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High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI

BACKGROUND: Atherosclerosis is prevalent in cardiovascular disease, but present imaging modalities have limited capabilities for characterizing lesion stage, progression and response to intervention. This study tests whether intravascular magnetic resonance imaging (IVMRI) measures of relaxation tim...

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Autores principales: Wang, Guan, Zhang, Yi, Hegde, Shashank Sathyanarayana, Bottomley, Paul A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694914/
https://www.ncbi.nlm.nih.gov/pubmed/29157260
http://dx.doi.org/10.1186/s12968-017-0399-6
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author Wang, Guan
Zhang, Yi
Hegde, Shashank Sathyanarayana
Bottomley, Paul A.
author_facet Wang, Guan
Zhang, Yi
Hegde, Shashank Sathyanarayana
Bottomley, Paul A.
author_sort Wang, Guan
collection PubMed
description BACKGROUND: Atherosclerosis is prevalent in cardiovascular disease, but present imaging modalities have limited capabilities for characterizing lesion stage, progression and response to intervention. This study tests whether intravascular magnetic resonance imaging (IVMRI) measures of relaxation times (T(1), T(2)) and proton density (PD) in a clinical 3 Tesla scanner could characterize vessel disease, and evaluates a practical strategy for accelerated quantification. METHODS: IVMRI was performed in fresh human artery segments and swine vessels in vivo, using fast multi-parametric sequences, 1–2 mm diameter loopless antennae and 200–300 μm resolution. T(1), T(2) and PD data were used to train a machine learning classifier (support vector machine, SVM) to automatically classify normal vessel, and early or advanced disease, using histology for validation. Disease identification using the SVM was tested with receiver operating characteristic curves. To expedite acquisition of T(1), T(2) and PD data for vessel characterization, the linear algebraic method (‘SLAM’) was modified to accommodate the antenna’s highly-nonuniform sensitivity, and used to provide average T(1), T(2) and PD measurements from compartments of normal and pathological tissue segmented from high-resolution images at acceleration factors of R ≤ 18-fold. The results were validated using compartment-average measures derived from the high-resolution scans. RESULTS: The SVM accurately classified ~80% of samples into the three disease classes. The ‘area-under-the-curve’ was 0.96 for detecting disease in 248 samples, with T(1) providing the best discrimination. SLAM T(1), T(2) and PD measures for R ≤ 10 were indistinguishable from the true means of segmented tissue compartments. CONCLUSION: High-resolution IVMRI measures of T(1), T(2) and PD with a trained SVM can automatically classify normal, early and advanced atherosclerosis with high sensitivity and specificity. Replacing relaxometric MRI with SLAM yields good estimates of T(1), T(2) and PD an order-of-magnitude faster to facilitate IVMRI-based characterization of vessel disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12968-017-0399-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-56949142017-11-27 High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI Wang, Guan Zhang, Yi Hegde, Shashank Sathyanarayana Bottomley, Paul A. J Cardiovasc Magn Reson Research BACKGROUND: Atherosclerosis is prevalent in cardiovascular disease, but present imaging modalities have limited capabilities for characterizing lesion stage, progression and response to intervention. This study tests whether intravascular magnetic resonance imaging (IVMRI) measures of relaxation times (T(1), T(2)) and proton density (PD) in a clinical 3 Tesla scanner could characterize vessel disease, and evaluates a practical strategy for accelerated quantification. METHODS: IVMRI was performed in fresh human artery segments and swine vessels in vivo, using fast multi-parametric sequences, 1–2 mm diameter loopless antennae and 200–300 μm resolution. T(1), T(2) and PD data were used to train a machine learning classifier (support vector machine, SVM) to automatically classify normal vessel, and early or advanced disease, using histology for validation. Disease identification using the SVM was tested with receiver operating characteristic curves. To expedite acquisition of T(1), T(2) and PD data for vessel characterization, the linear algebraic method (‘SLAM’) was modified to accommodate the antenna’s highly-nonuniform sensitivity, and used to provide average T(1), T(2) and PD measurements from compartments of normal and pathological tissue segmented from high-resolution images at acceleration factors of R ≤ 18-fold. The results were validated using compartment-average measures derived from the high-resolution scans. RESULTS: The SVM accurately classified ~80% of samples into the three disease classes. The ‘area-under-the-curve’ was 0.96 for detecting disease in 248 samples, with T(1) providing the best discrimination. SLAM T(1), T(2) and PD measures for R ≤ 10 were indistinguishable from the true means of segmented tissue compartments. CONCLUSION: High-resolution IVMRI measures of T(1), T(2) and PD with a trained SVM can automatically classify normal, early and advanced atherosclerosis with high sensitivity and specificity. Replacing relaxometric MRI with SLAM yields good estimates of T(1), T(2) and PD an order-of-magnitude faster to facilitate IVMRI-based characterization of vessel disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12968-017-0399-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-11-20 /pmc/articles/PMC5694914/ /pubmed/29157260 http://dx.doi.org/10.1186/s12968-017-0399-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Guan
Zhang, Yi
Hegde, Shashank Sathyanarayana
Bottomley, Paul A.
High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI
title High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI
title_full High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI
title_fullStr High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI
title_full_unstemmed High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI
title_short High-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular MRI
title_sort high-resolution and accelerated multi-parametric mapping with automated characterization of vessel disease using intravascular mri
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694914/
https://www.ncbi.nlm.nih.gov/pubmed/29157260
http://dx.doi.org/10.1186/s12968-017-0399-6
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