Cargando…
Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype
Blood-brain barrier (BBB) dysfunction might be an important component of many neurodegenerative disorders. In this study, we investigated its role in dementia using large clinical cohorts. The cerebrospinal fluid (CSF)/plasma albumin ratio (Qalb), an indicator of BBB (and blood-CSF barrier) permeabi...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754327/ https://www.ncbi.nlm.nih.gov/pubmed/28061383 http://dx.doi.org/10.1016/j.neurobiolaging.2016.11.017 |
_version_ | 1783290390807314432 |
---|---|
author | Janelidze, Shorena Hertze, Joakim Nägga, Katarina Nilsson, Karin Nilsson, Christer Wennström, Malin van Westen, Danielle Blennow, Kaj Zetterberg, Henrik Hansson, Oskar |
author_facet | Janelidze, Shorena Hertze, Joakim Nägga, Katarina Nilsson, Karin Nilsson, Christer Wennström, Malin van Westen, Danielle Blennow, Kaj Zetterberg, Henrik Hansson, Oskar |
author_sort | Janelidze, Shorena |
collection | PubMed |
description | Blood-brain barrier (BBB) dysfunction might be an important component of many neurodegenerative disorders. In this study, we investigated its role in dementia using large clinical cohorts. The cerebrospinal fluid (CSF)/plasma albumin ratio (Qalb), an indicator of BBB (and blood-CSF barrier) permeability, was measured in a total of 1015 individuals. The ratio was increased in patients with Alzheimer's disease, dementia with Lewy bodies or Parkinson's disease dementia, subcortical vascular dementia, and frontotemporal dementia compared with controls. However, this measure was not changed during preclinical or prodromal Alzheimer's disease and was not associated with amyloid positron emission tomography or APOE genotype. The Qalb was increased in diabetes mellitus and correlated positively with CSF biomarkers of angiogenesis and endothelial dysfunction (vascular endothelial growth factor, intracellular adhesion molecule 1, and vascular cell adhesion molecule 1). In healthy elderly, high body mass index and waist-hip ratio predicted increased Qalb 20 years later. In summary, BBB permeability is increased in major dementia disorders but does not relate to amyloid pathology or APOE genotype. Instead, BBB impairment may be associated with diabetes and brain microvascular damage. |
format | Online Article Text |
id | pubmed-5754327 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-57543272018-01-10 Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype Janelidze, Shorena Hertze, Joakim Nägga, Katarina Nilsson, Karin Nilsson, Christer Wennström, Malin van Westen, Danielle Blennow, Kaj Zetterberg, Henrik Hansson, Oskar Neurobiol Aging Article Blood-brain barrier (BBB) dysfunction might be an important component of many neurodegenerative disorders. In this study, we investigated its role in dementia using large clinical cohorts. The cerebrospinal fluid (CSF)/plasma albumin ratio (Qalb), an indicator of BBB (and blood-CSF barrier) permeability, was measured in a total of 1015 individuals. The ratio was increased in patients with Alzheimer's disease, dementia with Lewy bodies or Parkinson's disease dementia, subcortical vascular dementia, and frontotemporal dementia compared with controls. However, this measure was not changed during preclinical or prodromal Alzheimer's disease and was not associated with amyloid positron emission tomography or APOE genotype. The Qalb was increased in diabetes mellitus and correlated positively with CSF biomarkers of angiogenesis and endothelial dysfunction (vascular endothelial growth factor, intracellular adhesion molecule 1, and vascular cell adhesion molecule 1). In healthy elderly, high body mass index and waist-hip ratio predicted increased Qalb 20 years later. In summary, BBB permeability is increased in major dementia disorders but does not relate to amyloid pathology or APOE genotype. Instead, BBB impairment may be associated with diabetes and brain microvascular damage. Elsevier 2017-03 /pmc/articles/PMC5754327/ /pubmed/28061383 http://dx.doi.org/10.1016/j.neurobiolaging.2016.11.017 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Janelidze, Shorena Hertze, Joakim Nägga, Katarina Nilsson, Karin Nilsson, Christer Wennström, Malin van Westen, Danielle Blennow, Kaj Zetterberg, Henrik Hansson, Oskar Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype |
title | Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype |
title_full | Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype |
title_fullStr | Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype |
title_full_unstemmed | Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype |
title_short | Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype |
title_sort | increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or apoe genotype |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754327/ https://www.ncbi.nlm.nih.gov/pubmed/28061383 http://dx.doi.org/10.1016/j.neurobiolaging.2016.11.017 |
work_keys_str_mv | AT janelidzeshorena increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT hertzejoakim increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT naggakatarina increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT nilssonkarin increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT nilssonchrister increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT wennstrommalin increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT vanwestendanielle increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT blennowkaj increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT zetterberghenrik increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype AT hanssonoskar increasedbloodbrainbarrierpermeabilityisassociatedwithdementiaanddiabetesbutnotamyloidpathologyorapoegenotype |