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Updated: Mar 17, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Effect of cholesterol lowering treatment on plasma markers of endothelial dysfunction in chronic kidney disease
Angelo Zinellu1, Salvatore Sotgia1, Arduino A Mangoni2
1Department of Biomedical Sciences - University of Sassari, Sassari, Italy.
Insights
Cholesterol-lowering treatments significantly reduced asymmetric dimethylarginine (ADMA) in chronic kidney disease (CKD) patients. This improvement in endothelial dysfunction markers may be linked to reduced oxidative stress and inflammation.
Area of Science:
- Nephrology
- Cardiology
- Biochemistry
Background:
- Chronic kidney disease (CKD) is associated with high cardiovascular risk, driven by endothelial dysfunction.
- This dysfunction stems from a pro-inflammatory and pro-oxidative state characteristic of CKD.
Purpose of the Study:
- To investigate the impact of cholesterol-lowering therapies on endothelial dysfunction markers in CKD patients.
- Specifically examining asymmetric dimethylarginine (ADMA), vascular cell adhesion molecule (VCAM), and intercellular adhesion molecule (ICAM).
Main Methods:
- 30 CKD patients were randomized into three cholesterol-lowering treatment groups for 12 months.
- Measurements included plasma ADMA, Kynurenine/Tryptophan (Kyn/Trp) ratio, malondialdehyde (MDA), allantoin/uric acid (All/UA) ratio, VCAM, and ICAM.
- Treatments: simvastatin 40mg/day, ezetimibe/simvastatin 10/20mg/day, or ezetimibe/simvastatin 10/40mg/day.
Main Results:
- Cholesterol-lowering treatment significantly reduced plasma ADMA concentrations across all groups.
- A parallel significant decrease was observed in oxidative stress markers (MDA, All/UA ratio) and inflammation marker (Kyn/Trp ratio).
- No significant changes were noted in VCAM and ICAM plasma concentrations.
Conclusions:
- Cholesterol-lowering treatment effectively reduces ADMA levels in CKD patients, indicating improved endothelial function.
- The observed benefits may be mediated by a reduction in systemic oxidative stress and inflammation.
- Further research could explore the long-term cardiovascular implications.
Abstract:
The elevated cardiovascular morbidity and mortality in chronic kidney disease (CKD) is linked with endothelial dysfunction secondary to the pro-inflammatory and pro-oxidative state typical of this pathology. In consideration of the well-known pleiotropic effect of statins, we investigated the effect of cholesterol lowering treatment on endothelial dysfunction markers (MED), asymmetric dimethylarginine (ADMA), vascular cell (VCAM) and intercellular (ICAM) adhesion molecule. Plasma MED concentrations, inflammation and oxidative stress indices [Kynurenine/Tryptophan (Kyn/Trp) ratio, malondialdehyde (MDA) and allantoin/uric acid (All/UA) ratio] were measured in 30 CKD patients randomized to three cholesterol lowering regimens for 12 months (simvastatin 40mg/day, ezetimibe/simvastatin 10/20mg/day, or ezetimibe/simvastatin 10/40mg/day). Treatment significantly reduced ADMA concentrations in all patients [0.694μmol/L (0.606-0.761) at baseline vs. 0.622μmol/L (0.563-0.681) after treatment, p<0.001]. ADMA reduction was paralleled by a significant decrease of MDA, All/AU ratio and Kyn/Trp ratio, but not VCAM and ICAM plasma concentrations. Cholesterol lowering treatment was associated with a significant reduction in plasma ADMA concentrations in CKD patients. This might be mediated by reduced oxidative stress and inflammation.
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