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Hypertension and Alzheimer's disease: indirect effects through circle of Willis atherosclerosis.
- Source :
-
Brain communications [Brain Commun] 2020 Jul 21; Vol. 2 (2), pp. fcaa114. Date of Electronic Publication: 2020 Jul 21 (Print Publication: 2020). - Publication Year :
- 2020
-
Abstract
- Hypertension is common among older adults and is believed to increase susceptibility to Alzheimer's disease, but mechanisms underlying this relationship are unclear. Hypertension also promotes circle of Willis atherosclerosis, which contributes to cerebral hypoperfusion and arterial wall stiffening, two potential mechanisms linking hypertension to Alzheimer's disease. To examine the role of circle of Willis atherosclerosis in the association between hypertension and Alzheimer's disease neuropathology, we analysed post-mortem neuropathological data on 2198 decedents from the National Alzheimer's Coordinating Center database [mean (standard deviation) age at last visit 80.51 (1.95) and 47.1% female] using joint simultaneous (i.e. mediation) modelling. Within the overall sample and among Alzheimer's dementia decedents, hypertension was indirectly associated with increased neuritic plaques and neurofibrillary tangles through its association with circle of Willis atherosclerosis. Similar indirect effects were observed for continuous measures of systolic and diastolic blood pressure. These results suggest that hypertension may promote Alzheimer's disease pathology indirectly through intracranial atherosclerosis by limiting cerebral blood flow and/or dampening perivascular clearance. Circle of Willis atherosclerosis may be an important point of convergence between vascular risk factors, cerebrovascular changes and Alzheimer's disease neuropathology.<br /> (© The Author(s) (2020). Published by Oxford University Press on behalf of the Guarantors of Brain.)
Details
- Language :
- English
- ISSN :
- 2632-1297
- Volume :
- 2
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Brain communications
- Publication Type :
- Academic Journal
- Accession number :
- 33543127
- Full Text :
- https://doi.org/10.1093/braincomms/fcaa114