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Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study
Increasing evidence suggests a role for endothelial cell (EC) dysfunction in pathogenesis of cerebral small vessel disease. Commonly used medications including certain antihypertensives and statins have EC-stabilizing effects. We used individual patient data from completed acute stroke trials to ass...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773869/ https://www.ncbi.nlm.nih.gov/pubmed/31608006 http://dx.doi.org/10.3389/fneur.2019.01029 |
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author | Becker, Charlotte Elisabeth Quinn, Terence J. Williams, Anna |
author_facet | Becker, Charlotte Elisabeth Quinn, Terence J. Williams, Anna |
author_sort | Becker, Charlotte Elisabeth |
collection | PubMed |
description | Increasing evidence suggests a role for endothelial cell (EC) dysfunction in pathogenesis of cerebral small vessel disease. Commonly used medications including certain antihypertensives and statins have EC-stabilizing effects. We used individual patient data from completed acute stroke trials to assess whether prior exposure to EC-stabilizing medications was associated with lacunar stroke, using lacunar stroke as a clinical proxy for cerebral small vessel disease. Across 12,002 patients with relevant data, 2,855 (24%) had a lacunar stroke presentation. Univariable analyses suggested potential confounding from vascular diseases treated with EC-stabilizing medications. Initial multivariable logistic regression gave conflicting results when describing the independent association of exposure to EC-stabilizing medication and lacunar stroke in the complete population (O.R. 0.87, 95% C.I.: 0.77– 0.98) and limited to those taking any antihypertensive (O.R. 1.51, 95% C.I.: 1.21–1.88). Re-running the analyses including statins in the EC-stabilizing category suggested a beneficial effect of EC-stabilizing medication exposure on lacunar stroke incidence (O.R. 0.83, 95% C.I.: 0.73–0.93). These results align with recent pre-clinical data and would support interventional trials of EC-stabilizing medication for preventing cerebral small vessel disease. Our results also suggest that analyses of EC-stabilizing interventions need to adjust for potential endothelial effects of other co-prescribed medication. |
format | Online Article Text |
id | pubmed-6773869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67738692019-10-13 Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study Becker, Charlotte Elisabeth Quinn, Terence J. Williams, Anna Front Neurol Neurology Increasing evidence suggests a role for endothelial cell (EC) dysfunction in pathogenesis of cerebral small vessel disease. Commonly used medications including certain antihypertensives and statins have EC-stabilizing effects. We used individual patient data from completed acute stroke trials to assess whether prior exposure to EC-stabilizing medications was associated with lacunar stroke, using lacunar stroke as a clinical proxy for cerebral small vessel disease. Across 12,002 patients with relevant data, 2,855 (24%) had a lacunar stroke presentation. Univariable analyses suggested potential confounding from vascular diseases treated with EC-stabilizing medications. Initial multivariable logistic regression gave conflicting results when describing the independent association of exposure to EC-stabilizing medication and lacunar stroke in the complete population (O.R. 0.87, 95% C.I.: 0.77– 0.98) and limited to those taking any antihypertensive (O.R. 1.51, 95% C.I.: 1.21–1.88). Re-running the analyses including statins in the EC-stabilizing category suggested a beneficial effect of EC-stabilizing medication exposure on lacunar stroke incidence (O.R. 0.83, 95% C.I.: 0.73–0.93). These results align with recent pre-clinical data and would support interventional trials of EC-stabilizing medication for preventing cerebral small vessel disease. Our results also suggest that analyses of EC-stabilizing interventions need to adjust for potential endothelial effects of other co-prescribed medication. Frontiers Media S.A. 2019-09-25 /pmc/articles/PMC6773869/ /pubmed/31608006 http://dx.doi.org/10.3389/fneur.2019.01029 Text en Copyright © 2019 Becker, Quinn and Williams. http://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 Becker, Charlotte Elisabeth Quinn, Terence J. Williams, Anna Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study |
title | Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study |
title_full | Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study |
title_fullStr | Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study |
title_full_unstemmed | Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study |
title_short | Association Between Endothelial Cell Stabilizing Medication and Small Vessel Disease Stroke: A Case-Control Study |
title_sort | association between endothelial cell stabilizing medication and small vessel disease stroke: a case-control study |
topic | Neurology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6773869/ https://www.ncbi.nlm.nih.gov/pubmed/31608006 http://dx.doi.org/10.3389/fneur.2019.01029 |
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