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依折麦布/辛伐他汀与辛伐他汀单药治疗对代谢综合征患者血小板及炎症生物标志物的影响。

The effects of ezetimibe/simvastatin versus simvastatin monotherapy on platelet and inflammatory biomarkers in patients with metabolic syndrome.

作者信息

Miller Michael, DiNicolantonio James J, Can Mehmet, Grice Rachel, Damoulakis Abigail, Serebruany Victor L

机构信息

Department of Medicine, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

出版信息

Cardiology. 2013;125(2):74-7. doi: 10.1159/000347134. Epub 2013 May 7.

Abstract

In a randomized, double-blind, crossover study of 15 aspirin-naive patients (mean age 48.8 ± 10.2 years) with the metabolic syndrome, statin monotherapy (simvastatin 40 mg daily) was compared to combination therapy (simvastatin 40 mg and ezetimibe 10 mg daily) on biomarkers of inflammation and platelet activity. The addition of ezetimibe to simvastatin over a 4-week period was associated with reduced expression of CD141 (thrombomodulin; p = 0.02), platelet endothelial cell adhesion molecule (p < 0.0001) and CD51/61 (vitronectin receptor; p = 0.048) compared to statin monotherapy. Ezetimibe added to simvastatin improves several indices of platelet reactivity beyond statin monotherapy. However, the clinical relevance of these findings await results of the IMPROVE-IT trial (Improved Reduction of Outcomes: Vytorin Efficacy International Trial).

摘要

在一项针对15名初治阿司匹林的代谢综合征患者(平均年龄48.8±10.2岁)的随机、双盲、交叉研究中,比较了他汀类单药治疗(辛伐他汀每日40毫克)与联合治疗(辛伐他汀每日40毫克和依折麦布每日10毫克)对炎症和血小板活性生物标志物的影响。与他汀类单药治疗相比,在4周时间内,辛伐他汀联合依折麦布可使CD141(血栓调节蛋白;p=0.02)、血小板内皮细胞黏附分子(p<0.0001)和CD51/61(玻连蛋白受体;p=0.048)的表达降低。辛伐他汀联合依折麦布在改善血小板反应性的多项指标方面优于他汀类单药治疗。然而,这些发现的临床相关性有待IMPROVE-IT试验(改善转归:Vytorin疗效国际试验)的结果。

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