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Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity
Background: Atherosclerosis is a systemic inflammatory disease, with common inflammatory processes implicated in both atheroma vulnerability and blood-brain barrier disruption. This prospective multimodal imaging study aimed to measure directly the association between systemic atheroma inflammation...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438317/ https://www.ncbi.nlm.nih.gov/pubmed/34531813 http://dx.doi.org/10.3389/fneur.2021.690935 |
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author | Evans, Nicholas R. Tarkin, Jason M. Walsh, Jessica Chowdhury, Mohammed M. Patterson, Andrew J. Graves, Martin J. Rudd, James H. F. Warburton, Elizabeth A. |
author_facet | Evans, Nicholas R. Tarkin, Jason M. Walsh, Jessica Chowdhury, Mohammed M. Patterson, Andrew J. Graves, Martin J. Rudd, James H. F. Warburton, Elizabeth A. |
author_sort | Evans, Nicholas R. |
collection | PubMed |
description | Background: Atherosclerosis is a systemic inflammatory disease, with common inflammatory processes implicated in both atheroma vulnerability and blood-brain barrier disruption. This prospective multimodal imaging study aimed to measure directly the association between systemic atheroma inflammation (“atheroinflammation”) and downstream chronic cerebral small vessel disease severity. Methods: Twenty-six individuals with ischemic stroke with ipsilateral carotid artery stenosis of >50% underwent (18)fluoride-fluorodeoxyglucose-positron emission tomography within 2 weeks of stroke. Small vessel disease severity and white matter hyperintensity volume were assessed using 3-tesla magnetic resonance imaging also within 2 weeks of stroke. Results: Fluorodeoxyglucose uptake was independently associated with more severe small vessel disease (odds ratio 6.18, 95% confidence interval 2.1–18.2, P < 0.01 for the non-culprit carotid artery) and larger white matter hyperintensity volumes (coefficient = 14.33 mL, P < 0.01 for the non-culprit carotid artery). Conclusion: These proof-of-concept results have important implications for our understanding of the neurovascular interface and potential therapeutic exploitation in the management of systemic atherosclerosis, particularly non-stenotic disease previously considered asymptomatic, in order to reduce the burden of chronic cerebrovascular disease. |
format | Online Article Text |
id | pubmed-8438317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84383172021-09-15 Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity Evans, Nicholas R. Tarkin, Jason M. Walsh, Jessica Chowdhury, Mohammed M. Patterson, Andrew J. Graves, Martin J. Rudd, James H. F. Warburton, Elizabeth A. Front Neurol Neurology Background: Atherosclerosis is a systemic inflammatory disease, with common inflammatory processes implicated in both atheroma vulnerability and blood-brain barrier disruption. This prospective multimodal imaging study aimed to measure directly the association between systemic atheroma inflammation (“atheroinflammation”) and downstream chronic cerebral small vessel disease severity. Methods: Twenty-six individuals with ischemic stroke with ipsilateral carotid artery stenosis of >50% underwent (18)fluoride-fluorodeoxyglucose-positron emission tomography within 2 weeks of stroke. Small vessel disease severity and white matter hyperintensity volume were assessed using 3-tesla magnetic resonance imaging also within 2 weeks of stroke. Results: Fluorodeoxyglucose uptake was independently associated with more severe small vessel disease (odds ratio 6.18, 95% confidence interval 2.1–18.2, P < 0.01 for the non-culprit carotid artery) and larger white matter hyperintensity volumes (coefficient = 14.33 mL, P < 0.01 for the non-culprit carotid artery). Conclusion: These proof-of-concept results have important implications for our understanding of the neurovascular interface and potential therapeutic exploitation in the management of systemic atherosclerosis, particularly non-stenotic disease previously considered asymptomatic, in order to reduce the burden of chronic cerebrovascular disease. Frontiers Media S.A. 2021-08-31 /pmc/articles/PMC8438317/ /pubmed/34531813 http://dx.doi.org/10.3389/fneur.2021.690935 Text en Copyright © 2021 Evans, Tarkin, Walsh, Chowdhury, Patterson, Graves, Rudd and Warburton. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neurology Evans, Nicholas R. Tarkin, Jason M. Walsh, Jessica Chowdhury, Mohammed M. Patterson, Andrew J. Graves, Martin J. Rudd, James H. F. Warburton, Elizabeth A. Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity |
title | Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity |
title_full | Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity |
title_fullStr | Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity |
title_full_unstemmed | Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity |
title_short | Carotid Atheroinflammation Is Associated With Cerebral Small Vessel Disease Severity |
title_sort | carotid atheroinflammation is associated with cerebral small vessel disease severity |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438317/ https://www.ncbi.nlm.nih.gov/pubmed/34531813 http://dx.doi.org/10.3389/fneur.2021.690935 |
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