Experimental validation of the hyperpolarized 129Xe chemical shift saturation recovery technique in healthy volunteers and subjects with interstitial lung disease. Issue 1 (8th August 2014)
- Record Type:
- Journal Article
- Title:
- Experimental validation of the hyperpolarized 129Xe chemical shift saturation recovery technique in healthy volunteers and subjects with interstitial lung disease. Issue 1 (8th August 2014)
- Main Title:
- Experimental validation of the hyperpolarized 129Xe chemical shift saturation recovery technique in healthy volunteers and subjects with interstitial lung disease
- Authors:
- Stewart, Neil J.
Leung, General
Norquay, Graham
Marshall, Helen
Parra‐Robles, Juan
Murphy, Philip S.
Schulte, Rolf F.
Elliot, Charlie
Condliffe, Robin
Griffiths, Paul D.
Kiely, David G.
Whyte, Moira K.
Wolber, Jan
Wild, Jim M. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mrm25400-sec-0001" sec-type="section"> <title>Purpose</title> <p>To assess the sensitivity of the hyperpolarized <sup>129</sup>Xe chemical shift saturation recovery (CSSR) technique for noninvasive quantification of changes to lung microstructure and function in idiopathic pulmonary fibrosis (IPF) and systemic sclerosis (SSc).</p> </sec> <sec id="mrm25400-sec-0002" sec-type="section"> <title>Methods</title> <p>Ten healthy volunteers, four subjects with SSc and four with IPF were scanned at 1.5 T. A CSSR pulse sequence was implemented using binomial‐composite radiofrequency pulses to monitor <sup>129</sup>Xe magnetization in tissues and blood plasma (T/P) and red blood cells (RBCs). The dynamics of <sup>129</sup>Xe uptake into these compartments were fitted with three existing analytical models of gas diffusion to extract parameters of lung physiology. These parameters were quantitatively compared between models.</p> </sec> <sec id="mrm25400-sec-0003" sec-type="section"> <title>Results</title> <p>Uptake of xenon into the pulmonary capillaries was impaired in subjects with IPF and SSc. Statistically significant septal thickening was measured by <sup>129</sup>Xe CSSR in IPF patients. Preliminary data suggests age‐dependent alterations to septal thickness in healthy volunteers. These findings were reproduced using each of the literature models. CSSR‐derived parameters were compared<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="mrm25400-sec-0001" sec-type="section"> <title>Purpose</title> <p>To assess the sensitivity of the hyperpolarized <sup>129</sup>Xe chemical shift saturation recovery (CSSR) technique for noninvasive quantification of changes to lung microstructure and function in idiopathic pulmonary fibrosis (IPF) and systemic sclerosis (SSc).</p> </sec> <sec id="mrm25400-sec-0002" sec-type="section"> <title>Methods</title> <p>Ten healthy volunteers, four subjects with SSc and four with IPF were scanned at 1.5 T. A CSSR pulse sequence was implemented using binomial‐composite radiofrequency pulses to monitor <sup>129</sup>Xe magnetization in tissues and blood plasma (T/P) and red blood cells (RBCs). The dynamics of <sup>129</sup>Xe uptake into these compartments were fitted with three existing analytical models of gas diffusion to extract parameters of lung physiology. These parameters were quantitatively compared between models.</p> </sec> <sec id="mrm25400-sec-0003" sec-type="section"> <title>Results</title> <p>Uptake of xenon into the pulmonary capillaries was impaired in subjects with IPF and SSc. Statistically significant septal thickening was measured by <sup>129</sup>Xe CSSR in IPF patients. Preliminary data suggests age‐dependent alterations to septal thickness in healthy volunteers. These findings were reproduced using each of the literature models. CSSR‐derived parameters were compared with gold‐standard indicators of pulmonary function; diffusing capacity of carbon monoxide and pulmonary transit‐time.</p> </sec> <sec id="mrm25400-sec-0004" sec-type="section"> <title>Conclusions</title> <p>CSSR with hyperpolarized <sup>129</sup>Xe is sensitive to pathology‐induced degradation of lung structure/function and shows promise for quantification of disease severity and monitoring treatment response. Magn Reson Med 74:196–207, 2015. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Magnetic resonance in medicine. Volume 74:Issue 1(2015:Jul.)
- Journal:
- Magnetic resonance in medicine
- Issue:
- Volume 74:Issue 1(2015:Jul.)
- Issue Display:
- Volume 74, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 74
- Issue:
- 1
- Issue Sort Value:
- 2015-0074-0001-0000
- Page Start:
- 196
- Page End:
- 207
- Publication Date:
- 2014-08-08
- Subjects:
- Nuclear magnetic resonance -- Periodicals
Electron paramagnetic resonance -- Periodicals
616.07548 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1522-2594 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mrm.25400 ↗
- Languages:
- English
- ISSNs:
- 0740-3194
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5337.798000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4256.xml