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T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis

PURPOSE: In multiple sclerosis (MS) the sensitivity for detection of contrast enhancing lesions (CEL) in T1-weighted scans is essential for diagnostics and therapy decisions. The purpose of our study was to evaluate the sensitivity of T1w MPRAGE scans in comparison to T1w dark blood technique (T1-DB...

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Autores principales: Thaler, Christian, Schneider, Tanja, Sedlacik, Jan, Kutzner, Daniel, Stellmann, Jan-Patrick, Heesen, Christoph, Fiehler, Jens, Siemonsen, Susanne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552307/
https://www.ncbi.nlm.nih.gov/pubmed/28797082
http://dx.doi.org/10.1371/journal.pone.0183099
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author Thaler, Christian
Schneider, Tanja
Sedlacik, Jan
Kutzner, Daniel
Stellmann, Jan-Patrick
Heesen, Christoph
Fiehler, Jens
Siemonsen, Susanne
author_facet Thaler, Christian
Schneider, Tanja
Sedlacik, Jan
Kutzner, Daniel
Stellmann, Jan-Patrick
Heesen, Christoph
Fiehler, Jens
Siemonsen, Susanne
author_sort Thaler, Christian
collection PubMed
description PURPOSE: In multiple sclerosis (MS) the sensitivity for detection of contrast enhancing lesions (CEL) in T1-weighted scans is essential for diagnostics and therapy decisions. The purpose of our study was to evaluate the sensitivity of T1w MPRAGE scans in comparison to T1w dark blood technique (T1-DB) for CEL in MS. MATERIALS AND METHODS: 3T MR imaging was performed in 37 MS patients, including T2-weighted imaging, T1w MPRAGE before and after gadolinium injection (unenhanced-T1 and T1-CE) and T1-DB imaging. After gadolinium application, the T1-DB scan was performed prior to T1-CE. From unenhanced-T1 and T1-CE scans, subtraction images (T1-SUB) were calculated. The number of CEL was determined separately on T1-CE and T1-DB by two raters independently. Lesions only detected on T1-DB scans then were verified on T1-SUB. Only lesions detected by both raters were included in further analysis. RESULTS: In 16 patients, at least one CEL was detected by both rater, either on T1-CE or T1-DB. All lesions that were detected on T1-CE were also detected on T1-DB images. The total number of contrast enhancing lesions detected on T1-DB images (n = 54) by both raters was significantly higher than the corresponding number of lesions identified on T1-CE (n = 27) (p = 0.01); all of these lesions could be verified on SUB images. In 21 patients, no CEL was detected in any of the sequences. CONCLUSIONS: The application of T1-DB technique increases the sensitivity for CEL in MS, especially for those lesions that show only subtle increase in intensity after Gadolinium application but remain hypo- or iso-intense to surrounding tissue.
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spelling pubmed-55523072017-08-25 T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis Thaler, Christian Schneider, Tanja Sedlacik, Jan Kutzner, Daniel Stellmann, Jan-Patrick Heesen, Christoph Fiehler, Jens Siemonsen, Susanne PLoS One Research Article PURPOSE: In multiple sclerosis (MS) the sensitivity for detection of contrast enhancing lesions (CEL) in T1-weighted scans is essential for diagnostics and therapy decisions. The purpose of our study was to evaluate the sensitivity of T1w MPRAGE scans in comparison to T1w dark blood technique (T1-DB) for CEL in MS. MATERIALS AND METHODS: 3T MR imaging was performed in 37 MS patients, including T2-weighted imaging, T1w MPRAGE before and after gadolinium injection (unenhanced-T1 and T1-CE) and T1-DB imaging. After gadolinium application, the T1-DB scan was performed prior to T1-CE. From unenhanced-T1 and T1-CE scans, subtraction images (T1-SUB) were calculated. The number of CEL was determined separately on T1-CE and T1-DB by two raters independently. Lesions only detected on T1-DB scans then were verified on T1-SUB. Only lesions detected by both raters were included in further analysis. RESULTS: In 16 patients, at least one CEL was detected by both rater, either on T1-CE or T1-DB. All lesions that were detected on T1-CE were also detected on T1-DB images. The total number of contrast enhancing lesions detected on T1-DB images (n = 54) by both raters was significantly higher than the corresponding number of lesions identified on T1-CE (n = 27) (p = 0.01); all of these lesions could be verified on SUB images. In 21 patients, no CEL was detected in any of the sequences. CONCLUSIONS: The application of T1-DB technique increases the sensitivity for CEL in MS, especially for those lesions that show only subtle increase in intensity after Gadolinium application but remain hypo- or iso-intense to surrounding tissue. Public Library of Science 2017-08-10 /pmc/articles/PMC5552307/ /pubmed/28797082 http://dx.doi.org/10.1371/journal.pone.0183099 Text en © 2017 Thaler et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Thaler, Christian
Schneider, Tanja
Sedlacik, Jan
Kutzner, Daniel
Stellmann, Jan-Patrick
Heesen, Christoph
Fiehler, Jens
Siemonsen, Susanne
T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
title T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
title_full T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
title_fullStr T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
title_full_unstemmed T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
title_short T1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
title_sort t1w dark blood imaging improves detection of contrast enhancing lesions in multiple sclerosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5552307/
https://www.ncbi.nlm.nih.gov/pubmed/28797082
http://dx.doi.org/10.1371/journal.pone.0183099
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