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Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas
The apparent diffusion coefficient (ADC) derived from diffusion-weighted imaging (DWI) correlates inversely with tumor proliferation rates. High-grade gliomas are typically heterogeneous and the delineation of areas of high and low proliferation is impeded by partial volume effects and blurred borde...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
e-Med
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335334/ https://www.ncbi.nlm.nih.gov/pubmed/22487677 http://dx.doi.org/10.1102/1470-7330.2012.0010 |
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author | Simon, Dirk Fritzsche, Klaus H. Thieke, Christian Klein, Jan Parzer, Peter Weber, Marc-André Stieltjes, Bram |
author_facet | Simon, Dirk Fritzsche, Klaus H. Thieke, Christian Klein, Jan Parzer, Peter Weber, Marc-André Stieltjes, Bram |
author_sort | Simon, Dirk |
collection | PubMed |
description | The apparent diffusion coefficient (ADC) derived from diffusion-weighted imaging (DWI) correlates inversely with tumor proliferation rates. High-grade gliomas are typically heterogeneous and the delineation of areas of high and low proliferation is impeded by partial volume effects and blurred borders. Commonly used manual delineation is further impeded by potential overlap with cerebrospinal fluid and necrosis. Here we present an algorithm to reproducibly delineate and probabilistically quantify the ADC in areas of high and low proliferation in heterogeneous gliomas, resulting in a reproducible quantification in regions of tissue inhomogeneity. We used an expectation maximization (EM) clustering algorithm, applied on a Gaussian mixture model, consisting of pure superpositions of Gaussian distributions. Soundness and reproducibility of this approach were evaluated in 10 patients with glioma. High- and low-proliferating areas found using the clustering correspond well with conservative regions of interest drawn using all available imaging data. Systematic placement of model initialization seeds shows good reproducibility of the method. Moreover, we illustrate an automatic initialization approach that completely removes user-induced variability. In conclusion, we present a rapid, reproducible and automatic method to separate and quantify heterogeneous regions in gliomas. |
format | Online Article Text |
id | pubmed-3335334 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | e-Med |
record_format | MEDLINE/PubMed |
spelling | pubmed-33353342014-04-05 Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas Simon, Dirk Fritzsche, Klaus H. Thieke, Christian Klein, Jan Parzer, Peter Weber, Marc-André Stieltjes, Bram Cancer Imaging Original Article The apparent diffusion coefficient (ADC) derived from diffusion-weighted imaging (DWI) correlates inversely with tumor proliferation rates. High-grade gliomas are typically heterogeneous and the delineation of areas of high and low proliferation is impeded by partial volume effects and blurred borders. Commonly used manual delineation is further impeded by potential overlap with cerebrospinal fluid and necrosis. Here we present an algorithm to reproducibly delineate and probabilistically quantify the ADC in areas of high and low proliferation in heterogeneous gliomas, resulting in a reproducible quantification in regions of tissue inhomogeneity. We used an expectation maximization (EM) clustering algorithm, applied on a Gaussian mixture model, consisting of pure superpositions of Gaussian distributions. Soundness and reproducibility of this approach were evaluated in 10 patients with glioma. High- and low-proliferating areas found using the clustering correspond well with conservative regions of interest drawn using all available imaging data. Systematic placement of model initialization seeds shows good reproducibility of the method. Moreover, we illustrate an automatic initialization approach that completely removes user-induced variability. In conclusion, we present a rapid, reproducible and automatic method to separate and quantify heterogeneous regions in gliomas. e-Med 2012-04-05 /pmc/articles/PMC3335334/ /pubmed/22487677 http://dx.doi.org/10.1102/1470-7330.2012.0010 Text en © 2012 International Cancer Imaging Society |
spellingShingle | Original Article Simon, Dirk Fritzsche, Klaus H. Thieke, Christian Klein, Jan Parzer, Peter Weber, Marc-André Stieltjes, Bram Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
title | Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
title_full | Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
title_fullStr | Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
title_full_unstemmed | Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
title_short | Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
title_sort | diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3335334/ https://www.ncbi.nlm.nih.gov/pubmed/22487677 http://dx.doi.org/10.1102/1470-7330.2012.0010 |
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