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Updated: Jan 28, 2026

Author Spotlight: Standardization and Best Practices for Advancing Lung Imaging Using 129Xe MRI
Published on: November 21, 2023
Xenon-129 MRI detects ventilation deficits in paediatric stem cell transplant patients unable to perform spirometry
Laura L Walkup1,2,3, Kasiani Myers2,4, Javier El-Bietar2,4,5
1Center for Pulmonary Imaging Research, Division of Pulmonary Medicine and Dept of Radiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Insights
Hyperpolarized xenon-129 MRI detects lung ventilation deficits in pediatric HSCT patients, even those with normal spirometry. This advanced imaging method identifies early pulmonary abnormalities missed by standard lung function tests.
Area of Science:
- Medical Imaging
- Pulmonology
- Pediatric Hematology/Oncology
Background:
- Early detection of lung problems after stem cell transplants is difficult.
- Spirometry is often insensitive to early changes and challenging for children.
- Hyperpolarized 129Xe MRI offers a new approach to assess lung ventilation.
Purpose of the Study:
- To quantify regional lung ventilation abnormalities in pediatric HSCT patients using 129Xe MRI.
- To compare the sensitivity of 129Xe MRI to standard spirometry in this population.
- To evaluate 129Xe MRI's utility in detecting pulmonary changes in children unable to perform spirometry.
Main Methods:
- Paediatric allogeneic HSCT patients (n=23, ages 6-16) underwent 129Xe MRI.
- Regional ventilation was quantified using a breath-hold technique.
- Ventilation defect percentage (VDP) was compared to spirometry metrics (FEV1, FEV1/FVC, FEF25-75%).
Main Results:
- 129Xe MRI revealed a mean VDP of 10.5±9.4%.
- VDP correlated significantly with spirometry measures (p≤0.02).
- Ventilation deficits were found in patients with normal spirometry and in those unable to perform the test.
Conclusions:
- 129Xe MRI effectively detects lung ventilation deficits in pediatric HSCT patients.
- This imaging technique identifies abnormalities missed by spirometry, especially in non-compliant children.
- 129Xe MRI provides a valuable tool for assessing pulmonary involvement in this pediatric population.
Background:
Early detection of pulmonary morbidity following haematopoietic stem cell transplantation (HSCT) remains an important challenge for intervention, primarily due to the insensitivity of spirometry to early change, and in paediatrics, patient compliance provides additional challenges. Regional lung ventilation abnormalities in paediatric HSCT patients were quantified using hyperpolarised xenon-129 (129Xe) magnetic resonance imaging (MRI) and compared to spirometry.
Methods:
Medically stable, paediatric allogeneic HSCT patients (n=23, ages 6-16 years) underwent an outpatient MRI scan where regional ventilation was quantified with a breath-hold of hyperpolarised 129Xe gas. Ventilation deficits, regions of the lung that ventilate poorly due to obstruction, were quantified as a ventilation defect percentage (VDP) and compared to forced expiratory volume in 1 s (FEV1), FEV1/forced vital capacity (FVC) ratio, and forced expiratory flow at 25-75% of FVC (FEF25-75%) from spirometry using linear regression.
Results:
The mean±sd 129Xe VDP was 10.5±9.4% (range 2.6-41.4%). 129Xe VDP correlated with FEV1, FEV1/FVC ratio and FEF25-75% (p≤0.02 for all comparisons). Ventilation deficits were detected in patients with normal spirometry (i.e. FEV1 >80%), supporting the sensitivity of 129Xe MRI to early obstruction reported in other pulmonary conditions. Seven (30%) patients could not perform spirometry, yet ventilation deficits were observed in five of these patients, detecting abnormalities that otherwise may have gone undetected and untreated until advanced.
Conclusion:
Lung ventilation deficits were detected using hyperpolarised 129Xe gas MRI in asymptomatic paediatric HSCT patients and in a subgroup who were unable to perform reliable spirometry. 129Xe MRI provides a reliable imaging-based assessment of pulmonary involvement in this potentially difficult to diagnose paediatric population.
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