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T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients
BACKGROUND: Magnetic Resonance Imaging (MRI) is an established tool in diagnosing and evaluating disease activity in Multiple Sclerosis (MS). While clinical-radiological correlations are limited in general, hypointense T1 lesions (also known as Black Holes (BH)) have shown some promising results. Th...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676682/ https://www.ncbi.nlm.nih.gov/pubmed/26659852 http://dx.doi.org/10.1371/journal.pone.0144693 |
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author | Thaler, Christian Faizy, Tobias Sedlacik, Jan Holst, Brigitte Stellmann, Jan-Patrick Young, Kim Lea Heesen, Christoph Fiehler, Jens Siemonsen, Susanne |
author_facet | Thaler, Christian Faizy, Tobias Sedlacik, Jan Holst, Brigitte Stellmann, Jan-Patrick Young, Kim Lea Heesen, Christoph Fiehler, Jens Siemonsen, Susanne |
author_sort | Thaler, Christian |
collection | PubMed |
description | BACKGROUND: Magnetic Resonance Imaging (MRI) is an established tool in diagnosing and evaluating disease activity in Multiple Sclerosis (MS). While clinical-radiological correlations are limited in general, hypointense T1 lesions (also known as Black Holes (BH)) have shown some promising results. The definition of BHs is very heterogeneous and depends on subjective visual evaluation. OBJECTIVE: We aimed to improve clinical-radiological correlations by defining BHs using T1 relaxation time (T1-RT) thresholds to achieve best possible correlation between BH lesion volume and clinical disability. METHOD: 40 patients with mainly relapsing-remitting MS underwent MRI including 3-dimensional fluid attenuated inversion recovery (FLAIR), magnetization-prepared rapid gradient echo (MPRAGE) before and after Gadolinium (GD) injection and double inversion-contrast magnetization-prepared rapid gradient echo (MP2RAGE) sequences. BHs (BH(vis)) were marked by two raters on native T1-weighted (T1w)-MPRAGE, contrast-enhancing lesions (CE lesions) on T1w-MPRAGE after GD and FLAIR lesions (total-FLAIR lesions) were detected separately. BH(vis) and total-FLAIR lesion maps were registered to MP2RAGE images, and the mean T1-RT were calculated for all lesion ROIs. Mean T1 values of the cortex (CTX) were calculated for each patient. Subsequently, Spearman rank correlations between clinical scores (Expanded Disability Status Scale and Multiple Sclerosis Functional Composite) and lesion volume were determined for different T1-RT thresholds. RESULTS: Significant differences in T1-RT were obtained between all different lesion types with highest T1 values in visually marked BHs (BH(vis): 1453.3±213.4 ms, total-FLAIR lesions: 1394.33±187.38 ms, CTX: 1305.6±35.8 ms; p<0.05). Significant correlations between BH(vis)/total-FLAIR lesion volume and clinical disability were obtained for a wide range of T1-RT thresholds. The highest correlation for BH(vis) and total-FLAIR lesion masks were found at T1-RT>1500 ms (Expanded Disability Status Scale vs. lesion volume: r(BHvis) = 0.442 and r(total-FLAIR) = 0.497, p<0.05; Multiple Sclerosis Functional Composite vs. lesion volume: r(BHvis) = -0.53 and r(total-FLAIR) = -0.627, p<0.05). CONCLUSION: Clinical-radiological correlations in MS patients are increased by application of T1-RT thresholds. With the short acquisition time of the MP2RAGE sequences, quantitative T1 maps could be easily established in clinical studies. |
format | Online Article Text |
id | pubmed-4676682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46766822015-12-31 T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients Thaler, Christian Faizy, Tobias Sedlacik, Jan Holst, Brigitte Stellmann, Jan-Patrick Young, Kim Lea Heesen, Christoph Fiehler, Jens Siemonsen, Susanne PLoS One Research Article BACKGROUND: Magnetic Resonance Imaging (MRI) is an established tool in diagnosing and evaluating disease activity in Multiple Sclerosis (MS). While clinical-radiological correlations are limited in general, hypointense T1 lesions (also known as Black Holes (BH)) have shown some promising results. The definition of BHs is very heterogeneous and depends on subjective visual evaluation. OBJECTIVE: We aimed to improve clinical-radiological correlations by defining BHs using T1 relaxation time (T1-RT) thresholds to achieve best possible correlation between BH lesion volume and clinical disability. METHOD: 40 patients with mainly relapsing-remitting MS underwent MRI including 3-dimensional fluid attenuated inversion recovery (FLAIR), magnetization-prepared rapid gradient echo (MPRAGE) before and after Gadolinium (GD) injection and double inversion-contrast magnetization-prepared rapid gradient echo (MP2RAGE) sequences. BHs (BH(vis)) were marked by two raters on native T1-weighted (T1w)-MPRAGE, contrast-enhancing lesions (CE lesions) on T1w-MPRAGE after GD and FLAIR lesions (total-FLAIR lesions) were detected separately. BH(vis) and total-FLAIR lesion maps were registered to MP2RAGE images, and the mean T1-RT were calculated for all lesion ROIs. Mean T1 values of the cortex (CTX) were calculated for each patient. Subsequently, Spearman rank correlations between clinical scores (Expanded Disability Status Scale and Multiple Sclerosis Functional Composite) and lesion volume were determined for different T1-RT thresholds. RESULTS: Significant differences in T1-RT were obtained between all different lesion types with highest T1 values in visually marked BHs (BH(vis): 1453.3±213.4 ms, total-FLAIR lesions: 1394.33±187.38 ms, CTX: 1305.6±35.8 ms; p<0.05). Significant correlations between BH(vis)/total-FLAIR lesion volume and clinical disability were obtained for a wide range of T1-RT thresholds. The highest correlation for BH(vis) and total-FLAIR lesion masks were found at T1-RT>1500 ms (Expanded Disability Status Scale vs. lesion volume: r(BHvis) = 0.442 and r(total-FLAIR) = 0.497, p<0.05; Multiple Sclerosis Functional Composite vs. lesion volume: r(BHvis) = -0.53 and r(total-FLAIR) = -0.627, p<0.05). CONCLUSION: Clinical-radiological correlations in MS patients are increased by application of T1-RT thresholds. With the short acquisition time of the MP2RAGE sequences, quantitative T1 maps could be easily established in clinical studies. Public Library of Science 2015-12-11 /pmc/articles/PMC4676682/ /pubmed/26659852 http://dx.doi.org/10.1371/journal.pone.0144693 Text en © 2015 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Thaler, Christian Faizy, Tobias Sedlacik, Jan Holst, Brigitte Stellmann, Jan-Patrick Young, Kim Lea Heesen, Christoph Fiehler, Jens Siemonsen, Susanne T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients |
title | T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients |
title_full | T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients |
title_fullStr | T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients |
title_full_unstemmed | T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients |
title_short | T1- Thresholds in Black Holes Increase Clinical-Radiological Correlation in Multiple Sclerosis Patients |
title_sort | t1- thresholds in black holes increase clinical-radiological correlation in multiple sclerosis patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4676682/ https://www.ncbi.nlm.nih.gov/pubmed/26659852 http://dx.doi.org/10.1371/journal.pone.0144693 |
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