Plasma metabolomics reveals the shared and distinct metabolic disturbances associated with cardiovascular events in coronary artery disease.
Jiali LvChang PanYuping CaiXinyue HanCheng WangJingjing MaJiaojiao PangTonghui XuShuo WuTianzhang KouFandong RenZheng-Jiang ZhuTao ZhangJiali WangYu-Guo ChenPublished in: Nature communications (2024)
Risk prediction for subsequent cardiovascular events remains an unmet clinical issue in patients with coronary artery disease. We aimed to investigate prognostic metabolic biomarkers by considering both shared and distinct metabolic disturbance associated with the composite and individual cardiovascular events. Here, we conducted an untargeted metabolomics analysis for 333 incident cardiovascular events and 333 matched controls. The cardiovascular events were designated as cardiovascular death, myocardial infarction/stroke and heart failure. A total of 23 shared differential metabolites were associated with the composite of cardiovascular events. The majority were middle and long chain acylcarnitines. Distinct metabolic patterns for individual events were revealed, and glycerophospholipids alteration was specific to heart failure. Notably, the addition of metabolites to clinical markers significantly improved heart failure risk prediction. This study highlights the potential significance of plasma metabolites on tailed risk assessment of cardiovascular events, and strengthens the understanding of the heterogenic mechanisms across different events.
Keyphrases
- cardiovascular events
- coronary artery disease
- heart failure
- cardiovascular disease
- mass spectrometry
- left ventricular
- risk assessment
- percutaneous coronary intervention
- ms ms
- atrial fibrillation
- coronary artery bypass grafting
- acute heart failure
- human health
- cardiac resynchronization therapy
- liquid chromatography
- subarachnoid hemorrhage
- single cell
- aortic valve
- blood brain barrier
- high resolution mass spectrometry