Unfractionated heparin is associated with a lower rise of serum vascular cell adhesion molecule-1 in acute ischemic stroke patients

被引:34
作者
Chamorro, A
Cervera, A
Castillo, J
Dávalos, A
Aponte, JJ
Planas, AM
机构
[1] Hosp Clin Univ, Serv Neurol, Barcelona 08036, Spain
[2] Complejo Hosp Univ, Dept Neurol, Santiago De Compostela 15706, Spain
[3] Hosp Univ Doctor Josep Trueta, Neurol Sect, Girona 17001, Russia
[4] Hosp Clin Univ, Barcelona 08036, Spain
[5] CSIC, IIBB, Dept Pharmacol & Toxicol, Barcelona 08036, Spain
关键词
cerebrovascular disease; heparin; aspirin; cytokines; vascular cell adhesion molecule-1; inflammation; outcome;
D O I
10.1016/S0304-3940(02)00518-9
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We sought to assess the anti-inflammatory properties of unfractionated heparin (UFH) in patients with ischemic stroke treated within 24 h from the onset of symptoms. We studied prospectively 167 patients that received 1000 IU/h intravenous UFH (n = 70) or 300 mg oral aspirin (n = 97) at a mean treatment delay of 6.7 h. Repeated plasma levels of interleukin (IL)-6, IL-10, IL-4, tumor necrosis factor (TNF)-alpha, soluble intercellular adhesion molecule-1 (sICAM-1), and soluble vascular cell adhesion molecule-1 (sVCAM-1) were compared in both groups using multivariate analyses. Whereas TNF-alpha and sICAM-1 decreased at 48 h, IL-6, IL-4, and sVCAM-1 increased compared with baseline values (P < 0.01). The rise of sVCAM-1 levels at 48 h was significantly lower in patients treated with UFH (P = 0.017) and a two-fold increase of baseline sVCAM-1 was an independent predictor of poor outcome (odds ratio, 2.19,1.1-4.39). These results suggest that adjusted high-dose UFH has anti-inflammatory effects which might improve recovery if administered early after stroke onset. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:229 / 232
页数:4
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