CCTA Evaluation of SGLT2i-related Pericoronary Fat Changes in Non-diabetic ACS Patients Without HF

Overview

The goal of this clinical trial is to learn if dapagliflozin, a sodium-glucose cotransporter 2 inhibitor (SGLT2i), can reduce coronary artery inflammation in people with acute coronary syndrome (ACS) who do not have diabetes or heart failure. Coronary inflammation will be measured using the fat attenuation index (FAI), a marker derived from coronary CT angiography (CCTA) that quantifies inflammation in the fat tissue surrounding heart arteries. The main questions it aims to answer are: * Does dapagliflozin lower coronary artery inflammation as measured by FAI? * Does dapagliflozin slow the progression of coronary plaques? Researchers will compare participants who take dapagliflozin 10 mg daily plus standard therapy to those who receive standard therapy alone for 6 months. Participants will: * Undergo percutaneous coronary intervention (PCI) for ACS * Have a baseline CCTA scan at 1 month after PCI, at which point they will be randomly assigned to receive dapagliflozin or standard care alone * Have a follow-up CCTA scan at 6 months after randomization * Have blood tests at the time of PCI, at randomization, and at 6 months after randomization * Receive follow-up phone calls at 3 and 6 months after randomization

SCIENTIFIC BACKGROUND Residual inflammatory risk (RIR) has emerged as a major driver of adverse cardiovascular outcomes in patients with acute coronary syndrome (ACS), even after guideline-directed medical therapy and successful revascularization. Recent pooled analyses of the PROMINENT, REDUCE-IT, and STRENGTH trials demonstrated that high-sensitivity C-reactive protein (hsCRP), a marker of RIR, predicts future cardiovascular events more strongly than LDL-cholesterol in statin-treated patients. Pericoronary adipose tissue (PCAT) fat attenuation index (FAI), measured by coronary CT angiography (CCTA), has been validated as a novel imaging biomarker that directly quantifies coronary artery inflammation. When coronary inflammation occurs, PCAT undergoes characteristic morphological changes with decreased lipid content and increased water-to-fat ratio, resulting in higher CT attenuation values (shifting from approximately -190 Hounsfield Units toward -30 HU). The CRISP-CT study validated this imaging biomarker and demonstrated its prognostic value for cardiac mortality independent of conventional cardiovascular risk factors. SGLT2 inhibitors have established cardiovascular benefits in patients with diabetes or heart failure. Beyond glucose-lowering and diuretic effects, anti-inflammatory mechanisms may contribute to these benefits, including suppression of inflammatory cytokines such as interleukin-6 and monocyte chemoattractant protein-1, reduction of oxidative stress, and improvement of endothelial function. Clinical studies have shown that SGLT2 inhibitors reduce epicardial adipose tissue volume and may stabilize coronary plaques in diabetic patients. The EMPA-TROPISM study provided evidence that empagliflozin reduces epicardial adipose tissue volume even in non-diabetic patients with heart failure, suggesting glucose-independent mechanisms. KNOWLEDGE GAP The EMPACT-MI and DAPA-MI trials recently evaluated SGLT2 inhibitors in patients with acute myocardial infarction without diabetes or heart failure, with primary endpoints focused on clinical outcomes. Neither trial specifically assessed coronary inflammation using validated imaging biomarkers. Whether SGLT2 inhibitors exert measurable anti-inflammatory effects at the coronary arterial level in this population remains unknown. STUDY RATIONALE This study addresses this knowledge gap by employing CCTA-derived pericoronary fat attenuation index as a direct measure of coronary inflammation. The study population specifically excludes patients with diabetes and heart failure to isolate the potential anti-inflammatory effects of dapagliflozin from its established benefits in these conditions. Assessment of non-culprit vessels in patients with multivessel disease allows longitudinal evaluation of atherosclerotic changes without interference from prior intervention. STUDY TIMELINE Participants undergo PCI for ACS at enrollment. At 1 month post-PCI, eligible participants undergo baseline CCTA and are then randomized to receive either dapagliflozin plus standard therapy or standard therapy alone. This timing allows for stabilization of the acute coronary event before baseline imaging assessment. Follow-up CCTA is performed at 6 months post-randomization to evaluate changes in FAI and plaque characteristics. CLINICAL SIGNIFICANCE Current anti-inflammatory therapies for secondary prevention of coronary artery disease have significant limitations, including high cost and limited accessibility for monoclonal antibodies such as canakinumab, and gastrointestinal side effects with poor tolerability for low-dose colchicine. If this study demonstrates that SGLT2 inhibitors reduce coronary inflammation in non-diabetic patients without heart failure, it would expand therapeutic options for addressing residual inflammatory risk and potentially benefit a broader patient population beyond those with diabetes or heart failure.