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Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density

BACKGROUND: Proteins are major plaque components, and their degradation is related to the plaque instability. We sought to assess the feasibility of magnetization transfer (MT) magnetic resonance (MR) for identifying fibrin and collagen in carotid atherosclerotic plaques ex vivo. METHODS: Human caro...

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Autores principales: Qiao, Ye, Hallock, Kevin J, Hamilton, James A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278375/
https://www.ncbi.nlm.nih.gov/pubmed/22107813
http://dx.doi.org/10.1186/1532-429X-13-73
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author Qiao, Ye
Hallock, Kevin J
Hamilton, James A
author_facet Qiao, Ye
Hallock, Kevin J
Hamilton, James A
author_sort Qiao, Ye
collection PubMed
description BACKGROUND: Proteins are major plaque components, and their degradation is related to the plaque instability. We sought to assess the feasibility of magnetization transfer (MT) magnetic resonance (MR) for identifying fibrin and collagen in carotid atherosclerotic plaques ex vivo. METHODS: Human carotid artery specimens (n = 34) were obtained after resection from patients undergoing endarterectomy. MR was completed within 12 hr after surgery on an 11.7T MR microscope prior to fixation. Two sets of T1W spoiled gradient echo images were acquired with and without the application of a saturation pulse set to 10 kHz off resonance. The magnetization transfer ratio (MTR) was calculated, and the degree of MT contrast was correlated with histology. RESULTS: MT with appropriate calibration clearly detected regions with high protein density, which showed a higher MTR (thick fibers (collagen type I) (54 ± 8%)) compared to regions with a low amount of protein including lipid (46 ± 8%) (p = 0.05), thin fibers (collagen type III) (11 ± 6%) (p = 0.03), and calcification (6.8 ± 4%) (p = 0.02). Intraplaque hemorrhage (IPH) with different protein density demonstrated different MT effects. Old (rich in protein debris) and recent IPH (rich in fibrin) had a much higher MTR 69 ± 6% and 55 ± 9%, respectively, compared to fresh IPH (rich in intact red blood cells)(9 ± 3%). CONCLUSIONS: MT MR enhances plaque tissue contrast and identifies the protein-rich regions of carotid artery specimens. The additional information from MTR of IPH may provide important insight into the role of IPH on plaque stability, evolution, and the risk for future ischemic events.
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spelling pubmed-32783752012-02-14 Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density Qiao, Ye Hallock, Kevin J Hamilton, James A J Cardiovasc Magn Reson Research BACKGROUND: Proteins are major plaque components, and their degradation is related to the plaque instability. We sought to assess the feasibility of magnetization transfer (MT) magnetic resonance (MR) for identifying fibrin and collagen in carotid atherosclerotic plaques ex vivo. METHODS: Human carotid artery specimens (n = 34) were obtained after resection from patients undergoing endarterectomy. MR was completed within 12 hr after surgery on an 11.7T MR microscope prior to fixation. Two sets of T1W spoiled gradient echo images were acquired with and without the application of a saturation pulse set to 10 kHz off resonance. The magnetization transfer ratio (MTR) was calculated, and the degree of MT contrast was correlated with histology. RESULTS: MT with appropriate calibration clearly detected regions with high protein density, which showed a higher MTR (thick fibers (collagen type I) (54 ± 8%)) compared to regions with a low amount of protein including lipid (46 ± 8%) (p = 0.05), thin fibers (collagen type III) (11 ± 6%) (p = 0.03), and calcification (6.8 ± 4%) (p = 0.02). Intraplaque hemorrhage (IPH) with different protein density demonstrated different MT effects. Old (rich in protein debris) and recent IPH (rich in fibrin) had a much higher MTR 69 ± 6% and 55 ± 9%, respectively, compared to fresh IPH (rich in intact red blood cells)(9 ± 3%). CONCLUSIONS: MT MR enhances plaque tissue contrast and identifies the protein-rich regions of carotid artery specimens. The additional information from MTR of IPH may provide important insight into the role of IPH on plaque stability, evolution, and the risk for future ischemic events. BioMed Central 2011-11-22 /pmc/articles/PMC3278375/ /pubmed/22107813 http://dx.doi.org/10.1186/1532-429X-13-73 Text en Copyright ©2011 Qiao et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Qiao, Ye
Hallock, Kevin J
Hamilton, James A
Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
title Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
title_full Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
title_fullStr Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
title_full_unstemmed Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
title_short Magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
title_sort magnetization transfer magnetic resonance of human atherosclerotic plaques ex vivo detects areas of high protein density
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3278375/
https://www.ncbi.nlm.nih.gov/pubmed/22107813
http://dx.doi.org/10.1186/1532-429X-13-73
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AT hamiltonjamesa magnetizationtransfermagneticresonanceofhumanatheroscleroticplaquesexvivodetectsareasofhighproteindensity