Romain Froidevaux1, Markus Weiger1, Manuela Barbara Rösler1, David Otto Brunner1, Benjamin Emanuel Dietrich1, and Klaas Paul Pruessmann1
1Institute for Biomedical Engineering, ETH Zurich and University of Zurich, Zurich, Switzerland
Synopsis
With recent developments in gradient hardware even tissues with T2s
down to tens of microseconds have become accessible for MRI. Hence, mapping
signal decay or imaging short-T2 tissues selectively is of particular interest.
This can be performed using ultra-short echo time imaging with multiple TEs.
However, for typical resolutions this approach is limited to T2s down to
hundreds of microseconds.
In this work, the PETRA and HYFI techniques are utilized to map the signal
decay of samples with T2s down to 54 μs. Considerably larger scan efficiency is
obtained for the HYFI approach.
Introduction
Direct depiction of tissues with
transverse relaxation times T2 or T2* in the sub-millisecond range, such as
e.g. bone, teeth, or lung has a great potential for further expanding the
scientific and diagnostic value of MRI (1). With recent developments in
gradient hardware (2)
even tissues with T2s down to tens of microseconds, e.g. the myelin sheath (3),
have become accessible. In this context, mapping signal decay or imaging
short-T2 tissues selectively is of particular interest.
A common technique applied for
this purpose is radial ultra-short echo time (UTE) imaging with multiple TEs (4,5).
However, for typical resolutions the UTE approach is limited to T2s down to
hundreds of microseconds. Imaging of shorter T2s can be accomplished by
avoiding any gradient ramping after excitation with the radial zero echo time
(ZTE) technique (6)(Fig. 1a), yet preventing increasing TE and hence T2 weighting. The latter is possible
with single-point imaging (SPI)(7),
yet at the price of greatly reduced SNR efficiency.
In this work, the PETRA (8)(Fig. 1c) and HYFI (9)(Fig. 1d) techniques are utilized to enable mapping of very rapid signal decay.
Both approaches improve scan efficient by combining ZTE and SPI data using
different strategies while the option for T2 weighting is still available. These
features are employed here for mapping samples with T2s down to 54 μs, clearly demonstrating
highest efficiency for HYFI.Methods
Hardware
All experiments were performed on
a 3T Achieva MRI system (Philips Healthcare, Best, Netherlands), complemented
with dedicated short-T2-MRI hardware: a high-performance insert gradient
capable of reaching 200 mT/m at full duty cycle (2),
symmetrically biased transmit-receive switches with switching times of
approximately 3µs at 3T (10),
and a high-end spectrometer with up to 4 MHz acquisition bandwidth and short
digital filters with group delays down to 1.2µs (11).
A largely 1H-free RF loop coil was used for both transmission and reception (12).
Imaging
Data were acquired with HYFI and
PETRA (Fig. 1) where the inner k-space was increased so that it contains all
the k-space support but the outermost Nyquist interval. The acquisition of same
image geometry with increasing TE was obtained by increasing the dead time and reducing the
gradient accordingly. In PETRA and HYFI, the echo time is defined to be equal
to the dead time. For HYFI, the decay constant was set to A=0.1 for target T2=TE.
Images were reconstructed using
an iterative conjugate gradient algorithm complemented with a pulse profile
correction algorithm (13,14).
Samples
An imaging phantom with a range
of T2 values was created by filling six solutions of MnCl2 with concentrations
of 240,120,60,30,15 and 7.5 mMol into glass vials. For measurement of the
transverse relaxation times, the solutions were filled into glass spheres of
diameter 20mm to minimize susceptibility effects.Results
Fig. 2: The signal decay of each MnCl2
solution was fitted with single exponentials for three different data types: FIDs
and PETRA or HYFI echo series. They provide the indicated relaxation constants
with very good agreement especially in the short-T2 range. However,
HYFI seems to consistently underestimate T2 values as compared to PETRA.
Fig. 3: Two echo series of
similar image quality were obtained with HYFI and PETRA while HYFI required
only 37% of the scan time needed by PETRA.
Fig. 4: Weighted
subtractions(15)
of the shortest and one longer TE efficiently suppress long-T2 signals and
provide a large variety of short-T2 contrast in the sub-millisecond range. Only
a small edge artefact is observed for longer T2s (for both HYFI and PETRA).Discussion
Very
good agreement was obtained for T2s derived from FIDs and both mapping
approaches. Faster decay in FIDs at longer relaxation times indicates dephasing
due to residual inhomogeneity, which is reduced by separating locations in the
mapping techniques. Deviations between HYFI and PETRA are associated with the
different strategies used for the inner k-space. Indeed in HYFI, choosing TE
equal to the dead time slightly underestimates the actual time of acquisition of
the radial data points (as opposed to PETRA where all data are acquired at TE),
leading to somewhat lower T2 values. This might be addressed by a more
sophisticated data analysis.
Weighted subtractions of HYFI
data (Fig. 4) show great potential to introduce versatile contrast in the
short-T2 range while preserving acceptable scanning efficiency. This may be
especially interesting for direct imaging of the myelin sheath in which the
majority of the signal is expected to decay in less than a 100 µs(16,17).
The edge artifact in Fig. 4 will
require further investigation.
It may stem from gradient imperfections due to strong eddy currents occurring
at high-bandwidth, thus mostly affecting the shortest-TE image. Conclusion
Multi-TE HYFI imaging enables mapping
and T2-contrast generation for samples with ultra-short T2s down to tens of
microseconds. It proved to be significantly more time-efficient than its PETRA counterpart
relying on more SPI scanning. Further speed-up is possible by changing the partition
of inner and outer k-space but this requires careful consideration with respect
to mapping fidelity. The presented approach allows a large variety of T2 contrast
in the sub-millisecond range, suggesting applications in domains such as direct
depiction of the myelin sheath, bone or teeth imaging, as well as material
studies.Acknowledgements
No acknowledgement found.References
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