Galen Durant Reed1, JaeMo Park2, Junjie Ma2, Crystal Harrison2, Rolf Schulte3, Albert Chen 4, Salvador Pena2, Jeannie Baxter2, Kelley Derner2, Maida Tai2, Dean Sherry2, Vlad G Zaha2, and Craig R Malloy2
1GE Healthcare, Dallas, TX, United States, 2University of Texas Southwestern Medical Center, Dallas, TX, United States, 3GE Healthcare, Munich, Germany, 4GE Healthcare, Toronto, ON, Canada
Synopsis
Initial human hyperpolarized 13C cardiac imaging experiments
utilized a frequency-selective, single-shot spiral pulse sequence for encoding,
and a rigid 8 channel receiver array paired with a Helmholtz clamshell
transmitter. In phantom studies, we evaluate this RF hardware along with
flexible transmit / receiver designs and test these in healthy volunteers. Furthermore,
as pointed out previously, the detected circumferential distribution of [13C]bicarbonate
around the myocardium is often non-uniform in pigs, thus confounding the
translation of this technique for regional metabolism evaluation. We observed
this artifact in human volunteers and explore its possible sources.
Introduction
Understanding
the role of altered intermediary metabolism in heart disease is important to
addressing diverse clinical questions and new opportunities in therapy. In vivo
assessment of cardiac metabolism in human subjects is critical. Earlier studies
demonstrated imaging of [13C]bicarbonate in the human myocardium, a
direct index of pyruvate oxidation in the citric acid cycle [1]. Initial imaging studies utilized an MRI pulse
sequence consisting of a frequency-selective, single shot spiral in which one
or more slices were encoded during mid-diastole [2]. This acquisition was paired with the
clamshell-geometry radio frequency (RF) excitation Helmholtz coil [3] and the rigid, 8-channel paddle receivers. In
this study, we evaluated two additional transmit / receive RF coils for 13C
imaging over larger fields of view (FOV); initial transmit B1 profiles, SNR
profiles, and in vivo images are provided. As pointed out in reference [4], the detected circumferential distribution of [13C]bicarbonate in the myocardium is often non-uniform in pigs, thus confounding the
translation of this technique for regional metabolism evaluation. We observed
this artifact in human volunteers and explore its possible sources. Methods
Three 13C-tuned RF
transmit / receive configurations were tested to determine sensitivity, spatial
coverage, and transmitter homogeneity. A clamshell transmitter / 8 channel
rigid paddle [5]
(GE Healthcare, Waukesha, WI), a dual 20 cm loop (Pulseteq, Chobham, UK)
transceiver, and a flexible 8 channel array / vest transmitter (Clinical MR
Solutions, Brookfield, WI) were measured using the SNR-measurement protocol,
described in reference [6].
The protocol uses the natural abundance 13CH3 signal of
the widely-distributed dimethyl silicone phantoms. A saline-filled ring enclosing
the phantom provided RF loading. 2 sets of experiments were performed. In the
first set, both the clamshell and dual loop coils were measured over a 32-cm
FOV in a smaller 16 cm diameter phantom. In the second set of experiments, the
flexible 8 channel and dual loop coils were measured over a 48-cm FOV in a larger
22 cm diameter phantom. Images were acquired at
approximate flip angles of 45 and 90 degrees, 4s TR, and an flip angle map was
reconstructed. The 90 degree image signal was then normalized by the sine of
the estimated flip angle and noise to create a B1-normalized sensitivity map.
Human Imaging and
Dynamic Nuclear Polarization
Subjects were scanned on a GE MR750w MRI
system. The gradient shim values were calculated using a 14 cm FOV rectangular
region enclosing the entire heart. A 1H imaging protocol including
short-axis SSFP localizers and B0 maps were acquired with the body coil. A
pre-determined scaling was applied to determine the center frequency shift for in vivo [1-13C]lactate based
on in vivo 1H water
resonant frequency. A cardiac-triggered, spectral-spatial excite (3 cm slice
thickness), spiral readout gradient echo was adapted within the multi-nuclear
research pack framework [7].
The 50 ms spiral readout had a nominal 40 cm FOV, 1.2 cm resolution, peak
gradient amplitude 2.3 G/cm, and ramp rate of 74 G/cm/ms to conform to the restrictions
of the wide bore gradient system [1-13C]pyruvate polarization and QC
were performed via SPINLab polarizer. Injection was carried out over 12
seconds, and imaging initiated at the end of the infusion. One volunteer was imaged with both the dual
loop and the flexible 8 channel array. Results
Figure 1 shows flip angle and SNR maps acquired in phantoms
of the 3 coils studied. Due to its smaller transmitter size, the dual loop
showed much higher transmitter inhomogeneity than either the clamshell or the
8-channel flexible array. Both the 8-channel array and dual loop have larger
diameter receive elements, thus generating more uniform SNR profiles. The
profile of these coils at a depth within the phantom typical of posterior left
ventricle wall (15-20 cm) is at least 2x higher in both the dual loop and
flexible 8-channel compared to the clamshell. Cardiac B0 maps, SSFP localizer,
and [13C]bicarbonate are displayed in Figure 2. Note that the off-resonant
region in the B0 map corresponds to an SSFP band as well as dropout in the [13C]bicarbonate
image. [13C]bicarbonate images from the same volunteer using both
the dual loop and the flexible 8 channel array are shown in Figure 3. SNR of
the 8-channel array is comparable to the dual loop only when a small subset of
channels proximal to the anterior chest wall are used. Discussion
Phantom
measurements suggest that for imaging deeper tissue regions, the smaller
receive elements of paddle receiver were suboptimal. The 8-channel array and
the dual loop show comparable SNR distally, with the latter having a more
inhomogeneous B1 field. The 8-channel showed comparable SNR in vivo to the dual
loop only when a proximal subset of channels was selected, and this process can
easily be automated via coil subspace-selection methods such as singular value
decomposition [8]. Similar to the results in reference [4] in pigs, we observed non-uniform
circumferential [13C]bicarbonate distribution in the myocardium when
viewed on short axis. B0 mapping and SSFP imaging indicate that this is due to sup-optimal
shimming, thus suggesting the need for improved B0 shim routines. Acknowledgements
No acknowledgement found.References
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