About this trial
Both globally and nationally, heart disease remains the leading cause of death overall and across genders, with ischemic heart disease being the primary cause. It is now understood that multiple risk factors contribute to the development of this condition, notably type 2 diabetes mellitus and obesity, especially an increase in visceral fat. Among these, the role of epicardial fat volume in the presence of atheromatous plaques in patients with coronary artery disease has been emphasized, along with the link between its volume and the risk of ischemic cardiovascular events. Consequently, recent decades have seen focused research on the potential of epicardial fat as a marker for major adverse cardiac events and on strategies to reduce its volume as a treatment goal for patients with risk factors.
Selective sodium-glucose cotransporter 2 inhibitors are drugs that, beyond their antihyperglycemic effect, have demonstrated cardiovascular benefits through various mechanisms, including a reduction in epicardial fat. This was supported by a previous study conducted by our research group, although no statistically significant difference was found. On the other hand, GLP-1 agonists are effective drugs for weight control in patients with severe obesity. However, little research has been done on their effect on more localized fat, such as epicardial fat.
Eligibility criteria
Qualifiers
Criteria for the fourth definition of acute myocardial infarction with and without ST-segment elevation.
Diagnosed with type 2 diabetes.
Initial serum high-sensitivity CRP value > 2.0 mg/L.
Clinically obese.
Disqualifiers
Patients who have recently received immunosuppressive therapy
Patients with a history of ischemic heart disease
Known allergy to any of the medications used
Use of any of the study drugs more than 6 months prior to randomization
Trial design
Treatments tested in this trial
- Dapagliflozin 10 MG Oral Tablet
- Semaglutide (Rybelsus®)