Reproducibility of low-frequency MR elastography of the human brain
Florian Dittmann1, Sebastian Hirsch1, Jing Guo1, Jürgen Braun2, and Ingolf Sack1

1Institute of Radiology, Charité, Berlin, Germany, 2Department of Medical Informatics, Charité, Berlin, Germany

Synopsis

Since shear waves at low drive frequencies are nearly unaffected by attenuation, we introduce a brain MRE setup, which is based on remote excitation of intracranial shear waves by a pressurized-air actuator in the regime of 20 Hz. MRE-scans, which were repeated 27 times on three different days for each of six healthy volunteers, show differences between individuals as well as from day-to-day for the same individual. The investigation demonstrates that cerebral low frequency MRE provides a fast and reproducible novel source of mechanical information of brain tissue with less onerous head stimulation as required by conventional MRE.

Target audience

Physicists and physicians interested in magnetic resonance elastography (MRE).

Background

MRE is capable of generating image contrast based on the viscoelastic properties of tissue by inducing and detecting time harmonic shear waves in the body [1]. Recent work in MRE of the brain suggested the exploitation of low vibration frequencies since shear waves in the regime of 20 Hz are nearly unaffected by attenuation [2]. Furthermore, it was stated that low drive frequencies are less onerous to patients and volunteers than high frequencies, in particular when combined with remote wave excitation as proposed in [3]. Based on these reports, we introduce a low-frequency protocol for brain-MRE including a remote compressed-air actuator which is placed beneath the shoulders and we test the reproducibility of this protocol.

Purpose

To introduce low-frequency MRE of the brain based on remote excitation of intracranial shear waves by a pressurized-air actuator and to analyze reproducibility of this method as well as inter-subject variation and day-to-day variation of the brain shear modulus in the low frequency regime.

Methods

An MRE setup was developed utilizing a single shot spin-echo EPI sequence based on retrospective wave phase correction as detailed in [2], which ensures an uninterrupted shear wave propagation through the tissue with minimized image acquisition time. Intracranial shear waves were excited by a remote actuator placed under the shoulders of the volunteers and operated by 17.85, 20.00 and 22.73 Hz drive frequencies (56, 50 and 54 ms cycle time). The rubber membrane of the actuator (11 cm diameter) was vibrated by air pressure pulses supplied with compressed air of approximately 0.25 bar from a medical air pipeline and controlled by a high-speed electromagnetic valve [4]. Imaging parameters: 1.5T Siemens Sonata MR scanner, 15 consecutive coronal slices, 2 mm isotropic voxel size, 8 wave dynamics, 3 wave field components, rectangular 1st momentum nulled motion encoding gradient with 25 mT/m amplitude (38.4 ms duration), TR/TE=2500/92 ms, FoV=192×160 mm2, matrix size: 96×80, total measurement time including three frequencies: 3:06 min

To analyze the reproducibility of the method, six healthy volunteers were scanned on three days within one week. On each of the three days, nine MRE-repetitions were acquired in three sessions (in total 27 repetitions per subject). After the third and the sixth repetition of each day, the subject left and reentered the scanner, and actuator and subject were repositioned.

In addition to the MRE scans, a magnetization-prepared rapid gradient echo (MPRAGE) sequence (TR/TE=2110/4.4 ms, TI=1100 ms, flip angle 15°, 1 mm isotropic voxel size) was acquired before each session.

MRE data were analyzed by multifrequency dual elasto-visco (MDEV) inversion as described in [2] yielding a 3D parameter map corresponding to the magnitude |G*| of the complex shear modulus.

Results

Despite long scan times due to multiple repetitions, no discomfort was reported by any subject. As visualized by the three curl-components of the wave field at 20 Hz in Fig. 2 (bottom), high shear wave amplitudes were achieved throughout the whole brain. The |G*|-maps agree well to the anatomy. Figure 3 shows |G*|-values average within the cerebrum for the 27 scans of each subject. The variances along the repetitions are displayed in Table 1. The variance within one session (group averaged coefficient of variation CVmedian = 0.8%) was smaller than the variance within one day (group averaged CVmedian = 1.8%) and smaller than the total variance accounting for 27 measurements (2.5%). We note inter-subject differences raising the question to what extent |G*| reflects intrinsic structural differences between individual brains.

Discussion & Conclusion

Low frequency MRE vibrations were felt less intense than intrinsic scanner vibrations. Furthermore, the remote actuator does not require any space within the narrow geometry of head coils resulting in a flexible setup. Our method shows good test-retest reproducibility. Higher variances between days as compared to intra-day scans indicate the influence of day-to-day changes of brain viscoelasticity. Since low-frequency MRE is potentially more sensitive to fluid-solid interactions in poroelastic media, vascular effects may play a role here. This may contribute to the observed inter-subject differences and should be further investigated. Another source of variability is the delineation of regions which was done with the help of atlas-based image registration in our study. This approach neglects boundary effects near tissue interfaces [5].

In summary, cerebral low frequency MRE provides a novel source of mechanical information of brain tissue which is attainable in a fast and reproducible way with less onerous head stimulations as required by conventional MRE. The measured elastograms reveal individual and day-to-day variations of brain viscoelasticity requiring further investigations.

Acknowledgements

No acknowledgement found.

References

1. Muthupillai R, Ehman RL. Magnetic resonance elastography. Nat. Med. 1996;2:601–603.

2. Dittmann F, Hirsch S, Tzschätzsch H, Guo J, Braun J, Sack I. In vivo wideband multifrequency MR elastography of the human brain and liver. Magn. Reson. Med. 2015; doi: 10.1002/mrm.26006.

3. Fehlner A, Papazoglou S, McGarry MD, Paulsen KD, Guo J, Streitberger K-J, Hirsch S, Braun J, Sack I. Cerebral multifrequency MR elastography by remote excitation of intracranial shear waves. NMR Biomed. 2015;28:1426–1432.

4. Braun J, Hirsch S, Heinze T, Sack I. Feasibility of a new actuator type for magnetic resonance elastography based on transient air pressure impulses. In: Proc 23rd Annual Annual Meeting ISMRM. ; 2015.

5. Murphy MC, Huston J, Jack CR, Glaser KJ, Senjem ML, Chen J, Manduca A, Felmlee JP, Ehman RL. Measuring the characteristic topography of brain stiffness with magnetic resonance elastography. PLoS One 2013; 8:e81668.

Figures

Figure 1: Placement of passive pneumatic actuator below the shoulders

Figure 2: Coronal magnitude image (top left), |G*|-maps (top center) and three components of curl wave field at 20 Hz (bottom row) of one volunteer

Figure 3: Boxplots of mean |G*|-values within the cerebrum over the 27 repetitions for each of the six subjects

Table 1: Mean and standard deviation (STD) of |G*| and coefficient of variation (CV) for all repetitions, day-wise and session-wise for each of the six subjects



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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