Increased blood-brain barrier permeability is associated with dementia and diabetes but not amyloid pathology or APOE genotype Show others and affiliations
2017 (English) In: Neurobiology of Aging, ISSN 0197-4580, E-ISSN 1558-1497, Vol. 51, p. 104-112, article id S0197-4580(16)30304-9Article in journal (Refereed) Published
Abstract [en]
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.
Place, publisher, year, edition, pages Elsevier, 2017. Vol. 51, p. 104-112, article id S0197-4580(16)30304-9
Keywords [en]
APOE ε4, Amyloid, Blood-brain barrier, Dementia, Diabetes, Vascular pathology
National Category
Neurology
Identifiers URN: urn:nbn:se:liu:diva-162698 DOI: 10.1016/j.neurobiolaging.2016.11.017 ISI: 000397168600011 PubMedID: 28061383 Scopus ID: 2-s2.0-85007609372 OAI: oai:DiVA.org:liu-162698 DiVA, id: diva2:1379246
2019-12-162019-12-162024-05-02 Bibliographically approved