Metabolomics reveal dynamic changes in eicosanoid profile in patients with ST-elevation myocardial infarction after percutaneous coronary intervention.
Liuyang ZhangZhi DaiRuifeng GuoXiao WangWei GongJuanhui DuanZhiqing HeRu DingXu ZhangShaoping NieChun LiangPublished in: Clinical and experimental pharmacology & physiology (2021)
Eicosanoids play important roles in the cardiovascular system. The metabolic disorders involving some eicosanoids in the pathophysiologic process include myocardial infarction and myocardial ischaemia-reperfusion injury. Percutaneous coronary intervention (PCI) is often the first-choice strategy for acute ST-segment elevation myocardial infarction (STEMI) according to current guidelines. This study aimed to investigate the dynamic eicosanoid metabolic profile in STEMI patients after PCI. The eicosanoid profiles in plasma of 20 patients at seven times (30 minutes before surgery; 6, 12, 24, and 72 hours after surgery; 1 day before discharge; and 28 days after surgery) were studied by using metabolomics. Levels of PGE2, PGD2, and TXA2 were decreased significantly and EETs contents were increased significantly at 6 hours after PCI. EETs were hydrolysed to DHETs within a short time after surgery (12-72 hours). 20-HETE content was significantly increased. In samples taken at the time of discharge and at follow-up after discharge, LTB4 level continued to increase. This work suggests that change in content of some functional eicosanoids may be involved in cardiac injury and repair after PCI in a synergistic manner.
Keyphrases
- percutaneous coronary intervention
- st segment elevation myocardial infarction
- st elevation myocardial infarction
- acute myocardial infarction
- coronary artery bypass
- antiplatelet therapy
- acute coronary syndrome
- coronary artery disease
- coronary artery bypass grafting
- left ventricular
- atrial fibrillation
- mass spectrometry
- end stage renal disease
- liver failure
- newly diagnosed
- ejection fraction
- heart failure
- chronic kidney disease
- single cell
- gene expression
- hepatitis b virus
- drug induced
- intensive care unit
- patient reported outcomes
- brain injury
- cerebral ischemia
- cancer therapy
- genome wide