Why the study?
Does the presence of diabetes or concomitant use of CYP3A4-metabolized drugs increase the risk of MACE in patients receiving DAPT after PCI?
Does the presence of diabetes or concomitant use of CYP3A4-metabolized drugs increase the risk of MACE in patients receiving DAPT after PCI?
In patients receiving DAPT after PCI, diabetes and the concomitant use of CYP3A4-metabolized drugs are significant risk factors for major adverse cardiac events.
Diabetes and CYP3A4 drug use were associated with higher MACE on DAPT; leaves open whether these factors warrant tailored regimens or prospective trials.
Patients who received percutaneous coronary intervention (PCI) should be treated with dual anti-platelet therapy (DAPT). DAPT significantly lowers the risk of the incidence of major adverse cardiac events (MACE). However, the risk factors for the incidence of MACE are unclear. We investigated the relationship between the incidence of MACE in PCI treated patients who underwent combined therapy by clopidogrel and aspirin, and patient background, present clinical history, lifestyle, and concomitant drugs. Between the MACE symptom group and non-MACE group, there were no significant differences in terms of patient background and lifestyle. In the MACE-symptom group, the percentage of treatments using concomitant drugs that inhibits cytochrom P450 (CYP)3A4 activity was significantly higher than in the non-MACE group (odds ratio 2.70). The present study also demonstrated that diabetes was an important risk factor (odds ratio 3.16, P = 0.001) of MACE symptoms. A significant positive correlation was found between diabetes and hypertension morbidity, and the administration ratio of concurrent drugs with CYP3A4 inhibition activity. The present study suggests that diabetes morbidity may be associated with MACE symptoms in antiplatelet therapy with DAPT.
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Takeno et al. (2014) studied this question.
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