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Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities

The extent and spatial location of white matter hyperintensities (WMH) on brain MRI may be relevant to the development of cognitive decline in older persons. Here, we introduce a new method, known as the Multi-atlas based Detection and Localization (MADL), to evaluate WMH on fluid-attenuated inversi...

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Autores principales: Wu, Dan, Albert, Marilyn, Soldan, Anja, Pettigrew, Corinne, Oishi, Kenichi, Tomogane, Yusuke, Ye, Chenfei, Ma, Ting, Miller, Michael I., Mori, Susumu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444296/
https://www.ncbi.nlm.nih.gov/pubmed/30927606
http://dx.doi.org/10.1016/j.nicl.2019.101772
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author Wu, Dan
Albert, Marilyn
Soldan, Anja
Pettigrew, Corinne
Oishi, Kenichi
Tomogane, Yusuke
Ye, Chenfei
Ma, Ting
Miller, Michael I.
Mori, Susumu
author_facet Wu, Dan
Albert, Marilyn
Soldan, Anja
Pettigrew, Corinne
Oishi, Kenichi
Tomogane, Yusuke
Ye, Chenfei
Ma, Ting
Miller, Michael I.
Mori, Susumu
author_sort Wu, Dan
collection PubMed
description The extent and spatial location of white matter hyperintensities (WMH) on brain MRI may be relevant to the development of cognitive decline in older persons. Here, we introduce a new method, known as the Multi-atlas based Detection and Localization (MADL), to evaluate WMH on fluid-attenuated inversion recovery (FLAIR) data. This method simultaneously parcellates the whole brain into 143 structures and labels hyperintense areas within each WM structure. First, a multi-atlas library was established with FLAIR data of normal elderly brains; and then a multi-atlas fusion algorithm was developed by which voxels with locally abnormal intensities were detected as WMH. At the same time, brain segmentation maps were generated from the multi-atlas fusion process to determine the anatomical location of WMH. Areas identified using the MADL method agreed well with manual delineation, with an interclass correlation of 0.97 and similarity index (SI) between 0.55 and 0.72, depending on the total WMH load. Performance was compared to other state-of-the-art WMH detection methods, such as BIANCA and LST. MADL-based analyses of WMH in an older population revealed a significant association between age and WMH load in deep WM but not subcortical WM. The findings also suggested increased WMH load in selective brain regions in subjects with mild cognitive impairment compared to controls, including the inferior deep WM and occipital subcortical WM. The proposed MADL approach may facilitate location-dependent characterization of WMH in older individuals with memory impairment.
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spelling pubmed-64442962019-04-12 Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities Wu, Dan Albert, Marilyn Soldan, Anja Pettigrew, Corinne Oishi, Kenichi Tomogane, Yusuke Ye, Chenfei Ma, Ting Miller, Michael I. Mori, Susumu Neuroimage Clin Regular Article The extent and spatial location of white matter hyperintensities (WMH) on brain MRI may be relevant to the development of cognitive decline in older persons. Here, we introduce a new method, known as the Multi-atlas based Detection and Localization (MADL), to evaluate WMH on fluid-attenuated inversion recovery (FLAIR) data. This method simultaneously parcellates the whole brain into 143 structures and labels hyperintense areas within each WM structure. First, a multi-atlas library was established with FLAIR data of normal elderly brains; and then a multi-atlas fusion algorithm was developed by which voxels with locally abnormal intensities were detected as WMH. At the same time, brain segmentation maps were generated from the multi-atlas fusion process to determine the anatomical location of WMH. Areas identified using the MADL method agreed well with manual delineation, with an interclass correlation of 0.97 and similarity index (SI) between 0.55 and 0.72, depending on the total WMH load. Performance was compared to other state-of-the-art WMH detection methods, such as BIANCA and LST. MADL-based analyses of WMH in an older population revealed a significant association between age and WMH load in deep WM but not subcortical WM. The findings also suggested increased WMH load in selective brain regions in subjects with mild cognitive impairment compared to controls, including the inferior deep WM and occipital subcortical WM. The proposed MADL approach may facilitate location-dependent characterization of WMH in older individuals with memory impairment. Elsevier 2019-03-13 /pmc/articles/PMC6444296/ /pubmed/30927606 http://dx.doi.org/10.1016/j.nicl.2019.101772 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
Wu, Dan
Albert, Marilyn
Soldan, Anja
Pettigrew, Corinne
Oishi, Kenichi
Tomogane, Yusuke
Ye, Chenfei
Ma, Ting
Miller, Michael I.
Mori, Susumu
Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities
title Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities
title_full Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities
title_fullStr Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities
title_full_unstemmed Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities
title_short Multi-atlas based detection and localization (MADL) for location-dependent quantification of white matter hyperintensities
title_sort multi-atlas based detection and localization (madl) for location-dependent quantification of white matter hyperintensities
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6444296/
https://www.ncbi.nlm.nih.gov/pubmed/30927606
http://dx.doi.org/10.1016/j.nicl.2019.101772
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