the MIMOSA design applies two complementary modes 50 , 51 with the objective of homogenizing B1rms for CEST saturation. This effectively results in a solution equivalent to PUSH‐2, but for the special case of using two pre‐defined modes of the pTx coil.

5.1. PUSH performance for MTR imaging at 7T

Simulations show that in both 2D and 3D imaging (Figure 2) PUSH‐2 and ‐3 yield a strong improvement in the homogeneity of B1rms for all β achievable (within SAR limits) with CP mode, whereas with PUSH‐1 (static shimming) the improvements reduce as β increases. Remarkably, PUSH‐2 and ‐3 sustain these improvements beyond β achievable with CP mode, delivering higher and more uniform B1rms. For 2D imaging (Figure 3 and Supporting Information Figure S3), these improvements are more substantial in the inferior and middle axial slices of the brain, however the maximum β achievable with CP mode is considerably smaller for the inferior slices. For 3D imaging (Figure 4), these improvements are smaller, with B1rms decreasing from the middle toward the inferior and superior slices. In all simulations, two or three sub‐pulses yield very similar results, suggesting that two sub‐pulses are enough to explore the variability in the transmit sensitivity maps used, hence in most in vivo experiments a maximum of two sub‐pulses was used.

The 2D in vivo experiments shows up to four times more uniform MTR maps with PUSH‐2 (Figure 6), corroborated by the narrow distributions of MTR in WM (Figure 7). Higher maximum MTR is obtained with PUSH‐2, as expected from the simulations. Moreover, PUSH‐1 (static shimming) solutions for β=1.6μT have pathological contrast with “holes,” which is known to affect shimming solutions. 52 The 2D results are consistent across all subjects, with the MTR maps correlating very well with the respective B1rms maps. Some inter‐subject variability is observed for the maximum MTR achieved (Figure 7D), relating to the reference voltage of each subject (Supporting Information Figure S6). This is understandable since a higher reference voltage indicates the subject experiences a higher SAR per unit of achieved B1+ leaving less room for optimization.

The 3D in vivo experiments also show more homogeneous MTR maps with PUSH‐2 (Figure 8) but with a more modest 25% improvement in homogeneity. The distribution in WM shows smaller MTR values in the top and bottom slabs, agreeing with the respective B1rms distribution (Supporting Information Figure S7). This effect is also observed in the 3D simulations (Figure 4). A potential half‐way point between the 2D and 3D results would be to use a multi‐slab approach where saturation pulses are designed separately for each slab (although they are spatially non‐selective due to the broad semisolid lineshape) and are paired with slab selective excitation pulses.

5.2. Impact of RF coil design

While current pTx methods can use gradients to enhance spatial encoding of RF pulses designed to achieve rotations of magnetization, PUSH relies solely on the transmit sensitivity maps to homogenize the MT contrast. This is seen particularly in the performance of PUSH in 3D, where there is a persistent decrease in the achieved MTR in the superior and inferior regions. This is consistent with the limited coverage and lack of pTx control over B1+ variation in the z‐axis (head‐foot) from the circumferentially arranged transmit elements in the coil used. It is likely that the proposed method would benefit from alternative coil geometries, 10 for example, more channels and/or different distribution, to achieve a greater control of the mean squared B1+ spatial distribution.

For the coil used in this work, we found that more than two sub‐pulses do not improve the MT contrast homogeneity, but this may also prove not to be the case for alternative coil designs. More sub‐pulses might also be beneficial in the case where peak voltage is the active constraint, whereas in the current implementation with the sequence and hardware used, local SAR was always the most limiting.

5.3. Assumptions and future extensions

Although exchange (Equation 2) is neglected over the RF duration, its cumulative effect over the whole pulse sequence makes MTR sensitive to both saturation of the semisolid and rotation of the free water. 53 , 54 Thus, the excitation pulse can also affect MT contrast because (i) it applies some power (i.e., has an associated B1rms denoted βex) and (ii) it rotates the free water magnetization (by flip angle α), which then exchanges with the semisolid. Supporting Information Figure S2 suggests that for the scenario examined in this work the flip angle has a potentially greater effect on the MTR than βex, especially for higher flip angles. Hence, in order to focus only on the saturation pulses our experiments used a low excitation flip angle, as excitation pulses used CP mode. As a result, the observed MTR is highly correlated with the B1rms over the entire sequence; the contribution of excitation pulses to the B1rms is negligible. This simple embodiment is used as a means to illustrate the key concept; however, a future implementation might also consider designing uniform excitation pulses using methods such as kT‐points 23 or SPINS 24 potentially as part of a joint optimization problem (Equation 7). Likewise, it is not necessary to compute pulses in terms of the sequence B1rms as done here. Use of the RMS instead mean squared B1+ in Equation (12) has the advantage that, in the case of one sub‐pulse, it simplifies to a static shimming problem, making it a special case and allowing for a direct comparison. Likewise, averaging over the sequence TR rather than the pulse duration connects more closely to the expected SAR limits, 31 and MT contrast for sequences with short TR where the continuous wave approximation is still valid. 31 , 32 However, in sequences with long TR this approximation breaks down and different exchange times affect MT contrast, so it is more appropriate to consider B1+2 over the pulse duration (as in Equation 3) instead of over the TR (Equation 9).

Although gradient blips are observed not to affect the MT contrast, gradients applied during (as opposed to in between) RF pulses are expected to affect the semisolid saturation. According to Equation (3) the saturation depends on B1+2 but also on the absorption lineshape gωγΔBz,T2s. Thus, theoretically, it is also possible to control the saturation using applied gradients, which could be an avenue to explore, although this would require prior knowledge of the absorption lineshape. 21 , 55

6. CONCLUSIONS

This work proposed a novel RF pulse framework called pulse design for saturation homogeneity (PUSH) for design of RF pulses considering their saturation effect on semisolid magnetization relevant to magnetization transfer imaging. It was also demonstrated that adding gradient blips between RF sub pulses as commonly used by standard pTx methods does not affect the MT contrast; the “flip angle” of a saturation pulse is not a meaningful way of describing its operation.

The specific case demonstrated in this work was the design of off‐resonance saturation pulses where on‐resonance effects can be neglected. Simulations and in vivo experiments showed that, for the eight‐channel RF coil used in this work, PUSH can obtain up to 4 and 1.25 times more uniform MT contrast in 2D and 3D imaging, respectively, achieving monomodal distributions of MTR that correlate very well with the corresponding applied B1rms. Moreover, PUSH delivered higher B1rms than CP mode under the same SAR budget, thus also obtaining stronger contrast.

Supporting information

Figure S1. Mean squared B1+ (B1+2=β2) of each sub‐pulse for the PUSH‐1, ‐2 and ‐3 pulses optimized in the Simulations section 3.2 (middle axial slice, β=1μT). The first three columns show the sub‐pulse B1+2, whereas the last column shows the total B1+2 which is the sum of the contributions from all sub‐pulses. For PUSH‐2 and ‐3 the sub‐pulses are highly complementary, yielding very uniform total B1+2.

Figure S2. MTR simulations assuming an ideal homogeneous saturation pulse whilst alternately changing flip angle α and B1rms βex properties of the excitation pulse from spatially inhomogeneous to homogeneous. Simulations using target flip angle of (A) 5 and (B) 15, showing that for 5 any inhomogeneity in either α or βex induces small changes in MTR, whereas for 15 the induced changes are much larger, with α inhomogeneity being the largest confound. In these simulations the pattern from CP mode was used for the inhomogeneous profiles.

Figure S3. NRMSE of B1rms for the axial slice positioned as indicated by the red line in the sagittal plane in (B), comparing CP mode with the optimized PUSH solutions using 1, 2 and 3 sub‐pulses (curves for 2 and 3 sub‐pulses are superimposed due to nearly identical performance). The gray area represents β where CP mode reached the local SAR limits and its voltage is capped. Slice 12 corresponds to the solution in Figure 2A. To navigate through different slices this document needs to be open on a JavaScript‐supporting PDF viewer, such as Adobe Acrobat Reader.

Figure S4. Corresponding 2D B1rms maps for the MTR maps in Figure 6. Different rows correspond to different pulses (top row: CP mode; middle row: PUSH‐1; bottom row: PUSH‐2) and columns correspond to different β (increasing from left to right). Below each is the mean ± standard deviation of B1rms over the white matter mask also used in Figure 6.

Figure S5. Corresponding B1rms violin plot distributions for the MTR data in Figure 7. B1rms distributions for saturation pre‐pulses designed using β of (A) 0.7μT, (B) 1μT, (C) 1.3μT and (D) 1.6μT. The black line represents the mean B1rms. Subjects are sorted in increasing order of reference voltage, which is inversely proportional to the maximum β achievable with CP mode.

Figure S6. Mean MTR in WM (β=1.6μT) versus the reference voltage Vref associated to each subject. At the highest β all pulses are at the SAR limits and the mean MTR is indicative of the maximum MTR achieved.

Figure S7. Corresponding B1rms for the MTR data in Figure 8. (A) Transverse, coronal and sagittal planes of the 3D B1rms maps. The left column contains the B1rms maps using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± standard deviation of B1rms over the white matter mask also used in Figure 8. (B–D) Histograms of the B1rms distribution in white matter over three slabs: (B) top slab, (C) middle slab, and (D) bottom slab, as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend.

Figure S8. (A) Transverse, coronal and sagittal planes of the 3D MTR maps for subject E (β=1μT). The left column contains the MTR maps acquired using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± standard deviation of MTR over the white matter mask. (B–D) Histograms of the MTR distribution in white matter over three slabs: (B) top slab, (C) middle slab, and (D) bottom slab, as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend.

Figure S9. Corresponding B1rms for the MTR data in Figure S8. (A) Transverse, coronal and sagittal planes of the 3D B1rms maps. The left column contains the B1rms maps using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± standard deviation of B1rms over the white matter mask also used in Figure S8. (B–D) Histograms of the B1rms distribution in white matter over three slabs: (B) top slab, (C) middle slab, and (D) bottom slab, as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend.

ACKNOWLEDGMENTS

This research was funded in whole, or in part, by the Wellcome Trust [WT 203148/Z/16/Z]. For the purpose of open access, the author has applied a CC BY public copyright license to any Author Accepted Manuscript version arising from this submission. This work was supported by the Wellcome/EPSRC Centre for Medical Engineering [WT 203148/Z/16/Z] and by the National Institute for Health Research (NIHR) Biomedical Research Centre based at Guy's and St Thomas' NHS Foundation Trust and King's College London and/or the NIHR Clinical Research Facility, and funded by the King's College London & Imperial College London EPSRC Centre for Doctoral Training in Medical Imaging [EP/L015226/1]. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.

Leitão D, Tomi‐Tricot R, Bridgen P, et al. Parallel transmit pulse design for saturation homogeneity (PUSH) for magnetization transfer imaging at 7T . Magn Reson Med. 2022;88:180‐194. doi: 10.1002/mrm.29199

Funding information Engineering and Physical Sciences Research Council, EP/L015226/1; Wellcome Trust, WT 203148/Z/16/Z; Department of Health, EPSRC Centre for Doctoral Training in Medical Imaging, Imperial College London, King's College London, King's College London, Biomedical Research Centre, National Institute for Health Research, Wellcome, Wellcome Trust

DATA AVAILABILITY STATEMENT

According to UK research councils' Common Principles on Data Policy and Wellcome Trust's Policy on data, software and materials management and sharing, all simulated data supporting this study will be openly available at https://github.com/mriphysics/PUSH (hash 3ce6d8a was the version at time of submission). This excludes in‐vivo MRI data because of the terms of the ethical approval under which they were acquired, and proprietary code from SIEMENS but that can be shared upon request by agreement including the vendor.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Figure S1. Mean squared B1+ (B1+2=β2) of each sub‐pulse for the PUSH‐1, ‐2 and ‐3 pulses optimized in the Simulations section 3.2 (middle axial slice, β=1μT). The first three columns show the sub‐pulse B1+2, whereas the last column shows the total B1+2 which is the sum of the contributions from all sub‐pulses. For PUSH‐2 and ‐3 the sub‐pulses are highly complementary, yielding very uniform total B1+2.

Figure S2. MTR simulations assuming an ideal homogeneous saturation pulse whilst alternately changing flip angle α and B1rms βex properties of the excitation pulse from spatially inhomogeneous to homogeneous. Simulations using target flip angle of (A) 5 and (B) 15, showing that for 5 any inhomogeneity in either α or βex induces small changes in MTR, whereas for 15 the induced changes are much larger, with α inhomogeneity being the largest confound. In these simulations the pattern from CP mode was used for the inhomogeneous profiles.

Figure S3. NRMSE of B1rms for the axial slice positioned as indicated by the red line in the sagittal plane in (B), comparing CP mode with the optimized PUSH solutions using 1, 2 and 3 sub‐pulses (curves for 2 and 3 sub‐pulses are superimposed due to nearly identical performance). The gray area represents β where CP mode reached the local SAR limits and its voltage is capped. Slice 12 corresponds to the solution in Figure 2A. To navigate through different slices this document needs to be open on a JavaScript‐supporting PDF viewer, such as Adobe Acrobat Reader.

Figure S4. Corresponding 2D B1rms maps for the MTR maps in Figure 6. Different rows correspond to different pulses (top row: CP mode; middle row: PUSH‐1; bottom row: PUSH‐2) and columns correspond to different β (increasing from left to right). Below each is the mean ± standard deviation of B1rms over the white matter mask also used in Figure 6.

Figure S5. Corresponding B1rms violin plot distributions for the MTR data in Figure 7. B1rms distributions for saturation pre‐pulses designed using β of (A) 0.7μT, (B) 1μT, (C) 1.3μT and (D) 1.6μT. The black line represents the mean B1rms. Subjects are sorted in increasing order of reference voltage, which is inversely proportional to the maximum β achievable with CP mode.

Figure S6. Mean MTR in WM (β=1.6μT) versus the reference voltage Vref associated to each subject. At the highest β all pulses are at the SAR limits and the mean MTR is indicative of the maximum MTR achieved.

Figure S7. Corresponding B1rms for the MTR data in Figure 8. (A) Transverse, coronal and sagittal planes of the 3D B1rms maps. The left column contains the B1rms maps using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± standard deviation of B1rms over the white matter mask also used in Figure 8. (B–D) Histograms of the B1rms distribution in white matter over three slabs: (B) top slab, (C) middle slab, and (D) bottom slab, as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend.

Figure S8. (A) Transverse, coronal and sagittal planes of the 3D MTR maps for subject E (β=1μT). The left column contains the MTR maps acquired using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± standard deviation of MTR over the white matter mask. (B–D) Histograms of the MTR distribution in white matter over three slabs: (B) top slab, (C) middle slab, and (D) bottom slab, as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend.

Figure S9. Corresponding B1rms for the MTR data in Figure S8. (A) Transverse, coronal and sagittal planes of the 3D B1rms maps. The left column contains the B1rms maps using CP mode, middle column using PUSH‐1 and right column using PUSH‐2. Below each sagittal plane is the mean ± standard deviation of B1rms over the white matter mask also used in Figure S8. (B–D) Histograms of the B1rms distribution in white matter over three slabs: (B) top slab, (C) middle slab, and (D) bottom slab, as illustrated in (A) near the bottom right sagittal plane. Moving average plotted jointly with histograms to delineate distribution trend.

Data Availability Statement

According to UK research councils' Common Principles on Data Policy and Wellcome Trust's Policy on data, software and materials management and sharing, all simulated data supporting this study will be openly available at https://github.com/mriphysics/PUSH (hash 3ce6d8a was the version at time of submission). This excludes in‐vivo MRI data because of the terms of the ethical approval under which they were acquired, and proprietary code from SIEMENS but that can be shared upon request by agreement including the vendor.


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