Effects of simvastatin treatment on sICAM-1 and sE-selectin levels in hypercholesterolemic subjects
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- 作者：Sardo ; Maria A. ; Castaldo ; Maria ; Cinquegrani ; Maurizio ; Bonaiuto ; Michele ; Maesano ; Antonella ; et. al.
- 关键词：Hypercholesterolemia ; sICAM-1 ; sE-Selectin ; Simvastatin ; Endothelial activation ; Atherosclerosis
- 刊名：Atherosclerosis
- 出版年：2001
- 出版时间：March, 2001
- 年：2001
- 卷：155
- 期：1
- 页码：143-147
- 全文大小：138 K
文摘
This study was performed to determine whether the levels of soluble intercellular adhesion molecule-1 (sICAM-l) and soluble endothelial molecule-1 (sE-selectin) were elevated in subjects with hypercholesterolemia who presented with no other risk factors or evidence of atherosclerosis. The effects of administration of an HMG-CoA reductase inhibitor on the serum levels of these molecules were also examined. Forty hypercholesterolemic subjects (HCh) (19 males and 21 females), without hypertension or cardiovascular disease, received placebo for 4 weeks. The patients were then randomized in two groups; 20 of them (simvastatin group) were treated with simvastatin (20 mg/day) and the other 20 (placebo group) continued placebo administration. After 12 and 24 weeks of either simvastatin or placebo treatment, sICAM-1 and sE-selectin levels were measured. The same parameters were measured in 20 control subjects (C) with normal cholesterol levels, matched for sex and age. HCh had sICAM-1 basal values higher than C (352.4±57.9 ng/ml versus 114.9±89.6 ng/ml; P<0.001); however, sE-selectin basal values were not different in the two groups. No correlation was observed between HCh sICAM-1 levels and cholesterol levels (total and low-density lipoprotein). Furthermore, cholesterol-lowering treatment with simvastatin did not significantly diminish sICAM-1 levels. Our findings would support the hypothesis that patients with isolated hypercholesterolemia and without clinical atherosclerosis may be silent carriers of arterial subendothelial inflammation, expressed as an increase of sICAM-1.