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Published on: March 29, 2024
Relationship between high on aspirin platelet reactivity and oxidative stress in coronary artery by-pass grafted
Wiktor Kuliczkowski1, Ryszard Golanski, Michal Bijak
1aDepartment of Cardiology, Wroclaw Medical University, Wroclaw bDepartment of Cardiac Surgery, Medical University of Lodz cDepartment of General Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz dSilesian Center for Heart Diseases, Zabrze eDepartment of Haemostasis and Haemostatic Disorders, Medical University of Lodz, Lodz, Poland.
Abstract:
The aim of the study was to assess the responsiveness of blood platelets to acetylsalicylic acid (ASA) in patients following coronary artery bypass grafting (CABG) surgery with relation to oxidative and antioxidative plasma status. The study included 37 patients treated with the CABG procedure. During the first 24 h after CABG patients were given 300 mg of ASA with the following dose of 150 mg daily. The blood was collected before the procedure and 10 days after. Whole blood platelet aggregation induced with arachidonic acid, collagen and adenosine diphosphate (ADP) was performed together with whole blood generation of thromboxane B2 (TxB2). Oxidative stress was measured before and 10 days after CABG with total oxidative plasma status (TOS) and total antioxidative status of the plasma (TAS). TOS/TAS index was calculated. We observed a significant increase in the TOS and TOS/TAS index and ADP-induced aggregation 10 days after CABG in comparison with its level before operation. There was a significant decrease in the arachidonic acid-induced aggregation and serum TxB2 level. Patients with ADP-induced and collagen-induced aggregation in the upper quartile had significantly higher TOS and TOS/TAS index before (ADP) and after the operation (ADP and collagen). There were 19 patients (51%) with high on aspirin platelet reactivity after CABG who had also higher TOS and TOS/TAS index and lower TAS value in comparison with aspirin responders. Despite ASA use, increased oxidative stress after CABG can overcome its antiplatelet effect and increase platelet activation through other pathways.
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