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Assessing the feasibility of hyperpolarized 129 Xe multiple-breath washout MRI in pediatric cystic fibrosis.
Couch, Marcus J; Morgado, Felipe; Kanhere, Nikhil; Kowalik, Krzysztof; Rayment, Jonathan H; Ratjen, Felix; Santyr, Giles.
Afiliação
  • Couch MJ; Translational Medicine Program, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Morgado F; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
  • Kanhere N; Translational Medicine Program, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Kowalik K; Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.
  • Rayment JH; Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
  • Ratjen F; Translational Medicine Program, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Santyr G; Translational Medicine Program, Hospital for Sick Children, Toronto, Ontario, Canada.
Magn Reson Med ; 84(1): 304-311, 2020 07.
Article em En | MEDLINE | ID: mdl-31765507
ABSTRACT

PURPOSE:

To assess the feasibility of hyperpolarized 129 Xe multiple-breath washout MRI in pediatric cystic fibrosis (CF) participants with preserved lung function. Fractional ventilation (r), defined as the fractional gas replacement per breath, was mapped using 2 signal models (1) constant T1 and (2) variable T1 as a function of the hyperpolarized gas washout.

METHODS:

A total of 17 pediatric participants were recruited (mean age 11.7 ± 2.8 years), including 7 children with clinically stable CF and 10 aged-matched healthy controls. Pulmonary function tests were performed, including spirometry, to measure the forced expiratory volume in 1 second and nitrogen multiple-breath washout to measure the lung clearance index. Hyperpolarized 129 Xe MRI was performed during consecutive breaths of air following a single 129 Xe inhalation, and fractional ventilation maps were calculated.

RESULTS:

The forced expiratory volume in 1 second was similar in both groups (P = .32), but there was a statistically significant difference in lung clearance index between healthy and CF participants (P = .001). With variable T1 modeling, CF participants had a mean r of 0.44 ± 0.08 and healthy participants had a mean r of 0.37 ± 0.12 (P = .20). With constant T1 modeling, CF participants had a mean r' of 0.48 ± 0.08, and healthy participants had a mean r' of 0.43 ± 0.12 (P = .32). Therefore, assuming a constant T1 leads to a relative bias in r of 15.1% ± 6.4% and 20.8% ± 7.4% for CF and healthy participants, respectively (P = .12).

CONCLUSION:

This study demonstrates that hyperpolarized 129 Xe multiple-breath washout imaging is feasible in pediatric participants with CF, and inclusion of variable T1 modeling reduces bias in the fractional ventilation measurements.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fibrose Cística Tipo de estudo: Prognostic_studies Limite: Adolescent / Aged / Child / Humans Idioma: En Revista: Magn Reson Med Assunto da revista: DIAGNOSTICO POR IMAGEM Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Fibrose Cística Tipo de estudo: Prognostic_studies Limite: Adolescent / Aged / Child / Humans Idioma: En Revista: Magn Reson Med Assunto da revista: DIAGNOSTICO POR IMAGEM Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Canadá