Pierre Daudé1,2, Thomas Troalen3, Adèle L C Mackowiak4,5, Davide Piccini4,6, Jerôme Yerly4,5, Josef Pfeuffer7, Frank Kober1,2, Sylviane Confort Gouny1,2, Monique Bernard1,2, Matthias Stuber4,5, Jessica A M Bastiaansen4,5,8,9, and Stanislas Rapacchi1,2
1Aix-Marseille Univ, CNRS, CRMBM, Marseille, France, 2APHM, Hôpital Universitaire Timone, CEMEREM, Marseille, France, 3Siemens Healthcare SAS, Saint-Denis, France, 4Department of Diagnostic and Interventional Radiology, Lausanne University Hospital, Lausanne, Switzerland, 5Center for Biomedical Imaging, Lausanne, Switzerland, 6Advanced Clinical Imaging Technology, Siemens Healthcare, Lausanne, Switzerland, 7Siemens Healthcare, MR Application Development, Erlangen, Germany, 8Department of Diagnostic, Interventional and Pediatric Radiology, Bern University Hospital (Inselspital), Bern, Switzerland, 9Translational Imaging Center, sitem-insel, Bern, Switzerland
Synopsis
Free-running cardiac DIXON-MRI has potential for T2*/PDFF
quantification to explore cardiac fat accumulation and alteration in metabolic
diseases. DIXON at 3T suffers from rapid fat-water phase
accrual and inhomogeneous B0. Consequently, bipolar echoes, as opposed to monopolar,
are required to achieve equal/shorter than in-phase/out-of-phase echo spacing. However,
distortions occur between even and odd echoes due to gradients imperfections. Thus,
the existing framework was extended with a k-space trajectory correction based
on gradient impulse response function(GIRF). Both monopolar or bipolar echoes without GIRF
correction resulted in fat-water swaps and unreliable quantitative maps, that
were resolved using GIRF-corrected bipolar free-running DIXON.
Background
There is a
growing interest in probing cardiac fat which has been shown to influence pathophysiological
pathways towards cardiovascular degradation in metabolic diseases1. Chemical shift-encoded
(CSE) MRI enables high resolution mapping of proton density fat-fraction
(PDFF), non-invasive biomarker of fatty depots2 as well as the
quantification of T2* decay, which could further probe iron overload and
haemorrhage. Nevertheless, CSE-MRI or DIXON-MRI, while benefiting from
increased field-strength at 3T, remains challenging due to rapid phase accrual between water
and fat concomitant with inhomogeneous B03 in the heart. The free-running framework is a
novel approach for high-resolution cardiac imaging with fully respiratory and
cardiac self-gating, combined with a multidimensional Compressed Sensing
reconstruction4. We hypothesized that the free-running framework lays ground for high-resolution
cardiac DIXON-MRI at 3T. Only bipolar multi-echoes achieve short-enough
echo spacing at 3T but suffer from distortions between odd and even echoes due
to gradient imperfections. Thus, free-running DIXON was extended with k-space
trajectory correction using gradient impulse response function (GIRF), which enabled
high-resolution cardiac DIXON at 3T.
Methods
A custom-written prototype 3D radial spoiled gradient echo sequence was
implemented with multiple echoes and a phyllotaxis trajectory for integration
with the free-running framework4. Data were acquired on a 3T scanner (Vida, Siemens) with the spine coil
and an 18-channel body coil.
With a TR of 15ms, which is sufficient to quantify fatty acid
composition (FAC) parameters5 and T2* decay, 13 echoes (TE1/ΔTE = 1.12/1.07ms) in bipolar mode and 8 echoes
(TE1/ΔTE = 1.16/1.96ms) in monopolar mode were obtained. For a ten minutes acquisition, 40014 radial
views per echo (13 segments, 3078 Shots) were acquired with FOV=220mm at isotropic
1.5mm resolution, FA=5°, BW=1510 Hz/px for all echoes.
The system-specific Gradient system Impulse Response Function (GIRF) was measured using the 2-offcentered slices
method on a spherical phantom at isocenter6,7. The gradients (Fig1) were corrected using multiplication in the frequency domain between
the GIRF and the DIXON free-running gradients waveforms, and provided
the actual k-space trajectory.
Cardiac and respiratory motion signals were extracted from the first
echo of the superior-inferior projections4. Data were binned in 4 respiratory phases and 100ms-wide cardiac phases.
The 6D binned k-space data were reconstructed using the free-running compressed
sensing framework4. Based on 3D radial Nyquist criteria, individual free-running DIXON data
were accelerated by a factor R=26 for 8 cardiac phases and 4 respiratory state.
Complex images from each bin were processed for fat-water separation
using Iterative Decomposition of water and fat with Echo Asymmetry and Least
square Estimation (IDEAL) method with constrained extension8. Performances of the proposed
correction were evaluated on a phantom, on in vivo images and quantitative maps
(PDFF, R2*).Results
The GIRF correction revealed subtle
oscillations on gradient waveforms and roughly a shift of one sampled point in
k-space trajectory on even echoes(Fig1). Thus, strong radial artifacts appeared
between odd and even echoes images that were resolved with GIRF correction(Fig2).
Odd echoes were not impacted thanks to a sequence-level calibration for the 1st
echo and balanced errors between odd and even gradients.
At 3T, despite a high bandwidth and modest matrix
size, monopolar echoes were unable to reach an echo spacing shorter than the
required in-phase/out-of-phase 1.24ms delay (black markers in Fig. 3). Only
bipolar echoes achieved short-enough echo spacing (ΔTE=1.07ms). Additionally,
within TR=15ms, 13 bipolar echoes were acquired against 8 monopolar echoes only(Fig3).
Without GIRF correction, fat/water images were incorrectly
reconstructed (Fig4) with blurring at the apex and around the atria and massive
swaps between fat and water. On the contrary, GIRF corrected images were sharper
and fat/water swaps were not observed.
Whether in monopolar or in bipolar mode without
correction, PDFF and T2* maps were highly overestimated across the cardiac and
respiratory cycles (Fig5). In end-diastolic images, mean PDFF in the heart was
36%, 11% and more realistically 2% for monopolar mode, bipolar without correction
and for GIRF corrected bipolar respectively. This overestimation of fat was visible
at all motion states. Similarly, recurrent underestimations were observed in
R2* maps.Discussion
Aiming for high-resolution cardiac fat and water imaging, free-running
cardiac DIXON proved to require bipolar echoes at 3T. However, gradient
imperfections hampering the demanding high gradient throughput, a correction
with the system-specific GIRF was required to prevent radial-trajectory image
artifacts. Eventually, GIRF-corrected free-running provided fat/water
swaps-free motion-resolved volumes, paired with PDFF and T2* maps. Of note, quantitative
PDFF and T2* maps were also corrupted using a graph-cut algorithm9, confirming the image quality
were the culprit.
Providing full cardiac and respiratory cycles to
evaluate cardiac fat in metabolic diseases offers multiple benefits: 1/ to
study epicardial fat, systole is preferred when pericardium is thicker, 2/ B0 inhomogeneity
tends to be reduced during expiration, limiting local signal loss and phase accumulation
and 3/ variations of R2* along the cardiac cycle in the myocardium but also between
right and left ventricular blood pools hold interest to probe cardio-respiratory
status. Further investigation leveraging the 13 echoes could provide valuable
FAC characterization.Conclusion
This study aims at providing free-running
cardiac DIXON-MRI at 3T to enable high resolution PDFF and T2* mapping along
the cardiac and respiratory cycle to reliably study cardiac fat in metabolic
diseases.Acknowledgements
This project has received
financial support from the CNRS through a MITI program and was performed within
a laboratory member of France Life Imaging network. (grant
ANR-11-INBS-0006)References
1. Gaborit, B., Sengenes, C., Ancel, P., Jacquier, A. &
Dutour, A. Role of Epicardial Adipose Tissue in Health and Disease: A Matter of
Fat? in Comprehensive Physiology (ed. Terjung, R.) 1051–1082 (John Wiley
& Sons, Inc., 2017). doi:10.1002/cphy.c160034.
2. Reeder, S. B., Hu, H.
H. & Sirlin, C. B. Proton density fat-fraction: A standardized mr-based
biomarker of tissue fat concentration. J. Magn. Reson. Imaging 36,
1011–1014 (2012).
3. Rajiah, P. &
Bolen, M. A. Cardiovascular MR Imaging at 3 T: Opportunities, Challenges, and
Solutions. RadioGraphics 34, 1612–1635 (2014).
4. Di Sopra, L.,
Piccini, D., Coppo, S., Stuber, M. & Yerly, J. An automated approach to
fully self‐gated free‐running cardiac and respiratory motion‐resolved 5D
whole‐heart MRI. Magn Reson Med 82, 2118–2132 (2019).
5. Schneider, M. et
al. Accurate fatty acid composition estimation of adipose tissue in the
abdomen based on bipolar multi‐echo MRI. Magn. Reson. Med. 81,
2330–2346 (2019).
6. Campbell-Washburn, A.
E., Xue, H., Lederman, R. J., Faranesh, A. Z. & Hansen, M. S. Real-time
distortion correction of spiral and echo planar images using the gradient
system impulse response function: Real-Time Distortion Correction Framework for
Fast Imaging. Magn. Reson. Med. 75, 2278–2285 (2016).
7. Berzl,M.,Pfeuffer,J.
et al. Improved spiral trajectory correction using the gradient impulse
response function (GIRF). ISMRM 2017,933.
8. Bydder, M. et al.
Constraints in estimating the proton density fat fraction. Magnetic
Resonance Imaging 66, 1–8 (2020).
9. Andersson, J.,
Ahlström, H. & Kullberg, J. Water-fat separation incorporating spatial
smoothing is robust to noise. Magnetic Resonance Imaging 50,
78–83 (2018).