Sebastian Theilenberg1, Jakob Bindl1, Anna-Lisa Kofahl1, Carsten Urbach1, and Karl Maier1
1Helmholtz-Institut für Strahlen- und Kernphysik, University of Bonn, Bonn, Germany
Synopsis
Magnetic
resonance rheology is a novel method to create an imaging contrast based on the
mechanical properties of brain tissue. It is based on a short fall of the head
that creates a broadband excitation of the tissue. The resulting deflections of
the tissue elements are depicted using motion sensitive phase imaging. This
contribution presents measurements on agar phantoms as well as four meningioma
patients to show the feasibility of the method to depict local alterations of
the mechanical properties of the investigated material.
Introduction
Magnetic
Resonance Rheology (MRR)1 is a novel method to visualize the
mechanical properties of brain tissue. The main difference to the more common
magnetic resonance elastography is its means of excitation: MRR uses a short
fall of the head to create a global excitation of the brain tissue. The
introduced deflection of the tissue elements are measured using motion
sensitive MRI phase imaging.
We present measurements on two agar-based phantoms and a study on four patients
diagnosed with meningioma to show the feasibility of this method to visualize
locally different mechanical properties of the material based on the phase
contrast.Methods
MRR uses a
custom build lifting device (Fig. 1) adapted to a standard head coil of a
Siemens Avanto 1.5 T scanner. The patient’s head respectively the phantom is positioned
on a moveable shell that is lifted pneumatically to a height of approximately 1
mm. It is then dropped synchronized to an SE-EPI sequence equipped with two
identical trapezoidal motion encoding gradients2 (MEG) in the
direction of the falling motion on either side of the inversion pulse. The
falling motion excites a wide band of frequencies in the investigated material.
The resulting deflection is sampled by shifting the start of the falling motion
(parameter $$$\tau$$$) (Fig. 2).
The first
presented study was on two cylindrical phantoms each filled with two different
layers of agar based hydrogel3. One phantom consisted of two layers
with different agar concentration and thus different Young’s moduli, the second
phantom consisted of two layers of equal Young’s moduli but different density,
which was achieved by adding tungsten carbide powder to the hydrogel.
The second study was performed on four meningioma patients prior to surgery.
In both studies, phase images of one transversal slice with induced motion were
acquired at different tau values to examine the phase progression per voxel
with respect to tau. The imaging parameters were TR = 3000 ms resp. 3500 ms
(phantoms resp. meningioma patients), TE = 80 ms, matrix size: 112 x 128, voxel
size between 1.4 x 1.4 x 5 mm and 2 x 2 x 5 mm. The strength of the MEGs was G
= 34.8 mT/m, the length of one MEG was delta = 5 ms and the distance between
both MEGs was Delta = 45 ms. All measurements were accompanied by a measurement
with the same parameters but without induced motion of the head that served as
a baseline measurement.
The images
were post-processed by subtraction of the baseline, normalization to a
reference point and numerical phase unwrapping. As a measure of strain instead
of deflection, the gradient of the phase in the direction of the falling motion was calculated after
smoothing with a gaussian filter ($$$\sigma$$$ = 0.6).Results
The phase images
of the phantoms clearly show the different oscillatory behavior of the two
layers. This distinction is even easier in the calculated strain images (cf.
Fig 3). For the meningioma patients, the tumor regions of all four patients
show up in the motion images with a distinct signature of less deflection. In
the strain images, the tumor regions show reduced strain values (cf. Fig. 4)Discussion
The phantom
measurements showed that the signal measured in MRR is dependent both on the
elastic properties and the density of the material. In vivo, the typical phase
signal of an MRR measurement is a global oscillation of the brains hemispheres with
a higher deflection of tissue elements in the center of the hemisphere than
near to the meninges, as was shown in previous studies1. As
expected, the different mechanical properties of the meningioma tissue lead to
a different $$$\tau$$$-dependence of the measured phase in those regions. All
meningiomas were classified by the surgeons as significantly stiffer than
healthy tissue, which explains the lower strain values found in those regions.Conclusion
The
presented results show the feasibility of MRR to visualize local alterations of
the mechanical properties of brain tissue. To investigate the full potential of
this method, however, the number of patients in this study was too small.
Further research will address this, and will attempt to quantify the results of
MRR measurements with the aim to infer the mechanical properties of the
investigated brain tissue.Acknowledgements
The authors would like to thank Prof. Elke Hattingen and Dr. Bogdan Pintea for their valuable help with the study on meningioma patients and Dr. Jürgen Finsterbusch for the development of the MRI sequence.
References
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A-L, Theilenberg S., et al. Combining
Rheology and MRI: Imaging Healthy and Tumorous Brains Based on Mechanical
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diffusion measurements: spin echoes in the presence of a time-dependent field
gradient. J Chem Phys 1965;42:288-292.
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harmonic motion imaging: theory, simulations and experiments. Ultrasound Med
Biol 2003;29:1405–1413.