KyungPyo Hong1, Suvai Gunasekaran1, Mohammed Elbaz1, Aggelos K Katsaggelos2, Saman Nazarian3, Rod Passman4, Eugene Kholmovski5, and Daniel Kim1
1Radiology, Northwestern University Feinberg School of Medicine, Chicago, IL, United States, 2Electrical and Computer Engineering, Northwestern University Feinberg School of Medicine, Evanston, IL, United States, 3Medicine, Cardiology, Hospital of the University of Pennsylvania, Philadelphia, PA, United States, 4Medicine, Cardiology, Northwestern University Feinberg School of Medicine, Chicago, IL, United States, 5Biomedical Engineering, Johns Hopkins University, Baltimore, MD, United States
Synopsis
Keywords: Motion Correction, Arrhythmia, Late Gadolinium Enhancement
Previously described left atrial (LA) late gadolinium enhancement (LGE) using
a stack-of-stars k-space sampling pattern with XD-GRASP reconstruction may
produce blurry LA wall due to signal variation of inversion-recovery-prepared 1D
self-navigation caused by arrhythmia. We hypothesize 2D image self-navigation
would be less sensitive to arrhythmia for motion tracking in XD-GRASP framework.
In this study, we developed a free-breathing, LA LGE pulse sequence with
isotropic spatial resolution using a stack-of-stars sampling pattern and 2D
self-navigation and compared its performance against conventional 1D
self-navigation in patients with atrial fibrillation. Results show that 2D
self-navigation improves respiratory motion tracking compared with 1D.
INTRODUCTION
Late gadolinium enhancement (LGE)1 is the gold standard for evaluation of myocardial
fibrosis, including in the left atrium (LA)2. Our group has recently developed a free-breathing, LA LGE
pulse sequence using a stack-of-stars k-space sampling pattern with XD-GRASP3
reconstruction, which used 1D self-navigation (1D-navi) oriented along the
head-to-foot direction to track respiratory motion4. The 1D-navi signal
was acquired immediately before LGE readout and used to assign each LGE readout
into a respiratory state or bin using principal component analysis (PCA). However,
PCA coefficients were frequently contaminated by sources of signal variation, such as 1) irregular inversion-recovery (IR) due to arrythmia in patients with
atrial fibrillation (AF) and 2) 1D projection of body surface structures with
bright signals (e.g., subcutaneous fat) that superimposes onto the relevant anatomical
features (e.g., lung-liver interface) essential for tracking respiratory motion.
This problem often translates into inconsistent PCA coefficient resulting in
inaccurate respiratory motion tracking, which requires manual selection of a
PCA coefficient that best tracks motion. We hypothesize that 2D image
self-navigation (2D-navi) is less sensitive to signal variation of IR caused by
arrhythmia compared with 1D-navi. In this study, we developed a free-breathing,
LA LGE pulse sequence using a stack-of-stars sampling pattern with isotropic
spatial resolution and 2D-navi and compared its performance against 1D-navi in
patients with AF. Our benchmark for success was automation of XD-GRASP
reconstruction. METHODS
Pulse Sequence: We developed an IR 3D-isotropic
stack-of-stars pulse sequence with variable density along slice direction (i.e.,
kz) and added 1D-navi (oriented along superior-inferior [SI] direction) and
2D-navi (6 radial projections at the center of kz with angle
increment=32.0397°) acquisitions per heartbeat as shown in Figure 1. The
relevant imaging parameters were: FOV=336x336x120 mm3 (coronal plane),
reconstruction matrix=224x224x80, spatial resolution=1.5x1.5x1.5 mm3,
20% oversampling in kz (96 slices in total), flip angle=15°, TE/TR =2.11/4.76
msec, receiver bandwidth=421 Hz/pixel, spoiled gradient-echo readout, 21 radial
projections per heartbeat (or shot) along kz with variable density, LGE readout
duration=100 msec, projection angle increment of 8.3264° within shot and
32.0397° between shots, SPAIR fat suppression, ECG trigger every heartbeat, total
scan duration=600 heartbeats, 3 regional saturation bands to suppress bright
signals at the abdomen and arms. MRI Studies: We enrolled 9 patients with AF (7 males;
61.9 ± 12.3 yrs) and performed 3D-isotropic LA LGE at 20-30 min after
administration of 0.2 mmol/kg of gadobutrol (Gadavist, Bayer). During the scan,
all patients had arrhythmia ranging from light to severe (Min. and Max.
coefficient of variation in individual R-R intervals=4.1% and 35.4%,
respectively). The quiescent period of LA was identified using a free-breathing
cine scan in 4-chamber view. Optimal TI was identified using a single-shot TI
scout with 60 k-space ky-lines per shot with GRAPPA (R=2) at 5 consecutive
heartbeats, which matches the readout timing of our 3D LGE.
Image Reconstruction: We automated the XD-GRASP3 reconstruction
pipeline to select the second PCA coefficient from 1D-navi and 2D-navi. For
1D-navi, we used the same method as previously described4. For
2D-navi, we performed compressed sensing (CS) to reconstruct a low-resolution 2D
image (6 radial projections per frame per heartbeat) for 600 heartbeats, where temporal
and spatial total variations were used as sparsifying transforms with
regularization weights of 0.001 and 0.00025, respectively. Then we extracted
the half-size FOV at the center of the 2D images and averaged along the
left-right direction to create 1D-navi like signals capturing the respiratory
motions along SI direction while excluding unwanted signals. PCA was applied to
1D-navi and pseudo-1D-navi, and the second coefficient was selected and ascending-sorted
and then its corresponding LGE readouts were assigned equally into 6
respiratory bins (see Figure 2).
Image Analysis: We calculated blur metric (0=sharp;
1=blur)5 in each slice of 6 respiratory 3D-volumes
encapsulating the heart. We identified the top and bottom location of an
internal organ (e.g., spleen or liver) among 6 respiratory states and measured
the maximum displacement.
Statistical Analysis: We compared all measurements between
1D-navi and 2D-navi by using a paired t-test. P<0.05 was considered
statistically significant. RESULTS
Mean blur metric was not significantly
different between 1D-navi (0.1849±0.0110) and 2D-navi (0.1857±0.0117) results.
The maximum displacement was significantly (p<0.05) longer for 2D-navi (12.3±5.8
mm) than 1D-navi results (7.5±5.8 mm). The range of maximum displacement was
0.0 to 19.5 mm for 1D-navi and 6.0 to 24.0 mm for 2D-navi, respectively. Mean blur metric and maximum displacement of
1D-navi and 2D-navi were summarized in Table 1. Figure 3 shows maximum
displacement between respiratory state 1 and 6 in one patient where both
performed equally well, and another patient where 2D-navi outperformed 1D-navi (0.0
mm and 10.5 mm displacement in 1D-navi and 2D-navi, respectively). Figure 4 compares
representative LGE images at coronal, sagittal, and axial views between 1D-navi
and 2D-navi in patient #5. DISCUSSION
We demonstrated that 2D-navi improves
tracking respiratory motions in 3D-isotropic LA LGE using XD-GRASP compared
with conventional 1D-navi. This improved motion tracking with consistent PCA
signal processing enables automation of XD-GRASP image reconstruction. Future
study includes automated inline image reconstruction pipeline using Siemens FIRE
(Framework for Image Reconstruction Environments).CONCLUSION
2D image self-navigation produces
consistent PCA signal processing and improves tracking of respiratory motions,
thereby enabling automation of 3D-isotropic LA LGE reconstruction using
XS-GRASP. Acknowledgements
This study was partially funded by National Institutes of Health (R01HL116895, R21AG055954, R01HL151079, R21EB030806A1) and American Heart Association
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