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Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla
OBJECTIVE: To investigate the impact of a higher magnetic field strength of 3 Tesla (T) on the detection rate of cortical lesions in multiple sclerosis (MS) patients, in particular using a dedicated double inversion recovery (DIR) pulse sequence. METHODS: Thirty-four patients with clinically isolate...
Autores principales: | , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Springer-Verlag
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882050/ https://www.ncbi.nlm.nih.gov/pubmed/20094887 http://dx.doi.org/10.1007/s00330-009-1705-y |
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author | Simon, Birgit Schmidt, Stephan Lukas, Carsten Gieseke, Jürgen Träber, Frank Knol, Dirk L. Willinek, Winfried A. Geurts, Jeroen J. G. Schild, Hans H. Barkhof, Frederik Wattjes, Mike P. |
author_facet | Simon, Birgit Schmidt, Stephan Lukas, Carsten Gieseke, Jürgen Träber, Frank Knol, Dirk L. Willinek, Winfried A. Geurts, Jeroen J. G. Schild, Hans H. Barkhof, Frederik Wattjes, Mike P. |
author_sort | Simon, Birgit |
collection | PubMed |
description | OBJECTIVE: To investigate the impact of a higher magnetic field strength of 3 Tesla (T) on the detection rate of cortical lesions in multiple sclerosis (MS) patients, in particular using a dedicated double inversion recovery (DIR) pulse sequence. METHODS: Thirty-four patients with clinically isolated syndromes or definite MS were included. All patients underwent magnetic resonance imaging (MRI) at 1.5 T and 3 T, including T2-weighted turbo spin echo (TSE), fluid-attenuated inversion recovery (FLAIR) and DIR sequences. All images were analysed for focal lesions categorised according to their anatomical location. RESULTS: The total number of detected lesions was higher at 3 T across all pulse sequences. We observed significantly higher numbers of lesions involving the cortex at 3 T using a DIR sequence. DIR at 3 T showed 192% more pure intracortical (p < 0.001) and 30% more mixed grey matter-white matter lesions (p = 0.008). No significant increase in cortical lesions could be detected on the FLAIR and T2-weighted images. Using the T2-weighted and FLAIR sequences, significantly more lesions could be detected at 3 T in the infratentorial, periventricular and juxtacortical white matter. CONCLUSION: DIR brain MR imaging at 3 T substantially improves the sensitivity of the detection of cortical lesions compared with the standard magnetic field strength of 1.5 T. |
format | Text |
id | pubmed-2882050 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-28820502010-06-10 Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla Simon, Birgit Schmidt, Stephan Lukas, Carsten Gieseke, Jürgen Träber, Frank Knol, Dirk L. Willinek, Winfried A. Geurts, Jeroen J. G. Schild, Hans H. Barkhof, Frederik Wattjes, Mike P. Eur Radiol Neuro OBJECTIVE: To investigate the impact of a higher magnetic field strength of 3 Tesla (T) on the detection rate of cortical lesions in multiple sclerosis (MS) patients, in particular using a dedicated double inversion recovery (DIR) pulse sequence. METHODS: Thirty-four patients with clinically isolated syndromes or definite MS were included. All patients underwent magnetic resonance imaging (MRI) at 1.5 T and 3 T, including T2-weighted turbo spin echo (TSE), fluid-attenuated inversion recovery (FLAIR) and DIR sequences. All images were analysed for focal lesions categorised according to their anatomical location. RESULTS: The total number of detected lesions was higher at 3 T across all pulse sequences. We observed significantly higher numbers of lesions involving the cortex at 3 T using a DIR sequence. DIR at 3 T showed 192% more pure intracortical (p < 0.001) and 30% more mixed grey matter-white matter lesions (p = 0.008). No significant increase in cortical lesions could be detected on the FLAIR and T2-weighted images. Using the T2-weighted and FLAIR sequences, significantly more lesions could be detected at 3 T in the infratentorial, periventricular and juxtacortical white matter. CONCLUSION: DIR brain MR imaging at 3 T substantially improves the sensitivity of the detection of cortical lesions compared with the standard magnetic field strength of 1.5 T. Springer-Verlag 2010-01-22 2010 /pmc/articles/PMC2882050/ /pubmed/20094887 http://dx.doi.org/10.1007/s00330-009-1705-y Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Neuro Simon, Birgit Schmidt, Stephan Lukas, Carsten Gieseke, Jürgen Träber, Frank Knol, Dirk L. Willinek, Winfried A. Geurts, Jeroen J. G. Schild, Hans H. Barkhof, Frederik Wattjes, Mike P. Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla |
title | Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla |
title_full | Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla |
title_fullStr | Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla |
title_full_unstemmed | Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla |
title_short | Improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery MR imaging at 3 Tesla |
title_sort | improved in vivo detection of cortical lesions in multiple sclerosis using double inversion recovery mr imaging at 3 tesla |
topic | Neuro |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882050/ https://www.ncbi.nlm.nih.gov/pubmed/20094887 http://dx.doi.org/10.1007/s00330-009-1705-y |
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