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血清单核细胞趋化蛋白-1 谱作为心肌梗死后患者恢复的生物标志物。

Serum profiles of monocyte chemoattractant protein-1 as a biomarker for patients recovering from myocardial infarction.

机构信息

Department of Pathophysiology, Poznan University of Medical Sciences, Swiecickiego 6, 60-781, Poznan, Poland.

出版信息

Clin Res Cardiol. 2010 May;99(5):315-22. doi: 10.1007/s00392-010-0122-1. Epub 2010 Feb 7.

DOI:10.1007/s00392-010-0122-1
PMID:20140679
Abstract

BACKGROUND

Monocyte chemoattractant protein-1 (MCP-1) plays a key role in the pathogenesis of atherosclerosis and has been proposed as a biomarker for patients with cardiovascular disease.

METHODS

To assess its clinical usefulness, serum MCP-1 concentrations were measured in patients with ST-elevation myocardial infarction (MI) at admission, immediately after percutaneous coronary intervention (PCI), at 24 h, and after 6 months.

RESULTS

We found no differences in MCP-1 concentrations between patients with acute MI, patients with stable coronary artery disease and healthy individuals. Although median MCP-1 concentrations in patients with MI were similar at admission and after 6 months, there were significant differences between individuals in how MCP-1 levels changed with time. As demonstrated by comparing baseline quartiles of MCP-1, the levels of MCP-1 tended to increase in patients with low MCP-1 concentration at admission, and decrease in patients with initially high MCP-1 levels. We found an inverse correlation between MCP-1 concentration at baseline and the time to reperfusion, and detected a significant decrease in MCP-1 concentration immediately after PCI. We also observed lower MCP-1 concentrations over time in patients who developed restenosis within 6 months. However, we did not confirm the association between MCP-1 concentrations at baseline and a number of previously implicated demographic, clinical and laboratory criteria.

CONCLUSIONS

Our data demonstrate some new aspects of MCP-1 measurement in patients with MI, but do not corroborate many earlier observations.

摘要

背景

单核细胞趋化蛋白-1(MCP-1)在动脉粥样硬化的发病机制中起着关键作用,并被提议作为心血管疾病患者的生物标志物。

方法

为了评估其临床实用性,在入院时、经皮冠状动脉介入治疗(PCI)后即刻、24 小时和 6 个月时测量 ST 段抬高型心肌梗死(MI)患者的血清 MCP-1 浓度。

结果

我们发现在急性 MI 患者、稳定型冠状动脉疾病患者和健康个体之间,MCP-1 浓度没有差异。尽管 MI 患者的 MCP-1 中位数在入院时和 6 个月时相似,但个体间 MCP-1 水平随时间变化的差异很大。如通过比较 MCP-1 的基线四分位数,在入院时 MCP-1 浓度较低的患者中,MCP-1 水平趋于升高,而在初始 MCP-1 水平较高的患者中,MCP-1 水平下降。我们发现 MCP-1 浓度与再灌注时间之间存在负相关,并且在 PCI 后即刻 MCP-1 浓度显著下降。我们还观察到,在 6 个月内发生再狭窄的患者中,MCP-1 浓度随时间逐渐降低。然而,我们并未证实基线 MCP-1 浓度与之前提出的许多涉及人口统计学、临床和实验室标准的指标之间的关联。

结论

我们的数据表明 MCP-1 在 MI 患者中的测量存在一些新的方面,但不能证实许多早期观察结果。

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Impact of heterogeneity of human peripheral blood monocyte subsets on myocardial salvage in patients with primary acute myocardial infarction.人类外周血单核细胞亚群异质性对原发性急性心肌梗死患者心肌挽救的影响。
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