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Body Mass Index and Platelet Reactivity During Dual Antiplatelet Therapy With Clopidogrel or Ticagrelor
Matteo Nardin1, Monica Verdoia, Chiara Sartori
1*Division of Cardiology, Azienda Ospedaliera-Universitaria "Maggiore della Carità," Eastern Piedmont University, Novara, Italy; †Clinical Chemistry, Azienda Ospedaliera-Universitaria "Maggiore della Carità," Eastern Piedmont University, Novara, Italy; and ‡Department of Cardiology, UMC St Radboud, Nijmegen, The Netherlands.
Insights
Higher body mass index (BMI) is linked to increased platelet reactivity in patients on clopidogrel, a dual antiplatelet therapy (DAPT), but not in those on ticagrelor. This finding impacts managing high residual platelet reactivity (HRPR) in coronary artery disease.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Research
Background:
- Dual antiplatelet therapy (DAPT) is crucial for patients with acute coronary syndromes or after percutaneous coronary revascularization.
- High residual platelet reactivity (HRPR) during DAPT is associated with increased risks of stent thrombosis and ischemic events.
- The influence of body mass index (BMI) on platelet reactivity in patients on DAPT requires further investigation.
Purpose of the Study:
- To investigate the impact of body mass index (BMI) on platelet reactivity in patients undergoing dual antiplatelet therapy (DAPT).
- To determine if BMI influences the effectiveness of acetylsalicylic acid (ASA), clopidogrel, or ticagrelor in patients with coronary artery disease.
Main Methods:
- A cohort of 498 patients treated with ASA and either clopidogrel or ticagrelor for acute coronary syndromes or drug-eluting stent implantation were analyzed.
- Platelet reactivity was assessed using multiple-electrode aggregometry 30-90 days post-discharge.
- High residual platelet reactivity (HRPR) was defined based on adenosine diphosphate (ADP) and acetylsalicylic acid (ASPI) test results.
Main Results:
- Higher BMI was associated with increased platelet reactivity and a trend towards higher HRPR for ADP antagonists overall, but this was not statistically significant.
- In the clopidogrel subgroup, higher BMI was an independent predictor of HRPR (OR, 1.45; P=0.049).
- No significant impact of BMI on platelet reactivity or HRPR was observed in patients treated with ticagrelor or on acetylsalicylic acid (ASA).
Conclusions:
- Higher body mass index (BMI) is associated with increased platelet reactivity and HRPR in patients treated with clopidogrel as part of DAPT.
- The effectiveness of ticagrelor and ASA in achieving adequate platelet inhibition is not significantly influenced by BMI.
- These findings suggest that BMI may be a factor to consider when optimizing DAPT strategies, particularly with clopidogrel.
Introduction:
Dual antiplatelet therapy (DAPT) is considered essential in clinical management of patients undergoing percutaneous coronary revascularization or acute coronary syndromes. However, the optimal platelet inhibition is not always obtained, with high residual platelet reactivity (HRPR) increasing stent thrombosis and recurrent ischemic events. Aim of this study was to investigate the impact of body mass index (BMI) on platelet reactivity in patients on DAPT.
Methods:
We included patients treated with acetylsalycilic acid (ASA) (100-160 mg) and clopidogrel (75 mg) or ticagrelor (90 mg twice a day) for acute coronary syndromes or drug-eluting stent implantation. Platelet reactivity was assessed at 30-90 days postdischarge by multiple-electrode aggregometry. HRPR for adenosine diphosphate (ADP) antagonists was defined as ADP test results >417 AU*min. HRPR for ASA was considered for ASPI test >862 AU*min.
Results:
Our population is represented by 498 patients, 308 (61.8%) were treated with clopidogrel and 190 (38.2%) with ticagrelor. Overall, higher BMI was related with younger age (P = 0.003), higher prevalence of diabetes mellitus (P < 0.001), hypercholesterolemia (P = 0.017), hypertension (P < 0.001), chronic therapy with angiotensin-receptor blockers (P = 0.019), calcium channel blockers (P = 0.003). Higher values of BMI directly related with hemoglobin (P = 0.02), triglycerides (P < 0.001), glycemia (P = 0.035), HbA1c (P < 0.001), and inversely related with high-density lipoprotein cholesterol (P = 0.01). BMI did not influence the effectiveness of ASA, whereas it was associated to a nonsignificant trend for higher platelet reactivity (r = 0.08, P = 0.08) for ADP antagonists. In fact, 111 patients (22.3%) displayed HRPR at ADP test (>417 AU*min) with no statistically significant difference according to BMI {20.3% vs. 27.1% vs. 25.7%, P = 0.28; adjusted odds ratio [OR] [95% confidence interval (CI)] = 1.19 [0.86-1.64], P = 0.30}. However, results were different when considering separately patients receiving clopidogrel or ticagrelor. In the clopidogrel-treated subgroup, significantly higher ADP-mediated aggregation values were found in patients with higher BMI (r = 0.14, P = 0.023) that emerged as an independent predictor of HRPR with clopidogrel [OR (95% CI), 1.45 (1.01-2.12), P = 0.049]. On the contrary, no impact of BMI was observed in the ticagrelor-treated subgroup for platelet reactivity (r = -0.036, P = 0.62) or the prevalence of HRPR [adjusted OR (95% CI), 0.73 (0.39-1.36), P = 0.32].
Conclusions:
This study shows that among patients treated with DAPT for coronary artery disease, higher BMI is related to increased platelet reactivity and a higher prevalence of HRPR in clopidogrel-treated patients while not significantly influencing the effectiveness of ticagrelor or ASA.
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