Hyeonha Kim1, Seokwon Lee2, Jinil Park3, and Jang-Yeon Park1,2
1Department of Intelligent Precision Healthcare Convergence, Sungkyunkwan University, Suwan, Korea, Republic of, 2Department of Biomedical Engineering, Sungkyunkwan University, Suwan, Korea, Republic of, 3Biomedical Institute for Convergence at SKKU, Sungkyunkwan University, Suwon, Korea, Republic of
Synopsis
Lung MRI is getting more interest as an alternative to CT
because of no radiation exposure and expands its role of providing structural
information to functional information such as ventilation and perfusion. In
terms of 3D functional imaging, 3D ventilation mapping was already proposed,
but few studies have been done on 3D perfusion mapping. Here, we propose a 3D
pulmonary perfusion map using 3D UTE-MRI with retrospective respiratory and
cardiac gating. The proposed method provides high-resolution 3D regional
perfusion information of the lungs and will be useful for diagnosing diffusive
lung diseases along with ventilation map (e.g., V/Q ratio).
Introduction
MRI is emerging in lung diagnosis as an
alternative to CT due to its lack of exposure to ionizing radiation and good
soft-tissue contrast1, 2. MRI is also expanding its diagnostic role of providing structural
information of the lungs to functional information such as ventilation and
perfusion. Recently, a
2D ventilation and perfusion map acquisition method called
PREFUL (Phase-resolved functional lung) MRI has been proposed that does not require
breath hold as well as contrast agents3. However, while 3D ventilation mapping was proposed using 3D PREFUL-MRI4 and 3D ultrashort echo-time MRI (UTE-MRI)5, 6, but few studies have been done on 3D perfusion mapping. Here, we propose
a non-contrast-enhanced 3D pulmonary perfusion map using 3D UTE-MRI with
retrospective respiratory and cardiac gating. It was demonstrated by healthy
human lung imaging and compared with 2D PREFUL perfusion mapping. Methods
Experiments: This study was approved by
the Institutional Review Board of Sungkyunkwan University (2019-02-008). Experiments
were performed at Siemens 3T (Prisma) using a 26-channel reception coil. A
volume-selective 3D UTE sequence (VS-UTE) was used with fat suppression7. Scan
parameters were: TR/TE = 3.3/0.12ms, FOV = 360mm, number of projections = 150k,
matrix size = 440×440×440, isotropic resolution = 0.8mm. Two flip angles
(FA), 5°
and 2° were used to test whether more
proton-density weighting with a smaller flip angle is better for perfusion
sensitivity. PREFUL-MRI were performed using a 2D spoiled GRE sequence over a
temporal resolution of 650ms with the following scan parameters: TR/TE =
3.4/1.52ms, FOV = 360×360
mm2, matrix size = 192×192, slice
thickness = 15mm, FA = 5°, bandwidth =1530 Hz/px, and parallel imaging with acceleration factor of two.
Cardiac
phase-resolved images:
As a first step to creating a perfusion map, cardiac phase-resolved images were
acquired via retrospective respiratory and cardiac gating. Respiratory signals with
cardiac signals were acquired from self-navigating echoes (Fig.1A)8, 9 and cardiac
signals were extracted by bandpass filtering in the range of 0.8-1.5Hz (Fig.1B)10. Then, eight cardiac phase-resolved lung images
were reconstructed at the same end-expiration respiratory phase (Fig.1D). The
number of projections used for each cardiac-phase image reconstruction was set equal
to 15k.
Perfusion map: To obtain a perfusion map, a difference image was
first created by subtracting the minimum value from the maximum value of the voxel
in eight cardiac phase-resolved lung images after image registration. Then, the
perfusion map was calculated by dividing the difference image by the aorta value
of the pulmonary trunk that is assumed to be filled with full blood (100%) to represent the percentage of
blood filled in each voxel.Results
Figure 1D shows
the eight lung images with different cardiac phases reconstructed from 3D UTE-MRI
data. Despite under-sampled reconstruction via retrospective respiratory and
cardiac gating, they not only clearly show cardiac motions, including systolic
and diastolic, during the cardiac cycle, but also provide good image quality
sufficient for perfusion analysis, minimizing motion artifacts.
Figure 2 shows
the results of comparing the perfusion sensitivity under FA = 5° and 2° conditions. The difference between the maximum and
minimum mean intensity of the pulmonary artery was higher at FA = 2° (Δ=0.036;
7.03% in percent change) than at FA = 5° (Δ=0.023;
5.62% in percent change).
Figure 3 shows regional
perfusion maps from some representative slices of the proposed 3D UTE-MRI
perfusion map. As expected, the aorta and large vessels showed higher signal
intensities, and the lung parenchyma showed low but clear signal intensities.
Figure 4 shows
the 3D-UTE-MRI perfusion map versus the 2D PREFUL-MRI perfusion map obtained from the
same healthy subject. For a fair comparison with the 2D PREFUL perfusion map, a
MIP (maximum intensity projection) image was calculated to obtain the 3D-UTE-MRI
perfusion map with the same slice thickness (=15mm) as the 2D PREFUL perfusion map.
Although both show similar distributions of signal intensities, especially
around the large vessel areas including the aorta, the 3D-UTE-MRI perfusion map
shows a broader and more detailed distribution may be due to the advantage of 3D
perfusion mapping.Discussion and Conclusion
In this study, we proposed a novel 3D perfusion map of the lungs using
3D UTE-MRI that does not require breath hold as well as contrast agents. The
proposed 3D perfusion map is expected to provide 3D high resolution regional perfusion
information of the lungs and will be particularly useful for diagnosing diffusive
lung diseases such as COPD, Asthma, and interstitial lung disease (ILD). It can
also be used to provide a 3D ventilation/perfusion (V/Q) ratio map from the
same 3D UTE-MRI data along with the already proposed 3D ventilation map. At
this stage, this study has a couple of limitations: First, in addition to the 2D
PREFUL-MRI perfusion map used here, a more direct 3D lung perfusion mapping,
e.g., using 3D DCE-MRI and SPECT, is needed for further validation of the
proposed method. Second, because only healthy volunteers were considered in
this study, a large cohort of lung patients is needed to test the clinical utility
of the proposed method. Acknowledgements
This work was supported by the National Research Foundation of Korea
(NRF) grant funded by the Korea government (MSIT): NRF-2020R1A2B5B02002676 and NRF-2021R1A4A5032806.References
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