Maria Liljeroth1,
Suryanarayanan S. Kaushik2, Zackary I. Cleveland3, Jane
Stiles4, Lake D. Morrison4, Michael C. Foster5,
H. Page McAdams6, Bastiaan Driehuys
1Sir
Peter Mansfield Magnetic Resonance Center, University of Nottingham,
Nottingham, Nottinghamshire, United Kingdom; 2Biomedical
Engineering, Duke University, Durham, NC, United States; 3Center
for In Vivo Microscopy, Duke University, Durham, NC, United States; 4Pulmonary
Medicine, Duke University, Durham, NC, United States; 5Cdu Duke
Hospital Clinic, Duke University, Durham, NC, United States; 6Chest
Radiology, Duke University, Durham, NC, United States
Idiopathic pulmonary fibrosis (IPF); a disorder marked by thickening of the interstitial barrier between airspaces and red blood cells (RBCs), is in dire need of improved biomarkers to evaluate drug efficacy. Hyperpolarized Xe-129 dissolves well in blood and pulmonary tissue and can be detected separately in these compartments by its chemical shift, thereby providing vital information on gas transfer in the lung. We present evidence that Xe-129 uptake in RBCs is greatly reduced in an IPF subject relative to controls. Results show high reproducibility at 5 month follow-up, demonstrating the value of hyperpolarized Xe-129 transfer spectroscopy in IPF therapy evaluation.
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