Soluble CD40 ligand in acute coronary syndromes

被引:705
作者
Heeschen, C
Dimmeler, S
Hamm, CW
van den Brand, MJ
Boersma, E
Zeiher, AM
Simoons, ML
CAPTURE Study Investigators
机构
[1] c7E3 Fab Antiplatelet Therapy Unstable Refractory, Frankfurt, Germany
[2] Univ Frankfurt, Dept Internal Med 4, D-6000 Frankfurt, Germany
[3] Kerckhoff Heart Ctr, Bad Nauheim, Germany
[4] Erasmus Univ, Thoraxctr, NL-3000 DR Rotterdam, Netherlands
关键词
D O I
10.1056/NEJMoa022600
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: CD40 ligand is expressed on platelets and released from them on activation. We investigated the predictive value of soluble CD40 ligand as a marker for clinical outcome and the therapeutic effect of glycoprotein IIb/IIIa receptor inhibition in patients with acute coronary syndromes. Methods: Serum levels of soluble CD40 ligand were measured in 1088 patients with acute coronary syndromes who had previously been enrolled in a randomized trial comparing abciximab with placebo before coronary angioplasty and in 626 patients with acute chest pain. Results: The levels of soluble CD40 ligand were elevated (above 5.0 mug per liter) in 221 patients with acute coronary syndromes (40.6 percent). Among patients receiving placebo, elevated soluble CD40 ligand levels indicated a significantly increased risk of death or nonfatal myocardial infarction during six months of follow-up (adjusted hazard ratio as compared with patients with low levels of the ligand [less than or equal to5.0 mug per liter], 2.71; 95 percent confidence interval, 1.51 to 5.35; P=0.001). The prognostic value of this marker was validated in the patients with chest pain, among whom elevated soluble CD40 ligand levels identified those with acute coronary syndromes who were at high risk for death or nonfatal myocardial infarction (adjusted hazard ratio as compared with those with low levels of the ligand, 6.65; 95 percent confidence interval, 3.18 to 13.89; P<0.001). The increased risk in patients with elevated soluble CD40 ligand levels was significantly reduced by treatment with abciximab (adjusted hazard ratio as compared with those receiving placebo, 0.37; 95 percent confidence interval, 0.20 to 0.68; P=0.001), whereas there was no significant treatment effect of abciximab in patients with low levels of soluble CD40 ligand. Conclusions: In patients with unstable coronary artery disease, elevation of soluble CD40 ligand levels indicated an increased risk of cardiovascular events. Elevation of soluble CD40 ligand identifies a subgroup of patients at high risk who are likely to benefit from antiplatelet treatment with abciximab.
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页码:1104 / 1111
页数:8
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