Agazi Samuel Tesfai1, Johannes Fischer1, Ali Caglar Özen1, Sébastien Bär1,2, Patrick Eppenberger3, Lena Öhrström3, Frank Rühli3, Ute Ludwig1, and Michael Bock1
1Dept.of Radiology, Medical Physics, Medical Center University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany, 2Department of Neurosurgery, Section for Neuroelectronic Systems, University Medical Center Freiburg, Freiburg, Germany, 3Institute of Evolutionary Medicine, Faculty of Medicine, University of Zurich, Zurich, Switzerland
Synopsis
Ancient mummified samples have ultra-short T2*
which decreases with increasing field strength. Here, image quality and T2*
relaxation times are compared for different tissues of a mummified hand between
a clinical 3T and a preclinical 9.4T system using a 3D UTE sequence. Although T2*
is shorter at 9.4T, image quality was superior to 3T, justifying the benefits
of ultra-high fields (UHF).
Introduction
In paleoradiology, X-ray based non-invasive
imaging modalities such as CT are predominantly used to image the rare and
fragile ancient remains. MRI of specimen such as mummified samples is difficult
due to the low proton density and the extremely short T2* of the
mummified tissue. Thus, the attainable SNR and the spatial resolution are
limited with MRI, even though very long measurement times can be realized. To
overcome the rapid T2*decay, pulse sequences such as ultra-short
echo time (UTE) or pointwise encoding time
reduction with radial acquisition (PETRA) are
used. These sequences provide improved contrast of mummified tissue, and they
can be applied to quantify the relaxation times1-3. However, they depend heavily on suitable hardware
with dedicated RF coils4 and fast Tx/Rx switching as well as high
performance gradients to maximize SNR. Recently, MRI of ancient remains was
shown with custom-made gradient inserts5 at 3T. In this work, we investigate
the benefits of ultra-high field (UHF) at 9.4T against clinical fields (3T).Materials and Methods
An embalmed
ancient Egyptian mummified left hand (approx. 1500–1100 BC) was used for MRI measurements (former collection of musée d’Orbe, Switzerland; Fig.1). The hand was
imaged with a preclinical MRI system at 9.4T (Bruker BioSpec 94/20 USR,
Ettlingen, Germany) with a bore size of 20 cm, that offers a gradient system with
Gmax=724 mT/m and a slew
rate of 4570 T/(m s). A custom-built linear
Tx/Rx high pass birdcage coil (diameter: 9 cm, 8 legs, length: 13.5 cm, leg
length: 11.5cm, leg width: 9mm, Q-factor:144, f0=400 MHz) was used.
For comparison, MRI data of the same sample were acquired at a clinical 3T
system (PrismaFit, Siemens, Erlangen) with Gmax=80 mT/m
and a slew rate of 200 T/(m s) and a dedicated Tx/Rx low pass birdcage coil in
quadrature mode (f0=123.2 MHz, Q factor: 150).
At 9.4T, a 3D UTE sequence was used for imaging with
following parameters: TE
= 40, 80, 160, 320, 640 µs, TR=5 ms, FA=4°, FOV=80mm, 10 averages, reconstructed
to a matrix size of 1603, bandwidth of 625 Hz/Pixel, 80000 spokes,
an isotropic resolution of 0.5mm and TA of 68 min. A T2* map was calculated from the 5
different TEs by a mono-exponential fit. At 3T, a 3D UTE sequence was applied
with the following parameters: TE=70,
120, 250, 400, 800µs, TR=5ms, FoV=192mm, 10 averages, matrix size of 384³,
BW=625 Hz/Pixel, FA=16°, 80000 radial spokes, isotropic resolution of 0.5mm and TA=68 min.Results
A transverse slice at the base of the hand from
the data sets at 3T (TE=70µs) and 9.4T (TE=40µs) is marked and shown in Fig. 2.
Anatomical details such as the cortical bone, tendons, and skin with embalming
remnants are identifiable at both field strengths. The 9.4T system has a higher
performance gradient system, thus the images suffer less from T2*
induced blurring. Cortical bone (SNR9.4T=61, SNR3T=24)
and dorsal skin (SNR9.4T=66, SNR3T=35) yield the highest
SNR gain. For most tissues, the SNR is superior for the 9.4T system, despite
reduced T2* relaxation time.
Ulnar skin with embalming remnant gives the
highest SNR9.4T=143 compared to 119 at 3T. The T2* map
(Fig. 3) also shows the highest relaxation time for skin with embalming resin (T2*=431µs at 9.4T, T2*=556µs at 3T). The range of T2*
relaxation times is reduced to below 200µs for all tissues at 9.4T besides
ulnar skin, whereas at 3T the T2* relaxation times have a much broader
range (177µs to 556µs) (Table 1).Discussion
Imaging at a preclinical UHF MRI system provides
highly improved image quality in terms of SNR and image sharpness for short T2*
samples. Increased SNR unveils more anatomical details and alteration of T2*
relaxation time might also provide additional contrast insight. This is
possible due to improved hardware specifications which allow a much shorter TE
(40µs at 9.4T system compared to 70µs at clinical 3T) yielding an SNR
improvement of up to 20%. Additionally, preclinical systems employ much
stronger gradients than clinical systems. This enables
rapid encoding, shortening the readout time after RF excitation that increases
image sharpness of samples with very short T2*. Higher B0
field strength provides significant sensitivity gain for improved SNR. At
clinical systems, much more sequence optimization steps are required to obtain
high image quality such as ideal Ernst angle (using FA=4° at 3T - identical to
9.4T - the measured signal was extremely low). However, there are several
downsides such as the simultaneous decrease of T2* relaxation times
down to 50% compared to 3T, that reduces SNR. Another aspect is the smaller
bore size (20cm diameter) and and narrow range of gradient linearity
(approximately 5-6cm in z-direction) in comparison to clinical devices. This
requires precise placement in the iso-center of the scanner to circumvent any
off-center effects due to the radial sequence and to obtain full FoV coverage.
Thus, these space limitations constrain the measurements to smaller specimen.Conclusion
In summary, MRI of ancient remains can be
performed with improved image quality at ultra-high field systems despite the
shorter T2* times and the sample size limitations. These MRI
acquisitions with spatial resolution up to 0.5mm would allow a detailed
analysis of anatomical structures providing additional insight and supplement
other imaging modalities such as CT. Acknowledgements
Grant support from the
Deutsche Forschungsgemeinschaft (DFG) under grant numbers BO 3025/8-1 and UL
1187/6-1 is gratefully acknowledged.References
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