4.3 Review

Diabetes and antiplatelet therapy: from bench to bedside

Journal

CARDIOVASCULAR DIAGNOSIS AND THERAPY
Volume 8, Issue 5, Pages 594-609

Publisher

AME PUBL CO
DOI: 10.21037/cdt.2018.05.09

Keywords

Coronary artery disease (CAD); diabetes mellitus (DM); antiplatelet therapy (APT); thrombosis; bleeding

Funding

  1. Amgen
  2. AstraZeneca
  3. Bayer
  4. Biosensors
  5. CeloNova
  6. CSL Behring
  7. Daiichi-Sankyo
  8. Eisai
  9. Eli-Lilly
  10. Gilead
  11. Janssen
  12. Matsutani Chemical Industry Co.
  13. Merck
  14. Novartis
  15. Osprey Medical
  16. Renal Guard Solutions

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Diabetes mellitus (DM) is a metabolic disorder associated with accelerated atherogenesis and an increased risk of atherothrombotic complications. Multiple mechanisms contribute to the prothrombotic status which characterizes DM patients underscoring the importance of antiplatelet therapies used for secondary prevention in these patients. For many years, dual antiplatelet therapy (DAPT) with aspirin and the P2Y12 inhibitor clopidogrel has represented the mainstay of treatment following an acute coronary syndrome (ACS) or in patients undergoing percutaneous coronary interventions (PCI). Although DAPT reduces the incidence of atherothrombotic recurrences, these rates remain high in DM patients underscoring the need for more efficacious therapies. Oral platelet P2Y(12) receptor inhibitors with enhanced potency, such as prasugrel and ticagrelor, as well as antiplatelet therapies such as vorapaxar inhibiting the thrombin-mediated platelet signaling pathway, constitute treatment opportunities for patients with DM and have shown to be associated with a greater reduction in ischemic recurrences, albeit at the cost of more bleeding. This article reviews currently available antiplatelet agents and delivers an update on the advances and drawbacks of these agents used for secondary prevention in DM patients experiencing an ACS or undergoing PCI.

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