Literature DB >> 16253854

Hyperpolarized HHe 3 MRI of the lung in cystic fibrosis: assessment at baseline and after bronchodilator and airway clearance treatment.

Kimiknu Mentore1, Deborah K Froh, Eduard E de Lange, James R Brookeman, Alix O Paget-Brown, Talissa A Altes.   

Abstract

RATIONALE AND
OBJECTIVES: The purpose of this study is to determine hyperpolarized helium 3 (HHe) magnetic resonance (MR) findings of the lung in patients with cystic fibrosis (CF) compared with healthy subjects and determine whether HHe MR can detect changes after bronchodilator therapy or mechanical airway mucus clearance treatment.
MATERIALS AND METHODS: Thirty-one subjects, 16 healthy volunteers and 15 patients with CF, underwent HHe lung ventilation MR imaging and spirometry at baseline. Eight patients with CF then were treated with nebulized albuterol, after which a follow-up HHe MR scan was obtained. Subsequently, recombinant human deoxyribonuclease (DNase) treatment and chest physical therapy were performed in these eight subjects, followed by a third HHe MR scan. For each MR study, the number of ventilation defects was scored by a human reader.
RESULTS: Patients with CF had significantly more HHe MR ventilation defects per image than healthy subjects (mean, 8.2 defects in patients with CF vs 1.6 defects in healthy subjects; P < .05). Even the four subjects with CF with a normal forced expiratory volume in 1 second had significantly more ventilation defects than healthy subjects (mean, 6.5 defects in these patients with CF; P = .0002). After treatment with albuterol, there was a small, but statistically significant, decrease in number of ventilation defects (mean, 9.6-8.0 defects; P = .025). After DNase and chest physical therapy, there was a trend toward increasing ventilation defects (mean, 8.3 defects; P = .096), but with a residual net improvement relative to baseline.
CONCLUSION: In patients with CF, HHe MR ventilation defects correlate with spirometry, change with treatment, and are elevated in number in patients with CF with normal spirometry results. Thus, HHe MR appears to possess many of the characteristics required of a biomarker for pulmonary CF and may be useful in the evaluation of CF pulmonary disease severity or progression.

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Year:  2005        PMID: 16253854     DOI: 10.1016/j.acra.2005.07.008

Source DB:  PubMed          Journal:  Acad Radiol        ISSN: 1076-6332            Impact factor:   3.173


  31 in total

Review 1.  [MRI methods for pulmonary ventilation and perfusion imaging].

Authors:  G Sommer; G Bauman
Journal:  Radiologe       Date:  2016-02       Impact factor: 0.635

2.  Assessment of lung disease in children with cystic fibrosis using hyperpolarized 3-Helium MRI: comparison with Shwachman score, Chrispin-Norman score and spirometry.

Authors:  Edwin J R van Beek; Catherine Hill; Neil Woodhouse; Stanislao Fichele; Sally Fleming; Bridget Howe; Sandra Bott; Jim M Wild; Christopher J Taylor
Journal:  Eur Radiol       Date:  2006-08-29       Impact factor: 5.315

Review 3.  Functional imaging: CT and MRI.

Authors:  Edwin J R van Beek; Eric A Hoffman
Journal:  Clin Chest Med       Date:  2008-03       Impact factor: 2.878

Review 4.  Advancing CT and MR imaging of the lungs and airways in children: imaging into practice.

Authors:  Edward Y Lee
Journal:  Pediatr Radiol       Date:  2008-05

5.  Hyperpolarized 3helium magnetic resonance ventilation imaging of the lung in cystic fibrosis: comparison with high resolution CT and spirometry.

Authors:  Colm J McMahon; Jonathan D Dodd; Catherine Hill; Neil Woodhouse; Jim M Wild; Stan Fichele; Charles G Gallagher; Stephen J Skehan; Edwin J R van Beek; James B Masterson
Journal:  Eur Radiol       Date:  2006-07-27       Impact factor: 5.315

Review 6.  Ten years of chest MRI for patients with cystic fibrosis : Translation from the bench to clinical routine.

Authors:  Patricia Leutz-Schmidt; Monika Eichinger; Mirjam Stahl; Olaf Sommerburg; Jürgen Biederer; Hans-Ulrich Kauczor; Michael U Puderbach; Marcus A Mall; Mark O Wielpütz
Journal:  Radiologe       Date:  2019-12       Impact factor: 0.635

7.  Novel Thoracic MRI Approaches for the Assessment of Pulmonary Physiology and Inflammation.

Authors:  Jonathan P Brooke; Ian P Hall
Journal:  Adv Exp Med Biol       Date:  2021       Impact factor: 2.622

8.  A two-center analysis of hyperpolarized 129Xe lung MRI in stable pediatric cystic fibrosis: Potential as a biomarker for multi-site trials.

Authors:  Marcus J Couch; Robert Thomen; Nikhil Kanhere; Raymond Hu; Felix Ratjen; Jason Woods; Giles Santyr
Journal:  J Cyst Fibros       Date:  2019-03-25       Impact factor: 5.482

9.  Three-dimensional Isotropic Functional Imaging of Cystic Fibrosis Using Oxygen-enhanced MRI: Comparison with Hyperpolarized 3He MRI.

Authors:  Wei Zha; Scott K Nagle; Robert V Cadman; Mark L Schiebler; Sean B Fain
Journal:  Radiology       Date:  2018-10-23       Impact factor: 11.105

10.  Three-dimensional imaging of ventilation dynamics in asthmatics using multiecho projection acquisition with constrained reconstruction.

Authors:  James H Holmes; Rafael L O'Halloran; Ethan K Brodsky; Thorsten A Bley; Christopher J Francois; Julia V Velikina; Ronald L Sorkness; William W Busse; Sean B Fain
Journal:  Magn Reson Med       Date:  2009-12       Impact factor: 4.668

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