Activation of coagulation and hyperfibrinolysis in patients with aortic arch atheromatosis (Aortic AA) as a risk factor for cerebral ischemia

• Published in: Thrombosis and haemostasis Vol. 93; no. 4; p. 690
• Main Authors: Siemens, Hans-Joachim G, Mirau, Wladimir, Brueckner, Sabine, Jahn, Juergen, Roth-Isigkeit, Angela, Gutsche, Sven, Mitusch, Rolf, Sheikhzadeh, Abdolhamid
• Format: Journal Article
• Language: English
• Published: Germany 01.04.2005
• Subjects: Adult; Aged; Aged, 80 and over; Aortic Arch Syndromes - blood; Aortic Arch Syndromes - complications; Arteriosclerosis - blood; Arteriosclerosis - complications; Biomarkers - blood; Blood Coagulation; Brain Ischemia - etiology; Case-Control Studies; Female; Fibrinolysis; Humans; Male; Middle Aged; Risk Factors; Severity of Illness Index; Thrombophilia - blood
• ISSN: 0340-6245
• DOI: 10.1160/TH02-12-0320

In patients with cerebral ischemia, a frequent finding is atheromatous plaques in the ascending aorta and the aortic arch. Since we were able to demonstrate that patients with atrial fibrillation have an increased coagulatory activity, we wanted to evaluate a potential systemic activation of the coagulatory system in patients with aortic arch atheromatosis (Aortic AA). In 134 consecutive patients, we determined several parameters of the coagulatory and fibrinolytic systems as well as several thrombophilia risk factors and compared the results with 134 age- and sex-matched healthy controls. In 90 of the 134 patients, transesophageal echocardiography showed Aortic AA, and in the remaining 44 patients, there were no aortic findings. The Aortic AA group showed higher concentrations of thrombin-antithrombin (TAT) and plasmin-antiplasmin complexes (PAP). Further division into 4 subgroups of different severity (grade I: no plaques; grade II: plaques 2-5 mm, grade III: plaques > 5 mm, grade IV: mobile plaques), revealed increasing concentrations of fibrinogen, D-dimers and tissue-type plasminogen activator. The grade IV-group displayed the highest values in comparison to all other groups. In conclusion, Aortic AA as such is a risk factor for cerebral ischemia. It causes a systemically detectable activation of coagulation which substantially exceeds the values for controls. This observation is in accordance with our findings in patients with atrial fibrillation.