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Published on: October 19, 2016
Arterial Stiffness and the Canonical WNT/β-catenin Pathway
1Department of Epidemiology - Data - Biostatistics, Delegation of Clinical Research and Innovation, Foch Hospital, 92150, Suresnes, France. alexandre.g.vallee@gmail.com.
Insights
Arterial stiffness (AS), a risk factor for cardiovascular disease, is linked to the WNT/β-catenin pathway. This pathway
Area of Science:
- Cardiovascular Research
- Molecular Biology
- Pathophysiology
Background:
- Arterial stiffness (AS) is a significant predictor of cardiovascular morbidity and mortality, particularly in hypertensive patients.
- Key risk factors for AS include aging, hypertension, vascular calcification, inflammation, and diabetes mellitus.
- The WNT/β-catenin pathway plays a crucial role in various cellular processes and is implicated in the development of these risk factors.
Purpose of the Study:
- To review the role of the WNT/β-catenin pathway in the development of arterial stiffness.
- To explore the connection between WNT/β-catenin pathway deregulation and arterial stiffness markers.
Main Methods:
- Literature review focusing on studies investigating arterial stiffness and the WNT/β-catenin pathway.
- Analysis of existing research on risk factors for arterial stiffness and their molecular underpinnings.
Main Results:
- Arterial stiffness, measured by aortic pulse wave velocity (PWV), is elevated in conditions like peripheral artery disease.
- Increased PWV is associated with a higher risk of cardiovascular events.
- Deregulation of the WNT/β-catenin pathway, specifically the inactivation of its inhibitors DKK1 and sclerostin, is linked to arterial stiffness.
Conclusions:
- The WNT/β-catenin pathway is a key contributor to the development of arterial stiffness.
- Understanding this pathway's role offers potential therapeutic targets for managing cardiovascular risk associated with arterial stiffness.
Purpose Of Review:
Arterial stiffness (AS) was mainly associated with cardiovascular morbidity and mortality in a hypertensive patient. Some risk factors contribute to the development of AS, such as aging, high blood pressure, vascular calcification, inflammation, and diabetes mellitus. The WNT/β-catenin pathway is implicated in numerous signaling and regulating pathways, including embryogenesis, cell proliferation, migration and polarity, apoptosis, and organogenesis. The activation of the WNT/β-catenin pathway is associated with the development of these risk factors.
Recent Findings:
Aortic pulse wave velocity (PWV) is measured to determine AS, and in peripheral artery disease patients, PWV is higher than controls. An augmentation in PWV by 1 m/s has been shown to increase the risk of cardiovascular events by 14%. AS measured by PWV is characterized by the deregulation of the WNT/β-catenin pathway by the inactivation of its two inhibitors, i.e., DKK1 and sclerostin. Thus, this review focuses on the role of the WNT/β-catenin pathway which contributes to the development of arterial stiffness.
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