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基于核磁共振(NMR)的脂质组学揭示了红细胞(RBC)膜脂质组改变与冠状动脉狭窄的存在及严重程度之间的关联。

Nuclear Magnetic Resonance (NMR)-Based Lipidomics Reveal the Association of Altered Red Blood Cell (RBC) Membrane Lipidome with the Presence and the Severity of Coronary Artery Stenosis.

作者信息

Kastani Ioanna A, Soltani Paraskevi K, Baltogiannis Giannis G, Christou Georgios A, Bairaktari Eleni T, Kostara Christina E

机构信息

Laboratory of Clinical Chemistry, Faculty of Medicine, School of Health Sciences, University of Ioannina, 45110 Ioannina, Greece.

Private Practice, Ioannina & St. Luke's Hospital Thessaloniki, 55236 Thessaloniki, Greece.

出版信息

Molecules. 2024 Dec 26;30(1):36. doi: 10.3390/molecules30010036.

Abstract

Coronary heart disease (CHD) is the leading cause of morbidity and mortality worldwide despite significant improvements in diagnostic modalities. Emerging evidence suggests that erythrocytes, or red blood cells (RBCs), are one of the most important contributors to the events implicated in atherosclerosis, although the molecular mechanisms behind it are under investigation. We used NMR-based lipidomic technology to investigate the RBC lipidome in patients with CHD compared to those with normal coronary arteries (NCAs), all angiographically documented, and its correlation with coronary artery stenosis. Targeted and untargeted lipidomic analysis revealed that CHD patients presented significant lipid alterations in the RBC membrane, characterized by higher cholesterol, sphingolipids, saturated and monounsaturated fatty acids, lower phospholipids (glycerophospholipids and ether glycerolipids), and unsaturated and polyunsaturated fatty acids. These aberrations gradually distinguish the three subgroups of patients with mild, moderate, and severe coronary stenosis, potentially indicating their non-negligible involvement in the onset and progression of atherosclerosis. The comprehensive analysis of RBC-membrane-derived lipids with omics approaches could unravel specific lipid abnormalities taking place at the silent subclinical stage of atherosclerosis and could have the potential to identify patients with subtle, but still proatherogenic, abnormalities that may confer a higher risk for the development of CHD.

摘要

尽管诊断方式有了显著改进,但冠心病(CHD)仍是全球发病和死亡的主要原因。新出现的证据表明,红细胞是动脉粥样硬化相关事件的最重要促成因素之一,尽管其背后的分子机制仍在研究中。我们使用基于核磁共振的脂质组学技术,对经血管造影记录的冠心病患者与正常冠状动脉(NCA)患者的红细胞脂质组进行了研究,并探讨了其与冠状动脉狭窄的相关性。靶向和非靶向脂质组学分析显示,冠心病患者的红细胞膜存在显著的脂质改变,其特征是胆固醇、鞘脂、饱和脂肪酸和单不饱和脂肪酸含量较高,磷脂(甘油磷脂和醚甘油磷脂)以及不饱和脂肪酸和多不饱和脂肪酸含量较低。这些异常逐渐区分出轻度、中度和重度冠状动脉狭窄患者的三个亚组,这可能表明它们在动脉粥样硬化的发生和发展中有着不可忽视的作用。利用组学方法对红细胞膜衍生脂质进行综合分析,可能会揭示动脉粥样硬化无症状亚临床阶段发生的特定脂质异常,并有可能识别出存在细微但仍具有促动脉粥样硬化作用的异常情况的患者,这些异常可能会增加患冠心病的风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2435/11721324/f9849131966f/molecules-30-00036-g001.jpg

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