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Updated: Jul 20, 2026

Motor and Hippocampal Dependent Spatial Learning and Reference Memory Assessment in a Transgenic Rat Model of Alzheimer's Disease with Stroke
Published on: March 22, 2016
How do heart disease and stroke become risk factors for Alzheimer's disease?
1Institute of Pathology, Case Western Reserve School of Medicine, Gig Harbor, WA, USA. jcdelatorre@comcast.net
Insights
Heart disease and stroke contribute to chronic brain hypoperfusion (CBH), increasing Alzheimer's disease (AD) risk. Understanding this link aids in developing targeted therapies for AD prevention and treatment.
Area of Science:
- Neurology
- Cardiology
- Geriatrics
Background:
- Heart disease and stroke are leading global causes of death and disability.
- These conditions are significant risk factors for Alzheimer's disease (AD), particularly in the elderly.
Purpose of the Study:
- To review evidence linking chronic brain hypoperfusion (CBH) from heart disease and stroke to AD development.
Main Methods:
- Systematic review of existing research on cardiovascular risk factors and their impact on cerebral blood flow and AD.
Main Results:
- Multiple heart conditions (e.g., CABG, atrial fibrillation, valve damage, heart failure) and cerebrovascular issues (e.g., atherosclerosis, TIAs) are associated with CBH.
- Reduced cerebral perfusion, especially in older adults, elevates AD probability.
- Chronic CBH may trigger a neuronal energy crisis, leading to protein synthesis defects and hallmark AD pathologies like beta-amyloid plaques and neurofibrillary tangles.
Conclusions:
- Understanding the progression from heart disease/stroke to AD enhances knowledge of AD's underlying pathology.
- This understanding can guide the development of more precise therapeutic strategies for preventing, managing, or reversing dementia.
Background:
Heart disease and stroke are two of the major leading causes of death and disability in the world. Mainly affecting the elderly population, heart disease and stroke are important risk factors for Alzheimer's disease (AD).
Methods:
This review examines the evidence linking chronic brain hypoperfusion (CBH) produced by several types of heart disease and stroke on the development of AD.
Results:
The evidence indicates a strong association between such risk factors as coronary artery bypass surgery (CABG), atrial fibrillation, aortic/mitral valve damage, hypertension, hypotension, congestive heart failure, cerebrovascular-carotid atherosclerosis, and transient ischemic attacks in producing CBH. In people whose cerebral perfusion is already diminished by their advanced age, further cerebral blood flow reductions from heart-brain vascular-related risk factors, seemingly increases the probability of AD. The evidence also suggests that a neuronal energy crisis brought on by a relentless CBH is responsible for protein synthesis defects that later result in the classic AD neurodegenerative lesions such as the formation of excess beta-amyloid plaques and neurofibrillary tangles.
Conclusions:
Knowledge of how heart disease and stroke can progress to AD should provide a better understanding of the physiopathology characteristic of AD and also target more precise therapy in preventing, controlling or reversing this dementia.
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