Methods and potential biomarkers for the evaluation of endothelial dysfunction in chronic kidney disease: A critical approach |
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Authors: | Simona M. Hogas Luminita Voroneanu Dragomir N. Serban Liviu Segall Mihai M. Hogas Ionela Lacramioara Serban Adrian Covic |
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Affiliation: | 1. Department of Medical Laboratory Sciences, University of Delaware, Newark, Delaware,;2. Diabetes and Metabolic Research Center, Christiana Care Health System, Newark, Delaware,;3. Diabetes and Metabolic Diseases Center, Christiana Care Health System, Wilmington, Delaware,;4. Department of Radiology, Christiana Care Health System, Newark, Delaware, and 5Biostatistics Core Facility, University of Delaware, Newark, Delaware.;5. Biostatistics Core Facility, University of Delaware, Newark, Delaware. |
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Abstract: | The impressive cardiovascular morbidity and mortality of chronic kidney disease (CKD) patients is attributable in a significant proportion to endothelial dysfunction (ED), arterial stiffness, and vascular calcifications. Abnormal vascular reactivity in these patients is more pronounced compared with other high-risk populations, but remains undiagnosed in the usual clinical setting. We briefly review the most important causes and risk factors of ED, oxidative stress, and inflammation related to arterial stiffness. We describe the main methods of ED investigation and the importance of using potential biomarkers together with classic techniques for a more comprehensive assessment of this condition. These methods include evaluation of: forearm blood flow by plethysmography, skin microcirculation by laser Doppler, and flow-mediated vasodilation by Doppler ultrasound imaging. Applanation tonometry is an easy-to-handle tool that allows a clinically reliable assessment of arterial stiffness and is also useful in quantifying endothelium-dependent and -independent vascular reactivity. We also discuss the diagnostic and therapeutic impact of new markers of ED in the CKD population. Improvement of endothelial function is an important challenge for clinical practice, and there are relatively few therapeutical strategies available. Therefore, a combined biomarker and bedside investigational approach could be a starting point for developing optimal therapeutic tools. |
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