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过氧化物酶体增殖物激活受体γ激动剂罗格列酮可降低无糖尿病的冠心病患者的循环血小板活性。

Peroxisome proliferator-activated receptor-gamma agonist rosiglitazone reduces circulating platelet activity in patients without diabetes mellitus who have coronary artery disease.

作者信息

Sidhu Jagdip S, Cowan Dahlia, Tooze Jennifer A, Kaski Juan-Carlos

机构信息

Coronary Artery Disease Research Unit, Cardiological Sciences, St. George's Hospital Medical School, London, United Kingdom.

出版信息

Am Heart J. 2004 Jun;147(6):e25. doi: 10.1016/j.ahj.2003.12.035.

DOI:10.1016/j.ahj.2003.12.035
PMID:15199366
Abstract

BACKGROUND

Rosiglitazone, a peroxisome proliferator-activated receptor-gamma (PPAR-gamma) agonist, is used in the treatment of type 2 diabetes mellitus, and in vitro data has shown that it may have anti-platelet effects independent of its hypoglycemic effects. The aim of this study was to assess the effect of rosiglitazone on circulating platelet activity in patients without diabetes mellitus who had coronary artery disease.

METHODS

Ninety-two patients with stable, documented coronary artery disease without diabetes mellitus were studied. Patients were randomized (double-blind) to receive placebo or rosiglitazone for 12 weeks. Circulating platelet activity was measured at baseline and after 12 weeks of therapy with whole blood flow cytometry to quantify platelet P-selectin expression.

RESULTS

The percentage of P-selectin positive platelets was significantly reduced by rosiglitazone treatment compared with placebo (P =.04). In the rosiglitazone group, the percentage of P-selectin positive platelets (median with interquartile range) decreased from 0.1 % (0.05-0.24) to 0.05 % (0.01-0.15). Rosiglitazone treatment significantly reduced the insulin resistance index (HOMA-R) compared with placebo (P =.02). No significant correlation was observed between change in platelet activity and change in HOMA-R.

CONCLUSIONS

Rosiglitazone significantly reduces circulating platelet activity in patients without diabetes mellitus who have coronary artery disease. This effect appears to be independent of any insulin-sensitising effect.

摘要

背景

罗格列酮是一种过氧化物酶体增殖物激活受体γ(PPAR-γ)激动剂,用于治疗2型糖尿病,体外数据表明它可能具有独立于其降糖作用的抗血小板效应。本研究的目的是评估罗格列酮对无糖尿病的冠心病患者循环血小板活性的影响。

方法

对92例有稳定记录的无糖尿病的冠心病患者进行研究。患者被随机(双盲)分为接受安慰剂或罗格列酮治疗12周。在基线和治疗12周后,用全血流式细胞术测量循环血小板活性,以量化血小板P-选择素的表达。

结果

与安慰剂相比,罗格列酮治疗使P-选择素阳性血小板的百分比显著降低(P = 0.04)。在罗格列酮组中,P-选择素阳性血小板的百分比(中位数及四分位数间距)从0.1%(0.05 - 0.24)降至0.05%(0.01 - 0.15)。与安慰剂相比,罗格列酮治疗显著降低了胰岛素抵抗指数(HOMA-R)(P = 0.02)。未观察到血小板活性变化与HOMA-R变化之间存在显著相关性。

结论

罗格列酮可显著降低无糖尿病的冠心病患者的循环血小板活性。这种效应似乎独立于任何胰岛素增敏作用。

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