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Updated: Jun 27, 2026

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Published on: March 6, 2012
Cerivastatin, a hydroxymethylglutaryl coenzyme a reductase inhibitor, improves endothelial function in elderly
T Tsunekawa1, T Hayashi, H Kano
1Department of Geriatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan.
Insights
Short-term cerivastatin improved endothelial function in elderly diabetic patients by increasing nitric oxide and reducing oxidative stress, without altering lipid levels. This suggests potential antiatherosclerotic benefits.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Endocrinology
Background:
- The short-term effects of hydroxymethylglutaryl coenzyme A reductase inhibitors (statins) on endothelial function at non-lipid-lowering doses remain unclear.
- Endothelial dysfunction is a key factor in atherosclerosis, particularly in diabetic patients.
Purpose of the Study:
- To investigate the short-term effects of cerivastatin on endothelial function in elderly diabetic patients.
- To assess cerivastatin's impact on nitric oxide products, adhesion molecules, and oxidative stress markers.
Main Methods:
- A 3-day treatment with low-dose cerivastatin (0.15 mg/d) in 27 elderly diabetic patients.
- Assessment of endothelium-dependent (flow-mediated) and independent (nitroglycerin) vasodilation.
- Measurement of nitric oxide metabolites (nitrite/nitrate, cGMP), adhesion molecules (VCAM-1, ICAM-1), von Willebrand Factor, and 8-isoprostane.
Main Results:
- Cerivastatin significantly improved flow-mediated dilatation and increased plasma nitrite/nitrate and cGMP levels.
- No significant changes were observed in plasma lipid profiles or nitroglycerin-induced dilatation.
- Plasma 8-isoprostane and soluble vascular cell adhesion molecule-1 levels showed a tendency to decrease.
Conclusions:
- Short-term cerivastatin administration enhances endothelial function in elderly diabetic patients, independent of lipid-lowering effects.
- The observed improvement may be linked to increased nitric oxide bioavailability and reduced oxidative stress.
- These findings suggest potential short-term antiatherosclerotic benefits of statins at non-lipid-lowering doses.
Background:
The short-term effects of hydroxymethylglutaryl coenzyme A reductase inhibitors (statins) on endothelial function at doses that do not affect plasma lipid levels are not known.
Methods And Results:
We investigated the short-term effects of cerivastatin, a hydroxymethylglutaryl coenzyme A reductase inhibitor, on endothelial function and endothelium-related products in elderly diabetic patients. Twenty-seven elderly diabetic patients (aged 69.3+/-3.4 years), with or without mild hypercholesterolemia, were enrolled in this study, which tested cerivastatin treatment (0.15 mg/d) for 3 days. Endothelium-dependent flow-mediated dilatation, endothelium-independent dilatation by nitroglycerin in the brachial artery, nitric oxide-related products (nitrite/nitrate and cGMP), endothelium-related products (von Willebrand Factor, soluble vascular cell adhesion molecule-1, and soluble intercellular adhesion molecule-1), and a marker of oxidant stress (8-isoprostane) were assessed. Levels of plasma lipids were not changed before and after treatment with cerivastatin. Flow-mediated dilatation was significantly increased by cerivastatin treatment, as were plasma nitrite/nitrate levels (from 16.9+/-3.4 to 22.0+/-3.7 micromol/L, P<0.05) and cGMP values. The percent of nitroglycerin-induced dilatation was not changed. Plasma concentrations of 8-isoprostane decreased, and levels of soluble vascular cell adhesion molecule also tended to decrease with cerivastatin.
Conclusions:
Improvement of endothelial function was in line with antiatherosclerotic effects. Cerivastatin improved impaired endothelial function in the short-term without affecting lipid profiles in elderly diabetic patients. This effect may be partly due to upregulation of endothelial nitric oxide synthase.
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