RSNA 2011 

Abstract Archives of the RSNA, 2011


MSVP32-03

Comparison of Proton-MRI (MRI) and Contrast-enhanced MRI (CE-MRI) in Cystic Fibrosis (CF) to Detect Small Airways Disease

Scientific Formal (Paper) Presentations

Presented on November 29, 2011
Presented as part of MSVP32: Pediatric Radiology Series: Chest/Cardiovascular Imaging II

Participants

Pierluigi Ciet MD, Presenter: Nothing to Disclose
Piotr Alfred Wielopolski PhD, Abstract Co-Author: Nothing to Disclose
Sandra Lever, Abstract Co-Author: Nothing to Disclose
Els Van Der Wiel MD, Abstract Co-Author: Nothing to Disclose
Maarten H. Lequin MD, PhD, Abstract Co-Author: Nothing to Disclose
Harm Awm Tiddens MD, Abstract Co-Author: Nothing to Disclose
Giovanni Morana MD, Abstract Co-Author: Nothing to Disclose

PURPOSE

CF leads to early and chronic Lung structural changes. CT is the most sensitive technique to monitor CF-lung disease. Bronchiectasis(BE) and air-trapping (AT) are the most clinical relevant information that can be obtained. Unfortunately CT exposes the patient to radiation, so restricting its use. MRI is an attractive alternative to CT, but it has poorer spatial resolution for BE and AT. Hypo-perfusion (HP) is a clinical relevant alternative for AT since it identifies areas that do not contribute to gas exchange. Aims: 1) To compare the distribution/volume of HP on CE-MRI to AT on MRI: 2) To correlate distribution/volume of HP and AT to spirometry parameters related to small airway disease (FEF25, FEF75 and FEV/FVC ratio).

METHOD AND MATERIALS

In this 2 years cross-sectional study, 26 stable CF patients were enrolled (13 males, mean 14, range 8-18 yrs). MRI and spirometry were performed the same day as part of the routine annual examination. 1.5T MRI Scanner (Signa, General Electric). Protocol: SSFP 2D PD-w axial, coronal and sagittal (TR/TE/SL = 5.7/1.4/8mm ). GRE 3D-axial and -coronal (TR/TE/SL= 3/1/3mm; 0.1mmol/kg, Magnevist®Bayer). MRIs were anonymized and scored in random order with a semi-quantitative MRI-score. Descriptive statistics, T-test and Spearman correlation(r)were used.

RESULTS

2 patients were excluded for the analysis because of incomplete data. Mean AT score was 3.3 (range 0-8, SD 2,75). Mean HP score 4,4 (range 0-12, SD 3,94). Comparison of AT and HP scores showed that AT scores was decreased in 7 (29%), increased in 13 (51%) and unchanged in 17%(4). A significant relation was found between AT and HP (r=0.413; p=0.045). HP correlated negatively with FEF25 (r=-0.69; p=0.0001), FEF75(r=-0.46; p=0.02) and FEV/FVC(r=-0.51; p=0.01). AT correlated negatively with FEF75 (r=-0.48; p=0.016), but not with FEF25 and FEV/FVC. No significant differences were found between AT and HPs scores (p=0.17).

CONCLUSION

HP correlated better with spirometry parameters than AT did. Scores variations between MRI and CE-MRI suggest that AT zones do not always match with HP zones. CE-MRI is feasible and is potentially a clinical relevant parameter to monitor CF lung disease.

CLINICAL RELEVANCE/APPLICATION

Hypo-perfusion defects are more sensitive indicator of small airways disease progression than Air Trapping. CEMRI should be included routinely in CF follow-up to determine its impact in CF care.

Cite This Abstract

Ciet, P, Wielopolski, P, Lever, S, Van Der Wiel, E, Lequin, M, Tiddens, H, Morana, G, Comparison of Proton-MRI (MRI) and Contrast-enhanced MRI (CE-MRI) in Cystic Fibrosis (CF) to Detect Small Airways Disease.  Radiological Society of North America 2011 Scientific Assembly and Annual Meeting, November 26 - December 2, 2011 ,Chicago IL. http://archive.rsna.org/2011/11016724.html