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White matter damage due to pulsatile versus steady blood pressure differs by vascular territory: A cross-sectional analysis of the UK Biobank cohort study
Small vessel disease is associated with age, mean blood pressure (MAP) and blood pressure pulsatility (PP). We used data from the UK Biobank cohort study to determine the relative importance of MAP versus PP driving white matter injury within individual white matter tracts, particularly in the anter...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014677/ https://www.ncbi.nlm.nih.gov/pubmed/34775867 http://dx.doi.org/10.1177/0271678X211058803 |
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author | Wartolowska, Karolina A Webb, Alastair JS |
author_facet | Wartolowska, Karolina A Webb, Alastair JS |
author_sort | Wartolowska, Karolina A |
collection | PubMed |
description | Small vessel disease is associated with age, mean blood pressure (MAP) and blood pressure pulsatility (PP). We used data from the UK Biobank cohort study to determine the relative importance of MAP versus PP driving white matter injury within individual white matter tracts, particularly in the anterior and posterior vascular territory. The associations between blood pressure and diffusion indices in 27 major tracts were analysed using unadjusted and fully-adjusted general linear models and mixed-effect linear models. Blood pressure and neuroimaging data were available for 37,041 participants (mean age 64+/−7.5 years, 53% female). In unadjusted analyses, MAP and PP were similarly associated with diffusion indices in the anterior circulation. In the posterior circulation, the associations were weaker, particularly for MAP. In fully-adjusted analyses, MAP remained associated with all diffusion indices in the anterior circulation, independently of age. In the posterior circulation, the effect of MAP became protective. PP remained associated with greater mean diffusivity and extracellular free water diffusion in the anterior circulation and all diffusion indices in the posterior circulation. There was a significant interaction between PP and age. This implies discordant mechanisms for chronic white matter injury in different brain regions and potentially in the associated stroke risks. |
format | Online Article Text |
id | pubmed-9014677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-90146772022-04-19 White matter damage due to pulsatile versus steady blood pressure differs by vascular territory: A cross-sectional analysis of the UK Biobank cohort study Wartolowska, Karolina A Webb, Alastair JS J Cereb Blood Flow Metab Original Articles Small vessel disease is associated with age, mean blood pressure (MAP) and blood pressure pulsatility (PP). We used data from the UK Biobank cohort study to determine the relative importance of MAP versus PP driving white matter injury within individual white matter tracts, particularly in the anterior and posterior vascular territory. The associations between blood pressure and diffusion indices in 27 major tracts were analysed using unadjusted and fully-adjusted general linear models and mixed-effect linear models. Blood pressure and neuroimaging data were available for 37,041 participants (mean age 64+/−7.5 years, 53% female). In unadjusted analyses, MAP and PP were similarly associated with diffusion indices in the anterior circulation. In the posterior circulation, the associations were weaker, particularly for MAP. In fully-adjusted analyses, MAP remained associated with all diffusion indices in the anterior circulation, independently of age. In the posterior circulation, the effect of MAP became protective. PP remained associated with greater mean diffusivity and extracellular free water diffusion in the anterior circulation and all diffusion indices in the posterior circulation. There was a significant interaction between PP and age. This implies discordant mechanisms for chronic white matter injury in different brain regions and potentially in the associated stroke risks. SAGE Publications 2021-11-14 2022-05 /pmc/articles/PMC9014677/ /pubmed/34775867 http://dx.doi.org/10.1177/0271678X211058803 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Wartolowska, Karolina A Webb, Alastair JS White matter damage due to pulsatile versus steady blood pressure differs by vascular territory: A cross-sectional analysis of the UK Biobank cohort study |
title | White matter damage due to pulsatile versus steady blood pressure
differs by vascular territory: A cross-sectional analysis of the UK Biobank
cohort study |
title_full | White matter damage due to pulsatile versus steady blood pressure
differs by vascular territory: A cross-sectional analysis of the UK Biobank
cohort study |
title_fullStr | White matter damage due to pulsatile versus steady blood pressure
differs by vascular territory: A cross-sectional analysis of the UK Biobank
cohort study |
title_full_unstemmed | White matter damage due to pulsatile versus steady blood pressure
differs by vascular territory: A cross-sectional analysis of the UK Biobank
cohort study |
title_short | White matter damage due to pulsatile versus steady blood pressure
differs by vascular territory: A cross-sectional analysis of the UK Biobank
cohort study |
title_sort | white matter damage due to pulsatile versus steady blood pressure
differs by vascular territory: a cross-sectional analysis of the uk biobank
cohort study |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014677/ https://www.ncbi.nlm.nih.gov/pubmed/34775867 http://dx.doi.org/10.1177/0271678X211058803 |
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