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A typology of cerebral small vessel disease based on imaging markers

BACKGROUND: Lacunes, microbleeds, enlarged perivascular spaces (EPVS), and white matter hyperintensities (WMH) are brain imaging features of cerebral small vessel disease (SVD). Based on these imaging markers, we aimed to identify subtypes of SVD and to evaluate the validity of these markers as part...

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Autores principales: Sperber, Christoph, Hakim, Arsany, Gallucci, Laura, Seiffge, David, Rezny-Kasprzak, Beata, Jäger, Eugen, Meinel, Thomas, Wiest, Roland, Fischer, Urs, Arnold, Marcel, Umarova, Roza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511610/
https://www.ncbi.nlm.nih.gov/pubmed/37368130
http://dx.doi.org/10.1007/s00415-023-11831-x
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author Sperber, Christoph
Hakim, Arsany
Gallucci, Laura
Seiffge, David
Rezny-Kasprzak, Beata
Jäger, Eugen
Meinel, Thomas
Wiest, Roland
Fischer, Urs
Arnold, Marcel
Umarova, Roza
author_facet Sperber, Christoph
Hakim, Arsany
Gallucci, Laura
Seiffge, David
Rezny-Kasprzak, Beata
Jäger, Eugen
Meinel, Thomas
Wiest, Roland
Fischer, Urs
Arnold, Marcel
Umarova, Roza
author_sort Sperber, Christoph
collection PubMed
description BACKGROUND: Lacunes, microbleeds, enlarged perivascular spaces (EPVS), and white matter hyperintensities (WMH) are brain imaging features of cerebral small vessel disease (SVD). Based on these imaging markers, we aimed to identify subtypes of SVD and to evaluate the validity of these markers as part of clinical ratings and as biomarkers for stroke outcome. METHODS: In a cross-sectional study, we examined 1207 first-ever anterior circulation ischemic stroke patients (mean age 69.1 ± 15.4 years; mean NIHSS 5.3 ± 6.8). On acute stroke MRI, we assessed the numbers of lacunes and microbleeds and rated EPVS and deep and periventricular WMH. We used unsupervised learning to cluster patients based on these variables. RESULTS: We identified five clusters, of which the last three appeared to represent distinct late stages of SVD. The two largest clusters had no to only mild or moderate WMH and EPVS, respectively, and favorable stroke outcome. The third cluster was characterized by the largest number of lacunes and a likewise favorable outcome. The fourth cluster had the highest age, most pronounced WMH, and poor outcome. Showing the worst outcome, the fifth cluster presented pronounced microbleeds and the most severe SVD burden. CONCLUSION: The study confirmed the existence of different SVD types with different relationships to stroke outcome. EPVS and WMH were identified as imaging features of presumably early progression. The number of microbleeds and WMH severity appear to be promising biomarkers for distinguishing clinical subgroups. Further understanding of SVD progression might require consideration of refined SVD features, e.g., for EPVS and type of lacunes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-023-11831-x.
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spelling pubmed-105116102023-09-22 A typology of cerebral small vessel disease based on imaging markers Sperber, Christoph Hakim, Arsany Gallucci, Laura Seiffge, David Rezny-Kasprzak, Beata Jäger, Eugen Meinel, Thomas Wiest, Roland Fischer, Urs Arnold, Marcel Umarova, Roza J Neurol Original Communication BACKGROUND: Lacunes, microbleeds, enlarged perivascular spaces (EPVS), and white matter hyperintensities (WMH) are brain imaging features of cerebral small vessel disease (SVD). Based on these imaging markers, we aimed to identify subtypes of SVD and to evaluate the validity of these markers as part of clinical ratings and as biomarkers for stroke outcome. METHODS: In a cross-sectional study, we examined 1207 first-ever anterior circulation ischemic stroke patients (mean age 69.1 ± 15.4 years; mean NIHSS 5.3 ± 6.8). On acute stroke MRI, we assessed the numbers of lacunes and microbleeds and rated EPVS and deep and periventricular WMH. We used unsupervised learning to cluster patients based on these variables. RESULTS: We identified five clusters, of which the last three appeared to represent distinct late stages of SVD. The two largest clusters had no to only mild or moderate WMH and EPVS, respectively, and favorable stroke outcome. The third cluster was characterized by the largest number of lacunes and a likewise favorable outcome. The fourth cluster had the highest age, most pronounced WMH, and poor outcome. Showing the worst outcome, the fifth cluster presented pronounced microbleeds and the most severe SVD burden. CONCLUSION: The study confirmed the existence of different SVD types with different relationships to stroke outcome. EPVS and WMH were identified as imaging features of presumably early progression. The number of microbleeds and WMH severity appear to be promising biomarkers for distinguishing clinical subgroups. Further understanding of SVD progression might require consideration of refined SVD features, e.g., for EPVS and type of lacunes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-023-11831-x. Springer Berlin Heidelberg 2023-06-27 2023 /pmc/articles/PMC10511610/ /pubmed/37368130 http://dx.doi.org/10.1007/s00415-023-11831-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 Communication
Sperber, Christoph
Hakim, Arsany
Gallucci, Laura
Seiffge, David
Rezny-Kasprzak, Beata
Jäger, Eugen
Meinel, Thomas
Wiest, Roland
Fischer, Urs
Arnold, Marcel
Umarova, Roza
A typology of cerebral small vessel disease based on imaging markers
title A typology of cerebral small vessel disease based on imaging markers
title_full A typology of cerebral small vessel disease based on imaging markers
title_fullStr A typology of cerebral small vessel disease based on imaging markers
title_full_unstemmed A typology of cerebral small vessel disease based on imaging markers
title_short A typology of cerebral small vessel disease based on imaging markers
title_sort typology of cerebral small vessel disease based on imaging markers
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511610/
https://www.ncbi.nlm.nih.gov/pubmed/37368130
http://dx.doi.org/10.1007/s00415-023-11831-x
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