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Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging
Blood–brain barrier (BBB) leakage increases with age and is involved in the pathophysiology of cerebral small vessel disease (cSVD). We examined the relationship between BBB leakage and white matter hyperintensity (WMH) volume and cognition, in cSVD patients and healthy controls. Seventy-seven patie...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486901/ https://www.ncbi.nlm.nih.gov/pubmed/29572621 http://dx.doi.org/10.1007/s11682-018-9855-7 |
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author | Zhang, C. Eleana Wong, Sau May Uiterwijk, Renske Backes, Walter H. Jansen, Jacobus F. A. Jeukens, Cécile R. L. P. N. van Oostenbrugge, Robert J. Staals, Julie |
author_facet | Zhang, C. Eleana Wong, Sau May Uiterwijk, Renske Backes, Walter H. Jansen, Jacobus F. A. Jeukens, Cécile R. L. P. N. van Oostenbrugge, Robert J. Staals, Julie |
author_sort | Zhang, C. Eleana |
collection | PubMed |
description | Blood–brain barrier (BBB) leakage increases with age and is involved in the pathophysiology of cerebral small vessel disease (cSVD). We examined the relationship between BBB leakage and white matter hyperintensity (WMH) volume and cognition, in cSVD patients and healthy controls. Seventy-seven patients with clinically overt cSVD and thirty-nine age matched healthy controls underwent dynamic contract-enhanced and structural brain MRI and neuropsychological assessment. We quantified BBB leakage volume and rate in normal appearing white matter (NAWM), WMH and cortical grey matter (CGM). Larger leakage volume and lower leakage rate in WMH were associated with larger WMH volume in cSVD but not in controls. Higher leakage rate in NAWM was associated with lower scores on executive function and information processing speed in healthy controls, whereas no relation with cognition was found in cSVD patients. Our findings support the involvement of BBB leakage in cSVD and aging. They also suggest that the mechanism of cognitive dysfunction in cSVD is more complex and multifactorial in cSVD compared with normal aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11682-018-9855-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6486901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-64869012019-05-15 Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging Zhang, C. Eleana Wong, Sau May Uiterwijk, Renske Backes, Walter H. Jansen, Jacobus F. A. Jeukens, Cécile R. L. P. N. van Oostenbrugge, Robert J. Staals, Julie Brain Imaging Behav Original Research Blood–brain barrier (BBB) leakage increases with age and is involved in the pathophysiology of cerebral small vessel disease (cSVD). We examined the relationship between BBB leakage and white matter hyperintensity (WMH) volume and cognition, in cSVD patients and healthy controls. Seventy-seven patients with clinically overt cSVD and thirty-nine age matched healthy controls underwent dynamic contract-enhanced and structural brain MRI and neuropsychological assessment. We quantified BBB leakage volume and rate in normal appearing white matter (NAWM), WMH and cortical grey matter (CGM). Larger leakage volume and lower leakage rate in WMH were associated with larger WMH volume in cSVD but not in controls. Higher leakage rate in NAWM was associated with lower scores on executive function and information processing speed in healthy controls, whereas no relation with cognition was found in cSVD patients. Our findings support the involvement of BBB leakage in cSVD and aging. They also suggest that the mechanism of cognitive dysfunction in cSVD is more complex and multifactorial in cSVD compared with normal aging. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s11682-018-9855-7) contains supplementary material, which is available to authorized users. Springer US 2018-03-23 2019 /pmc/articles/PMC6486901/ /pubmed/29572621 http://dx.doi.org/10.1007/s11682-018-9855-7 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Zhang, C. Eleana Wong, Sau May Uiterwijk, Renske Backes, Walter H. Jansen, Jacobus F. A. Jeukens, Cécile R. L. P. N. van Oostenbrugge, Robert J. Staals, Julie Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
title | Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
title_full | Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
title_fullStr | Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
title_full_unstemmed | Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
title_short | Blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
title_sort | blood–brain barrier leakage in relation to white matter hyperintensity volume and cognition in small vessel disease and normal aging |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6486901/ https://www.ncbi.nlm.nih.gov/pubmed/29572621 http://dx.doi.org/10.1007/s11682-018-9855-7 |
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