Hana Hlavata1, Mauro Costagli2, Janine M Lupo3, Emiliano Perticaroli4, Michela Tosetti2, and Mirco Cosottini5
1IRCCS Stella Maris, Pisa, Italy, 2Imago 7 Research Center, IRCCS Stella Maris, Pisa, Italy, 3University of California San Francisco, San Francisco, CA, United States, 4Azienda Ospedaliero-Universitaria Pisana, Pisa, Italy, 5University of Pisa, Pisa, Italy
Synopsis
The
simultaneous depiction of both arterial and venous vasculature has recently
been demonstrated by using multi-echo sequences.
We quantitatively and qualitatively assessed the simultaneous
representation of intracranial arteries and veins at a higher resolution than
previously reported using a customized 3D spoiled gradient multi-echo sequence
at 7T.
Such custom sequence had an overall
better capability of depicting the arterial vasculature compared to conventional
time-of-flight (TOF) arteriography. On the contrary, veins were in general better
depicted by conventional susceptibility-weighted venography, however the custom
multi-echo sequence provided superior quality images of the superficial veins.
Introduction
The
simultaneous depiction of arterial and venous vasculature has recently
been demonstrated by using multi-echo sequences1—6. Here we assessed the
representation of intracranial arteries and veins at a higher
resolution than previously reported using a customized single-slab 3D spoiled
gradient multi-echo sequence at 7T6, and compared it to conventional
time-of-flight (TOF) arteriography and multi-echo susceptibility-weighted
venography.Methods
Images were
acquired with an MR950 7T system (GE Healthcare) equipped with a 32-ch receive head coil (Nova Medical). The same subject underwent the
following sequences, all prescribed axially with the same coverage of 50mm
along z, with (0.5mm)3
isotropic spatial resolution:
- meTOF: custom spoiled 3D gradient
multi-echo sequence6, single slab, with TE=3.0ms, 11.0ms, 18.9ms,
26.9ms, TR / FA / FOV / ReceiverBW =
40ms / 25deg / 3ms / 192mm / ±41.7kHz; acquisition matrix 384x384,
flow-compensated, ramp-excitation, ARC (Auto-calibrating recostruction for
Cartesian sampling) acceleration factor=3; scan duration=8’04’’. Data from the
first echo were used to produce arteriography images. The average of
T2*-weighted images from echoes 2~4 were used to produce venography images.
- TOF: product 3D time-of-flight multiple-overlapping
thin-slab acquisition with two slabs (12 overlapping locations), TR / FA / TE /
FOV / ReceiverBW = 19ms / 15deg / 3ms / 192mm / ±31.2kHz; acquisition matrix
384x384, flow-compensated, ramp-excitation, fat-saturation, ASSET (Array coil Spatial Sensitivity Encoding) acceleration factor=3;
scan duration=3’50’’.
- SWAN: product
susceptibility-weighted 3D gradient multi-echo sequence with TE=5.8ms, 12.4ms,
19.0ms, 25.6ms, 32.2ms, 38.8ms, TR / FA / FOV / ReceiverBW = 44.1ms / 15deg / 192mm
/ ±41.7kHz; matrix size=384x384, flow compensated, ASSET factor=3; scan
duration=5’21’’.
For
arteriography, 17 ROIs were manually drawn in different segments
of the cerebral arteires (medial, anterior and posterior segments), in the
carotid siphon, and basilar artery (Fig.1A). For venography, 16 ROIs
were drawn in the parenchyma adjacent to the rectal sinus and the perimesencephalic
and internal cerebral veins: in white matter, corpus callosum and pons Varolii
(Fig.1B). By using the data of two co-registered acquisitions of the same kind,
SNR was measured in each ROI with the difference method7, in meTOF’s
and TOF’s arteriograhies, as well as in meTOF’s and SWAN’s venographies.
Maximum
Intensity Projection (MIP) images were generated for arteriographies, while
Minimum Intensity Projection (mIP) images were generated for venographies, all
with thickness=8mm. 50 ROI pairs covered the vessels (either artery or vein)
and the respective adjacent parenchyma (Fig.1C), and were used to compute
Relative Contrast (RC)8.
Additional
sets of MIP and mIP images were generated with thickness = 30mm (Fig.2) and
were used by an expert neuroradiologist to qualitatively evaluate the
visualization of different vascular tracts with scores ranging between 0 and 4
(0 = no visualization of the tract; 4 excellent visualization).
Results
Quantitative
SNR measurements are reported in Fig.3. The arteriography based on the custom
meTOF sequence had an overall better SNR. The maximum difference was observed
in the anterior cerebral artery. In venography, SNR was, on average, 2.5 times
higher in SWAN than in the meTOF sequence.
RC measures
are shown in Fig.4. In arterial tracts RC was, on average, 7.4% higher in meTOF
than in conventional TOF. The RC in meTOF was higher in particular in proximal tracts,
while in distal arteries the RC was only 1.7% higher than in TOF. In venography,
RC was 4.8% higher in SWAN than in meTOF, but this
measure was biased by the measurements in deep veins, where RC in SWAN was 8.1%
higher than in meTOF. On the contrary, meTOF’s venography had a 27.3% higher RC
than SWAN when only superficial veins were considered.
The qualitative assessment scores are shown in
Fig.5.
Scores
attributed to images acquired with different techniques varied depending on the
tracts being examined.
Discussion and Conclusion
The custom multi-echo sequence6 had an overall better
capability of depicting the arterial vasculature compared to the conventional
TOF sequence, from both quantitative and qualitative standpoints, despite the use of one single slab and longer TR. On the contrary, veins
were better depicted by SWAN, possibly due to the larger number of echoes being
used; however the meTOF-based venography provided images with
satisfactory quality and, for superficial veins, it was superior to conventional
imaging.
The simultaneous acquisition of co-registered arterial and venous
vasculature at high resolution is therefore feasible and presents some
advantages with respect to conventional approaches.
It
is also worth noting that while the conventional TOF acquisition at 7T approached
the Specific Absorption Rate (SAR) time-average limit of 3.2W/kg imposed by International
Electrotechnical Commission (standard IEC-60601-2-33), the custom multi-echo
sequence used in this
study6
runs below such limits (SAR was about half that of TOF). In conclusion, this
technique could be a new valuable tool in clinical radiological settings for
studying neurovascular pathologies.Acknowledgements
No acknowledgement found.References
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