Soluble CD40 ligand is an early initiator of inflammation after coronary intervention

被引:40
作者
Aggarwal, A
Blum, A
Schneider, DJ
Sobel, BE
Dauerman, HL
机构
[1] Nebraska Heart Inst, Hastings, NE 68901 USA
[2] Poria Med Ctr, Dept Internal Med A, Lower Galilee, Israel
[3] Univ Vermont, Coll Med, Cardiol Unit, Burlington, VT USA
关键词
stent; inflammation; coronary artery disease;
D O I
10.1097/00019501-200412000-00003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background This prospective study evaluated the early increase in markers of inflammation after coronary stenting, and the predictors of early rise. Elevation of markers of inflammation after percutaneous coronary intervention correlates with an increased risk of adverse events. The role of soluble CD40 ligand (sCD40L) as a potential initiator of inflammation after stenting has not been described. Methods Seventy-five patients were treated with heparin alone (n = 25), or randomized to adjuvant treatment with eptifibatide (n = 26) or abciximab (n = 24) during stenting. Systemic blood was obtained before coronary stenting and at 10 min after stenting. C-reactive protein (CRP), interleukin (IL)-6, IL-1 receptor antagonist and sCD40L were determined by enzyme liberated immunosorbent assay. Results sCD40L exhibited the greatest relative rise (35%, P = 0.01 compared to concentrations before intervention) in the first 10 min after stenting. In a logistic regression model, an early increase in the concentration of sCD40L was predicted by baseline laboratory values (white blood count and sCD40L level before stenting) and procedural characteristics (number of stents and glycoprotein IIb-IIIa inhibitor assignment). Conclusions In conclusion, a systemic inflammatory response is detectable 10 min after coronary stent placement. The early increase in sCD40L suggests a possible role for this marker in the initiation of inflammation after coronary stenting. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:471 / 475
页数:5
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