Chemokines and Cardiovascular Risk

被引:173
作者
Aukrust, Pal [1 ,2 ]
Halvorsen, Bente [2 ]
Yndestad, Arne [2 ]
Ueland, Thor [2 ,3 ]
Oie, Erik [2 ,4 ]
Otterdal, Kari [2 ]
Gullestad, Lars [4 ]
Damas, Jan K. [2 ]
机构
[1] Univ Oslo, Rikshosp Univ Hosp, Dept Med, Sect Clin Immunol & Infect Dis, N-0027 Oslo, Norway
[2] Univ Oslo, Rikshosp Univ Hosp, Internal Med Res Inst, N-0027 Oslo, Norway
[3] Univ Oslo, Rikshosp Univ Hosp, Endocrinol Sect, N-0027 Oslo, Norway
[4] Univ Oslo, Rikshosp Univ Hosp, Dept Cardiol, N-0027 Oslo, Norway
关键词
chemokines; atherosclerosis; biomarkers; inflammation;
D O I
10.1161/ATVBAHA.107.161240
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Based on the importance of inflammation in atherogenesis, recent work has focused on whether plasma markers of inflammation can noninvasively diagnose and prognosticate atherosclerotic disorders. Although several studies support an important pathogenic role of chemokines in atherosclerosis, potentially representing attractive therapeutic targets in atherosclerotic disorders, this does not necessarily mean that chemokines are suitable parameters for risk prediction. In fact, the ability to reflect upstream inflammatory activity, stable levels in individuals, and high stability of the actual protein (eg, long half-life and negligible circadian variation) are additional important criteria for an ideal biomarker in cardiovascular disease. Although plasma/serum levels of certain chemokines (eg, interleukin-8/CXCL8 and monocyte chemoattractant protein-1/CCL2) have shown to be predictive for future cardiac events in some studies, their role as clinical biomarkers is unclear, and their ability to predict subclinical atherosclerosis has been disappointing. Further prospective studies, including a larger number of patients, are needed to make any firm conclusion. Based on the participation of several chemokines in atherogenesis, it is possible that in the future, combined measurements of multiple chemokines could reveal as a "signature of disease" that can serve as a highly accurate method to assess for the presence of atherosclerotic disease. (Arterioscler Thromb Vasc Biol. 2008;28:1909-1919)
引用
收藏
页码:1909 / 1919
页数:11
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