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Updated: Jun 17, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Effects of atorvastatin on arterial stiffness in chronic kidney disease: a randomised controlled trial
Robert G Fassett1, Iain K Robertson, Madeleine J Ball
1Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia. rfassett@mac.com
Insights
Atorvastatin therapy may slow the progression of arterial stiffness in patients with chronic kidney disease (CKD). This study found that aortic pulse wave velocity (PWV) increased in placebo patients but not in those treated with atorvastatin over three years.
Area of Science:
- Cardiovascular Medicine
- Nephrology
- Pharmacology
Background:
- Arterial stiffness, including augmentation index (AIx) and aortic pulse wave velocity (PWV), is a predictor of adverse outcomes in chronic kidney disease (CKD) stages 2-4.
- Statin therapy is known to have vascular benefits, but its long-term impact on arterial stiffness and central blood pressure in CKD patients remains under-researched.
Purpose of the Study:
- To evaluate the long-term effects of atorvastatin on arterial stiffness and central blood pressure in patients diagnosed with CKD.
- To determine if atorvastatin can mitigate the progression of arterial stiffness in this vulnerable patient group.
Main Methods:
- A randomized, double-blind trial involving 37 CKD patients (serum creatinine > 1.36 mg/dL) was conducted.
- Participants received either 10 mg of atorvastatin daily or a placebo for three years.
- Aortic PWV, AIx, and central/brachial blood pressures were measured every nine months.
Main Results:
- While aortic PWV significantly increased in the placebo group over three years, it did not show a significant increase in the atorvastatin group (p=0.05 vs. p=0.10).
- This indicates a potential 41% slowing in the rate of arterial stiffness increase with atorvastatin, though not statistically significant (p=0.48).
- No significant between-group differences were observed in the changes of AIx or central pulse pressure over the study period.
Conclusions:
- Arterial stiffness, as measured by aortic PWV, significantly worsened in CKD patients receiving a placebo over time.
- Atorvastatin treatment appeared to prevent the significant increase in aortic PWV observed in the placebo group, suggesting a protective effect on arterial stiffness.
Aim:
Central pulse pressure and measures of arterial stiffness (augmentation index (AIx) and aortic pulse wave velocity (PWV)) predict morbidity and mortality in patients with stage 2-4 chronic kidney disease (CKD). Although statin therapy may be of vascular benefit in patients with CKD, the long-term effect of statins on central pulse pressure and arterial stiffness has not been assessed in this patient population. Hence, the aim of this study was to assess the long-term effects of atorvastatin on arterial stiffness and central blood pressure in patients with CKD.
Methods:
We enrolled 37 patients with serum creatinine levels > 1.36 mg/dL into a randomized, double blind trial. Patients were allocated to receive 10 mg of atorvastatin per day (19) or placebo (18) for three years. Aortic PWV, AIx, estimated central and brachial blood pressures and were determined every nine months.
Results:
At baseline, there were no significant differences in aortic PWV, AIx, central or brachial blood pressures between atorvastatin-treated and placebo-treated patients. During the trial, aortic PWV significantly (p=0.05) increased in placebo-treated, but not (p=0.10) in atorvastatin-treated patients (0.51+/-0.95 vs. 0.30+/-0.75 m/sec/yr; p=0.48). This represented a 41% (but not statistically significant) slowing of the rate of increase in aortic stiffness. There were no significant changes between groups in the rate of change of AIx (atorvastatin -0.15+/-5.65 vs. placebo 0.39+/-5.38%/yr, p=0.53) or central pulse pressure (atorvastatin -2.32+/-7.46 vs. placebo -0.36+/-6.64 mmHg/yr p= 0.61).
Conclusion:
In patients with CKD arterial stiffness measured by aortic PWV showed a significant increase over time in placebo-treated patients but not in atorvastatin-treated patients.
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