Key result
In prediabetic patients with acute myocardial infarction, current metformin use was associated with a lower rate of Major Adverse Cardiac Events at 12 months compared to never-users, alongside reduced pericoronary fat inflammation.
Why the study?
Pericoronary adipose tissue inflammation may drive coronary plaque destabilization in prediabetes, but its features and the prognostic effects of metformin following AMI were unclear.
Does metformin reduce MACE and pericoronary fat inflammation in prediabetic patients with acute myocardial infarction undergoing CABG?
Observational (n=626)
Yes
Does metformin reduce MACE and pericoronary fat inflammation in prediabetic patients with acute myocardial infarction undergoing CABG?
Metformin use in prediabetic patients with acute myocardial infarction undergoing CABG is associated with reduced pericoronary fat inflammation and a lower rate of major adverse cardiac events at 12 months.
Answers are grounded in this paper and cite their sources.
Should not yet change practice in prediabetic AMI; leaves open confirmation of lower MACE by randomized trials.
BACKGROUND/OBJECTIVES: Pericoronary adipose tissue inflammation might lead to the development and destabilization of coronary plaques in prediabetic patients. Here, we evaluated inflammation and leptin to adiponectin ratio in pericoronary fat from patients subjected to coronary artery bypass grafting (CABG) for acute myocardial infarction (AMI). Furthermore, we compared the 12-month prognosis of prediabetic patients compared to normoglycemic patients (NG). Finally, the effect of metformin therapy on pericoronary fat inflammation and 12-months prognosis in AMI-prediabetic patients was also evaluated. METHODS: An observational prospective study was conducted on patients with first AMI referred for CABG. Participants were divided in prediabetic and NG-patients. Prediabetic patients were divided in two groups; never-metformin-users and current-metformin-users receiving metformin therapy for almost 6 months before CABG. During the by-pass procedure on epicardial coronary portion, the pericoronary fat was removed from the surrounding stenosis area. The primary endpoints were the assessments of Major-Adverse-Cardiac-Events (MACE) at 12-month follow-up. Moreover, inflammatory tone was evaluated by measuring pericoronary fat levels of tumor necrosis factor-α (TNF-α), sirtuin 6 (SIRT6), and leptin to adiponectin ratio. Finally, inflammatory tone was correlated to the MACE during the 12-months follow-up. RESULTS: The MACE was 9.1% in all prediabetic patients and 3% in NG-patients. In prediabetic patients, current-metformin-users presented a significantly lower rate of MACE compared to prediabetic patients never-metformin-users. In addition, prediabetic patients showed higher inflammatory tone and leptin to adiponectin ratio in pericoronary fat compared to NG-patients (P < 0.001). Prediabetic never-metformin-users showed higher inflammatory tone and leptin to adiponectin ratio in pericoronary fat compared to current-metformin-users (P < 0.001). Remarkably, inflammatory tone and leptin to adiponectin ratio was significantly related to the MACE during the 12-months follow-up. CONCLUSION: Prediabetes increase inflammatory burden in pericoronary adipose tissue. Metformin by reducing inflammatory tone and leptin to adiponectin ratio in pericoronary fat may improve prognosis in prediabetic patients with AMI. Trial registration Clinical Trial NCT03360981, Retrospectively Registered 7 January 2018.
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Sardu et al. (2019) conducted an observational in Acute myocardial infarction and multivessel coronary artery disease (n=626). Metformin vs. Never-metformin-users was evaluated on Major Adverse Cardiac Events (MACE) at 12 months. In prediabetic patients with acute myocardial infarction, current metformin use was associated with a lower rate of Major Adverse Cardiac Events at 12 months compared to never-users, alongside reduced pericoronary fat inflammation.
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