Expiratory lung MRI: a simple, sensitive method to quantify and visualise regional gas trapping in cystic fibrosis.

BACKGROUND

Computed tomography is the gold standard for visually assessing gas trapping, a hallmark of early lung disease in people with cystic fibrosis (pwCF), but its use is limited in children. Lung proton magnetic resonance imaging (¹H-MRI) offers a simple, non-ionising alternative. This work aimed to use breath-hold 1H-MRI to visualise and quantify gas trapping in pwCF.

METHODS

24 normal controls (9 adults, 15 children) and 27 pwCF underwent breath-hold 1H-MRI at residual volume (RV) and total lung capacity (TLC). For each participant, a threshold was defined from the TLC image and applied to the RV image to quantify low-signal areas, presumed to be gas trapping, as a gas trapping volume (GTV). An upper limit of normal (ULN) was defined based on the normal distribution of GTV, and GTV was compared to spirometry, body plethysmography, multiple breath washout and 129Xe Ventilation MRI.

RESULTS

Gas trapping was visualised in pwCF as regions of low signal intensity on RV images. Healthy volunteers had a median GTV of 2.93% (0.32-14.37%). PwCF had a GTV of 21.80% (2.04-82.68%) and FEV1 z-scores of -1.14 (-5.43, 2.17), with 14 having normal FEV1. The ULN of GTV was 7.01%; 9/14 pwCF with normal spirometry exceeded this. In pwCF, GTV is strongly correlated with FEV1 z-scores, 129Xe-MRI ventilation defect percentage, and gas trapping measured by body plethysmography (RV/TLC%).

CONCLUSIONS

Using a standard, easily implementable breath-hold 1H-MRI protocol, gas trapping in CF can be clearly visualised and quantified. Preliminary evidence shows lung function impairment in pwCF who have normal FEV1.