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Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes

BACKGROUND: Semi-quantitative evaluation of Modic changes (MCs) has recently been proposed as a way to standardise and increase repeatability of clinical studies. This study is aimed at developing semi-quantitative measures of enhancement, given by contrast agent injection, on T1-weighted images in...

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Autores principales: Tibiletti, Marta, Ciavarro, Cristina, Bari, Vlasta, McCall, Iain W., Urban, Jill P. G., Brayda-Bruno, Marco, Galbusera, Fabio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909339/
https://www.ncbi.nlm.nih.gov/pubmed/29708181
http://dx.doi.org/10.1186/s41747-017-0009-2
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author Tibiletti, Marta
Ciavarro, Cristina
Bari, Vlasta
McCall, Iain W.
Urban, Jill P. G.
Brayda-Bruno, Marco
Galbusera, Fabio
author_facet Tibiletti, Marta
Ciavarro, Cristina
Bari, Vlasta
McCall, Iain W.
Urban, Jill P. G.
Brayda-Bruno, Marco
Galbusera, Fabio
author_sort Tibiletti, Marta
collection PubMed
description BACKGROUND: Semi-quantitative evaluation of Modic changes (MCs) has recently been proposed as a way to standardise and increase repeatability of clinical studies. This study is aimed at developing semi-quantitative measures of enhancement, given by contrast agent injection, on T1-weighted images in MCs, and to investigate their reliability and relation with MC types. METHODS: Thirty-seven subjects suffering from low back pain underwent T1-weighted and T2-weighted turbo spin-echo sequences. Five minutes after the injection of a paramagnetic contrast agent, a second T1-weighted sequence was acquired. Regions of interest (ROIs) corresponding to MCs were selected manually on the unenhanced image; control ROIs in the “healthy” bone marrow were selected. For each ROI, the mean signal intensity (SI) of unenhanced pixels and the mean absolute and normalised difference in SI between unenhanced and contrast-enhanced pixels values were calculated. RESULTS: A total of 103 MCs were recognised and 61 were semi-quantitatively analysed: 16 type I, 34 type II and 11 type I/II. Regarding controls, MCs I showed a lower SI on the unenhanced T1-weighted images and a marked contrast enhancement (CE); MCs II showed a higher SI than controls on unenhanced images and a lower or comparable CE; and MCs I/II presented an intermediate SI on the unenhanced images and a marked CE. Inter-rater and intra-rater agreements were found to be excellent or substantial. CONCLUSIONS: Semi-quantitative measurements could differentiate MC types in terms of unenhanced SI and of CE with respect to “healthy” bone marrow.
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spelling pubmed-59093392018-04-24 Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes Tibiletti, Marta Ciavarro, Cristina Bari, Vlasta McCall, Iain W. Urban, Jill P. G. Brayda-Bruno, Marco Galbusera, Fabio Eur Radiol Exp Original Article BACKGROUND: Semi-quantitative evaluation of Modic changes (MCs) has recently been proposed as a way to standardise and increase repeatability of clinical studies. This study is aimed at developing semi-quantitative measures of enhancement, given by contrast agent injection, on T1-weighted images in MCs, and to investigate their reliability and relation with MC types. METHODS: Thirty-seven subjects suffering from low back pain underwent T1-weighted and T2-weighted turbo spin-echo sequences. Five minutes after the injection of a paramagnetic contrast agent, a second T1-weighted sequence was acquired. Regions of interest (ROIs) corresponding to MCs were selected manually on the unenhanced image; control ROIs in the “healthy” bone marrow were selected. For each ROI, the mean signal intensity (SI) of unenhanced pixels and the mean absolute and normalised difference in SI between unenhanced and contrast-enhanced pixels values were calculated. RESULTS: A total of 103 MCs were recognised and 61 were semi-quantitatively analysed: 16 type I, 34 type II and 11 type I/II. Regarding controls, MCs I showed a lower SI on the unenhanced T1-weighted images and a marked contrast enhancement (CE); MCs II showed a higher SI than controls on unenhanced images and a lower or comparable CE; and MCs I/II presented an intermediate SI on the unenhanced images and a marked CE. Inter-rater and intra-rater agreements were found to be excellent or substantial. CONCLUSIONS: Semi-quantitative measurements could differentiate MC types in terms of unenhanced SI and of CE with respect to “healthy” bone marrow. Springer International Publishing 2017-06-29 /pmc/articles/PMC5909339/ /pubmed/29708181 http://dx.doi.org/10.1186/s41747-017-0009-2 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.
spellingShingle Original Article
Tibiletti, Marta
Ciavarro, Cristina
Bari, Vlasta
McCall, Iain W.
Urban, Jill P. G.
Brayda-Bruno, Marco
Galbusera, Fabio
Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes
title Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes
title_full Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes
title_fullStr Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes
title_full_unstemmed Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes
title_short Semi-quantitative evaluation of signal intensity and contrast-enhancement in Modic changes
title_sort semi-quantitative evaluation of signal intensity and contrast-enhancement in modic changes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5909339/
https://www.ncbi.nlm.nih.gov/pubmed/29708181
http://dx.doi.org/10.1186/s41747-017-0009-2
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