Why the study?
The study was conducted to determine clinical and genetic factors predicting the development of dyspnea in patients receiving ticagrelor.
What clinical and genetic factors predict the development of ticagrelor-induced dyspnea in patients with acute myocardial infarction?
What clinical and genetic factors predict the development of ticagrelor-induced dyspnea in patients with acute myocardial infarction?
Lower platelet aggregation (ADP HS ≤19.5 U) and lower-dose or no atorvastatin are significant predictors of ticagrelor-induced dyspnea in patients with acute myocardial infarction.
Lower ADP HS aggregation and ABCB1 variants were associated with ticagrelor dyspnea; leaves open utility for risk stratification in ACS.
(1) Background: The aim of this study was to determine clinical and genetic factors predicting the development of dyspnea in patients receiving ticagrelor. (2) Methods: A total of 277 patients with acute myocardial infarction (with and without ST-segment elevation), who underwent coronary angiography and PTCA with stent implantation and treated with antiplatelet drugs (ticagrelor and aspirin), were enrolled in this study. Platelet aggregation (induction with high-sensitivity ADP, ADP HS) testing was performed using a MULTIPLATE analyzer and reagents for the determination of P2Y12 receptor activity. Venous blood samples were collected for genotyping. (3) Results: Patients experiencing ticagrelor-related dyspnea had lower ADP HS. ROC curve analysis showed that an ADP HS cut-off of ≤19.5 U was associated with the development of dyspnea. The ADP HS value of ≤19.5 U and any dose of atorvastatin lower than 80 mg (or no atorvastatin) increased the risk of dyspnea by more than 4 and 2 times, respectively (OR = 4.07, p ≤ 0.001 and OR = 2.25; p = 0.008). (4) Conclusion: A lower ADP HS value possibly indicates greater ticagrelor activity and a higher plasma concentration of this drug. Atorvastatin might have an impact on the occurrence of ticagrelor-related dyspnea by affecting ticagrelor metabolism. No impact of any genetic variant on the development of dyspnea was determined.
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Tamakauskas et al. (2022) studied this question.
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