Ozkan Doganay1,2, Tahreema N. Matin2, Brian Burns1,2, Rolf F. Schulte3, Fergus V. Gleeson1,2, and Daniel Bulte1,2
1Department of Oncology, University Of Oxford, OXFORD, United Kingdom, 2Department of Radiology, The Churchill Hospital, OXFORD, United Kingdom, 3General Electric Global Research, Munich, Germany
Synopsis
We implemented a spiral k-space sampling
approach for Dynamic hyperpolarized 129Xe Ventilation Imaging (DXeVI) of human lungs. The gas-inflow effect, susceptibility artifacts, spatial and temporal resolutions for capturing Gas Flow Patterns (GFPs) were quantified in the gas-flow phantom and compared
to corresponding simulated GFPs. DXeVI of GFPs are shown to be sensitive to small gas flow changes
between the anterior and posterior lung regions in healthy three subject. This
technique can potentially be used to detect and quantify ventilation
defects associated with early stage COPD or asthma to assess disease severity,
response to treatments and to identify disease progression.
Introduction:
The
purpose of this study was to develop and optimize a rapid Dynamic
hyperpolarized 129Xe Ventilation Imaging (DXeVI) technique using an
interleaved-spiral k-space sampling strategy. We aimed to investigate the feasibility
of capturing pulmonary Gas-Flow Patterns (GFPs) using DXeVIs during a ~3s Inhalation
Period (IP), ~5s Breath-Hold (BH), and ~3s Exhalation Period (EP). Static
ventilation imaging acquired during a BH interval with Hyperpolarized (HP) 129Xe-MRI
typically demonstrates homogeneous signal intensity throughout healthy lungs. Regions
of absent or relatively low signal are known as “ventilation defects” and
correspond to obstructed airflow1, 2. Previously, Dynamic Ventilation Imaging (DVI)
with HP 3He-MRI was reported to be sensitive to regional GFPs in
patients with lung disease including severe asthma, emphysema and cystic
fibrosis3. In this work, DVI with HP 129Xe-MRI
is presented using a rapid k-space sampling strategy to capture GFPs during a complete breath cycle.Theory:
Quantitative analysis of DVI GFPs was carried out by modelling
the loss of HP 129Xe magnetization as a function of RF pulses4 and finite element method modelling of 129Xe gas concentration cXe(r,t), solving the
Navier Stokes, diffusion and convection equations5. A simulation geometry was built
using similar dimensions to the gas-flow phantom geometry shown in Fig. 1(a). Simulated
GFPs were then calculated from H1 to H5. Methods:
The gas-inflow effect,
susceptibility artifacts, spatial, and temporal resolutions for capturing GFPs
were quantified in the gas-flow phantom (Fig. 1(a)) and compared to corresponding simulated GFPs. MRI was acquired using a GE 1.5T system, a
flexible vest-shaped transmit-receive RF coil, and nuclear enriched 129Xe
gas polarized to ~10%. DXeVI using the gas-flow phantom was acquired for a varying number of
interleaves (Nint=1, 2, 4, 8) on three healthy volunteers using:
(i) Nint=2 with the following parameters: FOV: 30×30 cm, matrix
size: 28×28, flip angle: 10o, slices: 13, slice thickness: 15 mm,
temporal resolution: 0.6 s/volume image; (ii) Nint=8 with the
following parameters: FOV: 30×30 cm, matrix size: 52×52, flip angle: 10o,
slices: 13, slice thickness: 15 mm, temporal resolution: 2.4 s/volume image.Results:
The change in simulated cXe(r,t) through the gas-flow phantom is shown in Fig.
1(a) 2s after the gas entered the inlet. As expected, the simulated and MR signal depends on the gas arrival time
to each ROI, H1 to H5. This is confirmed by comparing simulated GFPs to the
experimental GFPs in Fig 1(b). The Full Width at Half Maximum (FWHM) of the line
profiles in Fig. 1(b) corresponds to the spatial resolution and the average FWHM of
all peaks from H1 to H5 are measured to be 10.0±2.5 mm, 6.8±0.6 mm, 6.1±0.6
mm, and 5.5±0.5 mm for Nint=1, 2, 4, 8,
respectively. Representative coronal DXeVI for Nint=2 and slices 2
(anterior) and 6 (center) during the BH are averaged and shown in Fig. 2(a) and
(b). The corresponding GFPs from ROI-L and ROI-R (Fig. 2(a)) are shown in (c)
and (d). Spearman's correlations between two closely
spaced ROIs, ROI-L in
slices 2 and 3, were 0.99, 0.99, and 0.98; two distant ROIs, ROI-R in slice 2 and 6, were 0.90,
0.95, and 0.94 in three healthy subjects. Fig. 3(a) and (b) show Nint=8 images from the
same subject with higher spatial resolution than in Fig. 2(a) and (b) for Nint=2.Discussion:
The tradeoff between spatial and temporal
resolution, including the dependency on the number of interleaves was analyzed
using a flow-phantom. Although the highest temporal resolution per volume
image (0.3s) was achieved with Nint=1, the FWHM was larger by a
factor of two compared to Nint=8 due to susceptibility and T2*
blurring artifacts. The temporal resolution of Nint=2 (0.6s)
was four times better than Nint=8, allowing for detection
of GFPs during relatively short IP and EP intervals although images are of lower spatial resolution. This study has shown that regional GFPs are successfully detected using DXeVI in healthy volunteers. GFPs
correlate well when closely spaced ROIs were selected, e.g. Slices 2
and 3. GFPs from distant ROIs, e.g. ROI-L in slice 2 and ROI-R in slice 6,
correlate less well, confirming sensitivity of the technique to small changes in
ventilation from anterior to central region of healthy lungs.Conclusions:
DXeVI has potential clinical application in
obstructive lung disease where GFPs may be used to detect early stage disease with higher sensitivity than static imaging3. Furthermore
in patients with COPD or asthma, GFPs may indicate collateral ventilation associated
with ventilation defects. DXeVI may therefore present a unique non-invasive
method to help determine patient suitability and monitor efficacy of regional
treatments, for example lung volume reduction and airway bypass treatments.Acknowledgements
The authors thank Anthony McIntyre, Jennifer Lee, and Kenneth Jacop for practical assistance with HP 129Xe gas production and MR scans. References
1. G. Parraga, et al. Hyperpolarized He-3 ventilation defects and apparent diffusion
coefficients in chronic obstructive pulmonary disease - Preliminary results at
3.0 Tesla. Investigative Radiology 2007;42:384-391.
2. N.J. Stewart, et al. Feasibility of human lung ventilation imaging using highly polarized
naturally abundant xenon and optimized three-dimensional steady-state free
precession. Magnet Reson Med. 2015;74:346-352.
3. M. Salerno, et al. Dynamic
spiral MRI of pulmonary gas flow using hyperpolarized He-3: Preliminary studies
in healthy and diseased lungs. Magnet Reson Med. 2001;46:667-677.
4. H.E. Moller, et al. Signal
dynamics in magnetic resonance imaging of the lung with hyperpolarized noble
gases. Journal of Magnetic Resonance. 1998;135:133-143.
5. L. de Rochefort, et al. In vitro validation of computational fluid dynamic simulation in human
proximal airways with hyperpolarized 3He magnetic resonance phase-contrast
velocimetry. J Appl Physiol. 2007;102:2012-2023.