Acute coronary syndromes do not promote prolonged in vivo FXII-dependent prothrombotic activity

详细信息    查看全文

• 作者：Altieri ; Paola ; Devoto ; Emmanuela ; Spallarossa ; Paolo ; Rossettin ; Pierfranco ; Garibaldi ; Silvano ; et. al.
• 关键词：FXIIa ; Activated Factor XII ; CS ; contact system ; ACS ; acute coronary syndromes ; BMI ; body mass index ; IHD ; ischemic heart disease ; CHD ; coronary heart disease ; SA ; stable angina ; ACS ; acute coronary syndromes ; UA ; unstable angina ; nQ-MI ; non-Q myocardial
• 刊名：Thrombosis Research
• 出版年：2005
• 出版时间：2005
• 年：2005
• 卷：115
• 期：1-2
• 页码：65-72
• 全文大小：106 K

文摘

Background: Coagulation FXII is activated on contact with lipoprotein particles. It has been suggested that contact with subendothelial tissue provides an alternative biological surface for FXII activation. Our aim was to investigate whether activated FXII (FXIIa) is elevated in patients with coronary atherosclerosis, and whether disease status (acute phase or stable state) affects circulating levels of FXIIa. Methods: Circulating FXIIa levels were measured in the peripheral blood of 122 patients with coronary atherosclerosis (32, stable angina; 54, unstable angina; 36, nQ myocardial infarction) and in 45 age-matched subjects (Contr). Results: FXIIa levels (median, first and third quartiles; ng/ml) were higher in patients than in Contr: 1.61 (1.26aaa2.02) vs. 1.34 (1.13aaa1.81) (p<0.01). FXIIa levels were similar among patients with stable angina [1.66 (1.23aaa1.91)], unstable angina [1.53 (1.21aaa2.04)], and nQ myocardial infarction [1.75 (1.34aaa2.03)]. The three groups of patients had similar prevalence for most atherothrombotic risk factors; patients with stable angina had an increased severity of coronary disease, which did not explain the different levels of FXIIa. Fasting levels of triglycerides were the best predictor of FXIIa levels in our patients. Conclusions: The finding of similar FXIIa levels among patients in either acute or chronic phases of coronary atherosclerosis suggests that the initial arterial denudation and the acute-phase response associated to acute coronary syndromes are not major determinants for prolonged FXII activation.