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Alzheimer's disease is a vasocognopathy: a new term to describe its nature
1Institute of Pathology, Case Western Reserve University, Cleveland, OH, USA. jcdelatorre@cox.net
Insights
Alzheimer's disease (AD) is increasingly viewed as a vascular disorder, not just neurodegenerative. Reclassifying AD as a
Area of Science:
- Neurology
- Vascular Biology
- Neuroscience
Background:
- Alzheimer's disease (AD) and vascular dementia (VaD) share numerous risk factors and pathological markers.
- Cerebral hypoperfusion is linked to AD development and progression.
- Existing treatments improving cerebral perfusion show promise in lowering AD symptoms.
Purpose of the Study:
- To present evidence supporting the reclassification of Alzheimer's disease (AD) as a primary vascular disorder.
- To introduce the term 'vasocognopathy' to describe the vascular origins and cognitive impact of AD.
- To advocate for a paradigm shift in AD research and treatment strategies.
Main Methods:
- Multidisciplinary review of epidemiological, clinical, and pathological findings.
- Analysis of studies linking vascular risk factors to cerebral hypoperfusion.
- Examination of evidence for overlapping pathologies and symptoms in AD and VaD.
Main Results:
- Strong evidence links AD to cerebrovascular pathology, including hypoperfusion and infarction.
- Shared risk factors and pathological markers exist between AD and VaD.
- Cerebral hypoperfusion can induce neurodegenerative changes characteristic of AD.
Conclusions:
- Alzheimer's disease (AD) should be reclassified as a vascular disorder, termed 'vasocognopathy'.
- This reclassification necessitates a shift towards vascular-focused therapeutic strategies for AD.
- A vascular perspective offers potential for earlier diagnosis and more effective AD treatments.
Abstract:
Considerable evidence now indicates that Alzheimer's disease (AD) is a vascular disorder with neurodegenerative consequences. As a result, AD and vascular dementia (VaD) can each be described as a 'vasocognopathy'. The term better describes the origin of the disease (vaso: vessel/blood flow), its primary effect on a system (-cogno: relating to cognition) and its clinical course (-pathy: disorder). Evidence that AD is a vasocognopathy is partly supported by the following multidisciplinary findings: (1) epidemiologic studies linking AD and vascular risk factors to cerebral hypoperfusion; (2) evidence that AD and vascular dementia (VaD) share practically all reported risk factors; (3) evidence that pharmacotherapy which increases or improves cerebral perfusion lowers AD symptoms; (4) evidence of preclinical detection of AD candidates using regional cerebral perfusion and glucose uptake studies; (5) evidence of overlapping clinical symptoms in AD and VaD; (6) evidence of parallel cerebrovascular and neurodegenerative pathologic markers (including plaques and tangles) in AD and VaD; (7) evidence that cerebral infarction increases AD incidence by 50%; (8) evidence that chronic brain hypoperfusion can trigger hypometabolic, cognitive and neurodegenerative changes typical of AD; (9) evidence that most autopsied AD brains contain cerebrovascular pathology; (10) evidence that mild cognitive impairment (a transition stage for AD) converts to AD or VaD in 48% and 56% of cases, respectively, within several years. The collective evidence presented here poses a powerful argument for the re-classification of AD as a vascular disorder. Re-classification would allow a new strategy that could result in the tactical development and application of genuinely effective treatments, provide earlier diagnosis and reduce AD prevalence by focusing on the root of the problem.
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