Evaluation of neovessels in atherosclerotic plaques of rabbits using an albumin-binding intravascular contrast agent and MRI

Purpose To test whether B‐22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and macrophage density in atherosclerotic plaques of rabbits using MRI. Materials and Methods A T1‐weighted MRI of the aorta was acquired...

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Published in:Journal of magnetic resonance imaging Vol. 27; no. 6; pp. 1406 - 1411
Main Authors: Cornily, Jean-Christophe, Hyafil, Fabien, Calcagno, Claudia, Briley-Saebo, Karen C., Tunstead, James, Aguinaldo, Juan-Gilberto S., Mani, Venkatesh, Lorusso, Vito, Cavagna, Friedrich M., Fayad, Zahi A.
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Abstract Purpose To test whether B‐22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and macrophage density in atherosclerotic plaques of rabbits using MRI. Materials and Methods A T1‐weighted MRI of the aorta was acquired in 10 rabbits (7 atherosclerotic and 3 control rabbits) before and up to 2 h after intravenous injection of 100 μmol/kg of Gd‐DTPA or 75 μmol/kg of B‐22956/1. Plaque enhancement was measured at different time points. Immunohistochemistry was performed using anti‐CD 31 antibodies and anti‐RAM 11 antibodies to correlate to neovessel and macrophage density, respectively. Results MRI showed a significant plaque enhancement 2 h after B‐22956/1 versus Gd‐DTPA in the atherosclerotic group (39.75% versus 9.5%; P < 0.0001. Early atherosclerotic plaques (n = 146) enhancement positively correlates with neovessel density on corresponding histological sections (r = 0.42; P < 0.01). Enhancement of atherosclerotic plaques 2 h after injection of B‐22956/1 correlated with macrophage density (r = 0.71; P < 0.01). Conclusion Enhancement of atherosclerotic plaques with MRI correlated with neovessel density at early time points after the injection of B‐22956/1 and with macrophage density, at later time points. Hence, B‐22956/1‐enhanced MRI represents a promising imaging technique for the identification of “high‐risk” plaques. J. Magn. Reson. Imaging 2008;27:1406–1411. © 2008 Wiley‐Liss, Inc.
AbstractList To test whether B-22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and macrophage density in atherosclerotic plaques of rabbits using MRI. A T1-weighted MRI of the aorta was acquired in 10 rabbits (7 atherosclerotic and 3 control rabbits) before and up to 2 h after intravenous injection of 100 mumol/kg of Gd-DTPA or 75 mumol/kg of B-22956/1. Plaque enhancement was measured at different time points. Immunohistochemistry was performed using anti-CD 31 antibodies and anti-RAM 11 antibodies to correlate to neovessel and macrophage density, respectively. MRI showed a significant plaque enhancement 2 h after B-22956/1 versus Gd-DTPA in the atherosclerotic group (39.75% versus 9.5%; P < 0.0001. Early atherosclerotic plaques (n = 146) enhancement positively correlates with neovessel density on corresponding histological sections (r = 0.42; P < 0.01). Enhancement of atherosclerotic plaques 2 h after injection of B-22956/1 correlated with macrophage density (r = 0.71; P < 0.01). Enhancement of atherosclerotic plaques with MRI correlated with neovessel density at early time points after the injection of B-22956/1 and with macrophage density, at later time points. Hence, B-22956/1-enhanced MRI represents a promising imaging technique for the identification of "high-risk" plaques.
PURPOSETo test whether B-22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and macrophage density in atherosclerotic plaques of rabbits using MRI. MATERIALS AND METHODSA T1-weighted MRI of the aorta was acquired in 10 rabbits (7 atherosclerotic and 3 control rabbits) before and up to 2 h after intravenous injection of 100 mumol/kg of Gd-DTPA or 75 mumol/kg of B-22956/1. Plaque enhancement was measured at different time points. Immunohistochemistry was performed using anti-CD 31 antibodies and anti-RAM 11 antibodies to correlate to neovessel and macrophage density, respectively. RESULTSMRI showed a significant plaque enhancement 2 h after B-22956/1 versus Gd-DTPA in the atherosclerotic group (39.75% versus 9.5%; P < 0.0001. Early atherosclerotic plaques (n = 146) enhancement positively correlates with neovessel density on corresponding histological sections (r = 0.42; P < 0.01). Enhancement of atherosclerotic plaques 2 h after injection of B-22956/1 correlated with macrophage density (r = 0.71; P < 0.01). CONCLUSIONEnhancement of atherosclerotic plaques with MRI correlated with neovessel density at early time points after the injection of B-22956/1 and with macrophage density, at later time points. Hence, B-22956/1-enhanced MRI represents a promising imaging technique for the identification of "high-risk" plaques.
Purpose To test whether B‐22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and macrophage density in atherosclerotic plaques of rabbits using MRI. Materials and Methods A T1‐weighted MRI of the aorta was acquired in 10 rabbits (7 atherosclerotic and 3 control rabbits) before and up to 2 h after intravenous injection of 100 μmol/kg of Gd‐DTPA or 75 μmol/kg of B‐22956/1. Plaque enhancement was measured at different time points. Immunohistochemistry was performed using anti‐CD 31 antibodies and anti‐RAM 11 antibodies to correlate to neovessel and macrophage density, respectively. Results MRI showed a significant plaque enhancement 2 h after B‐22956/1 versus Gd‐DTPA in the atherosclerotic group (39.75% versus 9.5%; P < 0.0001. Early atherosclerotic plaques (n = 146) enhancement positively correlates with neovessel density on corresponding histological sections (r = 0.42; P < 0.01). Enhancement of atherosclerotic plaques 2 h after injection of B‐22956/1 correlated with macrophage density (r = 0.71; P < 0.01). Conclusion Enhancement of atherosclerotic plaques with MRI correlated with neovessel density at early time points after the injection of B‐22956/1 and with macrophage density, at later time points. Hence, B‐22956/1‐enhanced MRI represents a promising imaging technique for the identification of “high‐risk” plaques. J. Magn. Reson. Imaging 2008;27:1406–1411. © 2008 Wiley‐Liss, Inc.
PURPOSE: To test whether B-22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and macrophage density in atherosclerotic plaques of rabbits using MRI. MATERIALS AND METHODS: A T1-weighted MRI of the aorta was acquired in 10 rabbits (7 atherosclerotic and 3 control rabbits) before and up to 2 h after intravenous injection of 100 mumol/kg of Gd-DTPA or 75 mumol/kg of B-22956/1. Plaque enhancement was measured at different time points. Immunohistochemistry was performed using anti-CD 31 antibodies and anti-RAM 11 antibodies to correlate to neovessel and macrophage density, respectively. RESULTS: MRI showed a significant plaque enhancement 2 h after B-22956/1 versus Gd-DTPA in the atherosclerotic group (39.75% versus 9.5%; P < 0.0001. Early atherosclerotic plaques (n = 146) enhancement positively correlates with neovessel density on corresponding histological sections (r = 0.42; P < 0.01). Enhancement of atherosclerotic plaques 2 h after injection of B-22956/1 correlated with macrophage density (r = 0.71; P < 0.01). CONCLUSION: Enhancement of atherosclerotic plaques with MRI correlated with neovessel density at early time points after the injection of B-22956/1 and with macrophage density, at later time points. Hence, B-22956/1-enhanced MRI represents a promising imaging technique for the identification of "high-risk" plaques.
Author Calcagno, Claudia
Cornily, Jean-Christophe
Briley-Saebo, Karen C.
Fayad, Zahi A.
Tunstead, James
Lorusso, Vito
Cavagna, Friedrich M.
Hyafil, Fabien
Mani, Venkatesh
Aguinaldo, Juan-Gilberto S.
AuthorAffiliation 3 Department of Cardiology, Hôpital Bichat, Assistance Publique-Hopitaux de Paris, Paris, France
1 Imaging Science Laboratories, Mount Sinai School of Medicine, New York, New York
5 Bracco Imaging S.p.A., Milano, Italy
2 Department of Cardiology, Hôpital de la Cavale Blanche, CHU Brest, Brest, France
4 Department of Medicine and Michael A. Wiener Cardiovascular Institute, New York, New York
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Snippet Purpose To test whether B‐22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying...
To test whether B-22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying neovessel and...
PURPOSETo test whether B-22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying...
PURPOSE: To test whether B-22956/1, a novel intravascular contrast agent with a high affinity to serum albumin (Bracco Imaging SpA.), allowed quantifying...
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SourceType Open Access Repository
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SubjectTerms Albumins
Albumins - metabolism
Animals
Aorta, Abdominal
Aorta, Abdominal - pathology
Aorta, Abdominal - ultrastructure
Atherosclerosis
Atherosclerosis - diagnosis
Atherosclerosis - pathology
Contrast Media
Contrast Media - administration & dosage
Disease Models, Animal
Gadolinium DTPA
Human health and pathology
Image Enhancement
Image Enhancement - methods
Image Processing, Computer-Assisted
Image Processing, Computer-Assisted - methods
inflammation
Life Sciences
Magnetic Resonance Imaging
Magnetic Resonance Imaging - methods
Male
Neovascularization, Pathologic
Neovascularization, Pathologic - diagnosis
Neovascularization, Pathologic - pathology
Organometallic Compounds
plaque
Rabbits
Time Factors
Tissues and Organs
Title Evaluation of neovessels in atherosclerotic plaques of rabbits using an albumin-binding intravascular contrast agent and MRI
URI https://api.istex.fr/ark:/67375/WNG-WD7P7S6G-9/fulltext.pdf
https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fjmri.21369
https://www.ncbi.nlm.nih.gov/pubmed/18504763
https://search.proquest.com/docview/71619877
https://hal.univ-brest.fr/hal-00837632
https://pubmed.ncbi.nlm.nih.gov/PMC4415534
Volume 27
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