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Updated: Jul 28, 2025

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
New mechanisms involved in the development of cardiovascular disease in chronic kidney disease
Andrea Figuer1, Matilde Alique1, Gemma Valera1
1Departamento de Biología de Sistemas, Universidad de Alcalá (IRYCIS), Alcalá de Henares (Madrid), Spain.
Insights
Extracellular vesicles (EVs) contribute to cardiovascular disease (CVD) in chronic kidney disease (CKD) patients by causing endothelial damage. Targeting EVs may offer new diagnostic and therapeutic strategies for CKD-associated CVD.
Area of Science:
- Nephrology
- Cardiology
- Biomedical Sciences
Background:
- Chronic kidney disease (CKD) affects the elderly, often requiring renal replacement therapy.
- CKD patients experience increased oxidative stress, inflammation, and extracellular vesicle (EV) release, contributing to cardiovascular disease (CVD).
- EVs in CKD patients are elevated in plasma and altered in content, promoting endothelial dysfunction, senescence, and vascular calcification.
Purpose of the Study:
- To review classic and novel mechanisms of CVD development in CKD.
- To emphasize the critical role of EVs in CKD-associated cardiovascular pathologies.
- To explore the potential of EVs as diagnostic and therapeutic tools in CKD.
Main Methods:
- Literature review focusing on mechanisms of CVD in CKD.
- Emphasis on the role of extracellular vesicles (EVs) and their components (e.g., miRNAs).
- Analysis of EV involvement in endothelial dysfunction, vascular calcification, and thrombosis.
Main Results:
- EVs from CKD patients induce endothelial dysfunction, senescence, and vascular calcification.
- Altered EV content, including miRNAs, exacerbates endothelial dysfunction and thrombotic risks.
- EVs are implicated as key mediators in the premature development of CVD in CKD.
Conclusions:
- Extracellular vesicles play a significant role in the pathogenesis of cardiovascular disease in chronic kidney disease.
- Modulating EV release or content presents a promising avenue for diagnosing and treating CKD-associated CVD.
- Further research into EVs could lead to novel therapeutic strategies to mitigate cardiovascular risks in CKD patients.
Abstract:
Chronic kidney disease (CKD) is a pathology with a high worldwide incidence and an upward trend affecting the elderly. When CKD is very advanced, the use of renal replacement therapies is required to prolong its life (dialysis or kidney transplantation). Although dialysis improves many complications of CKD, the disease does not reverse completely. These patients present an increase in oxidative stress, chronic inflammation and the release of extracellular vesicles (EVs), which cause endothelial damage and the development of different cardiovascular diseases (CVD). CKD patients develop premature diseases associated with advanced age, such as CVD. EVs play an essential role in developing CVD in patients with CKD since their number increases in plasma and their content is modified. The EVs of patients with CKD cause endothelial dysfunction, senescence and vascular calcification. In addition, miRNAs free or transported in EVs together with other components carried in these EVs promote endothelial dysfunction, thrombotic and vascular calcification in CKD, among other effects. This review describes the classic factors and focuses on the role of new mechanisms involved in the development of CVD associated with CKD, emphasizing the role of EVs in the development of cardiovascular pathologies in the context of CKD. Moreover, the review summarized the EVs' role as diagnostic and therapeutic tools, acting on EV release or content to avoid the development of CVD in CKD patients.
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