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他汀类药物使用者的脂质生物标志物,通过冠状动脉计算机断层血管造影进行注释。

Lipid biomarkers in statin users with coronary artery disease annotated by coronary computed tomography angiography.

机构信息

Istituto di Fisiologia Clinica-CNR, via Giuseppe Moruzzi 1, 56124, Pisa, Italy.

Department of Cardiology, Leiden University Medical Center, Albinusdreef 2, 2333 ZA, Leiden, The Netherlands.

出版信息

Sci Rep. 2021 Jun 18;11(1):12899. doi: 10.1038/s41598-021-92339-0.

Abstract

Molecular markers are suggested to improve the diagnostic and prognostic accuracy in patients with coronary artery disease (CAD) beyond current clinical scores based on age, gender, symptoms and traditional risk factors. In this context, plasma lipids are emerging as predictors of both plaque composition and risk of future events. We aim to identify plasma lipid biomarkers associated to CAD indexes of stenosis severity, plaque lipid content and a comprensive score of CAD extent and its risk. We used a simple high performance liquid chromatography-tandem mass spectrometry method to identify 69 plasma lipids in 132 subjects referred to Coronary Computed Tomography Angiography (CCTA) for suspected CAD, all under statin treatment. Patients were stratified in groups using three different CCTA-based annotations: CTA-risk score, lipid plaque prevalence (LPP) ratio and the coronary artery disease-reporting and data system (CAD-RADS). We identified a common set of lipid biomarkers composed of 7 sphingomyelins and 3 phosphatidylethanolamines, which discriminates between high risk CAD patients and controls regardless of the CAD annotations used (CTA score, LPP ratio, or CAD-RADS). These results highlight the potential of circulating lipids as biomarkers of stenosis severity, non calcified plaque composition and overall plaque risk of events.

摘要

分子标志物被认为可以提高冠心病(CAD)患者的诊断和预后准确性,超越目前基于年龄、性别、症状和传统危险因素的临床评分。在这种情况下,血浆脂质作为斑块成分和未来事件风险的预测因子正在出现。我们旨在确定与 CAD 狭窄程度指数、斑块脂质含量以及 CAD 程度及其风险的综合评分相关的血浆脂质生物标志物。我们使用简单的高效液相色谱-串联质谱法在 132 名因疑似 CAD 而接受冠状动脉计算机断层扫描血管造影(CCTA)的患者中鉴定了 69 种血浆脂质,所有患者均接受他汀类药物治疗。患者根据三种不同的基于 CCTA 的注释进行分层:CTA 风险评分、脂质斑块患病率(LPP)比和冠状动脉疾病报告和数据系统(CAD-RADS)。我们确定了一组共同的脂质生物标志物,由 7 种神经鞘磷脂和 3 种磷脂酰乙醇胺组成,可区分高危 CAD 患者和对照组,无论使用哪种 CAD 注释(CTA 评分、LPP 比或 CAD-RADS)。这些结果强调了循环脂质作为狭窄严重程度、非钙化斑块成分和整体斑块事件风险的生物标志物的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab6/8213699/b510ddb04f19/41598_2021_92339_Fig1_HTML.jpg

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