Christian Anderson1, Charlie Wang1, Yuning Gu1, Mark Griswold1,2, Xin Yu1,2,3, and Chris Flask1,2,4
1Biomedical Engineering, Case Western Reserve University, Cleveland, OH, United States, 2Radiology, University Hospitals Cleveland Medical Center, Cleveland, OH, United States, 3Physiology and Biophysics, Case Western Reserve University, Cleveland, OH, United States, 4Pediatrics, University Hospitals Cleveland Medical Center, Cleveland, OH, United States
Synopsis
Preclinical quantitative MRI is susceptible to the motion
artifacts caused by the rapid respiratory motion and high heart rates present in small
animals. This can be alleviated through the use of gating/triggering but these
are difficult to implement in magnetic resonance fingerprinting due to the need
for dynamic, coherent signal evolutions. We propose a method for an
incremented phase encoding MRF acquisition that enhances motion
suppression in Cartesian MRF. This phase incremented strategy distributes
motion artifacts throughout the acquisition creating incoherent artifacts
allowing the MRF method to “see through” the artifacts and produce artifact
free T1 and T2 maps.
Purpose
The
presence of motion artifacts is of significant concern for preclinical MRI due
to the lack of breathholds and rapid breathing and heart rates in animal models. These
motion artifacts are typically limited with respiratory and/or cardiac gating1.
Unfortunately, gating in MRF is challenging as MRF requires dynamic, coherent
signal acquisitions. Prior preclinical studies have shown that Cartesian MRF
exhibits some inherent resistance to respiratory motion artifacts. However, these in vivo studies have also shown that Cartesian MRF is still subject
to major pulsatility artifacts as well as residual respiratory motion artifacts2.
In this study, we propose to implement a Cartesian MRF acquisition with
incremented phase encoding3,4 during each dynamic MRF acquisition to
introduce an additional temporal incoherence in order to “dephase” the motion
and pulsatility artifacts.Methods
Two
fully-sampled Cartesian FISP MRF5 acquisitions were implemented on a high field
(7T) Bruker small animal MRI scanner. The first acquisition was a standard Cartesian MRF implementation with a
constant phase encoding for each image of the 1024 images in the dynamic MRF
scan as described previously2. The second scan, termed Regularly Incremented
Phase Encoding MRF (RIPE-MRF), incorporated a time-varying incremented phase
encoding step across all of the 1024 images. These are visually demonstrated in
Figure 1. The repetition time (9.5-12
ms) and flip angle (0-70 degrees) profiles were the same for both MRF
acquisitions and similar to previous MRF implementations6.
We first obtained in vitro phantom MRF results to ensure the consistency
between the two MRF methods. We
then obtained in vivo MRF data of
mouse kidneys to qualitatively compare the motion artifact sensitivity for both
the standard Cartesian MRF and RIPE-MRF methods. The MRF data were acquired for
the same imaging slice and with no respiratory or cardiac gating. All MRF datasets
were matched on a pixel-by-pixel basis using the same MRF dictionary to
generate T1 and T2 maps.Results
The
in vitro MRF results from the standard Cartesian MRF and RIPE-MRF techniques
are shown in Figures 2 and 3. These two MRF methodologies generated similar T1 and T2
maps (Figure 2) with consistent T1 and T2 values between RIPE-MRF and standard Cartesian
MRF (Figure 3). In vivo MRF results for
the two MRF methods are shown in Figures 4 and 5. Composite MRF images were calculated by
performing a complex sum of the 1024 images for each MRF acquisition (Figure 4).
Interestingly, the composite image from the RIPE-MRF acquisition shows
significantly reduced artifact in comparison to the composite image from the
standard Cartesian MRF acquisition. From ROI analysis the artifact-to-noise
ratio in the composite images from standard Cartesian MRF was measured to be 12.758
and for the RIPE-MRF composite image the artifact-to-noise ratio was 1.620.
Similar reduction in motion and pulsatility artifact were observed in the in
vivo T1 and T2 maps (Figure 5).Discussion
In
this study, we have shown that incorporation of incremental phase encoding
during the dynamic MRF scan (RIPE-MRF) results in temporal incoherence of the
pulsatility and motion artifacts. By
incrementing the phase encoding lines of k-space, RIPE-MRF distributes the occurrence
of any motion artifacts and any variation in physiological state over the
entire acquisition rather than a single line of k-space. This temporal
incoherence resulted in a significant reduction in the level of artifact in both
the composite images (Figure 4) as well as the corresponding T1 and T2 maps
(Figure 5). In vitro results suggest that this reduction in motion/pulsatility
artifact does not significantly impact the accuracy of the T1 and T2 estimates
(Figures 2 and 3).Conclusion
The
proposed RIPE-MRF technique offers the opportunity to improve the quality of Cartesian
MRF results for imaging applications where motion and cardiac pulsatility are
problematic. The RIPE-MRF technique
allows Cartesian MRF acquisitions to be implemented without respiratory or
cardiac gating allowing for a more rapid acquisition with reduced complexity
and post-processing.Acknowledgements
NIH T32EB007509, NIH TL1TR000441, NHLBI R21 HL130839, Cystic Fibrosis FoundationReferences
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