Literature DB >> 20308459

Hyperpolarized 3He MR for sensitive imaging of ventilation function and treatment efficiency in young cystic fibrosis patients with normal lung function.

Elise Bannier1, Katarzyna Cieslar, Karim Mosbah, Françoise Aubert, François Duboeuf, Zahir Salhi, Sophie Gaillard, Yves Berthezène, Yannick Crémillieux, Philippe Reix.   

Abstract

PURPOSE: To assess the sensitivity of hyperpolarized helium 3 ((3)He) magnetic resonance (MR) imaging for the detection of peripheral airway obstruction in younger cystic fibrosis (CF) patients showing normal spirometric results (mean forced expiratory volume in 1 second [FEV(1)], 112% +/- 14.5 [standard deviation]) and to observe the immediate effects of a single chest physical therapy (CPT) session, thereby comparing two image quantification techniques.
MATERIALS AND METHODS: Ten pediatric CF patients (age range, 8-16 years) with normal spirometric results were included in this study after approval from the local research ethics committee. Spirometry followed by proton and hyperpolarized (3)He three-dimensional lung imaging were performed with a 1.5-T MR unit before and after 20 minutes of CPT. The number of ventilation defects per image (VDI) and the ventilated lung fraction (VF), defined as the ratio of ventilated lung volume divided by total lung volume, were quantified.
RESULTS: Ventilation defects were found in all patients (mean VDI, 5.1 +/- 1.9; mean global VF, 78.5% +/- 12.3; and mean peripheral VF, 75.5% +/- 17.1) despite normal spirometric results. After CPT, disparate changes in the distribution of ventilation defects were observed but the average VDI and VF did not change significantly (mean VDI, 5.1 +/- 1.1; mean global VF, 83.5% +/- 12.2; and mean peripheral VF, 80.3% +/- 12.2). There was no correlation between FEV(1) and VDI (rho = -0.041, P = .863) or global VF (rho = -0.196, P = .408) values but peripheral VF and VDI were correlated (rho = -0.563, P = .011).
CONCLUSION: Although spirometric results indicate normal lung function, the mean VDI in patients (5.1) found in this study is well above the VDI in healthy subjects (1.6) reported in the literature. A single CPT session induces disparate changes in the distribution and extent of ventilation defects. RSNA, 2010

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Year:  2010        PMID: 20308459     DOI: 10.1148/radiol.09090039

Source DB:  PubMed          Journal:  Radiology        ISSN: 0033-8419            Impact factor:   11.105


  17 in total

1.  Hyperpolarized 129Xe for investigation of mild cystic fibrosis lung disease in pediatric patients.

Authors:  Robert P Thomen; Laura L Walkup; David J Roach; Zackary I Cleveland; John P Clancy; Jason C Woods
Journal:  J Cyst Fibros       Date:  2016-07-29       Impact factor: 5.482

2.  Multireader Determination of Clinically Significant Obstruction Using Hyperpolarized 129Xe-Ventilation MRI.

Authors:  Lukas Ebner; Rohan S Virgincar; Mu He; Kingshuk R Choudhury; Scott H Robertson; Andreas Christe; Achille Mileto; Joseph G Mammarapallil; H Page McAdams; Bastiaan Driehuys; Justus E Roos
Journal:  AJR Am J Roentgenol       Date:  2019-02-19       Impact factor: 3.959

3.  Preliminary comparison of normalized T1 and non-contrast perfusion MRI assessments of regional lung disease in cystic fibrosis patients.

Authors:  Shannon B Donnola; Elliott C Dasenbrook; David Weaver; Lan Lu; Karishma Gupta; Anjali Prabhakaran; Xin Yu; James F Chmiel; Kimberly McBennett; Michael W Konstan; Mitchell L Drumm; Chris A Flask
Journal:  J Cyst Fibros       Date:  2015-12-22       Impact factor: 5.482

Review 4.  Hyperpolarized Gas Magnetic Resonance Lung Imaging in Children and Young Adults.

Authors:  Lucia Flors; John P Mugler; Eduard E de Lange; Grady W Miller; Jaime F Mata; Nick Tustison; Iulian C Ruset; F William Hersman; Talissa A Altes
Journal:  J Thorac Imaging       Date:  2016-09       Impact factor: 3.000

Review 5.  Current technology in the diagnosis of developmentally related lung disorders.

Authors:  Aaron Hamvas
Journal:  Neonatology       Date:  2012-06-01       Impact factor: 4.035

Review 6.  Current state of the art MRI for the longitudinal assessment of cystic fibrosis.

Authors:  Jason C Woods; Jim M Wild; Mark O Wielpütz; John P Clancy; Hiroto Hatabu; Hans-Ulrich Kauczor; Edwin J R van Beek; Talissa A Altes
Journal:  J Magn Reson Imaging       Date:  2019-12-17       Impact factor: 4.813

7.  Assessment of the influence of lung inflation state on the quantitative parameters derived from hyperpolarized gas lung ventilation MRI in healthy volunteers.

Authors:  Paul J C Hughes; Laurie Smith; Ho-Fung Chan; Bilal A Tahir; Graham Norquay; Guilhem J Collier; Alberto Biancardi; Helen Marshall; Jim M Wild
Journal:  J Appl Physiol (1985)       Date:  2018-11-09

8.  CFTR Modulator Therapies in Pediatric Cystic Fibrosis: Focus on Ivacaftor.

Authors:  Elizabeth L Kramer; John P Clancy
Journal:  Expert Opin Orphan Drugs       Date:  2016-09-13       Impact factor: 0.694

Review 9.  Novel imaging techniques for cystic fibrosis lung disease.

Authors:  Jennifer L Goralski; Neil J Stewart; Jason C Woods
Journal:  Pediatr Pulmonol       Date:  2021-02

10.  Semiautomated Ventilation Defect Quantification in Exercise-induced Bronchoconstriction Using Hyperpolarized Helium-3 Magnetic Resonance Imaging: A Repeatability Study.

Authors:  Wei Zha; David J Niles; Stanley J Kruger; Bernard J Dardzinski; Robert V Cadman; David G Mummy; Scott K Nagle; Sean B Fain
Journal:  Acad Radiol       Date:  2016-06-02       Impact factor: 5.482

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