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MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease

A protocol for evaluating ultrasmall superparamagnetic particles of iron oxide (USPIO) uptake and elimination in cerebral small vessel disease patients was developed and piloted. B(1)-insensitive R(1) measurement was evaluated in vitro. Twelve participants with history of minor stroke were scanned a...

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Autores principales: Thrippleton, Michael J., Blair, Gordon W., Valdes-Hernandez, Maria C., Glatz, Andreas, Semple, Scott I. K., Doubal, Fergus, Vesey, Alex, Marshall, Ian, Newby, David E., Wardlaw, Joanna M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387454/
https://www.ncbi.nlm.nih.gov/pubmed/30759756
http://dx.doi.org/10.3390/ijms20030776
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author Thrippleton, Michael J.
Blair, Gordon W.
Valdes-Hernandez, Maria C.
Glatz, Andreas
Semple, Scott I. K.
Doubal, Fergus
Vesey, Alex
Marshall, Ian
Newby, David E.
Wardlaw, Joanna M.
author_facet Thrippleton, Michael J.
Blair, Gordon W.
Valdes-Hernandez, Maria C.
Glatz, Andreas
Semple, Scott I. K.
Doubal, Fergus
Vesey, Alex
Marshall, Ian
Newby, David E.
Wardlaw, Joanna M.
author_sort Thrippleton, Michael J.
collection PubMed
description A protocol for evaluating ultrasmall superparamagnetic particles of iron oxide (USPIO) uptake and elimination in cerebral small vessel disease patients was developed and piloted. B(1)-insensitive R(1) measurement was evaluated in vitro. Twelve participants with history of minor stroke were scanned at 3-T MRI including structural imaging, and R(1) and R(2)* mapping. Participants were scanned (i) before and (ii) after USPIO (ferumoxytol) infusion, and again at (iii) 24–30 h and (iv) one month. Absolute and blood-normalised changes in R(1) and R(2)* were measured in white matter (WM), deep grey matter (GM), white matter hyperintensity (WMH) and stroke lesion regions. R(1) measurements were accurate across a wide range of values. R(1) (p < 0.05) and R(2)* (p < 0.01) mapping detected increases in relaxation rate in all tissues immediately post-USPIO and at 24–30 h. R(2)* returned to baseline at one month. Blood-normalised R(1) and R(2)* changes post-infusion and at 24–30 h were similar, and were greater in GM versus WM (p < 0.001). Narrower distributions were seen with R(2)* than for R(1) mapping. R(1) and R(2)* changes were correlated at 24–30 h (p < 0.01). MRI relaxometry permits quantitative evaluation of USPIO uptake; R(2)* appears to be more sensitive to USPIO than R(1). Our data are explained by intravascular uptake alone, yielding estimates of cerebral blood volume, and did not support parenchymal uptake. Ferumoxytol appears to be eliminated at 1 month. The approach should be valuable in future studies to quantify both blood-pool USPIO and parenchymal uptake associated with inflammatory cells or blood-brain barrier leak.
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spelling pubmed-63874542019-02-27 MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease Thrippleton, Michael J. Blair, Gordon W. Valdes-Hernandez, Maria C. Glatz, Andreas Semple, Scott I. K. Doubal, Fergus Vesey, Alex Marshall, Ian Newby, David E. Wardlaw, Joanna M. Int J Mol Sci Article A protocol for evaluating ultrasmall superparamagnetic particles of iron oxide (USPIO) uptake and elimination in cerebral small vessel disease patients was developed and piloted. B(1)-insensitive R(1) measurement was evaluated in vitro. Twelve participants with history of minor stroke were scanned at 3-T MRI including structural imaging, and R(1) and R(2)* mapping. Participants were scanned (i) before and (ii) after USPIO (ferumoxytol) infusion, and again at (iii) 24–30 h and (iv) one month. Absolute and blood-normalised changes in R(1) and R(2)* were measured in white matter (WM), deep grey matter (GM), white matter hyperintensity (WMH) and stroke lesion regions. R(1) measurements were accurate across a wide range of values. R(1) (p < 0.05) and R(2)* (p < 0.01) mapping detected increases in relaxation rate in all tissues immediately post-USPIO and at 24–30 h. R(2)* returned to baseline at one month. Blood-normalised R(1) and R(2)* changes post-infusion and at 24–30 h were similar, and were greater in GM versus WM (p < 0.001). Narrower distributions were seen with R(2)* than for R(1) mapping. R(1) and R(2)* changes were correlated at 24–30 h (p < 0.01). MRI relaxometry permits quantitative evaluation of USPIO uptake; R(2)* appears to be more sensitive to USPIO than R(1). Our data are explained by intravascular uptake alone, yielding estimates of cerebral blood volume, and did not support parenchymal uptake. Ferumoxytol appears to be eliminated at 1 month. The approach should be valuable in future studies to quantify both blood-pool USPIO and parenchymal uptake associated with inflammatory cells or blood-brain barrier leak. MDPI 2019-02-12 /pmc/articles/PMC6387454/ /pubmed/30759756 http://dx.doi.org/10.3390/ijms20030776 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Thrippleton, Michael J.
Blair, Gordon W.
Valdes-Hernandez, Maria C.
Glatz, Andreas
Semple, Scott I. K.
Doubal, Fergus
Vesey, Alex
Marshall, Ian
Newby, David E.
Wardlaw, Joanna M.
MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease
title MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease
title_full MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease
title_fullStr MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease
title_full_unstemmed MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease
title_short MRI Relaxometry for Quantitative Analysis of USPIO Uptake in Cerebral Small Vessel Disease
title_sort mri relaxometry for quantitative analysis of uspio uptake in cerebral small vessel disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6387454/
https://www.ncbi.nlm.nih.gov/pubmed/30759756
http://dx.doi.org/10.3390/ijms20030776
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