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Validation and comparison of two automated methods for quantifying brain white matter hyperintensities of presumed vascular origin
OBJECTIVES: White matter hyperintensities (WMH) are a common imaging finding indicative of cerebral small vessel disease. Lesion segmentation algorithms have been developed to overcome issues arising from visual rating scales. In this study, we evaluated two automated methods and compared them to vi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607266/ https://www.ncbi.nlm.nih.gov/pubmed/31612759 http://dx.doi.org/10.1177/0300060519880053 |
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author | Waymont, Jennifer M.J. Petsa, Chariklia McNeil, Chris J. Murray, Alison D. Waiter, Gordon D. |
author_facet | Waymont, Jennifer M.J. Petsa, Chariklia McNeil, Chris J. Murray, Alison D. Waiter, Gordon D. |
author_sort | Waymont, Jennifer M.J. |
collection | PubMed |
description | OBJECTIVES: White matter hyperintensities (WMH) are a common imaging finding indicative of cerebral small vessel disease. Lesion segmentation algorithms have been developed to overcome issues arising from visual rating scales. In this study, we evaluated two automated methods and compared them to visual and manual segmentation to determine the most robust algorithm provided by the open-source Lesion Segmentation Toolbox (LST). METHODS: We compared WMH data from visual ratings (Scheltens’ scale) with those derived from algorithms provided within LST. We then compared spatial and volumetric WMH data derived from manually-delineated lesion maps with WMH data and lesion maps provided by the LST algorithms. RESULTS: We identified optimal initial thresholds for algorithms provided by LST compared with visual ratings (Lesion Growth Algorithm (LGA): initial κ and lesion probability thresholds, 0.5; Lesion Probability Algorithm (LPA) lesion probability threshold, 0.65). LGA was found to perform better then LPA compared with manual segmentation. CONCLUSION: LGA appeared to be the most suitable algorithm for quantifying WMH in relation to cerebral small vessel disease, compared with Scheltens’ score and manual segmentation. LGA offers a user-friendly, effective WMH segmentation method in the research environment. |
format | Online Article Text |
id | pubmed-7607266 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-76072662020-11-13 Validation and comparison of two automated methods for quantifying brain white matter hyperintensities of presumed vascular origin Waymont, Jennifer M.J. Petsa, Chariklia McNeil, Chris J. Murray, Alison D. Waiter, Gordon D. J Int Med Res Special Issue: Cerebral Small Vessel Disease: Recent Trends OBJECTIVES: White matter hyperintensities (WMH) are a common imaging finding indicative of cerebral small vessel disease. Lesion segmentation algorithms have been developed to overcome issues arising from visual rating scales. In this study, we evaluated two automated methods and compared them to visual and manual segmentation to determine the most robust algorithm provided by the open-source Lesion Segmentation Toolbox (LST). METHODS: We compared WMH data from visual ratings (Scheltens’ scale) with those derived from algorithms provided within LST. We then compared spatial and volumetric WMH data derived from manually-delineated lesion maps with WMH data and lesion maps provided by the LST algorithms. RESULTS: We identified optimal initial thresholds for algorithms provided by LST compared with visual ratings (Lesion Growth Algorithm (LGA): initial κ and lesion probability thresholds, 0.5; Lesion Probability Algorithm (LPA) lesion probability threshold, 0.65). LGA was found to perform better then LPA compared with manual segmentation. CONCLUSION: LGA appeared to be the most suitable algorithm for quantifying WMH in relation to cerebral small vessel disease, compared with Scheltens’ score and manual segmentation. LGA offers a user-friendly, effective WMH segmentation method in the research environment. SAGE Publications 2019-10-15 /pmc/articles/PMC7607266/ /pubmed/31612759 http://dx.doi.org/10.1177/0300060519880053 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Special Issue: Cerebral Small Vessel Disease: Recent Trends Waymont, Jennifer M.J. Petsa, Chariklia McNeil, Chris J. Murray, Alison D. Waiter, Gordon D. Validation and comparison of two automated methods for quantifying brain white matter hyperintensities of presumed vascular origin |
title | Validation and comparison of two automated methods for quantifying
brain white matter hyperintensities of presumed vascular origin |
title_full | Validation and comparison of two automated methods for quantifying
brain white matter hyperintensities of presumed vascular origin |
title_fullStr | Validation and comparison of two automated methods for quantifying
brain white matter hyperintensities of presumed vascular origin |
title_full_unstemmed | Validation and comparison of two automated methods for quantifying
brain white matter hyperintensities of presumed vascular origin |
title_short | Validation and comparison of two automated methods for quantifying
brain white matter hyperintensities of presumed vascular origin |
title_sort | validation and comparison of two automated methods for quantifying
brain white matter hyperintensities of presumed vascular origin |
topic | Special Issue: Cerebral Small Vessel Disease: Recent Trends |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7607266/ https://www.ncbi.nlm.nih.gov/pubmed/31612759 http://dx.doi.org/10.1177/0300060519880053 |
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