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Blood, 15 January 2005, Vol. 105, No. 2, pp. 855-861.
Prepublished online as a Blood First Edition Paper on July 15, 2004; DOI 10.1182/blood-2004-01-0177.
Previous Article | Next Article 
Submitted January 15, 2004
Accepted July 2, 2004
Non-Invasive Measurement and Imaging of Liver Iron Concentrations Using Proton Magnetic Resonance
Timothy G St. Pierre*, Paul R Clark, Wanida Chua-anusorn, Adam J Fleming, Gary P Jeffrey, John K Olynyk, Pensri Pootrakul, Erin Robins, and Robert Lindeman
School of Physics, University of Western Australia, Perth, Western Australia, Australia
School of Medicine and Pharmacology, University of Western Australia, Perth, Western Australia, Australia; Department of Gastroenterology and Hepatology, Sir Charles Gairdner Hospital, Perth, Western Australia, Australia
School of Medicine and Pharmacology, University of Western Australia, Perth, Western Australia, Australia
Thalassemia Research Center, Mahidol University, Bangkok, Nakornpathom, Thailand
SKG Radiology, St John of God Hospital, Perth, Western Australlia, Australia
Department of Haematology, Prince of Wales Hospital, Sydney, New South Wales, Australia
* Corresponding author; email: stpierre{at}physics.uwa.edu.au.
Measurement of liver iron concentrations (LIC) is necessary for a range of iron loading disorders such as hereditary hemochromatosis, thalassemia, sickle cell disease, aplastic anemia, and myelodysplasia. Currently, chemical analysis of needle biopsy specimens is the most common accepted method of measurement. This study presents a readily available non-invasive method of measuring and imaging LIC in vivo using clinical 1.5 T magnetic resonance imaging units. Mean liver proton transverse relaxation rates (R2) were measured for 105 human subjects. A value for the LIC for each subject was obtained by chemical assay of a needle biopsy specimen. High degrees of sensitivity and specificity of R2 to biopsy LIC were found at the clinically significant LIC thresholds of 1.8, 3.2, 7.0 and 15.0 mg Fe/g dry tissue. A calibration curve relating liver R2 to LIC has been deduced from the data covering the range of LIC from 0.3 to 42.7 mg Fe/g dry tissue. Proton transverse relaxation rates in aqueous paramagnetic solutions were also measured on each magnetic resonance imaging unit to ensure instrument-independent results. Measurements of proton transverse relaxivity of aqueous MnCl2 phantoms on 13 different magnetic resonance imaging units using the method yielded a coefficient of variation of 2.1%.

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