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Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo

PURPOSE: There is currently no adequate method of mapping physiologic and pathophysiologic tissue albumin concentrations in human subjects. The objective of this study was to devise and evaluate a biomarker of regional albumin concentration using gadofosveset-enhanced MRI. THEORY AND METHODS: A bind...

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Autores principales: Richardson, Owen C, Bane, Octavia, Scott, Marietta LJ, Tanner, Steven F, Waterton, John C, Sourbron, Steven P, Carroll, Timothy J, Buckley, David L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296221/
https://www.ncbi.nlm.nih.gov/pubmed/24515975
http://dx.doi.org/10.1002/mrm.25128
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author Richardson, Owen C
Bane, Octavia
Scott, Marietta LJ
Tanner, Steven F
Waterton, John C
Sourbron, Steven P
Carroll, Timothy J
Buckley, David L
author_facet Richardson, Owen C
Bane, Octavia
Scott, Marietta LJ
Tanner, Steven F
Waterton, John C
Sourbron, Steven P
Carroll, Timothy J
Buckley, David L
author_sort Richardson, Owen C
collection PubMed
description PURPOSE: There is currently no adequate method of mapping physiologic and pathophysiologic tissue albumin concentrations in human subjects. The objective of this study was to devise and evaluate a biomarker of regional albumin concentration using gadofosveset-enhanced MRI. THEORY AND METHODS: A binding and relaxation model was devised and evaluated in vitro in solutions of albumin at 3.0 Tesla (T) and 4.7T. The method was evaluated in the heart in seven volunteers at 3.0T. RESULTS: MRI-derived estimates of albumin concentration were in good agreement with true values over the range 0.1–1.0 mM (Pearson correlation coefficients of 0.85 and 0.88 for 3.0T and 4.7T, respectively). The mean calculated albumin concentration in the myocardium for the volunteers was 0.02 mM (range, 0.01–0.03 mM). CONCLUSION: Accurate estimates of albumin concentration in vitro suggest this may be a viable noninvasive alternative to existing techniques. In the myocardium the MRI-derived estimates of albumin concentration indicate the practical feasibility of the technique but were below expected values. Gadofosveset-enhanced MR relaxometry has potential in providing biomarkers of regional albumin concentration; further evaluation is required before it can be used reliably in vivo. Magn Reson Med 73:244–253, 2015. © 2014 Wiley Periodicals, Inc.
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spelling pubmed-42962212015-01-21 Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo Richardson, Owen C Bane, Octavia Scott, Marietta LJ Tanner, Steven F Waterton, John C Sourbron, Steven P Carroll, Timothy J Buckley, David L Magn Reson Med Imaging Methodology—Full Papers PURPOSE: There is currently no adequate method of mapping physiologic and pathophysiologic tissue albumin concentrations in human subjects. The objective of this study was to devise and evaluate a biomarker of regional albumin concentration using gadofosveset-enhanced MRI. THEORY AND METHODS: A binding and relaxation model was devised and evaluated in vitro in solutions of albumin at 3.0 Tesla (T) and 4.7T. The method was evaluated in the heart in seven volunteers at 3.0T. RESULTS: MRI-derived estimates of albumin concentration were in good agreement with true values over the range 0.1–1.0 mM (Pearson correlation coefficients of 0.85 and 0.88 for 3.0T and 4.7T, respectively). The mean calculated albumin concentration in the myocardium for the volunteers was 0.02 mM (range, 0.01–0.03 mM). CONCLUSION: Accurate estimates of albumin concentration in vitro suggest this may be a viable noninvasive alternative to existing techniques. In the myocardium the MRI-derived estimates of albumin concentration indicate the practical feasibility of the technique but were below expected values. Gadofosveset-enhanced MR relaxometry has potential in providing biomarkers of regional albumin concentration; further evaluation is required before it can be used reliably in vivo. Magn Reson Med 73:244–253, 2015. © 2014 Wiley Periodicals, Inc. BlackWell Publishing Ltd 2015-01 2014-02-11 /pmc/articles/PMC4296221/ /pubmed/24515975 http://dx.doi.org/10.1002/mrm.25128 Text en © 2014 University of Leeds. Magnetic Resonance in Medicine published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Imaging Methodology—Full Papers
Richardson, Owen C
Bane, Octavia
Scott, Marietta LJ
Tanner, Steven F
Waterton, John C
Sourbron, Steven P
Carroll, Timothy J
Buckley, David L
Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo
title Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo
title_full Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo
title_fullStr Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo
title_full_unstemmed Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo
title_short Gadofosveset-Based Biomarker of Tissue Albumin Concentration: Technical Validation in Vitro and Feasibility in Vivo
title_sort gadofosveset-based biomarker of tissue albumin concentration: technical validation in vitro and feasibility in vivo
topic Imaging Methodology—Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296221/
https://www.ncbi.nlm.nih.gov/pubmed/24515975
http://dx.doi.org/10.1002/mrm.25128
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