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Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage

AIMS: Iron released from lysed red blood cells within the hematoma plays a role in intracerebral hemorrhage (ICH)‐related neurotoxicity. This study utilizes magnetic resonance imaging (MRI) to examine the time course, extent of erythrolysis, and its correlation with perihematomal iron accumulation a...

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Autores principales: Novakovic, Nemanja, Wilseck, Zachary M., Chenevert, Thomas L., Xi, Guohua, Keep, Richard F., Pandey, Aditya S., Chaudhary, Neeraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446214/
https://www.ncbi.nlm.nih.gov/pubmed/34145764
http://dx.doi.org/10.1111/cns.13693
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author Novakovic, Nemanja
Wilseck, Zachary M.
Chenevert, Thomas L.
Xi, Guohua
Keep, Richard F.
Pandey, Aditya S.
Chaudhary, Neeraj
author_facet Novakovic, Nemanja
Wilseck, Zachary M.
Chenevert, Thomas L.
Xi, Guohua
Keep, Richard F.
Pandey, Aditya S.
Chaudhary, Neeraj
author_sort Novakovic, Nemanja
collection PubMed
description AIMS: Iron released from lysed red blood cells within the hematoma plays a role in intracerebral hemorrhage (ICH)‐related neurotoxicity. This study utilizes magnetic resonance imaging (MRI) to examine the time course, extent of erythrolysis, and its correlation with perihematomal iron accumulation and white matter loss. METHODS: The feasibility of assessing proportional erythrolysis using T2* MRI was examined using pig blood phantoms with specified degrees of erythrolysis. Fifteen prospectively enrolled ICH patients had MRIs (3‐Tesla) at days 1–3, 14, and 30 (termed early, subacute, and late periods, respectively). Measurement was performed on T2*, 1/T2*, and fractional anisotropy (FA) maps. RESULTS: Pig blood phantoms showed a linear relationship between 1/T2* signal and percent erythrolysis. MRI on patients showed an increase in erythrolysis within the hematoma between the early and subacute phases after ICH, almost completing by day 14. Although perihematomal iron overload (IO) correlated with the erythrolysis extent and hematoma volume at days 14 and 30, perihematomal white matter (WM) loss significantly correlated with both, only at day 14. CONCLUSION: MRI may reliably assess the portion of the hematoma that lyses over time after ICH. Perihematomal IO and WM loss correlate with both the erythrolysis extent and hematoma volume in the early and subacute periods following ICH.
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spelling pubmed-84462142021-09-22 Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage Novakovic, Nemanja Wilseck, Zachary M. Chenevert, Thomas L. Xi, Guohua Keep, Richard F. Pandey, Aditya S. Chaudhary, Neeraj CNS Neurosci Ther Original Articles AIMS: Iron released from lysed red blood cells within the hematoma plays a role in intracerebral hemorrhage (ICH)‐related neurotoxicity. This study utilizes magnetic resonance imaging (MRI) to examine the time course, extent of erythrolysis, and its correlation with perihematomal iron accumulation and white matter loss. METHODS: The feasibility of assessing proportional erythrolysis using T2* MRI was examined using pig blood phantoms with specified degrees of erythrolysis. Fifteen prospectively enrolled ICH patients had MRIs (3‐Tesla) at days 1–3, 14, and 30 (termed early, subacute, and late periods, respectively). Measurement was performed on T2*, 1/T2*, and fractional anisotropy (FA) maps. RESULTS: Pig blood phantoms showed a linear relationship between 1/T2* signal and percent erythrolysis. MRI on patients showed an increase in erythrolysis within the hematoma between the early and subacute phases after ICH, almost completing by day 14. Although perihematomal iron overload (IO) correlated with the erythrolysis extent and hematoma volume at days 14 and 30, perihematomal white matter (WM) loss significantly correlated with both, only at day 14. CONCLUSION: MRI may reliably assess the portion of the hematoma that lyses over time after ICH. Perihematomal IO and WM loss correlate with both the erythrolysis extent and hematoma volume in the early and subacute periods following ICH. John Wiley and Sons Inc. 2021-06-17 /pmc/articles/PMC8446214/ /pubmed/34145764 http://dx.doi.org/10.1111/cns.13693 Text en © 2021 The Authors. CNS Neuroscience & Therapeutics Published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Novakovic, Nemanja
Wilseck, Zachary M.
Chenevert, Thomas L.
Xi, Guohua
Keep, Richard F.
Pandey, Aditya S.
Chaudhary, Neeraj
Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
title Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
title_full Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
title_fullStr Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
title_full_unstemmed Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
title_short Assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
title_sort assessing early erythrolysis and the relationship to perihematomal iron overload and white matter survival in human intracerebral hemorrhage
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8446214/
https://www.ncbi.nlm.nih.gov/pubmed/34145764
http://dx.doi.org/10.1111/cns.13693
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