Departments of Medicine "D" & "E", The Tel-Aviv Sourasky Medical Center, Tel Aviv, Israel.
Clin Res Cardiol. 2010 Oct;99(10):651-6. doi: 10.1007/s00392-010-0167-1. Epub 2010 May 15.
Previous studies have demonstrated the presence of increased erythrocyte aggregation (EA) in patients with acute coronary syndromes (ACS). We have presently explored the correlation between the time from symptom onset to the appearance of an inflammatory response and aggregated erythrocytes in the peripheral blood of ACS patients.
Consecutive individuals undergoing coronary catheterization at the Tel-Aviv Souraski medical center were enrolled. Matched controls were fitted for each case in order to compare the EA and inflammatory response in each time quartile from symptom onset. Linear regression models were fitted for wide-range C-reactive protein (wr-CRP), fibrinogen and for the Vacuum R a measure of EA, as the dependant variables and adjusted to multiple cardiovascular risk factors, relevant medications as well as to time from symptom onset to angiography.
The study population comprised 428 male patients, 223 with unstable angina and 205 with acute myocardial infarction (AMI). A significant time-dependant increase in the concentrations of inflammation-sensitive biomarkers as well as EA has been noted only in the AMI group. Time from onset of pain to angiography entered as a significant predictor of fibrinogen, wr-CRP, and VR (r (2) = 0.24, p < 0.001; r (2) = 0.18, p < 0.001; r (2) = 0.6, p = 0.04; respectively).
The results indicate that erythrocyte aggregation and inflammation increase as time from clinical symptom onset lengthens during the course of AMI.
先前的研究表明,急性冠脉综合征(ACS)患者存在红细胞聚集(EA)增加。我们目前探讨了 ACS 患者外周血中从症状发作到炎症反应和聚集红细胞出现的时间之间的相关性。
连续入组在特拉维夫 Souraski 医疗中心接受冠状动脉造影的个体。为每个病例匹配了匹配的对照组,以便比较每个时间四分位从症状发作开始的 EA 和炎症反应。线性回归模型拟合了宽范围 C 反应蛋白(wr-CRP)、纤维蛋白原和真空 R 作为 EA 的测量值,作为因变量,并调整了多种心血管危险因素、相关药物以及从症状发作到血管造影的时间。
研究人群包括 428 名男性患者,其中 223 名患有不稳定型心绞痛,205 名患有急性心肌梗死(AMI)。仅在 AMI 组中观察到炎症敏感生物标志物和 EA 的浓度呈显著时间依赖性增加。疼痛发作到血管造影的时间作为纤维蛋白原、wr-CRP 和 VR 的显著预测因子(r (2) = 0.24,p < 0.001;r (2) = 0.18,p < 0.001;r (2) = 0.6,p = 0.04;分别)。
结果表明,在 AMI 过程中,从临床症状发作到炎症反应和聚集红细胞出现的时间延长,红细胞聚集和炎症反应增加。