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Rapid single-breath hyperpolarized noble gas MRI-based biomarkers of airspace enlargement.

Authors :
Westcott A
Guo F
Parraga G
Ouriadov A
Source :
Journal of magnetic resonance imaging : JMRI [J Magn Reson Imaging] 2019 Jun; Vol. 49 (6), pp. 1713-1722. Date of Electronic Publication: 2018 Dec 21.
Publication Year :
2019

Abstract

Background: Multi-b diffusion-weighted hyperpolarized-gas MRI measures pulmonary airspace-enlargement using apparent diffusion coefficients (ADCs) and mean-linear-intercepts (L <subscript>m</subscript> ).<br />Purpose: To develop single-breath 3D multi-b diffusion-weighted <superscript>3</superscript> He and <superscript>129</superscript> Xe MRI using k-space undersampling. Rapid, cost-efficient, single-breath acquisitions may facilitate clinical translation.<br />Study Type: Prospective.<br />Subjects: We evaluated 12 participants, including nine subjects (mean age = 69 ± 9) who were included in the retrospective experiment and three chronic pulmonary obstruction disease (COPD) patients (mean age = 81 ± 6) who participated in the prospective study.<br />Field Strength: A whole-body 3 T 2D/3D fast gradient recall echo (FGRE) sequence.<br />Assessment: Hyperpolarized <superscript>3</superscript> He/ <superscript>129</superscript> Xe MRI, spirometry, plethysmography computed tomography (CT). We evaluated <superscript>129</superscript> Xe ADC/morphometry estimates by retrospectively undersampling previously acquired fully sampled multibreath, multi-b diffusion-weighted data. Next, we prospectively evaluated the feasibility of accelerated (AF = 7) <superscript>3</superscript> He MRI static-ventilation/T <subscript>2</subscript> * (extra short-TE, b = 0 image) and ADC/morphometry (five b-values) maps using a single gas-dose and 16-second breath-hold. To conservatively evaluate cost-improvement, we compared total costs of single vs. multiple <superscript>129</superscript> Xe doses.<br />Statistical Tests: Multivariate analysis of variance, independent t-tests and voxel-by-voxel basis difference test.<br />Results: For the retrospectively undersampled <superscript>129</superscript> Xe data, a nonsignificant mean difference for ADC/L <subscript>m</subscript> of 14%/12%, 12%/8%, and 11%/9% was observed (all, P > 0.4) between the fully sampled and accelerated data for the never-smoker, COPD, and alpha-1 antitrypsin deficiency (AATD) groups, respectively. The control never-smoker group had significantly lower ADC (P < 0.001) and L <subscript>m</subscript> (P < 0.001) than the COPD/AATD group for both fully sampled and accelerated data. For the prospectively acquired <superscript>3</superscript> He MRI data, static-ventilation, T <subscript>2</subscript> *, ADC, and morphometry maps were acquired using a single 16-second breath-hold scan and single gas dose. Accelerated imaging resulted in cost savings of ~$US 1000/patient, a conservative estimate based on <superscript>129</superscript> Xe MRI dose savings (single vs. five doses).<br />Data Conclusion: This is a proof-of-concept demonstration of accelerated (7×) morphometry that shows that less cost- and time-efficient multibreath methods that lead to variability and patient fatigue may be avoided in the future.<br />Level of Evidence: 2 Technical Efficacy: Stage 5 J. Magn. Reson. Imaging 2018.<br /> (© 2018 International Society for Magnetic Resonance in Medicine.)

Details

Language :
English
ISSN :
1522-2586
Volume :
49
Issue :
6
Database :
MEDLINE
Journal :
Journal of magnetic resonance imaging : JMRI
Publication Type :
Academic Journal
Accession number :
30578587
Full Text :
https://doi.org/10.1002/jmri.26574