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...

Descripción completa

Detalles Bibliográficos
Autores principales: Janelidze, Shorena, Hertze, Joakim, Nägga, Katarina, Nilsson, Karin, Nilsson, Christer, Wennström, Malin, van Westen, Danielle, Blennow, Kaj, Zetterberg, Henrik, Hansson, Oskar
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