Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance

Measurement of liver iron concentration (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 me...

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Published inBlood Vol. 105; no. 2; pp. 855 - 861
Main Authors St. Pierre, Timothy G., Clark, Paul R., Chua-anusorn, Wanida, Fleming, Adam J., Jeffrey, Gary P., Olynyk, John K., Pootrakul, Pensri, Robins, Erin, Lindeman, Robert
Format Journal Article
LanguageEnglish
Published Washington, DC Elsevier Inc 15.01.2005
The Americain Society of Hematology
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Abstract Measurement of liver iron concentration (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 noninvasive method of measuring and imaging LICs in vivo using clinical 1.5-T magnetic resonance imaging units. Mean liver proton transverse relaxation rates (R2) were measured for 105 humans. 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 LICs 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 LICs 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%.
AbstractList Measurement of liver iron concentration (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 noninvasive method of measuring and imaging LICs in vivo using clinical 1.5-T magnetic resonance imaging units. Mean liver proton transverse relaxation rates (R2) were measured for 105 humans. 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 LICs 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 LICs 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%.
Measurement of liver iron concentration (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 noninvasive method of measuring and imaging LICs in vivo using clinical 1.5-T magnetic resonance imaging units. Mean liver proton transverse relaxation rates (R2) were measured for 105 humans. 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 LICs 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 LICs 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%.Measurement of liver iron concentration (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 noninvasive method of measuring and imaging LICs in vivo using clinical 1.5-T magnetic resonance imaging units. Mean liver proton transverse relaxation rates (R2) were measured for 105 humans. 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 LICs 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 LICs 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%.
Author Clark, Paul R.
Olynyk, John K.
Lindeman, Robert
Pootrakul, Pensri
Robins, Erin
Chua-anusorn, Wanida
Fleming, Adam J.
St. Pierre, Timothy G.
Jeffrey, Gary P.
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– sequence: 2
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  fullname: Clark, Paul R.
– sequence: 3
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  fullname: Fleming, Adam J.
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  surname: Olynyk
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  surname: Lindeman
  fullname: Lindeman, Robert
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ISSN 0006-4971
IngestDate Fri Jul 11 11:54:43 EDT 2025
Wed Feb 19 02:30:18 EST 2025
Mon Jul 21 09:16:40 EDT 2025
Tue Jul 01 00:54:43 EDT 2025
Thu Apr 24 22:57:53 EDT 2025
Fri Feb 23 02:46:16 EST 2024
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Issue 2
Keywords Human
Overload
Digestive system
Liver
Magnetic resonance
Non invasive method
Proton
Exploration
Medical imagery
Iron
Language English
License This article is made available under the Elsevier license.
CC BY 4.0
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Snippet Measurement of liver iron concentration (LIC) is necessary for a range of iron-loading disorders such as hereditary hemochromatosis, thalassemia, sickle cell...
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SubjectTerms Biological and medical sciences
Biopsy
Chlorides
Humans
Investigative techniques, diagnostic techniques (general aspects)
Iron - metabolism
Iron Overload - metabolism
Iron Overload - pathology
Liver - metabolism
Liver - pathology
Magnetic Resonance Imaging - methods
Magnetic Resonance Imaging - standards
Manganese Compounds
Medical sciences
Metabolic diseases
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Phantoms, Imaging
Protons
Reproducibility of Results
Sensitivity and Specificity
Title Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance
URI https://dx.doi.org/10.1182/blood-2004-01-0177
https://www.ncbi.nlm.nih.gov/pubmed/15256427
https://www.proquest.com/docview/67341669
Volume 105
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