Gopal Varma1, Olivier M Girard2, Samira Mchinda2, Arnaud Guidon3, Dan W Rettmann4, Victor Carvalho2, Valentin H Prevost2, Pauline W Worters5, Marc R Lebel6, Guillaume Duhamel2, and David C Alsop1
1Division of MR Research, Radiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States, 2CNRS, CRMBM, UMR 7339, Aix Marseille Universite, Marseille, France, 3GE Healthcare, Boston, MA, United States, 4GE Healthcare, Rochester, MN, United States, 5GE Healthcare, Menlo Park, CA, United States, 6GE Healthcare, Calgary, AB, Canada
Synopsis
The inhomogeneous magnetization transfer
(ihMT) technique provides a myelin-sensitive signal and has been applied for 3D
acquisition in the steady-state. Sequences applied in a segmented fashion,
following some magnetization preparation, provide an advantage of allowing insertion
of additional modules, e.g. motion correction. An ihMT acquisition in the style
of the magnetization-prepared rapid gradient-echo sequence was designed based
on considerations of safety, hardware and optimizing the ihMT signal. Whole
brain 3D ihMT data with 2.4mm isotropic resolution was achieved in 6-7mins. IhMT
ratios between 15-20% were measured in white matter areas, and were not
significantly modified by inclusion of a prospective motion correction module.
Introduction
Inhomogeneous magnetization transfer (ihMT)
provides a contrast sensitive to myelinated structures1. Its signal is
correlated with myelin content as measured by fluorescence microscopy2,
and other MRI techniques that are surrogate measures of myelin3. State-of-the-art
3D ihMT relies on RF pulses applied off-resonance and readout(s) combined and
repeated to achieve a steady-state signal4. A preparatory module is
used to prepare the magnetization and allows rapid 3D acquisition in a
segmented fashion. Such magnetization preparation sequences allow the amount of
k-space sampled to be controlled
depending on motion or expected changes in signal. These sequences can also be
adapted to include prospective motion (PROMO) compensation or other modules5.
Recent developments show the maximum ihMT signal available can be greatly
enhanced with reduced RF duty cycles4. Whilst this allows for lower
SAR sequences, the maximum achievable pulse amplitude limits the ihMT signal. The
goal of this work is to demonstrate an ihMT prepared 3D gradient echo sequence
in the style of the magnetization-prepared rapid gradient-echo (MPRAGE) acquisition.Methods
Simulations were conducted for white
matter (WM) and grey matter (GM) tissues using numerical solution of the differential
equations of the two-pool model of MT (ode45, Matlab, MathWorks). Single
frequency off-resonance irradiation was simulated by inclusion of a dipolar
reservoir6. Values for rate and other quantitative MT parameters
were taken from prior literature at 3T7-8. Imaging was achieved with
a series of MT pulses applied at ±7kHz (B1,peak=150mG from scanner limitations) followed by rapid gradient-echoes (RAGEs), based on simulation results, repeated for a given k-space volume. RAGEs were simulated by multiplication of the free-pool longitudinal magnetization by the cosine of the flip angle (FA), assuming
perfect spoiling. Since ihMT involves separate single and dual frequency RF
preparations, an interleaved strategy was compared to acquisition of 3D
datasets with one preparation type in a sequential manner. Figure 1 illustrates
the strategies employed on a 3T clinical scanner (Discovery MR750, GE
Healthcare) for whole-brain ihMT. The repetition time between cycles of the MT
preparation plus RAGEs, TRRAGE was increased from 2 to 2.5s to include
the PROMO module. Whole brain ihMTRAGE data were acquired in healthy volunteers,
after informed consent, using a 32-channel head coil. IhMT was calculated as
twice the difference between the signals following single and dual frequency
RF, and ihMTR by dividing ihMT by the signal following zero power preparation.Results
Taking a fixed, low duty cycle of 5% for
the MT preparation, the simulated ihMT signal after 4s of irradiation for
different pulse widths was maximal for 5ms RF in GM and 95% of the maximum in
WM (Fig. 2a). Simulation of the ihMT following cycles of 5ms MT pulses repeated
every 100ms shows a steady-state is reached after 3s (Fig. 2b). However, the
ihMT is within 8 and 35% of the steady-state value, for WM and GM tissues
respectively, after a more reasonable 1s preparation. Although an interleaved
acquisition might reduce the interference of motion between the different
preparations, a reduction in ihMTR was observed in simulations and acquired
data (Figs. 2c-4). A significant difference (p<0.01 from paired one-tail
t-tests) between the ihMTRs from an interleaved and sequential implementation
was measured in: putamen; cerebellum; cerebral cortex; splenium of corpus
callosum; pons; and, midbrain regions of interest (Fig. 4). No significant
change in ihMTRs was found from inclusion of PROMO.Discussion
The results from simulations of the
ihMTRAGE sequence, accounting for scanner limitation information, allowed MPRAGE
like acquisition for whole brain ihMT. Lower ihMTRs from an interleaved
acquisition were close to that expected from simulation using a low duty cycle
preparation. IhMTR values lower than simulations predict were likely the result
of ihMT signal decay during acquisition and/or inaccurate parameter values
(Figs. 2,4). Simulation of RAGEs following MT preparation showed decreasing
ihMT with increasing FA and acquisition time. This result supported a
center-out k-space acquisition and
minimizing FA, but requires further consideration of signal-to-noise effects. Corpus
callosum ihMTRs were greater than those reported for a 3D steady-state
gradient-echo implementation4, likely due to the relatively
concentrated energy deposition scheme (B1,RMS~30mG over the preparation)
and dual frequency preparation by cosine modulation9. Simulations
provide a framework for optimization of ihMTRAGE based on tissue parameters and
other considerations, including duty cycle, the signal-to-noise for variable
FAs and different TRs of the RAGEs.Conclusion
A 3D ihMT sequence based on MPRAGE was
implemented for acquisition of 2.4mm isotropic data of the brain in scan times
of 6-7mins. Simulations of the sequence successfully anticipated the reduced
ihMTR values observed in an interleaved relative to sequential acquisition and
can guide further optimization of ihMTRAGE.Acknowledgements
No acknowledgement found.References
1. Varma G, Duhamel G, de Bazelaire C, et
al. Magnetization transfer from inhomogeneously broadened lines: A potential
marker for myelin. Magn Reson Med. 2015;73(2):614-622.
2. Prevost V, Girard O, Cayre M, et al.
Validation of inhomogeneous magnetization transfer (ihMT) as a myelin
biomarker. Proc. ISMRM 2017:4549.
3. Geeraert BL, Lebel RM, Mah AC, et al.
A comparison of inhomogeneous magnetization transfer, myelin volume fraction,
and diffusion tensor imaging measures in healthy children. NeuroImage.
2017;doi:10.10156/j.neuroimage.2017.09.019.
4. Mchinda S, Varma G, Prevost VH, et al.
Whole brain inhomogeneous magnetization transfer (ihMT) imaging: Sensitivity
enhancement within a steady-state gradient echo sequence. Magn Reson Med.
2017;doi:10.1002/mrm.26907.
5. White N, Roddey C, Shankaranarayanan
A, et al. PROMO: Real-time prospective motion correction in MRI using
image-based tracking. Magn Reson Med. 2010;63(1):91-105.
6. Varma G, Girard OM, Prevost VH, et al.
Interpretation of magnetization transfer from inhomogeneously broadened lines
(ihMT) in tissues as a dipolar order effect within motion restricted molecules.
J Magn Reson. 2015;260:67-76.
7. Stanisz GJ, Odrobina EE, Pun J, et al.
T1, T2 relaxation and magnetization transfer in tissue at 3T. Magn Reson Med.
2005;54(3):507-512.
8. Varma G, Girard OM, Prevost VH, et al.
In vivo measurement of a new source of contrast, the dipolar relaxation time, T1D,
using a modified inhomogeneous magnetization transfer (ihMT) sequence. Magn
Reson Med. 2017;78(4):1362-1372.
9. Prevost VH, Girard OM, Mchinda S, et
al. Optimization of inhomogeneous magnetization transfer (ihMT) MRI contrast
for preclinical studies using dipolar relaxation time (T1D)
filtering. 2017;doi:10.1002/nbm.3706.