AI Article Synopsis

  • The study examined the effects of diabetes mellitus (DM) on patients with acute coronary syndrome (ACS) and their 2-year health outcomes based on the type of antiplatelet therapy used.
  • Among the 1717 ACS patients, 38% had DM, and these patients were older, more often female, and had more health complications, with clopidogrel being the most prescribed medication.
  • Findings indicated that DM significantly increased the risk of major adverse cardiovascular events (MACEs) and overall mortality, with the use of ticagrelor or prasugrel linked to better outcomes compared to clopidogrel in diabetic patients.

Article Abstract

Aims: We investigated the impact of diabetes mellitus (DM) in acute coronary syndrome (ACS) patients, and the 2-year prognosis based on antiplatelet therapy.

Methods: This is a prospective and multicenter registry including hospitalized ACS patients. Clinical management and antiplatelet therapy at discharge were recorded. Bleeding events, all-cause mortality and major adverse cardiovascular events (MACEs) were recorded during 2-years and compared according to DM and the P2Y receptor inhibitor.

Results: From 1717 ACS patients, 653 (38%) had DM. Diabetic patients were older, more commonly females, with higher prevalence of comorbidities and more conservative management. After excluding antiplatelet monotherapy or oral anticoagulation, clopidogrel was prescribed in 59.6% of DM patients. Cox regression analysis showed that DM was an independent risk factor for MACE (aHR 1.39, 95% CI 1.05-1.83). The use of clopidogrel instead of ticagrelor/prasugrel was also independently associated with MACE (aHR 1.71, 95% CI 1.11-2.63), and all-cause mortality (aHR 2.47, 95% CI 1.23-4.96) in diabetic patients (log-rank p-values < 0.001).

Conclusions: In ACS patients, DM was associated with higher risk of MACE. In such patients, the use of ticagrelor/prasugrel reduced MACE and mortality compared to clopidogrel. Novel P2Y receptor inhibitors might be used as the first therapeutic choice in these high-risk patients.

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http://dx.doi.org/10.1016/j.diabres.2022.109215DOI Listing

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