Andrew David Scott1,2, Upasana Tayal1,2, Sonia Nielles-Vallespin1,3, Pedro Ferreira1,2, Xiaodong Zhong4, Frederick Epstein5, Sanjay Prasad1,2, and David Firmin1,2
1NIHR funded Cardiovascular Biomedical Research Unit, Royal Brompton Hospital, London, United Kingdom, 2National Heart and Lung Institute, Imperial College London, London, United Kingdom, 3National Heart Lung and Blood Institute, National Institutes of Health, Bethesda, MD, United States, 4MR R&D Collaborations, Siemens Healthcare, Atlanta, GA, United States, 5University of Virginia, Department of Biomedical Engineering, Charlottesville, VA, United States
Synopsis
Displacement encoding with stimulated
echoes (DENSE) can provide valuable strain information, but acquisitions are typically
too long for patient cohorts who have difficulty breath holding. In this work
we accelerate 2D cine spiral DENSE acquisitions by selectively exciting a small
field of view around the heart. We compare strain data derived from DENSE
acquired with unaccelerated and up to 2.5x acceleration in a cohort of healthy
subjects and show minimal differences when the acquisition is accelerated. We
also show an example from a patient with a myocardial infarction where the
accelerated DENSE data shows abnormal strain in the infarcted regions.Background
Displacement
encoding with stimulated echoes (DENSE) is an accurate and reproducible
1,2 technique for measuring myocardial strain
throughout the cardiac cycle. The strain maps provided could be valuable in
dilated cardiomyopathy (DCM) patients where strain has a prognostic value
3.
However, DENSE acquisitions typically require long breath holds which are
difficult for DCM patients or navigator gating which is time consuming and
prone to failure. In this work we accelerate DENSE acquisitions by selectively
exciting a volume of tissue around the heart. This allows fewer spiral
interleaves to be acquired without aliasing and, therefore a shorter breath
hold. We compare accelerated and unaccelerated DENSE in healthy volunteers and
demonstrate the utility of accelerated DENSE in an example patient.
Methods
A
cine spiral DENSE sequence4 was modified to selectively excite a
reduced field of view. A slice selective gradient was added to the first and
second RF pulses on the read and phase axes respectively (figure 1). An
improved excitation profile without increasing TE was achieved by making the
1st pulse asymmetric (peak at 81% of duration) and the 2nd pulse a time-reversed
copy of the first.
In-vivo 2D cine DENSE was performed in 8 normal
subjects (Siemens Skyra 3T) in a mid short-axis slice. Images were acquired
with variable flip angle (20o max), TE=1ms, fat suppression,
3.5x3.5mm2 spatial resolution, 1282 reconstruction matrix,
8mm slice thickness, TR=15ms, 30ms temporal resolution, 2 spirals/frame, 6ms spiral duration, 2
direction simple encoding (+reference) at 0.06cycles/mm, CSPAMM and
through-plane dephasing artifact suppression5 (0.08cycles/mm). Long,
medium and short acquisitions were performed with square fields of view/breath hold
durations of 360mm2/20RR-intervals (RR), 224mm2/14RR and
120mm2/8RR, respectively,
including 2RR-intervals
for a B0 field map in each case. The long acquisition used a similar field of view
to previous work performed without the zonal excitation and was used as a
reference4. Images were processed using the DENSE analysis tool from
the University of Virginia6. Peak and time-to-peak radial and circumferential strains measured globally over the left ventricle were compared between protocols using a Wilcoxon signed rank test (p<0.05 threshold) and by calculating the root mean square error between the strain-time curves.
Mid-ventricular short
axis spiral cine DENSE using the medium breath hold protocol was also performed in one patient diagnosed with dilated cardiomyopathy.
Results
Figure
2 shows example magnitude images in
one example volunteer acquired using long, medium and short acquisitions and the corresponding
strain curves are shown in figure 3. There is good agreement between the strain
curves from all three acquisitions. Global peak strain, time to peak strain and
the differences between acquisitions (long
acquisition as
reference, expressed as bias and root mean square error) are summarized in the table for radial and circumferential strain for all 8 volunteers. While there is a significant
under-estimation (p<0.01) of peak radial strain using the medium
acquisition, the magnitude of the difference is small (0.01). There were no
other significant differences and the medium and short breath hold acquisitions
appear to be equally accurate.
Upon
review of the patient data, a wall motion abnormality and late gadolinium
enhancement (LGE) indicated that the diagnosis was incorrect and the patient
had an extensive infarct. Figure 4 shows the strain curves derived from DENSE
with the corresponding LGE images. Radial and circumferential strain is reduced
with abnormal strain patterns in the infarcted regions of myocardium, while the
remote regions show relatively normal strains.
Discussion and conclusion
Spiral cine DENSE imaging
can be accelerated by up to a factor of 2.5 by selectively exciting and imaging
a small field of view around the heart. The associated loss of signal to noise
ratio is partly compensated for by imaging at 3T. This improvement allows 2D
acquisitions to be performed in a medium (~14s) or even short breath hold (~8s)
which most patients could sustain. The technique was demonstrated in a patient
with myocardial infarction. Segments of the heart with reduced strain were
found to correspond to regions of the heart with late gadolinium enhancement. In
future the same approach may be used to accelerate 2D long axis and 3D spiral
cine DENSE acquisitions.
Acknowledgements
This work was performed at the National Institute for Health Research funded Cardiovascular Biomedical Research Unit at the Royal Brompton Hospital and Imperial College London.References
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