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Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction

Myocardial infarction is one of the most common human cerebrovascular conditions and frequently leads to ischemic stroke. Evidence has indicated that magnetic resonance imaging (MRI) is a potential method for the diagnosis of patients with cardiovascular injury. However, the efficacy of MRI in diagn...

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Autores principales: Qin, Jiangjun, Zhou, Shuchang, Li, Zhiwei, Chen, Yinan, Qin, Qun, Ai, Tao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143907/
https://www.ncbi.nlm.nih.gov/pubmed/30233676
http://dx.doi.org/10.3892/etm.2018.6600
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author Qin, Jiangjun
Zhou, Shuchang
Li, Zhiwei
Chen, Yinan
Qin, Qun
Ai, Tao
author_facet Qin, Jiangjun
Zhou, Shuchang
Li, Zhiwei
Chen, Yinan
Qin, Qun
Ai, Tao
author_sort Qin, Jiangjun
collection PubMed
description Myocardial infarction is one of the most common human cerebrovascular conditions and frequently leads to ischemic stroke. Evidence has indicated that magnetic resonance imaging (MRI) is a potential method for the diagnosis of patients with cardiovascular injury. However, the efficacy of MRI in diagnosing patients with myocardial infarction requires to be improved. In the present study, a novel nano-size contrast agent, a chitosan/Fe(3)O(4)-enclosed albumin (CFEA), was introduced that was used to quantify blood volume and permeability in the infarcted myocardium. A total of 68 patients with suspected myocardial infarction were recruited to analyze the efficacy of MRI combined with CFEA (MRI-CFEA). All patients received diagnosis by MRI and MRI-CFEA. It was revealed that MRI-CFEA provided a higher signal intensity than MRI in the same patients. It was demonstrated that the diagnostic efficacy of MRI-CFEA for patients with myocardial infarction was higher than that of MRI (P<0.05). By MRI-CFEA, 50/68 of cases with myocardial infarction were diagnosed, providing a significantly higher diagnostic rate compared with the 38/68 of cases diagnosed by contrast-enhanced MRI (P<0.01). MRI-CFEA successfully discriminated the infarcted regions based on a decreased fractional blood volume and increased permeability-surface (PS) area product in the infarcted myocardium. A pharmacodynamics analysis indicated that CFEA was eliminated within 24 h in all individuals. In conclusion, the present study provided a novel method to diagnose infarcted myocardium for patients with myocardial infarction, providing an imaging biomarker for the assessment of endothelial dysfunction in the clinic.
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spelling pubmed-61439072018-09-19 Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction Qin, Jiangjun Zhou, Shuchang Li, Zhiwei Chen, Yinan Qin, Qun Ai, Tao Exp Ther Med Articles Myocardial infarction is one of the most common human cerebrovascular conditions and frequently leads to ischemic stroke. Evidence has indicated that magnetic resonance imaging (MRI) is a potential method for the diagnosis of patients with cardiovascular injury. However, the efficacy of MRI in diagnosing patients with myocardial infarction requires to be improved. In the present study, a novel nano-size contrast agent, a chitosan/Fe(3)O(4)-enclosed albumin (CFEA), was introduced that was used to quantify blood volume and permeability in the infarcted myocardium. A total of 68 patients with suspected myocardial infarction were recruited to analyze the efficacy of MRI combined with CFEA (MRI-CFEA). All patients received diagnosis by MRI and MRI-CFEA. It was revealed that MRI-CFEA provided a higher signal intensity than MRI in the same patients. It was demonstrated that the diagnostic efficacy of MRI-CFEA for patients with myocardial infarction was higher than that of MRI (P<0.05). By MRI-CFEA, 50/68 of cases with myocardial infarction were diagnosed, providing a significantly higher diagnostic rate compared with the 38/68 of cases diagnosed by contrast-enhanced MRI (P<0.01). MRI-CFEA successfully discriminated the infarcted regions based on a decreased fractional blood volume and increased permeability-surface (PS) area product in the infarcted myocardium. A pharmacodynamics analysis indicated that CFEA was eliminated within 24 h in all individuals. In conclusion, the present study provided a novel method to diagnose infarcted myocardium for patients with myocardial infarction, providing an imaging biomarker for the assessment of endothelial dysfunction in the clinic. D.A. Spandidos 2018-10 2018-08-13 /pmc/articles/PMC6143907/ /pubmed/30233676 http://dx.doi.org/10.3892/etm.2018.6600 Text en Copyright: © Qin et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Qin, Jiangjun
Zhou, Shuchang
Li, Zhiwei
Chen, Yinan
Qin, Qun
Ai, Tao
Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
title Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
title_full Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
title_fullStr Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
title_full_unstemmed Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
title_short Combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
title_sort combination of magnetic resonance imaging and targeted contrast agent for the diagnosis of myocardial infarction
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6143907/
https://www.ncbi.nlm.nih.gov/pubmed/30233676
http://dx.doi.org/10.3892/etm.2018.6600
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