Cardiometabolic risk factors and neurodegeneration: a review of the mechanisms underlying diabetes, obesity and hypertension in Alzheimer’s disease
Open accessAbstract
A growing body of evidence suggests that cardiometabolic risk factors play a significant role in Alzheimer’s disease (AD). Diabetes, obesity and hypertension are highly prevalent and can accelerate neurodegeneration and perpetuate the burden of AD. Insulin resistance and enzymes including insulin degrading enzymes are implicated in AD where breakdown of insulin is prioritised over amyloid-β. Leptin resistance and inflammation demonstrated by higher plasma and central nervous system levels of interleukin-6 (IL-6), IL-1β and tumour necrosis factor-α, are mechanisms connecting obesity and diabetes with AD. Leptin has been shown to ameliorate AD pathology and enhance long-term potentiation and hippocampal-dependent cognitive function. The renin-aldosterone angiotensin system, involved in hypertension, has been associated with AD pathology and neurotoxic reactive oxygen species, where angiotensin binds to specific angiotensin-1 receptors in the hippocampus and cerebral cortex. This review aims to consolidate the evidence behind putative processes stimulated by obesity, diabetes and hypertension, which leads to increased AD risk. We focus on how novel knowledge can be applied clinically to facilitate recognition of efficacious treatment strategies for AD.
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Patients with both type 2 diabetes and obesity face an elevated risk of neurodegenerative and cerebrovascular diseases, including dementia, Parkinson disease, and stroke.
“Patients with both conditions face an elevated risk of neurodegenerative and cerebrovascular diseases, including dementia, Parkinson disease, and stroke.5”
From Neurodegeneration and Stroke After Semaglutide and Tirzepatide in Patients With Diabetes and Obesity (2025) · cites this paper as [5]
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Alzheimer’s Disease: Exploring the Landscape of Cognitive Decline
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- Authors
- Patel, V., & Edison, P.
- Affiliations
- Imperial College London (GB)
- Corresponding author
- Edison, Paul
- ORCID
- Edison, Paul
- Venue
- Journal of Neurology, Neurosurgery & Psychiatry
- Publisher
- BMJ
- Published
- 2024-01-30
- Volume
- 95
- Issue
- 6
- Pages
- 581-589
- ISSN
- 0022-3050 (ISSN-L)
- 1468-330X
- PMC
- PMC11103343
- OpenAlex
- W4391346690
- Cited by
- 80
- References
- 7
- Citations by year
- 2026: 27 · 2025: 44 · 2024: 9
- FWCI
- 4.56
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Journal of Neurology Neurosurgery & Psychiatry (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- Novo Nordisk
- Higher Education Funding Council for England (N/A)
- Alzheimer's Research UK (N/A)
- Medical Research Council (N/A)
- Alzheimer’s Association US (N/A)
- GE Healthcare (N/A)
- Piramal Life Sciences (N/A)
- Alzheimer’s Drug Discovery Foundation (N/A)
- Topics
- Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
- Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
- Health Sciences › Medicine › Epidemiology › Adipokines, Inflammation, and Metabolic Diseases
- Keywords
- Alzheimer's disease, cardiometabolic risk factors, diabetes mellitus, obesity, hypertension, neurodegeneration, insulin resistance, insulin-degrading enzyme, amyloid-beta, leptin resistance, inflammation, interleukin-6, IL-1β, TNF-α, renin-angiotensin system, reactive oxygen species, hippocampus, long-term potentiation, cognitive function
- MeSH terms
- Cardiometabolic Risk Factors, Alzheimer Disease, Diabetes Mellitus, Humans, Hypertension, Insulin Resistance, Obesity, Renin-Angiotensin System
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