Inflammatory markers predict late cardiac events in patients who are exhausted after percutaneous coronary intervention

被引:41
作者
Kwaijtaal, M
van Diest, R
Bär, FW
van der Ven, AJ
Bruggeman, CA
de Baets, MH
Appels, A
机构
[1] Univ Hosp Maastricht, Dept Med Microbiol, NL-6202 AZ Maastricht, Netherlands
[2] Univ Maastricht, European Grad Sch Neurosci, Maastricht, Netherlands
[3] Univ Maastricht, Dept Psychiat & Neuropsychol, Maastricht, Netherlands
[4] Univ Maastricht, Dept Cardiol, Maastricht, Netherlands
[5] Univ Maastricht, Cardiovasc Res Inst Maastricht, Maastricht, Netherlands
[6] Univ Nijmegen, Med Ctr St Radboud, Dept Internal Med, Nijmegen, Netherlands
[7] Univ Hosp Maastricht, Dept Neurol, Maastricht, Netherlands
[8] Maastricht Univ, Dept Med Psychol, Maastricht, Netherlands
关键词
angioplasty; restenosis; inflammation;
D O I
10.1016/j.atherosclerosis.2005.02.022
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic inflammation is one of the main underlying mechanisms in the development of coronary artery disease (CAD). We investigated the prognostic value of inflammatory markers for cardiac events occurring more than 6 months after percutaneous coronary intervention (PCI), i.e. late cardiac events, furthermore we investigated the temporal stability of these markers. Exhausted patients (234) recently treated by successful PCI were studied. Serum samples collected about 6 weeks after PCI (baseline), 6 and 18 months after baseline were analyzed for CRP, IL-6, tumour necrosis factor (TNF-alpha), IL-10, IL-1ra, IL-8 and neopterin. In the mean cardiac follow-up of 24 months, 25 late cardiac events occurred. Cox proportional hazards analysis was used to determine the prognostic value. Elevated concentrations of IL-6 at baseline and 6 months later increased the risk of late cardiac events (RR 3.9, CI 1.7-9.0, p 0.00 and RR 3.6, CI 1.6-8.5. p 0.00). Elevated concentrations of CRP and IL-10 at baseline also increased the risk of late cardiac events (RR 2.5, CI 1.1-5.7, p 0.04 and RR 2.5, CI 1.1-5.6, p 0.03) as did IL-1 receptor antagonist at 6 months (RR 2.6, CI 1.1-6.1, p 0.04). Temporal stability was high for most markers, but highest for IL-6. These results support the assumption that chronic inflammation is a pathophysiological mechanism in the development of CAD. (c) 2005 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:341 / 348
页数:8
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