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Development and validation of a ceramide- and phospholipid-based cardiovascular risk estimation score for coronary artery disease patients

医学 冠状动脉疾病 内科学 普伐他汀 危险系数 心脏病学 疾病 置信区间 他汀类 队列 鞘脂 弗雷明翰风险评分 队列研究 胆固醇 神经酰胺 化学 细胞凋亡 生物化学
作者
Mika Hilvo,Peter J. Meikle,Eva Ringdal Pedersen,Grethe S. Tell,Indu Dhar,Hermann Brenner,Ben Schöttker,Mitja Lääperi,Dimple Kauhanen,Kaisa M. Koistinen,Antti Jylhä,Kevin Huynh,Natalie A. Mellett,Andrew Tonkin,David Sullivan,John Simes,Paul J. Nestel,Wolfgang Köenig,Dietrich Rothenbacher,Ottar Nygård
出处
期刊:European Heart Journal [Oxford University Press]
卷期号:41 (3): 371-380 被引量:221
标识
DOI:10.1093/eurheartj/ehz387
摘要

Abstract Aims Distinct ceramide lipids have been shown to predict the risk for cardiovascular disease (CVD) events, especially cardiovascular death. As phospholipids have also been linked with CVD risk, we investigated whether the combination of ceramides with phosphatidylcholines (PCs) would be synergistic in the prediction of CVD events in patients with atherosclerotic coronary heart disease in three independent cohort studies. Methods and results Ceramides and PCs were analysed using liquid chromatography–mass spectrometry (LC-MS) in three studies: WECAC (The Western Norway Coronary Angiography Cohort) (N = 3789), LIPID (Long-Term Intervention with Pravastatin in Ischaemic Disease) trial (N = 5991), and KAROLA (Langzeiterfolge der KARdiOLogischen Anschlussheilbehandlung) (N = 1023). A simple risk score, based on the ceramides and PCs showing the best prognostic features, was developed in the WECAC study and validated in the two other cohorts. This score was highly significant in predicting CVD mortality [multiadjusted hazard ratios (HRs; 95% confidence interval) per standard deviation were 1.44 (1.28–1.63) in WECAC, 1.47 (1.34–1.61) in the LIPID trial, and 1.69 (1.31–2.17) in KAROLA]. In addition, a combination of the risk score with high-sensitivity troponin T increased the HRs to 1.63 (1.44–1.85) and 2.04 (1.57–2.64) in WECAC and KAROLA cohorts, respectively. The C-statistics in WECAC for the risk score combined with sex and age was 0.76 for CVD death. The ceramide-phospholipid risk score showed comparable and synergistic predictive performance with previously published CVD risk models for secondary prevention. Conclusion A simple ceramide- and phospholipid-based risk score can efficiently predict residual CVD event risk in patients with coronary artery disease.
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