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Biomarkers Assessing Endothelial Dysfunction in Alzheimer's Disease.
Antía Custodia1,2, Marta Aramburu-Núñez1,2, Mariña Rodríguez-Arrizabalaga1
1NeuroAging Group (NEURAL), Clinical Neurosciences Research Laboratory (LINC), Health Research Institute of Santiago de Compostela (IDIS), 15706 Santiago de Compostela, Spain.
Alzheimer's disease (AD) involves endothelial dysfunction, impairing the blood-brain barrier (BBB). New biomarkers for this dysfunction may offer early AD diagnosis and novel therapeutic targets.
Area of Science:
- Neuroscience
- Vascular Biology
- Gerontology
Background:
- Alzheimer's disease (AD) is a leading cause of dementia in the elderly.
- Endothelial dysfunction is increasingly recognized as a critical factor in AD pathogenesis.
- Vascular risk factors contribute to blood-brain barrier (BBB) compromise in AD.
Purpose of the Study:
- To explore the role of endothelial dysfunction in Alzheimer's disease.
- To identify early biomarkers for endothelial dysfunction in AD.
- To investigate potential therapeutic targets for AD based on endothelial dysfunction.
Main Methods:
- Review of current evidence linking endothelial dysfunction and AD.
- Analysis of biomarker changes associated with BBB disruption.
- Exploration of neuroinflammatory and neurodegenerative pathways.
Main Results:
- Endothelial dysfunction compromises the BBB, allowing toxic substances into the brain.
- Increased adhesion molecules and endothelin-1 indicate vascular inflammation and BBB permeability.
- Neuroinflammation and astrogliosis result from BBB disruption, leading to neuronal degeneration.
Conclusions:
- Endothelial dysfunction is a significant contributor to cognitive decline in Alzheimer's disease.
- Biomarkers of endothelial dysfunction could serve as early diagnostic and prognostic markers for AD.
- Identifying these biomarkers opens avenues for new therapeutic strategies against AD.
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