| Literature DB >> 33572568 |
Efstratios Karagiannidis1, Andreas S Papazoglou1, Nikolaos Stalikas1, Olga Deda2,3, Eleftherios Panteris2,3, Olga Begou3,4, Georgios Sofidis1, Dimitrios V Moysidis1, Anastasios Kartas1, Evangelia Chatzinikolaou5, Kleoniki Keklikoglou5,6, Andreana Bompoti7, Helen Gika2,3, Georgios Theodoridis3,4, Georgios Sianos1.
Abstract
ST-elevation myocardial infarction (STEMI) remains one of the leading causes of mortality worldwide. The identification of novel metabolic and imaging biomarkers could unveil key pathophysiological mechanisms at the molecular level and promote personalized care in patients with acute coronary syndromes. We studied 38 patients with STEMI who underwent primary percutaneous coronary intervention and thrombus aspiration. We sought to correlate serum ceramide levels with micro-CT quantified aspirated thrombus volume and relevant angiographic outcomes, including modified TIMI thrombus grade and pre- or post-procedural TIMI flow. Higher ceramide C16:0 levels were significantly but weakly correlated with larger aspirated thrombus volume (Spearman r = 0.326, p = 0.046), larger intracoronary thrombus burden (TB; p = 0.030) and worse pre- and post-procedural TIMI flow (p = 0.049 and p = 0.039, respectively). Ceramides C24:0 and C24:1 were also significantly associated with larger intracoronary TB (p = 0.008 and p = 0.001, respectively). Receiver operating characteristic analysis demonstrated that ceramides C24:0 and C24:1 could significantly predict higher intracoronary TB (area under the curve: 0.788, 95% CI: 0.629-0.946 and 0.846, 95% CI: 0.706-0.985, respectively). In conclusion, serum ceramide levels were higher among patients with larger intracoronary and aspirated TB. This suggests that quantification of serum ceramides might improve risk-stratification of patients with STEMI and facilitate an individualized approach in clinical practice.Entities:
Keywords: ST-elevation myocardial infarction; ceramides; micro-CT; thrombus; thrombus aspiration
Year: 2021 PMID: 33572568 PMCID: PMC7911549 DOI: 10.3390/jpm11020089
Source DB: PubMed Journal: J Pers Med ISSN: 2075-4426