2004
DOI: 10.1002/mrm.20051
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Assessment of human pulmonary function using oxygen‐enhancedT1imaging in patients with cystic fibrosis

Abstract: Indirect qualitative MRI of pulmonary function is feasible using the paramagnetic effects of oxygen physically dissolved in blood. In this study, a more quantitative oxygen-enhanced pulmonary function test based on the slope of a plot of R 1 vs. oxygen concentration-the oxygen transfer function (OTF)-was developed and tested in a pool of five healthy volunteers and five patients with cystic fibrosis (CF). The lung T 1 relaxation rate, R 1 , under normoxic conditions (room air, 21% O 2 ), and the response to va… Show more

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Cited by 126 publications
(122 citation statements)
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“…Recent advances in proton MRI have enabled the identification of structural abnormalities such as onset of fibrosis, mucus plugging, bronchiectasis, and atelectasis in infants and adults with CF (10)(11)(12). Oxygen-enhanced proton MRI has also shown to be sensitive to regional aspects of function, namely, gas exchange in the adult CF lung (13).…”
mentioning
confidence: 99%
“…Recent advances in proton MRI have enabled the identification of structural abnormalities such as onset of fibrosis, mucus plugging, bronchiectasis, and atelectasis in infants and adults with CF (10)(11)(12). Oxygen-enhanced proton MRI has also shown to be sensitive to regional aspects of function, namely, gas exchange in the adult CF lung (13).…”
mentioning
confidence: 99%
“…Since molecular oxygen has a paramagnetic effect in the lung after diffusing through the alveolar-capillary barrier and dissolving into capillary blood (22), the correlation with the PFTs assessing alveolar-capillary gas exchange was expected. However, in this study, a new observation has been made.…”
Section: Discussionmentioning
confidence: 99%
“…MRI had similar quantitative www.interscience.wiley.com/journal/cmmi AEROSOLS AND GASEOUS CONTRAST AGENTS FOR MRI OF THE LUNG prediction to CT and had better qualitative predictions than CT or perfusion scintigraphy (80). T 1 maps were obtained in five patients with cystic fibrosis (77), showing inhomogeneous T 1 distribution in lung parenchyma. Areas of reduced T 1 matched with areas of reduced perfusion.…”
Section: Human Studiesmentioning
confidence: 96%