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Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Assessment of vascular function in patients with chronic kidney disease
Kristen L Jablonski1, Emily Decker1, Loni Perrenoud1
1Division of Renal Diseases and Hypertension, University of Colorado, Denver.
Insights
Patients with chronic kidney disease (CKD) exhibit vascular dysfunction, including impaired endothelium-dependent dilation and arterial stiffness. These non-traditional risk factors contribute to their elevated cardiovascular disease (CVD) risk.
Area of Science:
- Nephrology
- Cardiology
- Vascular Biology
Background:
- Patients with chronic kidney disease (CKD) face a higher risk of cardiovascular disease (CVD) than the general population.
- Traditional CVD risk factors only partially explain this increased risk.
- Vascular dysfunction, encompassing endothelial dysfunction and arterial stiffness, is a key non-traditional risk factor in CKD.
Purpose of the Study:
- To discuss methods for assessing vascular dysfunction in CKD patients.
- To highlight the role of impaired endothelium-dependent dilation (EDD) and arterial stiffness in CKD-related CVD risk.
- To explore the contribution of oxidative stress and reduced nitric oxide (NO) bioavailability to vascular dysfunction in CKD.
Main Methods:
- Assessing brachial artery flow-mediated dilation (FMDBA) to measure EDD.
- Measuring aortic pulse-wave velocity (aPWV) to assess large elastic artery stiffness.
- Analyzing vascular endothelial cell protein expression for oxidative stress markers via immunofluorescence.
Main Results:
- Patients with CKD demonstrate impaired FMDBA and increased aPWV.
- Both FMDBA and aPWV are independent predictors of cardiovascular events in CKD and non-CKD populations.
- Increased oxidative stress and reduced NO bioavailability are significant contributors to vascular dysfunction in CKD.
Conclusions:
- Vascular dysfunction is prevalent in CKD and contributes to CVD risk.
- Noninvasive measures like FMDBA and aPWV are valuable for risk assessment in CKD.
- Understanding cellular mechanisms, such as oxidative stress, is crucial for managing vascular complications in CKD.
Abstract:
Patients with chronic kidney disease (CKD) have significantly increased risk of cardiovascular disease (CVD) compared to the general population, and this is only partially explained by traditional CVD risk factors. Vascular dysfunction is an important non-traditional risk factor, characterized by vascular endothelial dysfunction (most commonly assessed as impaired endothelium-dependent dilation [EDD]) and stiffening of the large elastic arteries. While various techniques exist to assess EDD and large elastic artery stiffness, the most commonly used are brachial artery flow-mediated dilation (FMDBA) and aortic pulse-wave velocity (aPWV), respectively. Both of these noninvasive measures of vascular dysfunction are independent predictors of future cardiovascular events in patients with and without kidney disease. Patients with CKD demonstrate both impaired FMDBA, and increased aPWV. While the exact mechanisms by which vascular dysfunction develops in CKD are incompletely understood, increased oxidative stress and a subsequent reduction in nitric oxide (NO) bioavailability are important contributors. Cellular changes in oxidative stress can be assessed by collecting vascular endothelial cells from the antecubital vein and measuring protein expression of markers of oxidative stress using immunofluorescence. We provide here a discussion of these methods to measure FMDBA, aPWV, and vascular endothelial cell protein expression.
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