The balance between pro- and anti-inflammatory cytokines is associated with platelet aggregability in acute coronary syndrome patients

被引:66
|
作者
Gori, A. M. [1 ,2 ]
Cesari, F. [1 ,2 ]
Marcucci, R. [1 ,2 ]
Giusti, B. [1 ,2 ]
Paniccia, R. [1 ,2 ]
Antonucci, E. [1 ,2 ]
Gensini, G. F. [1 ,2 ,3 ,4 ]
Abbate, R. [1 ,2 ]
机构
[1] Univ Florence, Dept Med & Surg Crit Care, I-50134 Florence, Italy
[2] Univ Florence, Ctr Study Mol & Clin Level Chron Degenerat & Neop, I-50134 Florence, Italy
[3] Azienda Osped Univ Careggi, Dept Heart & Vessels, Florence, Italy
[4] Fdn Don Carlo Onlus IRCCS, Ctr S Maria Ulivi, Florence, Italy
关键词
Inflammation; Residual platelet reactivity; Anti-inflammatory cyto-chemokines; Pro-inflammatory cyto-chemokines; C-reactive protein; Von Willebrand factor; ASPIRIN RESISTANCE; INCREASED RISK; MYOCARDIAL-INFARCTION; CLOPIDOGREL; REACTIVITY; EVENTS; INTERVENTION; DETERMINANT; CHEMOKINES; ADHESION;
D O I
10.1016/j.atherosclerosis.2008.04.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Residual platelet reactivity (RPR) on antiplatelet therapy in ischemic heart disease patients is associated with adverse events. Clinical. cellular and pharmacogenetic factors may account for the variable response to antiplatelet treatment. Objective: We sought to explore the interplay of multiple pro-inflammatory and anti-inflammatory cytokines with platelet function in patients with acute coronary syndrome (ACS) undergoing percutaneous coronary intervention (PCI) on dual antiplatelet therapy. Methods: In 208 ACS patients undergoing PCI on dual antiplatelet therapy we measured platelet function by platelet aggregation with two agonists [1 mM arachidonic acid (AA) and 10 mu M ADPI. IL-1 beta, IL-1ra, IL-4, IL-6. IL-8, IL-10, IL-12, IP-10, IFN-gamma. MCP-1, MIP-1 alpha, MIP-1 beta. TNF-alpha, and VEGF levels were determined by using the Bio-Plex cytokine assay (Bio-Rad Laboratories Inc., Hercules, CA, USA). We defined patients with RPR those with platelet aggregation by AA >= 20% and/or ADP (10 mu mol) >= 70%. Results: We documented a significant association between IP-10, IFN-gamma, IL-4 and RPR by both AA- and ADP-induced platelet aggregation after adjustment for age, sex, cardiovascular risk factors. ejection fraction. BMI, vWF and CRP. Patients with pro-inflammatory cytokines not compensated by anti-inflammatory cytokines had higher risk of RPR by both AA and ADP (AA: OR = 3.85, 95% CI 1.52-9.74 ADP: OR = 2.49, 95% CI 1.33-4.68) with respect to patients with balanced anti-/pro-inflammatory cytokines. Patients with anti-inflammatory response overwhelming pro-inflammatory response have lower risk of RPR (AA: OR = 0.55, 95% CI 0.28-1.06: ADP: OR = 0.47, 95% CI 0.26-0.87). Conclusion: Our study provides new insights into the interplay of anti-/pro-inflammatory cytokines with platelet hyper-reactivity in high-risk patients. (C) 2008 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:255 / 262
页数:8
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