Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).

<h4>Objective</h4>Texture analysis is an alternative method to quantitatively assess MR-images. In this study, we introduce dynamic texture parameter analysis (DTPA), a novel technique to investigate the temporal evolution of texture parameters using dynamic susceptibility contrast enhan...

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Autores principales: Rajeev Kumar Verma, Johannes Slotboom, Mirjam Rachel Heldner, Frauke Kellner-Weldon, Raimund Kottke, Christoph Ozdoba, Christian Weisstanner, Christian Philipp Kamm, Roland Wiest
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Publicado: Public Library of Science (PLoS) 2013
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spelling oai:doaj.org-article:d2e64339333b4a89ae4d6ad9ff09b2582021-11-18T07:37:36ZCharacterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).1932-620310.1371/journal.pone.0067610https://doaj.org/article/d2e64339333b4a89ae4d6ad9ff09b2582013-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23874432/?tool=EBIhttps://doaj.org/toc/1932-6203<h4>Objective</h4>Texture analysis is an alternative method to quantitatively assess MR-images. In this study, we introduce dynamic texture parameter analysis (DTPA), a novel technique to investigate the temporal evolution of texture parameters using dynamic susceptibility contrast enhanced (DSCE) imaging. Here, we aim to introduce the method and its application on enhancing lesions (EL), non-enhancing lesions (NEL) and normal appearing white matter (NAWM) in multiple sclerosis (MS).<h4>Methods</h4>We investigated 18 patients with MS and clinical isolated syndrome (CIS), according to the 2010 McDonald's criteria using DSCE imaging at different field strengths (1.5 and 3 Tesla). Tissues of interest (TOIs) were defined within 27 EL, 29 NEL and 37 NAWM areas after normalization and eight histogram-based texture parameter maps (TPMs) were computed. TPMs quantify the heterogeneity of the TOI. For every TOI, the average, variance, skewness, kurtosis and variance-of-the-variance statistical parameters were calculated. These TOI parameters were further analyzed using one-way ANOVA followed by multiple Wilcoxon sum rank testing corrected for multiple comparisons.<h4>Results</h4>Tissue- and time-dependent differences were observed in the dynamics of computed texture parameters. Sixteen parameters discriminated between EL, NEL and NAWM (pAVG = 0.0005). Significant differences in the DTPA texture maps were found during inflow (52 parameters), outflow (40 parameters) and reperfusion (62 parameters). The strongest discriminators among the TPMs were observed in the variance-related parameters, while skewness and kurtosis TPMs were in general less sensitive to detect differences between the tissues.<h4>Conclusion</h4>DTPA of DSCE image time series revealed characteristic time responses for ELs, NELs and NAWM. This may be further used for a refined quantitative grading of MS lesions during their evolution from acute to chronic state. DTPA discriminates lesions beyond features of enhancement or T2-hypersignal, on a numeric scale allowing for a more subtle grading of MS-lesions.Rajeev Kumar VermaJohannes SlotboomMirjam Rachel HeldnerFrauke Kellner-WeldonRaimund KottkeChristoph OzdobaChristian WeisstannerChristian Philipp KammRoland WiestPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 8, Iss 7, p e67610 (2013)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Rajeev Kumar Verma
Johannes Slotboom
Mirjam Rachel Heldner
Frauke Kellner-Weldon
Raimund Kottke
Christoph Ozdoba
Christian Weisstanner
Christian Philipp Kamm
Roland Wiest
Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).
description <h4>Objective</h4>Texture analysis is an alternative method to quantitatively assess MR-images. In this study, we introduce dynamic texture parameter analysis (DTPA), a novel technique to investigate the temporal evolution of texture parameters using dynamic susceptibility contrast enhanced (DSCE) imaging. Here, we aim to introduce the method and its application on enhancing lesions (EL), non-enhancing lesions (NEL) and normal appearing white matter (NAWM) in multiple sclerosis (MS).<h4>Methods</h4>We investigated 18 patients with MS and clinical isolated syndrome (CIS), according to the 2010 McDonald's criteria using DSCE imaging at different field strengths (1.5 and 3 Tesla). Tissues of interest (TOIs) were defined within 27 EL, 29 NEL and 37 NAWM areas after normalization and eight histogram-based texture parameter maps (TPMs) were computed. TPMs quantify the heterogeneity of the TOI. For every TOI, the average, variance, skewness, kurtosis and variance-of-the-variance statistical parameters were calculated. These TOI parameters were further analyzed using one-way ANOVA followed by multiple Wilcoxon sum rank testing corrected for multiple comparisons.<h4>Results</h4>Tissue- and time-dependent differences were observed in the dynamics of computed texture parameters. Sixteen parameters discriminated between EL, NEL and NAWM (pAVG = 0.0005). Significant differences in the DTPA texture maps were found during inflow (52 parameters), outflow (40 parameters) and reperfusion (62 parameters). The strongest discriminators among the TPMs were observed in the variance-related parameters, while skewness and kurtosis TPMs were in general less sensitive to detect differences between the tissues.<h4>Conclusion</h4>DTPA of DSCE image time series revealed characteristic time responses for ELs, NELs and NAWM. This may be further used for a refined quantitative grading of MS lesions during their evolution from acute to chronic state. DTPA discriminates lesions beyond features of enhancement or T2-hypersignal, on a numeric scale allowing for a more subtle grading of MS-lesions.
format article
author Rajeev Kumar Verma
Johannes Slotboom
Mirjam Rachel Heldner
Frauke Kellner-Weldon
Raimund Kottke
Christoph Ozdoba
Christian Weisstanner
Christian Philipp Kamm
Roland Wiest
author_facet Rajeev Kumar Verma
Johannes Slotboom
Mirjam Rachel Heldner
Frauke Kellner-Weldon
Raimund Kottke
Christoph Ozdoba
Christian Weisstanner
Christian Philipp Kamm
Roland Wiest
author_sort Rajeev Kumar Verma
title Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).
title_short Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).
title_full Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).
title_fullStr Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).
title_full_unstemmed Characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (DTPA).
title_sort characterization of microcirculation in multiple sclerosis lesions by dynamic texture parameter analysis (dtpa).
publisher Public Library of Science (PLoS)
publishDate 2013
url https://doaj.org/article/d2e64339333b4a89ae4d6ad9ff09b258
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