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Ticagrelor as an Alternative Antiplatelet Therapy in Cardiac Patients Non-Sensitive to Aspirin
Hamzah Khan1, Reid Gallant2, Shubha Jain1
1Division of Vascular Surgery, St. Michael's Hospital, Toronto, ON M5B 1W8, Canada.
Insights
A significant portion of coronary artery disease patients are non-sensitive to aspirin therapy. This study found that these aspirin non-sensitive patients demonstrated sensitivity to ticagrelor, suggesting it as a viable alternative treatment.
Area of Science:
- Cardiology
- Pharmacology
- Hematology
Background:
- Aspirin (acetylsalicylic acid) is a primary antiplatelet medication for coronary artery disease (CAD).
- A notable percentage of CAD patients exhibit non-sensitivity to aspirin, increasing their risk of adverse cardiovascular events.
- Ticagrelor offers an alternative antiplatelet mechanism for patients unresponsive to aspirin.
Purpose of the Study:
- To identify patients with coronary artery disease who are non-sensitive to aspirin therapy.
- To evaluate the sensitivity of aspirin non-sensitive patients to ticagrelor.
Main Methods:
- Pilot study involving 38 CAD patients on 81 mg aspirin.
- Light-transmission aggregometry (LTA) used to assess platelet aggregation in response to arachidonic acid (for aspirin sensitivity) and adenosine diphosphate (ADP) (for ticagrelor sensitivity).
- Patients with ≥20% maximal platelet aggregation after arachidonic acid were deemed aspirin non-sensitive; those with ≥46% maximal aggregation after ADP were considered ticagrelor non-sensitive.
Main Results:
- 32% (12/38) of patients were identified as non-sensitive to their aspirin therapy.
- All patients (100%) demonstrated sensitivity to ticagrelor ex vivo.
- Aspirin non-sensitive patients were found to be sensitive to ticagrelor.
Conclusions:
- The study successfully identified aspirin non-sensitivity in CAD patients using LTA.
- Ticagrelor proved effective in all tested patients, including those non-sensitive to aspirin.
- Ticagrelor represents a potential alternative antiplatelet therapy for aspirin non-sensitive individuals with CAD.
Abstract:
Background and Objectives: Aspirin (acetylsalicylic acid-ASA) is a first-line antiplatelet therapy provided to patients with coronary artery disease (CAD). However, it has been demonstrated that 20-30% of these patients are non-sensitive to their ASA therapy. ASA non-sensitivity is a phenomenon where low-dose ASA (81-325 mg) does not completely inhibit arachidonic-acid-induced platelet aggregation, putting patients at risk of adverse cardio-thrombotic events. Ticagrelor is a P2Y12 receptor inhibitor and alternative antiplatelet that has been approved to reduce the risk of stroke, myocardial infarction, and overall cardiovascular-related death. In this study, we aimed to identify ASA non-sensitive patients and evaluate if they would be sensitive to ticagrelor. Materials and Methods: For this pilot study, thirty-eight patients with CAD taking 81 mg ASA were recruited. Blood samples were collected from each patient and platelet rich plasma (PRP) from each sample was isolated. Light-transmission aggregometry (LTA) was used to determine baseline ASA sensitivity in each patient using 0.5 mg/mL arachidonic acid as a platelet agonist. Patients with ≥20% maximal platelet aggregation after activation were considered ASA non-sensitive. Fresh PRP samples from all patients were then spiked with a clinical dosage of ticagrelor (3 μM-approximately equivalent to a loading dose of 180 mg ticagrelor). Sensitivity was determined using LTA and 5 μM ADP as a platelet agonist. Patients with ≥46% maximal platelet aggregation were considered ticagrelor non-sensitive. Results: Of the 38 CAD patients taking 81 mg ASA, 32% (12/38) were non-sensitive to their 81 mg ASA therapy. All 38 of the recruited patients (100%) were sensitive to ticagrelor ex vivo. In conclusion, we were able to identify ASA non-sensitivity using LTA and determine that ASA non-sensitive patients were sensitive to ticagrelor. Conclusions: Our results suggest that ticagrelor is a promising alternative therapy for patients who are non-sensitive to ASA.
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