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    Comparison of normal tissue R1 and R*2 modulation by oxygen and carbogen.

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    Authors
    O'Connor, James P B
    Naish, Josephine H
    Jackson, Alan
    Waterton, John C
    Watson, Yvonne
    Cheung, Susan
    Buckley, David L
    McGrath, Deirdre M
    Buonaccorsi, Giovanni A
    Mills, Samantha J
    Roberts, Caleb
    Jayson, Gordon C
    Parker, Geoff J M
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    Affiliation
    Imaging Science and Biomedical Engineering, University of Manchester, Manchester, UK.
    Issue Date
    2009-01
    
    Metadata
    Show full item record
    Abstract
    Magnetic resonance imaging has shown promise for evaluating tissue oxygenation. In this study differences in the tissue longitudinal relaxation rate (R(1)) and effective transverse relaxation rate (R(*)(2)), induced by inhalation of pure oxygen and carbogen, were evaluated in 10 healthy subjects. Significant reductions in R(1) were demonstrated following both oxygen and carbogen inhalation in the spleen (both P < 0.001), liver (P = 0.002 air vs. oxygen; P = 0.001 air vs. carbogen), skeletal muscle (both P < 0.001), and renal cortex (P = 0.005 air vs. oxygen; P = 0.008 air vs. carbogen). No significant change in R(*)(2) occurred following pure oxygen in any organ. However, a significant increase in R(*)(2) was observed in the spleen (P < 0.001), liver (P = 0.001), skeletal muscle (P = 0.026), and renal cortex (P = 0.001) following carbogen inhalation, an opposite effect to that observed in many studies of tumor pathophysiology. Changes in R(1) and R(*)(2) were independent of the gas administration order in the spleen and skeletal muscle. These findings suggest that the R(1) and R(*)(2) responses to hyperoxic gases are independent biomarkers of oxygen physiology.
    Citation
    Comparison of normal tissue R1 and R*2 modulation by oxygen and carbogen. 2009, 61 (1):75-83notMagn Reson Med
    Journal
    Magnetic Resonance in Medicine : official journal of the Society of Magnetic Resonance in Medicine / Society of Magnetic Resonance in Medicine
    URI
    http://hdl.handle.net/10541/53113
    DOI
    10.1002/mrm.21815
    PubMed ID
    19097212
    Type
    Article
    Language
    en
    ISSN
    1522-2594
    ae974a485f413a2113503eed53cd6c53
    10.1002/mrm.21815
    Scopus Count
    Collections
    All Paterson Institute for Cancer Research
    Medical Oncology

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