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 bindin...

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Published inMagnetic resonance in medicine Vol. 73; no. 1; pp. 244 - 253
Main Authors Richardson, Owen C., Bane, Octavia, Scott, Marietta L.J., Tanner, Steven F., Waterton, John C., Sourbron, Steven P., Carroll, Timothy J., Buckley, David L.
Format Journal Article
LanguageEnglish
Published United States Blackwell Publishing Ltd 01.01.2015
Wiley Subscription Services, Inc
BlackWell Publishing Ltd
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Summary: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.
Bibliography:istex:139B8D862CC43C55DA1BD3A32EFAFC31816AE945
ark:/67375/WNG-2NTG40LX-7
ArticleID:MRM25128
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.25128