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BackgroundMRI with xenon‐129 gas (Xe MRI) can assess airflow obstruction and heterogeneity in lung diseases. Specifically, Xe MRI may represent a sensitive modality for future therapeutic trials of cystic fibrosis (CF) therapies. The reproducibility of Xe MRI has not yet been assessed in the context of a multi‐site study.PurposeTo determine the same‐day repeatability and 28‐day reproducibility of Xe MRI in children with CF.Study TypeFour‐center prospective, longitudinal.PopulationThirty‐eight children (18 females, 47%), median interquartile range (IQR) age 12 (9–14) years old, with mild CF (forced expiratory volume in 1 second (FEV1) ≥85% predicted).Field Strength/Sequence3‐T, two‐dimensional (2D) gradient‐echo (GRE) sequence.AssessmentXe MRI, FEV1, and nitrogen multiple‐breath wash‐out for lung‐clearance index (LCI2.5) were performed. To assess same‐day reproducibility, Xe MRI was performed twice within the first visit, and procedures were repeated at 28 days. Xe hypoventilation was quantified using ventilation‐defect percentage (VDP) and reader‐defect volume (RDV). For VDP, hypoventilated voxels from segmented images were identified using a threshold of <60% mean whole‐lung signal and expressed as a percentage of the lung volume. For RDV, hypoventilation was identified by two trained readers and expressed as a percentage.Statistical TestsInter‐site comparisons were conducted using Kruskal–Wallis nonparametric tests with Dunn's multiple‐comparisons tests. Differences for individuals were assessed using Wilcoxon matched‐pairs tests. Bland–Altman tests were used to evaluate same‐day repeatability, 28‐day reproducibility, and inter‐reader agreement. A P‐value ≤0.05 was considered significant.ResultsMedian FEV1 %‐predicted was 96.8% (86%–106%), and median LCI2.5 was 6.6 (6.3–7.4). Xe MRI had high same‐day reproducibility (mean VDP difference 0.12%, 95% limits of agreement [−3.2, 3.4]; mean RDV difference 0.42% [−2.5, 3.3]). At 28 days, 26/31 participants (84%) fell within the same‐day 95% limits of agreement.Data ConclusionXe MRI may offer excellent same‐day and short‐term reproducibility.Evidence Level2Technical EfficacyStage 2
BackgroundMRI with xenon‐129 gas (Xe MRI) can assess airflow obstruction and heterogeneity in lung diseases. Specifically, Xe MRI may represent a sensitive modality for future therapeutic trials of cystic fibrosis (CF) therapies. The reproducibility of Xe MRI has not yet been assessed in the context of a multi‐site study.PurposeTo determine the same‐day repeatability and 28‐day reproducibility of Xe MRI in children with CF.Study TypeFour‐center prospective, longitudinal.PopulationThirty‐eight children (18 females, 47%), median interquartile range (IQR) age 12 (9–14) years old, with mild CF (forced expiratory volume in 1 second (FEV1) ≥85% predicted).Field Strength/Sequence3‐T, two‐dimensional (2D) gradient‐echo (GRE) sequence.AssessmentXe MRI, FEV1, and nitrogen multiple‐breath wash‐out for lung‐clearance index (LCI2.5) were performed. To assess same‐day reproducibility, Xe MRI was performed twice within the first visit, and procedures were repeated at 28 days. Xe hypoventilation was quantified using ventilation‐defect percentage (VDP) and reader‐defect volume (RDV). For VDP, hypoventilated voxels from segmented images were identified using a threshold of <60% mean whole‐lung signal and expressed as a percentage of the lung volume. For RDV, hypoventilation was identified by two trained readers and expressed as a percentage.Statistical TestsInter‐site comparisons were conducted using Kruskal–Wallis nonparametric tests with Dunn's multiple‐comparisons tests. Differences for individuals were assessed using Wilcoxon matched‐pairs tests. Bland–Altman tests were used to evaluate same‐day repeatability, 28‐day reproducibility, and inter‐reader agreement. A P‐value ≤0.05 was considered significant.ResultsMedian FEV1 %‐predicted was 96.8% (86%–106%), and median LCI2.5 was 6.6 (6.3–7.4). Xe MRI had high same‐day reproducibility (mean VDP difference 0.12%, 95% limits of agreement [−3.2, 3.4]; mean RDV difference 0.42% [−2.5, 3.3]). At 28 days, 26/31 participants (84%) fell within the same‐day 95% limits of agreement.Data ConclusionXe MRI may offer excellent same‐day and short‐term reproducibility.Evidence Level2Technical EfficacyStage 2
Background Lung prefusion and ventilation under physiological conditions have not been evaluated and visualized before. We aim to analyse pulmonary perfusion and ventilation between tidal and deep breathing in healthy individuals and compared differences between sexes and age groups with Phase-Resolved Functional Lung Magnetic Resonance Imaging (PREFUL- MRI).Methods This prospective observational study included healthy volunteers from May 2023 to May 2024. All participants underwent PREFUL-MRI in the supine position during tidal and deep-slow breathing using a balanced steady-state free-precession sequence. Perfusion-and ventilation-related metrics on PREFUL-MRI were analysed with an automated quantitative pipeline and compared between tidal and deep breathing, sexes and age groups.Results Eighty-seven healthy participants (47 men, mean age: 38.6 ± 12.3 years) were enrolled. Mean perfusion (7.7% vs. 6.0%, p < 0.001) and ventilation defects (8.6% vs. 5.1%, p = 0.002) were decreased, and mean ventilation (15.8% vs. 48.3%, p < 0.001) and perfusion defects (1.9% vs 7.9%, p = 0.001) increased during deep breathing compared with those during tidal breathing. Twenty-eight participants had increased lung perfusion while the other 59 people had reduced perfusion during tidal breathing. During tidal breathing, men exhibited higher mean ventilation (20.2% vs. 14.2%, p = 0.002) and more ventilation defects (9.5% vs. 6.3%, p = 0.022)than did women. Perfusion defects decreased in participants aged ≥ 45 years compared with those aged < 45 years (1.6% vs. 2.6%, p = 0.029). Mean flow-volume loop correlations were similar between tidal and deep breathing, sexes and age groups (p > 0.05).Conclusion PREFUL-MRI enables visually analysing lung perfusion and ventilation, thus enhancing our understanding of the physiological characteristics and alterations of lung.
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