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Multimodal exploration of the intracranial aneurysm wall

PURPOSE: Intracranial aneurysms (IAs) are pathological changes of the intracranial vessel wall, although clinical image data can only show the vessel lumen. Histology can provide wall information but is typically restricted to ex vivo 2D slices where the shape of the tissue is altered. METHODS: We d...

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Autores principales: Niemann, Annika, Tulamo, Riikka, Netti, Eliisa, Preim, Bernhard, Berg, Philipp, Cebral, Juan, Robertson, Anne, Saalfeld, Sylvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480333/
https://www.ncbi.nlm.nih.gov/pubmed/36877287
http://dx.doi.org/10.1007/s11548-023-02850-0
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author Niemann, Annika
Tulamo, Riikka
Netti, Eliisa
Preim, Bernhard
Berg, Philipp
Cebral, Juan
Robertson, Anne
Saalfeld, Sylvia
author_facet Niemann, Annika
Tulamo, Riikka
Netti, Eliisa
Preim, Bernhard
Berg, Philipp
Cebral, Juan
Robertson, Anne
Saalfeld, Sylvia
author_sort Niemann, Annika
collection PubMed
description PURPOSE: Intracranial aneurysms (IAs) are pathological changes of the intracranial vessel wall, although clinical image data can only show the vessel lumen. Histology can provide wall information but is typically restricted to ex vivo 2D slices where the shape of the tissue is altered. METHODS: We developed a visual exploration pipeline for a comprehensive view of an IA. We extract multimodal information (like stain classification and segmentation of histologic images) and combine them via 2D to 3D mapping and virtual inflation of deformed tissue. Histological data, including four stains, micro-CT data and segmented calcifications as well as hemodynamic information like wall shear stress (WSS), are combined with the 3D model of the resected aneurysm. RESULTS: Calcifications were mostly present in the tissue part with increased WSS. In the 3D model, an area of increased wall thickness was identified and correlated to histology, where the Oil red O (ORO) stained images showed a lipid accumulation and the alpha-smooth muscle actin (aSMA) stained images showed a slight loss of muscle cells. CONCLUSION: Our visual exploration pipeline combines multimodal information about the aneurysm wall to improve the understanding of wall changes and IA development. The user can identify regions and correlate how hemodynamic forces, e.g. WSS, are reflected by histological structures of the vessel wall, wall thickness and calcifications.
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spelling pubmed-104803332023-11-14 Multimodal exploration of the intracranial aneurysm wall Niemann, Annika Tulamo, Riikka Netti, Eliisa Preim, Bernhard Berg, Philipp Cebral, Juan Robertson, Anne Saalfeld, Sylvia Int J Comput Assist Radiol Surg Original Article PURPOSE: Intracranial aneurysms (IAs) are pathological changes of the intracranial vessel wall, although clinical image data can only show the vessel lumen. Histology can provide wall information but is typically restricted to ex vivo 2D slices where the shape of the tissue is altered. METHODS: We developed a visual exploration pipeline for a comprehensive view of an IA. We extract multimodal information (like stain classification and segmentation of histologic images) and combine them via 2D to 3D mapping and virtual inflation of deformed tissue. Histological data, including four stains, micro-CT data and segmented calcifications as well as hemodynamic information like wall shear stress (WSS), are combined with the 3D model of the resected aneurysm. RESULTS: Calcifications were mostly present in the tissue part with increased WSS. In the 3D model, an area of increased wall thickness was identified and correlated to histology, where the Oil red O (ORO) stained images showed a lipid accumulation and the alpha-smooth muscle actin (aSMA) stained images showed a slight loss of muscle cells. CONCLUSION: Our visual exploration pipeline combines multimodal information about the aneurysm wall to improve the understanding of wall changes and IA development. The user can identify regions and correlate how hemodynamic forces, e.g. WSS, are reflected by histological structures of the vessel wall, wall thickness and calcifications. Springer International Publishing 2023-03-06 2023 /pmc/articles/PMC10480333/ /pubmed/36877287 http://dx.doi.org/10.1007/s11548-023-02850-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Niemann, Annika
Tulamo, Riikka
Netti, Eliisa
Preim, Bernhard
Berg, Philipp
Cebral, Juan
Robertson, Anne
Saalfeld, Sylvia
Multimodal exploration of the intracranial aneurysm wall
title Multimodal exploration of the intracranial aneurysm wall
title_full Multimodal exploration of the intracranial aneurysm wall
title_fullStr Multimodal exploration of the intracranial aneurysm wall
title_full_unstemmed Multimodal exploration of the intracranial aneurysm wall
title_short Multimodal exploration of the intracranial aneurysm wall
title_sort multimodal exploration of the intracranial aneurysm wall
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10480333/
https://www.ncbi.nlm.nih.gov/pubmed/36877287
http://dx.doi.org/10.1007/s11548-023-02850-0
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