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Author Spotlight: Standardization and Best Practices for Advancing Lung Imaging Using 129Xe MRI
Published on: November 21, 2023
Hyperpolarised xenon-129 diffusion-weighted magnetic resonance imaging for assessing lung microstructure in
James A Eaden1,2, Nicholas D Weatherley1,2, Ho-Fung Chan1
1POLARIS, Department of Infection, Immunity and Cardiovascular Disease, University of Sheffield, Sheffield, UK.
Background:
Hyperpolarised 129-xenon (129Xe) magnetic resonance imaging (MRI) shows promise in monitoring the progression of idiopathic pulmonary fibrosis (IPF) due to the lack of ionising radiation and the ability to quantify functional impairment. Diffusion-weighted (DW)-MRI with hyperpolarised gases can provide information about lung microstructure. The aims were to compare 129Xe DW-MRI measurements with pulmonary function tests (PFTs), and to assess whether they can detect early signs of disease progression in patients with newly diagnosed IPF.
Methods:
This is a prospective, single-centre, observational imaging study of patients presenting with IPF to Northern General Hospital (Sheffield, UK). Hyperpolarised 129Xe DW-MRI was performed at 1.5 T on a whole-body General Electric HDx scanner and PFTs were performed on the same day as the MRI scan.
Results:
There was an increase in global 129Xe apparent diffusion coefficient (ADC) between the baseline and 12-month visits (mean 0.043 cm2·s-1, 95% CI 0.040-0.047 cm2·s-1 versus mean 0.045 cm2·s-1, 95% CI 0.040-0.049 cm2·s-1; p=0.044; n=20), with no significant change in PFTs over the same time period. There was also an increase in 129Xe ADC in the lower zone (p=0.027), and an increase in 129Xe mean acinar dimension in the lower zone (p=0.033) between the baseline and 12-month visits. 129Xe DW-MRI measurements correlated strongly with diffusing capacity of the lung for carbon monoxide (% predicted), transfer coefficient of the lung for carbon monoxide (KCO) and KCO (% predicted).
Conclusions:
129Xe DW-MRI measurements appear to be sensitive to early changes of microstructural disease that are consistent with progression in IPF at 12 months. As new drug treatments are developed, the ability to quantify subtle changes using 129Xe DW-MRI could be particularly valuable.
Insights
Hyperpolarized 129-xenon (129Xe) diffusion-weighted MRI detects early microstructural changes in idiopathic pulmonary fibrosis (IPF) progression within 12 months. This imaging technique shows promise for monitoring IPF, especially as new treatments emerge.
Area of Science:
- Pulmonary Medicine
- Radiology
- Medical Imaging
Background:
- Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease.
- Hyperpolarized 129-xenon (129Xe) MRI offers a non-ionizing method to assess lung microstructure and function.
- Diffusion-weighted (DW)-MRI with hyperpolarized gases can reveal insights into lung tissue changes.
Purpose of the Study:
- To compare 129Xe DW-MRI measurements with standard pulmonary function tests (PFTs) in IPF patients.
- To evaluate the ability of 129Xe DW-MRI to detect early signs of disease progression in newly diagnosed IPF.
- To assess the utility of 129Xe DW-MRI in monitoring IPF progression over 12 months.
Main Methods:
- A prospective, single-centre observational study involving patients with newly diagnosed IPF.
- Hyperpolarized 129Xe DW-MRI was performed at 1.5T.
- Pulmonary function tests (PFTs) were conducted concurrently with MRI scans.
Main Results:
- Global 129Xe apparent diffusion coefficient (ADC) significantly increased from baseline to 12 months (p=0.044).
- 129Xe ADC also increased in the lower lung zones (p=0.027), alongside an increased mean acinar dimension (p=0.033).
- 129Xe DW-MRI measurements showed strong correlations with diffusing capacity for carbon monoxide (DLCO) and transfer coefficient (KCO).
Conclusions:
- 129Xe DW-MRI measurements are sensitive to early microstructural disease progression in IPF at 12 months.
- The technique detected changes not evident in PFTs over the same period.
- Quantifying subtle changes with 129Xe DW-MRI may be valuable for monitoring IPF, especially with emerging therapies.
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