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Increase in blood–brain barrier leakage in healthy, older adults
Blood–brain barrier (BBB) breakdown can disrupt nutrient supply and waste removal, which affects neuronal functioning. Currently, dynamic contrast-enhanced (DCE) MRI is the preferred in-vivo method to quantify BBB leakage. Dedicated DCE MRI studies in normal aging individuals are lacking, which coul...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394987/ https://www.ncbi.nlm.nih.gov/pubmed/32601792 http://dx.doi.org/10.1007/s11357-020-00211-2 |
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author | Verheggen, Inge C. M. de Jong, Joost J. A. van Boxtel, Martin P. J. Gronenschild, Ed H. B. M. Palm, Walter M. Postma, Alida A. Jansen, Jacobus F. A. Verhey, Frans R. J. Backes, Walter H. |
author_facet | Verheggen, Inge C. M. de Jong, Joost J. A. van Boxtel, Martin P. J. Gronenschild, Ed H. B. M. Palm, Walter M. Postma, Alida A. Jansen, Jacobus F. A. Verhey, Frans R. J. Backes, Walter H. |
author_sort | Verheggen, Inge C. M. |
collection | PubMed |
description | Blood–brain barrier (BBB) breakdown can disrupt nutrient supply and waste removal, which affects neuronal functioning. Currently, dynamic contrast-enhanced (DCE) MRI is the preferred in-vivo method to quantify BBB leakage. Dedicated DCE MRI studies in normal aging individuals are lacking, which could hamper value estimation and interpretation of leakage rate in pathological conditions. Therefore, we applied DCE MRI to investigate the association between BBB disruption and age in a healthy sample. Fifty-seven cognitively and neurologically healthy, middle-aged to older participants (mean age: 66 years, range: 47–91 years) underwent MRI, including DCE MRI with intravenous injection of a gadolinium-based contrast agent. Pharmacokinetic modeling was applied to contrast concentration time-curves to estimate BBB leakage rate in each voxel. Subsequently, leakage rate was calculated in the white and gray matter, and primary (basic sensory and motor functions), secondary (association areas), and tertiary (higher-order cognition) brain regions. A difference in vulnerability to deterioration was expected between these regions, with especially tertiary regions being affected by age. Higher BBB leakage rate was significantly associated with older age in the white and gray matter, and also in tertiary, but not in primary or secondary brain regions. Even in healthy individuals, BBB disruption was stronger in older persons, which suggests BBB disruption is a normal physiologically aging phenomenon. Age-related increase in BBB disruption occurred especially in brain regions most vulnerable to age-related deterioration, which may indicate that BBB disruption is an underlying mechanism of normal age-related decline. Netherlands Trial Register number: NL6358, date of registration: 2017-03-24. |
format | Online Article Text |
id | pubmed-7394987 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-73949872020-08-18 Increase in blood–brain barrier leakage in healthy, older adults Verheggen, Inge C. M. de Jong, Joost J. A. van Boxtel, Martin P. J. Gronenschild, Ed H. B. M. Palm, Walter M. Postma, Alida A. Jansen, Jacobus F. A. Verhey, Frans R. J. Backes, Walter H. GeroScience Original Article Blood–brain barrier (BBB) breakdown can disrupt nutrient supply and waste removal, which affects neuronal functioning. Currently, dynamic contrast-enhanced (DCE) MRI is the preferred in-vivo method to quantify BBB leakage. Dedicated DCE MRI studies in normal aging individuals are lacking, which could hamper value estimation and interpretation of leakage rate in pathological conditions. Therefore, we applied DCE MRI to investigate the association between BBB disruption and age in a healthy sample. Fifty-seven cognitively and neurologically healthy, middle-aged to older participants (mean age: 66 years, range: 47–91 years) underwent MRI, including DCE MRI with intravenous injection of a gadolinium-based contrast agent. Pharmacokinetic modeling was applied to contrast concentration time-curves to estimate BBB leakage rate in each voxel. Subsequently, leakage rate was calculated in the white and gray matter, and primary (basic sensory and motor functions), secondary (association areas), and tertiary (higher-order cognition) brain regions. A difference in vulnerability to deterioration was expected between these regions, with especially tertiary regions being affected by age. Higher BBB leakage rate was significantly associated with older age in the white and gray matter, and also in tertiary, but not in primary or secondary brain regions. Even in healthy individuals, BBB disruption was stronger in older persons, which suggests BBB disruption is a normal physiologically aging phenomenon. Age-related increase in BBB disruption occurred especially in brain regions most vulnerable to age-related deterioration, which may indicate that BBB disruption is an underlying mechanism of normal age-related decline. Netherlands Trial Register number: NL6358, date of registration: 2017-03-24. Springer International Publishing 2020-06-29 /pmc/articles/PMC7394987/ /pubmed/32601792 http://dx.doi.org/10.1007/s11357-020-00211-2 Text en © The Author(s) 2020 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/. |
spellingShingle | Original Article Verheggen, Inge C. M. de Jong, Joost J. A. van Boxtel, Martin P. J. Gronenschild, Ed H. B. M. Palm, Walter M. Postma, Alida A. Jansen, Jacobus F. A. Verhey, Frans R. J. Backes, Walter H. Increase in blood–brain barrier leakage in healthy, older adults |
title | Increase in blood–brain barrier leakage in healthy, older adults |
title_full | Increase in blood–brain barrier leakage in healthy, older adults |
title_fullStr | Increase in blood–brain barrier leakage in healthy, older adults |
title_full_unstemmed | Increase in blood–brain barrier leakage in healthy, older adults |
title_short | Increase in blood–brain barrier leakage in healthy, older adults |
title_sort | increase in blood–brain barrier leakage in healthy, older adults |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7394987/ https://www.ncbi.nlm.nih.gov/pubmed/32601792 http://dx.doi.org/10.1007/s11357-020-00211-2 |
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