» Articles » PMID: 17984769

Assessment of Morphological MRI for Pulmonary Changes in Cystic Fibrosis (CF) Patients: Comparison to Thin-section CT and Chest X-ray

Abstract

Objectives: As pulmonary complications are life limiting in patients with cystic fibrosis (CF), repeated chest imaging [chest x-ray, computed tomography (CT)] is needed for follow up. With the continuously rising life expectancy of CF patients, magnetic resonance imaging (MRI) as a radiation-free imaging modality might become more and more attractive. The goal of this study was to prospectively assess the value of MRI for evaluation of morphologic pulmonary CF-changes in comparison to established imaging modalities.

Materials And Methods: Thirty-one CF patients (19 female, 12 male; mean age 16.7 years) with stable lung disease were examined by MRI: HASTE, coronal/transversal (TR/TE/alpha/TA: infinite/28 ms/180 degrees /18 s), multi-detector computed tomography (MDCT) (30 patients): 120 kV, dose modulated mAs, and chest x-ray (21 patients). Image evaluation: random order, 4 chest radiologists in consensus; chest x-ray: modified Chrispin-Norman score; CT and MRI: modified Helbich score. The maximal attainable score for chest x-ray was 34, for MRI and CT 25. Median scores, Pearson correlation coefficients, Bland-Altman plots, and concordance of MRI to CT on a lobar and segmental basis were calculated.

Results: The median MRI and MDCT scores were 13 (min 3, max 20) respectively 13.5 (min 0, max 20). The median chest x-ray score was 14 (min 5, max 32). Pearson correlation coefficients: MRI/CT = 0.80, P < 0.0001; MRI/chest x-ray = 0.63, P < 0.0018; chest x-ray/CT = 0.75, P < 0.0001. The median lobe related concordance was 80% for bronchiectasis, 77% for mucus plugging, 93%, for sacculation/abscesses, and 100% for collapse/consolidation.

Conclusions: Morphologic MRI of the lung in CF patients demonstrates comparable results to MDCT and chest x-ray. Because radiation exposure is an issue in CF patients, MRI might have the ability to be used as an appropriate alternative method for pulmonary imaging.

Citing Articles

Following, Seeing, and Understanding: Longitudinal Magnetic Resonance Imaging in Children with Cystic Fibrosis.

Eddy R, Parraga G Ann Am Thorac Soc. 2025; 22(1):39-40.

PMID: 40043192 PMC: 11708752. DOI: 10.1513/AnnalsATS.202411-1148ED.


Automated lung segmentation on chest MRI in children with cystic fibrosis.

Ringwald F, Wucherpfennig L, Hagen N, Mucke J, Kaletta S, Eichinger M Front Med (Lausanne). 2024; 11:1401473.

PMID: 39606627 PMC: 11600534. DOI: 10.3389/fmed.2024.1401473.


Comparing three-dimensional zero echo time (3D-ZTE) lung MRI and chest CT in the evaluation of systemic sclerosis-related interstitial lung disease.

Ufuk F, Kurnaz B, Peker H, Sagtas E, Ok Z, Cobankara V Eur Radiol. 2024; .

PMID: 39592487 DOI: 10.1007/s00330-024-11216-2.


Pulmonary Vascular Dysfunctions in Cystic Fibrosis.

Amoakon J, Mylavarapu G, Amin R, Naren A Physiology (Bethesda). 2024; 39(4).

PMID: 38501963 PMC: 11368519. DOI: 10.1152/physiol.00024.2023.


MDCT and MRI in Bronchiectasis in Older Children and Young Adults - A Non-Inferiority Trial.

Lokesh , Jana M, Naranje P, Bhalla A, Kabra S, Hadda V Indian J Pediatr. 2023; 92(2):116-122.

PMID: 38051445 DOI: 10.1007/s12098-023-04921-1.