Ventilation and perfusion assessed by functional MRI in children with CF: reproducibility in comparison to lung function.

Nyilas, Sylvia Meryl; Bauman, Grzegorz; Pusterla, Orso; Ramsey, Kathryn Angela; Singer, Florian; Stranzinger, Enno; Yammine, Sophie; Casaulta, Carmen; Bieri, Oliver; Latzin, Philipp (2019). Ventilation and perfusion assessed by functional MRI in children with CF: reproducibility in comparison to lung function. Journal of cystic fibrosis, 18(4), pp. 543-550. Elsevier 10.1016/j.jcf.2018.10.003

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BACKGROUND

Chronic lung diseases such as cystic fibrosis (CF) can be monitored by imaging and lung function modalities. Magnetic resonance imaging (MRI) techniques such as matrix pencil (MP) decomposition allows for evaluation of regional impairment of fractional ventilation (R) and relative perfusion (R). However, reproducibility of MP MRI outcomes in children with CF is unknown. We examined short-term variability of ventilation and perfusion impairment from MP MRI and compared this to lung function outcomes.

METHOD

Twenty-threeCF and 12 healthy school-aged children underwent MRI and lung function tests on the same day on two occasions 24 h apart. Global ventilation inhomogeneity was assessed by the lung clearance index (LCI) from nitrogen-multiple breath washout (N-MBW) technique. Intra-class-coefficient (ICC), percentage change, and Bland-Altman limits of agreement were evaluated to assess reproducibility.

RESULTS

Sixty-nine measurements from MP MRI and N-MBW were performed. The ICC between two visits for R, R and LCI ranged between 0.60 and 0.90 in individuals with CF and healthy controls. In individuals with CF, percentage of change between the visits was 0.02% for R, -1.11% for R and 2.91% for LCI and limits of agreement between visits were - 4.3% and 3.9% for R, -4.4% and 3.7% for R, and -2.6 and 3.0 for LCI.

CONCLUSIONS

Functional imaging is reproducible and short-term changes in R and R greater than ±4.4% can be considered clinical meaningful. Very good short-term reproducibility, and easy application without the need for breathing maneuvers or contrast agent, makes MP MRI a promising surveillance method for CF.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine
04 Faculty of Medicine > Department of Radiology, Neuroradiology and Nuclear Medicine (DRNN) > Institute of Diagnostic, Interventional and Paediatric Radiology
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Unit Childrens Hospital > Forschungsgruppe Pneumologie (Pädiatrie)
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > Unit Childrens Hospital
04 Faculty of Medicine > Department of Gynaecology, Paediatrics and Endocrinology (DFKE) > Clinic of Paediatric Medicine > Paediatric Pneumology

Graduate School:

Graduate School for Cellular and Biomedical Sciences (GCB)

UniBE Contributor:

Nyilas, Sylvia Meryl, Ramsey, Kathryn Angela, Singer, Florian, Stranzinger, Enno, Yammine, Sophie, Casaulta, Carmen, Latzin, Philipp

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1569-1993

Publisher:

Elsevier

Language:

English

Submitter:

Anette van Dorland

Date Deposited:

23 Jan 2019 14:42

Last Modified:

05 Dec 2022 15:18

Publisher DOI:

10.1016/j.jcf.2018.10.003

PubMed ID:

30348613

Uncontrolled Keywords:

Functional magnetic resonance imaging Lung function measurements Reproducibility

BORIS DOI:

10.7892/boris.120753

URI:

https://boris.unibe.ch/id/eprint/120753

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