Technical challenges in 3 T magnetic resonance spectroscopic imaging of the prostate—A single-institution experience
Brief Report

Technical challenges in 3 T magnetic resonance spectroscopic imaging of the prostate—A single-institution experience

Haesun Choi1, Michelle Underwood2, Piyaporn Boonsirikamchai3, Surena Matin4, Patricia Troncoso5, Jingfei Ma6

1Department of Diagnostic Radiology, 2Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA; 3Department of Diagnostic Radiology, King Chulalongkorn Memorial Hospital, Pathum Wan, Bangkok, Thailand; 4Department of Urology, 5Department of Pathology, 6Department of Imaging Physics, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

Correspondence to: Haesun Choi. The University of Texas MD Anderson Cancer Center, Department of Diagnostic Radiology, 1400 Pressler St., Unit 1473, Houston, TX 77030, USA. Email: hchoi@mdanderson.org.

Abstract: The magnetic resonance spectroscopic imaging (MRSI) is the only technique that is currently available in the clinical practice to provide the metabolic status of prostate tissue at the cellular level with a great potential to improve the clinical patient care. Increasing the field strength from 1.5 to 3 T can theoretically provide proportionately higher signal-to-noise ratio (SNR) and improve spectral separation between prostatic metabolite peaks. The technique, however, has been limited to a few academic institutions that are equipped with a team of experts primarily due to due to serious technical challenges in optimizing the spectral quality. High quality shimming is key to the successful MRSI acquisition. Without optimization of the increased field inhomogeneity and radiofrequency (RF) dielectric effect at 3 T, the spectral peak broadening and residual signal from the periprostatic fat tissue may render the overall spectra non-diagnostic. The purpose of this technical note is to present the practical steps of successful acquisition of 3 T MRSI and to address several important technical challenges in minimizing the effect of the increased magnetic field and RF field inhomogeneity in order to obtain highest possible spectral quality based on our initial experience in using 3 T MRSI prototype software.

Keywords: Prostate cancer; magnetic resonance spectroscopy; 3 T; magnetic field inhomogeneity; radiofrequency (RF) field inhomogeneity


Submitted Jul 13, 2014. Accepted for publication Jul 16, 2014.

doi: 10.3978/j.issn.2223-4292.2014.07.09


Introduction

Magnetic resonance imaging (MRI) has shown a significant impact on clinical decision making in prostate cancer management (1). In recent years, the multiparametric MRI, which includes any combination of dynamic contrast-enhanced (DCE) MRI, diffusion-weighted MRI (DWI), and magnetic resonance spectroscopic imaging (MRSI), has been advocated to better localize and characterize prostate cancer and to improve the specificity of conventional MRI in detecting prostate cancer, although each technique has its own limitations and all of them are continuously being evolving (1-5). The DWI and DCE-MRI have been relatively well accepted and cautiously incorporated into the routine clinical practice of prostate MRI in many imaging centers. In contrast, MRSI of the prostate is still restricted to only a few academic institutions, despite the fact that MRSI is the only imaging technique that can evaluate the status of tissue metabolism that is specific to prostate tissue (6-11). A major hindrance to the clinical acceptance of prostate MRSI is the technical challenge in acquiring high-quality MRSI data.

MRSI at 1.5 T is commercially available through major vendors, and its use has been relatively well established in clinical practice at major academic institutions where a team of experts are available. Increasing the field strength from 1.5 to 3 T can theoretically provide proportionately higher signal-to-noise ratio (SNR) and improve spectral separation between prostatic metabolite peaks (Figure 1) and, thus, help radiologists more accurately interpret the images. However, compared with 1.5 T MRSI, 3 T MRSI requires some changes in acquisition technique and scan parameters to achieve expected high spectral quality. First, the echo time (TE) must be decreased from approximately 130 ms to approximately 85 ms in order to avoid a potential spectral distortion from the strongly coupled citrate spin system. Additionally, special attention needs to be paid to the increased susceptibility-induced magnetic field inhomogeneity and strong radiofrequency (RF) dielectric effects at 3 T. Without optimization of the increased field inhomogeneity and RF dielectric effect, the spectral peak broadening and residual signal from the periprostatic fat tissue may render the overall spectra non-diagnostic (Figures 1,2).

Figure 1 Magnetic resonance spectrum of benign prostate tissue at 1.5 and 3 T. The spectra obtained at 1.5 T (A) and 3 T (B) demonstrate a spectral complex of choline, polyamine, and creatine peaks at 3.2, 3.1, and 3.0 ppm and a citrate peak at 2.6 ppm at 1.5 T (A). At 3 T (B), the Cho-Po-Cr complex is slightly broadened but otherwise similar to that at 1.5 T. Note the separation of citrate peaks and the substantially higher amplitude of all peaks at 3 T than at 1.5 T. Cho, choline; Po, polyamine; Cr, creatine; Ci, citrate.
Figure 2 Non-diagnostic prostate magnetic resonance spectrum due to contamination from periprostatic fat. The spectra from the mid-gland (A) demonstrates the strong fat signal dominating the citrate peaks in all voxels laterally (red box), affecting even the inner voxels (green box) to a lesser degree (B). The water spectral linewidth per prescan was 19 Hz, and transmit gain was 200.

In this technical note, we describe our preliminary experience of a prototype 3 T MRSI (GE Health Care: GE, Milwaukee, WI) of the prostate in patients and how to manage some of the technical challenges to achieve optimal spectral quality.


Technical note

At our institution, the 3 T prostate MRSI is performed with an endorectal coil (e-coil) (MEDRAD, Pittsburg, PA, USA) to maximize the SNR. Proper placement of the e-coil is essential: care should be taken to keep the e-coil as straight as possible toward the midline of the body of patient (or prostate) to ensure that the sensitive volume of the coil is congruent with the prostate within approximately ±12 degrees from the midline. To minimize the magnetic field inhomogeneity introduced by the prostate-air interface between the prostate and rectum and endorectal coil balloon, the coil is filled with about 50-100 mL of perfluorocarbon complex (PFC) (3 M, St. Paul, MN, USA) (12). The magnetic susceptibility of PFC closely matches that of the prostatic tissues without generating any detectable MR signal (13). The proper positioning of the e-coil is visually confirmed by the three plane localizers (Figure 3).

Figure 3 Optimal endorectal coil placement for 3 T magnetic resonance spectroscopic imaging of the prostate. The perfluorocarbon complex-filled endorectal coil is placed at the midline of the pelvis, immediately posterior to the prostate (A,B). The two “ears” (arrows) indicate the location of the coil element within the coil. Symmetric position of the “ears” on an axial localizer (A) can be used as a reference to confirm optimal coil placement. C, coil; P, prostate.

Once the position of the e-coil is confirmed, we acquire high-resolution (3 mm slice thickness without gap) T2-weighted images (T2WI) in three orthogonal planes before acquiring MRSI data. The MRSI acquisition parameters we typically use are repetition time (TR) =1,300 ms; TE =85 ms; number of excitations (NEX) =1; acquisition matrix =12×8×8; field of view =110×55×55 mm3; and a scan time of approximately 17 min.

The first step in prescribing an MRSI is to place a rectangular box of spectral volume of interest (VOI) on an axial T2WI on the largest cross-sectional area of the prostate. The size of the box is adjusted to maximize the coverage of the prostate with minimal inclusion of the periprostatic fat. A sagittal T2WI is used to further adjust the dimension of the VOI box along the superior-inferior direction to cover the prostate from the base to the apex, excluding the seminal vesicles in order to avoid spectral contamination from the seminal fluids (Figure 4). To further maximize the exclusion of the periprostatic fat, six very selective saturation (VSS) bands are placed (four over the axial image and two over the sagittal image) at the corners of the VOI to best conform the spectroscopic volume to the actual shape of the prostate (Figure 4).

Figure 4 Optimal placement of spectral VOI box and VSS bands on axial and sagittal T2 images. The spectral VOI (while box) is placed to conform to the largest segment of the prostate on a T2 axial image (A), excluding periprostatic fat as much as possible. The periprostatic fat is further excluded from four corners of the spectral VOI box by using the four VSS bands (yellow box). Note the position of the spectral VOI box including most of peripheral zone, from the apex to the base of the prostate, on a midline sagittal T2 image (B). One additional VSS band (green box) is placed inferiorly along the posterior surface of the prostate to further exclude the periprostatic fat, and one VSS band (red box) is placed superiorly to exclude the seminal vesicle. VOI, volume of interest; VSS, very selective saturation.

Once an appropriate VOI and the six VSS bands are placed, we perform an automatic prescan procedure that includes calibrating the transmit gains (TG) and receive gains, optimizing the magnetic field shimming, and calibrating the center transmit frequency. Optimum shimming of the magnetic field is key to the successful MRSI data acquisition. The quality of shimming can be checked by observing either the decay rate of the water free-induction decay signal or the shape of the water spectral peak in pure absorption mode after Fourier transformation. Alternatively, we can also display the water spectral peak in the magnitude mode and observe the full width at half maximum of the peak (in Hz). When the linewidth is suboptimal (e.g., >15 Hz), the settings for the three shimming gradients (along x, y, and z directions) can be adjusted manually to allow the free-induction decay signal to oscillate as far out as possible or to match the spectral shape in the pure absorption mode with that of the magnitude mode as closely as possible (Figure 5).

Figure 5 Prescan displays before and after manual shimming adjustment in 3 T magnetic resonance spectroscopic imaging of prostate.(A,B) The MR spectrum is displayed in magnitude (top) and pure absorption (bottom) modes before (A) and after (B) shimming adjustment. Current settings to the shimming gradients are adjusted to obtain the narrowest resonance peaks (B). (C,D) Alternatively, the water resonance peak (top right) and the water FID signal (bottom) can be displayed before (C) and after (D) offsetting the transmit center frequency by a fixed amount (e.g., 100 Hz). The current settings to the shimming gradients are adjusted so that the FID signal oscillates and extends to the longest duration (D). FID, free-induction decay.

Another setting that we find requires careful tuning at 3 T is the TG, which is used to control the RF power output. An incorrect TG setting will result in an inaccurate flip angle of the RF pulses, which can lead to incomplete fat suppression and compromised spectral quality. Increased dielectric effects and B1 field shading at 3 T can make this effect particularly pronounced, especially in large patients.

To mitigate the sensitivity of the RF inhomogeneity at 3 T, the prototype software we use has “voxelated TG” as a default option. Voxelated TG only uses the signals from a small region of interest in the prostate, which is sensitive to the e-coil, for the purpose of calibrating the TG. Compared with using the signal from the built-in body coil at 1.5 T, voxelated TG is less sensitive to B1-inhomogeneity. However, we found that, in certain patients, the automatic prescan using the voxelated TG failed to complete the procedure. The root cause of this failure that we identified was the insufficient signal from the small region of interest defined for the voxelated TG. One way to circumvent this difficulty is to increase the size of the spectral VOI box to increase the signal. Greater signal can be obtained by temporarily removing the VSS bands and increasing the actual size of the VOI box or even by turning off the voxelated TG so that the automatic prescan may be completed to obtain an initial TG setting (Figure 6). Using this TG setting as a starting value, we can manually prescan to find a final optimal TG value (typically 190) by gradually restoring the desired scan prescriptions (e.g., the VOI size and the placement of the VSS bands).

Figure 6 Resolution of incomplete shimming caused by suboptimal transmit gain in 3 T magnetic resonance spectroscopic imaging of the prostate. When the shimming fails to complete with standard placement (A) of spectral VOI box and VSS bands [note that the pure absorption graphic is inverted (bottom) mismatching with the magnitude mode (top)] (B), first, remove all VSS bands and open the VOI box (green box) to collect sufficient signal (C). Next, open the user CV page, type in “voxtg_on” under CV name, and change the current value (default value) to 0 (D). Then, place the VOI volume box and all VSS bands back onto the T2-weighted axial image by copying and pasting the original graphics to repeat the shimming procedure. Note the pure absorption mode (bottom) now matches the magnitude mode (top) (E), indicating that the shimming is successful.

Once the prescan settings are optimized, we can acquire high-quality spectra successfully.


Discussion

In endorectal MRSI at a higher field strength, the magnetic susceptibility-related field inhomogeneity from the prostate-air/rectum interface increases proportionally. Without a good magnetic field shimming, the increased spectral separation may not directly benefit the spectral quantitation. Filling the e-coil with PFC instead of air is the first step to improve the magnetic field inhomogeneity. PFC has similar physical properties to soft tissue and has been demonstrated to improve the field inhomogeneity substantially at 1.5 T (12) as well as at 3 T.

Another complexity in 3 T MRSI is the increased RF inhomogeneity owing to the shortened RF wavelength and increased dielectric effects at the higher magnetic field strength. At 1.5 T, the RF wavelength is typically much longer than the body size. As a result, the dielectric shading is minimal and using the built-in body RF coil for the TG setting is rarely a problem. At 3 T, however, the RF wavelength becomes comparable or even shorter than a typical body size. As a result careful tuning of TG becomes critical in obtaining an acceptable spectral quality. Poorly tuned TG will result in incorrect flip angle of the RF pulses, which can lead to incomplete fat suppression. While the voxelated TG option does help reduce the sensitivity of the RF to B1-inhomogeneity, in our experience, it is not always feasible to achieve the correct TG for every patient. Therefore, careful manual tuning by observing the residual fat signal is often necessary. In the manual prescan, the tuning steps we describe above allowed us to obtain an optimal TG setting that avoids the potential pitfalls of relying on signals from the built-in body RF coil.

Our experience is based on the software of a specific vendor. However, most of the technical challenges and technical solutions we have described in optimizing 3 T prostate MRSI data acquisition should be applicable to all 3 T scanners.

In summary, the 3 T can potentially improve the spectral quality of prostate MRSI. We presented our initial experience in using 3 T MRSI prototype software and some practical steps to address several important challenges in minimizing the effect of the increased magnetic field and RF field inhomogeneity in order to obtain optimal spectral quality.


Acknowledgements

We would like to acknowledge Mr. Kelly Duggan for his editorial support of images and Ms. Jill Designe for her editorial support of the manuscript.

Funding: The work was conducted with the fund from the United States Department of Defense. (Grant Number, PC061612; Award Number, W81XWH-07-1-0110). The funding agency has no involvement in study design, in the writing of the report, and in the decision to submit the paper for publication.

Disclosure: The authors declare no conflict of interest.


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Cite this article as: Choi H, Underwood M, Boonsirikamchai P, Matin S, Troncoso P, Ma J. Technical challenges in 3 T magnetic resonance spectroscopic imaging of the prostate—A single-institution experience. Quant Imaging Med Surg 2014;4(4):251-258. doi: 10.3978/j.issn.2223-4292.2014.07.09

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