Monocyte chemoattractant protein-1/CCL2 as a biomarker in acute coronary syndromes

被引:74
作者
Gonzalez-Quesada, Carlos [1 ]
Frangogiannis, Nikolaos G. [1 ]
机构
[1] Baylor Coll Med, Cardiovasc Sci Sect, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
HEALING MYOCARDIAL INFARCTS; HUMAN ENDOTHELIAL-CELLS; C-REACTIVE PROTEIN; E-KNOCKOUT MICE; PLASMA-LEVELS; REDUCES ATHEROSCLEROSIS; INFLAMMATORY RESPONSE; DEFICIENT MICE; SMOOTH-MUSCLE; TISSUE FACTOR;
D O I
10.1007/s11883-009-0021-y
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The CC chemokine monocyte chemoattractant protein (MCP)-1/CCL2 is involved in the formation, progression, and destabilization of atheromatous plaques and plays an essential role in postinfarction remodeling. These properties generated significant interest in the potential significance of MCP-1 as a biomarker in acute coronary syndromes (ACS). Emerging evidence suggests that MCP-1 plasma levels have prognostic value in the acute and chronic phase following ACS, providing information independent of standard clinical variables. The mechanisms responsible for adverse prognosis in patients with elevated plasma MCP-1 following ACS remain unknown. High plasma MCP-1 levels may reflect a higher burden of atherosclerotic disease, may exert prothrombotic effects resulting in recurrent coronary events, or may identify patients who mount a more intense cardiac inflammatory reaction following a coronary event, resulting in enhanced adverse remodeling. Beyond its prognostic significance, the MCP-1 axis may be an attractive target for therapy in patients with ACS.
引用
收藏
页码:131 / 138
页数:8
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