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.
Abstract

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