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Updated: Jul 13, 2026

Ultrasound Assessment of Endothelial-Dependent Flow-Mediated Vasodilation of the Brachial Artery in Clinical Research
Published on: October 22, 2014
Modulation of arterial reactivity using amlodipine and atorvastatin measured by ultrasound examination (MARGAUX)
François Charbonneau1, Todd J Anderson, Lawrence Title
1Department of Cardiovascular Sciences and the Libin Cardiovascular Institute, University of Calgary, Calgary, AB, Canada.
Insights
Atorvastatin improved endothelial function and reduced inflammation in coronary disease patients. Adding amlodipine did not provide further benefits on these measures.
Area of Science:
- Cardiology
- Vascular Biology
- Pharmacology
Background:
- Coronary artery disease (CAD) involves endothelial dysfunction.
- Statins like atorvastatin improve cardiovascular outcomes.
- The role of calcium channel blockers (CCBs) in enhancing endothelial function in CAD patients on statins is not fully understood.
Purpose of the Study:
- To investigate the impact of amlodipine on endothelial function in patients with coronary disease receiving atorvastatin.
- To assess changes in inflammatory markers alongside endothelial function.
Main Methods:
- A randomized, placebo-controlled trial involving 134 patients with coronary disease.
- Patients received atorvastatin titrated to achieve low-density lipoprotein cholesterol (LDL-C) below 2.5 mmol/L.
- Participants were then randomized to amlodipine (5-10 mg/day) or placebo for 12 months.
- Endothelial function was assessed via brachial artery flow-mediated dilation (FMD) using vascular ultrasound.
- Inflammatory markers including high-sensitivity C-reactive protein (hsCRP) and soluble vascular cell adhesion molecule-1 (sVCAM-1) were measured.
Main Results:
- Intensive LDL-C reduction with atorvastatin significantly decreased hsCRP and sVCAM-1 levels.
- Atorvastatin therapy alone led to a significant improvement in FMD.
- Amlodipine addition resulted in a modest reduction in blood pressure but did not further improve FMD or inflammatory markers.
- No significant changes in nitroglycerin-mediated dilation were observed.
Conclusions:
- Intensive LDL-C lowering with atorvastatin effectively improves endothelial function and reduces inflammation in patients with coronary disease.
- The addition of amlodipine to atorvastatin therapy does not confer additional benefits on endothelial function or inflammatory markers in this patient population.
Objective:
To evaluate the effect of the calcium channel blocker amlodipine on endothelial function in normotensive patients with coronary disease taking concomitant atorvastatin therapy.
Methods And Results:
Atorvastatin was titrated (10-80 mg/day) to maintain LDL-C<2.5 mmol/L and patients were randomized to receive amlodipine (5-10mg/day, n=64) or placebo (n=70) for 12 months. Brachial artery flow-mediated vasodilation (FMD) was assessed using vascular ultrasound. Inflammatory markers were also measured. At 12 months there was a significant decrease in mean low-density lipoprotein cholesterol (LDL-C) (4.4-2.1 mmol/L, P<0.0001), high-sensitivity C-reactive protein (hsCRP) (3.8-2.3mg/L, P<0.0001) and soluble vascular cell adhesion molecule-1 (sVCAM-1) (710-665 ng/mL, P<0.0001) for all patients, compared with baseline. Amlodipine was associated with a mean blood pressure reduction of 8/3 mm Hg (P<0.0001) whereas patients on placebo had no significant change. In the atorvastatin-placebo group, mean FMD increased (7.3-9.5%, P<0.05) with no change in nitroglycerin-mediated dilation. No further benefit on FMD or inflammatory markers was observed with the addition of amlodipine.
Conclusions:
Intensive reduction of LDL-C with atorvastatin improves endothelium-dependent vasodilation and reduces markers of inflammation in patients with coronary disease. Amlodipine was not associated with a significant additional benefit on these variables.
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