Inflammation-sensitive proteins and erythrocyte aggregation in atherothrombosis

被引:27
作者
Ben Assayag, E
Bornstein, N
Shapira, I
Mardi, T
Goldin, Y
Tolshinski, T
Vered, Y
Zakuth, V
Burke, M
Berliner, S
Bonet, DS
机构
[1] Tel Aviv Sourasky Med Ctr, Dept Internal Med D, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-64239 Tel Aviv, Israel
关键词
inflammation-sensitive proteins; erythrocyte aggregation;
D O I
10.1016/j.ijcard.2003.12.013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To find the relative contribution of various inflammation-sensitive proteins including fibrinogen, immunoglobulins (IgG, IgM and IgA), ceruloplasmin and high sensitivity C-reactive protein (hs-CRP) to the induction and/or maintenance of enhanced erythrocyte adhesiveness/aggregation in the peripheral blood of individuals with atherothrombotic risk factors. Methods: The degree of erythrocyte adhesiveness/aggregation was determined by a simple slide test and image analysis. In addition, we measured various inflammation-sensitive protein levels including fibrinogen, ceruloplasmin, immunoglobulins and hs-CRP in a group of 234 individuals with atherothrombotic risk factors and healthy ones. Pearson partial correlations and multiple linear regression analysis were performed. Results: Fibrinogen was found to be the major protein contributing to the enhanced erythrocyte adhesiveness/aggregation, explaining 30% of the model. Fibrinogen and IgG together explained 32.4% of the model. Other inflammation-sensitive proteins did not reach statistical significance and were excluded from the model. Conclusions: Among inflammation-sensitive proteins measured in our cohort, fibrinogen is the dominant contributor to erythrocyte adhesiveness/aggregation in the peripheral blood of individuals with atherothrombotic risk factors and healthy ones. These findings may pave the way for the development of therapeutic strategies directed at the attenuation of erythrocyte aggregability in individuals with atherothrombosis. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:271 / 276
页数:6
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