Seong Dae Yun1 and N. Jon Shah1,2,3,4
1Institute of Neuroscience and Medicine 4, INM-4, Forschungszentrum Juelich, Juelich, Germany, 2Institute of Neuroscience and Medicine 11, INM-11, JARA, Forschungszentrum Juelich, Juelich, Germany, 3JARA - BRAIN - Translational Medicine, Aachen, Germany, 4Department of Neurology, RWTH Aachen University, Aachen, Germany
Synopsis
Keywords: Contrast Mechanisms, Quantitative Imaging, 7T, Inversion-recovery EPI, Rapid T1 mapping, Submillimetre and Whole-brain
Knowledge
of T
1 relaxation time is of great interest for clinical diagnosis or
MRI sequence optimisation. For the quantitative measurement of T
1, the
inversion-recovery method is widely used due to its relatively good accuracy or
tolerance to B
1 inhomogeneity. However, 2D multi-slice- or 3D segmentation-based
readout methods often preclude the effect of different signal recovery
modulation depending on slice locations. Therefore, this work presents a
single-slice-based inversion-recovery 2D EPI method, combined with TR-external
EPI phase correction at 7T, to provide rapid, whole-brain T
1 mapping
with a voxel size of 0.73 × 0.73
mm
2.
Introduction
The
quantitative measurement of T1 relaxation time is of great interest
in the MR community as it can provide valuable information on physiological
state for clinical diagnosis or physical tissue parameters to optimise imaging
sequences.1-4 Previously, various methods have been presented for T1
mapping, and of these, the inversion-recovery method is considered a gold
standard method, as it can provide an enhanced accuracy or tolerance to B1
inhomogeneity when compared to other types of methods (e.g. variable flip
angle).1,5
However,
the approach of tracking the dynamic recovery of longitudinal magnetisation after
an inversion inherently requires a relatively long acquisition time, which can
significantly hinder the mapping of whole-brain T1 with high spatial
resolution. To effectively shorten its acquisition time, an inversion-recovery
method, the readout of which is implemented with echo-planar-imaging, namely
IR-EPI, was demonstrated using the 2D multi-slice-based or 3D segmented EPI regime.1,5,6
However, the acquisition of multiple slices in successive excitation loops within
the same T1 recovery period can impose a different signal recovery modulation
for each slice. That is, the earlier time point during the recovery may not be
effectively captured in the slice acquired at a later time point. Specifically,
this problem becomes more severe as the number of slices increases for larger
brain coverage.
Therefore,
this work presents a single-slice-based IR-EPI method (i.e. one inversion-recovery
per each slice) where the number of required inversion-recovery loops is reduced
by means of the multiband acceleration, resulting in a much shorter acquisition
time.7,8 Moreover, the EPI readout was further configured with the TR-external
EPI phase correction scheme (TRx) to substantially reduce the minimum TE
required for submillimetre resolution EPI.9,10Methods
Figure
1 shows a diagram of the proposed imaging sequence. The inversion-recovery loop
is repeated as many times as the number of slices, which can be reduced by the multiband
acceleration. Each inversion-recovery kernel starts with combined
saturation and inversion preparation pulses and subsequently performs dynamic
sampling only for a single slice or a group of slices in case of multiband acceleration.
This strategy ensures data at each slice location have identical inversion time
points. Here, each temporal point is acquired with 2D EPI combined with the TRx
scheme.
The feasibility of using the multiband and the TRx techniques
for IR-EPI was verified by comparing the signals from the following four sequences:
1) IR-EPI, 2) IR-Multiband EPI (IR-MEPI), 3) TRx-IR-EPI and 4) TRx-IR-MEPI. For
this comparison, low-resolution data sets from a uniform spherical phantom were
acquired without any acceleration condition (see Fig. 2a). Next, submillimetre-resolution
protocols were configured using IR-MEPI and TRx-IR-MEPI, each of which was
optimised to offer the highest possible spatial resolutions (0.97 × 0.97 mm2 and 0.73 ×
0.73 mm2,
respectively) under the imaging condition shown in Fig. 2b. Data sets from a healthy volunteer screened
with a standard safety procedure were acquired using the two submillimetre protocols.
All
experiments in this work were performed at a Siemens Magnetom Terra 7T scanner with a
1-Tx/32-Rx head coil.Results
Figures
3a-c depict the temporal signal evolution of the phantom data obtained from the
four different sequences. This result suggests that the use of the multiband or
TRx techniques has no significant impact on the behaviour of the signal
recovery. The very small difference observed in the above plots was also numerically
verified by computing the mean signal differences (see Fig. 3d). Figure 4 shows
T1 maps at a representative slice location obtained from IR-MEPI
(0.97 × 0.97 mm2)
and TRx-IR-MEPI (0.73 × 0.73
mm2). This result demonstrates the impact of the superior spatial
resolution achieved in TRx-IR-MEPI, resulting in a clearer delineation of the T1
values around the cortical ribbon. Figure 5 shows the T1 maps for all
the slices (75) from TRx-IR-MEPI, and depicts reliable T1 estimation
for all slice locations. The mean T1 values for whole-brain WM/GM
were computed as 1200.72/1640.30 ms for IR-MEPI and 1140.20/1617.19 ms for TRx-IR-MEPI,
both of which are in good agreement with those reported in previous
submillimetre T1 mapping studies obtained with MP2RAGE (1140/1653)5,
IR-Turbo-spin-echo (1017/1654)11 or IR-EPI (1170/1783)5
methods at 7T.Discussion and conclusions
This work demonstrates rapid, whole-brain T1
mapping using TRx-IR-MEPI
at 7T. The method was able to achieve a relatively large matrix size, consequently
resulting in a substantial improvement in the spatial resolution of T1
maps when compared to IR-MEPI. The achieved spatial resolution suggests its
potential use for cortical depth-dependent T1 quantification. The TE
employed here was 17.6 ms, which was also similar to the TEs (16~20 ms) employed
in the previous submillimetre IR-EPI study.5 However, in contrast, our
method is based on single-shot EPI, which can mitigate increased aliasing
artefacts, physiological noise or subject motion stemming from the multiple
shots typically seen in 2D multi-shot or 3D segmented EPI. For the submillimetre-protocols
tested here, the required time for the entire T1 recovery data (0.73 × 0.73 mm2 ×
75 slices × 60 time-points) was only 3.5 minutes, which was mainly the result
of the use of the multiband acceleration. In future works, a study with more
subjects including the inversion efficiency measurement12,13 is
planned for more quantitative analysis on TRx-IR-MEPI with improved T1 mapping
accuracy. Acknowledgements
No acknowledgement found.References
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