Cystic Fibrosis Clinical Trial
Official title:
Hyperpolarised 129Xe MRI for Non-invasive Assessment of Ventilation, Perfusion and the Alveolar Membrane - a Physiological Study in Healthy Volunteers & Cystic Fibrosis Patients
Chronic lung diseases show a gradual onset of irreversible lung damage which can lead to severe breathing problems and/or respiratory failure. Imaging is central to guiding treatment; however, current techniques are either inaccurate or involve exposure to radiation. Recent developments in lung magnetic resonance imaging (MRI) provide promise as a radiation-free alternative. However, conventional MRI cannot directly show changes in distribution of inhaled air or absorption of gas which are important signs of early lung disease. Recently MRI imaging of the inhaled gas contrast agent Xenon has been developed which can provide this important information. This study aims to determine how Xenon MRI can help determine air flow distribution and gas uptake in the lungs. The investigators will also be able to compare the information from patients with that from healthy volunteers. This should give insight into the processes involved in chronic lung diseases and help evaluate disease extent in patients.
Hyperpolarised gas MRI (3He and 129Xe) has enabled novel methods of in-vivo functional lung
imaging that do not rely on the use of ionising radiation. Hyperpolarised 129Xe (HP Xe) MRI
provides additional complementary information to 3He and 1H MRI and conventional lung imaging
modalities. By virtue of its solubility, the 129Xe contrast agent follows the gas exchange
pathways in the lungs, offering a direct means to explore regional ventilation-perfusion
(V/Q). The competing modality of nuclear medicine lung V/Q scans suffer from very poor
spatial resolution and a reliance on high doses of radiation via radio-nuclide inhalation.
Nuclear medicine is thus unsuitable for studies of basic physiology in healthy volunteers or
in longitudinal studies in lung disease patients.
The aims and objectives of this study are:
1. To assess the physiological differences in lung ventilation between the normal group
(volunteers) and the cystic fibrosis disease group
2. To evaluate differences in Xe diffusion across the alveolar membrane between the normal
group (volunteers) and the cystic fibrosis disease group
3. To understand the relationship between the extent of abnormal ventilation (and
ventilation-perfusion mismatch) on MRI and the results from conventional physiological
evaluation of lung function using pulmonary function tests (spirometry and gas exchange)
4. To understand the relationship between gas exchange as determined by HP Xe imaging with
the extent of ventilation perfusion mismatch on standard perfusion MRI
This is a physiological cross-sectional feasibility study comparing regional lung ventilation
and diffusion across the alveolar membrane in normal volunteers and cystic fibrosis. 15
healthy volunteers and 15 cystic fibrosis patients will be recruited. All imaging will take
place at Papworth Hospital.
Phase I: Volunteer study (n=15, aged 18-70)
Hyperpolarised 129Xe MRI scans will be performed in the MRI department at Papworth Hospital,
using a Siemens Avanto 1.5 Tesla system with 129Xe capability using a dedicated
transmit-receive RF coil.
Phase II: CF study (n=15, aged 18-70)
Patients already enrolled in the study 'Pulmonary magnetic resonance imaging in cystic
fibrosis: accuracy and reproducibility' (REC reference: 13/EE/0401; IRAS project ID: 73137)
will be invited to take part in this study too.
These patients, with CF in stable phase, will be evaluated with same day conventional MRI,
lung function tests and clinical scoring. The methodology of 129Xe MRI will be as described
above for healthy volunteers.
Morphological imaging: A combination of T1 and T2 weighted sequences will be used.
Hyperpolarized 129Xe MR imaging: For each subject, up to two deliveries of ≤ 1L doses of
hyperpolarised xenon will take place as follows:-
1. 129Xe ventilation imaging will provide further information on assessment of lung
ventilation volume using a volumetric gradient echo sequence.
2. Chemical shift saturation recovery (CSSR) spectroscopy with dissolved xenon will provide
an estimation of the fraction of 129Xe in tissue/interstitium and in red blood cells.
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