Synopsis
We made slice profile measurements and acquired 2D multi-gradient-echo data on a phantom in the presence of various through-plane gradients. The sinc-term correction for R2* mapping that is commonly used to compensate for the dephasing effects of these gradients was substantially outperformed by a correction based on the measured slice profiles. Our results highlight the importance of incorporating realistic slice profiles into the estimation of “intrinsic” R2* values, which may contain information about tissue structure at microscopic-to-mesoscopic spatial scales.Purpose
With the increasing popularity of field strengths of 3T and above, there has been a growing appreciation for the need to correct for the dephasing effects of through-plane gradients in 2D gradient-echo acquisitions
[1], since susceptibility gradients (e.g., due to air-tissue interfaces) are more prominent at higher fields. A sinc-term correction is often employed for this purpose
[2-5], based on the assumption of “ideal” rectangular slice profiles. Our goal here was to measure the slice profiles generated by typical 2D gradient-echo sequences on a clinical scanner and to compare the effectiveness of the sinc-term correction for R
2* mapping with a correction based on experimentally measured slice profiles.
Methods
A Siemens cylindrical phantom (1900 mL; 3.75g NiSO4×6H2O + 5g NaCl per 1000g distilled H2O) was scanned on a 1.5T Avanto MR system (Siemens Healthcare, Erlangen, Germany) with a 12-channel receive coil. The product multi-gradient-echo sequence (“gre”) was run with following parameters: FA=90°, TR=2 s, 12 unipolar gradient-echoes with TEs from 6 to 77.5 ms (BW=230 Hz/px), 2D acquisition with 15 axial slices with 4/2 mm slice thickness/gap and 2×2 mm2 in-plane voxel size (matrix=128×128). To investigate the effect of through-plane gradients, shim settings were deliberately adjusted in order to induce z-direction gradients of BGz = 0, 50, 100 or 200 µT/m. To measure slice profiles (BGz=0 only), the “gre” pulse-sequence code was modified to have the readout (RO) gradient in the same direction as the slice-select (SS) gradient (see Fig. 1a). All parameters were as above, except for the number of slices and the voxel size, which were reduced to 1 and 0.5×0.5 mm2, respectively (matrix=512×512; BW=570 Hz/px), with the increased resolution chosen here to provide a more fine-grained slice profile measurement.
For each voxel in a 50×50 mm2 region of interest (ROI) in the center of the phantom (for the 2×2 mm2 acquisitions described above), reference R2* values were obtained from straight-line fits to ln(S) versus TE for the BGz=0 data, where S(TE) is the signal magnitude at time TE, with monoexponential decay assumed. Through-plane gradients cause dephasing that modulates S(TE) with a multiplicative factor F(TE); for a rectangular slice profile, FRECT(TE)=sinc(γ2 BGz Δz TE), where γ is the gyromagnetic ratio and Δz is the nominal slice thickness[2]. Given measured slice profiles (MSP), an alternative modulation function FMSP(TE) was obtained via numerical integration, as described by Hernando et al[1]. Corrected R2* values were then obtained by dividing S(TE) by FRECT(TE) prior to fitting[2,3] (with care taken to avoid “divide-by-zero” issues) or alternatively by dividing by FMSP(TE) instead.
Results
Fig. 1 shows the result of the slice profile measurement on the cylindrical phantom—note the substantial departure from the “ideal” rectangular profile. For a central voxel in the 2×2 mm
2 data, Fig. 2 shows plots of signal magnitude
S versus
TE for BGz=0 (black curves), for which the decay is indeed monoexponential, and for BGz=200 µT/m (black dots). Multiplying the BGz=0 data by
FRECT and
FMSP results in the red and blue curves, respectively, with
FMSP clearly providing a much better agreement with the BGz=200 µT/m data. Fig. 3 shows a comparison of the corrected R
2* values obtained from using
FRECT versus
FMSP, with the latter in much closer agreement with the reference R
2* values (from the BGz=0 data) of
10.6±0.2 s
-1 in the green ROI shown in Fig. 2a.
Discussion
Failure to adequately correct for the effect of through-plane gradients in 2D gradient-echo acquisitions could obscure the “intrinsic” R
2* near air-tissue susceptibility interfaces, compromising information about field perturbations and therefore tissue structure at microscopic-to-mesoscopic spatial scales
[2]. We have shown here that sinc-term corrections fare poorly compared to corrections based on measured slice profiles when using the Siemens product “gre” sequence, which uses Hanning-filtered sinc waveforms for RF excitation pulses. We acknowledge that this discrepancy may be reduced with the use of custom RF pulses (e.g., SLR pulses
[6]) that may provide slice profiles that are closer to rectangular, or with the use of thinner slices. We remark that the considerations herein do not apply to 3D gradient-echo acquisitions, for which the effect of “through-plane” gradients (i.e., in the 2
nd phase-encoding direction) is very different
[7,8].
Acknowledgements
No acknowledgement found.References
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